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array:24 [ "pii" => "S1578219013001479" "issn" => "15782190" "doi" => "10.1016/j.adengl.2013.01.001" "estado" => "S300" "fechaPublicacion" => "2013-09-01" "aid" => "803" "copyright" => "Elsevier España, S.L. and AEDV" "copyrightAnyo" => "2012" "documento" => "article" "crossmark" => 0 "subdocumento" => "ssu" "cita" => "Actas Dermosifiliogr. 2013;104:598-616" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 17368 "formatos" => array:3 [ "EPUB" => 81 "HTML" => 12718 "PDF" => 4569 ] ] "Traduccion" => array:1 [ "es" => array:19 [ "pii" => "S0001731013000380" "issn" => "00017310" "doi" => "10.1016/j.ad.2013.01.003" "estado" => "S300" "fechaPublicacion" => "2013-09-01" "aid" => "803" "copyright" => "Elsevier España, S.L. y AEDV" "documento" => "article" "crossmark" => 0 "subdocumento" => "ssu" "cita" => "Actas Dermosifiliogr. 2013;104:598-616" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 19748 "formatos" => array:3 [ "EPUB" => 4 "HTML" => 14980 "PDF" => 4764 ] ] "es" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Documento de consenso</span>" "titulo" => "Acitretina: guía de uso en psoriasis" "tienePdf" => "es" "tieneTextoCompleto" => "es" "tieneResumen" => array:2 [ 0 => "es" 1 => "en" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "598" "paginaFinal" => "616" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Guidelines for the Use of Acitretin in Psoriasis" ] ] "contieneResumen" => array:2 [ "es" => true "en" => true ] "contieneTextoCompleto" => array:1 [ "es" => true ] "contienePdf" => array:1 [ "es" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figura 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1466 "Ancho" => 3266 "Tamanyo" => 405255 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Mecanismo de acción de los retinoides.</p> <p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">ADH: alcohol deshidrogenasa; COUP-TFII: <span class="elsevierStyleItalic">chicken ovalbumin upstream promoter-transcription factor <span class="elsevierStyleSmallCaps">ii</span></span>; CRBP: <span class="elsevierStyleItalic">cellular retinol binding proteins</span>; CYP: citocromo P 450 familia 26; FOG2: <span class="elsevierStyleItalic">friend of</span> GATA; GATA4: guanina, adenina, timina, adenina; LRAT: <span class="elsevierStyleItalic">lecitin retinol acetil transferasa</span>; RAR: <span class="elsevierStyleItalic">retinoic acid receptors</span>; RARE: <span class="elsevierStyleItalic">retinoic acid response elements</span>; RBP: <span class="elsevierStyleItalic">retinol binding proteins</span>; RDH: <span class="elsevierStyleItalic">retinal dehidrogenasa</span>; RXR: retinoid <span class="elsevierStyleSmallCaps">X</span> receptors; STRAT6: <span class="elsevierStyleItalic">stimulated by retinoic acid 6</span>.</p> <p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Fuente: Saurat<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a>; Siegenthaler et al.<a class="elsevierStyleCrossRef" href="#bib0725"><span class="elsevierStyleSup">145</span></a>; y Napoli<a class="elsevierStyleCrossRef" href="#bib0730"><span class="elsevierStyleSup">146</span></a>.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "G. 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Carretero, M. Ribera, I. Belinchón, J.M. Carrascosa, Ll. Puig, C. Ferrandiz, L. Dehesa, D. Vidal, F. Peral, E. Jorquera, A. Gonzalez-Quesada, C. Muñoz, J. Notario, F. Vanaclocha, J.C. Moreno" "autores" => array:16 [ 0 => array:4 [ "nombre" => "G." "apellidos" => "Carretero" "email" => array:1 [ 0 => "gcarrete@aedv.es" ] "referencia" => array:3 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 2 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">¿</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "M." "apellidos" => "Ribera" "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] ] ] 2 => array:3 [ "nombre" => "I." 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Acitretin fulfills a unique role in the strategies used to treat psoriasis because its mechanism of action is different from that of other systemic drugs. This distinction is the main reason for the continued usefulness of acitretin in the treatment of psoriasis despite the more than 35 years that have elapsed since it was first synthesized and the 25 years since it was first introduced in Spain. Acitretin continues to be useful as monotherapy and in combination with other systemic treatments or phototherapy, and its role as a rescue drug or in combination with biologic agents is particularly interesting, as has been shown by recent reviews on this topic.<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1–5</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">The retinoids are a group of nonsteroid hormone compounds related to retinol. These intracrine and paracrine mediators intervene in a wide range of essential biologic processes in vertebrates, including embryogenesis, morphogenesis, and organogenesis, the regulation of cell growth, differentiation, and apoptosis, as well as immune regulation.<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6–8</span></a> Retinoids exert their effects by binding to cytoplasmic proteins, which determine their intracellular distribution, and by binding to and/or activating nuclear receptors belonging to the superfamily of the ligand-inducible transcription factors, including steroid, vitamin D<span class="elsevierStyleInf">3</span>, and thyroid hormone receptors. There are 2 known families of retinoid nuclear receptors, the retinoic acid receptor (RAR) and the retinoid <span class="elsevierStyleSmallCaps">X</span> receptor (RXR), each one comprising 3 types and various isoforms. In normal skin, the concentration of RXR is 5 times that of RAR. Before binding to the nuclear response elements, which determine the transcription of the various retinoid-dependent genes, the activated retinoid receptors bind to form homodimers (RAR/RAR, RXR/RXR) or heterodimers (RAR/RXR, RAR/VDR or RXR/VDR); the target genes sensitive to therapeutic retinoids respond predominantly to the RXR/RAR heterodimers.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> The development of the retinoids currently on the market has mirrored the discovery of the specificity of action of different intranuclear receptors in an effort to reduce the toxicity and increase the specificity of action of these drugs.<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8,10–12</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The retinoids were first synthesized in the 1970s to assess their usefulness in skin cancer,<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a> and their use in dermatology was soon extended to the treatment of other proliferative diseases.<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a> In psoriasis, their usefulness arises from their effects on keratinization, cell proliferation and inflammation,<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">12,15–18</span></a> and immune regulation.<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">19,20</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">When first developed in 1972, the monoaromatic retinoid etretinate had a considerable impact on the systemic treatment of psoriasis and other disorders of keratinization because of its antiproliferative activity and effect on cell differentiation, especially in epithelial tissues.<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">9,21,22</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The introduction of etretinate, the first retinoid used to treat psoriasis, revolutionized psoriasis therapy, adding an interesting new option to the limited therapeutic arsenal available at that time for severe cases—essentially methotrexate and psoralen-UV-A (PUVA) therapy. The introduction of etretinate was also accompanied by a methodological revolution because the Psoriasis Area and Severity Index (PASI) was first used to assess the efficacy of the new retinoid in clinical trials.<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">23</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Like all the synthetic retinoids, etretinate is highly teratogenic, and this risk—further increased by the drug's long elimination half-life—greatly restricted its use in women of reproductive potential. As a result, etretinate was replaced in 1997 by its active metabolite, acitretin, a drug with similar efficacy but a shorter half-life. It was hoped that this shorter half-life would reduce the duration of the drug's teratogenic effects; however, it did not.</p><p id="par0035" class="elsevierStylePara elsevierViewall">Even though acitretin is used to treat many skin conditions, the present review will focus only on its usefulness in psoriasis. We felt it would be of interest to develop guidelines by consensus among the members of the Psoriasis Group of the Spanish Academy of Dermatology and Venereology.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Pharmacology</span><p id="par0040" class="elsevierStylePara elsevierViewall">Acitretin (C<span class="elsevierStyleInf">21</span>H<span class="elsevierStyleInf">26</span>O<span class="elsevierStyleInf">3</span>, PM 326.42934 [g/mol]) (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>) is a second-generation monoaromatic retinoid and a free acid form and active metabolite of its precursor etretinate. It has the advantage over its precursor of having a much shorter half-life.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0045" class="elsevierStylePara elsevierViewall">Despite their structural similarity, the 2 drugs have very different physical and chemical properties. Owing to its better pharmacokinetic profile, efficacy, and safety acitretin has now completely replaced etretinate.</p><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Mechanism of Action</span><p id="par0050" class="elsevierStylePara elsevierViewall">Acitretin acts by modulating the proliferation of epidermal keratinocytes. In hyperproliferative tissue, such as psoriasis plaques, acitretin has an antiproliferative effect, whereas in healthy tissues it induces proliferation.<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a> In psoriasis, this antiproliferative action reduces desquamation, erythema, and the overall thickness of the lesion. Some authors have also attributed retinoids a role in the modulation of the T-cell response,<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a> the inhibition of chemotaxis, and the activation of polymorphonuclear leukocytes.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a> Unlike other systemic antipsoriatic therapies, acitretin is not considered to be cytotoxic or immunosuppressive.</p><p id="par0055" class="elsevierStylePara elsevierViewall">Acitretin binds to RAR and RXR nuclear receptors, activating all 3 subtypes (α, β, and γ) and modulating the transcription of the genes that code for various proteins involved in the pathogenesis of psoriasis.<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a> Although retinoids act primarily by binding to nuclear receptors, they also act indirectly by antagonizing a number of transcription factors, competing with coactivator proteins which are essential for the activation of genes on which retinoids have no direct effect (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>).<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10,28,29</span></a> In addition to its direct mechanism of positive transcription, acitretin also exerts an indirect effect by inhibiting certain genes that regulate proliferation, angiogenesis, and inflammation in psoriasis.<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">12,30</span></a></p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0060" class="elsevierStylePara elsevierViewall">Although the specific action that derives from this acitretin-induced transcription and inhibition is not fully understood, various hypotheses have focused on 2 areas of action: the modification of the metabolism and action of endogenous retinoids,<a class="elsevierStyleCrossRefs" href="#bib0145"><span class="elsevierStyleSup">29,31</span></a> and the overall immune regulation of the inflammatory molecules and cells involved in psoriasis,<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">19,31,32</span></a> particularly helper T (T<span class="elsevierStyleInf">h</span>) 1 and T<span class="elsevierStyleInf">h</span>17 cells.<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">18,20,33</span></a> These theories would explain the mechanisms of action that make acitretin capable of reversing the pathological and clinical manifestations of plaque psoriasis.<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">18,34–37</span></a></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Absorption and Distribution</span><p id="par0065" class="elsevierStylePara elsevierViewall">The mean absolute bioavailability of acitretin is 59% (range, 36% to 95%). Absorption is linear up to 50<span class="elsevierStyleHsp" style=""></span>mg/d and nonlinear at higher doses. The rate and extent of absorption can be 2 to 5 times higher when acitretin is taken with food.<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">38,39</span></a></p><p id="par0070" class="elsevierStylePara elsevierViewall">Absorbed acitretin is transported bound to plasma proteins (95%)—mostly albumin—with the remainder binding to high-density lipoprotein, low-density lipoprotein, and very low-density lipoprotein.<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">38,40</span></a> The drug is distributed rapidly throughout the body and does not accumulate in any particular tissue. It is about 50 times less lipophilic than etretinate, and does not therefore tend to accumulate in adipose tissue.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Metabolism</span><p id="par0075" class="elsevierStylePara elsevierViewall">Acitretin is metabolized primarily by the liver, giving rise to 2 metabolites: 13-cis-acitretin and etretinate. The amount of 13-cis-acitretin formed is independent of dose, formulation, and administration with food. Steady state concentrations of acitretin and 13-cis-acitretin are reached after approximately 3 weeks of daily administration of acitretin.</p><p id="par0080" class="elsevierStylePara elsevierViewall">It has been found that etretinate is naturally produced from acitretin through a re-esterification process that varies in each individual.<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a> The amount of etretinate produced is very small, but this process is potentiated by the presence of ethanol through the action of a liver enzyme that catalyzes the ethyl esterification of acitretin to etretinate.<a class="elsevierStyleCrossRefs" href="#bib0085"><span class="elsevierStyleSup">17,43</span></a> Since the accumulation of etretinate in fatty tissue, and in the liver, kidney, brain, and testes, is 50 times greater than that of acitretin, retinoid activity can persist for a long time even after the patient has stopped taking acitretin.</p><p id="par0085" class="elsevierStylePara elsevierViewall">Once it has exerted its action on the target cell, the unused acitretin and etretinate are converted to polar metabolites by the enzymatic action of the cytochrome P450 complex.<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10,44</span></a></p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Half-life</span><p id="par0090" class="elsevierStylePara elsevierViewall">Chemically, acitretin and etretinate are very similar, with the only difference being that etretinate is the ethylester form of acitretin. This small chemical difference, however, results in major differences in the pharmacokinetic profiles of the 2 drugs. Etretinate, unlike acitretin, is an uncharged molecule and therefore highly lipophilic, a characteristic that leads to considerable accumulation of the drug in body fat. Acitretin, on the other hand, has a negative ionic charge and therefore accumulates less in adipose tissue. Its higher rate of clearance and lower volume of distribution means that it has a much shorter elimination half-life than etretinate (50<span class="elsevierStyleHsp" style=""></span>hours vs 120 days).<a class="elsevierStyleCrossRefs" href="#bib0225"><span class="elsevierStyleSup">45–47</span></a> In fact, this was the main reason why acitretin replaced etretinate in clinical practice.</p><p id="par0095" class="elsevierStylePara elsevierViewall">However, the hydrolysis that occurs naturally in the human body to convert etretinate to acitretin can be reversed in the presence of heavy alcohol consumption.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">46</span></a> Etretinate has been detected in the plasma of patients on monotherapy with acitretin, and since etretinate accumulates in adipose tissue and has a long half-life, its presence prolongs the teratogenic potential of acitretin.</p><p id="par0100" class="elsevierStylePara elsevierViewall">Larsen et al<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">46</span></a> reported that maximum plasma concentrations of acitretin were reached between 0.9 and 4.6<span class="elsevierStyleHsp" style=""></span>hours after oral administration, with an absorption half-life ranging from 0.2 to 1.7<span class="elsevierStyleHsp" style=""></span>hours and a distribution half-life of between 1.2 and 3.5<span class="elsevierStyleHsp" style=""></span>hours.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">46</span></a> In the same study, the elimination half-life of the drug after cessation of treatment varied between 16.5 and 111.1<span class="elsevierStyleHsp" style=""></span>hours (mean [SD], 47.1<span class="elsevierStyleHsp" style=""></span>hours [29.8]), while that of its metabolite (13-cis-acitretin) varied between 36.5 and 249.4<span class="elsevierStyleHsp" style=""></span>hours (mean [SD], 119.4 [7.4]).</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Excretion</span><p id="par0105" class="elsevierStylePara elsevierViewall">The conjugates produced by the metabolism of acitretin and its metabolite 13-cis-acitretin are eliminated by the kidney (16% to 53%) or excreted into bile and ultimately eliminated in feces (34% to 54%). Acitretin is eliminated within approximately 49<span class="elsevierStyleHsp" style=""></span>hours (range, 33 to 96<span class="elsevierStyleHsp" style=""></span>hours), its metabolite, 13-cis-acitretin within 63<span class="elsevierStyleHsp" style=""></span>hours (range, 28 to 157<span class="elsevierStyleHsp" style=""></span>hours), and etretinate within approximately 120 days (maximum up to 168 days).</p><p id="par0110" class="elsevierStylePara elsevierViewall">Trace amounts of acitretin are excreted in human milk (30–40<span class="elsevierStyleHsp" style=""></span>ng/mL),<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">48</span></a> and it is estimated that the infant would ingest only 1.5% of the maternal dose. Traces of the drug have also been found in seminal fluid at very low concentrations (12.5<span class="elsevierStyleHsp" style=""></span>ng/mL).</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Pharmacogenetics</span><p id="par0115" class="elsevierStylePara elsevierViewall">To date investigators have identified more than 20 genes that regulate the metabolism of retinoids, 6 genes that encode the nuclear receptors involved in signal transduction, and many others that code for regulators of this pathway.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">49</span></a> Further study and greater understanding of these genetic variations and isoforms will lead to a better understanding of the specific mechanism of action of the retinoids in general, and acitretin in particular.</p></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Indications</span><p id="par0120" class="elsevierStylePara elsevierViewall">The summary of product characteristics (SPC) for Neotigason specifies the following indications: severe extensive psoriasis that is resistant to other forms of therapy, palmoplantar pustular psoriasis, severe congenital ichthyosis, and severe Darier disease. Thanks to its to its lack of a direct immunosuppressive effect and its ability to achieve a very long-term response with continued therapy, and in spite of the slowness of clinical response, acitretin continues to have an important role in the treatment of psoriasis. Because of its ability to regulate keratinization, acitretin should be considered in the forms of psoriasis in which the desquamative component predominates over the inflammatory or infiltrative component.</p><p id="par0125" class="elsevierStylePara elsevierViewall">Acitretin is a first-line option in pustular psoriasis,<a class="elsevierStyleCrossRefs" href="#bib0250"><span class="elsevierStyleSup">50–52</span></a> especially the palmoplantar form,<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> and as a component of long-term treatment strategies involving combination, rotation, or sequential therapy.</p><p id="par0130" class="elsevierStylePara elsevierViewall">Although acitretin has traditionally been considered a first-line treatment for psoriatic erythroderma, it should be noted that this indication was established by comparison with etretinate<a class="elsevierStyleCrossRefs" href="#bib0270"><span class="elsevierStyleSup">54,55</span></a> under the assumption that the proven equivalence between etretinate and acitretin in the treatment of psoriasis vulgaris would also largely hold true for erythroderma.<a class="elsevierStyleCrossRefs" href="#bib0225"><span class="elsevierStyleSup">45,56</span></a> The use of acitretin in the treatment of erythroderma has not been studied directly and evidence demonstrating its value in this setting is scant.<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a> In our opinion, now that other faster acting and more effective first-line drugs are available (such as ciclosporin, for example), acitretin should no longer be considered a first-line option in psoriatic erythroderma.</p><p id="par0135" class="elsevierStylePara elsevierViewall">Because its mechanism of action does not involve immunosuppression, acitretin is recommended as a first-line systemic treatment in patients with melanoma, solid tumors, or lymphoproliferative malignancies, and in patients with human immunodeficiency virus infection.<a class="elsevierStyleCrossRefs" href="#bib0285"><span class="elsevierStyleSup">57,58</span></a> Acitretin is not indicated in the treatment of psoriatic arthritis.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a></p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Contraindications</span><p id="par0140" class="elsevierStylePara elsevierViewall">Acitretin is absolutely contraindicated in pregnancy and in patients who are allergic to the product or any of its components. It is relatively contraindicated in women of reproductive potential, women who are breastfeeding, patients with hepatic or renal impairment, patients with poorly controlled dyslipidemia, and patients receiving concomitant tetracyclines; in these groups of patients the risk-benefit ratio must be carefully assessed. <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a> summarizes the contraindications to acitretin treatment.</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Use and Special Precautions</span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Presentations</span><p id="par0145" class="elsevierStylePara elsevierViewall">The commercial preparation of acitretin (Neotigason) is available in 2 presentations: 10<span class="elsevierStyleHsp" style=""></span>mg and 25<span class="elsevierStyleHsp" style=""></span>mg capsules in boxes of 30 capsules.</p><p id="par0150" class="elsevierStylePara elsevierViewall">The inactive excipients are glucose, sodium ascorbate, cellulose, iron oxide black (E172), iron oxide yellow (E 172), iron oxide red (E 172), titanium dioxide (E 171), and gelatin.</p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Posology</span><p id="par0155" class="elsevierStylePara elsevierViewall">Acitretin is administered orally, preferably with food (to enhance absorption). The dose is not weight adjusted. Etretinate dosage was weight adjusted, which is perhaps why this information still appears in some acitretin guidelines.<a class="elsevierStyleCrossRef" href="#bib0295"><span class="elsevierStyleSup">59</span></a> The optimal therapeutic dose in monotherapy is between 25 and 50<span class="elsevierStyleHsp" style=""></span>mg/d.<a class="elsevierStyleCrossRefs" href="#bib0300"><span class="elsevierStyleSup">60,61</span></a> It can be administered in a single or twice-daily dose. Higher-doses (50–75<span class="elsevierStyleHsp" style=""></span>mg/d) are more effective, but the appearance of adverse effects usually makes it necessary to reduce the dose or discontinue treatment.<a class="elsevierStyleCrossRefs" href="#bib0305"><span class="elsevierStyleSup">61–63</span></a> In fact, no clinical trials have been carried out with doses higher than 75<span class="elsevierStyleHsp" style=""></span>mg/d. Doses under 25<span class="elsevierStyleHsp" style=""></span>mg/d may be indicated in combination therapy.</p><p id="par0160" class="elsevierStylePara elsevierViewall">A recent study that analyzed the findings of 2 pivotal clinical trials concluded that the differences in efficacy between a regimen of 25<span class="elsevierStyleHsp" style=""></span>mg/d and one of 50<span class="elsevierStyleHsp" style=""></span>mg/d do not justify the risk of the adverse effects that occur with the higher dose, and the authors recommended 25<span class="elsevierStyleHsp" style=""></span>mg/d for maintenance regimens.<a class="elsevierStyleCrossRefs" href="#bib0320"><span class="elsevierStyleSup">64,65</span></a></p><p id="par0165" class="elsevierStylePara elsevierViewall">Since the pharmacokinetics, efficacy, and adverse reaction profile of acitretin are subject to interindividual variations, it is not possible to establish a standard dose. The regimen must, therefore, be tailored on a case-by-case basis by adjusting the dose to obtain the best clinical outcome with the lowest possible occurrence of adverse events.<a class="elsevierStyleCrossRef" href="#bib0330"><span class="elsevierStyleSup">66</span></a></p><p id="par0170" class="elsevierStylePara elsevierViewall">Although the SPC for Neotigason continues to specify that treatment with acitretin for more than 6 months is contraindicated, neither the experience of years of use nor results from several retrospective studies indicate any substantial increase in adverse effects with longer term therapy.</p><p id="par0175" class="elsevierStylePara elsevierViewall">The recommended starting dosage for acitretin in plaque psoriasis is 10 to 20 <span class="elsevierStyleHsp" style=""></span>mg/d. This initial regimen should be continued for 4 weeks. Response to treatment should be assessed at 4 weeks, after which the dose should be gradually increased to achieve the best therapeutic effect with the fewest adverse effects (minimal effective dose). In general, the maintenance regimen in most series varies between 25 and 50<span class="elsevierStyleHsp" style=""></span>mg/d. Psoriatic lesions clear faster when the starting dose is higher, but such high-dose regimens also increase the risk of mucocutaneous adverse effects and consequently the risk of the patient stopping treatment due to poor tolerance of side effects. Initiating treatment at a high dosage (1<span class="elsevierStyleHsp" style=""></span>mg/kg/d) is currently only recommended for the treatment of generalized flares of pustular psoriasis.</p><p id="par0180" class="elsevierStylePara elsevierViewall">In some patients, psoriasis may worsen after the start of treatment, a phenomenon that manifests as more intense erythema and a greater spread of lesions, which later resolve.<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">61</span></a></p></span></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Efficacy</span><p id="par0185" class="elsevierStylePara elsevierViewall">Acitretin has be shown to be an effective treatment for psoriasis in both monotherapy and combination regimens.<a class="elsevierStyleCrossRefs" href="#bib0170"><span class="elsevierStyleSup">34–36,45,56,67</span></a> Accumulated experience with the drug and studies of its efficacy situate it in the group of less effective systemic antipsoriatic drugs, although no trials have directly compared acitretin with other antipsoriatic agents. The efficacy of acitretin, and most of its adverse effects, are dose-dependent and vary considerably from patient to patient. It usually takes 3 to 6 months to achieve maximum response.<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">38,53,61,62,68,69</span></a></p><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Plaque Psoriasis</span><p id="par0190" class="elsevierStylePara elsevierViewall">Very few studies have evaluated the short-term efficacy of acitretin in plaque psoriasis. A study that examined efficacy at 8 weeks in patients who received an initial dose of 10, 25, or 50<span class="elsevierStyleHsp" style=""></span>mg of acitretin reported a mean reduction in PASI of 61%, 79%, and 86%, respectively, in the 3 treatment groups as compared to 30% in the placebo group.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a></p><p id="par0195" class="elsevierStylePara elsevierViewall">The available studies on the efficacy of the drug have very varied designs and objectives. Overall, initial doses of between 40 and 50<span class="elsevierStyleHsp" style=""></span>mg/d have achieved a 50% reduction in PASI (PASI 50) in 66% to 85% of patients and a 75% reduction (PASI 75) in 34% to 52% of patients at 8 to 12 weeks. Higher dose regimens—up to 70<span class="elsevierStyleHsp" style=""></span>mg/d—were associated with adverse effects that make it difficult for patients to continue treatment.<a class="elsevierStyleCrossRefs" href="#bib0180"><span class="elsevierStyleSup">36,45,67,70</span></a></p><p id="par0200" class="elsevierStylePara elsevierViewall">Clinical experience has shown acitretin to be an ideal choice for long-term maintenance therapy because the clinical response is sustained and there is no significant loss of efficacy over time. The authors of a study that enrolled 63 patients in which efficacy was assessed following 12 months of treatment with acitretin reported that, of the 37 patients who completed the study, 89% had a PASI 50 response and 78.4% a PASI 75 response.<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a></p></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Pustular Psoriasis</span><p id="par0205" class="elsevierStylePara elsevierViewall">In generalized pustular psoriasis, acitretin is used at a dose of 0.5 to 1<span class="elsevierStyleHsp" style=""></span>mg/kg/d and treatment generally produces a rapid clinical response with clearing of the lesions within 10 days. The dose should then be tapered slowly until a maintenance dose of 10<span class="elsevierStyleHsp" style=""></span>mg/d is reached. Relapse on withdrawal of treatment is rare, and in such cases reintroduction of the drug restores the same efficacy. Acitretin is probably the first-line therapy in this form of psoriasis, with studies showing it to be effective in 84% of patients.<a class="elsevierStyleCrossRefs" href="#bib0250"><span class="elsevierStyleSup">50,71</span></a></p><p id="par0210" class="elsevierStylePara elsevierViewall">It is also considered to be among the first-line options for palmoplantar pustulosis, either in monotherapy or in combination with phototherapy.<a class="elsevierStyleCrossRef" href="#bib0360"><span class="elsevierStyleSup">72</span></a></p></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Nail Psoriasis</span><p id="par0215" class="elsevierStylePara elsevierViewall">Numerous isolated cases in the literature demonstrate the efficacy of acitretin in the treatment of nail psoriasis. In an open study of 36 patients with moderate to severe nail psoriasis treated with acitretin at a dose of 0.2 to 0.3<span class="elsevierStyleHsp" style=""></span>mg/kg/d for 6 months, a good response was observed, with a mean reduction in the Nail Psoriasis Severity Index (NAPSI) score of 41%.<a class="elsevierStyleCrossRef" href="#bib0365"><span class="elsevierStyleSup">73</span></a> Complete clearing of lesions was achieved in 9 patients (25%), and there was no improvement in 6 (11%). These findings prompted the authors to propose this low-dose regimen of acitretin as a therapeutic option for nail psoriasis because of its good tolerance profile and scant adverse effects. By contrast, no improvement was achieved in a recent open-label study of 30 patients with nail psoriasis treated with acitretin at 0.3<span class="elsevierStyleHsp" style=""></span>mg/kg/d during the first month and 0.5<span class="elsevierStyleHsp" style=""></span>mg/kg/d for a further 3 months.<a class="elsevierStyleCrossRef" href="#bib0370"><span class="elsevierStyleSup">74</span></a></p></span></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Toxicity and Adverse Reactions</span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Overview</span><p id="par0220" class="elsevierStylePara elsevierViewall">Most of the adverse effects of acitretin are dose-dependent and, in general, well tolerated at the recommended doses. Adverse clinical reactions and laboratory abnormalities occur less often with low-dose regimens (25<span class="elsevierStyleHsp" style=""></span>mg/d) than with high ones (50<span class="elsevierStyleHsp" style=""></span>mg/d).<a class="elsevierStyleCrossRefs" href="#bib0325"><span class="elsevierStyleSup">65,68</span></a> However, the toxic dose of acitretin is very close to the therapeutic dose, and for this reason most patients experience some adverse effects during the initial period of treatment while the dose is being adjusted. Such effects are usually reversible and disappear when the dose is reduced or treatment is interrupted, although in some cases they lead to discontinuation of treatment.</p><p id="par0225" class="elsevierStylePara elsevierViewall">The adverse effects most often associated with the use of acitretin are shown in <a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>.</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia></span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Toxicity by Organ and System</span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Mucocutaneous Effects</span><p id="par0230" class="elsevierStylePara elsevierViewall">The most common adverse effects associated with acitretin affect the skin and mucous membranes.<a class="elsevierStyleCrossRef" href="#bib0375"><span class="elsevierStyleSup">75</span></a> The effects are dose dependent and related to decreased sebum production, thinning of the stratum corneum, and impaired skin barrier function. Dryness of the lips and cheilitis occur in over 75% of patients. The next most common mucocutaneous effects are skin exfoliation or peeling, which can affect any part of the body but especially the palms and soles (in up to 50% of patients), rhinitis and epistaxis caused by drying of the nasal mucosa (up to 30%), and generalized xerosis, including xerophthalmia and xerostomia (Neotigason SPC).<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">76</span></a> Less common adverse effects include nail fragility, periungual pyogenic granuloma, and a condition called retinoid dermatitis, which presents as scaly erythematous plaques or follicular papules and/or vesicles, predominantly affecting the face, forearms, chest, flanks, and the dorsum of the hands. These lesions have the histologic features of nonspecific acute dermatitis<a class="elsevierStyleCrossRef" href="#bib0385"><span class="elsevierStyleSup">77</span></a> and must be distinguished from a psoriasis flare.<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">69</span></a> Some patients experience photosensitivity reactions due to thinning of the stratum corneum.</p><p id="par0235" class="elsevierStylePara elsevierViewall">These adverse effects usually only require symptomatic treatment, combining hydration and topical corticosteroids, or a temporary reduction in the dose of acitretin.</p><p id="par0240" class="elsevierStylePara elsevierViewall">During the initial weeks of treatment, an increase in hair loss may be observed, sometimes leading to transient diffuse alopecia caused by telogen effluvium (in up to 25% of patients). In such cases, a rapid decrease in the dose should be considered because it is otherwise unlikely that the patient will adhere to treatment. The rate of hair loss usually returns to normal within 6 to 8 weeks of the dose reduction. Changes in hair color and texture during treatment with acitretin have also been reported.<a class="elsevierStyleCrossRef" href="#bib0390"><span class="elsevierStyleSup">78</span></a></p></span><span id="sec0110" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Hepatic Effects</span><p id="par0245" class="elsevierStylePara elsevierViewall">Acitretin is hepatotoxic when used in the long term. Elevations in aspartate alanine aminotransferase, aspartate aminotransferase, and lactate dehydrogenase are seen in one-third of patients. These abnormalities are usually transient or reversible upon reduction of the dose or discontinuation of treatment.<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">76</span></a> If liver enzymes are persistently or excessively high, the possibility of acute toxic hepatitis should be investigated; this adverse effect is rare (0.26% of patients)<a class="elsevierStyleCrossRef" href="#bib0330"><span class="elsevierStyleSup">66</span></a> and also reversible upon cessation of treatment. There is anecdotal evidence of fatal progression from acitretin-induced acute toxic hepatitis to cirrhosis.<a class="elsevierStyleCrossRef" href="#bib0395"><span class="elsevierStyleSup">79</span></a></p><p id="par0250" class="elsevierStylePara elsevierViewall">The hepatotoxicity of acitretin is exacerbated by alcohol intake, obesity, diabetes, and certain hepatotoxic drugs. Of these, alcohol may have the greatest impact since it directly influences and modifies the metabolism of retinoids and is thought to be the factor that maximizes the severity of acitretin-associated hepatotoxicity.<a class="elsevierStyleCrossRef" href="#bib0400"><span class="elsevierStyleSup">80</span></a> Complete abstention from alcohol is therefore recommended during treatment with acitretin.</p></span><span id="sec0115" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Metabolic Effects</span><p id="par0255" class="elsevierStylePara elsevierViewall">One of the most common adverse effects of acitretin therapy, together with muscosal alterations, is an abnormal lipid profile. An increase in triglycerides is observed in up to 66% of patients, hypercholesterolemia in 33%, and a decrease in high density lipoprotein in up to 40% of patients.<a class="elsevierStyleCrossRefs" href="#bib0405"><span class="elsevierStyleSup">81,82</span></a> The changes in lipid levels are dose-related. In general, triglycerides levels tend to rise to between 2 and 3 times the upper limit of normal, rarely reaching levels associated with a risk of pancreatitis or eruptive xanthomas.<a class="elsevierStyleCrossRefs" href="#bib0345"><span class="elsevierStyleSup">69,81,82</span></a></p><p id="par0260" class="elsevierStylePara elsevierViewall">The risk of abnormal lipid levels and pancreatitis increases when there is a family history of hypertriglyceridemia, alcohol consumption, obesity, or diabetes.<a class="elsevierStyleCrossRefs" href="#bib0405"><span class="elsevierStyleSup">81,82</span></a></p><p id="par0265" class="elsevierStylePara elsevierViewall">In diabetic patients, acitretin treatment can alter glucose tolerance and lead to a disruption of glycemic control. Blood sugar levels should therefore be checked frequently in these patients, especially during the initial weeks of treatment. However, no increased risk of nondiabetic patients developing diabetes has been reported.<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">76</span></a></p></span><span id="sec0120" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Neurologic Effects Pseudotumor Cerebri</span><p id="par0270" class="elsevierStylePara elsevierViewall">In rare cases, pseudotumor cerebri or benign intracranial hypertension has been associated with the use of systemic retinoids.<a class="elsevierStyleCrossRef" href="#bib0415"><span class="elsevierStyleSup">83</span></a> This condition presents with headache, visual disturbance, nausea, and/or vomiting. Patients taking acitretin should be warned to contact their physicians if they experience any of these symptoms. An eye examination should be performed urgently and treatment with acitretin must be discontinued immediately if papilledema is observed.</p><p id="par0275" class="elsevierStylePara elsevierViewall">Pseudotumor cerebri was first reported in association with acitretin combined with tetracycline or minocycline,<a class="elsevierStyleCrossRefs" href="#bib0410"><span class="elsevierStyleSup">82,84</span></a> but it is also possible with acitretin used in isolation.<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">76</span></a></p></span><span id="sec0125" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Ophthalmologic Effects</span><p id="par0280" class="elsevierStylePara elsevierViewall">Xerophthalmia and eye irritation are relatively common adverse effects and may require the use of artificial tears, particularly in older patients (physiological xerophthalmia) and contact lens users. In some cases, ocular dryness is very severe and precludes the use of contact lenses during treatment. Other, much less common, side effects include the loss of eyelashes and decreased night vision. The onset of diplopia or blurred vision may be caused by papilledema and indicates the need for immediate withdrawal of acitretin (Neotigason SPC).<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">76</span></a></p></span><span id="sec0130" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0150">Musculoskeletal Effects</span><p id="par0285" class="elsevierStylePara elsevierViewall">Sustained treatment with acitretin is often associated with arthralgia and myalgia; these symptoms are usually mild and can be controlled with oral analgesics. It is recommended that patients on acitretin should avoid intense physical exercise to minimize the risk of such symptoms.</p><p id="par0290" class="elsevierStylePara elsevierViewall">Although early follow-up studies of patients treated with etretinate and acitretin reported a possible association with diffuse idiopathic skeletal hyperostosis,<a class="elsevierStyleCrossRef" href="#bib0425"><span class="elsevierStyleSup">85</span></a> clinical experience accumulated over the decades since acitretin was first used as an antipsoriatic treatment has demonstrated that this effect is very rare<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> (less than 1% of patients) and is primarily related to exacerbation of preexisting hyperostosis.<a class="elsevierStyleCrossRef" href="#bib0430"><span class="elsevierStyleSup">86</span></a> Acitretin is not associated with increased susceptibility to bone fractures.<a class="elsevierStyleCrossRef" href="#bib0435"><span class="elsevierStyleSup">87</span></a> Based on current data and the accumulated clinical evidence, it no longer appears reasonable to link acitretin to increased bone risk of any kind.<a class="elsevierStyleCrossRefs" href="#bib0260"><span class="elsevierStyleSup">52,53,88</span></a> Thus, we do not recommend performing bone tests before or during treatment except when a history of bone disease makes this advisable.</p></span><span id="sec0135" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0155">Retinoic Acid Syndrome</span><p id="par0295" class="elsevierStylePara elsevierViewall">Retinoic acid syndrome is a potentially fatal complication associated with the treatment of acute promyelocytic leukemia with all-trans retinoic acid therapy.<a class="elsevierStyleCrossRefs" href="#bib0445"><span class="elsevierStyleSup">89,90</span></a> The clinical features of this syndrome are as follows: fever, pulmonary infiltrates associated with respiratory distress, pleural or pericardial effusion, unexplained weight gain, ascites, impaired myocardial contractility, renal or hepatic insufficiency, episodic hypotension and, in some cases, coma. They typically occur in association with an elevated white blood cell count. The syndrome usually develops 7 to 10 days after start of treatment and is treated with high-dose corticosteroids. Although it is rarely associated with the use of acitretin, retinoic acid syndrome must be taken into account because some cases have been reported.<a class="elsevierStyleCrossRefs" href="#bib0455"><span class="elsevierStyleSup">91–93</span></a></p></span><span id="sec0140" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0160">Teratogenicity</span><p id="par0300" class="elsevierStylePara elsevierViewall">Acitretin is highly teratogenic (category <span class="elsevierStyleSmallCaps">X</span> in the US Food and Drug Administration [FDA] classification of fetal risk) and causes characteristic fetal malformations similar to those seen in hypervitaminosis A (retinoid embryopathy).<a class="elsevierStyleCrossRef" href="#bib0470"><span class="elsevierStyleSup">94</span></a></p><p id="par0305" class="elsevierStylePara elsevierViewall">The use of acitretin at any dose during pregnancy can cause spontaneous abortions and major fetal malformations, including meningomyelocele, meningoencephalocele, skeletal malformations, cardiovascular malformations, decreased cranial volume, facial dysmorphia, and malformations of the thymus. The risk is higher when the drug is administered between the third and sixth week of pregnancy.<a class="elsevierStyleCrossRefs" href="#bib0470"><span class="elsevierStyleSup">94,95</span></a></p><p id="par0310" class="elsevierStylePara elsevierViewall">Acitretin should not be taken by women who are pregnant or wish to become pregnant during treatment or up to 2 years after cessation of therapy according to the European Medicines Agency (Neotigason SPC) or up to 3 years according to the FDA (Soriatane SPC). Nor should it be prescribed to any woman of childbearing potential unless the prescribing physician considers the patient to be capable of using effective contraceptive methods during and after treatment.</p></span><span id="sec0145" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0165">Psychiatric Symptoms</span><p id="par0315" class="elsevierStylePara elsevierViewall">In 1997, the authors of a study on the safety of acitretin reported that its use was linked to depression in between 1% and 10% of cases (Soriatane SPC). However, the methodological shortcomings of that study and the fact that only 1 case—considered doubtful—of an association between acitretin and depression has been reported in the literature<a class="elsevierStyleCrossRef" href="#bib0480"><span class="elsevierStyleSup">96</span></a> raise doubts as to whether such an association really exists or whether the depression experienced by these patients is in fact due to the skin disease for which the acitretin treatment is prescribed. Nevertheless, and despite the fact that the relationship between isotretinoin—another retinoid—and depression and suicide has not been demonstrated either, the FDA has obliged manufacturers to include a warning about the risk of depression and suicide in the package insert for acitretin.<a class="elsevierStyleCrossRef" href="#bib0485"><span class="elsevierStyleSup">97</span></a></p></span></span></span><span id="sec0150" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0170">Safety</span><p id="par0320" class="elsevierStylePara elsevierViewall">Acitretin is a safe drug when it is correctly prescribed to the appropriate patient at the appropriate dose and when the patient is followed up regularly and the potential risks associated with toxicity are avoided, especially pregnancy in women.<a class="elsevierStyleCrossRefs" href="#bib0330"><span class="elsevierStyleSup">66,69</span></a><a class="elsevierStyleCrossRefs" href="#tbl0015">Tables 3 and 4</a> list the conditions required for the safe use of acitretin and the situations in which precautions are necessary.</p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia><elsevierMultimedia ident="tbl0020"></elsevierMultimedia><span id="sec0155" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0175">Patient Information</span><p id="par0325" class="elsevierStylePara elsevierViewall">Before starting treatment, patients should be well informed about the most common side effects of the drug because these can quickly lead to poor adherence to treatment. They should also understand that the clinical response may take time to appear and the physician should explain why acitretin has been prescribed in preference to other possible treatments. Patients who are given complete information and involved in the choice of drug are more likely to adhere to treatment.</p><p id="par0330" class="elsevierStylePara elsevierViewall">Women must be advised that they must avoid pregnancy during treatment with acitretin and for at least 2 to 3 years after cessation.</p><p id="par0335" class="elsevierStylePara elsevierViewall">Patients must be instructed to moisturize their skin and mucous membranes regularly and to use sunscreen and sunglasses to filter out UV radiation.</p><p id="par0340" class="elsevierStylePara elsevierViewall">They must be made aware that before taking any other medications they should inform the prescribing physician that they are taking acitretin; this precaution is essential to avoid toxicity (hepatotoxicity, hypervitaminosis A syndrome).</p><p id="par0345" class="elsevierStylePara elsevierViewall">The need for regular follow-up and testing to ensure the safety of treatment and make long-term use of the drug possible must be discussed with patients, and they must commit to this program.</p></span><span id="sec0160" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0180">Baseline Screening and Follow-up During Treatment</span><p id="par0350" class="elsevierStylePara elsevierViewall">Before starting a patient on treatment with acitretin, the physician must obtain a complete medical history (past history, comorbidities, concomitant medication, physical examination, prior course of psoriasis, type of psoriasis, and prior medication. In women, pregnancy must be ruled out and a contraceptive regimen put in place that must continue for at least 2 years after cessation of treatment according to the European label and 3 years according to the US label. Baseline blood count and biochemistry should be obtained; explorations should include liver and kidney function and lipid profile.<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">69</span></a></p><p id="par0355" class="elsevierStylePara elsevierViewall">Liver function and lipid levels should be reassessed a few weeks after start of treatment. The exact timing of this assessment will depend on the patient's risk profile and whether he/she is taking concomitant medication that might increase hepatotoxicity or lipid abnormalities. In our opinion, the first assessment during treatment should take place between 4 and 8 weeks and the standard program of monitoring check-ups should be initiated thereafter. In standard clinical practice, alterations in liver function and lipid values are not very common and monitoring every 6 months is sufficient.</p><p id="par0360" class="elsevierStylePara elsevierViewall">Regular radiographic investigation is not recommended except when there is evidence of bone toxicity.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a></p><p id="par0365" class="elsevierStylePara elsevierViewall">Clinical and laboratory parameters should be evaluated every 3 to 6 months (<a class="elsevierStyleCrossRef" href="#tbl0025">Table 5</a>).<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">69</span></a><a class="elsevierStyleCrossRef" href="#fig0015">Figure 3</a> is a sample treatment monitoring form.</p><elsevierMultimedia ident="tbl0025"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0280" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0185">Use in Patients with Cardiovascular Risk Factors and Metabolic Syndrome</span><p id="par0375" class="elsevierStylePara elsevierViewall">The decision to use acitretin in patients with cardiovascular risk must be very carefully weighed because of the associated risk of hypertriglyceridemia and the consequent increased risk of atherosclerosis. If acitretin is prescribed, it is always advisable to add lipid-lowering therapy<a class="elsevierStyleCrossRef" href="#bib0490"><span class="elsevierStyleSup">98</span></a> and to advise the patient to begin or further enhance a lifestyle designed to reduce cardiovascular risk factors.<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">69</span></a></p><p id="par0380" class="elsevierStylePara elsevierViewall">The use of acitretin in patients with metabolic syndrome must be considered on a case-by-case basis because of the risk of exacerbating the syndrome and increasing cardiovascular risk, and because the liver toxicity associated with acitretin is favored by obesity and diabetes. If the patient's lipid levels are affected, the dose should be reduced and lipid-lowering treatment should be added; in some cases, withdrawal of acitretin might even be considered.</p><p id="par0385" class="elsevierStylePara elsevierViewall">Hypertriglyceridemia and hyperglycemia can be managed by increasing physical exercise, introducing dietary changes, reducing alcohol intake, and pharmacotherapy.</p><p id="par0390" class="elsevierStylePara elsevierViewall">Increased efficacy of acitretin treatment has been reported in patients with type 2 diabetes mellitus taking pyoglitazone.<a class="elsevierStyleCrossRef" href="#bib0495"><span class="elsevierStyleSup">99</span></a> This may be a result of the anti-inflammatory and antiangiogenic effects of this oral hypoglycemic agent.<a class="elsevierStyleCrossRef" href="#bib0500"><span class="elsevierStyleSup">100</span></a> Pyoglitazone is a second-line oral antidiabetic agent and a first-line treatment in obese patients who cannot be treated with metformin. The prescription of this combination in a patient with psoriasis should involve an endocrinologist. It may occasionally be useful to take advantage of this synergistic effect in selected patients who have both psoriasis and diabetes.</p></span><span id="sec0165" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0190">Use in Patients With Impaired Liver Function</span><p id="par0395" class="elsevierStylePara elsevierViewall">Since acitretin is potentially hepatotoxic, it is relatively contraindicated in patients with hepatic impairment. If acitretin is used in such patients, liver enzymes must be monitored and the dose and regimen adjusted accordingly; alanine aminotransferase values should not exceed 4 to 5 times the upper limit of normal.</p><p id="par0400" class="elsevierStylePara elsevierViewall">Liver biopsy is never required since no association has been found between cumulative doses of acitretin and fibrosis or cirrhosis of the liver.<a class="elsevierStyleCrossRef" href="#bib0505"><span class="elsevierStyleSup">101</span></a> Habitual alcohol consumption, obesity, and diabetes exacerbate the hepatotoxic effect of acitretin and therefore increase the risk of such toxicity. In such cases, closer monitoring of liver function is required or the use of acitretin may be clearly contraindicated.</p></span><span id="sec0170" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0195">Use in Patients With Renal Impairment</span><p id="par0405" class="elsevierStylePara elsevierViewall">Acitretin is also contraindicated in patients with renal impairment (Neotigason SPC). Plasma concentrations of acitretin are lower in patients with severe kidney failure. Note that acitretin is not eliminated by dialysis.</p></span><span id="sec0175" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0200">Drug Interactions</span><p id="par0410" class="elsevierStylePara elsevierViewall">Logically, the concomitant use of acitretin with other drugs or substances having similar adverse effects can exacerbate these effects, or the action of acitretin may alter the function of other drugs taken concomitantly. Whenever acitretin is prescribed, all the drugs taken by the patient before and during treatment must be recorded.</p><p id="par0415" class="elsevierStylePara elsevierViewall">It is important to note that alcohol intake increases the hepatotoxicity of acitretin and favors the re-esterification of acitretin to etretinate, with the increased risk of teratogenicity that this implies (Neotigason SPC).<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">76</span></a> It is also important to note that acitretin reduces the anticontraceptive effect of drugs based on microdoses of progestogens and that these minipills should never be used to prevent pregnancy during treatment. Contraceptives that use a combination of estrogen and progesterone may be used since acitretin does not interfere with the action of these drugs.<a class="elsevierStyleCrossRef" href="#bib0510"><span class="elsevierStyleSup">102</span></a> The most important drug interactions are shown in <a class="elsevierStyleCrossRef" href="#tbl0030">Table 6</a>.</p><elsevierMultimedia ident="tbl0030"></elsevierMultimedia></span><span id="sec0180" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0205">Use in the Case of Infection and Vaccination</span><p id="par0420" class="elsevierStylePara elsevierViewall">Since acitretin is not a direct immunosuppressant it can be used in patients who are going to be vaccinated, whether with toxoids or with live, attenuated vaccines.</p></span><span id="sec0185" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0210">Use in Patients With Cancer and Immunocompromised Patients</span><p id="par0425" class="elsevierStylePara elsevierViewall">Acitretin is a psoriasis treatment suitable for use in patients with cancer or in immunocompromised patients because it is not an immunosuppressant and because retinoids have been shown to have a chemopreventive effect in promyelocytic leukemia,<a class="elsevierStyleCrossRef" href="#bib0515"><span class="elsevierStyleSup">103</span></a> precancerous and cancerous skin lesions,<a class="elsevierStyleCrossRefs" href="#bib0520"><span class="elsevierStyleSup">104–106</span></a> and hepatocellular carcinoma.<a class="elsevierStyleCrossRef" href="#bib0535"><span class="elsevierStyleSup">107</span></a> Consequently, acitretin may be indicated as a first-line systemic treatment in patients with psoriasis who also have melanoma, solid tumors, or lymphoproliferative disorders,<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">58</span></a> and in patients with human immunodeficiency virus infection.<a class="elsevierStyleCrossRefs" href="#bib0285"><span class="elsevierStyleSup">57,58</span></a></p></span><span id="sec0190" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0215">Use in Pregnant Women and Reproductive Considerations</span><p id="par0430" class="elsevierStylePara elsevierViewall">The use of acitretin during pregnancy is contraindicated because of the drug's teratogenicity and the risk that it may cause severe fetal malformations (independent of dose and timing of exposure).<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">76</span></a></p><p id="par0435" class="elsevierStylePara elsevierViewall">When acitretin is administered to woman of childbearing potential, contraception must start at least 1 month before start of treatment and must be maintained for 2 to 3 years after cessation of treatment. The minimum duration of contraception after cessation of treatment is specified as 2 years in the European SPC. The duration of this safety period has been calculated on the basis of evidence that 98% of the etretinate that may have been formed from the acitretin administered will be eliminated within 2 years. The 3-year contraception period after discontinuation of treatment specified in the US SPC (1 year longer than the calculation based on the half-life of the drug) has been established to increase the margin of safety, but is without pharmacologic basis.</p><p id="par0440" class="elsevierStylePara elsevierViewall">If acitretin is prescribed to women of reproductive potential, it is essential to ensure adequate contraception from at least 1 month before start of treatment throughout the entire period of treatment, and for at least 2 years after cessation of treatment. Contraceptive measures must also be adopted if the patient receives repeated cycles of treatment. These precautions must be taken even by women who normally do not use contraception because of a history of infertility. Alcohol consumption is strictly prohibited in women of childbearing age during treatment and for 2 months following withdrawal of treatment. In such cases, convincing evidence that the patient understands and accepts the potential risks of treatment is essential and the patient must sign informed consent authorizing the use of acitretin.</p><p id="par0445" class="elsevierStylePara elsevierViewall">Patients receiving acitretin must not donate blood during treatment or for 1 year following withdrawal of treatment to avoid all possible risk of teratogenicity in the eventual recipient of the donated blood. Nevertheless, a recent study that monitored the pregnancies of 18 women who accidentally received blood transfusions from individuals taking acitretin did not observe any fetal malformations or abnormalities during pregnancy.<a class="elsevierStyleCrossRef" href="#bib0540"><span class="elsevierStyleSup">108</span></a></p><p id="par0450" class="elsevierStylePara elsevierViewall">In male patients, acitretin has not been associated with abnormalities in spermatogenesis or the characteristics of spermatozoids.<a class="elsevierStyleCrossRef" href="#bib0545"><span class="elsevierStyleSup">109</span></a> No cases of fetal malformation have been reported in pregnancies following conception while the father was taking acitretin. The presence of acitretin metabolites in the seminal fluid of men being treated with acitretin appears to entail very little risk for the fetus. However, the data available are scant and acitretin therapy is usually avoided in males planning to have children.<a class="elsevierStyleCrossRef" href="#bib0550"><span class="elsevierStyleSup">110</span></a></p></span></span><span id="sec0195" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0220">Use in Breastfeeding Mothers</span><p id="par0455" class="elsevierStylePara elsevierViewall">The SPC contraindicates the use of acitretin in lactating mothers even though the quantities of drug excreted in maternal milk and the quantity that may be ingested by the infant are very small.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">48</span></a> This contraindication is based on initial concerns about the possibility of acitretin causing skeletal abnormalities and the results of animal studies performed at very high doses in which abnormalities were observed in the diaphyseal and spongy bone of offspring. However, since the risks of bone abnormalities have been minimized and relativized over time and the doses used in the studies in question were much higher than those recommended for use in humans, acitretin can be used in nursing mothers after careful consideration of the risk-benefit ratio in each case.<a class="elsevierStyleCrossRef" href="#bib0555"><span class="elsevierStyleSup">111</span></a></p></span><span id="sec0200" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0225">Pediatric Use</span><p id="par0460" class="elsevierStylePara elsevierViewall">The use of acitretin in children is also contraindicated based on data relating to long-term treatment with etretinate in childhood in which skeletal alterations were reported, including premature epiphyseal closure, skeletal hyperostosis, and extraosseus calcification. Based on the assumption that such changes could also appear in children taking acitretin—although this has not been demonstrated—the SPC for Neotigason advises against the use of acitretin in children. However, in light of the evidence available after nearly 2 decades of use, we believe that this contraindication is relative and that acitretin can be prescribed in specific cases as long as the risk-benefit ratio is favorable.</p><p id="par0465" class="elsevierStylePara elsevierViewall">In children, the dose of acitretin is weight-adjusted and the lowest possible dose is determined by the commercial availability of the drug in 10<span class="elsevierStyleHsp" style=""></span>mg doses. The recommended starting dosage is 0.5<span class="elsevierStyleHsp" style=""></span>mg/kg/d and this is escalated gradually taking into account the clinical response and the appearance of adverse effects. Doses in excess of 35<span class="elsevierStyleHsp" style=""></span>mg/d are only recommended in exceptional cases (Neotigason SPC). Once a clinical response is achieved, the dose should be reduced to the lowest effective maintenance regimen to avoid, as far as possible, long-term adverse effects.</p><span id="sec0205" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0230">Use in Elderly Patients</span><p id="par0470" class="elsevierStylePara elsevierViewall">The indications and regimens for the use of acitretin in older patients are the same as for adults in general. However, it should be remembered that older patients are more susceptible to cutaneous and mucosal xerosis and liver and kidney failure. Consequently, these adverse effects may appear at lower doses in these patients. The doses used should therefore be lower, particularly at the start of treatment, and these patients should be more closely monitored.</p></span><span id="sec0210" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0235">Use in Patients Undergoing Surgical Interventions</span><p id="par0475" class="elsevierStylePara elsevierViewall">The use of acitretin is not contraindicated in patients undergoing surgery, although the physician should carefully consider the possible benefits of reducing the dose or even temporarily suspending treatment with the drug to prevent possible postoperative complications associated with its adverse effects (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>).</p></span><span id="sec0215" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0240">Overdose</span><p id="par0480" class="elsevierStylePara elsevierViewall">The effects of accidental or intentional overdose with acitretin are similar to the manifestations of acute vitamin A toxicity, namely, severe headache, nausea or vomiting, drowsiness, irritability, and pruritus. These symptoms subside without treatment. Owing to the variable absorption of the drug, gastric lavage may be indicated in the initial hours following an overdose (Neotigason SPC).</p></span></span><span id="sec0220" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0245">Treatment Strategies for Acitretin in Psoriasis</span><span id="sec0225" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0250">Initial Dose Followed by Gradual Escalation</span><p id="par0485" class="elsevierStylePara elsevierViewall">Approaches that seek to achieve a rapid response at start of treatment with acitretin are generally counterproductive because they lead to the appearance of adverse effects, which eventually limit the use of the drug.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> The primary aim should be to identify the dose that each patient can tolerate and to maintain this regimen while waiting for a clinical response in the long term (the therapeutic objective should be assessed 3 to 6 months after start of treatment).</p><p id="par0490" class="elsevierStylePara elsevierViewall">Although the usual therapeutic dosage of acitretin is between 25 and 50<span class="elsevierStyleHsp" style=""></span>mg/d, it is preferable to start treatment with a lower dosage (between 10 and 25<span class="elsevierStyleHsp" style=""></span>mg/d)<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">61</span></a> and then tentatively raise the dose by 10<span class="elsevierStyleHsp" style=""></span>mg every 2 weeks until the adverse effects experienced by the patient make it advisable to refrain from further escalation.<a class="elsevierStyleCrossRefs" href="#bib0265"><span class="elsevierStyleSup">53,65</span></a> A useful sign is the appearance of cheilitis, which is an expression of the correct bioavailability of acitretin in each individual.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> Note that the individual variability associated with this drug means that low doses of acitretin may be effective.<a class="elsevierStyleCrossRef" href="#bib0320"><span class="elsevierStyleSup">64</span></a> Thus, gradual dose escalation is the optimal strategy for the correct use of this drug since this approach makes it possible to obtain the best clinical response with the least adverse effects.<a class="elsevierStyleCrossRef" href="#bib0340"><span class="elsevierStyleSup">68</span></a> The escalation approach also allows patients to gradually increase their tolerance of the potential and frequent adverse effects associated with acitretin and avoids the use of higher-than-necessary doses in some cases or doses that might lead to discontinuation of treatment in others.<a class="elsevierStyleCrossRefs" href="#bib0265"><span class="elsevierStyleSup">53,61</span></a></p><p id="par0495" class="elsevierStylePara elsevierViewall">Gradual dose escalation strategies take time, and attempts to shorten this time generally result in discontinuation of treatment before its long-term efficacy has been demonstrated. This gradual approach, which is the key to the correct management of therapy with acitretin in clinical practice, contrasts sharply with the strategies and responses we are accustomed to with other antipsoriatic drugs, some of which achieve dramatic results in a relatively short period.</p></span><span id="sec0230" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0255">Adjusted Dose and Maintenance Regimen</span><p id="par0500" class="elsevierStylePara elsevierViewall">Once the optimal dose has been achieved using the escalation strategy, and if an acceptable clinical response is achieved, it is normally possible to slightly reduce the dose to improve tolerance. Once again, this requires individualized dose adjustment achieved by gradually tapering the dose. Using this strategy it is often possible to maintain efficacy with low-dose regimens (10 to 25<span class="elsevierStyleHsp" style=""></span>mg/d; or 25<span class="elsevierStyleHsp" style=""></span>mg/48<span class="elsevierStyleHsp" style=""></span>h) for a very long period.<a class="elsevierStyleCrossRef" href="#bib0330"><span class="elsevierStyleSup">66</span></a></p></span><span id="sec0235" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0260">Combination Therapy</span><p id="par0505" class="elsevierStylePara elsevierViewall">There is evidence supporting the usefulness of combining acitretin with topical treatment, phototherapy, classic systemic therapies, and biologic agents, either as an initial drug to which a second treatment is added or as a second drug added to an already established regimen.<a class="elsevierStyleCrossRefs" href="#bib0560"><span class="elsevierStyleSup">112,113</span></a></p><p id="par0510" class="elsevierStylePara elsevierViewall">A recent study that analyzed the data on the prescription of acitretin recorded in the National Ambulatory Medical Care Survey found that in 62% of cases acitretin was prescribed concomitantly with another drug: topical corticosteroids (51%), calcipotriol (31%), biologic agents (6%), ciclosporin (5%), methotrexate (5%), and tazarotene (2%).<a class="elsevierStyleCrossRef" href="#bib0570"><span class="elsevierStyleSup">114</span></a><a class="elsevierStyleCrossRef" href="#tbl0035">Table 7</a> shows the different options for combination therapy with acitretin.</p><elsevierMultimedia ident="tbl0035"></elsevierMultimedia></span><span id="sec0240" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0265">Use in Combination with Topical Therapy</span><p id="par0515" class="elsevierStylePara elsevierViewall">The therapeutic efficacy of acitretin increases when it is combined with topical calcipotriol<a class="elsevierStyleCrossRefs" href="#bib0350"><span class="elsevierStyleSup">70,115,116</span></a> or topical corticosteroids.<a class="elsevierStyleCrossRefs" href="#bib0560"><span class="elsevierStyleSup">112,117</span></a> The combination with calcipotriol (1,25-dihydroxyvitamin D<span class="elsevierStyleInf">3</span>) is of particular interest since this drug also induces the transcription of certain genes.<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">28,118,119</span></a></p></span><span id="sec0245" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0270">Use in Combination With Phototherapy</span><p id="par0520" class="elsevierStylePara elsevierViewall">The association of oral retinoids and phototherapy is probably the most well-known and generally accepted combination therapy. The benefit of this combination was initially demonstrated with etretinate and PUVA therapy<a class="elsevierStyleCrossRefs" href="#bib0600"><span class="elsevierStyleSup">120,121</span></a> and, given the clinical equivalence of the 2 drugs, the results obtained with etretinate may be extrapolated to acitretin. Moreover, the combination of acitretin with UV-B, UV-A, or PUVA therapy has also been shown to be more effective than monotherapy with acitretin or phototherapy the use of a combination makes it possible to reduce the number of phototherapy sessions and the dose of acitretin required, thereby improving tolerance.<a class="elsevierStyleCrossRefs" href="#bib0260"><span class="elsevierStyleSup">52,66,122–124</span></a> Moreover the anticarcinogenic potential of the retinoids makes combination treatment safer than phototherapy alone.</p><p id="par0525" class="elsevierStylePara elsevierViewall">When clearing is used as a measure of efficacy, the result achieved with acitretin in combination with UV-B therapy (74%) is good and better than that achieved by monotherapy with either acitretin (42%) or UV-B (35% to 41%).<a class="elsevierStyleCrossRefs" href="#bib0330"><span class="elsevierStyleSup">66,125,126</span></a> The acitretin–PUVA combination has also been shown to be more effective than monotherapy with either treatment.<a class="elsevierStyleCrossRef" href="#bib0635"><span class="elsevierStyleSup">127</span></a> The acitretin–UV-B and acitretin–PUVA combinations have similar efficacy in the treatment of psoriasis.<a class="elsevierStyleCrossRef" href="#bib0640"><span class="elsevierStyleSup">128</span></a> UV-B, and particularly narrowband UV-B, is currently preferred to PUVA in combinations with acitretin because it does not produce the adverse effects associated with psoralens.</p><p id="par0530" class="elsevierStylePara elsevierViewall">When combination therapy is chosen from the outset, the recommended strategy is to administer acitretin at a low dose (for example 25<span class="elsevierStyleHsp" style=""></span>mg/d) for 2 weeks before starting phototherapy. When the patient is already receiving UV-B phototherapy but the therapeutic objective has not been achieved, 25<span class="elsevierStyleHsp" style=""></span>mg/d of acitretin may be prescribed. In such cases the dose of UV-B should be reduced by between 30% and 50% during the first week to prevent erythema. It is then gradually increased until clinical response is achieved with acceptable tolerance.<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">69</span></a> Once the lesions have cleared, the dose of acitretin should be maintained for 1 month before reducing either the dose of acitretin or the frequency of phototherapy sessions.<a class="elsevierStyleCrossRef" href="#bib0645"><span class="elsevierStyleSup">129</span></a></p></span><span id="sec0250" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0275">Use in Combination With Classic Systemic Treatments</span><p id="par0535" class="elsevierStylePara elsevierViewall">The association of acitretin and the immunosuppressive agents used to treat psoriasis is supported only by evidence from isolated case reports and series. Acitretin is the only systemic antipsoriatic agent that can be used in combination with another systemic drug without creating a regimen of 2 immunosuppressants, and consequently the only one that will not increase the risks arising from immunodeficiency.</p><p id="par0540" class="elsevierStylePara elsevierViewall">The combination of acitretin with methotrexate is effective,<a class="elsevierStyleCrossRef" href="#bib0650"><span class="elsevierStyleSup">130</span></a> particularly in the case of pustular psoriasis.<a class="elsevierStyleCrossRef" href="#bib0655"><span class="elsevierStyleSup">131</span></a> If, after starting acitretin at the usual doses a therapeutic response is not achieved within the established time frame (normally 3 to 6 months), weekly administration of methotrexate may be added at the usual doses. Once clinical improvement has been achieved, 1 of the 2 drugs may be discontinued<a class="elsevierStyleCrossRef" href="#bib0650"><span class="elsevierStyleSup">130</span></a> or the combination can be maintained at lower doses for both drugs.</p><p id="par0545" class="elsevierStylePara elsevierViewall">Given that both acitretin and methotrexate are hepatotoxic, close monitoring of liver function is essential. However, the concern about hepatotoxicity that initially motivated the formal contraindication to this combination in the Neotigason SPC is not usually a problem in clinical practice in our experience and in that of other authors,<a class="elsevierStyleCrossRef" href="#bib0560"><span class="elsevierStyleSup">112</span></a> and tolerance is generally good.<a class="elsevierStyleCrossRef" href="#bib0660"><span class="elsevierStyleSup">132</span></a></p><p id="par0550" class="elsevierStylePara elsevierViewall">The combination of acitretin and ciclosporin has also been used effectively in the treatment of psoriasis, although it is debatable whether it offers any advantage over monotherapy in terms of efficacy.<a class="elsevierStyleCrossRefs" href="#bib0665"><span class="elsevierStyleSup">133,134</span></a> In our clinical experience we have not observed any such advantage. Furthermore, prolonged use of this combination increases the risk of elevating cholesterol and triglyceride levels and of potentiating the toxicity of ciclosporin because acitretin inhibits the P-450 cytochrome, which is the principal inactivation pathway of ciclosporin. The combined use of acitretin and ciclosporin is more useful as a temporary overlap in the context of a sequential strategy (see below), or in selected cases of psoriatic erythroderma.<a class="elsevierStyleCrossRefs" href="#bib0675"><span class="elsevierStyleSup">135,136</span></a></p></span><span id="sec0255" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0280">Use in Combination with Biologic Therapy</span><p id="par0555" class="elsevierStylePara elsevierViewall">The combination of acitretin with the new selective immunosuppressants (biologics) is also a treatment option, especially in cases in which the biologic treatment has not achieved complete control of the disease and in which the antipsoriatic, but not immunosuppressive, action of acitretin may add the small degree of efficacy required to completely control the disease. Examples of such cases are patients with inflammatory bowel disease and psoriasis, patients with generalized psoriasis in whom therapy has not completely cleared lesions on the palms and soles, and patients with psoriasis previously treated with PUVA and ciclosporin who are on biologic treatment to reduce the risk of nonmelanoma skin cancer associated with immunosuppression.<a class="elsevierStyleCrossRefs" href="#bib0685"><span class="elsevierStyleSup">137–139</span></a></p><p id="par0560" class="elsevierStylePara elsevierViewall">A series of cases have recently been published of patients who responded to combinations of biologic drugs with acitretin.<a class="elsevierStyleCrossRefs" href="#bib0685"><span class="elsevierStyleSup">137,138,140,141</span></a> In these patients, the efficacy of monotherapy with a biologic agent was suboptimal and the addition of acitretin improved efficacy. These findings suggest that efficacy can be improved with no increase in toxicity, since acitretin is not an immunosuppressant. Furthermore, by using acitretin, physicians can reduce the dose of the biologic while maintaining response, enhancing safety, and above all reducing costs.</p><p id="par0565" class="elsevierStylePara elsevierViewall">A recent open-label retrospective study assessed the addition of a biologic agent in a series of patients who had a poor response to acitretin therapy.<a class="elsevierStyleCrossRef" href="#bib0690"><span class="elsevierStyleSup">138</span></a> As might be expected, the regimen was shown to be effective and is an example of the role acitretin can play in the era of biologic therapy. Because of its proven efficacy and very good long-term safety profile, acitretin may be another option to consider when choosing a combination strategy when a biologic drug does not achieve optimal efficacy or when response to biologic therapy diminishes. Moreover, acitretin is distinguished from ciclosporin, methotrexate, and the biologics in that its mechanism of action is not based on immunosuppression. To date, the tendency, perhaps influenced by the practice of rheumatologists, has been to use methotrexate with biologics as the first-line combination therapy, even in the absence of arthritis.</p></span><span id="sec0260" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0285">Sequential Therapy</span><p id="par0570" class="elsevierStylePara elsevierViewall">Sequential therapy has been established as a strategy for the long-term management of psoriasis to avoid the prolonged use of immunosuppressants and drugs with cumulative, organ-specific toxicity. The approach involves using a different drug as a maintenance regimen after the therapeutic objective has been achieved with the induction treatment; it can be a drug-sparing option in the long-term.<a class="elsevierStyleCrossRefs" href="#bib0080"><span class="elsevierStyleSup">16,142</span></a></p><p id="par0575" class="elsevierStylePara elsevierViewall">Acitretin is an ideal candidate for sequential strategies because of its capacity to maintain efficacy in the long term without direct immunosuppressive action. Moreover, in sequential approaches the slow response associated with acitretin treatment can be compensated for by starting treatment with a faster-acting and more effective antipsoriatic drug whose long-term use is limited by the risk of exceeding a maximum cumulative dose or even by financial considerations. The idea is that once improvement has been achieved with one treatment, it can be maintained using acitretin, preferably at low doses.<a class="elsevierStyleCrossRefs" href="#bib0330"><span class="elsevierStyleSup">66,143</span></a></p><p id="par0580" class="elsevierStylePara elsevierViewall">A classic sequential strategy involves using ciclosporin to clear the patient's psoriasis (clearing phase) and then adding a gradually escalating dose of acitretin (transition phase) to establish the maximum tolerated dose. The last step (maintenance phase) is to discontinue ciclosporin and maintain long-term monotherapy with acitretin.<a class="elsevierStyleCrossRef" href="#bib0710"><span class="elsevierStyleSup">142</span></a> Another variant of this strategy is to occasionally add UV-B or PUVA therapy in the case of a loss of response to monotherapy with acitretin (<a class="elsevierStyleCrossRef" href="#tbl0040">Table 8</a>).<a class="elsevierStyleCrossRef" href="#bib0330"><span class="elsevierStyleSup">66</span></a></p><elsevierMultimedia ident="tbl0040"></elsevierMultimedia></span><span id="sec0265" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0290">Intermittent Therapy</span><p id="par0585" class="elsevierStylePara elsevierViewall">Sudden interruption of acitretin therapy does not produce a rebound effect resulting in a flare.<a class="elsevierStyleCrossRef" href="#bib0720"><span class="elsevierStyleSup">144</span></a> This means that treatment with acitretin, whether as monotherapy or combination therapy, can be suspended at any time. Sustained remission of psoriasis after a prolonged period with therapeutic response can last 2 to 6 months.</p><p id="par0590" class="elsevierStylePara elsevierViewall">Because of these characteristics and the absence of any known antigen action or resistance, as long as a rapid clinical response is not required, acitretin is suitable for intermittent therapy, although this type of treatment regimen has not been assessed in clinical trials</p></span></span><span id="sec0270" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0295">Conclusions</span><p id="par0595" class="elsevierStylePara elsevierViewall">Acitretin is a second-generation synthetic retinoid that is effective in the systemic treatment of psoriasis, either in monotherapy or in combination or sequential regimens. Although it has a much shorter half-life than etretinate and does not accumulate in any particular tissue, its use is nonetheless contraindicated in pregnant women and women of childbearing age who plan to conceive within at least 2 years of cessation of treatment.</p><p id="par0600" class="elsevierStylePara elsevierViewall">Acitretin's efficacy in the treatment of psoriasis is mediated by the transcription and inhibition of specific genes, through which it influences the action of intracellular retinoids and exerts a primarily regulatory effect on the differentiation and proliferation of keratinocytes and, to a lesser degree, acts as an anti-inflammatory.</p><p id="par0605" class="elsevierStylePara elsevierViewall">Compared to other available systemic drugs (methotrexate, ciclosporin, and biologics), acitretin is less effective, but it nonetheless achieves significant clearing and can be used in the long term without risk of immunosuppression.</p><p id="par0610" class="elsevierStylePara elsevierViewall">In monotherapy, acitretin obtains a therapeutic response (PASI 75) in 40% to 50% of patients. The best results are achieved when the dose is gradually escalated to achieve the maximally effective dose, which varies in each individual.</p><p id="par0615" class="elsevierStylePara elsevierViewall">Acitretin is especially useful in the treatment of pustular psoriasis and the palmar and plantar forms of the disease. Its use in combination with phototherapy or in sequential therapy with ciclosporin is also of particular interest. When used in association with biologic drugs it offers a strategic advantage in the long-term management of psoriasis. Since it is not a direct immunosuppressant, acitretin can be used in patients in whom the risk of immunosuppression may limit the use of other antipsoriatic drugs.</p><p id="par0620" class="elsevierStylePara elsevierViewall">While it does not have a rapid onset of action, the value of acitretin in patients with psoriasis lies in its potential for very prolonged use as maintenance therapy after clearing has been achieved, or as a component of combination regimens.</p><p id="par0625" class="elsevierStylePara elsevierViewall">In summary, although acitretin is not usually a first-line option for clearing moderate to severe psoriasis, it should be considered in the overall long-term management of psoriasis as a maintenance treatment to prevent relapse; it can be very useful in specific circumstances and in certain clinical forms of the disease. The management of acitretin therapy may be more complicated than that of other drugs, but when used correctly it remains useful in the treatment of psoriasis even in the era of biologic therapies.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2,4</span></a><a class="elsevierStyleCrossRef" href="#tbl0045">Table 9</a> summarizes the use of acitretin in the treatment of psoriasis.</p><elsevierMultimedia ident="tbl0045"></elsevierMultimedia></span><span id="sec0275" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0300">Conflicts of Interest</span><p id="par0630" class="elsevierStylePara elsevierViewall">The authors deem that they have no conflicts of interest with respect to these guidelines. However, all those who participated in drawing up these guidelines have had and continue to have, to differing degrees, relationships with the pharmaceutical industry and have received financial support for conference attendance, clinical trials, or their work as scientific research consultants in relation to other antipsoriatic drugs.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:18 [ 0 => array:2 [ "identificador" => "xres261453" "titulo" => "Abstract" ] 1 => array:2 [ "identificador" => "xpalclavsec246066" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xres261452" "titulo" => "Resumen" ] 3 => array:2 [ "identificador" => "xpalclavsec246065" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:3 [ "identificador" => "sec0010" "titulo" => "Pharmacology" "secciones" => array:6 [ 0 => array:2 [ "identificador" => "sec0015" "titulo" => "Mechanism of Action" ] 1 => array:2 [ "identificador" => "sec0020" "titulo" => "Absorption and Distribution" ] 2 => array:2 [ "identificador" => "sec0025" "titulo" => "Metabolism" ] 3 => array:2 [ "identificador" => "sec0030" "titulo" => "Half-life" ] 4 => array:2 [ "identificador" => "sec0035" "titulo" => "Excretion" ] 5 => array:2 [ "identificador" => "sec0040" "titulo" => "Pharmacogenetics" ] ] ] 6 => array:2 [ "identificador" => "sec0045" "titulo" => "Indications" ] 7 => array:2 [ "identificador" => "sec0050" "titulo" => "Contraindications" ] 8 => array:3 [ "identificador" => "sec0055" "titulo" => "Use and Special Precautions" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0060" "titulo" => "Presentations" ] 1 => array:2 [ "identificador" => "sec0065" "titulo" => "Posology" ] ] ] 9 => array:3 [ "identificador" => "sec0070" "titulo" => "Efficacy" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0075" "titulo" => "Plaque Psoriasis" ] 1 => array:2 [ "identificador" => "sec0080" "titulo" => "Pustular Psoriasis" ] 2 => array:2 [ "identificador" => "sec0085" "titulo" => "Nail Psoriasis" ] ] ] 10 => array:3 [ "identificador" => "sec0090" "titulo" => "Toxicity and Adverse Reactions" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0095" "titulo" => "Overview" ] 1 => array:3 [ "identificador" => "sec0100" "titulo" => "Toxicity by Organ and System" "secciones" => array:9 [ 0 => array:2 [ "identificador" => "sec0105" "titulo" => "Mucocutaneous Effects" ] 1 => array:2 [ "identificador" => "sec0110" "titulo" => "Hepatic Effects" ] 2 => array:2 [ "identificador" => "sec0115" "titulo" => "Metabolic Effects" ] 3 => array:2 [ "identificador" => "sec0120" "titulo" => "Neurologic Effects Pseudotumor Cerebri" ] 4 => array:2 [ "identificador" => "sec0125" "titulo" => "Ophthalmologic Effects" ] 5 => array:2 [ "identificador" => "sec0130" "titulo" => "Musculoskeletal Effects" ] 6 => array:2 [ "identificador" => "sec0135" "titulo" => "Retinoic Acid Syndrome" ] 7 => array:2 [ "identificador" => "sec0140" "titulo" => "Teratogenicity" ] 8 => array:2 [ "identificador" => "sec0145" "titulo" => "Psychiatric Symptoms" ] ] ] ] ] 11 => array:3 [ "identificador" => "sec0150" "titulo" => "Safety" "secciones" => array:9 [ 0 => array:2 [ "identificador" => "sec0155" "titulo" => "Patient Information" ] 1 => array:2 [ "identificador" => "sec0160" "titulo" => "Baseline Screening and Follow-up During Treatment" ] 2 => array:2 [ "identificador" => "sec0280" "titulo" => "Use in Patients with Cardiovascular Risk Factors and Metabolic Syndrome" ] 3 => array:2 [ "identificador" => "sec0165" "titulo" => "Use in Patients With Impaired Liver Function" ] 4 => array:2 [ "identificador" => "sec0170" "titulo" => "Use in Patients With Renal Impairment" ] 5 => array:2 [ "identificador" => "sec0175" "titulo" => "Drug Interactions" ] 6 => array:2 [ "identificador" => "sec0180" "titulo" => "Use in the Case of Infection and Vaccination" ] 7 => array:2 [ "identificador" => "sec0185" "titulo" => "Use in Patients With Cancer and Immunocompromised Patients" ] 8 => array:2 [ "identificador" => "sec0190" "titulo" => "Use in Pregnant Women and Reproductive Considerations" ] ] ] 12 => array:2 [ "identificador" => "sec0195" "titulo" => "Use in Breastfeeding Mothers" ] 13 => array:3 [ "identificador" => "sec0200" "titulo" => "Pediatric Use" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0205" "titulo" => "Use in Elderly Patients" ] 1 => array:2 [ "identificador" => "sec0210" "titulo" => "Use in Patients Undergoing Surgical Interventions" ] 2 => array:2 [ "identificador" => "sec0215" "titulo" => "Overdose" ] ] ] 14 => array:3 [ "identificador" => "sec0220" "titulo" => "Treatment Strategies for Acitretin in Psoriasis" "secciones" => array:9 [ 0 => array:2 [ "identificador" => "sec0225" "titulo" => "Initial Dose Followed by Gradual Escalation" ] 1 => array:2 [ "identificador" => "sec0230" "titulo" => "Adjusted Dose and Maintenance Regimen" ] 2 => array:2 [ "identificador" => "sec0235" "titulo" => "Combination Therapy" ] 3 => array:2 [ "identificador" => "sec0240" "titulo" => "Use in Combination with Topical Therapy" ] 4 => array:2 [ "identificador" => "sec0245" "titulo" => "Use in Combination With Phototherapy" ] 5 => array:2 [ "identificador" => "sec0250" "titulo" => "Use in Combination With Classic Systemic Treatments" ] 6 => array:2 [ "identificador" => "sec0255" "titulo" => "Use in Combination with Biologic Therapy" ] 7 => array:2 [ "identificador" => "sec0260" "titulo" => "Sequential Therapy" ] 8 => array:2 [ "identificador" => "sec0265" "titulo" => "Intermittent Therapy" ] ] ] 15 => array:2 [ "identificador" => "sec0270" "titulo" => "Conclusions" ] 16 => array:2 [ "identificador" => "sec0275" "titulo" => "Conflicts of Interest" ] 17 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2012-11-18" "fechaAceptado" => "2013-01-20" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec246066" "palabras" => array:5 [ 0 => "Acitretin" 1 => "Guidelines" 2 => "Treatment" 3 => "Psoriasis" 4 => "Antipsoriasis systemic treatment" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec246065" "palabras" => array:5 [ 0 => "Acitretina" 1 => "Guía" 2 => "Tratamiento" 3 => "Psoriasis" 4 => "Tratamiento sistémico antipsoriásico" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Phototherapy, classic systemic treatments (methotrexate, acitretin, and ciclosporin), and biologic agents (etanercept, infliximab, adalimumab, and ustekinumab) constitute a broad therapeutic arsenal that increases the likelihood of achieving control of severe and extensive disease in patients with psoriasis. Acitretin continues to be a very valuable tool in both monotherapy, in which it is combined with other systemic treatments (classic or biologic), and in sequential therapy. Thanks to its lack of a direct immunosuppressive effect and its ability to achieve a long-term response, acitretin has an important role in the treatment of psoriasis, although this has not always been acknowledged in relevant treatment guidelines.</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">We present consensus guidelines for the use of acitretin in psoriasis drawn up by the Psoriasis Group of the Spanish Academy of Dermatology and Venereology. These guidelines provide a detailed account of acitretin, including pharmacological properties, indications and contraindications, adverse effects, and factors that should be taken into account to enhance the safe use of this drug. They also propose treatment strategies for use in routine clinical practice. The overall aim of these guidelines is to define the criteria for the use and management of acetretin in psoriasis.</p>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">La fototerapia y los tratamientos sistémicos clásicos (metotrexato, acitetrina, ciclosporina), junto con las denominadas terapias biológicas (etanercept, infliximab, adalimumab, ustekinumab), permiten al dermatólogo disponer de un arsenal terapéutico amplio que aumenta las posibilidades de control de pacientes con psoriasis grave y/o extensa. La acitretina sigue siendo de gran utilidad tanto en monoterapia como combinada con otros fármacos sistémicos (clásicos o «biológicos»), o en terapia secuencial. Se distingue por no ser inmunosupresor directo y mantener respuestas a muy largo plazo, lo que le confiere un papel relevante en el tratamiento de la psoriasis, que no siempre ha sido reconocido en las diversas guías terapéuticas de esta enfermedad.</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Se presenta una guía de uso de acitretina consensuada por los miembros del Grupo de Psoriasis de la Academia Española de Dermatología y Venereología, en la que se exponen de forma detallada aspectos de la farmacología del fármaco, sus indicaciones y contraindicaciones, su eficacia antipsoriásica, los efectos adversos asociados al fármaco, las acciones a tener en cuenta para aumentar la seguridad de su uso, y se propone diversas estrategias terapéuticas de aplicación en la práctica clínica habitual. El objetivo global es facilitar los criterios de indicación y manejo de la acitretina en pacientes con psoriasis.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0015">Please cite this article as: Carretero G, et al. Acitretina: guía de uso en psoriasis. Actas Dermosifiliogr. 2013;104:598–616.</p>" ] ] "multimedia" => array:12 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 909 "Ancho" => 1472 "Tamanyo" => 66918 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Chemical structure of acitretin.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1467 "Ancho" => 3266 "Tamanyo" => 283058 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Mechanism of action of retinoids. Abbreviations: ADH, alcohol dehydrogenase; COUP-TFII, chicken ovalbumin upstream promoter-transcription factor <span class="elsevierStyleSmallCaps">II</span>; CRABP, cellular retinoic acid-binding proteins; CRBP, cellular retinol-binding proteins; CYP, cytochrome P450, family 26; FOG2, friend of GATA; GATA4, guanine, adenine, thymine, adenine; LRAT, lecithin retinol acyltransferase; RAR, retinoic acid receptors; RARE, retinoic acid response elements; RBP, retinol binding protein; RDH, retinol dehydrogenase, RXR, retinoid <span class="elsevierStyleSmallCaps">X</span> receptors; STRA6, stimulated by retinoic acid 6.</p> <p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Source: Saurat<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a>; Siegenthaler et al.<a class="elsevierStyleCrossRef" href="#bib0725"><span class="elsevierStyleSup">145</span></a>; and Napoli.<a class="elsevierStyleCrossRef" href="#bib0730"><span class="elsevierStyleSup">146</span></a></p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 2642 "Ancho" => 3372 "Tamanyo" => 698584 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Treatment monitoring form for acitretin.</p>" ] ] 3 => array:7 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Relative contraindications</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Mild hepatic impairment (adjust dose) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Mild renal impairment (adjust dose) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Alcohol consumption (liver toxicity, re-esterification to etretinate) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Drug interactions (increases toxicity) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Concomitant organ toxic medication (increases toxicity) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Active infections (assess the possibility of acitretin toxicity exacerbating infection) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Poorly controlled dyslipidemia \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Metabolic syndrome \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Uncooperative or noncompliant patient \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Pediatric or elderly patient (lower tolerance for toxicity?) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Absolute contraindications</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Pregnancy (contraception starting 1 month before treatment and the patient must wait 2 years after cessation to become pregnant) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Severe liver failure \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Severe kidney failure \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Allergy to drug components \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab367498.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Contraindications to the Use of Acitretin.</p>" ] ] 4 => array:7 [ "identificador" => "tbl0010" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:3 [ "leyenda" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Adapted from Katz et al.<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">76</span></a> and Saurat.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a></p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Frequent \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Very Frequent \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Infrequent \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Very infrequent \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>• Rhinitis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>• Cheilitis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Xerostomia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Pancreatitis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>• Xerosis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>• Alopecia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Epistaxis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Exacerbation of inflammatory bowel disease \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>• Nail dystrophy \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>• Peeling \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Diffuse erythema \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Agranulocytosis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>• Pruritus \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Paronychia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Leukopenia \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Hyperestesic skin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Myopathy \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Sticky skin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Pseudotumor cerebri \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Xerophthalmia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Depression \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Arthralgia, myalgia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Retinoic acid syndrome \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Hyperostosis<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Reduced night vision \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Headache \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Toxic hepatitis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Nausea \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Edema of the face and limbs \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Abdominal pain \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Erythema multiforme \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Hyperlipidemia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Vasculitis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Photosensitivity \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Galactorrhea, gynecomastia \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Pulmonary fibrosis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">• Teratogenicity<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab367502.png" ] ] ] "notaPie" => array:2 [ 0 => array:3 [ "identificador" => "tblfn0005" "etiqueta" => "a" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Progression of preexisting lesions.</p>" ] 1 => array:3 [ "identificador" => "tblfn0010" "etiqueta" => "b" "nota" => "<p class="elsevierStyleNotepara" id="npar0010">If proper contraception is ensured.</p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Most Commonly Reported Adverse Effects Associated With Acitretin.</p>" ] ] 5 => array:7 [ "identificador" => "tbl0015" "etiqueta" => "Table 3" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Appropriate candidate selection \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Use of health screening protocol before treatment \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Review of the summaries of product characteristics for concomitant medications \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Precise prescribing after considering contraindications \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Gradual escalation of dose (indicative sign<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>cheilitis) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Protocolized follow-up and monitoring \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Patients must guarantee and commit to being available for follow up visits and periodic testing. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Good accessibility to health care personnel. \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab367496.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Measures for Enhancing the Safety of Treatment with Acitretin.</p>" ] ] 6 => array:7 [ "identificador" => "tbl0020" "etiqueta" => "Table 4" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Abbreviations: AIDS, acquired immunodeficiency syndrome; CHF, congestive heart failure; HIV, human immunodeficiency virus.</p><p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Adapted from Strober et al.<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">58</span></a></p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Indicated \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Risk/Benefit Assessment \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Not Indicated \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Obesity \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Type 2 diabetes mellitus \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Metabolic syndrome/dyslipidemia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Moderate to severe CHF \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Live vaccines \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Demyelinating disease \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Active granulomatous disease \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Pregnancy \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Lactation \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><<span class="elsevierStyleHsp" style=""></span>18 y/><span class="elsevierStyleHsp" style=""></span>65 y \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">At risk for infections \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">HIV/AIDS \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Chronic liver disease \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Hepatitis B virus carrier (asymptomatic) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Hepatitis C virus carrier (asymptomatic) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Renal insufficiency \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Psoriatic arthritis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Melanoma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Lymphoreticular neoplasia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Solid carcinoma \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">✓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab367500.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Evaluation of the Use of Acitretin in Situations of Risk.</p>" ] ] 7 => array:7 [ "identificador" => "tbl0025" "etiqueta" => "Table 5" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Medical history</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Type of psoriasis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Course of disease \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Arthitis/arthralgia \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Response to prior treatments \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Contraindications/risks \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Baseline workup</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Physical and dermatologic assessment \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Liver function \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Kidney function \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Lipid profile \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Blood sugar levels \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Viral infections \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Rule out pregnancy and prevent conception \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Follow-up monitoring</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Repeat physical and dermatologic assessment \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Liver function \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Kidney function \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Lipid profile \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Blood sugar levels \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Easy and direct line</span> o<span class="elsevierStyleItalic">f contact with the dermatology nursing staff</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab367503.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">Screening of Candidates Suitable for Treatment with Acitretin.</p>" ] ] 8 => array:7 [ "identificador" => "tbl0030" "etiqueta" => "Table 6" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Alcohol</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Increases hepatotoxicity \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Increases re-esterification of acitretin to etretinate (teratogenicity) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Tetracyclines</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Increases photosensitivity \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Risk of intracranial hypertension \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Minocycline</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Risk of intracranial hypertension \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Vitamin A (></span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">4,000-5,000 IU/d)</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Hypervitaminosis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Corticosteroids</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Altered lipid levels \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Risk of intracranial hypertension \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Methotrexate</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Potential hepatotoxicity \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Raises methotrexate levels \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Ciclosporin</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Alteration of lipid profile \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Increases cardiovascular risk \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Phenytoin</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Increases blood levels of phenytoin \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Oral antidiabetic agents</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Fluctuations in blood sugar levels \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Glibenclamide</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Reduces hypoglycemic effect of glibenclamide \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Progestogen contraceptives (in mini doses)</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Reduces contraceptive effect \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab367495.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">Drug Interactions With Acitretin.</p>" ] ] 9 => array:7 [ "identificador" => "tbl0035" "etiqueta" => "Table 7" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0095" class="elsevierStyleSimplePara elsevierViewall">Adapted from Lebwohl et al.<a class="elsevierStyleCrossRef" href="#bib0560"><span class="elsevierStyleSup">112</span></a></p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Starting with Acitretin and Adding a Second Drug</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Acitretin</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">+</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">methotrexate</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Full doses of both drugs can be administered \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Acitretin may be withdrawn abruptly \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Monitor hepatotoxicity \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Acitretin</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">+</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">ciclosporin</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Full doses of the both drugs can be administered \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Acitretin can be withdrawn abruptly \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Monitor lipid profile \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Acitretin</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">+</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">phototherapy</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Acitretin at normal doses, reduce phototherapy dose by 50% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Discontinue acitretin when clearing is achieved \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Starting with Another Drug, Adding Acitretin</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Methotrexate</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">+</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">acitretin</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Taper dosage of methotrexate over 2-3 mo to 7.5<span class="elsevierStyleHsp" style=""></span>mg/wk \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Introduce acitretin at full dose \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Monitor hepatotoxicity \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Ciclosporin</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">+</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">acitretin</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Full dose of ciclosporin \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Add acitretin at low daily doses (or every 48 <span class="elsevierStyleHsp" style=""></span>h) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Gradually increase dose of acitretin, depending on the clinical response \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Once response has been obtained, taper dose of ciclosporin over 3-4 months \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Maintain acitretin therapy \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Monitor alterations in lipid profile \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Phototherapy</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">+</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">acitretin</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Reduce phototherapy dose to 50% a week before introducing acitretin \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Add acitretin at 10-25<span class="elsevierStyleHsp" style=""></span>mg/d \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Gradually increase phototherapy dose according to response and phototoxicity \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Increase acitretin to an acceptable dose (most common maximum dosage is 25<span class="elsevierStyleHsp" style=""></span>mg/d) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Maintain acitretin and phototherapy until clearing is achieved \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Biologics</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">+</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">acitretin</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Maintain dose of tumor necrosis factor inhibitor \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Add acitretin at a low dose \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Gradually escalate dose of acitretin according to response \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab367499.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">Classic Acitretin Combination Strategies.</p>" ] ] 10 => array:7 [ "identificador" => "tbl0040" "etiqueta" => "Table 8" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0105" class="elsevierStyleSimplePara elsevierViewall">Adapted from Koo<a class="elsevierStyleCrossRef" href="#bib0710"><span class="elsevierStyleSup">142</span></a> and Lebwohl et al.<a class="elsevierStyleCrossRef" href="#bib0560"><span class="elsevierStyleSup">112</span></a></p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Phase 1</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Induction with ciclosporin</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Start ciclosporin at 5<span class="elsevierStyleHsp" style=""></span>mg/kg/d \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Continue with ciclosporin at 5<span class="elsevierStyleHsp" style=""></span>mg/kg/d \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Phase 2A</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Achieve clearing</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Introduce acitretin at a low dose and escalate gradually to the maximum tolerated dose \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Phase 2B</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Maintain clearing</span> (><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">6-7 mo)</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Gradually taper ciclosporin to <span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>1<span class="elsevierStyleHsp" style=""></span>mg/kg/d \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Maintain acitretin dose \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Phase 3A</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Consolidate clearing with acitretin monotherapy</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Withdraw ciclosporin \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Maintain treatment with acitretin \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleBold">Phase 3B</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleItalic">Long-term clearing Adjustment for fluctuations</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Maintain acitretin dose \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>Add phototherapy if required \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab367497.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0100" class="elsevierStyleSimplePara elsevierViewall">Sequential Therapy with Ciclosporin and Acitretin.</p>" ] ] 11 => array:7 [ "identificador" => "tbl0045" "etiqueta" => "Table 9" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:1 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Indications</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Generalized pustular psoriasis and palmoplantar psoriasis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Psoriatic erythroderma \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Psoriasis vulgaris (single-drug, combination, and sequential therapy) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Contraindications</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Absolute: pregnancy, allergy to any of its components, severe hepatic or renal impairment \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Relative: rental or hepatic impairment, metabolic syndrome \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Mechanism of Action</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Genetic transduction through the activation of specific nuclear receptors \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Acts on keratinization, cell proliferation, and inflammation \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Immune modulation \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Pharmacology</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Half-life of 50<span class="elsevierStyleHsp" style=""></span>h (its metabolite 13-cis-acitretin 90<span class="elsevierStyleHsp" style=""></span>h; and etretinate 120<span class="elsevierStyleHsp" style=""></span>d) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Does not accumulate in tissue \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Renal and fecal excretion via bile \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Is converted to etretinate by re-esterification (accelerated by alcohol) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Efficacy</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Slow response \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Assess achievement of therapeutic objective at 3-6 mo \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Short term (12 wks): PASI 50 in 80%/PASI 75 in 52% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Long-term (12 mo) PASI 50 in 89%/PASI 75 in 78% \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Dosing</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>The initial dosage of acitretin should be between 10 and 25<span class="elsevierStyleHsp" style=""></span>mg/d \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Dose increase every other week (indicative sign: appearance of cheilitis or xerosis) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>The optimal dosage is between 25 and 50<span class="elsevierStyleHsp" style=""></span>mg/d \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Once the desired clinical response has been achieved, consider gradually reducing the dose until the minimum effective dosage is achieved. This can then be maintained for long periods (10-25<span class="elsevierStyleHsp" style=""></span>mg/24<span class="elsevierStyleHsp" style=""></span>h, 25<span class="elsevierStyleHsp" style=""></span>mg/48<span class="elsevierStyleHsp" style=""></span>h) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Toxicity</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Severe: teratogenicity, hepatotoxicity, dyslipidemia (cardiovascular risk) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Mild: mucositis, xerosis, alopecia, laminar scaling, myalgia, photosensitivity, epistaxis, paronychia, nausea, abdominal pain, sticky skin (see <a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Safety</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Ensure correct patient screening and selection \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Patient information and education \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Use dose in therapeutic range \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Individualized dose adjustment guided by the appearance of adverse effects \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Strategies</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Monotherapy \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Combination therapy \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Sequential therapy (ciclosporin sparing) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Combinations</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Acitretin<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>phototherapy \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Acitretin<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>methotrexate \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Acitretin<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>biologic agent \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Acitretin<span class="elsevierStyleHsp" style=""></span>+<span class="elsevierStyleHsp" style=""></span>topical calcipotriol \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Screening and Monitoring</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Baseline physical examination and medical history \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Rule out pregnancy (fertile women) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Identification of contraindications and comorbidities at baseline and regularly thereafter \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Check the list of concomitant medications the patient is taking \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Baseline and regular laboratory workup according to protocol (see attached sample treatment monitoring form, for example) \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab367501.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0110" class="elsevierStyleSimplePara elsevierViewall">Use of Acitretin in Psoriasis.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:146 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Acitretin" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.annder.2011.10.001" "Revista" => array:6 [ …6] ] ] ] ] ] 1 => array:3 [ "identificador" => "bib0010" "etiqueta" => "2" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Acitretin in dermatology: A review" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 2 => array:3 [ "identificador" => "bib0015" "etiqueta" => "3" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Acitretin revisited" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 3 => array:3 [ "identificador" => "bib0020" "etiqueta" => "4" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Acitretin revisited in the era of biologics" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.3109/09546630903578582" "Revista" => array:6 [ …6] ] ] ] ] ] 4 => array:3 [ "identificador" => "bib0025" "etiqueta" => "5" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1111/j.1365-2133.2010.09755.x" "Revista" => array:6 [ …6] ] ] ] ] ] 5 => array:3 [ "identificador" => "bib0030" "etiqueta" => "6" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Retinoids: Biological function and use in the treatment of dermatological diseases. Expert opinion investigational" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ …5] ] ] ] ] ] 6 => array:3 [ "identificador" => "bib0035" "etiqueta" => "7" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Retinoids: Transport, metabolism and mechanism of action" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 7 => array:3 [ "identificador" => "bib0040" "etiqueta" => "8" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Recent developments in receptor-selective retinoids" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 8 => array:3 [ "identificador" => "bib0045" "etiqueta" => "9" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Update on retinoid therapy of psoriasis in: an update on the use of retinoids in dermatology" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1111/j.1529-8019.2006.00082.x" "Revista" => array:6 [ …6] ] ] ] ] ] 9 => array:3 [ "identificador" => "bib0050" "etiqueta" => "10" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Retinoids: Mechanisms of action" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/S0151-9638(10)70036-3" "Revista" => array:7 [ …7] ] ] ] ] ] 10 => array:3 [ "identificador" => "bib0055" "etiqueta" => "11" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Biología de los receptores de los retinoides" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ …5] ] ] ] ] ] 11 => array:3 [ "identificador" => "bib0060" "etiqueta" => "12" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Rational design of receptor-selective retinoids" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 12 => array:3 [ "identificador" => "bib0065" "etiqueta" => "13" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Therapeutic effects of an aromatic acid analog on chemically induced skin papilomas and carcinomas of mice" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 13 => array:3 [ "identificador" => "bib0070" "etiqueta" => "14" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Vitamin A and retinoids, from nutrition to pharmacotherapy in dermatology and oncology" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 14 => array:3 [ "identificador" => "bib0075" "etiqueta" => "15" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Retinoic acid improves epidermal morphogenesis" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 15 => array:3 [ "identificador" => "bib0080" "etiqueta" => "16" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Retinoids" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 16 => array:3 [ "identificador" => "bib0085" "etiqueta" => "17" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Advances in psoriasis therapy" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ …6] ] ] ] ] ] 17 => array:3 [ "identificador" => "bib0090" "etiqueta" => "18" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Comparative study of histopathological and immunohistochemical findings in skin biopsies from patients with psoriasis before and after treatment with acitretin" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ …5] ] ] ] ] ] 18 => array:3 [ "identificador" => "bib0095" "etiqueta" => "19" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Cellular actions of etretinate in psoriasis: Enhanced epidermal differentiation and reduced cell-mediated inflammation are unexpected outcomes" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ …5] ] ] ] ] ] 19 => array:3 [ "identificador" => "bib0100" "etiqueta" => "20" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Acitretin exerted a greater influence on T-helper (Th)1 and Th17 than on Th2 cells in treatment of psoriasis vulgaris" "autores" => array:1 [ …1] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ …5] ] ] ] ] ] 20 => array:3 [ "identificador" => 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año/Mes | Html | Total | |
---|---|---|---|
2024 Noviembre | 86 | 18 | 104 |
2024 Octubre | 842 | 142 | 984 |
2024 Septiembre | 1037 | 139 | 1176 |
2024 Agosto | 1115 | 174 | 1289 |
2024 Julio | 1217 | 123 | 1340 |
2024 Junio | 988 | 124 | 1112 |
2024 Mayo | 778 | 102 | 880 |
2024 Abril | 741 | 74 | 815 |
2024 Marzo | 889 | 156 | 1045 |
2024 Febrero | 987 | 100 | 1087 |
2024 Enero | 1129 | 121 | 1250 |
2023 Diciembre | 903 | 128 | 1031 |
2023 Noviembre | 852 | 101 | 953 |
2023 Octubre | 668 | 93 | 761 |
2023 Septiembre | 631 | 94 | 725 |
2023 Agosto | 532 | 56 | 588 |
2023 Julio | 426 | 92 | 518 |
2023 Junio | 461 | 56 | 517 |
2023 Mayo | 542 | 78 | 620 |
2023 Abril | 381 | 47 | 428 |
2023 Marzo | 382 | 80 | 462 |
2023 Febrero | 321 | 49 | 370 |
2023 Enero | 248 | 70 | 318 |
2022 Diciembre | 197 | 63 | 260 |
2022 Noviembre | 94 | 59 | 153 |
2022 Octubre | 63 | 47 | 110 |
2022 Septiembre | 46 | 44 | 90 |
2022 Agosto | 44 | 58 | 102 |
2022 Julio | 41 | 64 | 105 |
2022 Junio | 35 | 42 | 77 |
2022 Mayo | 295 | 62 | 357 |
2022 Abril | 352 | 95 | 447 |
2022 Marzo | 369 | 108 | 477 |
2022 Febrero | 317 | 60 | 377 |
2022 Enero | 390 | 104 | 494 |
2021 Diciembre | 467 | 80 | 547 |
2021 Noviembre | 445 | 84 | 529 |
2021 Octubre | 550 | 107 | 657 |
2021 Septiembre | 865 | 101 | 966 |
2021 Agosto | 549 | 99 | 648 |
2021 Julio | 413 | 87 | 500 |
2021 Junio | 423 | 127 | 550 |
2021 Mayo | 415 | 124 | 539 |
2021 Abril | 811 | 189 | 1000 |
2021 Marzo | 572 | 126 | 698 |
2021 Febrero | 373 | 110 | 483 |
2021 Enero | 351 | 78 | 429 |
2020 Diciembre | 294 | 82 | 376 |
2020 Noviembre | 214 | 84 | 298 |
2020 Octubre | 185 | 73 | 258 |
2020 Septiembre | 201 | 63 | 264 |
2020 Agosto | 181 | 97 | 278 |
2020 Julio | 173 | 79 | 252 |
2020 Junio | 141 | 118 | 259 |
2020 Mayo | 203 | 139 | 342 |
2020 Abril | 197 | 124 | 321 |
2020 Marzo | 90 | 186 | 276 |
2020 Febrero | 8 | 90 | 98 |
2020 Enero | 4 | 67 | 71 |
2019 Diciembre | 4 | 53 | 57 |
2019 Noviembre | 4 | 53 | 57 |
2019 Octubre | 0 | 61 | 61 |
2019 Septiembre | 5 | 54 | 59 |
2019 Agosto | 4 | 38 | 42 |
2019 Julio | 4 | 67 | 71 |
2019 Junio | 13 | 75 | 88 |
2019 Mayo | 8 | 158 | 166 |
2019 Abril | 16 | 128 | 144 |
2019 Marzo | 1 | 45 | 46 |
2019 Febrero | 2 | 24 | 26 |
2019 Enero | 2 | 12 | 14 |
2018 Diciembre | 2 | 5 | 7 |
2018 Noviembre | 4 | 6 | 10 |
2018 Octubre | 15 | 0 | 15 |
2018 Septiembre | 7 | 57 | 64 |
2018 Agosto | 0 | 121 | 121 |
2018 Julio | 0 | 70 | 70 |
2018 Junio | 0 | 72 | 72 |
2018 Mayo | 0 | 67 | 67 |
2018 Abril | 0 | 76 | 76 |
2018 Marzo | 120 | 67 | 187 |
2018 Febrero | 639 | 48 | 687 |
2018 Enero | 536 | 66 | 602 |
2017 Diciembre | 494 | 64 | 558 |
2017 Noviembre | 593 | 128 | 721 |
2017 Octubre | 559 | 69 | 628 |
2017 Septiembre | 440 | 52 | 492 |
2017 Agosto | 427 | 54 | 481 |
2017 Julio | 466 | 73 | 539 |
2017 Junio | 422 | 86 | 508 |
2017 Mayo | 451 | 120 | 571 |
2017 Abril | 493 | 310 | 803 |
2017 Marzo | 398 | 228 | 626 |
2017 Febrero | 547 | 196 | 743 |
2017 Enero | 364 | 160 | 524 |
2016 Diciembre | 363 | 185 | 548 |
2016 Noviembre | 456 | 181 | 637 |
2016 Octubre | 514 | 217 | 731 |
2016 Septiembre | 532 | 77 | 609 |
2016 Agosto | 490 | 76 | 566 |
2016 Julio | 285 | 57 | 342 |
2016 Junio | 10 | 53 | 63 |
2016 Mayo | 10 | 56 | 66 |
2016 Abril | 4 | 10 | 14 |
2016 Marzo | 2 | 16 | 18 |
2016 Febrero | 8 | 7 | 15 |
2016 Enero | 4 | 8 | 12 |
2015 Diciembre | 12 | 6 | 18 |
2015 Noviembre | 16 | 3 | 19 |
2015 Octubre | 8 | 10 | 18 |
2015 Septiembre | 1 | 14 | 15 |
2015 Agosto | 7 | 9 | 16 |
2015 Julio | 300 | 2 | 302 |
2015 Junio | 243 | 21 | 264 |
2015 Mayo | 221 | 47 | 268 |
2015 Abril | 255 | 30 | 285 |
2015 Marzo | 277 | 22 | 299 |
2015 Febrero | 185 | 14 | 199 |
2015 Enero | 108 | 13 | 121 |
2014 Diciembre | 118 | 15 | 133 |
2014 Noviembre | 115 | 24 | 139 |
2014 Octubre | 101 | 13 | 114 |
2014 Septiembre | 86 | 20 | 106 |
2014 Agosto | 90 | 17 | 107 |
2014 Julio | 87 | 20 | 107 |
2014 Junio | 78 | 13 | 91 |
2014 Mayo | 126 | 24 | 150 |
2014 Abril | 74 | 12 | 86 |
2014 Marzo | 91 | 26 | 117 |
2014 Febrero | 79 | 21 | 100 |
2014 Enero | 78 | 22 | 100 |
2013 Diciembre | 56 | 13 | 69 |
2013 Noviembre | 67 | 30 | 97 |
2013 Octubre | 76 | 38 | 114 |
2013 Septiembre | 38 | 41 | 79 |
2013 Agosto | 1 | 0 | 1 |