Botulinum toxin type B: a new therapy for axillary hyperhidrosis

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Summary

Primary axillary hyperhidrosis is a disorder affecting mainly adolescents with significant adverse effects on quality of life. No ideal treatment exists, although recent data has demonstrated Botulinum toxin type A (Botox) as a treatment option. However, antibody formation may lead to loss of clinical benefit over time. Botulinum toxin type B (Neurobloc) has recently been introduced and may induce less immunogenic response.

Objective

To investigate the efficacy of Neurobloc for axillary hyperhidrosis.

Method

Thirteen patients (22 axillae) were recruited to the study. The hyperhidrotic area was defined using the iodine-starch test then measured and photographed. 5000 MU of Neurobloc was administered subdermally. Patients were reviewed at 4, 8 and 12 weeks to assess outcome objectively (hyperhidrotic area measurements and photographs) and subjectively (sweat production and patient satisfaction).

Results

There was a significant reduction in hyperhidrotic area at follow-up compared to baseline. Mean percentage reduction in hyperhidrotic area was 84, 87 and 81% at 4, 8 and 12 weeks (p=0.001, paired t test). Patient satisfaction was 100% throughout. Subjective mean percentage reduction in sweat production was 98, 96 and 90 at 4, 8 and 12 weeks. Side effects were minimal.

Conclusion

Neurobloc is an effective treatment for axillary hyperhidrosis.

Section snippets

Study design

Flow diagram of participant selection

Full ethical approval for the project was granted.

Procedure

The hyperhidrotic area for treatment was defined by Minor's iodine starch test under standardised conditions. The area of demarcation was marked, measured and photographed (Photo 1). The marked area was divided into equal sections. A total of 5000 units of botulinum toxin type B were injected subdermally into each axilla. The botulinum toxin was diluted with 0.9% saline and distributed into five 1 ml insulin

Participants

A total of 13 patients (22 axillae) were entered into the trial (Table 1). Three patients did not satisfy the study criteria.

Efficacy

All patients responded to treatment with a rapid onset of improvement of symptoms within one day. After injection of botulinum toxin type B, all patients had a significant reduction in hyperhidrotic area at 4, 8 and 12 weeks compared to baseline (Graph 1, p=0.0001).

The mean hyperhidrotic area at baseline was 88.1 cm2 (Graph 2). There was a reduction in mean hyperhidrotic

Primary findings

Our results show significant reduction in hyperhidrotic area and improvement in reported patient symptoms compared to baseline following injection of 5000 MU of botulinum toxin type B intradermally into the axillae of patients with primary axillary hyperhidrosis. The onset of action was rapid and the effects were maintained for the duration of the trial follow-up. These results are comparable with other studies investigating the efficacy of botulinum toxin type A for axillary hyperhidrosis.9, 10

Acknowledgements

Vascular Unit, Aberdeen Royal Infirmary. Funding from Elan pharmaceuticals.

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Presented at British Association of Plastic Surgeons Summer Meeting 2003.

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