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Long-term results of oxybutynin use in treating facial hyperhidrosis
Wolosker, Nelson; Teivelis, Marcelo Passos; Krutman, Mariana; Campbell, Taiz Pereira Dozono de Almeida; Kauffman, Paulo; Campos, José Ribas de; Puech-Leão, Pedro.
Afiliação
  • Wolosker, Nelson; Hospital Israelita Albert Einstein. São Paulo. BR
  • Teivelis, Marcelo Passos; Hospital Israelita Albert Einstein. São Paulo. BR
  • Krutman, Mariana; Hospital Israelita Albert Einstein. São Paulo. BR
  • Campbell, Taiz Pereira Dozono de Almeida; Hospital Israelita Albert Einstein. São Paulo. BR
  • Kauffman, Paulo; Hospital Israelita Albert Einstein. São Paulo. BR
  • Campos, José Ribas de; Hospital Israelita Albert Einstein. São Paulo. BR
  • Puech-Leão, Pedro; Hospital Israelita Albert Einstein. São Paulo. BR
An. bras. dermatol ; 89(6): 912-916, Nov-Dec/2014. tab, graf
Artigo em Inglês | LILACS | ID: lil-727646
Biblioteca responsável: BR1.1
ABSTRACT

BACKGROUND:

Facial hyperhidrosis can lead to serious emotional distress. Video-assisted thoracic sympathectomy resolves symptoms effectively, though it may be associated with compensatory hyperhidrosis, which may be more common in patients undergoing resection of the second thoracic ganglion. Oxybutynin has been used as a pharmacological approach to facial hyperhidrosis but the long-term results of this treatment are unclear.

OBJECTIVE:

To evaluate the use of low oxybutynin doses in facial hyperhidrosis patients for at least six months.

METHODS:

61 patients were monitored for over six months and assessed according to the following variables impact of hyperhidrosis on quality of life (QOL) before treatment and after six weeks, evolution of facial hyperhidrosis after six weeks and at the last consultation, complaints of dry mouth after six weeks and on last return visit, and improvement at other hyperhidrosis sites.

RESULTS:

Patients were monitored for 6 to 61 months (median=17 months). Thirty-six (59%) were female. Age ranged from 17-74 (median45). Pre-treatment QOL was poor/very poor in 96.72%. After six weeks, 100% of patients improved QOL. Comparing results after six weeks and on the last visit, 91.8% of patients maintained the same category of improvement in facial hyperhidrosis, 3.3% worsened and 4.9% improved. Dry mouth complaints were common but not consistent throughout treatment. More than 90% of patients presented moderate/great improvement at other hyperhidrosis sites.

CONCLUSION:

Patients who had a good initial response to treatment maintained a good response long-term, did not display tachiphylaxis and experienced improvement on other hyperhidrosis sites. .
Assuntos


Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Antagonistas Muscarínicos / Hiperidrose / Ácidos Mandélicos Tipo de estudo: Estudo de avaliação Aspecto: Preferência do paciente Limite: Adolescente / Adulto / Idoso / Feminino / Humanos / Masculino Idioma: Inglês Revista: An. bras. dermatol Assunto da revista: Dermatologia Ano de publicação: 2014 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: Hospital Israelita Albert Einstein/BR

Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Assunto principal: Antagonistas Muscarínicos / Hiperidrose / Ácidos Mandélicos Tipo de estudo: Estudo de avaliação Aspecto: Preferência do paciente Limite: Adolescente / Adulto / Idoso / Feminino / Humanos / Masculino Idioma: Inglês Revista: An. bras. dermatol Assunto da revista: Dermatologia Ano de publicação: 2014 Tipo de documento: Artigo País de afiliação: Brasil Instituição/País de afiliação: Hospital Israelita Albert Einstein/BR
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