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Long-term results of the use of oxybutynin for the treatment of axillary hyperhidrosis.
Wolosker, Nelson; Teivelis, Marcelo Passos; Krutman, Mariana; de Paula, Rafael Pessanha; Kauffman, Paulo; de Campos, José Ribas M; Puech-Leão, Pedro.
Afiliación
  • Wolosker N; Hospital Israelita Albert Einstein-HIAE, São Paulo, São Paulo, Brazil; Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo-HCFMUSP, São Paulo, São Paulo, Brazil.
  • Teivelis MP; Hospital Israelita Albert Einstein-HIAE, São Paulo, São Paulo, Brazil. Electronic address: dr.marcelo@consultoriovasculares.med.br.
  • Krutman M; Hospital Israelita Albert Einstein-HIAE, São Paulo, São Paulo, Brazil.
  • de Paula RP; Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo-HCFMUSP, São Paulo, São Paulo, Brazil.
  • Kauffman P; Hospital Israelita Albert Einstein-HIAE, São Paulo, São Paulo, Brazil.
  • de Campos JR; Hospital Israelita Albert Einstein-HIAE, São Paulo, São Paulo, Brazil; Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo-HCFMUSP, São Paulo, São Paulo, Brazil.
  • Puech-Leão P; Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo-HCFMUSP, São Paulo, São Paulo, Brazil.
Ann Vasc Surg ; 28(5): 1106-12, 2014 Jul.
Article en En | MEDLINE | ID: mdl-24512855
ABSTRACT

BACKGROUND:

Axillary hyperhidrosis (AH) is a common disease, with a significant impact on quality of life (QOL). Good short-term results are reported with oxybutynin, but longer follow-up data are lacking. We evaluated its effectiveness in a large series of patients who were not surgically treated and who had at least 6 months of follow-up.

METHODS:

From September 2007 to September 2013, 431 consecutive patients were enrolled in "pharmacological first" protocol for treatment of AH with oxybutynin. Thirty-four patients were lost to follow-up, and data are available for 397 patients treated for at least 6 weeks. Data at the start of the protocol, 6 weeks after beginning treatment, and at final visit were analyzed.

RESULTS:

One hundred fourteen patients (28.7%) did not improve and were referred for surgery (sympathectomy). Eight patients (2.01%) presented significant side effects (e.g. dry mouth) and discontinued therapy. Twenty-six patients (9.4%) preferred surgery over pharmacologic treatment. Sixty-two patients have not yet been under treatment for 6 months. The 181 patients with more than 6 months of follow-up (median 17 months, range 6-72) were analyzed as follows 82.9% of patients presented moderate or great improvement in AH and 89% of patients presented improvement in other sites of hyperhidrosis after a median of 17 months.

CONCLUSIONS:

In patients with good initial response to oxybutynin, >80% presented moderate or great improvement in axillary and in other sites of excessive sweating. Results were particularly better in women and those who presented better QOL after 6 weeks.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sudoración / Hiperhidrosis / Ácidos Mandélicos Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Vasc Surg Asunto de la revista: ANGIOLOGIA Año: 2014 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sudoración / Hiperhidrosis / Ácidos Mandélicos Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Vasc Surg Asunto de la revista: ANGIOLOGIA Año: 2014 Tipo del documento: Article País de afiliación: Brasil