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Botulinum toxin A for the treatment of neurogenic detrusor overactivity in multiple sclerosis patients
Deffontaines-Rufin, S; Weil, M; Verollet, D; Peyrat, L; Amarenco, G.
  • Deffontaines-Rufin, S; Hôpital TENON. Service d'urologie. Service de Rééducation Neurologique et d'Explorations Périnéales. Paris. FR
  • Weil, M; Hôpital TENON. Service d'urologie. Service de Rééducation Neurologique et d'Explorations Périnéales. Paris. FR
  • Verollet, D; Hôpital TENON. Service d'urologie. Service de Rééducation Neurologique et d'Explorations Périnéales. Paris. FR
  • Peyrat, L; Hôpital TENON. Service d'urologie. Service de Rééducation Neurologique et d'Explorations Périnéales. Paris. FR
  • Amarenco, G; Hôpital TENON. Service d'urologie. Service de Rééducation Neurologique et d'Explorations Périnéales. Paris. FR
Int. braz. j. urol ; 37(5): 642-648, Sept.-Oct. 2011. tab
Artículo en Inglés | LILACS | ID: lil-608134
ABSTRACT

PURPOSE:

Neurogenic detrusor overactivity (NDO) is common in patients who suffer from multiple sclerosis (MS). When the usual pharmacological treatment fails, botulinum toxin type A (BTX-A) injections can be proposed. The safety and efficacy of this treatment are already well known, but only a few studies focus on its use in patients with MS. MATERIALS AND

METHODS:

Seventy-one patients with MS underwent their first BTX-A injection for refractory NDO. They had clinical and urodynamic cystometry assessment before and three months after injection. The patients were divided in three groups according to treatment efficacy full success (total urinary continence, no overactive detrusor), improvement, or total failure (urge incontinence and overactive detrusor).

RESULTS:

77 percent of the patients had clinical improvement or full success of the treatment with a reduction of their urgency and incontinence. Significant urodynamic improvement after treatment was shown on different parameters volume at first involuntary bladder contraction (p = 0.0000001), maximum cystometric capacity (p = 0.0035), maximum detrusor pressure (p = 0.0000001). 46 percent of the patients were in the "full success" group. 31 percent of the patients had a partial improvement. 23 percent of the patients had no efficacy of the treatment. Duration of MS was a predictive factor of treatment failure (p = 0.015).

CONCLUSIONS:

Despite that a full success was obtained in 46 percent of the cases, BTX-A injection therapy failed to treat refractory NDO in 23 percent of patients suffering from MS. Duration of the disease was a predictive factor for an inefficient treatment. The injection therapy should be considered as soon as oral anticholinergic drugs fail to reduce NDO.
Asunto(s)


Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Vejiga Urinaria Neurogénica / Toxinas Botulínicas Tipo A / Vejiga Urinaria Hiperactiva / Esclerosis Múltiple / Fármacos Neuromusculares Tipo de estudio: Estudio observacional / Estudio pronóstico / Factores de riesgo Límite: Femenino / Humanos / Masculino Idioma: Inglés Revista: Int. braz. j. urol Asunto de la revista: Urología Año: 2011 Tipo del documento: Artículo País de afiliación: Francia Institución/País de afiliación: Hôpital TENON/FR

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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Vejiga Urinaria Neurogénica / Toxinas Botulínicas Tipo A / Vejiga Urinaria Hiperactiva / Esclerosis Múltiple / Fármacos Neuromusculares Tipo de estudio: Estudio observacional / Estudio pronóstico / Factores de riesgo Límite: Femenino / Humanos / Masculino Idioma: Inglés Revista: Int. braz. j. urol Asunto de la revista: Urología Año: 2011 Tipo del documento: Artículo País de afiliación: Francia Institución/País de afiliación: Hôpital TENON/FR