“…Further studies are needed to determine if lower BTX-A doses will have the same bene¢cial e¡ects, while avoiding the need for intermittent selfcatheterization or other forms of urinary drainage. In the present study, the duration of the BTX-A e¡ect in idiopathic as well as in neurogenic detrusor overactivity was similar to that observed by Kuo [2004] but less than reported in other studies [Schurch et al, 2000a,b;Radziszewski and Borkowski, 2002;Schulte-Baukloh et al, 2002Chancellor et al, 2003;Loch et al, 2003;Riccabona et al, 2004;Schmid et al, 2004]. Although di¡erences in baseline characteristicsöespecially in the neurogenic group considering that our study included only two patients with spinal cord injury and none with myelomeningoceleömay be assumed, the exact reason for this phenomenon remains unclear.…”
BTX-A injections into the detrusor have a significant and comparable but temporally limited effect in idiopathic and neurogenic detrusor overactivity resistant to anticholinergic treatment.
“…Further studies are needed to determine if lower BTX-A doses will have the same bene¢cial e¡ects, while avoiding the need for intermittent selfcatheterization or other forms of urinary drainage. In the present study, the duration of the BTX-A e¡ect in idiopathic as well as in neurogenic detrusor overactivity was similar to that observed by Kuo [2004] but less than reported in other studies [Schurch et al, 2000a,b;Radziszewski and Borkowski, 2002;Schulte-Baukloh et al, 2002Chancellor et al, 2003;Loch et al, 2003;Riccabona et al, 2004;Schmid et al, 2004]. Although di¡erences in baseline characteristicsöespecially in the neurogenic group considering that our study included only two patients with spinal cord injury and none with myelomeningoceleömay be assumed, the exact reason for this phenomenon remains unclear.…”
BTX-A injections into the detrusor have a significant and comparable but temporally limited effect in idiopathic and neurogenic detrusor overactivity resistant to anticholinergic treatment.
“…Les études suivantes [20,21] ont confirmé l'efficacité de cette technique dans cette indication, avec des doses moindres que dans les vessies neurogènes (200 UI Botox ® en quarante sites) et avec environ 60 % d'amélioration (mais 20 % de rétention transitoire) évaluée sur des échelles de symptômes et de qualité de vie (UDI/IIQ). D'autres études sont désormais disponibles [22][23][24][25], faisant état de 80 % de succès clinique et urodynamique pour des doses allant de 100 à 300 UI Botox ® , avec des taux de rétention de 5 %.…”
Section: Tb Et Autres Indications Périnéalesunclassified
Service de Rééducation neurologique et d'Explorations périnéales, Hôpital Rothschild, Assistance Publique-Hôpitaux de Paris, Unité Inserm U731/Université Pierre-et-Marie-Curie, 33 boulevard de Picpus, 75571 Paris Cedex 12 Résumé : La toxine botulique (TB) est une nouvelle et prometteuse technique de traitement d'une grande variété de troubles du bas appareil urinaire et du périnée. La TB a été initialement proposée dans le traitement des hyperactivités détrusoriennes neurologiques et des dyssynergies vésico-sphinctériennes. Désormais, elle est essayée dans d'autres troubles urologiques (instabilité vésicale idiopathique, dyssynergie fonctionnelle, hypertrophie bénigne de la prostate, cystite interstitielle) et périnéaux (anisme, vaginisme).Abstract: Botulinum toxin (BT) is a novel and promising treatment for a variety of lower urinary tract dysfunctions and perineal disorders. Botulinum toxin was initially applied in the bladder of patients with spinal neurogenic detrusor overactivity and in cases of detrusor external sphincter dyssynergia. Now, application of botulinum toxin is extended to the treatment of other urological disorders including non-neurogenic detrusor overactivity, non-relaxing urethral sphincter, detrusor underactivity, benign prostatic hyperplasia, interstitial cystitis and other perineal disorders (anismus, vaginismus).
“…Radziszewski and Borkowski [2002] [abstract] reported that intradetrusal injections with botulinum toxin A 300 U [Dysport, Ipsen Ltd, Slough, Berkshire, UK; it is generally considered that 1 U of Botox is equivalent to 3^4 U of Dysport: Odergren et al, 1998], in 12 patients with IDO refractory to anticholinergics, improved symptoms such as frequency, urgency, and incontinence as well as increasing mean maximum cystometric capacity (321.2^408.3 ml). Similarly, Loch et al [2003] [abstract] has reported successful outcomes using an intradetrusal injection of 200 U (Botox, Allergan) in his series of patients with NDO and IDO with urge incontinence. Zermann et al [2001] [abstract] performed intradetrusal injections of the botulinum toxin A into the trigone of seven patients with urgency-frequency-syndrome refractory to anticholinergics.…”
Application of botulinum toxin in the lower urinary tract has produced promising results in treating lower urinary tract dysfunction, which needs further evaluation with randomised, placebo-controlled trials.
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