Springer Nature medical video. Intradetrusor botulinum toxin injection / produced by Springer Nature.

Botulinum toxin-A is a potent neurotoxin produced by Clostridium botulinum that is an effective, minimally invasive treatment option for patients with pharmacologically refractory overactive bladder (OAB). OAB is a syndrome that is characterised by urgency and frequency with or without urgency urina...

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Format: Video
Language:English
Published: Dordrecht, South Holland : Springer Nature, 2022.
Series:Springer Nature Medical Video
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Online Access:Click for online access

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520 |a Botulinum toxin-A is a potent neurotoxin produced by Clostridium botulinum that is an effective, minimally invasive treatment option for patients with pharmacologically refractory overactive bladder (OAB). OAB is a syndrome that is characterised by urgency and frequency with or without urgency urinary incontinence (UUI). Its prevalence among the global population approaches 11 % and the female to male ratio is approximately 3:2. OAB is associated with significant decrease in quality of life (QoL) in terms of health. Initial treatment for OAB includes conservative and oral pharmacological treatments. Onabotulinum toxin A (BoNT-A), is the only licensed formulation of botulinum toxin A, for idiopathic UUI at 100 units with the small risk of urinary retention (approximately 10%). Therefore patients should be able and willing to perform intermittent catheterization, before administration. In addition, the injections must be repeated on average every 6 to 9 months. This video gives a comprehensive overview of understanding the concept, evaluation and selection of patient, detailed operative technique with clear demonstration of tips to avoid potential complications and postoperative care. It will be helpful for all those specialists, who are dealing with Female Urology (Urogynecologists, female urologists, minimally invasive pelvic surgeons, reconstructive surgeons, general urologists, general gynecologists, medical students, residents, patients). It is included as the third line management for Urge urinary incontinence, in most of the recently published standard guidelines and is US Food and Drug Administration (FDA) approved. 
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