Eilber Karyn S, Brucker Benjamin M, Pezzella Andrea, Lucente Vincent, Benson Kevin, Kennelly Michael J
Department of Urology, Cedars-Sinai Medical Center, Los Angeles, CA 90211, USA.
Departments of Urology and Obstetrics and Gynecology, New York University Langone Health, New York, NY 10016, USA.
Toxins (Basel). 2025 Apr 21;17(4):207. doi: 10.3390/toxins17040207.
OnabotulinumtoxinA is an FDA-approved treatment for adults with overactive bladder (OAB) who have an inadequate response to, or are intolerant of, oral pharmacotherapies including anticholinergics or beta-3 agonists. However, procedural practices of onabotulinumtoxinA intradetrusor injection vary among practitioners and can affect patient experience. To address this, a panel of six high-volume intravesical onabotulinumtoxinA providers with 100 years of combined experience convened to discuss the best office practices when treating patients with OAB. These key best practices include counseling patients on available OAB therapies, including onabotulinumtoxinA, at the initial consultation in accordance with established AUA and SUFU guidelines in a way that is easily understood. An office setting is preferred over a hospital or surgery center when performing the procedure. Staff involvement, from scheduling to post-procedure, is essential for establishing the relationships necessary to optimize patient experience and encourage compliance and retreatment. Experts generally recommend using a viscous lidocaine bladder instillation for an anesthetic 15 min prior to the reconstitution of onabotulinumtoxinA with 5 to 10 mL of normal saline. A range of one to 20 injection sites is acceptable, with a smaller number preferred. Starting in the lower bladder, experts recommend using a slower speed of injection to improve distribution and decrease patient discomfort. Subsequent treatments should be regularly scheduled at six-month intervals with the option of re-treating earlier if symptoms return, but no sooner than 12 weeks. For office intravesical onabotulinumtoxinA procedures, optimization of the patient experience by the physician and their staff, starting with the initial visit through the post-treatment follow-up, is key to long-term patient compliance.
A型肉毒毒素是一种经美国食品药品监督管理局(FDA)批准的治疗方法,用于治疗膀胱过度活动症(OAB)的成人患者,这些患者对包括抗胆碱能药物或β-3激动剂在内的口服药物治疗反应不佳或不耐受。然而,A型肉毒毒素膀胱逼尿肌内注射的操作方法在不同从业者之间存在差异,这可能会影响患者体验。为了解决这个问题,由六位经验丰富的高剂量膀胱内注射A型肉毒毒素提供者组成的小组(他们总共拥有100年的经验)召开会议,讨论治疗OAB患者时的最佳门诊操作方法。这些关键的最佳操作方法包括在初次咨询时,按照美国泌尿外科学会(AUA)和美国女性泌尿外科医师协会(SUFU)既定的指南,以易于理解的方式向患者介绍可用的OAB治疗方法,包括A型肉毒毒素。进行该操作时,门诊环境比医院或手术中心更可取。从安排预约到术后护理,工作人员的参与对于建立优化患者体验、鼓励依从性和再次治疗所需的关系至关重要。专家通常建议在将A型肉毒毒素用5至10毫升生理盐水复溶前15分钟,使用粘性利多卡因膀胱灌注进行麻醉。一到二十个注射部位的范围都是可以接受的,较少的数量更可取。从膀胱下部开始,专家建议使用较慢的注射速度,以改善药物分布并减轻患者不适。后续治疗应定期每六个月安排一次,如果症状复发,可以选择提前再次治疗,但最早不早于12周。对于门诊膀胱内注射A型肉毒毒素的操作,医生及其工作人员从初次就诊到治疗后随访对患者体验进行优化,是患者长期依从性的关键。