Department of Obstetrics and Gynecology, Duke University, Durham, North Carolina, USA.
Department of Obstetrics and Gynecology, University of New Mexico, Albuquerque, New Mexico, USA.
Eur Urol. 2018 Jul;74(1):66-73. doi: 10.1016/j.eururo.2018.02.011. Epub 2018 Feb 24.
Urgency urinary incontinence (UUI) is a chronic condition for which sacral neuromodulation (SNM) (InterStim/Medtronic) and onabotulinumtoxinA (BTX) (BotoxA/Allergan) are utilized. These therapies have not been compared over extended time.
To compare UUI episodes (UUIE) over 24 mo following SNM or BTX.
DESIGN, SETTING, AND PARTICIPANTS: Multicenter, open-label, randomized, extension trial (February 2012-July 2016) at nine US medical centers involving 386 women with ≥6 UUIE over 3 d inadequately managed by medications. Participants were clinical responders to treatment: ≥50% reduction in UUIEs after SNM placement or 1 mo post BTX.
SNM (n=194) versus 200 U BTX (n=192). SNM reprogrammings occurred throughout the 24 mo. After 6 mo, two additional BTX injections were allowed.
Primary outcome: change in mean daily UUIE over 24 mo.
no UUIE, ≥75% and ≥50% UUIE reduction; Overactive Bladder Questionnaire Short Form; Urinary Distress Inventory short form; Incontinence Impact Questionnaire; Patient Global Impression of Improvement; Overactive Bladder Satisfaction of Treatment Questionnaire; and adverse events (AEs). Primary analysis used a linear mixed model.
Outcome data were available for 260/298 (87%) clinical responders. No difference in decreased mean UUIE was found over 24 mo (-3.88 vs -3.50 episodes/d,95% confidence interval [CI]=-0.14-0.89; p=0.15), with no differences in UUI resolution, ≥75% or ≥50% UUIE reduction. BTX group maintained higher satisfaction (mean difference=-9.14, 95% CI=-14.38--3.90; p<0.001), treatment endorsement (mean difference=-12.16, 95% CI=-17.7--6.63; p<0.001) through 24 mo. Other secondary measures did not differ. Recurrent urinary tract infections (UTIs) were higher after BTX (24% vs 10%; p<0.01), 6% required intermittent catheterization post second injection. SNM revision and removals occurred in 3% and 9% patients, respectively.
Both treatments offered sustainable UUI improvement, and higher BTX dosing had low clean intermittent catheterization rates, but with UTI risk. SNM revision/removal rates were low due to standardized lead placement with strict treatment response definitions.
We compared a large group of US women with severe urgency urinary incontinence (UUI) who received sacral neuromodulation (InterStim) or onabotulinumtoxinA (Botox A) therapy during a 2-yr period. We found that both therapies had similar success in reducing UUI symptoms, and adverse events were low. However, women in the BotoxA group had higher satisfaction and endorsement with their treatment, but with a higher chance of a urinary tract infection. We conclude that both therapies offer sustained reduction in daily incontinence over 2 yr.
急迫性尿失禁(UUI)是一种慢性疾病,可采用骶神经调节(SNM)(InterStim/Medtronic)和注射用肉毒毒素 A(BTX)(BotoxA/Allergan)进行治疗。这两种治疗方法在较长时间内尚未进行比较。
比较 SNM 或 BTX 治疗后 24 个月的 UUI 发作(UUIE)。
设计、地点和参与者:这是一项多中心、开放标签、随机、扩展试验(2012 年 2 月至 2016 年 7 月),在美国 9 家医疗中心进行,涉及 386 名女性,这些女性患有≥6 次的 UUI,且在药物治疗下不能得到充分控制,持续时间至少 3 天。参与者为治疗的临床应答者:SNM 放置后或 BTX 注射后 1 个月 UUIE 减少≥50%。
SNM(n=194)与 200U BTX(n=192)。在整个 24 个月中对 SNM 进行重新编程。6 个月后,允许再进行两次 BTX 注射。
主要结局:24 个月内平均每日 UUIE 的变化。次要结局:无 UUIE、≥75%和≥50%的 UUIE 减少;膀胱过度活动症问卷短表;尿失禁困扰量表;尿失禁对生活质量的影响问卷;患者总体改善印象;膀胱过度活动症治疗满意度问卷;以及不良事件(AE)。主要分析采用线性混合模型。
对 260/298(87%)临床应答者的结局数据进行了分析。在 24 个月内,UUIE 减少的平均值没有差异(-3.88 与-3.50 次/天,95%置信区间[-0.14,0.89];p=0.15),UUI 缓解、≥75%或≥50%的 UUIE 减少没有差异。BTX 组的满意度(平均差值=-9.14,95%置信区间[-14.38,-3.90];p<0.001)和治疗认可(平均差值=-12.16,95%置信区间[-17.7,-6.63];p<0.001)在 24 个月内保持较高水平。其他次要措施没有差异。BTX 组(24%比 10%)发生复发性尿路感染(UTI)的比例更高(p<0.01),6%的患者在第二次注射后需要间歇性导尿。SNM 修订和移除分别发生在 3%和 9%的患者中。
这两种治疗方法均能持续改善 UUI,BTX 高剂量治疗的清洁间歇性导尿率较低,但有 UTI 风险。由于采用了标准化的导联放置,并严格定义了治疗反应,SNM 修订/移除率较低。
我们比较了一组来自美国的严重急迫性尿失禁(UUI)女性患者,她们在 2 年期间接受了骶神经调节(InterStim)或注射用肉毒毒素 A(BotoxA)治疗。我们发现,这两种治疗方法在减少 UUI 症状方面都有相似的效果,不良事件发生率较低。然而,BTX 组的女性对治疗的满意度和认可程度更高,但发生尿路感染的几率更高。我们的结论是,这两种治疗方法都能在 2 年内持续减少每日失禁次数。