Department of Surgery and Epidemiology and Biostatistics, Western University, London, Ontario, Canada.
Department of Urology, University Hospital, Ostrava, Czech Republic.
Neurourol Urodyn. 2024 Apr;43(4):803-810. doi: 10.1002/nau.25439. Epub 2024 Mar 13.
Our objective was to conduct an individual patient data meta-analysis (IPDMA) of the two published randomized placebo-controlled trials of mirabegron in people with neurogenic lower urinary tract dysfunction (NLUTD) due to spinal cord injury (SCI) or multiple sclerosis (MS).
We identified two randomized, placebo-controlled trials. We extracted individual patient data from the trials and evaluated two primary outcomes: change in maximum cystometric capacity and change in the patient perception of bladder condition (PPBC). We also evaluated several secondary outcomes related to urodynamic function and quality of life. We conducted three exploratory analyses to test hypotheses based on our clinical experiences with mirabegron in NLUTD. Analysis of covariance with adjustment for baseline values was used for the statistical analysis.
Our IPDMA included 98 patients from the two trials. The results showed that mirabegron was associated with a significant improvement in maximum cystometric capacity (+41 mL, p = 0.04) and in the PPBC (-0.8, p < 0.01) compared to placebo. Secondary outcomes including peak neurogenic detrusor overactivity pressure (-20 cm HO, p < 0.01), incontinence-QOL score (+12, p < 0.01), and 24 h pad weights (-79 g, p = 0.04) also improved significantly compared to placebo. Exploratory analyses found similar improvements in people with MS and SCI; some outcomes improved to a greater degree among people with incomplete SCI, or SCIs that were below T7.
Our IPDMA provides evidence supporting the use of mirabegron in patients with NLUTD due to SCI or MS. Further work evaluating differential responses in people with different SCI lesion characteristics may be warranted.
我们的目的是对两项已发表的米拉贝隆治疗脊髓损伤(SCI)或多发性硬化症(MS)相关神经源性下尿路功能障碍(NLUTD)的随机安慰剂对照试验进行个体患者数据荟萃分析(IPDMA)。
我们确定了两项随机、安慰剂对照试验。我们从这些试验中提取了个体患者数据,并评估了两个主要结局:最大膀胱容量的变化和患者对膀胱状况的感知(PPBC)的变化。我们还评估了与尿动力学功能和生活质量相关的几个次要结局。我们进行了三项探索性分析,以根据我们在 NLUTD 中使用米拉贝隆的临床经验检验假设。使用协方差分析并根据基线值进行调整进行统计分析。
我们的 IPDMA 纳入了两项试验中的 98 名患者。结果表明,与安慰剂相比,米拉贝隆治疗后最大膀胱容量显著增加(+41ml,p=0.04),PPBC 显著改善(-0.8,p<0.01)。与安慰剂相比,其他次要结局也有显著改善,包括高峰神经源性逼尿肌过度活动压力(-20cmH2O,p<0.01)、尿失禁生活质量评分(+12,p<0.01)和 24 小时尿垫重量(-79g,p=0.04)。探索性分析发现,MS 和 SCI 患者的改善情况相似;在不完全性 SCI 或 T7 以下 SCI 患者中,某些结局的改善程度更大。
我们的 IPDMA 提供了米拉贝隆治疗 SCI 或 MS 相关 NLUTD 患者的证据。可能需要进一步评估不同 SCI 病变特征患者的不同反应。