Marchand Greg, Masoud Ahmed Taher, Govindan Malini, Ware Kelly, King Alexa, Ruther Stacy, Brazil Giovanna, Cieminski Kaitlynne, Calteux Nicolas, Coriell Catherine, Ulibarri Hollie, Parise Julia, Arroyo Amanda, Chen Diana, Pierson Maria, Rafie Rasa, Sainz Katelyn
Marchand Institute for Minimally Invasive Surgery, Mesa, AZ (Drs Marchand, Masoud, and Govindan, MsesWare, King, Ruther, Brazil, andCieminski, MrCalteux, MsesCoriell, Ulibarri, Parise, and Arroyo, and Dr Sainz).
Fayoum University Faculty of Medicine, Fayoum, Egypt (Dr Masoud).
AJOG Glob Rep. 2021 Dec 10;2(1):100042. doi: 10.1016/j.xagr.2021.100042. eCollection 2022 Feb.
While widely used for the treatment of chronic pelvic pain, limited data exists on efficacy of gabapentin, especially in the subgroup of women suffering from chronic pelvic pain without a known diagnosis, such as endometriosis.
This study aimed to assess the efficacy of gabapentin when administered to women with chronic pelvic pain without another diagnosis.
We performed a Systematic Review and Meta Analysis including all controlled clinical trials addressing the use of gabapentin for the treatment of chronic pelvic pain without another diagnosis. We searched PubMed, Scopus, Web of Science, ClinicalTrials.Gov, MEDLINE, and The Cochrane Library from inception of each database to April 30, 2021. We included all the studies that fulfilled the following criteria: (1) population: women suffering from chronic pelvic pain without another identified diagnosis (such as endometriosis); (2) intervention: gabapentin (regardless of the dosage); (3) comparator:placebo; (4) outcomes: pain score (visual analog scale) after 3 months and pain score (visual analog scale) after 6 months as primary outcomes; and (5) study design: we only included randomized or controlled clinical trials. Our exclusion criteria included (1) uncontrolled clinical trials, (2) studies that did not report data or measures for any of our selected outcomes, (3) studies that included patients with surgically or clinically diagnosed endometriosis, or (4) studies with no full-text manuscript available. Risk of bias assessment was performed using the Cochrane risk of bias tool. We analyzed dichotomous outcomes as percentages and totals, whereas continuous outcomes were analyzed using mean difference, standard deviations, and relative 95% confidence intervals using the inverse variance method.
We included 4 placebo-controlled randomized controlled trials. Analysis was hindered because half of the studies (n=2) used the visual analog scale pain score and the other half (n=2) used the numerical rating scale. The analysis showed that when compared with the placebo, gabapentin significantly lowered the visual analog scale pain score at 3 months (mean difference, 0.79; 1.23 to 0.35; =.005) and 6 months (mean difference, 1.68; 2.30 to 1.05; =.001) and the numerical rating scale pain score at 3 months (mean difference, 0.20; 0.25 to 0.15; =.001). However, in terms of the numerical rating scale pain score after 6 months, the 2 groups showed no significant difference (mean difference, 0.27; 0.80 to 0.26; =.32).
Gabapentin may hold benefit for the management of chronic pelvic pain, with significant improvement in pain seen in both scales at 3 months when compared with the placebo, but only in the visual analog scale group at 6 months of usage. Secondary to the differences in the nature of the 2 scales, a further weighted combined analysis was not possible.
虽然加巴喷丁广泛用于治疗慢性盆腔疼痛,但关于其疗效的数据有限,尤其是在患有慢性盆腔疼痛但未明确诊断(如子宫内膜异位症)的女性亚组中。
本研究旨在评估加巴喷丁用于无其他诊断的慢性盆腔疼痛女性的疗效。
我们进行了一项系统评价和荟萃分析,纳入所有探讨加巴喷丁用于治疗无其他诊断的慢性盆腔疼痛的对照临床试验。我们检索了从每个数据库建立至2021年4月30日的PubMed、Scopus、Web of Science、ClinicalTrials.Gov、MEDLINE和Cochrane图书馆。我们纳入了所有符合以下标准的研究:(1)研究对象:患有慢性盆腔疼痛但无其他明确诊断(如子宫内膜异位症)的女性;(2)干预措施:加巴喷丁(无论剂量);(3)对照:安慰剂;(4)结局指标:3个月后的疼痛评分(视觉模拟量表)和6个月后的疼痛评分(视觉模拟量表)作为主要结局指标;(5)研究设计:我们仅纳入随机或对照临床试验。我们的排除标准包括:(1)非对照临床试验;(2)未报告我们所选任何结局指标数据或测量值的研究;(3)纳入手术或临床诊断为子宫内膜异位症患者的研究;(4)无全文手稿的研究。使用Cochrane偏倚风险工具进行偏倚风险评估。我们将二分法结局分析为百分比和总数,而连续结局则使用逆方差法分析平均差、标准差和相对95%置信区间。
我们纳入了4项安慰剂对照的随机对照试验。分析受到阻碍,因为一半的研究(n = 2)使用视觉模拟量表疼痛评分,另一半(n = 2)使用数字评定量表。分析表明,与安慰剂相比,加巴喷丁在3个月时显著降低了视觉模拟量表疼痛评分(平均差,0.79;1.23至0.35;P = 0.005)和6个月时的评分(平均差,1.68;2.30至1.05;P = 0.001),以及3个月时的数字评定量表疼痛评分(平均差,0.20;0.25至0.15;P = 0.001)。然而,在6个月后的数字评定量表疼痛评分方面,两组无显著差异(平均差,0.27;0.80至0.26;P = 0.32)。
加巴喷丁可能对慢性盆腔疼痛的管理有益,与安慰剂相比,在3个月时两种量表的疼痛均有显著改善,但仅在使用6个月时视觉模拟量表组有改善。由于两种量表性质不同,无法进行进一步的加权合并分析。