Department of Anesthesiology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, 12 Jichang Road, Guangzhou, Guangdong, 510405, People's Republic of China.
Int Urogynecol J. 2022 May;33(5):1071-1081. doi: 10.1007/s00192-021-05017-0. Epub 2022 Jan 11.
Chronic pelvic pain (CPP) affects 2.1-24% of women, causing physical and psychological damage to women around the world. Based on the efficacy of gabapentin in the treatment of chronic pain, we conducted this study to evaluate the efficacy and safety of gabapentin in reducing pain in women with CPP.
Systematic searches were performed in the electronic databases of PubMed, Embase, Web of Science, Scopus, Cochrane, and Clinicalkey databases. Studies focused on comparing the efficacy of gabapentin and placebo in the treatment of female CPP patients were included. RevMan 5.4 was used to analyze the results and risk of bias. Two investigators independently selected eligible studies and extracted related pain scores and side effects for meta-analysis.
In total, 4 RCTs were enrolled in the meta-analysis, totaling 425 patients. Among patients receiving gabapentin, the average pain scores in 3 and 6 months were significantly lower than those in the placebo group(p < 0.00001). The results showed that there was no statistical difference between gabapentin and placebo in the reduction of pain scores from baseline(p = 0.41). The incidence of side effects in the gabapentin group was significantly higher than that in the placebo group (p < 0.00001).
This systematic review and meta-analysis demonstrated that for women with CPP, gabapentin was significantly different from placebo in average pain scores at 3 and 6 months. However, the two drugs did not differ in the reduction in pain scores from baseline. Gabapentin can bring more significant side effects, whether they are common side effects or serious side effects.
慢性盆腔疼痛(CPP)影响 2.1-24%的女性,给全球女性带来身体和心理伤害。基于加巴喷丁治疗慢性疼痛的疗效,我们进行了这项研究,以评估加巴喷丁降低 CPP 女性疼痛的疗效和安全性。
在 PubMed、Embase、Web of Science、Scopus、Cochrane 和 Clinicalkey 数据库中进行系统检索。纳入了比较加巴喷丁和安慰剂治疗女性 CPP 患者疗效的研究。使用 RevMan 5.4 分析结果和偏倚风险。两名调查员独立选择合格的研究,并提取相关疼痛评分和副作用进行荟萃分析。
共有 4 项 RCT 纳入荟萃分析,总计 425 名患者。接受加巴喷丁治疗的患者,3 个月和 6 个月时的平均疼痛评分明显低于安慰剂组(p<0.00001)。结果表明,加巴喷丁与安慰剂在基线时疼痛评分的降低方面无统计学差异(p=0.41)。加巴喷丁组的副作用发生率明显高于安慰剂组(p<0.00001)。
本系统评价和荟萃分析表明,对于 CPP 女性,加巴喷丁在 3 个月和 6 个月时的平均疼痛评分与安慰剂显著不同。然而,两种药物在基线时疼痛评分的降低方面没有差异。加巴喷丁可能带来更显著的副作用,无论是常见副作用还是严重副作用。