Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Beijing University of Chinese Medicine, Beijing, China.
BMC Complement Med Ther. 2020 Oct 7;20(1):303. doi: 10.1186/s12906-020-03097-x.
Intrahepatic cholestasis of pregnancy (ICP) is a pregnancy complication whose range has been calculated to be between 0.01 and 15.6% all around the world. We wanted to systematically evaluate the effect and safety of oral herbal medicine on treatment for ICP.
Details of the methods could be found in the registered protocol on PROSPERO (CRD42018096013). Trials assessing the effectiveness of herbal medicine for ICP were searched from seven electronic databases from inception to 28th February 2020. RevMan 5.3 software was used to perform all statistical analysis. Meta-analysis, additional analysis, Trial Sequential Analysis (TSA) and Grading of Recommendations Assessment, Development and Evaluation (GRADE) were conducted if data permitted.
Totally 43 randomized controlled trials with 3556 patients were included. Meta-analysis showed potential good adjunctive effect of herbal medicine on decreasing the pruritus scores (MD -0.58, 95% CI - 0.79 to - 0.36), the serum TBA scores (MD - 3.99 μmol/L, 95% CI - 4.24 to - 3.74) on the basis with Ursodesoxycholic acid. Compared to the medicine alone, significantly lower incidence of fetal distress (RR 0.41, 95% CI 0.32 to 0.51), asphyxia neonatorum (RR 0.35, 95%CI 0.25 to 0.49), cesarean section (RR 0.73, 95% CI 0.63 to 0.85), postpartum hemorrhage (RR 0.45, 95% CI 0.28 to 0.72) were observed in the combination group. But the comparison between herbal medicine and medicine showed inconsistent results among trials. Insufficient information could be used to evaluate the safety of herbal medicine for ICP.
This review found the current evidence may support the effectiveness of combination of herbal medicine and conventional medicine for decreasing the maternal pruritus scores, the serum TBA, and the number of fetal distress, or asphyxia neonatorum events related to this condition (which was supported by TSA results). Since there were obvious statistical and clinical heterogeneity among trials, and the methodological quality of the included studies was poor, the level of the evidence could only be defined as "very low" according to the GRADE criteria. Further high quality studies are still needed to testify the effectiveness and safety of herbal medicine for ICP.
妊娠肝内胆汁淤积症(ICP)是一种妊娠并发症,其全球范围的发病率估计在 0.01%至 15.6%之间。我们旨在系统评估口服草药治疗 ICP 的疗效和安全性。
详细方法可在 PROSPERO(CRD42018096013)注册方案中找到。从七个电子数据库中检索了评估草药治疗 ICP 有效性的试验,检索时间从成立到 2020 年 2 月 28 日。如果数据允许,使用 RevMan 5.3 软件进行所有统计分析。如果数据允许,进行荟萃分析、附加分析、试验序贯分析(TSA)和推荐评估、制定和评估(GRADE)分级。
总共纳入了 43 项随机对照试验,共 3556 名患者。荟萃分析显示,在熊去氧胆酸基础上,草药联合治疗可能对降低瘙痒评分(MD-0.58,95%CI-0.79 至-0.36)和血清总胆汁酸(TBA)评分(MD-3.99μmol/L,95%CI-4.24 至-3.74)具有潜在的良好辅助作用。与单独用药相比,联合用药组胎儿窘迫(RR0.41,95%CI0.32 至 0.51)、新生儿窒息(RR0.35,95%CI0.25 至 0.49)、剖宫产(RR0.73,95%CI0.63 至 0.85)和产后出血(RR0.45,95%CI0.28 至 0.72)的发生率显著降低。但草药与药物的比较结果在各试验中不一致。由于缺乏足够的信息,无法评估 ICP 患者使用草药的安全性。
本综述发现,目前的证据可能支持在常规药物治疗的基础上联合使用草药来降低产妇瘙痒评分、血清 TBA 水平以及与该疾病相关的胎儿窘迫或新生儿窒息事件的发生率(这一结果得到了 TSA 结果的支持)。由于试验之间存在明显的统计学和临床异质性,且纳入研究的方法学质量较差,根据 GRADE 标准,证据水平只能定义为“极低”。仍需要高质量的研究来验证草药治疗 ICP 的有效性和安全性。