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固肾安胎丸联合地屈孕酮治疗先兆流产的疗效与安全性:一项系统评价和Meta分析

Efficacy and safety of Gushen Antai Pills combined with dydrogesterone in the treatment of threatened miscarriage: a systematic review and meta-analysis.

作者信息

Chen Kai, Liu Xiaoxia, Meng Xianhua, Li Hui, Yang Chenchen, Wang Xiaohong

机构信息

Department of Obstetrics and Gynecology, Jinan City People's Hospital, People's Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.

出版信息

Front Pharmacol. 2023 Jun 2;14:1138968. doi: 10.3389/fphar.2023.1138968. eCollection 2023.

Abstract

Despite some progress has been made in the pathogenesis and treatment of threatened miscarriage (TM), conventional treatment remains suboptimal. Thus, complementary medicine gradually become a new treatment option for treating threatened miscarriage. Gushen Antai Pills GAP), a classic prescription of Traditional Chinese medicine (TCM), has became a popular complementary therapy to conventional western medicine (dydrogesterone) in treating threatened miscarriage in recent years. However, a systematic summary and analysis for its therapeutic effects is lacking. This meta-analysis aimed to systematically evaluate the effectiveness and safety of Gushen Antai Pills combined with dydrogesterone in the treatment of threatened miscarriage. A systematic search across seven electronic databases was conducted from inception to 17 September 2022. Studies were included if they were randomized controlled trials (RCTs) evaluating the effect of integrating Gushen Antai Pills and dydrogesterone in patients with threatened miscarriage, and reported the outcomes of interest. All statistical analyses were conducted using the Revman5.3 and Stata 13 software. The GRADE system was used to evaluate the quality of evidence. Ten eligible randomized controlled trials involving 950 participants were contained in this meta-analysis. The pooled analysis showed that Gushen Antai Pills combined with dydrogesterone can significantly reduce the incidence of early pregnancy loss (RR: 0.29; 95% CI: 0.19-0.42; < 000001) and alleviate clinical symptoms (RR: 1.39; 95% CI: 1.22-1.59; < 000001), compared with treatment of dydrogesterone alone. Also, meta-analysis indicated that integrating Gushen Antai Pills and dydrogesterone is more effective than using dydrogesterone alone in improving hormone levels (serum levels of progesterone, -HCG and estradiol) for women with threatened miscarriage (all < 000001). Meanwhile, the combined effects with significant heterogeneity also showed favorable consistency in the sensitivity analyses, indicating a good stability of present results. Moreover, no significant differences between Gushen Antai Pills combined with dydrogesterone and control group on adverse events was identified. The overall GRADE qualities were low to moderate. The overall available evidence suggested that Gushen Antai Pills combined with dydrogesterone had significant effects in improving pregnancy success rate, clinical symptoms and hormone levels for women with threatened miscarriage, with considerable safety and reliability. However, due to the partial heterogeneity, suboptimal quality and high risk of bias of some included studies, further rigorously designed randomized controlled trials are required. identifier https://INPLASY2022120035, https://inplasy.com/inplasy-2022-12-0035/.

摘要

尽管在先兆流产(TM)的发病机制和治疗方面已取得一些进展,但传统治疗仍不尽人意。因此,补充医学逐渐成为治疗先兆流产的一种新的治疗选择。固肾安胎丸(GAP)是一种经典的中药方剂,近年来已成为治疗先兆流产时一种流行的与传统西药(地屈孕酮)联合使用的补充疗法。然而,目前缺乏对其治疗效果的系统总结和分析。本荟萃分析旨在系统评价固肾安胎丸联合地屈孕酮治疗先兆流产的有效性和安全性。从建库至2022年9月17日,对七个电子数据库进行了系统检索。纳入的研究需为评估固肾安胎丸与地屈孕酮联合治疗对先兆流产患者疗效的随机对照试验(RCT),并报告感兴趣的结局。所有统计分析均使用Revman5.3和Stata 13软件进行。采用GRADE系统评估证据质量。本荟萃分析纳入了10项符合条件的随机对照试验,共950名参与者。汇总分析表明,与单独使用地屈孕酮治疗相比,固肾安胎丸联合地屈孕酮可显著降低早期妊娠丢失的发生率(RR:0.29;95%CI:0.19 - 0.42;P < 0.000001)并缓解临床症状(RR:1.39;95%CI:1.22 - 1.59;P < 0.000001)。此外,荟萃分析表明,对于先兆流产女性,固肾安胎丸与地屈孕酮联合使用在改善激素水平(血清孕酮、β - HCG和雌二醇水平)方面比单独使用地屈孕酮更有效(所有P < 0.000001)。同时,合并效应虽有显著异质性,但在敏感性分析中也显示出良好的一致性,表明当前结果具有良好的稳定性。此外,未发现固肾安胎丸联合地屈孕酮与对照组在不良事件方面存在显著差异。总体GRADE质量为低到中等。总体现有证据表明,固肾安胎丸联合地屈孕酮在提高先兆流产女性的妊娠成功率、改善临床症状和激素水平方面具有显著效果,且具有相当的安全性和可靠性。然而,由于部分异质性、纳入研究质量欠佳以及偏倚风险较高,仍需要进一步设计严谨的随机对照试验。标识符:https://INPLASY2022120035,https://inplasy.com/inplasy - 2022 - 12 - 0035/

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8275/10275364/ba89839d0d20/fphar-14-1138968-g001.jpg

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