米索前列醇治疗不全流产的疗效、安全性和可接受性:系统回顾与元分析》。

Thiago Menezes da Silva, Moema Alves Guerra de Araujo, Ana Carolina Zimmermann Simões, Ronnier de Oliveira, Kleyton Santos de Medeiros, Ayane Cristine Sarmento, Robinson Dias de Medeiros, Ana Paula Ferreira Costa, Ana Katherine Gonçalves
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引用次数: 0

摘要

目的:评估米索前列醇治疗不全流产的有效性、安全性和可接受性:评估米索前列醇治疗不全流产的疗效、安全性和可接受性:在PubMed、Scopus、Embase、Web of Science、Cochrane Library和临床试验数据库(clinicaltrials.gov)中检索相关文章,并结合专题医学主题词和文本词制定检索策略。最后一次检索于 2022 年 7 月 4 日进行。没有语言限制:纳入的随机临床试验对象包括妊娠期在6/7周以内、诊断为不全流产的患者,这些患者至少接受了所研究的3种治疗方法中的一种。共筛选出 8087 项研究:使用Review Manager V.5.1 统计软件包(英国牛津 Cochrane Collaboration)对数据进行综合。对于二分结果,每项研究都得出了几率比(OR)和 95% 置信区间(CI)。试验结果之间的异质性采用标准检验I2统计量进行评估:米索前列醇与医用真空吸引术(MVA)相比,MVA 组的完全流产率更高(OR = 0.16;95%CI = 0.07-0.36)。大出血或大量出血在米索前列醇组更常见(OR = 3.00;95%CI = 1.96-4.59),但治疗后疼痛在接受 MVA 治疗的患者中更常见(OR = 0.65;95%CI = 0.52-0.80)。在治疗的总体可接受性方面,没有观察到有统计学意义的差异:结论:米索前列醇是一种安全的选择,患者接受度较高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy, Safety, and Acceptability of Misoprostol in the Treatment of Incomplete Miscarriage: A Systematic Review and Meta-analysis.

Objective:  To assess the efficacy, safety, and acceptability of misoprostol in the treatment of incomplete miscarriage.

Data sources: The PubMed, Scopus, Embase, Web of Science, Cochrane Library, and Clinical Trials databases (clinicaltrials.gov) were searched for the relevant articles, and search strategies were developed using a combination of thematic Medical Subject Headings terms and text words. The last search was conducted on July 4, 2022. No language restrictions were applied.

Selection of studies:  Randomized clinical trials with patients of gestational age up to 6/7 weeks with a diagnosis of incomplete abortion and who were managed with at least 1 of the 3 types of treatment studied were included. A total of 8,087 studies were screened.

Data collection:  Data were synthesized using the statistical package Review Manager V.5.1 (The Cochrane Collaboration, Oxford, United Kingdom). For dichotomous outcomes, the odds ratio (OR) and 95% confidence interval (CI) were derived for each study. Heterogeneity between the trial results was evaluated using the standard test, I2 statistic.

Data synthesis:  When comparing misoprostol with medical vacuum aspiration (MVA), the rate of complete abortion was higher in the MVA group (OR = 0.16; 95%CI = 0.07-0.36). Hemorrhage or heavy bleeding was more common in the misoprostol group (OR = 3.00; 95%CI = 1.96-4.59), but pain after treatment was more common in patients treated with MVA (OR = 0.65; 95%CI = 0.52-0.80). No statistically significant differences were observed in the general acceptability of the treatments.

Conclusion:  Misoprostol has been determined as a safe option with good acceptance by patients.

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