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Supplementation with progestogens in the first trimester of pregnancy to prevent miscarriage in women with unexplained recurrent miscarriage: a systematic review and meta-analysis of randomized, controlled trials

机译:怀孕前三个月补充孕激素对不明原因复发性流产妇女的预防性婚姻:随机对照试验的系统评价和荟萃分析

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摘要

OBJECTIVE:udTo investigate whether treatment with progestogens in the first trimester of pregnancy would decrease the incidence of miscarriage in women with a history of unexplained recurrent miscarriage.ududDESIGN:udSystematic review and meta-analysis.ududSETTING:udNot applicable.ududPATIENT(S):udWomen with a history of unexplained recurrent miscarriage.ududINTERVENTION(S):udRandomized, controlled trials were identified by searching electronic databases. We included randomized, controlled trials comparing supplementation with progestogens (i.e., intervention group) in the first trimester of pregnancy with control (either placebo or no treatment) in women with a history of recurrent miscarriage. All types of progestogens, including natural P and synthetic progestins, were analyzed.ududMAIN OUTCOME MEASURE(S):udThe primary outcome was the incidence of miscarriage. The summary measures were reported as relative risk (RR) with 95% confidence interval (CI).ududRESULT(S):udTen trials including 1,586 women with recurrent miscarriage were analyzed. Eight studies used placebo as control and were double-blind. Regarding the intervention, two RCTs used natural P, whereas the other eight studies used progestins: medroxyprogesterone, cyclopentylenol ether of progesterone, dydrogesterone, or 17-hydroxyprogesterone caproate. Pooled data from the 10 trials showed that women with a history of unexplained recurrent miscarriage who were randomized to the progestogens group in the first trimester and before 16 weeks had a lower risk of recurrent miscarriage (RR 0.72, 95% CI 0.53-0.97) and higher live birth rate (RR 1.07, 95% CI 1.02-1.15) compared with those who did not. No statistically significant differences were found in the other secondary outcomes, including preterm birth (RR 1.09, 95% CI 0.71-1.66), neonatal mortality (RR 1.80, 95% CI 0.44-7.34), and fetal genital abnormalities (RR 1.68, 95% CI 0.22-12.62).ududCONCLUSION(S):udOur findings provide evidence that supplementation with progestogens may reduce the incidence of recurrent miscarriages and seem to be safe for the fetuses. Synthetic progestogens, including weekly IM 17-hydroxyprogesterone caproate, but not natural P, were associated with a lower risk of recurrent miscarriage. Given the limitations of the studies included in our meta-analysis, it is difficult to recommend route and dose of progestogen therapy. Further head-to-head trials of P types, dosing, and route of administration are required.
机译:目的: ud为调查妊娠前三个月是否接受孕激素治疗是否会降低具有无法解释的反复流产史的女性流产的发生率。 ud ud设计: ud系统评价和荟萃分析。 ud ud设置: ud不适用。 ud ud患者: ud具有无法解释的反复流产史的妇女。 ud udINTERVENTION(S): ud通过搜索电子数据库确定了随机对照试验。我们纳入了一项随机对照试验,比较了有反复流产史的孕妇在妊娠头三个月补充孕激素(即干预组)和对照(安慰剂或未治疗)的情况。分析了所有类型的孕激素,包括天然P和合成孕激素。 ud ud主要观察指标: ud主要结果是流产的发生率。报告的简易措施为相对危险度(RR),置信区间(CI)为95%。 ud udRESULT(S): udTen试验共分析了1,586例反复流产的妇女。八项研究使用安慰剂作为对照,并且是双盲的。关于干预措施,两项RCT使用天然P,而其他八项研究使用孕激素:甲羟孕酮,孕酮的环戊烯醇醚,孕酮或孕酮己酸17-羟孕酮。来自10项试验的汇总数据显示,具有无法解释的反复流产史的妇女,在孕早期和16周之前被随机分配到孕激素组中,复发流产的风险较低(RR 0.72,95%CI 0.53-0.97),并且与未出生者相比,活产率更高(RR 1.07,95%CI 1.02-1.15)。在其他次要结局中,包括早产(RR 1.09,95%CI 0.71-1.66),新生儿死亡率(RR 1.80,95%CI 0.44-7.34)和胎儿生殖器异常(RR 1.68,95),在统计学上均无统计学差异。 %CI 0.22-12.62)。 ud ud结论(S): ud我们的发现提供了证据,证明补充孕激素可以减少反复流产的发生率,并且对于胎儿来说是安全的。人工合成的孕激素(包括每周一次的IM 17-羟己孕酮己酸酯,但非天然的P)与复发性流产的风险较低有关。考虑到我们荟萃分析中所包括研究的局限性,很难推荐孕激素治疗的途径和剂量。还需要进一步进行P型,剂量和给药途径的面对面试验。

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