17‐Hydroxyprogesterone caproate in triplet pregnancy: an individual patient data meta‐analysis

• Published in: BJOG : an international journal of obstetrics and gynaecology Vol. 123; no. 5; pp. 682 - 690
• Main Authors: Combs, CA, Schuit, E, Caritis, SN, Lim, AC, Garite, TJ, Maurel, K, Rouse, D, Thom, E, Tita, AT, Mol, BWJ
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.04.2016
• Subjects: 17‐Hydroxyprogesterone caproate; Female; Humans; Hydroxyprogesterones - therapeutic use; Meta-analysis; multiple gestation; Pregnancy; Pregnancy, Triplet; Premature birth; Premature Birth - prevention & control; preterm birth prevention; Progestins - therapeutic use; progestogens; Treatment Outcome; triplet pregnancy; triplet pregnancy; multiple gestation; preterm birth prevention; progestogens; 17-Hydroxyprogesterone caproate
• ISSN: 1470-0328; 1471-0528
• DOI: 10.1111/1471-0528.13779

Background Preterm birth complicates almost all triplet pregnancies and no preventive strategy has proven effective. Objective To determine, using individual patient data (IPD) meta‐analysis, whether the outcome of triplet pregnancy is affected by prophylactic administration of 17‐hydroxyprogesterone caproate (17OHPc). Search strategy We searched literature databases, trial registries and references in published articles. Selection criteria Randomised controlled trials (RCTs) of progestogens versus control that included women with triplet pregnancies. Data collection and analysis Investigators from identified RCTs collaborated on the protocol and contributed their IPD. The primary outcome was a composite measure of adverse perinatal outcome. The secondary outcome was the rate of birth before 32 weeks of gestation. Other pre‐specified outcomes included randomisation‐to‐delivery interval and rates of birth at <24, <28 and <34 weeks of gestation. Main results Three RCTs of 17OHPc versus placebo included 232 mothers with triplet pregnancies and their 696 offspring. Risk‐of‐bias scores and between‐study heterogeneity were low. Baseline characteristics were comparable between 17OHPc and placebo groups. The rate of the composite adverse perinatal outcome was similar among those treated with 17OHPc and those treated with placebo (34 and 35%, respectively; risk ratio [RR] 0.98, 95% confidence interval [95% CI] 0.79–1.2). The rate of birth at <32 weeks was also similar in the two groups (35 and 38%, respectively; RR 0.92, 95% CI 0.55–1.56). There were no significant between‐group differences in perinatal mortality rate, randomisation‐to‐delivery interval, or other specified outcomes. Conclusion Prophylactic 17OHPc given to mothers with triplet pregnancies had no significant impact on perinatal outcome or pregnancy duration. Tweetable 17‐Hydroxyprogesterone caproate had no significant impact on the outcome or duration of triplet pregnancy. Tweetable 17‐Hydroxyprogesterone caproate had no significant impact on the outcome or duration of triplet pregnancy.