Spong Catherine Y, Meis Paul J, Thom Elizabeth A, Sibai Baha, Dombrowski Mitchell P, Moawad Atef H, Hauth John C, Iams Jay D, Varner Michael W, Caritis Steve N, O'Sullivan Mary J, Miodovnik Menachem, Leveno Kenneth J, Conway Deborah, Wapner Ronald J, Carpenter Marshall, Mercer Brian, Ramin Susan M, Thorp John M, Peaceman Alan M, Gabbe Steven
National Institute of Child Health and Human Development, Bethesda, MD, USA.
Am J Obstet Gynecol. 2005 Sep;193(3 Pt 2):1127-31. doi: 10.1016/j.ajog.2005.05.077.
Preterm birth occurs in 1 of 8 pregnancies and may result in significant morbidity and mortality. 17-alpha hydroxyprogesterone caproate (17-OHP caproate) has been found to be efficacious in reducing the risk of subsequent preterm delivery in women who have had a previous spontaneous preterm birth (sPTB). This analysis was undertaken to evaluate if 17-OHP caproate therapy works preferentially depending on the gestational age at previous spontaneous delivery. We hypothesized that treatment with 17-OHP caproate is more effective in prolonging pregnancy depending on the gestational age of the earliest previous preterm birth (20-27.9, 28-33.9 vs 34-36.9 weeks).
This was a secondary analysis of 459 women with a previous sPTB enrolled in a randomized controlled trial evaluating 17-OHP caproate versus placebo. Effectiveness of 17-OHP caproate for pregnancy prolongation was evaluated based on gestational age at earliest previous delivery according to clinically relevant groupings (20-27.9, 28-33.9, and 34-36.9 weeks). Statistical analysis included the chi-square, Fisher exact, and Kruskal-Wallis tests, logistic regression, and survival analysis using proportional hazards.
Gestational age at earliest previous delivery was similar between women treated with 17-OHP caproate or placebo (P = .1). Women with earliest delivery at 20 to 27.9 weeks and at 28 to 33.9 weeks delivered at significantly more advanced gestational age if treated with 17-OHP caproate than with placebo (median 37.3 vs 35.4 weeks, P = .046 and 38.0 vs 36.7 weeks, P = .004, respectively) and were less likely to deliver <37 weeks (42% vs 63%, P = .026 and 34% vs 56%, P = .005, respectively). Those with earliest delivery at 34 to 36.9 weeks were not significantly different between 17-OHP caproate or control.
17-OHP caproate therapy given to prevent recurrent PTB is associated with a prolongation of pregnancy overall, and especially for women with a previous spontaneous PTB at <34 weeks.
每8次妊娠中就有1次发生早产,早产可能导致严重的发病和死亡。已发现己酸17-α羟孕酮(17-OHP己酸酯)在降低既往有自发性早产(sPTB)的女性再次发生早产的风险方面有效。进行该分析是为了评估17-OHP己酸酯治疗是否根据既往自发性分娩时的孕周而具有优先疗效。我们假设,根据最早一次既往早产的孕周(20 - 27.9周、28 - 33.9周与34 - 36.9周),17-OHP己酸酯治疗在延长孕周方面更有效。
这是对459例既往有sPTB且参与评估17-OHP己酸酯与安慰剂对照的随机对照试验的女性进行的二次分析。根据临床相关分组(20 - 27.9周、28 - 33.9周和34 - 36.9周),基于最早一次既往分娩时的孕周评估17-OHP己酸酯延长孕周的有效性。统计分析包括卡方检验、Fisher精确检验、Kruskal-Wallis检验、逻辑回归以及使用比例风险的生存分析。
接受17-OHP己酸酯或安慰剂治疗的女性最早一次既往分娩时的孕周相似(P = 0.1)。最早在20至27.9周分娩以及在28至33.9周分娩的女性,若接受17-OHP己酸酯治疗,其分娩时的孕周显著大于接受安慰剂治疗者(中位数分别为37.3周对35.4周,P = 0.046;38.0周对36.7周,P = 0.004),且分娩孕周<37周的可能性较小(分别为42%对63%,P = 0.026;34%对56%,P = 0.005)。最早在34至36.9周分娩的女性,17-OHP己酸酯组与对照组之间无显著差异。
给予17-OHP己酸酯预防复发性早产总体上与孕周延长相关,尤其是对于既往有<34周自发性早产的女性。