Progestogens for preterm birth prevention: a systematic review and meta-analysis by drug route

被引:10
|
作者
Edwards, Digna R. Velez [1 ,2 ]
Likis, Frances E. [3 ,4 ]
Andrews, Jeffrey C. [1 ,2 ]
Woodworth, Alison L. [5 ]
Jerome, Rebecca N. [6 ,7 ]
Fonnesbeck, Christopher J. [8 ]
McKoy, J. Nikki [4 ]
Hartmann, Katherine E. [1 ,2 ,3 ]
机构
[1] Vanderbilt Epidemiol Ctr, Inst Med & Publ Hlth, Nashville, TN 37203 USA
[2] Vanderbilt Univ, Med Ctr, Dept Obstet & Gynecol, Nashville, TN 37232 USA
[3] Vanderbilt Evidence Based Practice Ctr, Inst Med & Publ Hlth, Nashville, TN USA
[4] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USA
[5] Dept Pathol Microbiol & Immunol, Nashville, TN USA
[6] Dept Biomed Informat, Nashville, TN USA
[7] Vanderbilt Univ, Med Ctr, Eskind Biomed Lib, Nashville, TN USA
[8] Vanderbilt Univ, Med Ctr, Dept Biostat, Nashville, TN USA
基金
美国医疗保健研究与质量局;
关键词
Preterm birth; Meta-analysis; Review; Pregnancy; Progestogen; ALPHA-HYDROXYPROGESTERONE CAPROATE; DOUBLE-BLIND; 17-ALPHA-HYDROXYPROGESTERONE CAPROATE; MICRONIZED PROGESTERONE; VAGINAL PROGESTERONE; MAINTENANCE THERAPY; WOMEN; LABOR; MULTICENTER; TRIAL;
D O I
10.1007/s00404-013-2789-9
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Purpose Progestogen has been investigated as a preventive intervention among women with increased preterm birth risk. Our objective was to systematically review the effectiveness of intramuscular (IM), vaginal, and oral progestogens for preterm birth and neonatal death prevention. Methods We included articles published from January 1966 to January 2013 and found 27 randomized trials with data for Bayesian meta-analysis. Results Across all studies, only vaginal and oral routes were effective at reducing preterm births (IM risk ratio [RR] 0.95, 95 % Bayesian credible interval [BCI]: 0.88-1.03; vaginal RR 0.87, 95 % BCI: 0.80-0.94; oral RR 0.64, 95 % BCI: 0.49-0.85). However, when analyses were limited to only single births all routes were effective at reducing preterm birth (IM RR 0.77, 95 % BCI: 0.69-0.87; vaginal RR 0.80, 95 % BCI: 0.69-0.91; oral RR 0.66, 95 % BCI: 0.47-0.84). Only IM progestogen was effective at reducing neonatal deaths (IM RR 0.78, 95 % BCI: 0.56-0.99; vaginal RR 0.75, 95 % BCI: 0.45-1.09; oral RR 0.72, 95 % BCI: 0.09-1.74). Vaginal progestogen was effective in reducing neonatal deaths when limited to singletons births. Conclusions All progestogen routes reduce preterm births but not neonatal deaths. Future studies are needed that directly compare progestogen delivery routes.
引用
收藏
页码:1059 / 1066
页数:8
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