17 alpha-hydroxyprogesterone caproate to prevent prematurity in nulliparas with cervical length less than 30 mm

被引:61
作者
Grobman, William A. [1 ]
Thom, Elizabeth A. [2 ]
Spong, Catherine Y. [17 ]
Iams, Jay D. [3 ]
Saade, George R. [4 ]
Mercer, Brian M. [5 ]
Tita, Alan T. N. [6 ]
Rouse, Dwight J. [7 ]
Sorokin, Yoram [8 ]
Wapner, Ronald J. [9 ]
Leveno, Kenneth J. [10 ]
Blackwell, Sean [11 ]
Esplin, M. Sean [12 ]
Tolosa, Jorge E. [13 ]
Thorp, John M., Jr. [14 ]
Caritis, Steve N. [15 ]
Van Dorsten, J. Peter [16 ]
机构
[1] Northwestern Univ, Chicago, IL 60611 USA
[2] George Washington Univ, Ctr Biostat, Washington, DC USA
[3] Ohio State Univ, Columbus, OH 43210 USA
[4] Univ Texas Med Branch, Galveston, TX USA
[5] Case Western Reserve Univ, Metrohlth Med Ctr, Cleveland, OH USA
[6] Univ Alabama Birmingham, Birmingham, AL USA
[7] Brown Univ, Providence, RI 02912 USA
[8] Wayne State Univ, Detroit, MI USA
[9] Columbia Univ, New York, NY USA
[10] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
[11] Univ Texas Hlth Sci Ctr Houston, Houston, TX USA
[12] Univ Utah, Hlth Sci Ctr, Salt Lake City, UT USA
[13] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[14] Univ N Carolina, Chapel Hill, NC USA
[15] Univ Pittsburgh, Pittsburgh, PA USA
[16] Med Univ S Carolina, Charleston, SC 29425 USA
[17] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Bethesda, MD USA
关键词
nulliparous; progesterone; progestogen; short cervix; PRETERM BIRTH; DOUBLE-BLIND; 17-ALPHA-HYDROXYPROGESTERONE CAPROATE; WEEKS GESTATION; RISK; PROGESTERONE; WOMEN; PREDICTION; DELIVERY;
D O I
10.1016/j.ajog.2012.09.013
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
OBJECTIVE: We sought to evaluate whether 17 alpha-hydroxyprogesterone caproate (17-OHP) reduces preterm birth (PTB) in nulliparous women with a midtrimester cervical length (CL) <30 mm. STUDY DESIGN: In this multicenter randomized controlled trial, nulliparous women with a singleton gestation between 16 and 22 3/7 weeks with an endovaginal CL <30 mm (<10th percentile in this population) were randomized to weekly intramuscular 17-OHP (250 mg) or placebo through 36 weeks. The primary outcome was PTB <37 weeks. RESULTS: The frequency of PTB did not differ between the 17-OHP (n = 327) and placebo (n = 330) groups (25.1% vs 24.2%; relative risk, 1.03; 95% confidence interval, 0.79-1.35). There also was no difference in the composite adverse neonatal outcome (7.0% vs 9.1%; relative risk, 0.77; 95% confidence interval, 0.46-1.30). CONCLUSION: Weekly 17-OHP does not reduce the frequency of PTB in nulliparous women with a midtrimester CL <30 mm.
引用
收藏
页码:390.e1 / 390.e8
页数:8
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