Clindamycin to reduce preterm birth in a low resource setting: a randomised placebo-controlled clinical trial

被引:15
作者
Bellad, M. B. [1 ]
Hoffman, M. K. [2 ]
Mallapur, A. A. [3 ,4 ]
Charantimath, U. S. [1 ]
Katageri, G. M. [3 ,4 ]
Ganachari, M. S. [5 ,6 ]
Kavi, A. [1 ]
Ramdurg, U. Y. [3 ,4 ]
Bannale, S. G. [3 ,4 ]
Revankar, A. P. [1 ]
Sloan, N. L. [2 ]
Kodkany, B. S. [1 ]
Goudar, S. S. [1 ]
Derman, R. J. [7 ]
机构
[1] JN Med Coll, KLE Acad Higher Educ & Res, Belgaum, Karnataka, India
[2] Christiana Care Hlth Syst, Dept Obstet & Gynecol, Newark, DE USA
[3] S Nijalingappa Med Coll, Bagalkot, Karnataka, India
[4] HSK Hosp & Res Ctr, Bagalkot, Karnataka, India
[5] KLE Acad Higher Educ, JNMC Univ Campus, Belgaum, Karnataka, India
[6] Res Coll Pharm, JNMC Univ Campus, Belgaum, Karnataka, India
[7] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
关键词
clindamycin; prematurity; vaginal flora; MATERNAL-FETAL MEDICINE; BACTERIAL VAGINOSIS; NATIONAL-INSTITUTE; CHILD-HEALTH; GRAM STAIN; DELIVERY; PREGNANCY; WOMEN; METRONIDAZOLE; ULTRASOUND;
D O I
10.1111/1471-0528.15290
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
ObjectiveTo determine whether oral clindamycin reduces the risk of preterm birth (PTB) in women with abnormal vaginal microflora as evidenced by a vaginal pH 5.0. DesignRandomised double-blind placebo-controlled trial. SettingRural southern India. PopulationPregnant women with a singleton fetus between 13(+0/7) weeks and 20(+6/7) weeks. MethodsPregnant women were recruited during prenatal visits in Karnataka, India, from October 2013 to July 2015. Women were required to have a singleton fetus between 13(+0/7) weeks and 20(+6/7) weeks and an elevated vaginal pH (5.0) by colorimetric assessment. Participants were randomised to either oral clindamycin 300 mg twice daily for 5 days or an identical-appearing placebo. Main outcome measuresThe primary outcome was the incidence of PTB, defined as delivery before 37(+0/7) weeks. ResultsOf the 6476 screened women, 1727 women were randomised (block randomised in groups of six; clindamycin n = 866, placebo n = 861). The demographic, reproductive, and anthropomorphometric characteristics of the study groups were similar. Compliance was high, with over 94% of capsules being taken. The rate of PTB before 37 weeks was comparable between the two groups [clindamycin 115/826 (13.9%) versus placebo 111/806 (13.8%), between-group difference 0.2% (95% CI -3.2 to 3.5%, P = 0.93)], as was PTB at less than 34 weeks [clindamycin 40/826 (4.8%) versus placebo group 37/806 (4.6%), between-group difference 0.3% (95% CI -1.8 to 2.3%, P = 0.81)]. No differences were detected in the incidence of birthweight of<2500 g, <1500 g, miscarriage, stillbirth or neonatal death. ConclusionIn this setting, oral clindamycin did not decrease PTB among women with vaginal pH 5.0. Tweetable abstractOral clindamycin between 13(+0/7) and 20(+6/7) weeks does not prevent preterm birth in women with a vaginal pH 5.0. Tweetable abstract Oral clindamycin between 13(+0/7) and 20(+6/7) weeks does not prevent preterm birth in women with a vaginal pH 5.0.
引用
收藏
页码:1601 / 1609
页数:9
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