Vaginal Progesterone for Pregnancy Prolongation After Arrested Preterm Labor

Author:

Nachum Zohar12,Ganor Paz Yael345,Massalha Manal12,Wated Malak1,Harel Noa6,Yefet Enav67

Affiliation:

1. Department of Obstetrics and Gynecology, Emek Medical Center, Afula, Israel

2. Ruth and Bruce Rappaport Faculty of Medicine, Technion–Israel Institute of Technology, Haifa, Israel

3. Department of Obstetrics and Gynecology, Wolfson Medical Center, Holon, Israel

4. Department of Obstetrics and Gynecology, Samson Assuta Ashdod University Hospital, Ashdod, Israel

5. Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

6. Department of Obstetrics and Gynecology, Tzafon Medical Center, Poriya, Israel

7. Azrieli Faculty of Medicine, Bar-Ilan University, Safed, Israel

Abstract

ImportanceWomen with arrested preterm labor (APTL) are at very high risk for spontaneous preterm delivery (SPTD), the leading cause of neonatal mortality and morbidity. To date, no maintenance therapy has been found to be effective for pregnancy prolongation. A few clinical trials with considerable methodological limitations have demonstrated some efficacy for 400 mg vaginal micronized progesterone (VMP) in women with APTL.ObjectiveTo investigate the effectiveness of daily 400 mg VMP for the prolongation of pregnancy after APTL.Design, Setting, and ParticipantsThis randomized clinical trial was conducted between December 19, 2018, and February 27, 2023, in 3 university-affiliated medical centers in Israel. Participants included women with singleton and twin pregnancies after APTL following tocolysis at 24 weeks 0 days to 34 weeks 0 days’ gestation. Women with a history of preterm delivery or asymptomatic cervical shortening in the current pregnancy were excluded.InterventionsParticipants were randomly allocated to receive VMP 200 mg twice a day or no treatment until 36 weeks 6 days’ gestation.Main Outcomes and MeasuresThe primary end points were mean number of days from study enrollment to delivery and the rate of SPTD prior to 37 weeks’ gestation.ResultsA total of 129 participants were enrolled (65 in the VMP group and 64 in the no-treatment group). Mean (SD) age was 27.6 (5.1) years. Between the VMP and no-treatment groups, there was no difference in pregnancy prolongation (mean [SD], 40.0 [17.8] vs 37.4 [20.3] days; P = .44) and the rate of SPTD (16 [25%] vs 19 [30%]; relative risk, 0.8; 95% CI, 0.5-1.5; P = .52). In twin pregnancies, including 12 and 15 pairs in the VMP and no-treatment groups, respectively, VMP prolonged pregnancy (mean [SD], 43.7 [18.1] vs 26.1 [15.2] days; P = .02), postponed the delivery week (36.5 [1.4] vs 34.7 [2.2] weeks; P = .01), shortened the length of stay in the neonatal intensive care unit (4.9 [10.6] vs 13.2 [18.5] days; P = .03) and overall hospital stay (8.3 [9.6] vs 15.1 [17.2] days; P = .03), and was associated with a higher birth weight (2444 [528] vs 2018 [430] g; P = .01).Conclusions and RelevanceThese findings show that VMP given in a dosage of 200 mg twice a day following APTL is not an effective treatment to prolong pregnancy or prevent SPTD. However, VMP demonstrated beneficial effects in twin pregnancies, warranting further investigation.Trial RegistrationClinicalTrials.gov Identifier: NCT02430233

Publisher

American Medical Association (AMA)

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