Am J Perinatol 2024; 41(S 01): e2081-e2088
DOI: 10.1055/s-0043-1770703
Original Article

Persistent Bacterial Vaginosis and Risk for Spontaneous Preterm Birth

Authors

  • Yair J. Blumenfeld

    1   Department of Obstetrics & Gynecology, Stanford University School of Medicine, Stanford, California
  • Ivana Marić

    2   Department of Pediatrics, Stanford University School of Medicine, March of Dimes Prematurity Research Center, Stanford, California
  • David K. Stevenson

    2   Department of Pediatrics, Stanford University School of Medicine, March of Dimes Prematurity Research Center, Stanford, California
  • Ronald S. Gibbs

    1   Department of Obstetrics & Gynecology, Stanford University School of Medicine, Stanford, California
  • Gary M. Shaw

    2   Department of Pediatrics, Stanford University School of Medicine, March of Dimes Prematurity Research Center, Stanford, California

Funding This work was supported by the March of Dimes Prematurity Research Center at Stanford University (grant number: 22-FY22-003) and the Maternal and Child Health Research Institute, Stanford University (grant number: 1265282-110-UANAF).
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Abstract

Objective The aim of this study was to determine the association between persistent bacterial vaginosis (BV) in pregnancy and risk for spontaneous preterm birth (sPTB).

Study Design Retrospective data from IBM MarketScan Commercial Database were analyzed. Women aged between 12 and 55 years with singleton gestations were included and linked to an outpatient medications database and medications prescribed during the pregnancy were analyzed. BV in pregnancy was determined based on both a diagnosis of BV and treatment with metronidazole and/or clindamycin, and persistent treatment of BV was defined as BV in more than one trimester or BV requiring more than one antibiotic prescription. Odds ratios were calculated comparing sPTB frequencies in those with BV, or persistent BV, to women without BV in pregnancy. Survival analysis using Kaplan–Meier curves for the gestational age at delivery was also performed.

Results Among a cohort of 2,538,606 women, 216,611 had an associated International Classification of Diseases, 9th Revision or 10th Revision code for diagnosis of BV alone, and 63,817 had both a diagnosis of BV and were treated with metronidazole and/or clindamycin. Overall, the frequency of sPTB among women treated with BV was 7.5% compared with 5.7% for women without BV who did not receive antibiotics. Relative to those without BV in pregnancy, odds ratios for sPTB were highest in those treated for BV in both the first and second trimester (1.66 [95% confidence interval [CI]: 1.52, 1.81]) or those with three or more prescriptions in pregnancy (1.48 [95% CI: 1.35, 1.63].

Conclusion Persistent BV may have a higher risk for sPTB than a single episode of BV in pregnancy.

Key Points

  • Persistent BV beyond one trimester may increase the risk for sPTB.

  • Persistent BV requiring more than one prescription may increase the risk for sPTB.

  • Almost half of antibiotic prescriptions treating BV in pregnancy are filled after 20 weeks gestation.

Data Availability Statement

IBM MarketScan Research Databases are available to purchase by Federal, nonprofit, academic, pharmaceutical, and other researchers. Use of the data is contingent on completing a data use agreement and purchasing the data needed to support the study. More information about licensing the IBM MarketScan Research Databases is available at: https://www.ibm.com/products/marketscan-research-databases .


Authors' Contributions

Y.J.B., I.M., and G.M.S. were involved in the conception and planning of the study, data analysis, and manuscript development. D.K.S. was involved in planning the study, data analysis, and manuscript development. R.S.G. was involved in data analysis and manuscript development.


Ethical Approval

This project was deemed exempt by the Stanford Institutional Review Board for Human Subjects.


Supplementary Material



Publication History

Received: 16 August 2022

Accepted: 19 May 2023

Article published online:
28 June 2023

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