Publication

Stillbirth Associated With Infection in a Diverse U.S. Cohort.

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Last modified
  • 06/25/2025
Type of Material
Authors
    Jessica M Page, University of Utah Health Sciences, Salt Lake City, and Intermountain Health Care, Murray, Utah; RTI International, Research Triangle Park, North Carolina; the University of Virginia Healthcare, Charlottesville, Virginia; the University of Texas Medical Branch at Galveston, Galveston, Texas; Columbia University, New York, New York; the University of Texas Health Science Center at Houston, Houston, Texas; Rollins School of Public Health, Emory University, Atlanta, Georgia; the University of Texas at Austin, Austin, and the University of Texas Health Science Center at San Antonio, San Antonio, Texas; and Yale School of Medicine, New Haven, Connecticut.Tyler Bardsley, University of Utah Health SciencesVanessa Thorsten, RTI International, Research Triangle ParkAmanda A Allshouse, University of Utah Health SciencesMichael W Varner, University of Utah Health SciencesMichelle P Debbink, University of Utah Health SciencesDonlad J Dudley, University of Virginia HealthcareGeorge R Saade, University of Texas Medical Branch at GalvestonRobert L Goldenberg, Columbia UniversityBarbara Stoll, Emory UniversityCarol Hogue, Emory UniversityRadek Bukowski, University of Texas at AustinDeborah Conway, University of Texas Health Science Center at San AntonioUma M Reddy, Yale School of MedicineRobert M Silver, University of Utah Health Sciences
Language
  • English
Date
  • 2019-12
Publisher
  • Emory University Libraries
Publication Version
Copyright Statement
  • The American College of Obstetricians and Gynecologists
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 134
Issue
  • 6
Start Page
  • 1187
End Page
  • 1196
Supplemental Material (URL)
Abstract
  • OBJECTIVE: To better characterize infection-related stillbirth in terms of pathogenesis and microbiology. METHODS: We conducted a secondary analysis of 512 stillbirths in a prospective, multisite, geographically, racially and ethnically diverse, population-based study of stillbirth in the United States. Cases underwent evaluation that included maternal interview, chart abstraction, biospecimen collection, fetal autopsy, and placental pathology. Recommended evaluations included syphilis and parvovirus serology. Each case was assigned probable and possible causes of death using the INCODE Stillbirth Classification System. Cases where infection was assigned as a probable or possible cause of death were reviewed. For these cases, clinical scenario, autopsy, maternal serology, culture results, and placental pathology were evaluated. RESULTS: For 66 (12.9%) cases of stillbirth, infection was identified as a probable or possible cause of death. Of these, 36% (95% CI 35-38%) were categorized as a probable and 64% (95% CI 62-65%) as a possible cause of death. Infection-related stillbirth occurred earlier than non-infection-related stillbirth (median gestational age 22 vs 28 weeks, P=.001). Fetal bacterial culture results were available in 47 cases (71%), of which 35 (53%) grew identifiable organisms. The predominant species were Escherichia coli (19, 29%), group B streptococcus (GBS) (8, 12%), and enterococcus species (8, 12%). Placental pathology revealed chorioamnionitis in 50 (76%), funisitis in 27 (41%), villitis in 11 (17%), deciduitis in 35 (53%), necrosis in 27 (41%), and viral staining in seven (11%) cases. Placental pathology found inflammation or evidence of infection in 65 (99%) cases and fetal autopsy in 26 (39%) cases. In infection-related stillbirth cases, the likely causative nonbacterial organisms identified were parvovirus in two (3%) cases, syphilis in one (2%) case, cytomegalovirus (CMV) in five (8%) cases, and herpes in one (2%) case. CONCLUSION: Of infection-related stillbirth cases in a large U.S. cohort, E coli, GBS, and enterococcus species were the most common bacterial pathogens and CMV the most common viral pathogen.
Author Notes
  • Robert M. Silver, MD, Department of Obstetrics and Gynecology, University of Utah School of Medicine, 30 North 1900 East, Room 2B308, Salt Lake City, Utah 84132. Email: bsilver@hsc.utah.edu. phone: (801) 585-3857, fax: (801) 585-2594
Keywords
Research Categories
  • Health Sciences, Public Health
  • Health Sciences, Medicine and Surgery

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