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Association between acquiring SARS-CoV-2 during pregnancy and post-acute sequelae of SARS-CoV-2 infection: RECOVER electronic health record cohort analysis.
Bruno, Ann M; Zang, Chengxi; Xu, Zhengxing; Wang, Fei; Weiner, Mark G; Guthe, Nick; Fitzgerald, Megan; Kaushal, Rainu; Carton, Thomas W; Metz, Torri D.
  • Bruno AM; Department of Obstetrics and Gynecology, University of Utah Health, Salt Lake City, UT, USA.
  • Zang C; Department of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.
  • Xu Z; Department of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.
  • Wang F; Department of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.
  • Weiner MG; Department of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.
  • Guthe N; RECOVER Patient, Caregiver, or Community Advocate Representative, New York, NY, USA.
  • Fitzgerald M; RECOVER Patient, Caregiver, or Community Advocate Representative, New York, NY, USA.
  • Kaushal R; Department of Population Health Sciences, Weill Cornell Medicine, New York, NY, USA.
  • Carton TW; Louisiana Public Health Institute, New Orleans, LA, USA.
  • Metz TD; Department of Obstetrics and Gynecology, University of Utah Health, Salt Lake City, UT, USA.
EClinicalMedicine ; 73: 102654, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38828129
ABSTRACT

Background:

Little is known about post-acute sequelae of SARS-CoV-2 infection (PASC) after acquiring SARS-CoV-2 infection during pregnancy. We aimed to evaluate the association between acquiring SARS-CoV-2 during pregnancy compared with acquiring SARS-CoV-2 outside of pregnancy and the development of PASC.

Methods:

This retrospective cohort study from the Researching COVID to Enhance Recovery (RECOVER) Initiative Patient-Centred Clinical Research Network (PCORnet) used electronic health record (EHR) data from 19 U.S. health systems. Females aged 18-49 years with lab-confirmed SARS-CoV-2 infection from March 2020 through June 2022 were included. Validated algorithms were used to identify pregnancies with a delivery at >20 weeks' gestation. The primary outcome was PASC, as previously defined by computable phenotype in the adult non-pregnant PCORnet EHR dataset, identified 30-180 days post-SARS-CoV-2 infection. Secondary outcomes were the 24 component diagnoses contributing to the PASC phenotype definition. Univariable comparisons were made for baseline characteristics between individuals with SARS-CoV-2 infection acquired during pregnancy compared with outside of pregnancy. Using inverse probability of treatment weighting to adjust for baseline differences, the association between SARS-CoV-2 infection acquired during pregnancy and the selected outcomes was modelled. The incident risk is reported as the adjusted hazard ratio (aHR) with 95% confidence intervals.

Findings:

In total, 83,915 females with SARS-CoV-2 infection acquired outside of pregnancy and 5397 females with SARS-CoV-2 infection acquired during pregnancy were included in analysis. Non-pregnant females with SARS-CoV-2 infection were more likely to be older and have comorbid health conditions. SARS-CoV-2 infection acquired in pregnancy as compared with acquired outside of pregnancy was associated with a lower incidence of PASC (25.5% vs 33.9%; aHR 0.85, 95% CI 0.80-0.91). SARS-CoV-2 infection acquired in pregnant females was associated with increased risk for some PASC component diagnoses including abnormal heartbeat (aHR 1.67, 95% CI 1.43-1.94), abdominal pain (aHR 1.34, 95% CI 1.16-1.55), and thromboembolism (aHR 1.88, 95% CI 1.17-3.04), but decreased risk for other diagnoses including malaise (aHR 0.35, 95% CI 0.27-0.47), pharyngitis (aHR 0.36, 95% CI 0.26-0.48) and cognitive problems (aHR 0.39, 95% CI 0.27-0.56).

Interpretation:

SARS-CoV-2 infection acquired during pregnancy was associated with lower risk of development of PASC at 30-180 days after incident SARS-CoV-2 infection in this nationally representative sample. These findings may be used to counsel pregnant and pregnant capable individuals, and direct future prospective study.

Funding:

National Institutes of Health (NIH) Other Transaction Agreement (OTA) OT2HL16184.
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