Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Testing and Detection During Peripartum Hospitalizations Among a Multicenter Cohort of Pregnant Persons: March 2020-February 2021.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
08 02 2023
Historique:
received: 03 06 2022
pubmed: 13 8 2022
medline: 11 2 2023
entrez: 12 8 2022
Statut: ppublish

Résumé

Identifying severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections during peripartum hospitalizations is important to guide care, implement prevention measures, and understand infection burden. This cross-sectional analysis used electronic health record data from hospitalizations during which pregnancies ended (peripartum hospitalizations) among a cohort of pregnant persons at 3 US integrated healthcare networks (sites 1-3). Maternal demographic, medical encounter, SARS-CoV-2 testing, and pregnancy and neonatal outcome information was extracted for persons with estimated delivery and pregnancy end dates during March 2020-February 2021 and ≥1 antenatal care record. Site-stratified multivariable logistic regression was used to identify factors associated with testing and compare pregnancy and neonatal outcomes among persons tested. Among 17 858 pregnant persons, 10 863 (60.8%) had peripartum SARS-CoV-2 testing; 222/10 683 (2.0%) had positive results. Testing prevalence varied by site and was lower during March-May 2020. Factors associated with higher peripartum SARS-CoV-2 testing odds were Asian race (adjusted odds ratio [aOR]: 1.36; 95% confidence interval [CI]: 1.03-1.79; referent: White) (site 1), Hispanic or Latino ethnicity (aOR: 1.33; 95% CI: 1.08-1.64) (site 2), peripartum Medicaid coverage (aOR: 1.33; 95% CI: 1.06-1.66) (site 1), and preterm hospitalization (aOR: 1.69; 95% CI: 1.19-2.39 [site 1]; aOR: 1.39; 95% CI: 1.03-1.88 [site 2]). Findings highlight potential disparities in SARS-CoV-2 peripartum testing by demographic and pregnancy characteristics. Testing practice variations should be considered when interpreting studies relying on convenience samples of pregnant persons testing positive for SARS-CoV-2. Efforts to address testing differences between groups could improve equitable testing practices and care for pregnant persons with SARS-CoV-2 infections.

Sections du résumé

BACKGROUND
Identifying severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections during peripartum hospitalizations is important to guide care, implement prevention measures, and understand infection burden.
METHODS
This cross-sectional analysis used electronic health record data from hospitalizations during which pregnancies ended (peripartum hospitalizations) among a cohort of pregnant persons at 3 US integrated healthcare networks (sites 1-3). Maternal demographic, medical encounter, SARS-CoV-2 testing, and pregnancy and neonatal outcome information was extracted for persons with estimated delivery and pregnancy end dates during March 2020-February 2021 and ≥1 antenatal care record. Site-stratified multivariable logistic regression was used to identify factors associated with testing and compare pregnancy and neonatal outcomes among persons tested.
RESULTS
Among 17 858 pregnant persons, 10 863 (60.8%) had peripartum SARS-CoV-2 testing; 222/10 683 (2.0%) had positive results. Testing prevalence varied by site and was lower during March-May 2020. Factors associated with higher peripartum SARS-CoV-2 testing odds were Asian race (adjusted odds ratio [aOR]: 1.36; 95% confidence interval [CI]: 1.03-1.79; referent: White) (site 1), Hispanic or Latino ethnicity (aOR: 1.33; 95% CI: 1.08-1.64) (site 2), peripartum Medicaid coverage (aOR: 1.33; 95% CI: 1.06-1.66) (site 1), and preterm hospitalization (aOR: 1.69; 95% CI: 1.19-2.39 [site 1]; aOR: 1.39; 95% CI: 1.03-1.88 [site 2]).
CONCLUSIONS
Findings highlight potential disparities in SARS-CoV-2 peripartum testing by demographic and pregnancy characteristics. Testing practice variations should be considered when interpreting studies relying on convenience samples of pregnant persons testing positive for SARS-CoV-2. Efforts to address testing differences between groups could improve equitable testing practices and care for pregnant persons with SARS-CoV-2 infections.

Identifiants

pubmed: 35959949
pii: 6663759
doi: 10.1093/cid/ciac657
pmc: PMC9384720
doi:

Types de publication

Multicenter Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e51-e59

Subventions

Organisme : CDC HHS
ID : 75D30120C08150
Pays : United States

Informations de copyright

Published by Oxford University Press on behalf of Infectious Diseases Society of America 2022.

Déclaration de conflit d'intérêts

Potential conflicts of interest. A. L. N. received research funding from Pfizer and Vir Biotechnology for unrelated studies (paid to their institution). F. M. participates on data safety monitoring boards for Pfizer (includes a stipend for the author), Moderna (paid to author), Meissa (includes a stipend for the author), Virometix (unpaid participation), and the National Institutes of Health (unpaid participation) and reports grants or contracts from Pfizer (Pediatric COVID-19 Vaccine Study; payment to their institution), Gilead (Pediatric Remdesivir Study; payment to their institution), and the National Institutes of Health (COVID-19 vaccines in pregnant women and Acute Flacid Myelitis Natural History Study; payment to their institution) and royalties or licenses for Up to Date on various chapters and editing (paid to author). M. G. reports several internal grants from Kaiser Permanente Northern California Division of Research for research funding (paid to their institution). M. S. reports other financial or nonfinancial interests from the CDC as a government employee who performed co-authorship duties as part of regular employment. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Auteurs

Miranda J Delahoy (MJ)

COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Flor Munoz (F)

Baylor College of Medicine, Houston, Texas, USA.

De-Kun Li (DK)

Kaiser Permanente Northern California, Oakland, California, USA.

Carmen Sofia Arriola (CS)

COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Nanette Lee Bond (NL)

Baylor College of Medicine, Houston, Texas, USA.

Michael Daugherty (M)

COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Jeannette Ferber (J)

Kaiser Permanente Northern California, Oakland, California, USA.

Nickolas Ferguson (N)

Abt Associates, Rockville, Maryland, USA.

Louise Hadden (L)

Abt Associates, Rockville, Maryland, USA.

Jillian T Henderson (JT)

Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon, USA.

Stephanie A Irving (SA)

Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon, USA.

Mary Juergens (M)

Abt Associates, Rockville, Maryland, USA.

Venkatesh Kancharla (V)

Baylor College of Medicine, Houston, Texas, USA.

Mara Greenberg (M)

Department of Obstetrics and Gynecology, Kaiser Permanente Oakland Medical Center, Oakland, California, USA.

Roxana Odouli (R)

Kaiser Permanente Northern California, Oakland, California, USA.

Gabriella Newes-Adeyi (G)

Abt Associates, Rockville, Maryland, USA.

Erin G Nicholson (EG)

Baylor College of Medicine, Houston, Texas, USA.

Lawrence Reichle (L)

Abt Associates, Rockville, Maryland, USA.

Momodou Sanyang (M)

Baylor College of Medicine, Houston, Texas, USA.

Margaret Snead (M)

COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Fatimah S Dawood (FS)

COVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Allison L Naleway (AL)

Center for Health Research, Kaiser Permanente Northwest, Portland, Oregon, USA.

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