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SARS-CoV-2 and pregnancy outcomes under universal and non-universal testing in Sweden: register-based nationwide cohort study
The Clinical Epidemiology Division, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden: Department of Women’s Health, Karolinska University Hospital, Stockholm, Sweden.
The Clinical Epidemiology Division, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden; Statens Serum Institut, Copenhagen, Denmark.
The Clinical Epidemiology Division, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden; Department of Women’s Health, Karolinska University Hospital, Stockholm, Sweden.
Division of Infectious Diseases, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden; Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.
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2022 (English)In: British Journal of Obstetrics and Gynecology, ISSN 1470-0328, E-ISSN 1471-0528, Vol. 129, no 2, p. 282-290Article in journal (Refereed) Published
Abstract [en]

Objective: To assess associations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and pregnancy outcomes considering testing policy and test-positivity-to-delivery interval.

Design: Nationwide cohort study.

Setting: Sweden.

Population: From the Pregnancy-Register we identified 88 593 singleton births, 11 March 2020-31 January 2021, linked to data on SARS-CoV-2-positivity from the Public Health Agency, and information on neonatal care admission from the Neonatal Quality Register. Adjusted odds ratios (aORs) were estimated stratified by testing-policy and test-positivity-to-delivery interval.

Main outcome measures: Five-minute Apgar score, neonatal care admission, stillbirth and preterm birth.

Results: During pregnancy, SARS-CoV-2 test-positivity was 5.4% (794/14 665) under universal testing and 1.9% (1402/73 928) under non-universal testing. There were generally lower risks associated with SARS-CoV-2 under universal than non-universal testing. In women testing positive >10 days from delivery, generally no significant differences in risk were observed under either testing policy. Neonatal care admission was more common (15.3% versus 8.0%; aOR 2.24, 95% CI 1.62-3.11) in women testing positive <= 10 days before delivery under universal testing. There was no significant association with 5-minute Apgar score below 7 (1.0% versus 1.7%; aOR 0.64, 95% CI 0.24-1.72) or stillbirth (0.3% versus 0.4%; aOR 0.72, 95% CI 0.10-5.20). Compared with term births (2.1%), test-positivity was higher in medically indicated preterm birth (5.7%; aOR 2.70, 95% CI 1.60-4.58) but not significantly increased in spontaneous preterm birth (2.3%; aOR 1.12, 95% CI 0.62-2.02).

Conclusions: Testing policy and timing of test-positivity impact associations between SARS-CoV-2-positivity and pregnancy outcomes. Under non-universal testing, women with complications near delivery are more likely to be tested than women without complications, thereby inflating any association with adverse pregnancy outcomes compared with findings under universal testing.

Tweetable abstract: Testing policy and time from SARS-CoV-2 infection to delivery influence the association with pregnancy outcomes.

Place, publisher, year, edition, pages
John Wiley & Sons, 2022. Vol. 129, no 2, p. 282-290
Keywords [en]
Apgar, coronavirus disease 2019, neonatal care, preterm birth, severe acute respiratory syndrome coronavirus 2, stillbirth, universal
National Category
Gynaecology, Obstetrics and Reproductive Medicine
Identifiers
URN: urn:nbn:se:oru:diva-95696DOI: 10.1111/1471-0528.16990ISI: 000719875700001PubMedID: 34706148Scopus ID: 2-s2.0-85119174926OAI: oai:DiVA.org:oru-95696DiVA, id: diva2:1615956
Funder
Swedish Society of Medicine, 2020-937944NordForsk, 105545Region Stockholm, ALF 2020-0443The Karolinska Institutet's Research Foundation, ALF 2020-0443
Note

Funding agency:

Childhood Foundation of the Swedish Order of Freemasons [MNo]

Available from: 2021-12-01 Created: 2021-12-01 Last updated: 2025-02-11Bibliographically approved

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Ludvigsson, Jonas F.

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