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Meta-Analysis
. 2022 Apr 19;327(15):1469-1477.
doi: 10.1001/jama.2022.3271.

Association of SARS-CoV-2 Vaccination During Pregnancy With Pregnancy Outcomes

Affiliations
Meta-Analysis

Association of SARS-CoV-2 Vaccination During Pregnancy With Pregnancy Outcomes

Maria C Magnus et al. JAMA. .

Abstract

Importance: Data about the safety of vaccines against SARS-CoV-2 during pregnancy are limited.

Objective: To examine the risk of adverse pregnancy outcomes after vaccination against SARS-CoV-2 during pregnancy.

Design, setting, and participants: This registry-based retrospective cohort study included 157 521 singleton pregnancies ending after 22 gestational weeks from January 1, 2021, until January 12, 2022 (Sweden), or January 15, 2022 (Norway). The Pregnancy Register in Sweden and the Medical Birth Registry of Norway were linked to vaccination and other registries for identification of exposure and background characteristics.

Exposures: Data on mRNA vaccines-BNT162b2 (Pfizer-BioNTech) and mRNA-1273 (Moderna)-and 1 viral vector vaccine-AZD1222 (AstraZeneca)-were collected from national vaccination registries.

Main outcomes and measures: The risk of preterm birth and stillbirth was evaluated using Cox regression models, with gestational day as the time metric and vaccination as a time-dependent exposure variable. The risk of small for gestational age, low Apgar score, and neonatal care admission was evaluated using logistic regression. Random-effects meta-analysis was used to combine results between countries.

Results: Among the 157 521 singleton births included in the study (103 409 in Sweden and 54 112 in Norway), the mean maternal age at the time of delivery was 31 years, and 28 506 (18%) were vaccinated against SARS-CoV-2 (12.9% with BNT162b2, 4.8% with mRNA-1273, and 0.3% with AZD1222) while pregnant. A total of 0.7%, 8.3%, and 9.1% of individuals delivering were vaccinated during the first, second, and third trimester, respectively. Vaccination against SARS-CoV-2 was not significantly associated with increased risk of preterm birth (6.2 vs 4.9 per 10 000 pregnancy days; adjusted hazard ratio [aHR], 0.98 [95% CI, 0.91 to 1.05]; I2 = 0%; P for heterogeneity = .60), stillbirth (2.1 vs 2.4 per 100 000 pregnancy days; aHR, 0.86 [95% CI, 0.63 to 1.17]), small for gestational age (7.8% vs 8.5%; difference, -0.6% [95% CI, -1.3% to 0.2%]; adjusted OR [aOR], 0.97 [95% CI, 0.90 to 1.04]), low Apgar score (1.5% vs 1.6%; difference, -0.05% [95% CI, -0.3% to 0.1%]; aOR, 0.97 [95% CI, 0.87 to 1.08]), or neonatal care admission (8.5% vs 8.5%; difference, 0.003% [95% CI, -0.9% to 0.9%]; aOR, 0.97 [95% CI, 0.86 to 1.10]).

Conclusions and relevance: In this population-based study conducted in Sweden and Norway, vaccination against SARS-CoV-2 during pregnancy, compared with no SARS-CoV-2 vaccination during pregnancy, was not significantly associated with an increased risk of adverse pregnancy outcomes. The majority of the vaccinations were with mRNA vaccines during the second and third trimesters of pregnancy, which should be considered in interpreting the findings.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Ljung reported receiving personal fees from Pfizer outside the submitted work and being employed at the Swedish Medical Products Agency. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Development of Cohorts in a Study of Pregnancy Outcomes With and Without SARS-CoV-2 Vaccination
Figure 2.
Figure 2.. Cumulative Incidence Curves of the Risk of Preterm Birth, Very Preterm Birth, and Stillbirth According to SARS-CoV-2 Vaccination
All pregnancies were observed from 22 completed gestational weeks until event or 32 completed gestational weeks (very preterm birth), 37 completed gestational weeks (preterm birth), or end of pregnancy (stillbirth). Analyses were adjusted for age at start of pregnancy, parity, education level, living with a partner, household income (Norway only), whether the individual had tested positive for SARS-CoV-2, and underlying chronic condition. The I2 heterogeneity statistic for the difference in the estimates between Sweden and Norway was 0% (P = .60) for preterm birth, 59% (P = .12) for very preterm birth, and 0% (P = .71) for stillbirth. Combining the estimates for Sweden and Norway in a random-effects meta-analysis, the adjusted hazard ratio was 0.98 (95% CI, 0.91 to 1.05) for preterm birth, 0.91 (95% CI, 0.63 to 1.31) for very preterm birth, and 0.86 (95% CI, 0.63 to 1.17) for stillbirth.
Figure 3.
Figure 3.. Odds Ratios of Low Apgar Score at 5 Minutes, Small for Gestational Age, and Neonatal Care Admission According to Vaccination Against SARS-CoV-2 During Pregnancy
Adjusted for age at start of pregnancy, parity, education level, living with a partner, household income (Norway only), whether the individual had tested positive for SARS-CoV-2, and underlying chronic condition. The I2 heterogeneity statistic for difference in the estimates between Sweden and Norway was 0% (P = .93) for low Apgar score, 39% (P = .20) for small for gestational age, and 80% (P = .03) for neonatal care admission. The vertical dashed lines indicate the values for the meta-analyzed effect estimates.

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