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Obstetric and Early Neonatal Outcomes Following Second and Third COVID-19 Vaccination in Pregnancy
Ravit Peretz-Machluf1, Mayan Gilboa2, Shiran Bookstein-Peretz1
1Department of Obstetrics and Gynecology, Sheba Medical Center, Tel Hashomer, Israel, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Insights
The COVID-19 booster vaccine (BNT162b2) is safe for pregnant women, showing no increased adverse obstetric or neonatal outcomes. Booster vaccination during pregnancy is associated with fewer urgent cesarean deliveries.
Area of Science:
- Obstetrics and Gynecology
- Infectious Diseases
- Vaccinology
Background:
- Pregnant individuals face higher risks for severe COVID-19.
- While data on two COVID-19 vaccine doses exist, information on booster doses in pregnancy is limited.
- The BNT162b2 (Pfizer/BioNTech) mRNA vaccine is widely used.
Purpose of the Study:
- To compare obstetric and early neonatal outcomes in pregnant women receiving a COVID-19 booster vaccine versus those with only two doses.
- To assess the safety and efficacy of the BNT162b2 vaccine booster during pregnancy.
Main Methods:
- A cross-sectional study compared pregnant women vaccinated with two BNT162b2 doses to those who received a third (booster) dose.
- Outcomes analyzed included obstetric and early neonatal parameters.
Main Results:
- 84 pregnant women received the booster dose, and 139 received two doses.
- The booster group received the vaccine earlier in pregnancy (212 vs. 315 weeks).
- No significant differences in obstetric or neonatal outcomes were observed, except for lower urgent cesarean delivery rates in the booster group (aOR 0.21, P=0.039).
Conclusions:
- The BNT162b2 COVID-19 booster vaccine is safe for use during pregnancy.
- Booster vaccination does not increase the rate of adverse obstetric or early neonatal outcomes.
- The booster dose may be associated with a reduced need for urgent cesarean deliveries.
Background:
Pregnant women are at higher risk for severe coronavirus disease 2019 (COVID-19). Since the release of the BNT162b2 messenger RNA vaccine (Pfizer/BioNTech), there has been accumulated data about the three vaccine doses. However, information regarding obstetric and neonatal outcomes of pregnant women vaccinated with the third (booster) vaccine is limited and primarily retrospective.
Objectives:
To evaluate the obstetric and early neonatal outcomes of pregnant women vaccinated during pregnancy with the COVID-19 booster vaccine compared to pregnant women vaccinated only by the first two doses.
Methods:
We conducted a cross-sectional study of pregnant women who received the BNT162b2 vaccine during pregnancy. Obstetric and neonatal outcomes were compared between pregnant women who received only the first two doses of the vaccine to those who also received the booster dose.
Results:
Overall, 139 pregnant women were vaccinated during pregnancy with the first two doses of the vaccine and 84 with the third dose. The third dose group received the vaccine earlier during their pregnancy compared to the two doses group (212 vs. 315 weeks, respectively, P < 0.001). No differences in obstetric and early neonatal outcomes between the groups were found except for lower rates of urgent cesarean delivery in the third dose group (adjusted odds ratio 0.21; 95% confidence interval 0.048-0.926, P = 0.039).
Conclusions:
Compared to the first two doses of the BNT162b2 vaccine given in pregnancy, the booster vaccination is safe and not associated with an increased rate of adverse obstetric and early neonatal outcomes.
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