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Reductions in stillbirths and preterm birth in COVID-19-vaccinated women: a multicenter cohort study of vaccination uptake and perinatal outcomes.
Am J Obstet Gynecol. 2022 Nov 03 [Online ahead of print]AJ

Abstract

BACKGROUND

COVID-19 infection in pregnancy is associated with a higher risk of progression to severe disease, but vaccine uptake by pregnant women is hindered by persistent safety concerns. COVID-19 vaccination in pregnancy has been shown to reduce stillbirth, but its relationship with preterm birth is uncertain.

OBJECTIVE

This study aimed to measure the rate of COVID-19 vaccine uptake among women giving birth in Melbourne, Australia, and to compare perinatal outcomes by vaccination status.

STUDY DESIGN

This was a retrospective multicenter cohort study conducted after the June 2021 government recommendations for messenger RNA COVID-19 vaccination during pregnancy. Routinely collected data from all 12 public maternity hospitals in Melbourne were extracted on births at ≥20 weeks' gestation from July 1, 2021 to March 31, 2022. Maternal sociodemographic characteristics were analyzed from the total birth cohort. Perinatal outcomes were compared between vaccinated and unvaccinated women for whom weeks 20 to 43 of gestation fell entirely within the 9-month data collection period. The primary outcomes were the rates of stillbirth and preterm birth (spontaneous and iatrogenic) in singleton pregnancies of at least 24 weeks' gestation, after exclusion of congenital anomalies. Secondary perinatal outcomes included the rate of congenital anomalies among infants born at ≥20 weeks' gestation and birthweight ≤third centile and newborn intensive care unit admissions among infants born without congenital anomalies at ≥24 weeks' gestation. We calculated the adjusted odds ratio of perinatal outcomes among vaccinated vs unvaccinated women using inverse propensity score-weighting regression adjustment with multiple covariates; P<.05 was considered statistically significant.

RESULTS

Births from 32,536 women were analyzed: 17,365 (53.4%) were vaccinated and 15,171 (47.6%) were unvaccinated. Vaccinated women were more likely to be older, nulliparous, nonsmoking, not requiring an interpreter, of higher socioeconomic status, and vaccinated against pertussis and influenza. Vaccination status also varied by region of birth. Vaccinated women had a significantly lower rate of stillbirth compared with unvaccinated women (0.2% vs 0.8%; adjusted odds ratio, 0.18; 95% confidence interval, 0.09-0.37; P<.001). Vaccination was associated with a significant reduction in total preterm births at <37 weeks (5.1% vs 9.2%; adjusted odds ratio, 0.60; 95% confidence interval, 0.51-0.71; P<.001), spontaneous preterm birth (2.4% vs 4.0%; adjusted odds ratio, 0.73; 95% confidence interval, 0.56-0.96; P=.02), and iatrogenic preterm birth (2.7% vs 5.2%; adjusted odds ratio, 0.52; 95% confidence interval, 0.41-0.65; P<.001). Infants born to vaccinated mothers also had lower rates of admission to the neonatal intensive care unit. There was no significant increase in the rate of congenital anomalies or birthweight ≤3rd centile in vaccinated women. Vaccinated women were significantly less likely to have an infant with a major congenital anomaly compared with the unvaccinated group (2.4% vs 3.0%; adjusted odds ratio, 0.72; 95% confidence interval, 0.56-0.94; P=.02). This finding remained significant even when the analysis was restricted to women vaccinated before 20 weeks' gestation.

CONCLUSION

COVID-19 vaccination during pregnancy was associated with a reduction in stillbirth and preterm birth, and not associated with any adverse impact on fetal growth or development. Vaccine coverage was substantially influenced by known social determinants of health.

Authors+Show Affiliations

Department of Obstetrics and Gynaecology, Melbourne Medical School, The University of Melbourne, Melbourne, Australia; Reproductive Epidemiology Group, Murdoch Children's Research Institute, Melbourne, Australia; Department of Obstetrics and Gynaecology, Mercy Hospital for Women, Mercy Health, Melbourne, Australia; Department of Obstetrics and Gynaecology, The Northern Hospital, Northern Health, Melbourne, Australia. Electronic address: lisa.hui@unimelb.edu.au.Department of Obstetrics and Gynaecology, Melbourne Medical School, The University of Melbourne, Melbourne, Australia; Reproductive Epidemiology Group, Murdoch Children's Research Institute, Melbourne, Australia; Center for Alcohol Policy Research, La Trobe University, Melbourne, Australia.Department of Obstetrics and Gynaecology, Monash Health, Melbourne, Australia; Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia; Department of Obstetrics and Gynaecology, Frankston Hospital, Peninsula Health, Melbourne, Australia; Harvard T.H. School of Public Health, Harvard University, Cambridge, MA.Department of Obstetrics and Gynaecology, Mercy Hospital for Women, Mercy Health, Melbourne, Australia.Department of Obstetrics and Gynaecology, Melbourne Medical School, The University of Melbourne, Melbourne, Australia; Department of Obstetrics and Gynaecology, Mercy Hospital for Women, Mercy Health, Melbourne, Australia.Department of Obstetrics and Gynaecology, Melbourne Medical School, The University of Melbourne, Melbourne, Australia; Department of Maternal-Fetal Medicine, Joan Kirner Women's and Children's Hospital, Western Health, Melbourne, Australia.Department of Obstetrics and Gynaecology, Monash Health, Melbourne, Australia; Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia.Department of Obstetrics and Gynaecology, Melbourne Medical School, The University of Melbourne, Melbourne, Australia; Department of Obstetrics and Gynaecology, Royal Women's Hospital, Melbourne, Australia.Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia; Department of Obstetrics and Gynaecology, Box Hill Hospital, Eastern Health, Melbourne, Australia.Department of Obstetrics and Gynaecology, Frankston Hospital, Peninsula Health, Melbourne, Australia.Department of Obstetrics and Gynaecology, Monash Health, Melbourne, Australia; Department of Obstetrics and Gynaecology, Monash University, Melbourne, Australia.Department of Obstetrics and Gynaecology, Melbourne Medical School, The University of Melbourne, Melbourne, Australia; Department of Obstetrics and Gynaecology, Mercy Hospital for Women, Mercy Health, Melbourne, Australia.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

36336084

Citation

Hui, Lisa, et al. "Reductions in Stillbirths and Preterm Birth in COVID-19-vaccinated Women: a Multicenter Cohort Study of Vaccination Uptake and Perinatal Outcomes." American Journal of Obstetrics and Gynecology, 2022.
Hui L, Marzan MB, Rolnik DL, et al. Reductions in stillbirths and preterm birth in COVID-19-vaccinated women: a multicenter cohort study of vaccination uptake and perinatal outcomes. Am J Obstet Gynecol. 2022.
Hui, L., Marzan, M. B., Rolnik, D. L., Potenza, S., Pritchard, N., Said, J. M., Palmer, K. R., Whitehead, C. L., Sheehan, P. M., Ford, J., Mol, B. W., & Walker, S. P. (2022). Reductions in stillbirths and preterm birth in COVID-19-vaccinated women: a multicenter cohort study of vaccination uptake and perinatal outcomes. American Journal of Obstetrics and Gynecology. https://doi.org/10.1016/j.ajog.2022.10.040
Hui L, et al. Reductions in Stillbirths and Preterm Birth in COVID-19-vaccinated Women: a Multicenter Cohort Study of Vaccination Uptake and Perinatal Outcomes. Am J Obstet Gynecol. 2022 Nov 3; PubMed PMID: 36336084.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Reductions in stillbirths and preterm birth in COVID-19-vaccinated women: a multicenter cohort study of vaccination uptake and perinatal outcomes. AU - Hui,Lisa, AU - Marzan,Melvin B, AU - Rolnik,Daniel L, AU - Potenza,Stephanie, AU - Pritchard,Natasha, AU - Said,Joanne M, AU - Palmer,Kirsten R, AU - Whitehead,Clare L, AU - Sheehan,Penelope M, AU - Ford,Jolyon, AU - Mol,Ben W, AU - Walker,Susan P, Y1 - 2022/11/03/ PY - 2022/06/30/received PY - 2022/10/25/revised PY - 2022/10/30/accepted PY - 2022/11/7/pubmed PY - 2022/11/7/medline PY - 2022/11/6/entrez KW - COVID-19 KW - cohort studies KW - pregnancy outcome KW - premature birth KW - stillbirth KW - vaccination JF - American journal of obstetrics and gynecology JO - Am J Obstet Gynecol N2 - BACKGROUND: COVID-19 infection in pregnancy is associated with a higher risk of progression to severe disease, but vaccine uptake by pregnant women is hindered by persistent safety concerns. COVID-19 vaccination in pregnancy has been shown to reduce stillbirth, but its relationship with preterm birth is uncertain. OBJECTIVE: This study aimed to measure the rate of COVID-19 vaccine uptake among women giving birth in Melbourne, Australia, and to compare perinatal outcomes by vaccination status. STUDY DESIGN: This was a retrospective multicenter cohort study conducted after the June 2021 government recommendations for messenger RNA COVID-19 vaccination during pregnancy. Routinely collected data from all 12 public maternity hospitals in Melbourne were extracted on births at ≥20 weeks' gestation from July 1, 2021 to March 31, 2022. Maternal sociodemographic characteristics were analyzed from the total birth cohort. Perinatal outcomes were compared between vaccinated and unvaccinated women for whom weeks 20 to 43 of gestation fell entirely within the 9-month data collection period. The primary outcomes were the rates of stillbirth and preterm birth (spontaneous and iatrogenic) in singleton pregnancies of at least 24 weeks' gestation, after exclusion of congenital anomalies. Secondary perinatal outcomes included the rate of congenital anomalies among infants born at ≥20 weeks' gestation and birthweight ≤third centile and newborn intensive care unit admissions among infants born without congenital anomalies at ≥24 weeks' gestation. We calculated the adjusted odds ratio of perinatal outcomes among vaccinated vs unvaccinated women using inverse propensity score-weighting regression adjustment with multiple covariates; P<.05 was considered statistically significant. RESULTS: Births from 32,536 women were analyzed: 17,365 (53.4%) were vaccinated and 15,171 (47.6%) were unvaccinated. Vaccinated women were more likely to be older, nulliparous, nonsmoking, not requiring an interpreter, of higher socioeconomic status, and vaccinated against pertussis and influenza. Vaccination status also varied by region of birth. Vaccinated women had a significantly lower rate of stillbirth compared with unvaccinated women (0.2% vs 0.8%; adjusted odds ratio, 0.18; 95% confidence interval, 0.09-0.37; P<.001). Vaccination was associated with a significant reduction in total preterm births at <37 weeks (5.1% vs 9.2%; adjusted odds ratio, 0.60; 95% confidence interval, 0.51-0.71; P<.001), spontaneous preterm birth (2.4% vs 4.0%; adjusted odds ratio, 0.73; 95% confidence interval, 0.56-0.96; P=.02), and iatrogenic preterm birth (2.7% vs 5.2%; adjusted odds ratio, 0.52; 95% confidence interval, 0.41-0.65; P<.001). Infants born to vaccinated mothers also had lower rates of admission to the neonatal intensive care unit. There was no significant increase in the rate of congenital anomalies or birthweight ≤3rd centile in vaccinated women. Vaccinated women were significantly less likely to have an infant with a major congenital anomaly compared with the unvaccinated group (2.4% vs 3.0%; adjusted odds ratio, 0.72; 95% confidence interval, 0.56-0.94; P=.02). This finding remained significant even when the analysis was restricted to women vaccinated before 20 weeks' gestation. CONCLUSION: COVID-19 vaccination during pregnancy was associated with a reduction in stillbirth and preterm birth, and not associated with any adverse impact on fetal growth or development. Vaccine coverage was substantially influenced by known social determinants of health. SN - 1097-6868 UR - https://www.unboundmedicine.com/medline/citation/36336084/Reductions_in_stillbirths_and_preterm_birth_in_COVID_19_vaccinated_women:_a_multicenter_cohort_study_of_vaccination_uptake_and_perinatal_outcomes_ DB - PRIME DP - Unbound Medicine ER -