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COVID-19 Vaccination and Preterm Birth: Current Evidence and Gaps

Authors:

Abstract

This review article examines current evidence on COVID-19 vaccination in pregnant women, focusing on its safety, efficacy, and impact on preventing infectious complications, particularly preterm birth. Numerous studies indicate that maternal vaccination is safe and effective in mitigating the risk of severe SARS-CoV-2-related infections, including a reduced incidence of premature deliveries. The vaccine's immune response supports in-trauterine stability, reducing disease-related inflammatory effects. Additionally, maternal vaccination facilitates antibody transfer to the fetus, potentially offering newborns protection in their initial months of life. While findings to date consistently highlight substantial benefits, several gaps remain. These include comparative analyses of different vaccine types, effects in high-risk pregnancies, and the longevity of immunity provided by booster doses. Further research is needed across diverse and vulnerable populations to broaden the global applicability of vaccination recommendations. This review supports the continued promotion of COVID-19 vaccination for pregnant women as a critical public health strategy. Effective communication strategies are essential to enhance vaccine uptake and reduce hesitancy. Expanding longitudinal studies on the effects of maternal vaccination will be pivotal for refining guidelines and supporting informed decision-making by healthcare providers and pregnant individuals.
Research Article
ISSN: 2574 -1241 DOI: 10.26717/BJSTR.2025.60.009460
COVID-19 Vaccination and Preterm Birth: Current
Evidence and Gaps
Copyright@ : Irami Araújo-Filho | Biomed J Sci & Tech Res | BJSTR.MS.ID.009460. 52662
Amália Cinthia Meneses do Rêgo1 and Irami Araújo-Filho1,2*
1Institute of Teaching, Research, and Innovation, Liga Contra o Câncer, Full Professor of the Postgraduate Program in Biotechnology at Potiguar
University, Potiguar University (UnP), Brazil
2Full Professor, Department of Surgery, Potiguar University. Ph.D. in Health Science, Brazil
*Corresponding author: Irami Araújo-Filho, Postgraduate Program in Biotechnology at Potiguar University/ UnP, Full Professor Department
of Surgery, Federal University of Rio Grande do Norte. Full Professor, Department of Surgery, Potiguar University. Ph.D. in Health Science/
Natal-RN, Brazil
ABSTRACT
This review article examines current evidence on COVID-19 vaccination in pregnant women, focusing on its
-
ies indicate that maternal vaccination is safe and effective in mitigating the risk of severe SARS-CoV-2-related
infections, including a reduced incidence of premature deliveries. The vaccine’s immune response supports in-

-

  

of vaccination recommendations. This review supports the continued promotion of COVID-19 vaccination for


 -
nant individuals.
Keywords: COVID-19; Vaccines; Pregnancy; Immunization; Sars-Cov-2; Pregnancy Complications; Premature
Birth
ARTICLE INFO
Received: January 27, 2025
Published: 
Citation: Amália Cinthia Meneses do
Rêgo and Irami Araújo-Filho. COV-
ID-19 Vaccination and Preterm Birth:
    
J Sci & Tech Res 60(3)-2025. BJSTR.
MS.ID.009460.
Introduction
       
  -
       
       -
-
  


-
cal impairments, and weakened immune responses, often necessitat-

   
  
    
        
further intensify during pregnancy. The immune system of preg-
        
   
       
with immunological changes intrinsic to pregnancy, may heighten
        
     -
tive measures to reduce the risks and complications associated with
COVID-19 among pregnant populations.
Copyright@ : Irami Araújo-Filho | Biomed J Sci & Tech Res | BJSTR.MS.ID.009460.
Volume 60- Issue 3 DOI: 10.26717/BJSTR.2025.60.009460
52663
   -
tial in mitigating the adverse effects of the pandemic on maternal and
       
         
  
However, pregnant women were frequently excluded from early clini-
-
-
dicate that COVID-19 vaccination is generally safe for pregnant women

the incidence of adverse pregnancy outcomes, including preterm

-
nation in preventing prematurity, particularly in different gestational
-
explored aspect in the literature is the effect of maternal vaccination


distinct clinical characteristics and corresponding risks of neonatal
      
-
tion, supporting the development of more precise and individualized

      

  
-
ly mRNA and inactivated vaccines, and the different dosing sched-
         
     -
vated vaccines remain an essential option, especially in developing
     
-
-


especially in regions where logistical and economic factors limit vac-

on preterm infants exposed in utero represents an emerging area of
interest. Initial studies primarily examine immediate neonatal out-
    
However, limited information regarding these children’s neurocogni-
tive and immunological development over their early years is avail-
      -
ment of preterm neonates exposed to maternal vaccination highlights
-

Therefore, research focusing on these long-term outcomes is es-
sential to provide a more comprehensive view of the implications of
 -
cy of COVID-19 vaccination in pregnant women who have conditions
 -
   
     
        -
ture provides limited insights into COVID-19 vaccination in pregnant
women with such conditions, hindering the development of tailored

-
  -


-
uterine environment, helping protect the fetus and reduce the likeli-

through which maternal immunization confers this protection remain
  -
cal for understanding how vaccination prevents pregnancy complica-


The emergence of new SARS-CoV-2 variants, such as Delta and


-
mission and virulence characteristics, which may alter the immune
-
cine effectiveness against these variants is essential to ensure con-
tinued protection for pregnant women and their infants as the virus

is fundamental to sustained maternal and neonatal health protection



     
developing countries where socioeconomic constraints and health-
        
-


on COVID-19 vaccination and prematurity is relevant for various de-
-


-

  
       -
cation strategies that promote adherence. Informed approaches that
Copyright@ : Irami Araújo-Filho | Biomed J Sci & Tech Res | BJSTR.MS.ID.009460. 52664
Volume 60- Issue 3 DOI: 10.26717/BJSTR.2025.60.009460

       
Vaccination during pregnancy is a relatively new preventive strategy,
-

neonatal outcomes associated with maternal vaccination is critical, as

-
  

-

        
-

        


        -
tion in pregnancy, numerous questions remain unanswered. Contin-

type, maternal health conditions, and viral variants, is essential for a
more comprehensive understanding of COVID-19 vaccination effects
 
        
          

 -
ments and remaining data gaps. By synthesizing existing knowledge
and identifying critical areas for future research, this review aims to
    
guide ongoing investigations on maternal vaccination, ultimately en-
hancing understanding of how COVID-19 immunization during preg-

Methods
This review study was designed to assess the effectiveness of
COVID-19 vaccination among pregnant women and its role in miti-
gating infectious complications during pregnancy, with a particular
emphasis on prematurity-related outcomes. A systematic literature

-

          

“COVID-19,” “Vaccines,” “Pregnancy,” “Immunization,” “SARS-CoV-2,
“Pregnancy Complications, Infectious,” and “Premature Birth.” Bool-
     
ensure the comprehensive retrieval of studies relevant to this topic.
Inclusion criteria for this review span a range of study designs, in-
cluding randomized clinical trials, cohort studies, case-control stud-
ies, cross-sectional studies, case series, systematic reviews, and
       
analysis of vaccinated versus unvaccinated pregnant women, focus-
-
 
potential long-term health implications for neonates. Two reviewers


  -
olution was sought through discussion; if necessary, a third reviewer
-
   -
iations during the selection process. Data extraction was conducted
following a standardized protocol, with key data points collected on
       -
comes related to COVID-19 vaccination during pregnancy. Thematic
   
     -
   

as the implications for neonatal health in the long term. Additionally,

       
       -
vides a comprehensive synthesis of current literature, offering in-
sights into the strengths and limitations of COVID-19 vaccination for
pregnant women. By identifying existing knowledge gaps and propos-
 


and child across diverse healthcare environments.
Results and Discussion
      
     -
  -
gests that SARS-CoV-2 infection during pregnancy heightens the risk
 

the intrauterine environment, increasing the chances of premature
       
        -
 

and fetus from adverse outcomes. Thus, understanding the complex
-
-


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Volume 60- Issue 3 DOI: 10.26717/BJSTR.2025.60.009460
52665
       -
ness in reducing the severity of COVID-19. However, few studies have
directly compared mRNA vaccines with inactivated vaccines, such as
      
This lack of comparative data limits our understanding of whether
  
prematurity.
Table 1: COVID-19 Vaccination - Pregnancy and Prematurity.
Author Study Results
Blakeway, et al. [1] Retrospective Cohort
This study found that COVID-19 vaccination during pregnancy posed no signicant safety risks.
Vaccinated pregnant women showed a reduced incidence of severe COVID-19 complications, in-
cluding a lower rate of preterm births. These results support vaccination as a preventive measure to
reduce adverse pregnancy outcomes associated with COVID-19 infection.
Carbone, et al. [2] Systematic Review &
Meta-analysis
This meta-analysis across multiple studies revealed that maternal COVID-19 vaccination is linked
to a reduced risk of adverse neonatal outcomes, including prematurity and low birth weight. The
ndings underscore the value of maternal immunization to improve neonatal health outcomes by
mitigating the risks associated with maternal SARS-CoV-2 infection.
Jamieson, et al. [3] Review
This review highlighted the protective effects of COVID-19 vaccination in pregnant women, empha-
sizing reduced risks of maternal and neonatal complications due to COVID-19. It strongly supports
vaccination as part of routine prenatal care to safeguard maternal and newborn health by prevent-
ing severe infection-related outcomes.
Male [4] Narrative Review
This study explored the immunological benets of maternal COVID-19 vaccination, particularly
the potential for antibody transfer from mother to fetus, which could offer early-life protection for
newborns. The review suggests that maternal vaccination provides passive immunity to the fetus,
shielding infants from SARS-CoV-2 in early infancy.
Rahmati, et al. [5] Systematic Review &
Meta-analysis
This systematic review conrmed that COVID-19 vaccination in pregnant women lowers both infec-
tion rates and the severity of outcomes, indirectly decreasing the risk of prematurity. The ndings
advocate for incorporating COVID-19 vaccination into prenatal care as it reduces risks associated
with maternal infection and improves neonatal health outcomes.
Kalafat, et al. [7] Cohort Study
Findings showed that vaccinated pregnant women had signicantly lower rates of stillbirth
and preterm birth compared to their unvaccinated counterparts. This study supports the role of
COVID-19 vaccination in reducing pregnancy complications and highlights the need for public
health policies that encourage maternal vaccination.
Du, et al. [10] Cohort Study
This study examined the safety of inactivated COVID-19 vaccines administered in the rst trimester,
concluding there were no adverse effects on pregnancy outcomes. It reinforces the safety of early
vaccination with inactivated vaccines, supporting its use even at early gestational stages without
increased risk of complications.
Lipkind, et al. [11] Population-based
Study
In this large-scale study, no increased risk for preterm or small-for-gestational-age births was found
in vaccinated women, providing robust evidence for the safety of COVID-19 vaccination in preg-
nancy across diverse populations. The study highlights that vaccination does not increase the risk of
adverse pregnancy outcomes.
Shaee, et al. [12] Meta-analysis
A meta-analysis conrming that COVID-19 vaccination during pregnancy does not negatively
affect neonatal outcomes, such as birth weight or gestational age. It supports the safety of vaccina-
tion across all pregnancy trimesters and advocates for maternal immunization as part of standard
prenatal care.
Jaswa, et al. [13] Longitudinal Cohort
This cohort study investigated early neurodevelopmental outcomes in infants exposed to COVID-19
vaccination in utero, nding no adverse effects on cognitive or motor development at 12-18 months.
The study supports the safety of maternal vaccination, showing no negative impact on early child-
hood developmental milestones.
Zhao, et al. [14] Cohort Study
Examined outcomes in pregnancies where inactivated COVID-19 vaccines were administered before
conception, reporting no association with adverse outcomes. These results conrm the safety of
preconception vaccination, indicating no increased risk for complications later in pregnancy.
Fell, et al. [17] Retrospective Cohort
Analysis from a large retrospective cohort study showed a marked reduction in preterm birth
and stillbirth rates among vaccinated mothers, especially among high-risk pregnancies. The study
supports COVID-19 vaccination as a means to improve neonatal survival by preventing SARS-CoV-
2-related adverse outcomes in pregnant women.
Goldshtein, et al. [18] Cohort Study
Results from this cohort study found that maternal vaccination with the BNT162b2 mRNA vaccine
was associated with favorable neonatal outcomes, including the potential enhancement of early-life
immunity through antibody transfer. Findings suggest that vaccination may provide neonates with
some protection against SARS-CoV-2 infection after birth.
Copyright@ : Irami Araújo-Filho | Biomed J Sci & Tech Res | BJSTR.MS.ID.009460. 52666
Volume 60- Issue 3 DOI: 10.26717/BJSTR.2025.60.009460
Hui, et al. [20] Cohort Study
The study found that vaccinated pregnant women had signicantly lower rates of stillbirth and
preterm birth than those unvaccinated, underscoring the importance of maternal vaccination pro-
grams as a strategy to reduce adverse pregnancy outcomes during the pandemic.
Zhang, et al. [25] Meta-analysis
This meta-analysis focused on neonatal outcomes, reporting reduced respiratory complications,
including lower rates of respiratory distress in infants born to vaccinated mothers. Findings support
maternal vaccination for its potential positive impact on neonatal respiratory health, contributing to
healthier neonatal outcomes.
Darwin, et al. [26] Retrospective Cohort
This U.S.-based cohort study found signicant reductions in preterm births among vaccinated
pregnant women. Results underscore the protective effect of COVID-19 vaccination in preventing
preterm births and related neonatal complications, positioning vaccination as a crucial preventive
intervention for maternal and child health.
Note: Source: Authors.
       -

  
   
to guide recommendations in settings where vaccine choice is con-

regimen is also critically important in developing effective maternal
 -

  -
 
     -

 
        -
 
  -

are commonly studied, the long-term effects of maternal vaccination
       
-
derstanding the implications of maternal immunization on neurocog-

This research is critical, as it may reveal whether vaccination
during pregnancy supports neonatal immune resilience over time or
       

        
       -
cinated neonates could also elucidate whether maternal vaccination
confers indirect protection against infections in early infancy-a peri-
-
-


effect would reinforce the value of maternal immunization. Addition-
-
mune-related metrics, would provide a comprehensive view of ma-
  
women with high-risk conditions, such as gestational hypertension
  
      

prematurity risk, and vaccination could provide an additional safe-

        -
groups remains limited, complicating the creation of targeted guide-
lines. Future studies should prioritize including high-risk pregnant
populations to determine whether immunization strategies should

         
pregnancy. Research into immune response variations across tri-

        
-
derstanding how timing affects fetal immunity is especially relevant
for optimizing vaccination protocols and could yield insights that re-

impact on placental function and development is a vital yet underex-
plored area. The placenta is essential for nutrient transfer and fetal

health, including vascular function and immune interactions, could

  
-
   


-

  -
ing respiratory diseases and neonatal infections during pregnancy,
highlighting the importance of maternal immunization against infec-

if COVID-19 vaccines similarly offer protective effects, especially in
 
    
Copyright@ : Irami Araújo-Filho | Biomed J Sci & Tech Res | BJSTR.MS.ID.009460.
Volume 60- Issue 3 DOI: 10.26717/BJSTR.2025.60.009460
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of SARS-CoV-2 variants, such as Delta and Omicron, poses additional
  
-

indicates that the immune response in vaccinated pregnant women
might vary depending on the circulating variant, emphasizing the
-
ies on the effectiveness of different vaccine formulations and dosing
  -
tion protocols to ensure consistent protection for pregnant women
        

       
          -
      -

        -
       

among pregnant women, ultimately increasing vaccination rates and
      
-
ally. Many studies on vaccination and prematurity are conducted in
-

      

must include diverse populations from the underrepresented areas
 -
  

    -
-
nicities.
Research in underserved regions and among varied demograph-

     -

 
-
-

-





data on COVID-19 vaccination in pregnancy are promising, many
questions remain. Research addressing critical gaps—such as optimal
vaccine types, ideal dose schedules, interactions with maternal health
-
      


-

For instance, studies exploring rates of congenital infections, re-
spiratory distress, and NICU admissions among vaccinated mothers’
infants could add depth to our understanding of maternal vaccina-

       
  -
posed to COVID-19 vaccination in utero, particularly regarding neu-
rocognitive and immune development, are critical for assessing the
  
       
-
-
 
in pregnant women represents a vital intervention to mitigate risks
       


timing, maternal immune responses across viral variants, and specif-
-
      
-
tational age are essential to ensure maternal vaccination guidelines


Conclusion
This review underscores the critical role of COVID-19 vaccina-
tion in pregnancy as a protective measure for maternal and neonatal
   
safe and effective in mitigating severe infectious complications during
 -

     
with SARS-CoV-2 infection. Furthermore, vaccination facilitates ma-
      
  
-
nant women, further research is needed to address the remaining
 -
ferent vaccine types, outcomes in high-risk pregnancies, and the im-
-
tion. Additionally, further investigation into varied and underserved
-
Copyright@ : Irami Araújo-Filho | Biomed J Sci & Tech Res | BJSTR.MS.ID.009460. 52668
Volume 60- Issue 3 DOI: 10.26717/BJSTR.2025.60.009460
lines. Current evidence supports continuing COVID-19 vaccination

      
trust and reduce vaccine hesitancy to maximize coverage.
-
-
care providers and pregnant individuals to make well-informed, safe
decisions.
Acknowledgments
The authors thank the Federal University of Rio Grande do Norte,
         
study.
Conict of Interest

References
1.             

Gynecol 226(2): 236.e1-236.e14.
2.             
(2022) COVID-19 vaccine and pregnancy outcomes: A systematic review

3. Jamieson DJ, Rasmussen SA (2022) An update on COVID-19 and pregnan-

4. Male V (2022) SARS-CoV-2 infection and COVID-19 vaccination in preg-

5.     
COVID-19 vaccination during pregnancy on SARS-CoV-2 infection and
maternal and neonatal outcomes: A systematic review and meta-analysis.
Rev Med Virol 33(3): e2434.
6. 
-

7. -

             


9. 
-

10. 
vaccination against COVID-19 and neonatal outcomes during Omicron:

11. Zhao Y, Zhao Y, Su X, Zhou Y, Zhang Z, et al. (2023) No association of vacci-
 -

Chinese pregnant women J Med Virol 95(4).
12.    
et al. (2022) Receipt of COVID-19 vaccine during pregnancy and preterm
    -


13. 
al. (2023) COVID-19 vaccination during pregnancy: a systematic review

14. 

preterm. JAMA Netw Open 7(1).
15. 
exposure to maternal COVID-19 vaccination and offspring neurodevelop-

16. -
   
multicenter cohort study of vaccination uptake and perinatal outcomes.

17. 
of COVID-19 on infant health. Proc Natl Acad Sci U S A 120(49).
  


19. 
-
inantly Black population. J Matern Fetal Neonatal Med 36(1): 2196364.
20. 
and meta-analysis of neonatal outcomes of COVID-19 vaccination in preg-
nancy. Pediatr Res 94(1): 34-42.
21.           

22. 
-

23.         



24. -

and early infant outcomes. JAMA Pediatr 176(5): 470-477.
25.   -
pact of COVID-19 and vaccination during pregnancy on placenta-mediated

26.         -
stetric outcomes in women with rheumatic disease and COVID-19 in the
context of vaccination status. Rheumatology (Oxford) 62(4): 1621-1626.
27.        
-

 
and adverse perinatal outcomes: a systematic review and meta-analysis.

29. -

30. -
Copyright@ : Irami Araújo-Filho | Biomed J Sci & Tech Res | BJSTR.MS.ID.009460.
Volume 60- Issue 3 DOI: 10.26717/BJSTR.2025.60.009460
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tematic review and meta-analysis of the effectiveness and perinatal out-
comes of COVID-19 vaccination in pregnancy. Nat Commun 13(1): 2414.
31.               
COVID-19 vaccination during pregnancy with adverse neonatal and ma-
        
Health 11: 1044031.
32. 
-
stet Gynecol MFM 3(6): 100467.
33. -
son & Johnson/Janssen post-COVID vaccine hematological adverse events
-

    

34. 
COVID-19 vaccination safety and effectiveness during pregnancy: interim
  

35. -
tion during pregnancy: do healthcare workers recommend vaccination

36. -
-
demic: a protocol for timely, adaptive monitoring of perinatal outcomes in

37. -


     



39. -
ciation of SARS-CoV-2 vaccination during pregnancy with pregnancy out-
comes. JAMA 327(15): 1469-1477.
40. 
Perinatal outcomes and Sinopharm BBIBP-CorV vaccination during preg-

41. 


42.             
Surveillance systems for monitoring vaccination coverage with vaccines
        

43. 
vaccination on symptomatic infection and related symptoms among

44. -
cination and transmission patterns among pregnant and postnatal wom-

Hong Kong Med J 30(1): 16-24.
45.     -
nation during early pregnancy: A single-center prospective cohort study
of Chinese pregnant women. Hum Vaccin Immunother 19(2): 2226995.
46. Vidal MJ, Martínez Solanas È, Mendoza S, Sala N, Jané M, et al. (2023) Im-

and epidemiological features. Gac Sanit 37:102332.
47. Piekos SN, Hwang YM, Roper RT, Sorensen T, Price ND, et al. (2023) The
   
        
e594-e606.
      


49. Akgül F, Tüzer C, Arslan Y, Sevim B (2023) COVID-19 infection during preg-
nancy: A retrospective study in a city in the Southeastern region of Turkey.

50. 

neonatal outcomes. Vaccines (Basel) 11(11): 1710.
51. 
Peripartum outcomes associated with COVID-19 vaccination during preg-
nancy: a systematic review and meta-analysis. JAMA Pediatr 176(11):

52. Yang C, Zheng Z, Zheng P, Chen J, Huang Q, et al. (2023) Inactivated
COVID-19 vaccines in the peri-pregnancy period: evaluation of safety for

53. 
       

54.             
         -
ta-analysis. Vaccines (Basel) 12(1): 102.
55. Meghani M, Razzaghi H, Pingali C, Crane B, Naleway A, et al. (2021)
COVID-19 vaccination coverage among pregnant women during pregnan-
    

56. 
-

57. 
vaccination on symptomatic infection and related symptoms among

 


59.         -
stetric outcomes in women with rheumatic disease and COVID-19 in the
context of vaccination status. Rheumatology (Oxford) 62(4):1621-1626.
60. 
   
-
spir Med 10(12): 1129-1136.
61.     -
nation during early pregnancy: A single-center prospective cohort study
of Chinese pregnant women. Hum Vaccin Immunother 19(2): 2226995.
62. -
tematic review and meta-analysis of the effectiveness and perinatal out-
comes of COVID-19 vaccination in pregnancy. Nat Commun 13(1): 2414.
Copyright@ : Irami Araújo-Filho | Biomed J Sci & Tech Res | BJSTR.MS.ID.009460. 52670
Volume 60- Issue 3 DOI: 10.26717/BJSTR.2025.60.009460
63.   -
pact of COVID-19 and vaccination during pregnancy on placenta-mediated

64. 
exposure to maternal COVID-19 vaccination and offspring neurodevelop-

65. -
   
multicenter cohort study of vaccination uptake and perinatal outcomes.

66. 


67. 
al. (2023) COVID-19 vaccination during pregnancy: a systematic review

 Zhao Y, Zhao Y, Su X, Zhou Y, Zhang Z, et al. (2023) No association of vacci-
 -

Chinese pregnant women. J Med Virol 95(4).
69.    
et al. (2022) Receipt of COVID-19 vaccine during pregnancy and preterm
    -


70.  


71.           -
pact of COVID-19 on infant health. Proc Natl Acad Sci U S A 120(49):
e2311573120.
72. 
-

73. 
vaccination against COVID-19 and neonatal outcomes during Omicron:

74. 
-

75.            


76.        
-

77.             

Gynecol 226(2): 236.e1-236.e14.
             
(2022) COVID-19 vaccine and pregnancy outcomes: A systematic review

79.       

 -

 Male V (2022) SARS-CoV-2 infection and COVID-19 vaccination in preg-

 Jamieson DJ, Rasmussen SA (2022) An update on COVID-19 and pregnan-

 
-

     
COVID-19 vaccination during pregnancy on SARS-CoV-2 infection and
maternal and neonatal outcomes: A systematic review and meta-analysis.
Rev Med Virol 33(3): e2434.
       



 -
tematic review and meta-analysis of the effectiveness and perinatal out-
comes of COVID-19 vaccination in pregnancy. Nat Commun 13(1): 2414.
 Zhao Y, Su X, Zhou Y, Zhang Z, Zhang Y, et al. (2023) No association of vac-
-

Chinese pregnant women. J Med Virol 95(4).
 -

and early infant outcomes. JAMA Pediatr 176(5): 470-477.
 


90. -
-
demic: a protocol for timely, adaptive monitoring of perinatal outcomes in

Copyright@ : Irami Araújo-Filho | Biomed J Sci & Tech Res | BJSTR.MS.ID.009460.
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Article
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Vaccination plays a crucial role in preventing and controlling SARS-CoV-2 infections as well as their associated adverse outcomes. But there is a notable lack of research on the effectiveness of COVID-19 vaccination in children, particularly those young preterm-born children, who are more vulnerable to severe outcomes from SARS-CoV-2 infection. We aimed to determine the effect of vaccination with inactivated vaccines BBIBP-CorV and CoronaVac on symptomatic COVID-19 infection and related symptoms in preterm-born children aged 3–7 years after relaxation of the COVID-19 prevention and control measures in December 2022 in China. We performed a retrospective cohort study involving 242 preterm-born children aged 3–7 years and the data were collected in March 2023. Logistic regression models and modified Poisson regression models combined with entropy balancing were used to explore the associations of vaccination against SARS-CoV-2 with symptomatic COVID-19, specific symptoms, and persistent symptoms one month after recovery from COVID-19. Of the 242 recruited preterm-born children, 156 (64.5%) were vaccinated with inactivated vaccines BBIBP‐CorV and CoronaVac. After entropy balancing, the covariates were balanced between the vaccinated and the unvaccinated groups, with standardized mean difference < 0.001. Vaccination with the said SARS-CoV-2 vaccines lowered the risk of developing symptomatic COVID-19 in preterm-born children (risk ratio [RR] = 0.783; 95% confidence interval [CI]: (0.711, 0.861). Likewise, COVID-19 vaccination was associated with a decline in the risk of pneumonia (odds ratio [OR] = 0.318; 95% CI 0.110, 0.913), fever (RR = 0.710; 95% CI 0.635, 0.794), high fever (RR = 0.542; 95% CI 0.297, 0.988), sore throat (OR = 0.304; 95% CI 0.139, 0.664), and persistent symptoms (RR = 0.425; 95% CI 0.182, 0.993). Immunization with inactivated vaccines BBIBP‐CorV and CoronaVac provides protection against symptomatic COVID-19 for preterm-born children 3–7 years.
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Background After the outbreak of COVID-19, a huge part of the health care services was dedicated to preventing and treating this disease. In case of COVID-19 infection, severe COVID-19 is reported more in pregnant individuals. Afterward, Vaccination against SARS-CoV-2 became a hot topic due to known effects in preventing severe COVID-19 during pregnancy. Vaccination of pregnant individuals started in August 2021 with the Sinopharm vaccine in Iran. The aim of current study was to determine the incidence of perinatal outcomes in women who were vaccinated during pregnancy. Method This retrospective cohort study included 129,488 singleton births from March 21, 2021, until March 21, 2022, in Tehran, Iran. The data was obtained from the Iranian Maternal and Neonatal (IMaN) Network and the Maternal Vaccination Registry. Adverse perinatal outcomes investigated in this study include preterm birth, extremely preterm birth, low birth weight, very low birth weight, intrauterine growth restriction, stillbirth, neonatal intensive care unit admission, congenital anomaly, neonatal death and low 5-minute Apgar score. The risk of all perinatal outcomes was evaluated using multiple logistic regression. The analysis was done using STATA version 14. Results Of all 129,488 singleton births included in this study, 17,485 (13.5%) were vaccinated against SARS-CoV-2 (all with Sinopharm (BBIBP-CorV)). The exposure to the Sinopharm vaccine during pregnancy caused a significant decrease in the incidence of preterm birth (P =0.006, OR=0.91 [95% CI, 0.85 to 0.97]), extremely preterm birth (P =<0.001,OR=0.55 [95% CI, 0.45 to 0.66]), and stillbirth (P =<0.001, OR=0.60 [95% CI, 0.47 to 0.76]). Exposure to vaccination during the first trimester was associated with an increased risk of preterm birth (P =0.01, OR=1.27 [95% CI, 1.04 to 1.55]) Maternal vaccination during pregnancy was not associated with an increased risk of other adverse perinatal outcomes included in this study. Conclusion The finding of this population-based study indicated no adverse pregnancy outcome due to vaccination with the Sinopharm vaccine during the second and third trimesters of pregnancy. Overall risk of adverse pregnancy outcomes were lower in the vaccinated individuals compared to the unvaccinated group. Also, vaccination during the first trimester was associated with an increased risk of preterm birth.
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During the coronavirus diseases 2019 (COVID-19) pandemic, the safety and efficacy of vaccination during pregnancy, particularly regarding the risk of preterm birth, have been a subject of concern. This systematic review aims to evaluate the impact of COVID-19 vaccination on preterm birth risk and to inform clinical practice and public health policies. Following PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines, a database search included PubMed, Embase, and Scopus, conducted up until October 2023. Inclusion criteria focused on studies that examined COVID-19 vaccination during pregnancy and its correlation with preterm birth, defined as a birth before 37 weeks of gestation. Six studies met these criteria, encompassing 35,612 patients. A quality assessment was performed using the Newcastle–Ottawa Scale and the Cochrane Collaboration’s tool, with the risk of bias evaluated via a funnel plot analysis and an Egger’s regression test. The studies demonstrated geographical diversity, mainly from Israel, Romania, and the United States, with a blend of prospective and retrospective designs. The patient cohort’s mean age was 31.2 years, with common comorbidities such as gestational diabetes and obesity affecting 9.85% of the total population. The vaccination types varied across the studies, with BNT162b2 being the most used. The results indicated a low heterogeneity among the included studies, evidenced by a Cochran’s Q statistic of 2.10 and an I2 statistic of 13%. The meta-analysis yielded a pooled odds ratio (OR) for a preterm birth risk post-vaccination of approximately 1.03 (95% CI: 0.82–1.30), suggesting no significant increase in preterm birth risk was associated with COVID-19 vaccination. Notable findings included a low preterm birth rate (as low as 0.6% and up to 6.1%) with minimal differences in neonatal outcomes, such as birth weight and APGAR (appearance, pulse, grimace, activity, and respiration) scores between vaccinated and unvaccinated groups. This study concludes that a COVID-19 vaccination during pregnancy does not significantly increase the risk of preterm birth. These findings are crucial for reassuring healthcare providers and pregnant women about the safety of COVID-19 vaccines and supporting their use in public health strategies during the pandemic.
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Importance COVID-19 vaccine–derived antibodies in pregnant people may protect infants from severe infection in the first 6 months of life via transplacental antibody transfer. Few data exist on maternally derived SARS-CoV-2 antibodies in preterm compared with full-term infants in association with vaccination timing. Objective To compare SARS-CoV-2 anti-Spike (anti-S) antibody levels in preterm and full-term infants in the context of vaccine dose timing before delivery. Design, Setting, and Participants This prospective cohort study enrolled pregnant individuals and collected paired maternal and cord blood samples at delivery at the University of Washington between February 1, 2021, and January 31, 2023. Participants who had received at least 2 doses of a messenger RNA COVID-19 vaccine before delivery and did not have a history of prior COVID-19 infection or detectable anti–SARS-CoV-2 nucleocapsid antibodies were included. Exposures Timing of the last vaccine dose and preterm or full-term gestational age at delivery. Main Outcomes and Measures Paired maternal and cord samples were tested for anti-S antibody, and linear regression was used to evaluate associations between preterm delivery and anti-S antibody levels. Covariates included timing of last dose, number of doses, insurance status, and immunosuppressing medications. Results A total of 220 participants (median [IQR] age, 34 [32-37] years; 212 [96.4%] female) with 36 preterm and 184 full-term deliveries were studied. Before delivery, 121 persons received 2 vaccine doses and 99 persons received 3 or more vaccine doses. The geometric mean concentration of maternal anti-S antibodies was 674 (95% CI, 577-787) after 2 doses and 8159 (95% CI, 6636-10 032) after 3 or more doses ( P < .001). The cord anti-S antibody geometric mean concentration was 1000 (95% CI, 874-1144) after 2 doses and 9992 (95% CI, 8381-11 914) after 3 or more doses ( P < .001). After adjustment for vaccine timing and number of doses before delivery, no association was found between preterm delivery and cord anti-S antibody levels (β = 0.44; 95% CI, −0.06 to 0.94). Conclusions and Relevance In this prospective cohort study of pregnant individuals with preterm and full-term deliveries, receipt of 3 or more compared with 2 doses of COVID-19 vaccine before delivery resulted in 10-fold higher cord anti-S antibody levels. Maternal antibody concentration appeared more important than delivery gestational age in determining cord anti-S antibody levels. The number of doses and timing considerations for COVID-19 vaccine in pregnancy should include individuals at risk for preterm delivery.
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In utero exposure to COVID-19 infection may lead to large intergenerational health effects. The impact of infection exposure has likely evolved since the onset of the pandemic as new variants emerge, immunity from prior infection increases, vaccines become available, and vaccine hesitancy persists, such that when infection is experienced is as important as whether it is experienced. We examine the changing impact of COVID-19 infection on preterm birth and the moderating role of vaccination. We offer the first plausibly causal estimate of the impact of maternal COVID-19 infection by using population data with no selectivity, universal information on maternal COVID-19 infection, and linked sibling data. We then assess change in this impact from 2020 to 2023 and evaluate the protective role of COVID-19 vaccination on infant health. We find a substantial adverse effect of prenatal COVID-19 infection on the probability of preterm birth. The impact was large during the first 2 y of the pandemic but had fully disappeared by 2022. The harmful impact of COVID-19 infection disappeared almost a year earlier in zip codes with high vaccination rates, suggesting that vaccines might have prevented thousands of preterm births. The findings highlight the need to monitor the changing consequences of emerging infectious diseases over time and the importance of mitigation strategies to reduce the burden of infection on vulnerable populations.
Article
OBJECTIVE To evaluate maternal and neonatal outcomes by type of antihypertensive used in participants of the CHAP (Chronic Hypertension in Pregnancy) trial. METHODS We conducted a planned secondary analysis of CHAP, an open-label, multicenter, randomized trial of antihypertensive treatment compared with standard care (no treatment unless severe hypertension developed) in pregnant patients with mild chronic hypertension (blood pressure 140–159/90–104 mm Hg before 20 weeks of gestation) and singleton pregnancies. We performed three comparisons based on medications prescribed at enrollment: labetalol compared with standard care, nifedipine compared with standard care, and labetalol compared with nifedipine. Although active compared with standard care groups were randomized, medication assignment within the active treatment group was not random but based on clinician or patient preference. The primary outcome was the occurrence of superimposed preeclampsia with severe features, preterm birth before 35 weeks of gestation, placental abruption, or fetal or neonatal death. The key secondary outcome was small for gestational age (SGA) neonates. We also compared medication adverse effects between groups. Relative risks (RRs) and 95% CIs were estimated with log binomial regression to adjust for confounding. RESULTS Of 2,292 participants analyzed, 720 (31.4%) received labetalol, 417 (18.2%) received nifedipine, and 1,155 (50.4%) received no treatment. The mean gestational age at enrollment was 10.5±3.7 weeks; nearly half of participants (47.5%) identified as non-Hispanic Black; and 44.5% used aspirin. The primary outcome occurred in 217 (30.1%), 130 (31.2%), and 427 (37.0%) in the labetalol, nifedipine, and standard care groups, respectively. Risk of the primary outcome was lower among those receiving treatment (labetalol use vs standard adjusted RR 0.82, 95% CI, 0.72–0.94; nifedipine use vs standard adjusted RR 0.84, 95% CI, 0.71–0.99), but there was no significant difference in risk when labetalol was compared with nifedipine (adjusted RR 0.98, 95% CI, 0.82–1.18). There were no significant differences in SGA or serious adverse events between participants receiving labetalol and those receiving nifedipine. CONCLUSION No significant differences in predetermined maternal or neonatal outcomes were detected on the basis of the use of labetalol or nifedipine for treatment of chronic hypertension in pregnancy. CLINICAL TRIAL REGISTRATION ClinicalTrials.gov, NCT02299414.
Article
Introduction: Vaccination is a key strategy to control the coronavirus disease 2019 (COVID-19) pandemic. Safety concerns strongly influence vaccine hesitancy. Disease transmission during pregnancy could exacerbate risks of preterm birth and perinatal mortality. This study examined patterns of vaccination and transmission among pregnant and postnatal women during the fifth wave of COVID-19 in Hong Kong. Methods: The Antenatal Record System and Clinical Management System of the Hospital Authority was used to retrieve information concerning the demographic characteristics, vaccination history, COVID-19 status, and obstetric outcomes of women who were booked for delivery at Queen Mary Hospital in Hong Kong and had attended the booking antenatal visit from 1 July 2021 to 30 June 2022. Results: Among 2396 women in the cohort, 2006 (83.7%), 1843 (76.9%), and 831 (34.7%) had received the first, second, and third doses of COVID-19 vaccine, respectively. Among 1012 women who had received the second dose, 684 (67.6%) women were overdue for their third dose. There were 265 (11.1%) reported COVID-19 cases. Women aged 20 to 29 years had a low vaccination rate but the highest disease rate (19.1%). The disease rate was more than tenfold higher in women who had no (20.3%) or incomplete (18.8%) vaccination, compared with women who had complete vaccination (2.1%; P<0.001). Conclusion: Acceptance of COVID-19 vaccination was low in pregnant women. Urgent measures are needed to promote vaccination among pregnant women before the next wave of COVID-19.
Article
Objective: Assess the risk associated with COVID-19 in pregnant women on maternal and neonatal outcomes in Catalonia (Spain) in 2020, before the beginning of COVID-19 vaccination campaign. Method: Cross-sectional descriptive study with all pregnant women (41,560) and their live newborns (42,097) (1st March to 31st December 2020). Women were classified: positive and negative COVID-19 diagnosis during pregnancy. The outcomes analysed were complications during pregnancy, gestational age, admission of newborns to neonatal intensive care unit (NICU) and birth weight. Associations among positive COVID-19 and maternal and infant variables were measured with logistic regression models. Results were expressed as odds ratios and 95% confidence intervals. Models were adjusted for nationality, maternal age, socioeconomic status, type of pregnancy and type of centre where the delivery occurred (public or private management hospital). Results: A total of 696 women (1.7%) were diagnosed with COVID-19 during pregnancy. Women with COVID-19 were 4.37 times more likely to have complications during pregnancy (4.37; 3.52-5.40). A total of 713 newborns (1.7%) were from mothers with COVID-19. A positive diagnosis of COVID-19 increased the risk of preterm birth (1.41; 1.03-1.89), admission to NICU (1.40; 1.06-1.82) and low birth weight (1.35; 0.99-1.80) in babies. Conclusions: Pregnant women with COVID-19 had higher risk of developing complications during pregnancy and their newborns were more likely to be admitted to NICU and had prematurity.