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Safety of COVID-19 vaccines, their components or their platforms for pregnant women: A rapid review
Agustin Ciapponi; Ariel Bardach; Agustina Mazzoni; Tomas Alconada; Steven A. Anderson; Fernando J. Argento; Jamile Ballivian; Karin Bok; Daniel Comande; Emily Erbelding; Erin Goucher; Beate Kampmann; Ruth Karron; Flor M. Munoz; Maria Carolina Palermo; Edward P.K. Parker; Federico Rodriguez Cairoli; Maria Victoria Santa; Andy Stergachis; Gerald Voss; Xu Xiong; Natalia Zamora; Sabra Zaraa; Mabel Berrueta; Pierre M. Buekens.
Afiliação
  • Agustin Ciapponi; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Ariel Bardach; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Agustina Mazzoni; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Tomas Alconada; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Steven A. Anderson; US Food & Drug Administration
  • Fernando J. Argento; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Jamile Ballivian; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Karin Bok; National Institute of Allergy and Infectious Diseases; National Institutes of Health
  • Daniel Comande; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Emily Erbelding; National Institute of Allergy and Infectious Diseases
  • Erin Goucher; School of Public Health and Tropical Medicine, Tulane University, New Orleans, USA
  • Beate Kampmann; "The Vaccine Centre, London School of Hygiene and Tropical Medicine, London WC1E 7HT, UK; Vaccines & Immunity Theme, MRC Unit The Gambia at the London School o
  • Ruth Karron; Bloomberg School of Public Health, Johns Hopkins University
  • Flor M. Munoz; Baylor College of Medicine; Texas Children's Hospital
  • Maria Carolina Palermo; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Edward P.K. Parker; The Vaccine Centre, London School of Hygiene and Tropical Medicine, London WC1E 7HT, UK
  • Federico Rodriguez Cairoli; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Maria Victoria Santa; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Andy Stergachis; School of Pharmacy and School of Public Health, University of Washington, Seattle, WA USA
  • Gerald Voss; TuBerculosis Vaccine Initiative (TBVI, Lelystad, The Netherlands)
  • Xu Xiong; School of Public Health and Tropical Medicine, Tulane University, New Orleans, USA
  • Natalia Zamora; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Sabra Zaraa; School of Pharmacy, University of Washington, Seattle, USA.
  • Mabel Berrueta; Instituto de Efectividad Clinica y Sanitaria (IECS-CONICET), Buenos Aires, Argentina
  • Pierre M. Buekens; School of Public Health and Tropical Medicine, Tulane University, New Orleans, USA
Preprint em Inglês | medRxiv | ID: ppmedrxiv-21258283
ABSTRACT
BackgroundPregnant women with COVID-19 are at an increased risk of severe COVID-19 illness as well as adverse pregnancy and birth outcomes. Many countries are vaccinating or considering vaccinating pregnant women with limited available data about the safety of this strategy. Early identification of safety concerns of COVID-19 vaccines, including their components, or their technological platforms is therefore urgently needed. MethodsWe conducted a rapid systematic review, as the first phase of an ongoing full systematic review, to evaluate the safety of COVID-19 vaccines in pregnant women, including their components, and their technological platforms (whole virus, protein, viral vector or nucleic acid) used in other vaccines, following the Cochrane methods and the PRISMA statement for reporting (PROSPERO-CRD42021234185). We searched literature databases, COVID-19 and pregnancy registries from inception February 2021 without time or language restriction and explored the reference lists of relevant systematic reviews retrieved. We selected studies of any methodological design that included at least 50 pregnant women or pregnant animals exposed to the vaccines that were selected for review by the COVAX MIWG in August 2020 or their components or platforms included in the COVID-19 vaccines, and evaluated adverse events during pregnancy and the neonatal period. Pairs of reviewers independently selected studies through the COVIDENCE web software and performed the data extraction through a previously piloted online extraction form. Discrepancies were resolved by consensus. ResultsWe identified 6768 records, 256 potentially eligible studies were assessed by full-text, and 37 clinical and non-clinical studies (38 reports, involving 2,397,715 pregnant women and 56 pregnant animals) and 12 pregnancy registries were included. Most studies (89%) were conducted in high-income countries. The most frequent study design was cohort studies (n=21), followed by surveillance studies, randomized controlled trials, and registry analyses. Most studies (76%) allowed comparisons between vaccinated and unvaccinated pregnant women (n=25) or animals (n=3) and reported exposures during the three trimesters of pregnancy. The most frequent exposure was to AS03 adjuvant in the context of A/H1N1 pandemic influenza vaccines (n=24), followed by aluminum-based adjuvants (n=11). Aluminum phosphate was used in Respiratory Syncytial Virus Fusion candidate vaccines (n=3) and Tdap vaccines (n=3). Different aluminum-based adjuvants were used in hepatitis vaccines. The replication-deficient simian adenovirus ChAdOx1 was used for a Rift Valley fever vaccine. Only one study reported exposure to messenger RNA (mRNA) COVID-19 vaccines that also used lipid nanoparticles. Except for one preliminary report about A/H1N1 influenza vaccination (adjuvant AS03) - corrected by the authors in a more thorough analysis, all studies concluded that there were no safety concerns. ConclusionThis rapid review found no evidence of pregnancy-associated safety concerns of COVID-19 vaccines that were selected for review by the COVAX MIWG or of their components or platforms when used in other vaccines. However, the need for further data on several vaccine platforms and components is warranted given their novelty. Our findings support current WHO guidelines recommending that pregnant women may consider receiving COVID-19 vaccines, particularly if they are at high risk of exposure or have comorbidities that enhance the risk of severe disease.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct / Review / Revisão sistemática Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Cohort_studies / Experimental_studies / Estudo observacional / Estudo prognóstico / Rct / Review / Revisão sistemática Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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