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Post-marketing active surveillance of Guillain Barré Syndrome following COVID-19 vaccination in persons aged ≥12 years in Italy: A multi-database self-controlled case series study.
Morciano, Cristina; Spila Alegiani, Stefania; Menniti Ippolito, Francesca; Belleudi, Valeria; Trifirò, Gianluca; Zanoni, Giovanna; Puccini, Aurora; Sapigni, Ester; Mores, Nadia; Leoni, Olivia; Monaco, Giuseppe; Clagnan, Elena; Zappetti, Cristina; Bovo, Emanuela; Cutillo, Maria; Da Cas, Roberto; Massari, Marco.
Afiliação
  • Morciano C; Pharmacoepidemiology and Pharmacosurveillance Unit, National Centre for Drug Research and Evaluation, Istituto Superiore di Sanità (National Institute of Health), Rome, Italy.
  • Spila Alegiani S; Pharmacoepidemiology and Pharmacosurveillance Unit, National Centre for Drug Research and Evaluation, Istituto Superiore di Sanità (National Institute of Health), Rome, Italy.
  • Menniti Ippolito F; Pharmacoepidemiology and Pharmacosurveillance Unit, National Centre for Drug Research and Evaluation, Istituto Superiore di Sanità (National Institute of Health), Rome, Italy.
  • Belleudi V; Department of Epidemiology ASL Roma 1, Lazio Regional Health Service, Rome, Italy.
  • Trifirò G; Department of Diagnostics and Public Health, University of Verona, Verona, Italy.
  • Zanoni G; Immunology Unit, University Hospital, Verona, Italy.
  • Puccini A; Hospital Assistance Service, General Directorate for Personal Care, Health and Welfare, Emilia-Romagna Region, Bologna, Italy.
  • Sapigni E; Hospital Assistance Service, General Directorate for Personal Care, Health and Welfare, Emilia-Romagna Region, Bologna, Italy.
  • Mores N; Institute of Pharmacology, Pharmacovigilance, Policlinico Universitario A. Gemelli, Catholic University of Sacred Heart, Rome, Italy.
  • Leoni O; Department of Health of Lombardy Region, Epidemiology Observatory, Milan, Italy.
  • Monaco G; Department of Health of Lombardy Region, Epidemiology Observatory, Milan, Italy.
  • Clagnan E; Regional Health Authority, Friuli Venezia Giulia Region, Udine, Italy.
  • Zappetti C; Central Directorate for Health, Social Policies, Friuli Venezia Giulia Region, Trieste, Italy.
  • Bovo E; Veneto Tumour Registry, Azienda Zero, Padova, Italy.
  • Cutillo M; Pharmacoepidemiology and Pharmacosurveillance Unit, National Centre for Drug Research and Evaluation, Istituto Superiore di Sanità (National Institute of Health), Rome, Italy.
  • Da Cas R; Pharmacoepidemiology and Pharmacosurveillance Unit, National Centre for Drug Research and Evaluation, Istituto Superiore di Sanità (National Institute of Health), Rome, Italy.
  • Massari M; Pharmacoepidemiology and Pharmacosurveillance Unit, National Centre for Drug Research and Evaluation, Istituto Superiore di Sanità (National Institute of Health), Rome, Italy.
PLoS One ; 19(1): e0290879, 2024.
Article em En | MEDLINE | ID: mdl-38241309
ABSTRACT

BACKGROUND:

Recently published studies have reported association of COVID-19 vaccine ChAdOx1-S (Vaxzevria) with Guillain Barré Syndrome (GBS). Less is known about the safety of other COVID-19 vaccines with respect to GBS outcome. This study investigated the association of COVID-19 vaccines with GBS in more than 15 million persons aged ≥12 years in Italy.

METHODS:

Study population was all individuals aged ≥12 years who received at least one dose of COVID-19 vaccines, admitted to emergency care/hospital for GBS from 27 December 2020-30 September 2021 in Italy. Identification of GBS cases and receipt of at least one dose of mRNA-1273 (Elasomeran), BNT162b2 (Tozinameran), ChAdOx1-S (Vaxzevria) and Ad26.COV2.S (Janssen) through record linkage between regional health care and vaccination registries. Relative Incidence (RI) was estimated Self-controlled case series method adapted to event-dependent exposure using in the 42-day exposure risk period after each dose compared with other observation periods.

RESULTS:

Increased risk of GBS was found after first (RI = 6.83; 95% CI 2.14-21.85) and second dose (RI = 7.41; 2.35-23.38) of mRNA-1273 and first dose of ChAdOx1-S (RI = 6.52; 2.88-14.77). Analysis by age found an increased risk among those aged≥60 years after first (RI = 8.03; 2.08-31.03) and second dose (RI = 7.71; 2.38-24.97) of mRNA-1273. The first dose of ChAdOx1-S was associated with GBS in those aged 40-59 (RI = 4.50; 1.37-14.79) and in those aged ≥ 60 years (RI = 6.84; 2.56-18.28).

CONCLUSIONS:

mRNA-1273 and ChAdOx1-S vaccines were associated with an increased risk of GBS however this risk resulted in a small number of excess cases. Limitations were loss of GBS outpatient cases and imprecision of the estimates in the subgroup analysis due to a low number of events.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Screening_studies Limite: Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Screening_studies Limite: Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article