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High-Dose Quadrivalent Influenza Vaccine for Prevention of Cardiovascular and Respiratory Hospitalizations in Older Adults.
Palmu, Arto A; Pepin, Stephanie; Syrjänen, Ritva K; Mari, Karine; Mallett Moore, Tamala; Jokinen, Jukka; Nieminen, Heta; Kilpi, Terhi; Samson, Sandrine I; De Bruijn, Iris.
Afiliação
  • Palmu AA; Finnish Institute for Health and Welfare (THL), Tampere, Finland.
  • Pepin S; Global Clinical Development, Sanofi, Marcy L'Etoile, France.
  • Syrjänen RK; Finnish Institute for Health and Welfare (THL), Tampere, Finland.
  • Mari K; Biostatistics Global Clinical Development, Sanofi, Marcy L'Etoile, France.
  • Mallett Moore T; Global Pharmacovigilance, Sanofi, Swiftwater, Pennsylvania, USA.
  • Jokinen J; Finnish Institute for Health and Welfare (THL), Helsinki, Finland.
  • Nieminen H; Finnish Institute for Health and Welfare (THL), Tampere, Finland.
  • Kilpi T; Finnish Institute for Health and Welfare (THL), Helsinki, Finland.
  • Samson SI; Global Medical Affairs, Sanofi, Lyon, France.
  • De Bruijn I; Global Clinical Development, Sanofi, Marcy L'Etoile, France.
Influenza Other Respir Viruses ; 18(4): e13270, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38569647
ABSTRACT

BACKGROUND:

We assessed the relative vaccine effectiveness (rVE) of high-dose quadrivalent influenza vaccine (QIV-HD) versus standard-dose quadrivalent influenza vaccine (QIV-SD) in preventing respiratory or cardiovascular hospitalizations in older adults.

METHODS:

FinFluHD was a phase 3b/4 modified double-blind, randomized pragmatic trial. Enrolment of 121,000 adults ≥65 years was planned over three influenza seasons (October to December 2019-2021). Participants received a single injection of QIV-HD or QIV-SD. The primary endpoint was first occurrence of an unscheduled acute respiratory or cardiovascular hospitalization (ICD-10 primary discharge J/I codes), from ≥14 days post-vaccination until May 31. The study was terminated after one season due to COVID-19; follow-up data for 2019-2020 are presented.

RESULTS:

33,093 participants were vaccinated (QIV-HD, n = 16,549; QIV-SD, n = 16,544); 529 respiratory or cardiovascular hospitalizations (QIV-HD, n = 257; QIV-SD, n = 272) were recorded. The rVE of QIV-HD versus QIV-SD to prevent respiratory/cardiovascular hospitalizations was 5.5% (95% CI, -12.4 to 20.7). When prevention of respiratory and cardiovascular hospitalizations were considered separately, rVE estimates of QIV-HD versus QIV-SD were 5.4% (95% CI, -28.0 to 30.1) and 7.1% (95% CI, -15.0 to 25.0), respectively. Serious adverse reactions were <0.01% in both groups.

CONCLUSIONS:

Despite insufficient statistical power due to the impact of COVID-19, rVE point estimates demonstrated a trend toward a benefit of QIV-HD over QIV-SD. QIV-HD was associated with lower respiratory or cardiovascular hospitalization rates than QIV-SD, with a comparable safety profile. Adequately powered studies conducted over multiple influenza seasons are needed to determine statistical significance of QIV-HD compared with QIV-SD against preventing respiratory and cardiovascular hospitalizations. TRIAL REGISTRATION ClinicalTrials.gov number NCT04137887.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Influenza / Influenza Humana / COVID-19 Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Influenza / Influenza Humana / COVID-19 Idioma: En Ano de publicação: 2024 Tipo de documento: Article