TY - JOUR
T1 - High-Dose Versus Standard-Dose Influenza Vaccine and Cardiovascular Outcomes in Older Adults
T2 - The FLUNITY-HD Prespecified Pooled Analysis
AU - Johansen, Niklas Dyrby
AU - Modin, Daniel
AU - Pardo-Seco, Jacobo
AU - Rodriguez-Tenreiro-Sánchez, Carmen
AU - Loiacono, Matthew M
AU - Harris, Rebecca C
AU - Dufournet, Marine
AU - van Aalst, Robertus
AU - Chit, Ayman
AU - Larsen, Carsten Schade
AU - Larsen, Lykke
AU - Wiese, Lothar
AU - Dalager-Pedersen, Michael
AU - Claggett, Brian L
AU - Janstrup, Kira Hyldekær
AU - Duran-Parrondo, Carmen
AU - Piñeiro-Sotelo, Marta
AU - Cribeiro-González, Martín
AU - Conde-Pájaro, Mónica
AU - Mirás-Carballal, Susana
AU - González-Pérez, Juan-Manuel
AU - Solomon, Scott D
AU - Sivapalan, Pradeesh
AU - Martel, Cyril Jean-Marie
AU - Jensen, Jens Ulrik Stæhr
AU - Martinón-Torres, Federico
AU - Biering-Sørensen, Tor
AU - DANFLU-2 Study Group and the GALFLU Trial Team
A2 - Davidovski, Filip Soeskov
PY - 2026/3/17
Y1 - 2026/3/17
N2 - BACKGROUND: The high-dose inactivated influenza vaccine (HD-IIV) has demonstrated superior protection against a range of hospitalization end points versus standard-dose inactivated influenza vaccine (SD-IIV), but its effectiveness against specific cardiovascular outcomes and in those with pre-existing cardiovascular disease (CVD) is not well elucidated.METHODS: In a prespecified secondary analysis of the FLUNITY-HD (Pooled Analysis of Methodologically Harmonized Pragmatic Randomized Trials of High-Dose vs. Standard-Dose Influenza Vaccine Against Severe Clinical Outcomes) individual-level pooled data set integrating 2 methodologically harmonized pragmatic, individually randomized trials conducted in Denmark and Spain, we investigated the relative vaccine effectiveness of HD-IIV versus SD-IIV against severe cardiovascular outcomes and according to pre-existing CVD among adults ≥65 years of age. Data were primarily obtained from routine health care databases, with follow-up from 14 days after vaccination to May 31 the following year.RESULTS: The pooled data set encompassed 466 320 individually randomized participants, of whom 107 700 (23.1%) had a history of CVD. HD-IIV reduced the incidence of hospitalization for influenza or pneumonia, cardiorespiratory disease, laboratory-confirmed influenza, and any cause compared with SD-IIV, irrespective of the presence or absence of pre-existing CVD (
P
interaction>0.66 for all outcomes). Compared with the SD-IIV group, the HD-IIV group had a significantly lower incidence of hospitalization for any CVD (HD-IIV, 1.15%, versus SD-IIV, 1.24%; relative vaccine effectiveness, 6.6% [95% CI, 1.6-11.4];
P=0.010), hospitalization for any respiratory disease (HD-IIV, 0.92%, versus SD-IIV, 0.98%; relative vaccine effectiveness, 6.5% [95% CI, 0.7-11.9];
P=0.027), and hospitalization for heart failure (HD-IIV, 0.11%, versus SD-IIV, 0.15%; relative vaccine effectiveness, 21.3% [95% CI, 7.6-33.0];
P=0.003).
CONCLUSIONS: In a prespecified pooled analysis of 466 320 individually randomized older adults, HD-IIV reduced the incidence of a wide range of severe cardiovascular and respiratory outcomes compared with SD-IIV, with consistent findings regardless of previous history of CVD. Among cardiovascular outcomes, the protective effect of HD-IIV versus SD-IIV was particularly pronounced against hospitalization for heart failure.REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT06506812.
AB - BACKGROUND: The high-dose inactivated influenza vaccine (HD-IIV) has demonstrated superior protection against a range of hospitalization end points versus standard-dose inactivated influenza vaccine (SD-IIV), but its effectiveness against specific cardiovascular outcomes and in those with pre-existing cardiovascular disease (CVD) is not well elucidated.METHODS: In a prespecified secondary analysis of the FLUNITY-HD (Pooled Analysis of Methodologically Harmonized Pragmatic Randomized Trials of High-Dose vs. Standard-Dose Influenza Vaccine Against Severe Clinical Outcomes) individual-level pooled data set integrating 2 methodologically harmonized pragmatic, individually randomized trials conducted in Denmark and Spain, we investigated the relative vaccine effectiveness of HD-IIV versus SD-IIV against severe cardiovascular outcomes and according to pre-existing CVD among adults ≥65 years of age. Data were primarily obtained from routine health care databases, with follow-up from 14 days after vaccination to May 31 the following year.RESULTS: The pooled data set encompassed 466 320 individually randomized participants, of whom 107 700 (23.1%) had a history of CVD. HD-IIV reduced the incidence of hospitalization for influenza or pneumonia, cardiorespiratory disease, laboratory-confirmed influenza, and any cause compared with SD-IIV, irrespective of the presence or absence of pre-existing CVD (
P
interaction>0.66 for all outcomes). Compared with the SD-IIV group, the HD-IIV group had a significantly lower incidence of hospitalization for any CVD (HD-IIV, 1.15%, versus SD-IIV, 1.24%; relative vaccine effectiveness, 6.6% [95% CI, 1.6-11.4];
P=0.010), hospitalization for any respiratory disease (HD-IIV, 0.92%, versus SD-IIV, 0.98%; relative vaccine effectiveness, 6.5% [95% CI, 0.7-11.9];
P=0.027), and hospitalization for heart failure (HD-IIV, 0.11%, versus SD-IIV, 0.15%; relative vaccine effectiveness, 21.3% [95% CI, 7.6-33.0];
P=0.003).
CONCLUSIONS: In a prespecified pooled analysis of 466 320 individually randomized older adults, HD-IIV reduced the incidence of a wide range of severe cardiovascular and respiratory outcomes compared with SD-IIV, with consistent findings regardless of previous history of CVD. Among cardiovascular outcomes, the protective effect of HD-IIV versus SD-IIV was particularly pronounced against hospitalization for heart failure.REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT06506812.
KW - effectiveness
KW - high-dose
KW - hospitalization
KW - individual participant data
KW - individual randomization
KW - influenza
KW - meta-analysis
KW - pooled analysis
KW - pragmatic
KW - randomized controlled trial
KW - registry
KW - vaccine
UR - https://www.scopus.com/pages/publications/105033857266
U2 - 10.1161/CIRCULATIONAHA.125.077801
DO - 10.1161/CIRCULATIONAHA.125.077801
M3 - Journal article
C2 - 41212981
SN - 0009-7322
VL - 153
SP - 798
EP - 806
JO - Circulation
JF - Circulation
IS - 11
ER -