Association of post-vaccination adverse reactions after influenza vaccine with mortality and cardiopulmonary outcomes in patients with high-risk cardiovascular disease: the INVESTED trial.

All-cause death Cardiopulmonary hospitalizations High-risk cardiovascular disease Influenza vaccine Post-vaccination adverse reactions

Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
Feb 2023
Historique:
revised: 05 10 2022
received: 11 07 2022
accepted: 07 10 2022
pubmed: 7 11 2022
medline: 3 3 2023
entrez: 6 11 2022
Statut: ppublish

Résumé

Influenza vaccination is associated with reduced cardiopulmonary morbidity and mortality among patients with heart failure or recent myocardial infarction. The immune response to vaccination frequently results in mild adverse reactions (AR), which leads to vaccine hesitancy. This post hoc analysis explored the association between vaccine-related AR and morbidity and mortality in patients with high-risk cardiovascular disease. The INVESTED trial randomized 5260 patients with recent heart failure hospitalization or acute myocardial infarction to high-dose trivalent or standard-dose quadrivalent inactivated influenza vaccine. We examined the association between vaccine-related AR and adverse clinical outcomes across both treatment groups in propensity-adjusted models. Among 5210 participants with available information on post-vaccination symptoms, 1968 participants (37.8%) experienced a vaccine-related AR. Compared to those without AR, post-vaccination AR, most commonly injection site pain (60.3%), were associated with lower risk for the composite of all-cause death or cardiopulmonary hospitalization (hazard ratio [HR] 0.83, 95% confidence interval [CI] 0.75-0.92, p < 0.001), cardiopulmonary hospitalizations (HR 0.85 [95% CI 0.76-0.95], p = 0.003), all-cause death (HR 0.77 [95% CI 0.62-0.96], p = 0.02), cardiovascular hospitalizations (HR 0.88 [95% CI 0.78-0.99], p = 0.03) and non-cardiopulmonary hospitalizations (HR 0.80 [95% CI 0.69-0.92], p = 0.003). While mild (76.4%) and moderate (20.6%) AR were most common and together associated with lower risk for the primary outcome (HR 0.81 [95% CI 0.74-0.90], p < 0.001), severe AR (2.9%) were related to increased risk (HR 1.68 [95% CI 1.17-2.42], p = 0.005). Mild to moderate post-vaccination reactions after influenza vaccine were associated with reduced risk of cardiopulmonary hospitalizations and all-cause mortality in patients with high-risk cardiovascular disease, while severe reactions may indicate increased risk. Mild to moderate AR to influenza vaccination may be a marker of immune response and should not deter future vaccinations.

Identifiants

pubmed: 36335639
doi: 10.1002/ejhf.2716
pmc: PMC10292027
mid: NIHMS1855785
doi:

Substances chimiques

Influenza Vaccines 0

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

299-310

Subventions

Organisme : NHLBI NIH HHS
ID : U01 HL130163
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL130204
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01HL130163
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01HL130204
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022 European Society of Cardiology.

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Auteurs

Alexander Peikert (A)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Brian L Claggett (BL)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

KyungMann Kim (K)

Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI, USA.

Jacob A Udell (JA)

Peter Munk Cardiac Centre, University Health Network and Women's College Hospital, University of Toronto, Toronto, ONT, Canada.

Jacob Joseph (J)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Medicine, Boston, MA, USA.

Akshay S Desai (AS)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Michael E Farkouh (ME)

Peter Munk Cardiac Centre, University Health Network, University of Toronto, Toronto, ONT, Canada.

Sheila M Hegde (SM)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Adrian F Hernandez (AF)

Department of Medicine, Duke University, Durham, NC, USA.

Deepak L Bhatt (DL)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

J Michael Gaziano (JM)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Medicine, Boston, MA, USA.

H Keipp Talbot (HK)

Department of Medicine, Vanderbilt University, Nashville, TN, USA.

Clyde Yancy (C)

Department of Medicine, Northwestern University, Chicago, IL, USA.

Inder Anand (I)

Department of Medicine, University of Minnesota, Minneapolis VA Health Care System, Minneapolis, MN, USA.

Lu Mao (L)

Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, WI, USA.

Lawton S Cooper (LS)

National Heart, Lung, and Blood Institute, Bethesda, MD, USA.

Scott D Solomon (SD)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Orly Vardeny (O)

Department of Medicine, University of Minnesota, Minneapolis VA Health Care System, Minneapolis, MN, USA.

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