Risk of new-onset heart failure and heart failure exacerbations following COVID-19, influenza, or respiratory syncytial virus hospitalization

BACKGROUND: While acute respiratory-viral-infection (RVI) is associated with elevated short-term risk of concurrent cardiac events, less is known regarding subsequent heart-failure (HF) risk post-RVI hospitalisation. We evaluated risk of HF post-hospitalisation for influenza/COVID-19/respiratory-syncytial-virus(RSV). METHODS: Population-based retrospective cohort study, including all adult Singaporeans (≥18 years) hospitalised for influenza/COVID-19/RSV (01/01/2017-30/08/2023); stratified by pre-existing HF. Risks of acute HF (new-onset/readmission) post-RVI-hospitalisation was compared against controls (orthopaedic hospitalisations) using overlap-weighted competing-risks-regression. HF was ascertained using national healthcare-claims data. Analyses were further stratified by RVI type and vaccination status. RESULTS: Amongst individuals without pre-existing HF (N=59,408) hospitalised for RVI (influenza/COVID-19/RSV), overall risk of new-onset HF up to 180 days post-hospitalisation was elevated versus controls (adjusted-hazards-ratio, aHR=1.45[95%CI=1.26-1.67]). Risk of new-onset HF was observed up to 180 days post-hospitalisation for specific RVIs (RSV: aHR=2.03[95%CI=1.26-3.25]; COVID-19: aHR=1.36[95%CI=1.16-1.60]; influenza: aHR=1.62[95%CI=1.28-2.06]); however, risk was not significantly increased amongst influenza hospitalisations vaccinated <365 days prior (aHR=1.47[95%CI=0.82-2.64]). In HF patients (N=4163) hospitalised for RVI(influenza/COVID-19/RSV), risk of HF readmission was similarly increased (aHR=1.28[95%CI=1.08-1.52]). No increased risk of HF readmission post-COVID-19 was observed amongst individuals who received ≥4 COVID-19 vaccine doses (aHR=0.86[95%CI=0.59-1.27]), or who were vaccinated <180 days prior (aHR=0.97[95%CI=0.79-1.20]). Similarly, risk of HF readmission post-influenza was not significantly increased amongst individuals vaccinated <365 days prior (aHR=1.63[95%CI=0.94-2.82]). Elevated risk of HF readmission post-RVI hospitalisation predominantly accrued in older patients (≥70 years). CONCLUSIONS: RVIs can contribute to post-acute risk of new-onset HF and HF readmissions. Vaccination represents an opportunity for HF prevention amongst at-risk individuals.

Authors

Publication Details

Journal
UCL Discovery (University College London)
Published
2025-11-06
Primary Topic
Respiratory viral infections research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Risk of new-onset heart failure and heart failure exacerbations following COVID-19, influenza, or respiratory syncytial virus hospitalization

Khung Keong Yeo, Kelvin Bryan Tan, David Chien Boon Lye, Jonathan Yap et al.
UCL Discovery (University College London)
Respiratory viral infections research
article

Risk of new-onset heart failure and heart failure exacerbations following COVID-19, influenza, or respiratory syncytial virus hospitalization

Khung Keong Yeo, Kelvin Bryan Tan, David Chien Boon Lye, Jonathan Yap, Mark Yan Yee Chan, Jue Tao Lim, Derek J Hausenloy, Enoch Xueheng Loy, Raymond Wong, Calvin J Chiew, Russell Jingxian Li, Shir Lynn Lim, Nicholas Ngiam, Liang En Wee
article en

Abstract

BACKGROUND: While acute respiratory-viral-infection (RVI) is associated with elevated short-term risk of concurrent cardiac events, less is known regarding subsequent heart-failure (HF) risk post-RVI hospitalisation. We evaluated risk of HF post-hospitalisation for influenza/COVID-19/respiratory-syncytial-virus(RSV). METHODS: Population-based retrospective cohort study, including all adult Singaporeans (≥18 years) hospitalised for influenza/COVID-19/RSV (01/01/2017-30/08/2023); stratified by pre-existing HF. Risks of acute HF (new-onset/readmission) post-RVI-hospitalisation was compared against controls (orthopaedic hospitalisations) using overlap-weighted competing-risks-regression. HF was ascertained using national healthcare-claims data. Analyses were further stratified by RVI type and vaccination status. RESULTS: Amongst individuals without pre-existing HF (N=59,408) hospitalised for RVI (influenza/COVID-19/RSV), overall risk of new-onset HF up to 180 days post-hospitalisation was elevated versus controls (adjusted-hazards-ratio, aHR=1.45[95%CI=1.26-1.67]). Risk of new-onset HF was observed up to 180 days post-hospitalisation for specific RVIs (RSV: aHR=2.03[95%CI=1.26-3.25]; COVID-19: aHR=1.36[95%CI=1.16-1.60]; influenza: aHR=1.62[95%CI=1.28-2.06]); however, risk was not significantly increased amongst influenza hospitalisations vaccinated <365 days prior (aHR=1.47[95%CI=0.82-2.64]). In HF patients (N=4163) hospitalised for RVI(influenza/COVID-19/RSV), risk of HF readmission was similarly increased (aHR=1.28[95%CI=1.08-1.52]). No increased risk of HF readmission post-COVID-19 was observed amongst individuals who received ≥4 COVID-19 vaccine doses (aHR=0.86[95%CI=0.59-1.27]), or who were vaccinated <180 days prior (aHR=0.97[95%CI=0.79-1.20]). Similarly, risk of HF readmission post-influenza was not significantly increased amongst individuals vaccinated <365 days prior (aHR=1.63[95%CI=0.94-2.82]). Elevated risk of HF readmission post-RVI hospitalisation predominantly accrued in older patients (≥70 years). CONCLUSIONS: RVIs can contribute to post-acute risk of new-onset HF and HF readmissions. Vaccination represents an opportunity for HF prevention amongst at-risk individuals.

UCL Discovery (University College London)
Good health and well-being
Openalex Percentile: Top 27%
Respiratory viral infections research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.