Systematic Review of the Association of the Hospital Frailty Risk Score with Mortality in Patients with Cerebrovascular and Cardiovascular Disease.

Frailty cardiovascular disease cerebrovascular disease hospital frailty risk score mortality systematic review

Journal

Current cardiology reviews
ISSN: 1875-6557
Titre abrégé: Curr Cardiol Rev
Pays: United Arab Emirates
ID NLM: 101261935

Informations de publication

Date de publication:
29 Feb 2024
Historique:
received: 26 08 2023
revised: 26 11 2023
accepted: 14 12 2023
medline: 1 3 2024
pubmed: 1 3 2024
entrez: 1 3 2024
Statut: aheadofprint

Résumé

There is limited systematic data on the association between the Hospital Frailty Risk Score (HFRS) and characteristics and mortality in patients with cerebrovascular and cardiovascular disease (CVD). This systematic review aimed to summarise the use of the HFRS in describing the prevalence of frailty in patients with CVD, the clinical characteristics of patients with CVD, and the association between frailty on the likelihood of mortality in patients with CVD. A systematic literature search for observational studies using terms related to CVD, cerebrovascular disease, and the HFRS was conducted using 6 databases in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Studies were appraised using the Newcastle-Ottawa Scale (NOS). Seventeen observational studies were included, all rated 'good' quality according to the NOS. One study investigated 5 different CVD cohorts (atrial fibrillation (AF), heart failure (HF), hypotension, hypertension, and chronic ischemic heart disease), 1 study investigated 2 different CVD cohorts (AF and acute myocardial infarction (AMI)), 6 studies investigated HF, 3 studies investigated AMI, 4 studies investigated stroke, 1 study investigated AF, and 1 study investigated cardiac arrest. Increasing frailty risk category was associated with increased age, female sex, and non-white racial group across all CVD. Increasing frailty risk category is also associated with increased length of hospital stay, total costs, and increased odds of 30-day all-cause mortality across all CVD. The HFRS is an efficient and effective tool for stratifying frailty in patients with CVD and predicting adverse health outcomes.

Sections du résumé

BACKGROUND BACKGROUND
There is limited systematic data on the association between the Hospital Frailty Risk Score (HFRS) and characteristics and mortality in patients with cerebrovascular and cardiovascular disease (CVD). This systematic review aimed to summarise the use of the HFRS in describing the prevalence of frailty in patients with CVD, the clinical characteristics of patients with CVD, and the association between frailty on the likelihood of mortality in patients with CVD.
METHODS METHODS
A systematic literature search for observational studies using terms related to CVD, cerebrovascular disease, and the HFRS was conducted using 6 databases in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. Studies were appraised using the Newcastle-Ottawa Scale (NOS).
RESULTS RESULTS
Seventeen observational studies were included, all rated 'good' quality according to the NOS. One study investigated 5 different CVD cohorts (atrial fibrillation (AF), heart failure (HF), hypotension, hypertension, and chronic ischemic heart disease), 1 study investigated 2 different CVD cohorts (AF and acute myocardial infarction (AMI)), 6 studies investigated HF, 3 studies investigated AMI, 4 studies investigated stroke, 1 study investigated AF, and 1 study investigated cardiac arrest. Increasing frailty risk category was associated with increased age, female sex, and non-white racial group across all CVD. Increasing frailty risk category is also associated with increased length of hospital stay, total costs, and increased odds of 30-day all-cause mortality across all CVD.
CONCLUSIONS CONCLUSIONS
The HFRS is an efficient and effective tool for stratifying frailty in patients with CVD and predicting adverse health outcomes.

Identifiants

pubmed: 38425103
pii: CCR-EPUB-138875
doi: 10.2174/011573403X276647240217112151
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Balamrit Singh Sokhal (BS)

School of Medicine, Keele University, Keele, Staffordshire, ST5 5BG, United Kingdom.
Keele Cardiovascular Research Group, Centre for Prognosis Research, Keele University, ST5 5BG, United Kingdom.

Sowmya Prasanna Kumar Menon (SPK)

School of Medicine, Keele University, Keele, Staffordshire, ST5 5BG, United Kingdom.

Charles Willes (C)

School of Medicine, Keele University, Keele, Staffordshire, ST5 5BG, United Kingdom.

Nadia Corp (N)

School of Medicine, Keele University, Keele, Staffordshire, ST5 5BG, United Kingdom.

Andrija Matetić (A)

Keele Cardiovascular Research Group, Centre for Prognosis Research, Keele University, ST5 5BG, United Kingdom.
Department of Cardiology, University Hospital of Split, Split 21000, Croatia.

Christian Mallen (C)

School of Medicine, Keele University, Keele, Staffordshire, ST5 5BG, United Kingdom.

Mamas Mamas (M)

Keele Cardiovascular Research Group, Centre for Prognosis Research, Keele University, ST5 5BG, United Kingdom.

Classifications MeSH