Evidence map›Paper›PMID 42846148›Full record

ArticleInternational journal of general medicine2026

Fried Frailty Phenotype and 6-Month Risk of First All-Cause Rehospitalisation Among Older Outpatients with Heart Failure and LVEF >40%: A Multicentre Prospective Cohort Study.

Huan Thanh Nguyen, Duyen Hoang Mai Nguyen, Linh Nu Ngoc Doan, Tra Thanh Nguyen, Huy Quang Nguyen, Loi Phuc Luu

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Article in International journal of general medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Huan Thanh NguyenDepartment of Geriatrics and Gerontology, School of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh, Vietnam.ORCID 0000-0002-5086-7273
Duyen Hoang Mai NguyenDepartment of Geriatrics and Gerontology, School of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh, Vietnam.
Linh Nu Ngoc DoanDepartment of Geriatrics and Gerontology, School of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh, Vietnam.
Tra Thanh NguyenInstitute for Applied Research in Health Sciences and Aging (ARiHA), Thong Nhat Hospital, Ho Chi Minh, Vietnam.
Huy Quang NguyenDepartment of Geriatrics and Gerontology, School of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh, Vietnam.
Loi Phuc LuuComprehensive Geriatrics and Older Adults Leading Research Group, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh, Vietnam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Heart failure (HF) with left ventricular ejection fraction (LVEF) >40% is common in older adults and carries a substantial risk of post-discharge rehospitalisation. However, the prognostic association of the Fried frailty phenotype with short-term rehospitalisation remains incompletely characterised. Methods: We conducted a multicentre prospective cohort study of adults aged ≥60 years with HF and LVEF >40% who were enrolled 1-3 months after HF hospitalisation at two tertiary HF outpatient clinics in Ho Chi Minh City, Vietnam. Frailty was assessed at enrolment using the Fried frailty phenotype and defined as meeting ≥3 criteria. For prognostic analyses, robust and pre-frail participants were combined into a non-frail group and compared with frail participants. Participants were followed for 6 months from enrolment to ascertain first all-cause rehospitalisation. Cox proportional hazards regression assessed the association between frailty and rehospitalisation, and the incremental prognostic contribution of frailty was evaluated using Harrell's C-statistic and the likelihood-ratio test. Results: Among 313 participants, the median age was 72.0 years (interquartile range, 66.0-81.0), 53.4% were male, and 190 (60.7%) were frail. First all-cause rehospitalisation occurred in 118 participants (37.7%): 33 of 123 non-frail participants (26.8%) and 85 of 190 frail participants (44.7%). Frailty was associated with a higher risk of rehospitalisation in univariable analysis (HR, 1.89; 95% CI, 1.27-2.83) and after adjustment for prespecified covariates (adjusted HR, 1.80; 95% CI, 1.09-2.95; p = 0.021). Adding frailty increased Harrell's C-statistic from 0.717 to 0.723, corresponding to a change of 0.006 (95% CI, -0.004 to 0.027), and improved overall model fit according to the likelihood-ratio test (p = 0.017). Conclusion: Frailty was common and associated with a higher 6-month risk of first all-cause rehospitalisation among older outpatients with HF and LVEF >40%. Adding frailty improved overall model fit, whereas the estimated change in discrimination was small and its confidence interval included no improvement. The models were not internally or externally validated; independent validation is warranted.

Indexed as

frailtyfried frailty phenotypeheart failureolder adultsrehospitalisation

Identifiers

PMID42846148
PMCPMC13643380

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.