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Frailty related all-cause mortality or hospital readmission among adults aged 65 and older with stage-B heart failure inpatients
BACKGROUND: Frailty increases the adverse outcomes of clinical heart failure; however, the relationship between frailty and stage-B heart failure (SBHF) remains unknown. We aimed to explore the epidemiology and predictive value of frailty in older adults with SBHF. METHODS: A prospective cohort of S...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885474/ https://www.ncbi.nlm.nih.gov/pubmed/33593292 http://dx.doi.org/10.1186/s12877-021-02072-6 |
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author | Zheng, Pei-Pei Yao, Si-Min He, Wei Wan, Yu-Hao Wang, Hua Yang, Jie-Fu |
author_facet | Zheng, Pei-Pei Yao, Si-Min He, Wei Wan, Yu-Hao Wang, Hua Yang, Jie-Fu |
author_sort | Zheng, Pei-Pei |
collection | PubMed |
description | BACKGROUND: Frailty increases the adverse outcomes of clinical heart failure; however, the relationship between frailty and stage-B heart failure (SBHF) remains unknown. We aimed to explore the epidemiology and predictive value of frailty in older adults with SBHF. METHODS: A prospective cohort of SBHF inpatients aged 65 years or older who were hospitalized between September 2018 and February 2019 and were followed up for 6 months were included. SBHF was defined as systolic abnormality, structural abnormality (left ventricular enlargement, left ventricular hypertrophy, wall motion abnormalities, valvular heart disease), or prior myocardial infarction. Frailty was assessed by the Fried frailty phenotype. Multivariable Cox proportional hazards regression was used to explore the independent risk and prognostic factors. RESULTS: Data of 443 participants (age: 76.1 ± 6.79 years, LVEF: 62.8 ± 4.92%, men: 225 [50.8%], frailty: 109 [24.6%]) were analyzed. During the 6-month follow-up, 83 (18.7%) older SBHF inpatients experienced all-cause mortality or readmission, and 29 (6.5%) of them developed clinical HF. Frail individuals had a 1.78–fold (95%CI: 1.02–3.10, P = 0.041) higher risk of 6-month mortality or readmission and a 2.83–fold (95%CI 1.24–6.47, P = 0.014) higher risk of developing clinical HF, independent of age, sex, left ventricular ejection fraction, and N-terminal pro-B-type natriuretic peptide level. CONCLUSIONS: Frailty is common in older SBHF inpatients and should be considered to help identify individuals with an increased risk of mortality or readmission, and developing clinical HF. TRIAL REGISTRATION: ChiCTR1800017204. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-021-02072-6. |
format | Online Article Text |
id | pubmed-7885474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78854742021-02-17 Frailty related all-cause mortality or hospital readmission among adults aged 65 and older with stage-B heart failure inpatients Zheng, Pei-Pei Yao, Si-Min He, Wei Wan, Yu-Hao Wang, Hua Yang, Jie-Fu BMC Geriatr Research Article BACKGROUND: Frailty increases the adverse outcomes of clinical heart failure; however, the relationship between frailty and stage-B heart failure (SBHF) remains unknown. We aimed to explore the epidemiology and predictive value of frailty in older adults with SBHF. METHODS: A prospective cohort of SBHF inpatients aged 65 years or older who were hospitalized between September 2018 and February 2019 and were followed up for 6 months were included. SBHF was defined as systolic abnormality, structural abnormality (left ventricular enlargement, left ventricular hypertrophy, wall motion abnormalities, valvular heart disease), or prior myocardial infarction. Frailty was assessed by the Fried frailty phenotype. Multivariable Cox proportional hazards regression was used to explore the independent risk and prognostic factors. RESULTS: Data of 443 participants (age: 76.1 ± 6.79 years, LVEF: 62.8 ± 4.92%, men: 225 [50.8%], frailty: 109 [24.6%]) were analyzed. During the 6-month follow-up, 83 (18.7%) older SBHF inpatients experienced all-cause mortality or readmission, and 29 (6.5%) of them developed clinical HF. Frail individuals had a 1.78–fold (95%CI: 1.02–3.10, P = 0.041) higher risk of 6-month mortality or readmission and a 2.83–fold (95%CI 1.24–6.47, P = 0.014) higher risk of developing clinical HF, independent of age, sex, left ventricular ejection fraction, and N-terminal pro-B-type natriuretic peptide level. CONCLUSIONS: Frailty is common in older SBHF inpatients and should be considered to help identify individuals with an increased risk of mortality or readmission, and developing clinical HF. TRIAL REGISTRATION: ChiCTR1800017204. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12877-021-02072-6. BioMed Central 2021-02-16 /pmc/articles/PMC7885474/ /pubmed/33593292 http://dx.doi.org/10.1186/s12877-021-02072-6 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Zheng, Pei-Pei Yao, Si-Min He, Wei Wan, Yu-Hao Wang, Hua Yang, Jie-Fu Frailty related all-cause mortality or hospital readmission among adults aged 65 and older with stage-B heart failure inpatients |
title | Frailty related all-cause mortality or hospital readmission among adults aged 65 and older with stage-B heart failure inpatients |
title_full | Frailty related all-cause mortality or hospital readmission among adults aged 65 and older with stage-B heart failure inpatients |
title_fullStr | Frailty related all-cause mortality or hospital readmission among adults aged 65 and older with stage-B heart failure inpatients |
title_full_unstemmed | Frailty related all-cause mortality or hospital readmission among adults aged 65 and older with stage-B heart failure inpatients |
title_short | Frailty related all-cause mortality or hospital readmission among adults aged 65 and older with stage-B heart failure inpatients |
title_sort | frailty related all-cause mortality or hospital readmission among adults aged 65 and older with stage-b heart failure inpatients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885474/ https://www.ncbi.nlm.nih.gov/pubmed/33593292 http://dx.doi.org/10.1186/s12877-021-02072-6 |
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