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Prognostic impact of hospital‐acquired disability in elderly patients with heart failure

AIMS: Functional decline is associated with worse outcomes in patients with elderly heart failure (HF), but little is known about the prognostic impact of hospital‐acquired disability (HAD) during hospital stay after acute HF. The present study examines the prognostic significance of HAD in the pred...

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Autores principales: Saitoh, Masakazu, Takahashi, Yuta, Okamura, Daisuke, Akiho, Mitsutoshi, Suzuki, Hidetoshi, Noguchi, Naoki, Yamaguchi, Yukito, Hori, Kentaro, Adachi, Yuichi, Takahashi, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120367/
https://www.ncbi.nlm.nih.gov/pubmed/33838022
http://dx.doi.org/10.1002/ehf2.13356
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author Saitoh, Masakazu
Takahashi, Yuta
Okamura, Daisuke
Akiho, Mitsutoshi
Suzuki, Hidetoshi
Noguchi, Naoki
Yamaguchi, Yukito
Hori, Kentaro
Adachi, Yuichi
Takahashi, Tetsuya
author_facet Saitoh, Masakazu
Takahashi, Yuta
Okamura, Daisuke
Akiho, Mitsutoshi
Suzuki, Hidetoshi
Noguchi, Naoki
Yamaguchi, Yukito
Hori, Kentaro
Adachi, Yuichi
Takahashi, Tetsuya
author_sort Saitoh, Masakazu
collection PubMed
description AIMS: Functional decline is associated with worse outcomes in patients with elderly heart failure (HF), but little is known about the prognostic impact of hospital‐acquired disability (HAD) during hospital stay after acute HF. The present study examines the prognostic significance of HAD in the prediction of all‐cause mortality in elderly patients who admitted for acute HF. METHODS AND RESULTS: This retrospective study was performed in 1941 elderly patients aged ≥65 years or older from the cardiovascular physiotherapy for acute HF patients in the Tokyo metropolitan area registry and excluded those who died in hospital. HAD was defined as any decline in the Barthel index (BI) before discharge compared with the BI within 1 month before hospital admission. The primary outcome of this study was all‐cause death and HF readmission. A total of 565 (29%) deaths and 789 (41%) HF readmission occurred over a median follow‐up period of 1.7 years. A total of 476 patients (25%) had HAD during hospital stay after acute HF. In multivariable analysis, HAD predicted all‐cause death [hazard ratio (HR): 1.772; 95% confidence interval (CI): 1.450–2.167; P < 60; 0.001] and with risk of HF readmission (HR: 1.193; 95% CI: 1.005–1.416; P = 0.043) after adjusting for the Meta‐analysis Global Group in Chronic Heart Failure risk score. CONCLUSIONS: Hospital‐acquired disability is associated with an increased risk of all‐cause death and readmission for HF in elderly patients with acute HF.
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spelling pubmed-81203672021-05-21 Prognostic impact of hospital‐acquired disability in elderly patients with heart failure Saitoh, Masakazu Takahashi, Yuta Okamura, Daisuke Akiho, Mitsutoshi Suzuki, Hidetoshi Noguchi, Naoki Yamaguchi, Yukito Hori, Kentaro Adachi, Yuichi Takahashi, Tetsuya ESC Heart Fail Original Research Articles AIMS: Functional decline is associated with worse outcomes in patients with elderly heart failure (HF), but little is known about the prognostic impact of hospital‐acquired disability (HAD) during hospital stay after acute HF. The present study examines the prognostic significance of HAD in the prediction of all‐cause mortality in elderly patients who admitted for acute HF. METHODS AND RESULTS: This retrospective study was performed in 1941 elderly patients aged ≥65 years or older from the cardiovascular physiotherapy for acute HF patients in the Tokyo metropolitan area registry and excluded those who died in hospital. HAD was defined as any decline in the Barthel index (BI) before discharge compared with the BI within 1 month before hospital admission. The primary outcome of this study was all‐cause death and HF readmission. A total of 565 (29%) deaths and 789 (41%) HF readmission occurred over a median follow‐up period of 1.7 years. A total of 476 patients (25%) had HAD during hospital stay after acute HF. In multivariable analysis, HAD predicted all‐cause death [hazard ratio (HR): 1.772; 95% confidence interval (CI): 1.450–2.167; P < 60; 0.001] and with risk of HF readmission (HR: 1.193; 95% CI: 1.005–1.416; P = 0.043) after adjusting for the Meta‐analysis Global Group in Chronic Heart Failure risk score. CONCLUSIONS: Hospital‐acquired disability is associated with an increased risk of all‐cause death and readmission for HF in elderly patients with acute HF. John Wiley and Sons Inc. 2021-04-10 /pmc/articles/PMC8120367/ /pubmed/33838022 http://dx.doi.org/10.1002/ehf2.13356 Text en © 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research Articles
Saitoh, Masakazu
Takahashi, Yuta
Okamura, Daisuke
Akiho, Mitsutoshi
Suzuki, Hidetoshi
Noguchi, Naoki
Yamaguchi, Yukito
Hori, Kentaro
Adachi, Yuichi
Takahashi, Tetsuya
Prognostic impact of hospital‐acquired disability in elderly patients with heart failure
title Prognostic impact of hospital‐acquired disability in elderly patients with heart failure
title_full Prognostic impact of hospital‐acquired disability in elderly patients with heart failure
title_fullStr Prognostic impact of hospital‐acquired disability in elderly patients with heart failure
title_full_unstemmed Prognostic impact of hospital‐acquired disability in elderly patients with heart failure
title_short Prognostic impact of hospital‐acquired disability in elderly patients with heart failure
title_sort prognostic impact of hospital‐acquired disability in elderly patients with heart failure
topic Original Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120367/
https://www.ncbi.nlm.nih.gov/pubmed/33838022
http://dx.doi.org/10.1002/ehf2.13356
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