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Prognostic impact of follow‐up serum albumin after acute myocardial infarction

AIMS: Previous studies have suggested that low serum albumin (LSA) at admission for acute myocardial infarction (AMI) is associated with adverse in‐hospital outcomes. The aim of this study was to investigate whether LSA in the remote phase after AMI is prognostic for long‐term outcomes. METHODS AND...

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Autores principales: Yoshioka, Goro, Tanaka, Atsushi, Nishihira, Kensaku, Natsuaki, Masahiro, Kawaguchi, Atsushi, Watanabe, Nozomi, Shibata, Yoshisato, Node, Koichi
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/PMC8712885/
https://www.ncbi.nlm.nih.gov/pubmed/34612008
http://dx.doi.org/10.1002/ehf2.13640
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author Yoshioka, Goro
Tanaka, Atsushi
Nishihira, Kensaku
Natsuaki, Masahiro
Kawaguchi, Atsushi
Watanabe, Nozomi
Shibata, Yoshisato
Node, Koichi
author_facet Yoshioka, Goro
Tanaka, Atsushi
Nishihira, Kensaku
Natsuaki, Masahiro
Kawaguchi, Atsushi
Watanabe, Nozomi
Shibata, Yoshisato
Node, Koichi
author_sort Yoshioka, Goro
collection PubMed
description AIMS: Previous studies have suggested that low serum albumin (LSA) at admission for acute myocardial infarction (AMI) is associated with adverse in‐hospital outcomes. The aim of this study was to investigate whether LSA in the remote phase after AMI is prognostic for long‐term outcomes. METHODS AND RESULTS: This was a single‐centre, retrospective study of consecutive patients admitted for AMI from 2008 to 2016. Serum albumin concentrations were measured serially at admission and 1 year after discharge in Japanese patients. Occurrence of a composite of hospitalization for heart failure and cardiovascular death was the primary endpoint. The prognostic impact of remote LSA, defined as a serum albumin level < 3.8 g/dL at 1 year after discharge, was investigated with a multivariate‐adjusted Cox model. Among 1424 subjects analysed, 289 (20.3%) had LSA at admission, and 165 (11.6%) had LSA at 1 year after discharge. During follow‐up (median: 4.1 years), the primary endpoint occurred in 31/165 (18.8%) patients with remote LSA and 42/1259 (3.3%) patients without it [adjusted hazard ratio (aHR), 2.76; 95% confidence interval (CI), 1.32 to 5.72; P = 0.007]. The all‐cause death rate was 29.7% (49/165) in patients with remote LSA and 4.3% (54/1259) in patients without it (aHR, 4.02; 95% CI, 2.36 to 6.87; P < 0.001). The prognostic impact of remote LSA was consistent across albumin status in the acute phase of AMI. CONCLUSIONS: Regardless of albumin status in the acute phase of AMI, LSA in the remote phase after AMI was significantly associated with long‐term adverse outcomes.
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spelling pubmed-87128852022-01-04 Prognostic impact of follow‐up serum albumin after acute myocardial infarction Yoshioka, Goro Tanaka, Atsushi Nishihira, Kensaku Natsuaki, Masahiro Kawaguchi, Atsushi Watanabe, Nozomi Shibata, Yoshisato Node, Koichi ESC Heart Fail Original Articles AIMS: Previous studies have suggested that low serum albumin (LSA) at admission for acute myocardial infarction (AMI) is associated with adverse in‐hospital outcomes. The aim of this study was to investigate whether LSA in the remote phase after AMI is prognostic for long‐term outcomes. METHODS AND RESULTS: This was a single‐centre, retrospective study of consecutive patients admitted for AMI from 2008 to 2016. Serum albumin concentrations were measured serially at admission and 1 year after discharge in Japanese patients. Occurrence of a composite of hospitalization for heart failure and cardiovascular death was the primary endpoint. The prognostic impact of remote LSA, defined as a serum albumin level < 3.8 g/dL at 1 year after discharge, was investigated with a multivariate‐adjusted Cox model. Among 1424 subjects analysed, 289 (20.3%) had LSA at admission, and 165 (11.6%) had LSA at 1 year after discharge. During follow‐up (median: 4.1 years), the primary endpoint occurred in 31/165 (18.8%) patients with remote LSA and 42/1259 (3.3%) patients without it [adjusted hazard ratio (aHR), 2.76; 95% confidence interval (CI), 1.32 to 5.72; P = 0.007]. The all‐cause death rate was 29.7% (49/165) in patients with remote LSA and 4.3% (54/1259) in patients without it (aHR, 4.02; 95% CI, 2.36 to 6.87; P < 0.001). The prognostic impact of remote LSA was consistent across albumin status in the acute phase of AMI. CONCLUSIONS: Regardless of albumin status in the acute phase of AMI, LSA in the remote phase after AMI was significantly associated with long‐term adverse outcomes. John Wiley and Sons Inc. 2021-10-05 /pmc/articles/PMC8712885/ /pubmed/34612008 http://dx.doi.org/10.1002/ehf2.13640 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-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Yoshioka, Goro
Tanaka, Atsushi
Nishihira, Kensaku
Natsuaki, Masahiro
Kawaguchi, Atsushi
Watanabe, Nozomi
Shibata, Yoshisato
Node, Koichi
Prognostic impact of follow‐up serum albumin after acute myocardial infarction
title Prognostic impact of follow‐up serum albumin after acute myocardial infarction
title_full Prognostic impact of follow‐up serum albumin after acute myocardial infarction
title_fullStr Prognostic impact of follow‐up serum albumin after acute myocardial infarction
title_full_unstemmed Prognostic impact of follow‐up serum albumin after acute myocardial infarction
title_short Prognostic impact of follow‐up serum albumin after acute myocardial infarction
title_sort prognostic impact of follow‐up serum albumin after acute myocardial infarction
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712885/
https://www.ncbi.nlm.nih.gov/pubmed/34612008
http://dx.doi.org/10.1002/ehf2.13640
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