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Impact of the clinical frailty scale on mid-term mortality in patients with ST-elevated myocardial infarction
BACKGROUND: “Frailty” is associated with poor prognosis in ST-elevated myocardial infarction (STEMI). However, there is little data regarding the impact of the Canadian Study of Health and Aging Clinical Frailty Scale (CFS), a simple and semiquantitative tool for assessing frailty, on mid-term morta...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437299/ https://www.ncbi.nlm.nih.gov/pubmed/30963094 http://dx.doi.org/10.1016/j.ijcha.2019.02.014 |
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author | Yoshioka, Naoki Takagi, Kensuke Morita, Yasuhiro Yoshida, Ruka Nagai, Hiroaki Kanzaki, Yasunori Furui, Koichi Yamauchi, Ryota Komeyama, Shotaro Sugiyama, Hiroki Tsuboi, Hideyuki Morishima, Itsuro |
author_facet | Yoshioka, Naoki Takagi, Kensuke Morita, Yasuhiro Yoshida, Ruka Nagai, Hiroaki Kanzaki, Yasunori Furui, Koichi Yamauchi, Ryota Komeyama, Shotaro Sugiyama, Hiroki Tsuboi, Hideyuki Morishima, Itsuro |
author_sort | Yoshioka, Naoki |
collection | PubMed |
description | BACKGROUND: “Frailty” is associated with poor prognosis in ST-elevated myocardial infarction (STEMI). However, there is little data regarding the impact of the Canadian Study of Health and Aging Clinical Frailty Scale (CFS), a simple and semiquantitative tool for assessing frailty, on mid-term mortality in STEMI patients. METHODS: A total of 354 consecutive STEMI patients (mean age 69.8 ± 12.4 years; male 76.6%) who underwent percutaneous intervention between July 2014 and March 2017 were retrospectively reviewed. The study endpoint was mid-term mortality according to the CFS classification. Furthermore, in order to clarify the impact of CFS upon admission on mid-term mortality, the independent predictors of all-cause death were evaluated. RESULTS: Patients were categorized into three groups (CFS 1–3, n = 281; CFS 4–5, n = 62; and CFS 6–7, n = 11). During the study period (median 474 days), all-cause death was observed in 39 patients. After multivariate Cox regression analysis, higher CFS (adjusted hazard ratio [HR] 2.34, 95% confidence interval [CI] 1.43–3.85, p < 0.001), higher Killip score (adjusted HR 2.46, 95%CI 1.30–5.78, p = 0.002), and lower serum albumin level (adjusted HR 4.29, 95%CI 2.16–8.51, p < 0.001) were significantly associated with an increased risk of all-cause death. CONCLUSION: In conclusion, severe frailty was associated with mid-term mortality in STEMI patients who underwent PCI. |
format | Online Article Text |
id | pubmed-6437299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-64372992019-04-08 Impact of the clinical frailty scale on mid-term mortality in patients with ST-elevated myocardial infarction Yoshioka, Naoki Takagi, Kensuke Morita, Yasuhiro Yoshida, Ruka Nagai, Hiroaki Kanzaki, Yasunori Furui, Koichi Yamauchi, Ryota Komeyama, Shotaro Sugiyama, Hiroki Tsuboi, Hideyuki Morishima, Itsuro Int J Cardiol Heart Vasc Original Paper BACKGROUND: “Frailty” is associated with poor prognosis in ST-elevated myocardial infarction (STEMI). However, there is little data regarding the impact of the Canadian Study of Health and Aging Clinical Frailty Scale (CFS), a simple and semiquantitative tool for assessing frailty, on mid-term mortality in STEMI patients. METHODS: A total of 354 consecutive STEMI patients (mean age 69.8 ± 12.4 years; male 76.6%) who underwent percutaneous intervention between July 2014 and March 2017 were retrospectively reviewed. The study endpoint was mid-term mortality according to the CFS classification. Furthermore, in order to clarify the impact of CFS upon admission on mid-term mortality, the independent predictors of all-cause death were evaluated. RESULTS: Patients were categorized into three groups (CFS 1–3, n = 281; CFS 4–5, n = 62; and CFS 6–7, n = 11). During the study period (median 474 days), all-cause death was observed in 39 patients. After multivariate Cox regression analysis, higher CFS (adjusted hazard ratio [HR] 2.34, 95% confidence interval [CI] 1.43–3.85, p < 0.001), higher Killip score (adjusted HR 2.46, 95%CI 1.30–5.78, p = 0.002), and lower serum albumin level (adjusted HR 4.29, 95%CI 2.16–8.51, p < 0.001) were significantly associated with an increased risk of all-cause death. CONCLUSION: In conclusion, severe frailty was associated with mid-term mortality in STEMI patients who underwent PCI. Elsevier 2019-03-11 /pmc/articles/PMC6437299/ /pubmed/30963094 http://dx.doi.org/10.1016/j.ijcha.2019.02.014 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Paper Yoshioka, Naoki Takagi, Kensuke Morita, Yasuhiro Yoshida, Ruka Nagai, Hiroaki Kanzaki, Yasunori Furui, Koichi Yamauchi, Ryota Komeyama, Shotaro Sugiyama, Hiroki Tsuboi, Hideyuki Morishima, Itsuro Impact of the clinical frailty scale on mid-term mortality in patients with ST-elevated myocardial infarction |
title | Impact of the clinical frailty scale on mid-term mortality in patients with ST-elevated myocardial infarction |
title_full | Impact of the clinical frailty scale on mid-term mortality in patients with ST-elevated myocardial infarction |
title_fullStr | Impact of the clinical frailty scale on mid-term mortality in patients with ST-elevated myocardial infarction |
title_full_unstemmed | Impact of the clinical frailty scale on mid-term mortality in patients with ST-elevated myocardial infarction |
title_short | Impact of the clinical frailty scale on mid-term mortality in patients with ST-elevated myocardial infarction |
title_sort | impact of the clinical frailty scale on mid-term mortality in patients with st-elevated myocardial infarction |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437299/ https://www.ncbi.nlm.nih.gov/pubmed/30963094 http://dx.doi.org/10.1016/j.ijcha.2019.02.014 |
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