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The impact of left ventricular diastolic dysfunction for the prognosis in patients with lower extremity arterial disease
AIMS: Lower extremity arterial disease (LEAD) and left ventricular diastolic dysfunction (LVDD) share many risk factors, but the characteristics of LVDD and its association with prognosis in patients with LEAD have not been fully examined. METHODS AND RESULTS: We investigated the impact of LVDD on t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524108/ https://www.ncbi.nlm.nih.gov/pubmed/32578966 http://dx.doi.org/10.1002/ehf2.12839 |
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author | Lee, Jen‐Kuang Hwang, Juey‐Jen Chiang, Fu‐Tien Wu, Cho‐Kai |
author_facet | Lee, Jen‐Kuang Hwang, Juey‐Jen Chiang, Fu‐Tien Wu, Cho‐Kai |
author_sort | Lee, Jen‐Kuang |
collection | PubMed |
description | AIMS: Lower extremity arterial disease (LEAD) and left ventricular diastolic dysfunction (LVDD) share many risk factors, but the characteristics of LVDD and its association with prognosis in patients with LEAD have not been fully examined. METHODS AND RESULTS: We investigated the impact of LVDD on the clinical outcomes in LEAD patients. LVDD was classified according to the newest suggested classification by the American Society of Echocardiography. Survival analysis for mortality (primary endpoint) and major adverse cardiac events (MACE; secondary endpoint) was calculated with all clinical variables and adjusted by multivariate Cox regression. We consecutively enrolled 221 controls and 464 LEAD patients from outpatient clinics and hospitals. The prevalence of LVDD was proportional to the severity of LEAD defined by the Rutherford class. The difference of LVDD severity is significant when compared with the control and LEAD patients or LEAD patients who underwent endovascular therapy (EVT), and it is also proportional to the LEAD severity. The grade of LVDD was a significant factor in predicting MACE and mortality in LEAD patients after multivariate Cox regression analysis [hazard ratio (HR) = 2.11, 95% CI = 1.47–2.83, P = 0.026; HR = 1.47, 95% CI = 1.02–2.02, P = 0.041]. This impact remained significant in LEAD patients who underwent EVT. CONCLUSIONS: The degree of LVDD may predict MACE and mortality in LEAD patients. Whether early identification of LVDD in LEAD patients is helpful warrants further large‐scale prospective randomized studies. |
format | Online Article Text |
id | pubmed-7524108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75241082020-10-02 The impact of left ventricular diastolic dysfunction for the prognosis in patients with lower extremity arterial disease Lee, Jen‐Kuang Hwang, Juey‐Jen Chiang, Fu‐Tien Wu, Cho‐Kai ESC Heart Fail Original Research Articles AIMS: Lower extremity arterial disease (LEAD) and left ventricular diastolic dysfunction (LVDD) share many risk factors, but the characteristics of LVDD and its association with prognosis in patients with LEAD have not been fully examined. METHODS AND RESULTS: We investigated the impact of LVDD on the clinical outcomes in LEAD patients. LVDD was classified according to the newest suggested classification by the American Society of Echocardiography. Survival analysis for mortality (primary endpoint) and major adverse cardiac events (MACE; secondary endpoint) was calculated with all clinical variables and adjusted by multivariate Cox regression. We consecutively enrolled 221 controls and 464 LEAD patients from outpatient clinics and hospitals. The prevalence of LVDD was proportional to the severity of LEAD defined by the Rutherford class. The difference of LVDD severity is significant when compared with the control and LEAD patients or LEAD patients who underwent endovascular therapy (EVT), and it is also proportional to the LEAD severity. The grade of LVDD was a significant factor in predicting MACE and mortality in LEAD patients after multivariate Cox regression analysis [hazard ratio (HR) = 2.11, 95% CI = 1.47–2.83, P = 0.026; HR = 1.47, 95% CI = 1.02–2.02, P = 0.041]. This impact remained significant in LEAD patients who underwent EVT. CONCLUSIONS: The degree of LVDD may predict MACE and mortality in LEAD patients. Whether early identification of LVDD in LEAD patients is helpful warrants further large‐scale prospective randomized studies. John Wiley and Sons Inc. 2020-06-24 /pmc/articles/PMC7524108/ /pubmed/32578966 http://dx.doi.org/10.1002/ehf2.12839 Text en © 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology This is an open access article under the terms of the http://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 Lee, Jen‐Kuang Hwang, Juey‐Jen Chiang, Fu‐Tien Wu, Cho‐Kai The impact of left ventricular diastolic dysfunction for the prognosis in patients with lower extremity arterial disease |
title | The impact of left ventricular diastolic dysfunction for the prognosis in patients with lower extremity arterial disease |
title_full | The impact of left ventricular diastolic dysfunction for the prognosis in patients with lower extremity arterial disease |
title_fullStr | The impact of left ventricular diastolic dysfunction for the prognosis in patients with lower extremity arterial disease |
title_full_unstemmed | The impact of left ventricular diastolic dysfunction for the prognosis in patients with lower extremity arterial disease |
title_short | The impact of left ventricular diastolic dysfunction for the prognosis in patients with lower extremity arterial disease |
title_sort | impact of left ventricular diastolic dysfunction for the prognosis in patients with lower extremity arterial disease |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524108/ https://www.ncbi.nlm.nih.gov/pubmed/32578966 http://dx.doi.org/10.1002/ehf2.12839 |
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