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Modified frailty as a novel factor in predicting the response to cardiac resynchronization in the elderly population
BACKGROUND: The response to cardiac resynchronization therapy (CRT) is an important element of the treatment of advanced heart failure, especially in the geriatric population. The aim of the study was to examine the impact of frailty syndrome on the response to treatment with CRT. METHODS: Two hundr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394238/ https://www.ncbi.nlm.nih.gov/pubmed/30880925 http://dx.doi.org/10.2147/CIA.S193577 |
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author | Mlynarska, Agnieszka Mlynarski, Rafal Marcisz, Czeslaw Golba, Krzysztof S |
author_facet | Mlynarska, Agnieszka Mlynarski, Rafal Marcisz, Czeslaw Golba, Krzysztof S |
author_sort | Mlynarska, Agnieszka |
collection | PubMed |
description | BACKGROUND: The response to cardiac resynchronization therapy (CRT) is an important element of the treatment of advanced heart failure, especially in the geriatric population. The aim of the study was to examine the impact of frailty syndrome on the response to treatment with CRT. METHODS: Two hundred and forty-six patients of 60 years or older (aged 73.35±6.95; 22.4% women) with an implanted CRT were included in this single-center prospective study. There was a 12-month follow-up. The Tilburg Frailty Indicator was used to determine frailty (5 or more points). The response to CRT was evaluated based on an analysis of clinical criteria. RESULTS: One hundred and sixty-nine of 246 (68.9%) patients were found to be clinical CRT responders. Frailty syndrome was recognized in 173 (70.32%). There were 63.0% responders in the frailty-affected group, whereas there were statistically more responders (79.5%) in the robust group (P=0.0116). In the logistic regression, frailty emerged as an independent predictor of the response to CRT (OR=0.81, 95% CI=0.71–0.92; P=0.0008). The area under the curve of the ROC curve for frailty in the responders to CRT was 0.62. The cut-off value for a designation of frailty was 6 (P=0.0014). CONCLUSION: Frailty is a novel independent factor that can be used to predict the clinical response to CRT in the elderly population. Modifying the level of recognition in the Tilburg Frailty Indicator can improve the prediction of a response to CRT. |
format | Online Article Text |
id | pubmed-6394238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63942382019-03-15 Modified frailty as a novel factor in predicting the response to cardiac resynchronization in the elderly population Mlynarska, Agnieszka Mlynarski, Rafal Marcisz, Czeslaw Golba, Krzysztof S Clin Interv Aging Original Research BACKGROUND: The response to cardiac resynchronization therapy (CRT) is an important element of the treatment of advanced heart failure, especially in the geriatric population. The aim of the study was to examine the impact of frailty syndrome on the response to treatment with CRT. METHODS: Two hundred and forty-six patients of 60 years or older (aged 73.35±6.95; 22.4% women) with an implanted CRT were included in this single-center prospective study. There was a 12-month follow-up. The Tilburg Frailty Indicator was used to determine frailty (5 or more points). The response to CRT was evaluated based on an analysis of clinical criteria. RESULTS: One hundred and sixty-nine of 246 (68.9%) patients were found to be clinical CRT responders. Frailty syndrome was recognized in 173 (70.32%). There were 63.0% responders in the frailty-affected group, whereas there were statistically more responders (79.5%) in the robust group (P=0.0116). In the logistic regression, frailty emerged as an independent predictor of the response to CRT (OR=0.81, 95% CI=0.71–0.92; P=0.0008). The area under the curve of the ROC curve for frailty in the responders to CRT was 0.62. The cut-off value for a designation of frailty was 6 (P=0.0014). CONCLUSION: Frailty is a novel independent factor that can be used to predict the clinical response to CRT in the elderly population. Modifying the level of recognition in the Tilburg Frailty Indicator can improve the prediction of a response to CRT. Dove Medical Press 2019-02-25 /pmc/articles/PMC6394238/ /pubmed/30880925 http://dx.doi.org/10.2147/CIA.S193577 Text en © 2019 Mlynarska et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Mlynarska, Agnieszka Mlynarski, Rafal Marcisz, Czeslaw Golba, Krzysztof S Modified frailty as a novel factor in predicting the response to cardiac resynchronization in the elderly population |
title | Modified frailty as a novel factor in predicting the response to cardiac resynchronization in the elderly population |
title_full | Modified frailty as a novel factor in predicting the response to cardiac resynchronization in the elderly population |
title_fullStr | Modified frailty as a novel factor in predicting the response to cardiac resynchronization in the elderly population |
title_full_unstemmed | Modified frailty as a novel factor in predicting the response to cardiac resynchronization in the elderly population |
title_short | Modified frailty as a novel factor in predicting the response to cardiac resynchronization in the elderly population |
title_sort | modified frailty as a novel factor in predicting the response to cardiac resynchronization in the elderly population |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394238/ https://www.ncbi.nlm.nih.gov/pubmed/30880925 http://dx.doi.org/10.2147/CIA.S193577 |
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