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Do co-morbidities, frailty and functional status identify patients who may not benefit from ICD therapy?
FUNDING ACKNOWLEDGEMENTS: Type of funding sources: Private grant(s) and/or Sponsorship. Main funding source(s): Boston Scientific ISR lite. BACKGROUND: In carefully selected patients, Implantable Cardioverter Defibrillators reduce all-cause mortality by reducing the burden of sudden cardiac death. M...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207408/ http://dx.doi.org/10.1093/europace/euad122.416 |
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author | Wilson, D G James, S X Power, D F Sharma-Oates, A Lord, J M Roberts, P R Morgan, J M |
author_facet | Wilson, D G James, S X Power, D F Sharma-Oates, A Lord, J M Roberts, P R Morgan, J M |
author_sort | Wilson, D G |
collection | PubMed |
description | FUNDING ACKNOWLEDGEMENTS: Type of funding sources: Private grant(s) and/or Sponsorship. Main funding source(s): Boston Scientific ISR lite. BACKGROUND: In carefully selected patients, Implantable Cardioverter Defibrillators reduce all-cause mortality by reducing the burden of sudden cardiac death. Most patients who have an ICD implant do not receive life-prolonging therapy from it. Little research has been undertaken to determine which patients benefit the least from ICD therapy. As patients age and accumulate comorbidities, the risk of death increases and the benefit of ICDs diminishes. PURPOSE: We sought to evaluate the impact of comorbidity, frailty, functional status on death prior to ICD therapy as this group has the least to gain from ICD therapy. METHODS: A prospective, multicentre, observational study involving 15 English hospitals was undertaken. Patients were eligible for inclusion for the study if they were scheduled to have a de novo, replacement or an upgrade to a high-energy device (transvenous or subcutaneous ICD or CRT-D). Baseline characteristics were collected including age, gender, device type, LV function, medication, baseline bloods if available and were asked to complete a frailty assessment, Fried score; a functional status questionnaire (EQ5D5L), Charlson Co-morbidity Score and EQ5D5L data were calculated. RESULTS: In total, 662 patients were enrolled, mean age 65.6 (IQR 65-75) years, 77.3% male, 55.9% de novo implants, 33.4% replacements and 10.5% upgrade. Overall, 32% were for a secondary prevention indication, 49.% had a single or dual chamber transvenous ICD, 45.3% had a CRT-D and 5% had an S-ICD) implanted. A total of 63 patients (9.5%) died across this period, of these, 54 died without receiving appropriate therapy. Frailty was present in 83/662 (12.5%) and severe co-morbidity was present in 69/662 (10.4%). The overall survival probability estimated to be 90.2% at 2.5 years, and was 68% in frail patients. Figure 1. Multivariate predictors of death with no appropriate therapy were identified and a risk score comprising frailty, severe co-morbidity, age >70 years, eGFR <60 ml/min/1.73 m2 EQ5D5L <0.6 was developed. Table 1. The model performance was: sensitivity= 80.7%; specificity = 81.6%; precision 27.3%; accuracy 81.6% and AUC 0.81. CONCLUSION: Frailty and severe co-morbidity are powerful, independent predictors of death with no appropriate in ICD/CRT-D recipients. [Figure: see text] [Figure: see text] |
format | Online Article Text |
id | pubmed-10207408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102074082023-05-25 Do co-morbidities, frailty and functional status identify patients who may not benefit from ICD therapy? Wilson, D G James, S X Power, D F Sharma-Oates, A Lord, J M Roberts, P R Morgan, J M Europace 14.2 - Implantable Cardioverter-Defibrillator (ICD) FUNDING ACKNOWLEDGEMENTS: Type of funding sources: Private grant(s) and/or Sponsorship. Main funding source(s): Boston Scientific ISR lite. BACKGROUND: In carefully selected patients, Implantable Cardioverter Defibrillators reduce all-cause mortality by reducing the burden of sudden cardiac death. Most patients who have an ICD implant do not receive life-prolonging therapy from it. Little research has been undertaken to determine which patients benefit the least from ICD therapy. As patients age and accumulate comorbidities, the risk of death increases and the benefit of ICDs diminishes. PURPOSE: We sought to evaluate the impact of comorbidity, frailty, functional status on death prior to ICD therapy as this group has the least to gain from ICD therapy. METHODS: A prospective, multicentre, observational study involving 15 English hospitals was undertaken. Patients were eligible for inclusion for the study if they were scheduled to have a de novo, replacement or an upgrade to a high-energy device (transvenous or subcutaneous ICD or CRT-D). Baseline characteristics were collected including age, gender, device type, LV function, medication, baseline bloods if available and were asked to complete a frailty assessment, Fried score; a functional status questionnaire (EQ5D5L), Charlson Co-morbidity Score and EQ5D5L data were calculated. RESULTS: In total, 662 patients were enrolled, mean age 65.6 (IQR 65-75) years, 77.3% male, 55.9% de novo implants, 33.4% replacements and 10.5% upgrade. Overall, 32% were for a secondary prevention indication, 49.% had a single or dual chamber transvenous ICD, 45.3% had a CRT-D and 5% had an S-ICD) implanted. A total of 63 patients (9.5%) died across this period, of these, 54 died without receiving appropriate therapy. Frailty was present in 83/662 (12.5%) and severe co-morbidity was present in 69/662 (10.4%). The overall survival probability estimated to be 90.2% at 2.5 years, and was 68% in frail patients. Figure 1. Multivariate predictors of death with no appropriate therapy were identified and a risk score comprising frailty, severe co-morbidity, age >70 years, eGFR <60 ml/min/1.73 m2 EQ5D5L <0.6 was developed. Table 1. The model performance was: sensitivity= 80.7%; specificity = 81.6%; precision 27.3%; accuracy 81.6% and AUC 0.81. CONCLUSION: Frailty and severe co-morbidity are powerful, independent predictors of death with no appropriate in ICD/CRT-D recipients. [Figure: see text] [Figure: see text] Oxford University Press 2023-05-24 /pmc/articles/PMC10207408/ http://dx.doi.org/10.1093/europace/euad122.416 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | 14.2 - Implantable Cardioverter-Defibrillator (ICD) Wilson, D G James, S X Power, D F Sharma-Oates, A Lord, J M Roberts, P R Morgan, J M Do co-morbidities, frailty and functional status identify patients who may not benefit from ICD therapy? |
title | Do co-morbidities, frailty and functional status identify patients who may not benefit from ICD therapy? |
title_full | Do co-morbidities, frailty and functional status identify patients who may not benefit from ICD therapy? |
title_fullStr | Do co-morbidities, frailty and functional status identify patients who may not benefit from ICD therapy? |
title_full_unstemmed | Do co-morbidities, frailty and functional status identify patients who may not benefit from ICD therapy? |
title_short | Do co-morbidities, frailty and functional status identify patients who may not benefit from ICD therapy? |
title_sort | do co-morbidities, frailty and functional status identify patients who may not benefit from icd therapy? |
topic | 14.2 - Implantable Cardioverter-Defibrillator (ICD) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207408/ http://dx.doi.org/10.1093/europace/euad122.416 |
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