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Evaluation of MADIT II risk stratification score among registry of heart failure patients with primary prevention ICD/CRTD device

FUNDING ACKNOWLEDGEMENTS: Type of funding sources: None. BACKGROUND: Current guidelines advocate primary prevention ICD implantation for all symptomatic heart failure (HF) patients with low LVEF. As most patients will not use their device during lifetime, a score delineating subgroups with different...

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Autores principales: Rav Acha, M, Wube, O W, Tovia-Brodie, O T B, Michowitz, Y M, Ilan, M A, Ovdat, T A, Klempfner, R K, Goldenberg, I G, Glikson, M G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207569/
http://dx.doi.org/10.1093/europace/euad122.431
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author Rav Acha, M
Wube, O W
Tovia-Brodie, O T B
Michowitz, Y M
Ilan, M A
Ovdat, T A
Klempfner, R K
Goldenberg, I G
Glikson, M G
author_facet Rav Acha, M
Wube, O W
Tovia-Brodie, O T B
Michowitz, Y M
Ilan, M A
Ovdat, T A
Klempfner, R K
Goldenberg, I G
Glikson, M G
author_sort Rav Acha, M
collection PubMed
description FUNDING ACKNOWLEDGEMENTS: Type of funding sources: None. BACKGROUND: Current guidelines advocate primary prevention ICD implantation for all symptomatic heart failure (HF) patients with low LVEF. As most patients will not use their device during lifetime, a score delineating subgroups with differential ICD benefit is crucial. The MADIT Risk Stratification Score (MRSS) based on 5 parameters including: age>70, Creatinine >1.4 mg/dl, QRS width >120ms, presence of AF, and NYHA >2, was developed for this purpose. OBJECTIVE: Evaluate MRSS among Israeli nationwide registry of HF patients implanted with prophylactic ICD/CRTD. Endpoints included overall mortality, sustained ventricular arrhythmia (VA), and competing risk of arrhythmic (VA-related) versus non-arrhythmic death, a surrogate for potential ICD survival benefit. METHODS: Study based on comprehensive registry of ICD/CRTDs implanted in Israel between 2011-2018. All registry patients were categorized into MRSS-based risk-groups (low-risk- MRSS 0, intermediate-risk- MRSS 1-5, very high-risk (VHR) group defined by Creatinine >2.5mg/dL). Univariate and Kaplan Meier analysis used to evaluate the association of risk groups with study endpoints. RESULTS: 2177 HF patients, implanted with a primary prevention ICD (1255, 58%) or CRTD (922, 42%) were included. There were 189 (8.7%) patients with sustained VA and 316 (14.5%) deaths during median follow-up (F/U) period of 2.5 years. A significant correlation was found between MRSS-based risk subgroups and overall mortality (p 0.001). However, MRSS association with sustained VA was weak (p 0.2). Notably, the MRSS-based very high-risk (VHR) subgroup had an exceptionally high mortality but low VA incidence. Competing risk of arrhythmic versus non-arrhythmic death revealed a large and significant ICD survival benefit among the low and intermediate MRSS-based risk subgroups, with 10.2 and 12.3 months survival gained over 3-year F/U period among these subgroups, respectively (p 0.001). The VHR subgroup in contrast, showed a minimal non-significant ICD survival benefit. CONCLUSIONS: Use of MRSS among a contemporary real-world registry of HF patients revealed subgroups with differing ICD survival benefit, suggesting it as a universal tool to predict ICD survival benefit. MRSS-based VHR subgroup may not gain survival benefit from prophylactic ICD implant.
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spelling pubmed-102075692023-05-25 Evaluation of MADIT II risk stratification score among registry of heart failure patients with primary prevention ICD/CRTD device Rav Acha, M Wube, O W Tovia-Brodie, O T B Michowitz, Y M Ilan, M A Ovdat, T A Klempfner, R K Goldenberg, I G Glikson, M G Europace 14.2 - Implantable Cardioverter-Defibrillator (ICD) FUNDING ACKNOWLEDGEMENTS: Type of funding sources: None. BACKGROUND: Current guidelines advocate primary prevention ICD implantation for all symptomatic heart failure (HF) patients with low LVEF. As most patients will not use their device during lifetime, a score delineating subgroups with differential ICD benefit is crucial. The MADIT Risk Stratification Score (MRSS) based on 5 parameters including: age>70, Creatinine >1.4 mg/dl, QRS width >120ms, presence of AF, and NYHA >2, was developed for this purpose. OBJECTIVE: Evaluate MRSS among Israeli nationwide registry of HF patients implanted with prophylactic ICD/CRTD. Endpoints included overall mortality, sustained ventricular arrhythmia (VA), and competing risk of arrhythmic (VA-related) versus non-arrhythmic death, a surrogate for potential ICD survival benefit. METHODS: Study based on comprehensive registry of ICD/CRTDs implanted in Israel between 2011-2018. All registry patients were categorized into MRSS-based risk-groups (low-risk- MRSS 0, intermediate-risk- MRSS 1-5, very high-risk (VHR) group defined by Creatinine >2.5mg/dL). Univariate and Kaplan Meier analysis used to evaluate the association of risk groups with study endpoints. RESULTS: 2177 HF patients, implanted with a primary prevention ICD (1255, 58%) or CRTD (922, 42%) were included. There were 189 (8.7%) patients with sustained VA and 316 (14.5%) deaths during median follow-up (F/U) period of 2.5 years. A significant correlation was found between MRSS-based risk subgroups and overall mortality (p 0.001). However, MRSS association with sustained VA was weak (p 0.2). Notably, the MRSS-based very high-risk (VHR) subgroup had an exceptionally high mortality but low VA incidence. Competing risk of arrhythmic versus non-arrhythmic death revealed a large and significant ICD survival benefit among the low and intermediate MRSS-based risk subgroups, with 10.2 and 12.3 months survival gained over 3-year F/U period among these subgroups, respectively (p 0.001). The VHR subgroup in contrast, showed a minimal non-significant ICD survival benefit. CONCLUSIONS: Use of MRSS among a contemporary real-world registry of HF patients revealed subgroups with differing ICD survival benefit, suggesting it as a universal tool to predict ICD survival benefit. MRSS-based VHR subgroup may not gain survival benefit from prophylactic ICD implant. Oxford University Press 2023-05-24 /pmc/articles/PMC10207569/ http://dx.doi.org/10.1093/europace/euad122.431 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)
Rav Acha, M
Wube, O W
Tovia-Brodie, O T B
Michowitz, Y M
Ilan, M A
Ovdat, T A
Klempfner, R K
Goldenberg, I G
Glikson, M G
Evaluation of MADIT II risk stratification score among registry of heart failure patients with primary prevention ICD/CRTD device
title Evaluation of MADIT II risk stratification score among registry of heart failure patients with primary prevention ICD/CRTD device
title_full Evaluation of MADIT II risk stratification score among registry of heart failure patients with primary prevention ICD/CRTD device
title_fullStr Evaluation of MADIT II risk stratification score among registry of heart failure patients with primary prevention ICD/CRTD device
title_full_unstemmed Evaluation of MADIT II risk stratification score among registry of heart failure patients with primary prevention ICD/CRTD device
title_short Evaluation of MADIT II risk stratification score among registry of heart failure patients with primary prevention ICD/CRTD device
title_sort evaluation of madit ii risk stratification score among registry of heart failure patients with primary prevention icd/crtd device
topic 14.2 - Implantable Cardioverter-Defibrillator (ICD)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207569/
http://dx.doi.org/10.1093/europace/euad122.431
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