Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart Diseases
Introduction: Inherited cardiovascular diseases are an important cause of sudden cardiac death (SD). The use of risk scores identify high risk patients who would benefit from an implantable cardioverter-defibrillators (ICDs). The development of automated devices for out-of-hospital cardiac arrest im...
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Frontiers Media S.A.
2021-03-01
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Series: | Frontiers in Cardiovascular Medicine |
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Online Access: | https://www.frontiersin.org/articles/10.3389/fcvm.2021.634300/full |
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English |
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DOAJ |
author |
Juan P. Hernández del Rincón Juan P. Hernández del Rincón Juan P. Hernández del Rincón Mari C. Olmo Conesa Mari C. Olmo Conesa Ana Rodríguez Serrano Helena García Pulgar David López Cuenca David López Cuenca Carmen Muñoz Esparza Carmen Muñoz Esparza Marina Navarro Peñalver Marina Navarro Peñalver Juan José Santos Mateo Juan José Santos Mateo Elisa Nicolás Rocamora Elisa Nicolás Rocamora Elisa Nicolás Rocamora Cristina Gil Ortuño Cristina Gil Ortuño María Sabater-Molina María Sabater-Molina María Sabater-Molina María Sabater-Molina María Sabater-Molina Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Francisco Pastor Quirante Francisco Pastor Quirante Francisco Pastor Quirante |
spellingShingle |
Juan P. Hernández del Rincón Juan P. Hernández del Rincón Juan P. Hernández del Rincón Mari C. Olmo Conesa Mari C. Olmo Conesa Ana Rodríguez Serrano Helena García Pulgar David López Cuenca David López Cuenca Carmen Muñoz Esparza Carmen Muñoz Esparza Marina Navarro Peñalver Marina Navarro Peñalver Juan José Santos Mateo Juan José Santos Mateo Elisa Nicolás Rocamora Elisa Nicolás Rocamora Elisa Nicolás Rocamora Cristina Gil Ortuño Cristina Gil Ortuño María Sabater-Molina María Sabater-Molina María Sabater-Molina María Sabater-Molina María Sabater-Molina Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Francisco Pastor Quirante Francisco Pastor Quirante Francisco Pastor Quirante Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart Diseases Frontiers in Cardiovascular Medicine sudden cardiac death cardiomyopathy channelopathy inherited cardiovascular diseases prevented sudden cardiac death |
author_facet |
Juan P. Hernández del Rincón Juan P. Hernández del Rincón Juan P. Hernández del Rincón Mari C. Olmo Conesa Mari C. Olmo Conesa Ana Rodríguez Serrano Helena García Pulgar David López Cuenca David López Cuenca Carmen Muñoz Esparza Carmen Muñoz Esparza Marina Navarro Peñalver Marina Navarro Peñalver Juan José Santos Mateo Juan José Santos Mateo Elisa Nicolás Rocamora Elisa Nicolás Rocamora Elisa Nicolás Rocamora Cristina Gil Ortuño Cristina Gil Ortuño María Sabater-Molina María Sabater-Molina María Sabater-Molina María Sabater-Molina María Sabater-Molina Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Juan Ramón Gimeno Blanes Francisco Pastor Quirante Francisco Pastor Quirante Francisco Pastor Quirante |
author_sort |
Juan P. Hernández del Rincón |
title |
Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart Diseases |
title_short |
Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart Diseases |
title_full |
Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart Diseases |
title_fullStr |
Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart Diseases |
title_full_unstemmed |
Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart Diseases |
title_sort |
prevented sudden cardiac death and neurologic recovery in inherited heart diseases |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cardiovascular Medicine |
issn |
2297-055X |
publishDate |
2021-03-01 |
description |
Introduction: Inherited cardiovascular diseases are an important cause of sudden cardiac death (SD). The use of risk scores identify high risk patients who would benefit from an implantable cardioverter-defibrillators (ICDs). The development of automated devices for out-of-hospital cardiac arrest improves early resuscitation. The objective of the study is to quantify prevented SD and the neurological recovery of patients with inherited cardiovascular diseases.Methods: Two hundred fifty-seven cases of SD (age 42 ± 18 years, 79.4% men) of non-ischemic cardiac cause were prospectively collected during the study period (2009–17). Fifty three (20.6%) had a resuscitated cardiac arrest (RCA) (age 40 ± 18 years, 64.2% male). Epidemiological, clinical and autopsy aspects were analyzed. Prevented SD was defined as a combination of RCA and appropriate ICD therapy cases.Results: An autopsy was performed in 157/204 (77.0%) cases who died. There were 19 (12.1%) cases with a negative autopsy. The diagnosis of cardiomyopathy and channelopathy was 58.0 and 18.7%, respectively. Female sex and confirmed or suspected channelopathy were associated with successful resuscitation. The percentage of prevented SD remained low during the study period (mean 35.6%). 60.4% of RCA cases presented good neurological outcome. There was no association between neurological recovery and therapeutic hypothermia, but there was association with time of resuscitation (min).Conclusion: A fifth part of non-ischemic cardiac arrests were resuscitated. Female sex and channelopathies were more prevalent among RCA. Two thirds of RCA had a good neurological recovery. |
topic |
sudden cardiac death cardiomyopathy channelopathy inherited cardiovascular diseases prevented sudden cardiac death |
url |
https://www.frontiersin.org/articles/10.3389/fcvm.2021.634300/full |
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doaj-bcb5029e839b456ca7557e700b22fcd42021-03-15T04:35:30ZengFrontiers Media S.A.Frontiers in Cardiovascular Medicine2297-055X2021-03-01810.3389/fcvm.2021.634300634300Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart DiseasesJuan P. Hernández del Rincón0Juan P. Hernández del Rincón1Juan P. Hernández del Rincón2Mari C. Olmo Conesa3Mari C. Olmo Conesa4Ana Rodríguez Serrano5Helena García Pulgar6David López Cuenca7David López Cuenca8Carmen Muñoz Esparza9Carmen Muñoz Esparza10Marina Navarro Peñalver11Marina Navarro Peñalver12Juan José Santos Mateo13Juan José Santos Mateo14Elisa Nicolás Rocamora15Elisa Nicolás Rocamora16Elisa Nicolás Rocamora17Cristina Gil Ortuño18Cristina Gil Ortuño19María Sabater-Molina20María Sabater-Molina21María Sabater-Molina22María Sabater-Molina23María Sabater-Molina24Juan Ramón Gimeno Blanes25Juan Ramón Gimeno Blanes26Juan Ramón Gimeno Blanes27Juan Ramón Gimeno Blanes28Juan Ramón Gimeno Blanes29Francisco Pastor Quirante30Francisco Pastor Quirante31Francisco Pastor Quirante32Instituto de Medicina Legal y Ciencias Forenses, Murcia, SpainDepartamento de Medicina Legal, Universidad de Murcia, Murcia, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainDepartamento de Medicina Interna, Universidad de Murcia, Murcia, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainDepartamento de Medicina Interna, Universidad de Murcia, Murcia, SpainEuropean Reference Networks (Guard-Heart), Amsterdam, NetherlandsRed de investigación Cardiovascular (CIBERCV), Instituto de Salud Carlos III, Madrid, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainUnidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, SpainDepartamento de Medicina Interna, Universidad de Murcia, Murcia, SpainEuropean Reference Networks (Guard-Heart), Amsterdam, NetherlandsRed de investigación Cardiovascular (CIBERCV), Instituto de Salud Carlos III, Madrid, SpainInstituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, SpainServicio de Anatomía Patológica, Hospital General Universitario Reina Sofía, Murcia, SpainDepartamento de Anatomia Patologica, Universidad de Murcia, Murcia, SpainIntroduction: Inherited cardiovascular diseases are an important cause of sudden cardiac death (SD). The use of risk scores identify high risk patients who would benefit from an implantable cardioverter-defibrillators (ICDs). The development of automated devices for out-of-hospital cardiac arrest improves early resuscitation. The objective of the study is to quantify prevented SD and the neurological recovery of patients with inherited cardiovascular diseases.Methods: Two hundred fifty-seven cases of SD (age 42 ± 18 years, 79.4% men) of non-ischemic cardiac cause were prospectively collected during the study period (2009–17). Fifty three (20.6%) had a resuscitated cardiac arrest (RCA) (age 40 ± 18 years, 64.2% male). Epidemiological, clinical and autopsy aspects were analyzed. Prevented SD was defined as a combination of RCA and appropriate ICD therapy cases.Results: An autopsy was performed in 157/204 (77.0%) cases who died. There were 19 (12.1%) cases with a negative autopsy. The diagnosis of cardiomyopathy and channelopathy was 58.0 and 18.7%, respectively. Female sex and confirmed or suspected channelopathy were associated with successful resuscitation. The percentage of prevented SD remained low during the study period (mean 35.6%). 60.4% of RCA cases presented good neurological outcome. There was no association between neurological recovery and therapeutic hypothermia, but there was association with time of resuscitation (min).Conclusion: A fifth part of non-ischemic cardiac arrests were resuscitated. Female sex and channelopathies were more prevalent among RCA. Two thirds of RCA had a good neurological recovery.https://www.frontiersin.org/articles/10.3389/fcvm.2021.634300/fullsudden cardiac deathcardiomyopathychannelopathyinherited cardiovascular diseasesprevented sudden cardiac death |