Frontiers in Cardiovascular Medicine (Mar 2021)
Prevented Sudden Cardiac Death and Neurologic Recovery in Inherited Heart Diseases
- 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
Affiliations
- Juan P. Hernández del Rincón
- Instituto de Medicina Legal y Ciencias Forenses, Murcia, Spain
- Juan P. Hernández del Rincón
- Departamento de Medicina Legal, Universidad de Murcia, Murcia, Spain
- Juan P. Hernández del Rincón
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- Mari C. Olmo Conesa
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- Mari C. Olmo Conesa
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- Ana Rodríguez Serrano
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- Helena García Pulgar
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- David López Cuenca
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- David López Cuenca
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- Carmen Muñoz Esparza
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- Carmen Muñoz Esparza
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- Marina Navarro Peñalver
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- Marina Navarro Peñalver
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- Juan José Santos Mateo
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- Juan José Santos Mateo
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- Elisa Nicolás Rocamora
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- Elisa Nicolás Rocamora
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- Elisa Nicolás Rocamora
- Departamento de Medicina Interna, Universidad de Murcia, Murcia, Spain
- Cristina Gil Ortuño
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- Cristina Gil Ortuño
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- María Sabater-Molina
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- María Sabater-Molina
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- María Sabater-Molina
- Departamento de Medicina Interna, Universidad de Murcia, Murcia, Spain
- María Sabater-Molina
- European Reference Networks (Guard-Heart), Amsterdam, Netherlands
- María Sabater-Molina
- Red de investigación Cardiovascular (CIBERCV), Instituto de Salud Carlos III, Madrid, Spain
- Juan Ramón Gimeno Blanes
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- Juan Ramón Gimeno Blanes
- Unidad de Cardiopatías Hereditarias, Servicio de Cardiología, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain
- Juan Ramón Gimeno Blanes
- Departamento de Medicina Interna, Universidad de Murcia, Murcia, Spain
- Juan Ramón Gimeno Blanes
- European Reference Networks (Guard-Heart), Amsterdam, Netherlands
- Juan Ramón Gimeno Blanes
- Red de investigación Cardiovascular (CIBERCV), Instituto de Salud Carlos III, Madrid, Spain
- Francisco Pastor Quirante
- Instituto Murciano, de Investigación Biosanitaria (IMIB), Murcia, Spain
- Francisco Pastor Quirante
- Servicio de Anatomía Patológica, Hospital General Universitario Reina Sofía, Murcia, Spain
- Francisco Pastor Quirante
- Departamento de Anatomia Patologica, Universidad de Murcia, Murcia, Spain
- DOI
- https://doi.org/10.3389/fcvm.2021.634300
- Journal volume & issue
-
Vol. 8
Abstract
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.
Keywords
- sudden cardiac death
- cardiomyopathy
- channelopathy
- inherited cardiovascular diseases
- prevented sudden cardiac death