Cardiomiopatía cirrótica – ¿Realidad clínica o simple curiosidad académica? Revisión.

Parte 1: definición, epidemiología, anatomía patológica y clínica

Autores/as

  • Hugo R. Ramos, M.D., Ph.D. Facultad de Ciencias MédicasUniversidad Nacional de Cordoba. Instituto Modelo de Cardiologia
  • Mario H. Altieri, MD Service de Médecine, Centre Hospitalier Marguerite de Lorraine, Mortagne au Perche, France

DOI:

https://doi.org/10.31053/1853.0605.v81.n1.44416

Palabras clave:

cirrosis hepática, cardiomiopatía, insuficiencia cardíaca, trasplante hepático

Resumen

La cirrosis avanzada puede provocar alteraciones miocárdicas que constituyen el síndrome de Cardiomiopatía Cirrótica definido como la disfunción cardíaca asociada con cirrosis hepática en ausencia de enfermedad cardíaca preexistente. Su prevalencia es variable de acuerdo a lo reportado por diferentes grupos de investigación debido a que puede mantenerse subclínica o latente hasta que la pone de manifiesto una situación de estrés como una cirugía, hemorragia, infección, trasplante hepático o shunt porto-sistémico intrahepático transyugular. El objetivo de esta revisión es discutir la definición, los fundamentos anátomo-patológicos, fisiopatología, manifestaciones clínicas, criterios de diagnóstico, importancia de los estudios con imágenes, relevancia clínica, tratamiento farmacológico y trasplante hepático.

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Biografía del autor/a

Hugo R. Ramos, M.D., Ph.D., Facultad de Ciencias MédicasUniversidad Nacional de Cordoba. Instituto Modelo de Cardiologia

Egresado de la Universidad Nacional de Córdoba. Especialista en Clínica Médica, Especialista en Cardiología (CMPC y UNC), Especialista en Medicina de Emergencias (CMPC). Doctor en Medicina y Cirugía FCM, UNC. Prof. Asociado en la Cátedra de Clínica Médica I, UHMI 2 del Hospital San Roque, FCM, UNC. Ex Jefe del Depto de Clínica Médica del Hospital Municipal de Urgencias de Córdoba, Cardiólogo en Instituto Modelo de Cardiología de Córdoba.  Campo de investigación: biomarcadores cardíacos, insuficiencia cardíaca, amiloidosis cardíaca, cardiopatía isquémica. ORCID ID: https://orcid.org/0000-0001-6772-903X

Mario H. Altieri, MD, Service de Médecine, Centre Hospitalier Marguerite de Lorraine, Mortagne au Perche, France

Egresado de la Universidad Nacional de Córdoba. Especialista en Medicina Interna y Terapia Intensiva (CMPC), Especialista en Terapia Intensiva (Francia). Ex Prof. de Medicina Intensiva de la Universidad Católica de Córdoba. Ex Director del programa Medicob de trasplante de Hígado, Caen, Francia. Miembro fundador del Cirrhotic Cardiomyopathy Consortium. Ex Miembro del Comité Ejecutivo de la International Liver Transplant Society (ILTS) para problemas cardiovasculares y cirrosis. ORCID ID: https://orcid.org/0000-0003-4164-1771.

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Publicado

2024-03-27

Cómo citar

1.
Ramos H, Altieri M. Cardiomiopatía cirrótica – ¿Realidad clínica o simple curiosidad académica? Revisión. : Parte 1: definición, epidemiología, anatomía patológica y clínica. Rev Fac Cien Med Univ Nac Cordoba [Internet]. 27 de marzo de 2024 [citado 27 de abril de 2024];81(1):178-95. Disponible en: https://revistas.unc.edu.ar/index.php/med/article/view/44416

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