Cardiac Dysautonomia Predicts Long-Term Survival in Hereditary Transthyretin Amyloidosis After Liver Transplantation | Zendy

Vincent Algalarrondo | Zendy; Térésa Antonini | Zendy; Marie Théaudin | Zendy; Denis Chemla | Zendy; Anouar Benmalek | Zendy; Catherine Lacroix | Zendy; Denis Castaing | Zendy; Cécile Cauquil | Zendy; S. Dinanian | Zendy; Ludivine Eliahou | Zendy; Didier Samuel | Zendy; David Adams | Zendy; Dominique Le Guludec | Zendy; Michel Slama | Zendy; François Rouzet | Zendy

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Cardiac Dysautonomia Predicts Long-Term Survival in Hereditary Transthyretin Amyloidosis After Liver Transplantation

Author(s) -

Vincent Algalarrondo,

Térésa Antonini,

Marie Théaudin,

Denis Chemla,

Anouar Benmalek,

Catherine Lacroix,

Denis Castaing,

Cécile Cauquil,

S. Dinanian,

Ludivine Eliahou,

Didier Samuel,

David Adams,

Dominique Le Guludec,

Michel Slama,

François Rouzet

Publication year - 2016

Publication title -

jacc. cardiovascular imaging

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.79

H-Index - 120

eISSN - 1936-878X

pISSN - 1876-7591

DOI - 10.1016/j.jcmg.2016.07.008

Subject(s) - dysautonomia , medicine , cardiology , heart rate variability , liver transplantation , transthyretin , univariate analysis , heart transplantation , heart failure , heart rate , transplantation , disease , multivariate analysis , blood pressure

This study sought to compare techniques evaluating cardiac dysautonomia and predicting the risk of death of patients with hereditary transthyretin amyloidosis (mATTR) after liver transplantation (LT).

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