Clinical Profile of Patients with Hypertrophic Cardiomyopathy at a University Hospital

pp. 345-351

Authors

  • Aníbal M. Arias Institute of Cardiovascular Medicine – Hospital Italiano de Buenos Aires. Department of Cardiology
  • Rodrigo P. Bagnati Institute of Cardiovascular Medicine – Hospital Italiano de Buenos Aires. Department of Cardiology
  • Diego Pérez de Arenaza Institute of Cardiovascular Medicine – Hospital Italiano de Buenos Aires. Department of Cardiology
  • Pablo F. Oberti Institute of Cardiovascular Medicine – Hospital Italiano de Buenos Aires. Department of Cardiology
  • Mariano L. Falconi Institute of Cardiovascular Medicine – Hospital Italiano de Buenos Aires. Department of Cardiology
  • Rodolfo Pizarro Institute of Cardiovascular Medicine – Hospital Italiano de Buenos Aires. Department of Cardiology
  • Gonzalo Díaz Babio Institute of Cardiovascular Medicine – Hospital Italiano de Buenos Aires. Department of Cardiology
  • Luciano O. Lucas Institute of Cardiovascular Medicine – Hospital Italiano de Buenos Aires. Department of Cardiology
  • Ricardo García Mónaco Instituto de Medicina Cardiovascular - Hospital Italiano de Buenos Aires. Diagnostic Imaging Unit
  • César A. Belziti Institute of Cardiovascular Medicine – Hospital Italiano de Buenos Aires. Department of Cardiology

DOI:

https://doi.org/10.7775/rac.es.v82.i5.3368

Keywords:

Hypertrophic cardiomyopathy, Diagnosis, Treatment, Prognosis

Abstract

Introduction: Hypertrophic cardiomyopathy is the most frequent genetic cardiomyopathy, and there is no available information on baseline characteristics and outcomes of patients with this disease in our country.
Objective: To describe the clinical profile of patients with hypertrophic cardiomyopathy and to identify predictors of adverse outcomes.
Methods: One hundred and forty-three patients with hypertrophic cardiomyopathy at the Hospital Italiano of Buenos Aires between 2005 and 2011 were included in the study.
Results: Median age was 66 years and 52% were women. Most patients presented an asymmetric distribution (92%) and 60% had dynamic obstruction. Mortality was 5.59% at a median follow-up of 2.11 years [25-75 IQR (0.75-3.70)]. The most prevalent symptom was dyspnea (36%), followed by angina (17%) and syncope (14%). Dynamic obstruction, moderate or severe mitral regurgitation, left atrial diameter, and female gender were independently associated with dyspnea. Dynamic obstruction was independently associated with angina. Maximum wall thickness was directly and independently associated with syncope, while ejection fraction and left ventricular hypertrophy or negative T in the electrocardiogram presented an inverse relationship. Mortality was independently associated with hospitalization for decompensated heart failure.
Conclusion: Similar to previous studies, our population shows that hypertrophic cardiomyopathy is a heterogeneous disease. A prospective study is necessary to validate the risk predictors assessed in this study.

Published

2025-09-23

Issue

Section

ORIGINAL ARTICLES

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