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Clinical characteristics and outcome of end stage hypertrophic cardiomyopathy: Role of age and heart failure phenotypes.
Musumeci, Beatrice; Tini, Giacomo; Biagini, Elena; Merlo, Marco; Calore, Chiara; Ammirati, Enrico; Zampieri, Mattia; Russo, Domitilla; Grilli, Giulia; Santolamazza, Caterina; Vio, Riccardo; Rubino, Marta; Ditaranto, Raffaello; Del Franco, Annamaria; Sormani, Paola; Parisi, Vanda; Monda, Emanuele; Francia, Pietro; Cipriani, Alberto; Limongelli, Giuseppe; Sinagra, Gianfranco; Olivotto, Iacopo; Boni, Luca; Autore, Camillo.
Afiliação
  • Musumeci B; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Italy.
  • Tini G; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Italy.
  • Biagini E; Cardiology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Italy; European Reference Network for Rare, Low Prevalence, and Complex Diseases of the Heart (ERN GUARD-Heart), Italy.
  • Merlo M; Cardiothoracovascular Department, Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI), University of Trieste, Italy.
  • Calore C; Dipartimento di Scienze Cardio-Toraco-Vascolari e Sanità pubblica-Università di Padova, Italy.
  • Ammirati E; De Gasperis Cardio Center, Milano, Italy.
  • Zampieri M; Cardiomyopathy Unit, Careggi University Hospital, Florence, Italy.
  • Russo D; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Italy.
  • Grilli G; Cardiothoracovascular Department, Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI), University of Trieste, Italy.
  • Santolamazza C; De Gasperis Cardio Center, Milano, Italy.
  • Vio R; Dipartimento di Scienze Cardio-Toraco-Vascolari e Sanità pubblica-Università di Padova, Italy.
  • Rubino M; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, Naples, Italy.
  • Ditaranto R; Cardiology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Italy; Department of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.
  • Del Franco A; Cardiomyopathy Unit, Careggi University Hospital, Florence, Italy.
  • Sormani P; De Gasperis Cardio Center, Milano, Italy.
  • Parisi V; Cardiology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Italy; Department of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Italy.
  • Monda E; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, Naples, Italy.
  • Francia P; Department of Clinical and Molecular Medicine, Sapienza University of Rome, Italy.
  • Cipriani A; Dipartimento di Scienze Cardio-Toraco-Vascolari e Sanità pubblica-Università di Padova, Italy.
  • Limongelli G; Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, Naples, Italy.
  • Sinagra G; Cardiothoracovascular Department, Azienda Sanitaria Universitaria Giuliano Isontina (ASUGI), University of Trieste, Italy.
  • Olivotto I; Cardiomyopathy Unit, Careggi University Hospital, Florence, Italy.
  • Boni L; Epidemiologia Clinica, Istituto di Ricovero e Cura a Carattere Scientifico (IRCSS) Ospedale Policlinico San Martino-IST Nord CBA, Genova, Italy.
  • Autore C; Department of Cardiology and Respiratory Sciences, San Raffaele Cassino (FR), Italy. Electronic address: camillo.autore@sanraffaele.it.
Int J Cardiol ; 400: 131784, 2024 Apr 01.
Article em En | MEDLINE | ID: mdl-38242504
ABSTRACT

BACKGROUND:

A minority of patients with hypertrophic cardiomyopathy (HCM) presents advanced heart failure (HF) during their clinical course, in the context of left ventricular (LV) remodeling with reduced LV ejection fraction (LVEF), or of severe diastolic dysfunction without impaired LVEF. Aim of this study was to describe a multicentric end stage (ES) HCM population and analyze clinical course and outcome among its different phenotypes.

METHODS:

Data of all HCM patients from 7 Italian referral centres were retrospectively evaluated. ES was diagnosed in presence of LVEF <50% (ES-rEF) or NYHA functional class ≥II with severe diastolic dysfunction (ES-pEF). Outcomes were HCM-related and all-cause mortality; combined arrhythmic events; advanced HF treatments.

RESULTS:

Study population included 331 ES patients; 87% presented ES-rEF and 13% ES-pEF. At ES recognition, patients with ES-pEF were more commonly females, had more frequently NYHA III/IV, atrial fibrillation and greater maximal LV wall thickness. Over a median follow-up of 5.6 years, 83 (25%) patients died, 46 (15%) experienced arrhythmic events and (26%) 85 received advanced HF treatments. Incidence of HCM-related and all-cause mortality, and of combined arrhythmic events did not differ in ES-pEF and ES-rEF patients, but ES-pEF patients were less likely to receive advanced HF treatments. Older age at ES recognition was an independent predictor of increased HCM-related mortality (p = 0.01) and reduced access to advanced HF treatments (p < 0.0001).

CONCLUSIONS:

Two different HCM-ES phenotypes can be recognized, with ES-pEF showing distinctive features at ES recognition and receiving less frequently advanced HF treatments. Older age at ES recognition has a major impact on outcomes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiomiopatia Hipertrófica / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans Idioma: En Revista: Int J Cardiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiomiopatia Hipertrófica / Insuficiência Cardíaca Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans Idioma: En Revista: Int J Cardiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália