Prognostic implications of different clinical profiles in hypertrophic cardiomyopathy.
| Title: | Prognostic implications of different clinical profiles in hypertrophic cardiomyopathy. |
|---|---|
| Authors: | Russo D; Unit of Cardiology, Department of Clinical and Molecular Medicine, Faculty of Medicine and Psychology, Sant'Andrea Hospital, Sapienza University, Rome, Italy.; Sclafani M; Unit of Cardiology, Department of Clinical and Molecular Medicine, Faculty of Medicine and Psychology, Sant'Andrea Hospital, Sapienza University, Rome, Italy.; Tini G; Unit of Cardiology, Department of Clinical and Molecular Medicine, Faculty of Medicine and Psychology, Sant'Andrea Hospital, Sapienza University, Rome, Italy.; Musumeci MB; Unit of Cardiology, Department of Clinical and Molecular Medicine, Faculty of Medicine and Psychology, Sant'Andrea Hospital, Sapienza University, Rome, Italy.; Arcari L; Unit of Cardiology, Madre Giuseppina Vannini Hospital, Rome, Italy.; Limite LR; Unit of Arrhythmia and Electrophysiology Laboratories, Department of Cardiology and Cardiothoracic Surgery, San Raffaele Hospital, Milan, Italy.; Francia P; Unit of Cardiology, Department of Clinical and Molecular Medicine, Faculty of Medicine and Psychology, Sant'Andrea Hospital, Sapienza University, Rome, Italy.; Autore C; Unit of Cardiology, Department of Clinical and Molecular Medicine, Faculty of Medicine and Psychology, Sant'Andrea Hospital, Sapienza University, Rome, Italy - camillo.autore@uniroma1.it. |
| Source: | Minerva cardiology and angiology [Minerva Cardiol Angiol] 2022 Apr; Vol. 70 (2), pp. 189-206. Date of Electronic Publication: 2021 Oct 29. |
| Publication Type: | Journal Article; Review |
| Language: | English |
| Journal Info: | Publisher: Minerva medica Country of Publication: Italy NLM ID: 101776555 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2724-5772 (Electronic) Linking ISSN: 27245683 NLM ISO Abbreviation: Minerva Cardiol Angiol Subsets: MEDLINE |
| Imprint Name(s): | Original Publication: Torino : Minerva medica, [2021]- |
| MeSH Terms: | Atrial Fibrillation*/diagnosis ; Cardiomyopathy, Hypertrophic*/complications ; Cardiomyopathy, Hypertrophic*/diagnosis ; Cardiomyopathy, Hypertrophic*/genetics ; Ventricular Dysfunction, Left*/complications; Humans ; Myocardium ; Prognosis |
| Abstract: | Hypertrophic cardiomyopathy (HCM) is a myocardial genetic disease relatively common in the general population with heterogenous clinical presentation, natural history and prognosis. About 60% of HCM patients have a stable clinical course, while others may experience a variety of HCM-related complications which follows relatively independent pathways, and that can be distinguished in different subgroups. These subgroups are represented by patients with left ventricular outflow tract obstruction; patients with end-stage disease and reduced or preserved systolic function; patients with apical hypertrophy; patients with apical aneurysm; patients with atrial fibrillation, patients at high risk of sudden death and patients with preclinical HCM. The purpose of this review was to describe each of these clinical profiles with its prognostic implications. |
| Entry Date(s): | Date Created: 20211029 Date Completed: 20220413 Latest Revision: 20220413 |
| Update Code: | 20260130 |
| DOI: | 10.23736/S2724-5683.21.05752-5 |
| PMID: | 34713676 |
| Database: | MEDLINE |
Journal Article; Review