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May 31, 2010European Heart Journal232 citationsOpen Access

Clinicopathological profiles of progressive heart failure in hypertrophic cardiomyopathy

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PMPaola MelaciniCBCristina BassoAAAnnalisa Angelini

Key Result

Non-obstructive HCM with preserved systolic function had the most accelerated progression to advanced heart failure and adverse outcomes compared with other HCM profiles (P=0.04).

Key Points

  • This research aims to define profiles of severe progressive heart failure in patients with hypertrophic cardiomyopathy.
  • Assessment of clinical and morphological features in 293 hypertrophic cardiomyopathy patients.
  • Median follow-up of 6 years (inter-quartile range 2-11 years).
  • Analysis of gross and histopathological features in 12 deceased patients.
  • 50 patients (17%) developed severe progressive heart failure, with 18 patients dying or requiring transplantation.
  • Three heart failure profiles identified: end-stage systolic dysfunction (30%), left ventricular outflow obstruction (22%), and non-obstructive with preserved function (48%).
  • Atrial fibrillation contributed to heart failure in 32 patients (64%), particularly associated with accelerated progression to advanced heart failure.

Study Design

Type

Cohort (n=293)

Structured PICO

P
Population
293 consecutive patients with hypertrophic cardiomyopathy (HCM)
O
Outcome
Development of severe progressive heart failure symptoms, death, or heart transplantationhard clinical

Advanced heart failure in HCM presents in three distinct profiles, with atrial fibrillation being a major contributor and non-obstructive preserved systolic function showing the most rapid progression.

Abstract

AIMS: Hypertrophic cardiomyopathy (HCM) is an important cause of heart failure-related disability over a wide range of ages. Profiles of severe progressive heart failure symptoms and death, or heart transplantation deserve more complete definition within large patient cohorts. METHODS AND RESULTS: Clinical and morphological features of heart failure were assessed in 293 consecutive HCM patients over a median follow-up of 6 (inter-quartile range 2-11) years. Gross and histopathological features were analysed in 12 patients for whom the heart was available for inspection. Of the 293 patients, 50 (17%) developed severe progressive heart failure, including 18 who died or were transplanted. Three profiles of heart failure were identified predominantly associated with: (i) end-stage systolic dysfunction (ejection fraction <50%) (15; 30%); (ii) left ventricular (LV) outflow obstruction at rest (11; 22%); and (iii) non-obstructive with preserved systolic function (24; 48%). Overall, atrial fibrillation (AF) contributed to heart failure in 32 patients (64%) among the three profiles. Compared with other patients, those non-obstructive with preserved systolic function had earlier onset of heart failure symptoms mainly due to diastolic dysfunction, and the most accelerated progression to advanced heart failure and adverse outcome (P = 0.04). Thrombi were identified in the left atrial appendage of five gross heart specimens all belonging to patients with AF, including three of which were unrecognized clinically and had previously embolized. Extensive myocardial scarring with LV remodelling was evident in all end-stage patients; no or only focal scars were present in other patients. CONCLUSION: Profiles of advanced heart failure in HCM are due to diverse pathophysiological mechanisms, including LV outflow obstruction and diastolic or global systolic ventricular dysfunction. Atrial fibrillation proved to be the most common disease variable associated with progressive heart failure. Recognition of the heterogeneous pathophysiology of heart failure in HCM is relevant, given the targeted management strategies necessary in this disease.

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Cite This Study

Melacini et al. (2010) conducted a cohort in Hypertrophic cardiomyopathy (n=293). Non-obstructive HCM with preserved systolic function had the most accelerated progression to advanced heart failure and adverse outcomes compared with other HCM profiles (P=0.04).

synapsesocial.com/papers/6a0a949d700cef80f8708e07https://doi.org/10.1093/eurheartj/ehq136
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