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Short- and Long-Term Outcomes of Obstructive and Non-Obstructive Hypertrophic Cardiomyopathy: A Systematic Review and
Hui Zhen Lo1, Chen Ee Low2, Chun En Yau3
1Peninsula Health, Frankston, Vic, Australia.
Insights
Obstructive hypertrophic cardiomyopathy (HOCM) increases sudden cardiac death risk compared to non-obstructive (NOCM) forms. While NOCM patients face higher overall mortality incidence, HOCM is linked to increased heart failure mortality.
Area of Science:
- Cardiology
- Genetics
- Public Health
Background:
- Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac condition.
- Risk factors and outcomes for obstructive (HOCM) and non-obstructive (NOCM) hypertrophic cardiomyopathy are not fully understood.
- This study investigates mortality in HOCM versus NOCM patients.
Purpose of the Study:
- To compare mortality risks and incidence between obstructive and non-obstructive hypertrophic cardiomyopathy.
- To identify specific risk factors for all-cause and HCM-specific mortality.
- To provide a comprehensive analysis of outcomes in HCM subtypes.
Main Methods:
- A systematic review and meta-analysis adhering to PRISMA guidelines.
- Searched PubMed, SCOPUS, and Embase databases for studies from 2001 to 2023.
- Utilized random effects meta-analyses and meta-regressions for primary analysis.
Main Results:
- Included 61 studies with 52,020 participants.
- Sudden cardiac death (SCD) risk was significantly higher in HOCM versus NOCM patients (RR 1.69).
- NOCM patients had higher incidence of all-cause, HCM-related, and SCD mortality; HOCM patients had higher heart failure-related mortality.
Conclusions:
- Obstructive hypertrophic cardiomyopathy is associated with a significantly higher risk of sudden cardiac death.
- Non-obstructive hypertrophic cardiomyopathy presents a higher incidence of all-cause, HCM-related, and sudden cardiac death mortality.
- Heart failure-related mortality is the primary concern in obstructive hypertrophic cardiomyopathy.
Background:
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac condition, but the risk factors and outcomes of patients with obstructive (HOCM) and non-obstructive hypertrophic cardiomyopathy (NOCM) remain unclear. This systematic review and meta-analysis was conducted to investigate the risk ratio (RR), incidence, and risk factors of all-cause and HCM-specific mortality.
Methods:
This PRISMA-adherent systematic review involved a systematic search of PubMed, SCOPUS, and Embase for studies published from 1 January 2001 to 31 August 2023 that reported outcomes of patients with HOCM and NOCM. Random effects meta-analyses and meta-regressions were used for primary analysis.
Results:
Sixty-one observational studies with 52,020 participants were included. All-cause, HCM-related, and heart failure-related mortality had no difference in HOCM vs NOCM patients (RR 0.85, 95% CI 0.58-1.25), (RR 0.95, 95% CI 0.68-1.32), and (RR 0.95, 95% CI 0.58-1.58), respectively. Sudden cardiac death (SCD) was significantly higher in HOCM vs NOCM patients (RR 1.69, 95% CI 1.19-2.42). Incidence of all-cause mortality (NOCM 95.47, 95% CI 63.96-140.18 vs HOCM 65.75, 95% CI 48.04-89.37) per 1,000 observations, HCM-related mortality (NOCM 59.72, 95% CI 41.91-84.42 vs HOCM 55.51, 95% CI 39.42-77.64), and SCD (NOCM 32.17, 95% CI 22.42-45.96 vs HOCM: 25.39 95% CI 15.24-42.01) were higher in NOCM patients, while heart failure-related mortality (HOCM 55.51, 95% CI 39.42-77.64 vs NOCM 30.04, 95% CI 14.78-60.11) was higher in HOCM patients.
Conclusions:
The RR of SCD was significantly higher in HOCM vs NOCM patients. All-cause mortality, HCM-related mortality, and SCD were of higher incidence in NOCM patients. Only heart failure-related mortality was higher in HOCM patients.
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