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Long-term outcome of nonobstructive versus obstructive hypertrophic cardiomyopathy: A systematic review and
Francesco Pelliccia1, Vincenzo Pasceri2, Giuseppe Limongelli3
1Department Attilio Reale, Sapienza University, Rome, Italy.
Insights
Long-term mortality for nonobstructive hypertrophic cardiomyopathy (HCM) is significant and similar to obstructive HCM (HOCM). This finding challenges the notion that nonobstructive HCM carries a low risk, emphasizing the need for careful monitoring in all HCM patients.
Area of Science:
- Cardiology
- Clinical Medicine
- Public Health
Background:
- Hypertrophic cardiomyopathy (HCM) prognosis varies significantly among patients.
- Nonobstructive HCM (NOCM) is often considered lower-risk than obstructive HCM (HOCM).
- Existing data on NOCM may be biased due to tertiary center referral patterns.
Purpose of the Study:
- To conduct a systematic review and meta-analysis of published literature on HCM.
- To compare presenting features and long-term outcomes between NOCM and HOCM.
- To evaluate the mortality risk associated with NOCM versus HOCM.
Main Methods:
- Searched MEDLINE/PubMed, EMBASE, and Cochrane databases up to December 31, 2016.
- Included 20 studies with a total of 7731 patients (5058 NOCM, 2673 HOCM).
- Analyzed primary endpoints of HCM-related overall mortality and yearly cardiac death rates, plus sudden and heart failure deaths.
Main Results:
- Annual HCM-related mortality was 1.55% for NOCM and 1.77% for HOCM (RR: 0.89; 95% CI: 0.68-1.17; p=0.40).
- Five studies showed higher mortality in HOCM, three in NOCM, and twelve found no significant difference.
- No statistically significant difference in mortality was observed between NOCM and HOCM groups.
Conclusions:
- Long-term mortality in nonobstructive HCM is not negligible.
- The mortality risk for NOCM is comparable to that of obstructive HCM.
- These findings suggest NOCM patients require careful management and monitoring akin to HOCM patients.
Background:
Prognosis of hypertrophic cardiomyopathy (HCM) is particularly heterogeneous. Patients with nonobstructive HCM (NOCM) are thought to be at relatively low-risk as compared with obstructive HCM (HOCM) with no need of major treatment options. However, available evidence of NOCM comes mainly from tertiary centers where a referral bias is likely to occur. Aim of this study was to perform a systematic review and meta-analysis of the published literature on hypertrophic cardiomyopathy (HCM) in order to outline differences in presenting features and long-term outcome between NOCM and HOCM.
Methods:
MEDLINE/Pubmed, EMBASE and Cochrane databases up to December 31, 2016, and reviewed cited references to identify relevant studies were used. The primary endpoints were HCM-related overall mortality rate and yearly rate of cardiac death. Other endpoints were incidences of sudden and congestive heart failure deaths.
Results:
A total of 20 studies entered the meta-analysis on the long-term outcome of NOCM vs HOCM. They included a total of 7731 patients, 5058 patients with NOCM (65%) and 2673 patients with HOCM (35%). During the follow-up, annual mortality related to HCM averaged 1.55% in NOCM and 1.77% in HOCM (Relative Risk: 0.89, 95% confidence intervals: 0.68 to 1.17, p=0.40). Overall, 5 studies reported significantly higher mortality for HOCM, 3 higher mortality for NOCM, and 12 no significant differences.
Conclusion:
This large study-level meta-analysis shows that long-term mortality of patients with NOCM is not negligible and not significantly different from HOCM.
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