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Size Matters. Prevalence and Clinical Implications of Left Ventricular Apical Aneurysms in Hypertrophic
Katie Linden1,2, Nathan Green3, Alison Muir2
1Queen's University Belfast Wellcome-Wolfson Institute for Experimental Medicine Belfast UK.
Insights
Left ventricular apical aneurysms (LVAAs) occur in 3% of hypertrophic cardiomyopathy patients. Bigger LVAAs (>2 cm) significantly increase risks of sudden cardiac death, systemic embolization, and left ventricular thrombi.
Area of Science:
- Cardiology
- Medical Research
Background:
- Hypertrophic cardiomyopathy (HCM) is a significant cause of sudden cardiac death.
- Left ventricular apical aneurysm (LVAA) is a potential complication of HCM.
- The prevalence and clinical impact of LVAA in HCM require further elucidation.
Purpose of the Study:
- To systematically review the literature on LVAA prevalence in HCM.
- To determine the association of LVAA with adverse outcomes including sudden cardiac death, systemic embolization, and heart failure.
Main Methods:
- Systematic review and meta-analysis of longitudinal, observational studies.
- Searches included MEDLINE and manual searches up to August 2023.
- Random-effects model used for data pooling.
Main Results:
- Pooled prevalence of LVAA in HCM was 3% (95% CI, 2%-5%).
- Bigger LVAAs (≥2 cm) were associated with significantly higher risks of sudden cardiac death (OR 4.65), left ventricular thrombi (OR 10.92), and a trend towards higher systemic emboli.
- Small LVAAs (<2 cm) showed a lower prevalence of adverse events compared to bigger LVAAs.
Conclusions:
- Patients with bigger LVAAs (>2 cm) face the highest risk of poor outcomes in HCM.
- Targeted primary prevention strategies for sudden cardiac death and systemic embolization may benefit patients with bigger LVAAs.
Background:
The aim of this study was to systematically review the recently published literature and determine the prevalence of left ventricular apical aneurysm (LVAA) formation in hypertrophic cardiomyopathy and its association with sudden cardiac death, systemic embolization, and heart failure.
Methods:
The protocol was registered with the International Prospective Register of Systematic Reviews (registration number: CRD42023453640). MEDLINE and manual searches for articles published up to August 2023 were performed. Longitudinal, observational cohorts of unselected adult patients with hypertrophic cardiomyopathy were considered. Data were pooled using a random-effects model.
Results:
A total of 321 articles fulfilled the search criteria, and 10 retrospective observational studies were selected for the meta-analysis. The pooled prevalence of LVAA was 3% (95% CI, 2%-5%), and 57% of LVAAs were small (<2 cm). Small LVAAs had a lower prevalence of sudden cardiac death end points (4.71% [95% CI, 1.5%-9%) than bigger (≥2 cm) LVAAs (22% [95% CI, 15%-31%), with an odds ratio of 4.65 (95% CI, 2.14-10.10). The prevalence of systemic emboli was also higher in bigger LVAAs (17% [95% CI, 9%-28%) when compared with small LVAA (9% [95% CI, 4%-16%), with an odds ratio of 1.78 (95% CI, 0.53-5.99). Left ventricular thrombi were also more frequently detected in bigger LVAAs (30% [95% CI, 20%-42%) than small LVAAs (2% [95% CI, 0%-6%), with an odds ratio of 10.92 (95% CI, 3.75-31.84). There are scant data on heart failure deaths.
Conclusions:
The available data suggest that patients with bigger LVAAs (>2 cm) have the highest risk of poor outcomes and could be preferentially targeted for primary prevention of sudden cardiac death and systemic embolization.
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