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Published on: June 14, 2016
Apical hypertrophic cardiomyopathy: prevalence and correlates of apical outpouching
Josepha Binder1, Christine H Attenhofer Jost, Kyle W Klarich
1Department of Cardiology, Medical University, Graz, Austria.
Insights
Apical hypertrophic cardiomyopathy (ApHCM) patients with apical outpouching showed no increased risk of major cardiac events. Cardiac complications were common but not linked to apical outpouching in this ApHCM analysis.
Area of Science:
- Cardiology
- Cardiovascular Imaging
- Genetics
Background:
- Apical hypertrophic cardiomyopathy (ApHCM) is characterized by apical wall thickening.
- Apical outpouching, including wall motion abnormalities and aneurysms, has been described in ApHCM.
- The clinical significance of apical outpouching in ApHCM remains unclear.
Purpose of the Study:
- To investigate the prevalence and clinical implications of apical outpouching in patients with ApHCM.
- To determine if apical outpouching is associated with adverse cardiac events in ApHCM patients.
Main Methods:
- Retrospective analysis of 193 patients diagnosed with ApHCM between 1976 and 2006.
- Evaluation of apical outpouching using echocardiography, including contrast-enhanced studies.
- Assessment of clinical outcomes, including mortality, sudden cardiac death, and arrhythmias during follow-up.
Main Results:
- Apical outpouching was identified in 15% of ApHCM patients, with higher prevalence (28%) in contrast echocardiography.
- Patients with apical outpouching had more diastolic gradients, prolonged QT intervals, increased apical wall thickness, and family history of sudden cardiac death.
- No significant difference in overall mortality, sudden cardiac death, or other major adverse cardiac events was observed between ApHCM patients with and without apical outpouching.
Conclusions:
- Cardiac complications are frequent in ApHCM patients.
- Apical outpouching in ApHCM does not appear to be associated with an increased risk of major adverse cardiac events in this study.
- Further research is needed to fully understand the impact of true apical aneurysms in ApHCM.
Background:
Apical outpouching, including wall motion abnormalities and aneurysms, has been described in apical hypertrophic cardiomyopathy (ApHCM).
Methods:
Between 1976 and 2006, 193 patients with ApHCM (120 men; overall mean age, 61 ± 17 years) were evaluated.
Results:
Apical outpouching was found in 29 patients (15%) and in 22 of the 78 patients (28%) imaged with contrast echocardiography. Six patients had apical aneurysms, and 23 patients had hypokinesis with apical dilatation but no wall thinning. Apical outpouching was more common in patients with diastolic gradients out of the apex (P < .001), corrected QT interval prolongation (P < .001), increased apical wall thickness (P = .01), and family histories of sudden cardiac death (P = .03). Sudden cardiac death, resuscitated cardiac arrest, or discharge of an automated internal cardiac defibrillator, or a combination, was observed in 11 patients (6%) during follow-up. Atrial fibrillation (28%), ventricular tachycardia (20%), and stroke (11%) were also relatively common in this study. No difference was observed in overall mortality rate comparing patients with ApHCM with and without apical outpouching. Similarly, no differences were found in the rates of sudden cardiac death, resuscitated cardiac arrest, and discharge of an automated internal cardiac defibrillator. The impact of true aneurysms was not assessed in this study.
Conclusions:
Cardiac complications appear commonly in patients with ApHCM, but they did not seem to be related to apical outpouching in the present analysis.
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