Related Experiment Video
Updated: Jun 19, 2026

A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
Published on: May 16, 2020
[Clinical study of idiopathic dilated cardiomyopathy complicated by left ventricular aneurysm]
Shu-dong Xia1, Bi-feng Wu, Jian-mei Jin
1Department of Cardiology, First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310003, China.
Insights
Left ventricular aneurysm (LVA) is rare in idiopathic dilated cardiomyopathy (IDCM). Patients with LVA show worse heart function and more arrhythmias compared to those without.
Area of Science:
- Cardiology
- Cardiovascular Research
- Heart Failure Research
Context:
- Idiopathic dilated cardiomyopathy (IDCM) is a significant cause of heart failure.
- Left ventricular aneurysm (LVA) formation is a potential complication, though its incidence and impact in IDCM are not well-defined.
Purpose:
- To investigate the hemodynamic and electrophysiological effects of LVA in patients with IDCM.
- To compare patients with IDCM and LVA (I + L) against those with IDCM but without LVA (I - L).
Summary:
- A retrospective review of 998 IDCM patients identified 6 (0.60%) with LVA.
- The LVA group exhibited higher LV peak-systolic pressure, larger LV end-diastolic volume, and a trend towards lower LV ejection fraction.
- Ventricular arrhythmias were more frequent in IDCM patients with LVA.
Impact:
- LVA is a rare but significant finding in IDCM.
- LVA is associated with adverse hemodynamic profiles, impaired systolic function, and increased arrhythmia burden.
- These findings highlight the importance of monitoring for LVA in IDCM patients.
Objective:
To examine the hemodynamic and electrophysiological influence of left ventricular aneurysm (LVA) formation in patients with idiopathic dilated cardiomyopathy (IDCM).
Methods:
All hospital records were retrospectively reviewed from IDCM patients admitted to our hospital between 2003 and 2008. Patients with coronary angiography evidenced ischemic cardiomyopathy were excluded. IDCM patients with LVA (I + L) diagnosed by left ventriculography were enrolled. Twelve age-, gender- and left-ventricular-diameter- matched patients with IDCM without LVA served as control group (I - L).
Results:
Six out of 998 patients with IDCM were confirmed to have LVA (0.60%). The LV peak-systolic pressure was higher in the I + L group than in I - L group [ (130 +/- 10) mm Hg (1 mm Hg = 0.133 kPa) vs. (117 +/-9) mm Hg, P < 0.05]. The LV end-diastolic volume was significantly larger in the I + L group than in I-L group[ (272 +/- 57) ml vs. (207 +/- 60) ml, P < 0.05]. The LV ejection fraction was slightly lower in the I + L group than in I - L group [ (27 +/- 9)% vs. (35 +/- 6)%, P = 0. 09]. Ventricular arrhythmia occurred more frequently in I + L group than in I - L group.
Conclusion:
LVA formation in IDCM was a rare phenomenon. IDCM patients with LVA seem to have higher LV peak-systolic pressure, larger end-diastolic volume, worse LV systolic function and more frequent ventricular arrhythmia than those without LVA.
Related Concept Videos
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Aortic Regurgitation II: Clinical Features and Diagnostic Tests
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy I: Introduction and Classification
