Key result
Adult isolated LVNC presents with a triad of heart failure, arrhythmias, and embolic events.
Why the study?
Isolated left ventricular noncompaction (ILVNC) is a cardiomyopathy with increased risk for sudden cardiac death that requires organized insight into its disease process, diagnosis, and management in adults.
Clinical review describes the diagnostic features and prognosis of isolated left ventricular noncompaction in adults, highlighting risks of progressive heart failure and arrhythmias.
Isolated left ventricular noncompaction (ILVNC) is a cardiomyopathy that was first described in 1926 as a "spongy myocardium." The disorder results from intrauterine arrest of compaction of the loose interwoven meshwork of the fetal myocardial primordium and subsequent persistence of deep trabecular recesses in the myocardial wall. The classical clinical presentation is a triad of heart failure, arrhythmias, and embolic events from mural thrombi. ILVNC has been associated with several autosomal dominant, X-linked, and mitochondrial genetic mutations that are also shared among other cardiomyopathies. Over the past decade, ILVNC has been subject to intensive research, as it increases the risk for sudden cardiac death. This review focuses on the current understanding of ILVNC in adult populations and attempts to provide organized insight into the disease process, screening, diagnosis, management, role of device therapy, and prognosis.
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Hussein et al. (2015) conducted a review in Isolated left ventricular noncompaction (ILVNC). Isolated left ventricular noncompaction was evaluated. Isolated left ventricular noncompaction in adults presents with a triad of heart failure, arrhythmias, and embolic events, requiring comprehensive screening, diagnosis, and management.
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