Among 21 patients with mildly dilated cardiomyopathy followed for 6.8 years, 9 experienced cardiac events, with elevated left ventricular end-diastolic pressure predicting poor outcomes.
Cohort (n=21)
Patients with mildly dilated cardiomyopathy and impaired hemodynamics at diagnosis have a poor long-term prognosis and require careful follow-up despite mild left ventricular dilatation.
The long-term prognosis of patients with mildly dilated cardiomyopathy (MDCM) was investigated in 21 patients. MDCM was defined as left ventricular ejection fraction < or = 40% and left ventricular end-diastolic volume < or = 120 ml/m2 by left ventriculography. During a follow-up period of 6.8+/-3.7 years, there were 9 cardiac events (5 heart failure deaths, 2 sudden deaths, and 2 re-hospitalizations for heart failure). Only in the patients without cardiac events was there a significant decrease in left ventricular size (end-diastolic dimension decreased from 58+/-6 mm to 50+/-8 mm, p<0.001) and an improvement in systolic function (fractional shortening increased from 17+/-5% to 26+/-11%, p=0.007). However, left atrial dilation was observed in the patients with an event (from 39+/-5 mm to 43+/-5 mm, p=0.02). Based on proportional hazard analysis, left ventricular end-diastolic pressure and mean pulmonary artery pressure at diagnosis and left atrial dimension at the time of follow-up were significant predictors of poor outcome. A subset of patients with MDCM has impaired hemodynamics at diagnosis, left atrial dilation at follow-up and a poor prognosis, and must be followed carefully even if the left ventricular dilatation is mild.
Kitaoka et al. (Tue,) conducted a cohort in Mildly dilated cardiomyopathy (n=21). Among 21 patients with mildly dilated cardiomyopathy followed for 6.8 years, 9 experienced cardiac events, with elevated left ventricular end-diastolic pressure predicting poor outcomes.