Lewis A B
Division of Cardiology, Childrens Hospital Los Angeles, CA 90054-0700.
Am Heart J. 1994 Jul;128(1):133-6. doi: 10.1016/0002-8703(94)90019-1.
Mortality of pediatric patients with idiopathic dilated cardiomyopathy (IDC) is highest during the first 1 to 2 years the child is first seen. The echocardiograms of 72 infants and children with IDC were reviewed to determine whether left ventricular shortening fraction (LVSF), end-diastolic dimension, and wall mass were helpful in predicting outcome. Patients who were alive at last follow-up (group 1) were compared to those who died or required heart transplant (group 2). None of the indexes obtained at first examination were predictive of survival. Shortening fraction had improved significantly at follow-up 1 to 6 months after first examination in group 1 (15.1 +/- 0.9 to 24.4 +/- 1.8, p < 0.001) but remained unchanged in group 2 (14.1 +/- 1.5 to 15.3 +/- 3.2). No significant trends were noted in left ventricular end-diastolic dimension or wall mass. The 1- and 5-year actuarial survival for all patients was 75% and 60%, respectively. Persistent depression of LVSF < 15% was associated with a significantly lower survival rate (1-year 46%; 5-year 29%) compared to patients in whom follow-up LVSF was > 15% (1-year 97%; 5-year 90%; p < 0.05). It is concluded that the follow-up LVSF obtained at least 1 month after first examination is helpful in identifying pediatric patients who would benefit from early cardiac transplantation.
特发性扩张型心肌病(IDC)患儿的死亡率在首次就诊后的最初1至2年内最高。回顾了72例IDC婴幼儿和儿童的超声心动图,以确定左心室缩短分数(LVSF)、舒张末期内径和心肌重量是否有助于预测预后。将最后一次随访时存活的患者(第1组)与死亡或需要心脏移植的患者(第2组)进行比较。首次检查时获得的所有指标均不能预测生存情况。第1组在首次检查后1至6个月的随访中缩短分数有显著改善(从15.1±0.9提高到24.4±1.8,p<0.001),但第2组保持不变(从14.1±1.5到15.3±3.2)。左心室舒张末期内径或心肌重量未发现显著趋势。所有患者的1年和5年精算生存率分别为75%和60%。与随访LVSF>15%的患者相比,LVSF持续低于15%与显著较低的生存率相关(1年46%;5年29%)(1年97%;5年90%;p<0.05)。结论是,首次检查后至少1个月获得的随访LVSF有助于识别可从早期心脏移植中获益的儿科患者。