کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2944641 1577108 2014 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Recovery of Echocardiographic Function in Children With Idiopathic Dilated Cardiomyopathy : Results From the Pediatric Cardiomyopathy Registry
ترجمه فارسی عنوان
بازیابی عملکرد اکوکاردیوگرافی در کودکان مبتلا به کاردیومیوپاتی کبدی ایدیوپاتیک: نتایج حاصل از ثبت کاردیومیوپاتی کودکان
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی کاردیولوژی و پزشکی قلب و عروق
چکیده انگلیسی

ObjectivesThis study sought to determine the incidence and predictors of recovery of normal echocardiographic function among children with idiopathic dilated cardiomyopathy (DCM).BackgroundMost children with idiopathic DCM have poor outcomes; however, some improve.MethodsWe studied children <18 years of age from the Pediatric Cardiomyopathy Registry who had both depressed left ventricular (LV) function (fractional shortening or ejection fraction z-score <–2) and LV dilation (end-diastolic dimension [LVEDD] z-score >2) at diagnosis and who had at least 1 follow-up echocardiogram 30 days to 2 years from the initial echocardiogram. We estimated the cumulative incidence and predictors of normalization.ResultsAmong 868 children who met the inclusion criteria, 741 (85%) had both echocardiograms. At 2 years, 22% had recovered normal LV function and size; 51% had died or undergone heart transplantation (median, 3.2 months), and 27% had persistently abnormal echocardiograms. Younger age (hazard ratio [HR]: 0.92; 95% confidence interval [CI]: 0.88 to 0.97) and lower LVEDD z-score (HR: 0.78; 95% CI: 0.70 to 0.87) independently predicted normalization. Nine children (9%) with normal LV function and size within 2 years of diagnosis later underwent heart transplantation or died.ConclusionsDespite marked LV dilation and depressed function initially, children with idiopathic DCM can recover normal LV size and function, particularly those younger and with less LV dilation at diagnosis. Investigations related to predictors of recovery, such as genetic associations, serum markers, and the impact of medical therapy or ventricular unloading with assist devices are important next steps. Longer follow-up after normalization is warranted as cardiac failure can recur. (Pediatric Cardiomyopathy Registry; NCT00005391)

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of the American College of Cardiology - Volume 63, Issue 14, 15 April 2014, Pages 1405–1413
نویسندگان
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