Prediction of postnatal clinical course in primary congenital dilated cardiomyopathy
Prediction of postnatal clinical course in primary congenital dilated cardiomyopathy
复制标题
原发性先天性扩张型心肌病产后临床病程的预测
DOI:
10.1111/ped.14029
复制
发表时间:
2019
影响因子:
1.4
通讯作者:
Kato Taichi
中科院分区:
文献类型:
--
作者:
Yamamoto Hidenori;Fukasawa Yoshie;Ohashi Naoki;Yokoyama Takehiko;Suzuki Kazutaka;Ota Takaya;Yasuda Kazushi;Omoya Kentaro;Takahashi Yoshiyuki;Kato Taichi
BackgroundThe aim of this study was to investigate the prediction of postnatal prognosis using fetal and perinatal data in patients with primary congenital dilated cardiomyopathy (PCDCM), and to estimate the incidence of this disease.MethodsWe examined correlations between fetal or perinatal data and postnatal clinical course in a multicenter retrospective study of eight patients with PCDCM. Incidence was calculated in a population‐based study.ResultsAll patients developed heart failure at a median of 8 days (range, 0–43 days), and six patients died or required extracorporeal artificial heart therapy at a median of 67 days (range, 0–92 days). The cardiothoracic area ratio from fetal echocardiography, the Apgar score, and the standard deviation of birth weight correlated significantly with the date at onset of heart failure. However, no data correlated with survival. Cumulative incidence of PCDCM was calculated as 1.21 per 100 000 total births (95% confidence interval, 0.37 to 2.06).ConclusionsPrimary congenital dilated cardiomyopathy has a poor prognosis, but cardiothoracic area ratio from fetal echocardiography, body weight at birth, and Apgar score correlate with the timing of the onset of heart failure, and these indicators might therefore be useful for peri‐ and postnatal management.
登录
查看更多内容
影响因子:
37.8
作者:
D. Sahn
通讯作者:
D. Sahn
影响因子:
3
作者:
Y. Yinon;S. Yagel;J. Hegesh;B. Weisz;S. Mazaki‐Tovi;S. Lipitz;R. Achiron
通讯作者:
R. Achiron
影响因子:
1
作者:
H. Nagasawa
通讯作者:
H. Nagasawa
影响因子:
2.1
作者:
V. Fesslova;M. Mongiovì;S. Pipitone;J. Brankovic;L. Villa
通讯作者:
L. Villa