Impact of prenatal diagnosis of complex congenital heart disease on neonatal and infant morbidity and mortality

被引:50
作者
Chakraborty, Abhishek [1 ]
Gorla, Sudheer R. [1 ]
Swaminathan, Sethuraman [1 ]
机构
[1] Univ Miami, Miller Sch Med, Jackson Mem Hosp, Dept Pediat,Div Pediat Cardiol, 1611 NW 12th Ave,NW Room 109, Miami, FL 33136 USA
关键词
FETAL ECHOCARDIOGRAPHY; DELAYED DIAGNOSIS; GREAT-ARTERIES; 2ND TRIMESTER; PREVALENCE; TRANSPOSITION; POPULATION; OUTCOMES; TRENDS;
D O I
10.1002/pd.5351
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Objectives The objective of this study was to analyze the benefits associated with prenatal diagnosis of complex congenital heart disease (CHD) on preoperative morbidity, 30-day and 1-year mortality in this population. Method Results This was a retrospective review of patients with complex CHD born at our tertiary care center over a 10-year period. Date analysis using Student t test and chi-square test. The overall rate of prenatal detection of complex CHD was 68.1%. A steady increase in the number of complex CHD diagnosed prenatally was noted during the study period. The prenatal diagnosis of complex CHD was associated with significant reduction in the incidence of the following preoperative parameters: antibiotic use, mechanical ventilation, inotropic support, hepatic and renal dysfunction, and acidosis. These beneficial effects were more significant in ductal-dependent cardiac anomalies. However, there were no neonatal and infant survival benefits in association with prenatal diagnosis. Conclusion Prenatal diagnosis of complex CHD leads to improved preoperative morbidity, especially in patients with ductal-dependent cardiac anomalies. No survival benefits were noted with prenatal diagnosis of complex CHD.
引用
收藏
页码:958 / 963
页数:6
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