Abstract

BackgroundPrenatal cardiac screening is of great importance as it contributes to appropriate neonatal management and helps parents to make a decision regarding their pregnancy. The aim of our study was to evaluate the efficiency of a newly proposed screening protocol in the detection of fetal congenital heart disease (CHD).MethodsThis was a prospective study. A total of 52 cases of confirmed CHD fetuses and 248 cases of randomly selected normal fetuses were included in the study. Two sonographers with similar experience performed the cardiac screenings under two different protocols independently. The conventional protocol (Protocol A) paid greater attention to the four-chamber view and the outflow tract views. A 6-month training program was provided to sonographers performing scans under the new protocol (Protocol B), which emphasized systematically evaluating fetal cardiac anatomy and hemodynamics. Color Doppler was mandatory and some ultrasonic signs for special cardiac anomalies were also introduced into this protocol.ResultsProtocol B detected more cardiac anomalies than did Protocol A (96.2 % vs. 61.5 %, P < 0.01). Specifically, Protocol B was superior to Protocol A in detecting cardiac malpositions, abnormal systemic and pulmonary venous connection, right aortic arch, transposition of the great arteries, and congenital corrected transposition of the great arteries. By visualizing flow disturbance and retrograde flow with color Doppler, Protocol B was better than Protocol A in screening valvular associated malformations, such as pulmonary atresia, pulmonary stenosis, tricuspid dysplasia, etc. For the normal fetuses, Protocol B was better than Protocol A in reducing the false-positive detection of septal defects.ConclusionsThe current study introduces an enhanced protocol for fetal cardiac screening, under which the obstetric screening sonographers systematically identify fetal cardiac anatomy and hemodynamics. A short-term training program makes it possible for the screening sonographers to become familiar with the new protocol, and its value has been confirmed due to improvements made in screening efficiency.Electronic supplementary materialThe online version of this article (doi:10.1186/s12884-016-0933-9) contains supplementary material, which is available to authorized users.

Highlights

  • Prenatal cardiac screening is of great importance as it contributes to appropriate neonatal management and helps parents to make a decision regarding their pregnancy

  • All cases were confirmed by autopsy findings, operative findings, fetal/postnatal echocardiography, or by phone calls in order to acquire the information from routine infant physical examination reports

  • 52 cases of fetal congenital heart disease (CHD) were included in the current study, of which five cases were from the routine screening pregnancies

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Summary

Introduction

Prenatal cardiac screening is of great importance as it contributes to appropriate neonatal management and helps parents to make a decision regarding their pregnancy. The aim of our study was to evaluate the efficiency of a newly proposed screening protocol in the detection of fetal congenital heart disease (CHD). Fetal echocardiography is undoubtedly the best method currently available to diagnose congenital cardiac anomalies prenatally [7]. It is not practical for fetal echocardiographers to make a diagnosis for every fetus during routine obstetric scans. When CHD is suspected, patients should be referred for comprehensive cardiac examination by a fetal echocardiographer. To this end, highly efficient screening might lead to a high detection rate for fetal CHD

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