Although not all newborns with Ebstein's anomaly present with severe cardiomegaly in utero, some of them cannot live after birth because of the lung hypoplasia. T o clarifi the relationship between the intrauterine cardiomegaly and the outcome of the patients with Ebstein$ anomaly or tricuspid valve dysplasia, we calculated the ratio of the area of the heart against the thorax (CTAR) in the transverse view of the thorax at the level of the cardiac four-chamber view in the fetal echocardiogram and compared it to the outcome. The study population consisted of four patients with Ebstein's anomaly and one patient with tricuspid valve dysplasia who were diagnosed i n utero. The ranges obtained from 53 normal fetal cases were 20% 5 8% (mean t 2 SD) at below 20 week's gestation, 25% 2 10% at the gestational age of 21 to 30 weeks, and 29% 2 6.4% at the gestational age of 31 to 40 weeks. The CTARs of these five cases measured 81.6%, 51 %, 55.2%, 47.5%, and 75.6%, respectively, and were abnormully higher than the normal value. Two fetuses died i n utero with severe hydrops fetalis. Two fetuses whose cardiothoracic ratios by chest X ray were 100% died at twelve hours of life. One patient died at 11 0 days. The cross-sectional area of the thorax was smaller than the normal range in 3 (cases 1, 4, and 5) out of these 5 cases. Thus, we conclude that fetal Ebstein's anomaly and tricuspid valve dysplasia associated with massive tricuspid regurgitation with a large CTAR ratio (higher than 50%) and small thoracic cross-sectional area has a very poor prognosis both prenatally and neonatally. (ECHOCARDIOGRAPHY, Volume 11, May 1994) prenatal diagnosis, lung hypoplasia, Ebsteids anomaly, tricuspid dysplasia, cardiothoracic area ratio (CTAR) Ebstein's anomaly is known to have a very wide spectrum of clinical features from a case with an almost normal life span to a case of intrauterine fetal death.'s2 Tricuspid valve dysplasia is a very rare congenital anomaly with very severe regurgitation of the tricuspid valve showing gelatinous nodules and short chordae tendineae of the tricuspid valve and no features of Ebstein's a n~r n a l y .~.~ We have experienced five cases with severe prenatal tricuspid regurgitation, four of whom had Ebstein's anomaly and one who had tricuspid valve dysplasia. We studied the accuracy of prenatal diagnosis of these cases to evaluate the usefulness of prenatal diagnosis of Ebstein's anomaly and tricuspid valve dysplasia. Then, the cardiothoracic area ratio (CTAR) was measured and compared to the normal value in order to assess the severity and outcome of the disease ( Table 1).
Diagnostic AccuracyThe gestational period at diagnosis ranged from 23 weeks and 2 days (case 1) to 36 weeks showed massive tricuspid valve regurgitation