Reversed shunting across the ductus arteriosus or atrial septum in utero heralds severe congenital heart disease

被引:69
作者
Berning, RA
Silverman, NH
Villegas, M
Sahn, DJ
Martin, GR
Rice, MJ
机构
[1] UNIV CALIF SAN FRANCISCO, SAN FRANCISCO, CA 94143 USA
[2] OREGON HLTH SCI UNIV, PORTLAND, OR 97201 USA
[3] CHILDRENS NATL MED CTR, WASHINGTON, DC 20010 USA
关键词
D O I
10.1016/0735-1097(95)00446-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. This study was performed to define the significance of Doppler color flow mapping in demonstrating reversal of the direction of the normal physiologic flow across the atrial septum and ductus arteriosus in the human fetus. Background. Reversal of the physiologic shunting across the ductus arteriosus or atrial septum in utero (i.e., left to right) can be readily identified by Doppler color flow mapping, complemented by pulsed and continuous wave Doppler information. Methods. We reviewed echocardiograms recorded at our three institutions from 1988 to 1993, which displayed reversal of how by Doppler color flow in 53 fetuses of gestational age 18 weeks to term. The diagnoses were confirmed by postnatal echocardiography, operation or autopsy. Reversal of shunting was consistently associated with severe heart disease. Results. Reversed atrial shunting was found with severe left heart obstructive lesions, including 19 with hypoplastic left heart syndrome, 3 with critical aortic stenosis, 2 with double outlet right ventricle and 1 each with an interrupted aortic arch, atrioventricular septal defect and severe left ventricular dysfunction due to dilated cardiomyopathy. Reversed ductus arteriosus shunting,vas found with severe right heart obstructive lesions, including nine fetuses with pulmonary atresia, six with severe obstructive tricuspid valve abnormalities, five with severe tetralogy of Fallot, four with Ebstein's anomaly and two with single ventricle and pulmonary stenosis. Associated cardiac lesions were common in both groups. Only 3 of the 15 infants who were delivered alive from the reverse ductus arteriosus shunt group and 4 of 12 from the reverse atrial shunt group still survive. Conclusions. The finding of reversed flow by Doppler color flow mapping during fetal life provides a key to subsequent accurate diagnosis and denotes a spectrum of diseases with a very poor prognosis.
引用
收藏
页码:481 / 486
页数:6
相关论文
共 18 条
  • [1] PRENATAL SCREENING FOR CONGENITAL HEART-DISEASE
    ALLAN, LD
    CRAWFORD, DC
    CHITA, SK
    TYNAN, MJ
    [J]. BRITISH MEDICAL JOURNAL, 1986, 292 (6537) : 1717 - 1719
  • [2] EVALUATION OF FETAL STRUCTURAL HEART-DISEASE USING COLOR FLOW MAPPING
    CHIBA, Y
    KANZAKI, T
    KOBAYASHI, H
    MURAKAMI, M
    [J]. ULTRASOUND IN MEDICINE AND BIOLOGY, 1990, 16 (03) : 221 - 229
  • [3] FETAL ECHOCARDIOGRAPHIC SCREENING FOR CONGENITAL HEART-DISEASE - THE IMPORTANCE OF THE 4-CHAMBER VIEW
    COPEL, JA
    PILU, G
    GREEN, J
    HOBBINS, JC
    KLEINMAN, CS
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1987, 157 (03) : 648 - 655
  • [4] COPEL JA, 1991, OBSTET GYN CLIN N AM, V18, P845
  • [5] COPEL JA, 1991, OBSTET GYNECOL, V78, P1
  • [6] PRENATAL DETECTION OF CONGENITAL HEART-DISEASE - FACTORS AFFECTING OBSTETRIC MANAGEMENT AND SURVIVAL
    CRAWFORD, DC
    CHITA, SK
    ALLAN, LD
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1988, 159 (02) : 352 - 356
  • [7] FETAL ECHOCARDIOGRAPHY .7. DOPPLER COLOR FLOW MAPPING - A NEW TECHNIQUE FOR THE DIAGNOSIS OF CONGENITAL HEART-DISEASE
    DEVORE, GR
    HORENSTEIN, J
    SIASSI, B
    PLATT, LD
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1987, 156 (05) : 1054 - 1064
  • [8] FRIEDMAN AH, 1993, SEMIN PERINATOL, V17, P76
  • [9] PRENATAL-DIAGNOSIS OF AORTIC ATRESIA BY COLOR DOPPLER FLOW MAPPING
    GEMBRUCH, U
    CHATTERJEE, M
    BALD, R
    ELDERING, G
    GOCKE, H
    URBAN, AE
    HANSMANN, M
    [J]. PRENATAL DIAGNOSIS, 1990, 10 (04) : 211 - 217
  • [10] COLOR DOPPLER FLOW MAPPING OF FETAL HEART
    GEMBRUCH, U
    CHATTERJEE, MS
    BALD, R
    REDEL, DA
    HANSMANN, M
    [J]. JOURNAL OF PERINATAL MEDICINE, 1991, 19 (1-2) : 27 - 32