Am J Perinatol 2001; 18(7): 363-372
DOI: 10.1055/s-2001-18696
ORIGINAL ARTICLES

Copyright © 2001 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA. Tel.: +1(212) 584-4662

Perinatal Management of Fetal Cardiac Anomalies in a Specialized Obstetric-Pediatrics Center

Véronique Mirlesse1 , Adriano Cruz1 , Jérome Le Bidois2 , Patricia Diallo1 , Laurent Fermont2 , François Kieffer3 , Jean François Magny3 , François Jacquemard1 , Ronaldo Levy1 , Marcel Voyer3 , Fernand Daffos1
  • 1Service de Médecine fœtale, Institut de Puériculture, Paris. France
  • 2Centre de cardiologie périnatale, Institut de Puériculture, Paris. France
  • 3Service de Réanimation néonatale, Institut de Puériculture, Paris. France
Further Information

Publication History

Publication Date:
03 December 2001 (online)

ABSTRACT

Perinatal teams dealing with fetal heart disease frequently wonder which pregnancies might be terminated, and when delivery should take place in a specialized surrounding. We present a retrospective study of 229 fetuses, in which prenatal ultrasound showed a cardiac anomaly not compatible with a standard maternity ward delivery. One hundred nineteen pregnancies were terminated (group I) while 110 pregnancies led to the birth of a live baby (group II). Pathology in group I was discovered earlier than in group II (24 vs. 29.3 weeks' gestation; p <0.01), and associated malformations or chromosomal anomalies were much more frequent in group I (80/119 vs. 9/110; p <0.001). Among live born babies, three infants with transposition of the great arteries underwent Rashkind atrioseptostomy in the delivery room. With a minimum follow-up of 12 months, 69 children (63%) have undergone surgery. Among 92 survivors (1 child is lost to follow-up), 78 (71%) are asymptomatic and 14 symptomatic.

Early prenatal diagnosis of fetal heart anomalies significantly facilitates prenatal work-up and perinatal care. We present the types of pathology having led to termination and define the situations in which children are at risk of perinatal hemodynamic compromise.

REFERENCES

  • 1 Allan L, Baker E J. Prenatal diagnosis and correction of congenital heart defects.  Br J Hosp Med . 1993;  50 513-522
  • 2 Rychik J, Tian Z Y, Fogel M A, Joshi V, Rose N C, Jacobs M L. The single ventricle heart in the fetus: accuracy of prenatal diagnosis and outcome.  J Perinatol . 1997;  17 183-188
  • 3 De Vigan C, Goujard J, Vodovar V, Uzan S. Management of the fetus with correctable malformation in Paris maternity units: evolution 1985-1994.  Fetal Diagn Ther . 1997;  12 216-220
  • 4 Kirk J S, Comstock C H, Lee W, Smith R S, Riggs T W, Weinhouse E. Sonographic screening to detect fetal cardiac anomalies: a 5-years experience with 111 abnormal cases.  Obstet Gynecol . 1997;  89 227-232
  • 5 Brook M M, Silverman N H, Villegas M. Cardiac ultrasonography in structural abnormalities and arrhythmias: recognition and treatment.  West J Med . 1993;  159 286-300
  • 6 Gembruch U. Prenatal diagnosis of congenital heart disease.  Prenat Diagn . 1997;  17 1283-1298
  • 7 Montana E, Khoury M J, Cragan J D, Sharma S, Dhar P, Fyfe D. Trends and outcome after prenatal diagnosis of congenital cardiac malformations by fetal echocardiography in a well defined birth population, Atlanta, Georgia, 1990-1994.  J Am Coll Cardiol . 1996;  28 1805-1809
  • 8 Copel J A, Tan A S, Kleinman C S. Does prenatal diagnosis of congenital heart disease alter short-term outcome?.  Ultrasound Obstet Gynecol . 1997;  10 237-241
  • 9 Eapen R S, Rowland D G, Franklin W H. Effect of prenatal diagnosis of critical left heart obstruction on perinatal morbidity and mortality.  Am J Perinatol . 1998;  15 237-242
  • 10 Bonnet D, Coltri A, Butera G. Detection of transposition of the great arteries in fetuses reduces neonatal morbidity and mortality.  Circulation . 1999;  99 916-918
  • 11 Bitar F F, Byrum C J, Kveselis D A, Lawrence D A, Smith F C. In utero management of hydrops fetalis caused by critical aortic stenosis.  Am J Perinatol . 1997;  14 389-391
  • 12 . .  Journal Officiel de la République Française . 1975;  75 17
  • 13 . .  Journal Officiel de la République Française . 1994;  94 647
  • 14 . .  Journal Officiel de la République Française Décret . 1997;  95 578
  • 15 Hertzberg B S, Kliewer M A, Lile R L. Antenatal ultrasonographic findings in the CHARGE association.  J Ultrasound Med . 1994;  13 238-242
  • 16 Devriendt K, Van Schoubroeck D, Eyskens B. Polyhydramnios as a prenatal symptom of the Digeorge/Velo-cardio-facial syndrome.  Prenat Diagn . 1998;  18 68-72
  • 17 Cesko I, Hajdu J, Toth T, Marton T, Papp C, Papp Z. Ivemark syndrome with asplenia in siblings.  J Pediatr . 1997;  130 822-824
  • 18 Ellis I H, Yale C, Thomas R, Garrett C, Winter R M. Three sibs with microcephaly, congenital heart disease, lung segmentation defects and unilateral absent kidney: a new recessive multiple congenital anomaly syndrome?.  Clin Dysmorphol . 1996;  5 129-134
  • 19 Fyfe D E, Meyer K B, Case C L. Sonographic assesment of fetal cardiac arrhythmias.  Seminars in ultrasound, CT and MRI . 1993;  14 286-297
    >