Skip to main content
Top
Published in: Pediatric Cardiology 8/2012

01-12-2012 | Original Article

Ebstein’s Anomaly and Tricuspid Valve Dysplasia: Prognosis After Diagnosis In Utero

Authors: E. Barre, I. Durand, T. Hazelzet, N. David

Published in: Pediatric Cardiology | Issue 8/2012

Login to get access

Abstract

Tricuspid valve malformation is a rare congenital heart disease. Prenatal diagnosis of Ebstein’s anomaly (EA) and tricuspid valve dysplasia (TVD) is associated with high mortality. There are conflicting reports concerning accurate prognostication after diagnosis in utero. The aim of our study was to assess prognostic factors based on our experience. We reviewed 37 fetuses between 1984 and June 2010 comprising 26 cases of EA and 11 cases of TVD. There were 10 terminations, 5 intrauterine deaths, 8 neonatal deaths, and 14 survivors. We found that the major prognostic factor for outcome was the flow pattern through the pulmonary valve on the first echocardiogram. Retrograde flow was strongly correlated with fetal or neonatal death (p = 8 × 10−5), and anterograde flow predicted good outcome (p = 8 × 10−5). In contrast, cardiothoracic indexes, right to left-ventricular ratio, and Celermajer index were not useful prognostic markers. The Simpson Andrews Sharland score, which was more complex, was well correlated with our series. Flow through the pulmonary valve on the first echocardiogram is a simple and excellent prognostic factor when major tricuspid valve disease is diagnosed in utero. Fetuses should be monitored throughout pregnancy, particularly those with retrograde ductus arteriosus, because several hemodynamic factors may worsen the prognosis.
Literature
1.
go back to reference Andrews RE, Simpson JM, Sharland GK, Sullivan ID, Yates RWM (2006) Outcome after preterm delivery of infants antenatally diagnosed with congenital heart disease. J Pediatr 148(2):213–216PubMedCrossRef Andrews RE, Simpson JM, Sharland GK, Sullivan ID, Yates RWM (2006) Outcome after preterm delivery of infants antenatally diagnosed with congenital heart disease. J Pediatr 148(2):213–216PubMedCrossRef
2.
go back to reference Andrews RE, Tibby SM, Sharland GK, Simpson JM (2008) Prediction of outcome of tricuspid valve malformations diagnosed during fetal life. Am J Cardiol 101(7):1046–1050PubMedCrossRef Andrews RE, Tibby SM, Sharland GK, Simpson JM (2008) Prediction of outcome of tricuspid valve malformations diagnosed during fetal life. Am J Cardiol 101(7):1046–1050PubMedCrossRef
3.
go back to reference Atz AM, Munoz RA, Adatia I, Wessel DL (2003) Diagnostic and therapeutic uses of inhaled nitric oxide in neonatal Ebstein’s anomaly. Am J Cardiol 91(7):906–908PubMedCrossRef Atz AM, Munoz RA, Adatia I, Wessel DL (2003) Diagnostic and therapeutic uses of inhaled nitric oxide in neonatal Ebstein’s anomaly. Am J Cardiol 91(7):906–908PubMedCrossRef
4.
go back to reference Berning RA, Silverman NH, Villegas M, Sahn DJ, Martin GR, Rice MJ (1996) Reversed shunting across the ductus arteriosus or atrial septum in utero heralds severe congenital heart disease. J Am Coll Cardiol 2:481–486CrossRef Berning RA, Silverman NH, Villegas M, Sahn DJ, Martin GR, Rice MJ (1996) Reversed shunting across the ductus arteriosus or atrial septum in utero heralds severe congenital heart disease. J Am Coll Cardiol 2:481–486CrossRef
5.
go back to reference Celermajer DS, Cullen S, Sullivan ID, Spiegelhalter DJ, Wyse RK, Deanfield JE (1992) Outcome in neonates with Ebstein’s anomaly. J Am Coll Cardiol 19(5):1041–1046PubMedCrossRef Celermajer DS, Cullen S, Sullivan ID, Spiegelhalter DJ, Wyse RK, Deanfield JE (1992) Outcome in neonates with Ebstein’s anomaly. J Am Coll Cardiol 19(5):1041–1046PubMedCrossRef
6.
go back to reference Flores Arizmendi A, Fernández Pineda L, Quero Jiménez C, Maître Azcárate MJ, Herráiz Sarachaga I, Urroz E et al (2004) The clinical profile of Ebstein’s malformation as seen from the fetus to the adult in 52 patients. Cardiol Young 14(1):55–63PubMed Flores Arizmendi A, Fernández Pineda L, Quero Jiménez C, Maître Azcárate MJ, Herráiz Sarachaga I, Urroz E et al (2004) The clinical profile of Ebstein’s malformation as seen from the fetus to the adult in 52 patients. Cardiol Young 14(1):55–63PubMed
7.
go back to reference Freedom RM, Jaeggi E, Perrin D, S-Joon Yoo, Anderson RH (2006) The “wall-to-wall” heart in the patient with pulmonary atresia and intact ventricular septum. Cardiol Young 16(1):18–29PubMedCrossRef Freedom RM, Jaeggi E, Perrin D, S-Joon Yoo, Anderson RH (2006) The “wall-to-wall” heart in the patient with pulmonary atresia and intact ventricular septum. Cardiol Young 16(1):18–29PubMedCrossRef
8.
go back to reference Jaquiss RDB, Imamura M (2007) Management of Ebstein’s anomaly and pure tricuspid insufficiency in the neonate. Semin Thorac Cardiovasc Surg 19(3):258–263PubMedCrossRef Jaquiss RDB, Imamura M (2007) Management of Ebstein’s anomaly and pure tricuspid insufficiency in the neonate. Semin Thorac Cardiovasc Surg 19(3):258–263PubMedCrossRef
9.
go back to reference Khositseth A, Khowsathit P (1999) Factors affecting mortality in Ebstein’s anomaly of the tricuspid valve. J Med Assoc Thai 82(Suppl 1):S10–S15PubMed Khositseth A, Khowsathit P (1999) Factors affecting mortality in Ebstein’s anomaly of the tricuspid valve. J Med Assoc Thai 82(Suppl 1):S10–S15PubMed
10.
go back to reference Khositseth A, Danielson GK, Dearani JA, Munger TM, Porter CJ (2004) Supraventricular tachyarrhythmias in Ebstein anomaly: management and outcome. J Thorac Cardiovasc Surg 128(6):826–833PubMedCrossRef Khositseth A, Danielson GK, Dearani JA, Munger TM, Porter CJ (2004) Supraventricular tachyarrhythmias in Ebstein anomaly: management and outcome. J Thorac Cardiovasc Surg 128(6):826–833PubMedCrossRef
11.
go back to reference McElhinney DB, Salvin JW, Colan SD, Thiagarajan R, Crawford EC, Marcus EN et al (2005) Improving outcomes in fetuses and neonates with congenital displacement (Ebstein’s malformation) or dysplasia of the tricuspid valve. Am J Cardiol 96(4):582–586PubMedCrossRef McElhinney DB, Salvin JW, Colan SD, Thiagarajan R, Crawford EC, Marcus EN et al (2005) Improving outcomes in fetuses and neonates with congenital displacement (Ebstein’s malformation) or dysplasia of the tricuspid valve. Am J Cardiol 96(4):582–586PubMedCrossRef
12.
go back to reference Moran AM, Crowley D, Pinette MG, Wax JR (2008) Reversible right ventricular dysfunction and functional pulmonary atresia in the human fetus. J Ultrasound Med 27(3):487–491PubMed Moran AM, Crowley D, Pinette MG, Wax JR (2008) Reversible right ventricular dysfunction and functional pulmonary atresia in the human fetus. J Ultrasound Med 27(3):487–491PubMed
13.
go back to reference Paranon S, Acar P (2008) Ebstein’s anomaly of the tricuspid valve: from fetus to adult: congenital heart disease. Heart 94(2):237–243PubMedCrossRef Paranon S, Acar P (2008) Ebstein’s anomaly of the tricuspid valve: from fetus to adult: congenital heart disease. Heart 94(2):237–243PubMedCrossRef
14.
go back to reference Pavlova M, Fouron JC, Drblik SP, van Doesburg NH, Bigras JL, Smallhorn J et al (1998) Factors affecting the prognosis of Ebstein’s anomaly during fetal life. Am Heart J 135(6 Pt 1):1081–1085PubMedCrossRef Pavlova M, Fouron JC, Drblik SP, van Doesburg NH, Bigras JL, Smallhorn J et al (1998) Factors affecting the prognosis of Ebstein’s anomaly during fetal life. Am Heart J 135(6 Pt 1):1081–1085PubMedCrossRef
15.
go back to reference Roberson DA, Silverman NH (1989) Ebstein’s anomaly: echocardiographic and clinical features in the fetus and neonate. J Am Coll Cardiol 14(5):1300–1307PubMedCrossRef Roberson DA, Silverman NH (1989) Ebstein’s anomaly: echocardiographic and clinical features in the fetus and neonate. J Am Coll Cardiol 14(5):1300–1307PubMedCrossRef
16.
go back to reference Wald RM, Adatia I, Van Arsdell GS, Hornberger LK (2005) Relation of limiting ductal patency to survival in neonatal Ebstein’s anomaly. Am J Cardiol 96(6):851–856PubMedCrossRef Wald RM, Adatia I, Van Arsdell GS, Hornberger LK (2005) Relation of limiting ductal patency to survival in neonatal Ebstein’s anomaly. Am J Cardiol 96(6):851–856PubMedCrossRef
17.
go back to reference Yeager SB, Parness IA, Sanders SP (1988) Severe tricuspid regurgitation simulating pulmonary atresia in the fetus. Am Heart J 115(4):906–908PubMedCrossRef Yeager SB, Parness IA, Sanders SP (1988) Severe tricuspid regurgitation simulating pulmonary atresia in the fetus. Am Heart J 115(4):906–908PubMedCrossRef
Metadata
Title
Ebstein’s Anomaly and Tricuspid Valve Dysplasia: Prognosis After Diagnosis In Utero
Authors
E. Barre
I. Durand
T. Hazelzet
N. David
Publication date
01-12-2012
Publisher
Springer-Verlag
Published in
Pediatric Cardiology / Issue 8/2012
Print ISSN: 0172-0643
Electronic ISSN: 1432-1971
DOI
https://doi.org/10.1007/s00246-012-0355-z

Other articles of this Issue 8/2012

Pediatric Cardiology 8/2012 Go to the issue