Outcome of staged reconstructive surgery for hypoplastic left heart syndrome following antenatal diagnosis

BACKGROUND AND AIMS Staged reconstructive surgery has radically altered the prognosis of hypoplastic left heart syndrome (HLHS). Antenatal diagnosis allows for appropriate counselling, and time to consider treatment options. We report outcome from a centre where most cases are antenatally diagnosed and delivered on site. METHODS Information was collated on 188 consecutive cases of HLHS between 1995 and 2000, including timing of diagnosis, outcome of pregnancy, and age and outcome at each stage of surgery. At Guy's Hospital, 174 cases were diagnosed antenatally, of whom 50 underwent surgery. Fourteen others (five diagnosed antenatally at other centres, and nine diagnosed postnatally) also underwent surgery. RESULTS Survival after stage I (the Norwood operation) was 52% (33/64). Postoperative survival after stage II (the hemi-Fontan operation, performed in 29), and stage III (the Fontan operation, performed in 10), was 100%. Two late deaths occurred 3 and 10 months after stage II, giving overall survival of 48% (31/64). At follow up, three children have neurological impairment, and one had poor right ventricular function necessitating cardiac transplantation. CONCLUSIONS Antenatal diagnosis allows informed decisions about treatment options, and facilitates preoperative care. Mortality following stage I is high, irrespective of timing of diagnosis, but medium term outcome for survivors is good.

[1]  Y. Orime,et al.  Hypoplastic left heart syndrome: "Which is the best operative strategy?". , 1998, Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia.

[2]  W. Gersony,et al.  Survival and risk factor analysis for the Norwood procedure for hypoplastic left heart syndrome. , 1997, The American journal of cardiology.

[3]  K. Gauvreau,et al.  Comparison of outcome when hypoplastic left heart syndrome and transposition of the great arteries are diagnosed prenatally versus when diagnosis of these two conditions is made only postnatally. , 1999, The American journal of cardiology.

[4]  E. Colvin,et al.  Prenatally diagnosed hypoplastic left heart syndrome--outcomes after postnatal surgery. , 1999, The Journal of maternal-fetal medicine.

[5]  M. Tynan,et al.  The natural history of the hypoplastic left heart syndrome. , 1989, International journal of cardiology.

[6]  Diane E Spicer,et al.  Hypoplastic left-heart syndrome , 2001, The Lancet.

[7]  R. Uehara,et al.  Hypoplastic left heart syndrome: duration of survival without surgical intervention. , 1999, American heart journal.

[8]  J. Huhta,et al.  Diagnosis, transport, and outcome in fetuses with left ventricular outflow tract obstruction. , 1991, The Journal of thoracic and cardiovascular surgery.

[9]  F. Raymond,et al.  Fetal echocardiography as a predictor of chromosomal abnormality , 1997, The Lancet.

[10]  E. Blackstone,et al.  Outcome after a "perfect" Fontan operation. , 1990, Circulation.

[11]  A. Reiss,et al.  Syndrome , 1990, Biological Psychiatry.

[12]  D. Pieroni,et al.  Neurodevelopmental outcome of infants with hypoplastic left heart syndrome. , 1995, The Journal of pediatrics.

[13]  J. Simpson,et al.  Hypoplastic left heart syndrome. Willingness to initiate treatment is crucial. , 1997, BMJ.

[14]  A. Cook,et al.  Prospective diagnosis of 1,006 consecutive cases of congenital heart disease in the fetus. , 1994, Journal of the American College of Cardiology.

[15]  N. Silverman,et al.  Does Prenatal Diagnosis of Hypoplastic Left Heart Syndrome Lead to Improved Surgical Outcome , 1998 .

[16]  R. Holder,et al.  Outcome after prenatal diagnosis of hypoplastic left-heart syndrome: a case series , 2000, The Lancet.

[17]  L. Allan,et al.  Outcome after prenatal diagnosis of the hypoplastic left heart syndrome , 1998, Heart.

[18]  M. D. de Leval,et al.  The modified Norwood procedure for hypoplastic left heart syndrome: early to intermediate results of 120 patients with particular reference to aortic arch repair. , 1999, The Journal of thoracic and cardiovascular surgery.

[19]  E. Hey,et al.  Death in infancy from unrecognised congenital heart disease. , 1994, Archives of disease in childhood.

[20]  W. Norwood,et al.  Physiologic repair of aortic atresia-hypoplastic left heart syndrome. , 1983, The New England journal of medicine.

[21]  S. Paridon,et al.  Exercise Performance Following Repair of Hypoplastic Left Heart Syndrome: A Comparison with Other Types of Fontan Patients , 1997, Pediatric Cardiology.

[22]  R. Caldwell,et al.  Surgical management of hypoplastic left heart syndrome. , 1996, The Annals of thoracic surgery.