Two-year general and neurodevelopmental outcome after neonatal complex cardiac surgery in patients with deletion 22q11.2: A comparative study

Journal of Thoracic and Cardiovascular Surgery

Volumn 134, Issue 3, 2007, Pages 772-779

  Atallah, Joseph ^a,g   Joffe, Ari R ^a,g   Robertson, Charlene M T ^a,d,g   Leonard, Norma ^b,g   Blakley, Patricia M ^e,g   Nettel Aguirre, Alberto ^f,g   Sauve, Reg S ^f,g   Ross, David B ^c,g   Rebeyka, Ivan M ^c,g  

^a Departments of Pediatrics

^b Medical Genetics ^*

^c Surgery

^d UNIVERSITY OF ALBERTA   (Canada)

^e GLENROSE REHABILITATION HOSPITAL   (Canada)

^f UNIVERSITY OF SASKATCHEWAN   (Canada)

^g UNIVERSITY OF CALGARY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AGE DISTRIBUTION; AORTA ARCH INTERRUPTION; ARTICLE; CAUSE OF DEATH; CHILD DEVELOPMENT; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; FALLOT TETRALOGY; FEMALE; GENETIC ASSOCIATION; HEART SURGERY; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; MALE; MENTAL DEVELOPMENT; MULTIPLE REGRESSION; MULTIVARIATE ANALYSIS; PATENT DUCTUS ARTERIOSUS; PRESCHOOL CHILD; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT; RATING SCALE; RISK FACTOR; SCORING SYSTEM; SOCIAL STATUS; STATISTICAL SIGNIFICANCE; TREATMENT OUTCOME; UNIVARIATE ANALYSIS;

CARDIAC SURGICAL PROCEDURES; CHILD DEVELOPMENT; CHROMOSOME DELETION; FEMALE; FOLLOW-UP STUDIES; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; NERVOUS SYSTEM; PSYCHOMOTOR PERFORMANCE; RISK FACTORS; TIME FACTORS;

EID: 34548171231     PISSN: 00225223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jtcvs.2007.03.007     Document Type: Article

References (29)

1. Wernovsky G., Shillingford A.J., and Gaynor J.W. Central nervous system outcomes in children with complex congenital heart disease. Curr Opin Cardiol. 20 (2005) 90-94
2. Dittrich H., Buhrer C., Grimmer I., Dittrich S., Abdul-Khaliq H., and Lange P.E. Neurodevelopment at 1 year of age in infants with congenital heart disease. Heart. 89 (2003) 436-441
3. Robertson D.R., Justo R.N., Burke C.J., Pohlner P.G., Graham P.L., and Colditz P.B. Perioperative predictors of developmental outcome following cardiac surgery in infancy. Cardiol Young. 14 (2004) 389-395
4. Robertson C.M., Joffe A.R., Sauve R.S., Rebeyka I.M., Phillipos E.Z., Dyck J.D., et al. Outcomes from an interprovincial program of newborn open heart surgery. J Pediatr. 144 (2004) 86-92
5. Freed D.H., Robertson C.M.T., Sauve R.S., Joffe A.R., Rebeyka I.M., Ross D.B., et al. Intermediate-term outcomes of the arterial switch operation for transposition of the great arteries in neonates: alive but well?. J Thorac Cardiovasc Surg. 132 (2006) 845-852
6. Forbess J.M., Visconti K.J., Hancock-Friesen C., Howe R.C., Bellinger D.C., and Jonas R.A. Neurodevelopmental outcome after congenital heart surgery: results from an institutional registry. Circulation. 106 12 Suppl 1 (2002) I95-I102
7. Maharasingam M., Ostman-Smith I., and Pike M.G. A cohort study of neurodevelopmental outcome in children with DiGeorge syndrome following cardiac surgery. Arch Dis Child. 88 (2003) 61-64
8. Swillen A., Feys H., Adriaens T., Nelissen L., Mertens L., Gewillig M., et al. Early motor development in young children with 22q11 deletion syndrome and a conotruncal heart defect. Dev Med Child Neurol. 47 (2005) 797-802
9. Yobb T.M., Somerville M.J., Willatt L., Firth H.V., Harrison K., MacKenzie J., et al. Microduplication and triplication of 22q11.2: a highly variable syndrome. Am J Hum Genet 76 (2005) 865-876
10. Carey A.H., Kelly D., Halford S., Wadey R., Wilson D., Goodship J., et al. Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome. Am J Hum Genet. 51 (1992) 964-970
11. Blishen B.R. The 1981 Socioeconomic Index for Occupations in Canada. Can Rev Soc Anth 24 (1987) 465-488
12. Bax M.C.O. Terminology and classifications of cerebral palsy. Dev Med Child Neurol 6 (1964) 259-297
13. Bayley N. Manual: Bayley Scales of Infant Development. 2nd ed (1993), Psychological Corp, San Antonio
14. Botto L.D., May K., Fernhoff P.M., Correa A., Coleman K., Rasmussen S.A., et al. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population. Pediatrics. 112 1Pt1 (2003) 101-107
15. Perez E., and Sullivan K.E. Chromosome 22q11.2 deletion syndrome (DiGeorge and velocardiofacial syndromes). Curr Opin Pediatr. 14 (2002) 678-683
16. Robin N.H., and Shprintzen R.J. Defining the clinical spectrum of deletion 22q11.2. J Pediatr. 47 (2005) 90-96
17. Marino B., Digilio M.C., Toscano A., Giannotti A., and Dallapiccla B. Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11. Genet Couns. 10 (1999) 25-33
18. Boudjemline Y., Fermont L., Le Bidois J., Lyonnet S., Sidi D., and Bonnet D. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study. J Pediatr. 138 (2001) 520-524
19. Volpe P., Paladini D., Marasini M., Buonadonna A.L., Russo M.G., Caruso G., et al. Common arterial trunk in the fetus: characteristics, associations, and outcome in a multicentre series of 23 cases. Heart. 89 (2003) 1437-1441
20. Goldmuntz E., Clark B.J., Mitchell L.E., Jawad A.F., Cuneo B.F., Reed L., et al. Frequency of 22q11 deletions in patients with conotruncal defects. J Am Coll Cardiol. 32 (1998) 492-498
21. Mahle W.T., Crisalli J., Coleman K., Campbell R.M., Tam V.K., Vincent R.N., et al. Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect. Ann Thorac Surg. 76 (2003) 567-571
22. Gerdes M., Solot C., Wang P.P., Moss E., LaRossa D., Randall P., et al. Cognitive and behavioral profile of preschool children with chromosome 22q11.2 deletion. Am J Med Genet. 85 (1999) 127-133
23. Gerdes M., Solot C., Wang P.P., McDonald-McGinn D.M., and Zackai E.H. Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion. Genet Med. 3 (2001) 40-44
24. Niklasson L., Rasmussen P., Oskarsdottir S., and Gillberg C. Attention deficits in children with 22q.11 deletion syndrome. Dev Med Child Neurol. 47 (2005) 803-807
25. Campbell L.E., Daly E., Toal F., Stevens A., Azuma R., Catani M., et al. Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study. Brain. 129 Pt5 (2006) 1218-1228
26. van Amelsvoort T., Daly E., Henry J., Robertson D., Ng V., Owen M., et al. Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. Arch Gen Psychiatry. 61 (2004) 1085-1096
27. Anaclerio S., Di Ciommo V., Michielon G., Digilio M.C., Formigari R., Picchio F.M., et al. Conotruncal heart defects: impact of genetic syndromes on immediate operative mortality. Ital Heart J. 5 (2004) 624-628
28. Iserin L., de Lonlay P., Viot G., Sidi D., Kachaner J., Munnich A., et al. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies. Eur J Pediatr. 157 (1998) 881-884
29. Driscoll D.A. Prenatal diagnosis of the 22q11.2 deletion syndrome. Genet Med. 3 (2001) 14-18