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Pattern of head circumference growth following bidirectional Glenn in infants with single ventricle heart disease

Published online by Cambridge University Press:  11 December 2020

Stephanie Y Tseng*
Affiliation:
Department of Pediatrics, University of Cincinnati College of Medicine, Division of Cardiology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
Julia Anixt
Affiliation:
Department of Pediatrics, University of Cincinnati College of Medicine, Division of Developmental and Behavioral Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
Jareen Meinzen-Derr
Affiliation:
Department of Pediatrics, University of Cincinnati College of Medicine, Division of Biostatistics and Epidemiology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
Cameron Thomas
Affiliation:
Department of Pediatrics, University of Cincinnati College of Medicine, Division of Neurology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
David S Cooper
Affiliation:
Department of Pediatrics, University of Cincinnati College of Medicine, Division of Cardiology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
Haleh C Heydarian
Affiliation:
Department of Pediatrics, University of Cincinnati College of Medicine, Division of Cardiology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
*
Author for correspondence: Stephanie Y. Tseng, MD, The Heart Institute, Cincinnati Children’s Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH45229, USA. Tel: +1 513-636-7981; Fax: +1 513-803-4493. E-mail: Stephanie.Tseng@cchmc.org

Abstract

Background:

Infants with single ventricle congenital heart disease demonstrate increasing head growth after bidirectional Glenn; however, the expected growth trajectory has not been well described.

Aims:

1) We will describe the pattern of head circumference growth in the first year after bidirectional Glenn. 2) We will determine if head growth correlates with motor developmental outcomes approximately 12 months after bidirectional Glenn.

Methods:

Sixty-nine single ventricle patients underwent bidirectional Glenn between 2010 and 2016. Patients with structural brain abnormalities, grade III–IV intra-ventricular haemorrhage, significant stroke, or obstructive hydrocephalus were excluded. Head circumference and body weight measurements from clinical encounters were evaluated. Motor development was measured with Psychomotor Developmental Index of the Bayley Scales of Infant Development, Third Edition. Generalised estimating equations assessed change in head circumference z-scores from baseline (time of bidirectional Glenn) to 12 months post-surgery.

Results:

Mean age at bidirectional Glenn was 4.7 (2.3) months and mean head circumference z-score based on population-normed data was −1.13 (95% CI −1.63, −0.63). Head circumference z-score increased to 0.35 (95% CI −0.20, 0.90) (p < 0.0001) 12 months post-surgery. Accelerated head growth, defined as an increase in z-score of >1 from baseline to 12 months post-surgery, was present in 46/69 (66.7%) patients. There was no difference in motor Psychomotor Developmental Index scores between patients with and without accelerated head growth.

Conclusion:

Single ventricle patients demonstrated a significant increase in head circumference after bidirectional Glenn until 10–12 months post-surgery, at which time growth stabilised. Accelerated head growth did not predict sub-sequent motor developmental outcomes.

Type
Original Article
Copyright
© The Author(s), 2020. Published by Cambridge University Press

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References

Daymont, C, Neal, A, Prosnitz, A and Cohen, MS. Growth in children with congenital heart disease. Pediatrics 2013; 131: e236e242.CrossRefGoogle ScholarPubMed
Miller, SP, McQuillen, PS, Hamrick, S, et al. Abnormal brain development in newborns with congenital heart disease. N Engl J Med 2007; 357: 19281938.CrossRefGoogle ScholarPubMed
Shillingford, AJ, Ittenbach, RF, Marino, BS, et al. Aortic morphometry and microcephaly in hypoplastic left heart syndrome. Cardiol Young 2007; 17: 189195.CrossRefGoogle ScholarPubMed
Manzar, S, Nair, AK, Pai, MG, Al-Khusaiby, SM. Head size at birth in neonates with transposition of great arteries and hypoplastic left heart syndrome. Saudi Med J 2005; 26: 453456.Google ScholarPubMed
Hangge, PT, Cnota, JF, Woo, JG, et al. Microcephaly is associated with early adverse neurologic outcomes in hypoplastic left heart syndrome. Pediatr Res 2013; 74: 6167.CrossRefGoogle ScholarPubMed
Hinton, RB, Andelfinger, G, Sekar, P, et al. Prenatal head growth and white matter injury in hypoplastic left heart syndrome. Pediatr Res 2008; 64: 364369.CrossRefGoogle ScholarPubMed
Limperopoulos, C, Tworetzky, W, McElhinney, DB. et al. Brain volume and metabolism in fetuses with congenital heart disease: evaluation with quantitative magnetic resonance imaging and spectroscopy. Circulation 2010; 121: 2633.CrossRefGoogle ScholarPubMed
Donofrio, MT, Bremer, YA, Schieken, RM, et al. Autoregulation of cerebral blood flow in fetuses with congenital heart disease: the brain sparing effect. Pediatr Cardiol 2003; 24: 436443.CrossRefGoogle ScholarPubMed
Feinstein, JA, Benson, DW, Dubin, AM, et al. Hypoplastic left heart syndrome: current considerations and expectations. J Am Coll Cardiol 2012; 59: S1S42.CrossRefGoogle ScholarPubMed
Morgan, CD, Wolf, MS, Le, TM, et al. Cerebral ventriculomegaly after the bidirectional Glenn (BDG) shunt: a single-institution retrospective analysis. Childs Nerv Syst 2015; 31: 21312134.CrossRefGoogle ScholarPubMed
Ravishankar, C, Zak, V, Williams, IA, et al. Association of impaired linear growth and worse neurodevelopmental outcome in infants with single ventricle physiology: a report from the pediatric heart network infant single ventricle trial. J Pediatr 2013; 162: 250256 e252.CrossRefGoogle ScholarPubMed
Marino, BS, Lipkin, PH, Newburger, JW, et al. Neurodevelopmental outcomes in children with congenital heart disease: evaluation and management: a scientific statement from the American Heart Association. Circulation 2012; 126: 11431172.CrossRefGoogle ScholarPubMed
Miller, TA, Zak, V, Shrader, P, et al. Growth asymmetry, head circumference, and neurodevelopmental outcomes in infants with single ventricles. J Pediatr 2016; 168: 220225 e221.CrossRefGoogle ScholarPubMed
Medoff-Cooper, B, Irving, SY, Hanlon, AL, et al. The Association among feeding mode, growth, and developmental outcomes in infants with complex congenital heart disease at 6 and 12 months of age. J Pediatr 2016; 169: 154159 e151.CrossRefGoogle ScholarPubMed
Group WHOMGRS. WHO child growth standards based on length/height, weight and age. Acta Paediatr Suppl 2006; 450: 7685.Google Scholar
Fenton, TR, Kim, JH. A systematic review and meta-analysis to revise the Fenton growth chart for preterm infants. BMC Pediatr 2013; 13: 59.CrossRefGoogle ScholarPubMed
Bayley, N The Bayley Scales of Infant Development - III. The Psychological Corporation, San Antonio, TX, 2006.Google Scholar
Ackerman, LL, Kralik, SF, Daniels, Z, et al. Alterations in cerebral ventricle size in children with congenital heart disease. Childs Nerv Syst 2018; 34: 22332240.CrossRefGoogle ScholarPubMed
Trachsel, T, Balmer, C, Wahlander, H, et al. Does superior caval vein pressure impact head growth in Fontan circulation? Cardiol Young 2016; 26: 13271332.CrossRefGoogle ScholarPubMed
Fogel, MA, Li, C, Elci, OU, et al. Neurological injury and cerebral blood flow in single ventricles throughout staged surgical reconstruction. Circulation 2017; 135: 671682.CrossRefGoogle ScholarPubMed
Bellinger, DC, Watson, CG, Rivkin, MJ, et al. Neuropsychological status and structural brain imaging in adolescents with single ventricle who underwent the Fontan procedure. J Am Heart Assoc 2015; 4: e002302.CrossRefGoogle ScholarPubMed
Mussatto, KA, Hoffmann, RG, Hoffman, GM, et al. Risk and prevalence of developmental delay in young children with congenital heart disease. Pediatrics 2014; 133: e570e577.CrossRefGoogle ScholarPubMed
Newburger, JW, Sleeper, LA, Bellinger, DC, et al. Early developmental outcome in children with hypoplastic left heart syndrome and related anomalies: the single ventricle reconstruction trial. Circulation 2012; 125: 20812091.CrossRefGoogle ScholarPubMed