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Developmental language trajectories in children with critical CHD

Published online by Cambridge University Press:  26 March 2025

Alexa C. Escapita
Affiliation:
Department of Obstetrics and Gynecology, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Anna Caroline Gregg
Affiliation:
Arkansas Children’s Hospital Northwest, Springdale, AR, USA
Kelsey Lambou
Affiliation:
Department of Surgery, University of Kansas Medical Center, Kansas City, Kansas, USA
Heather Watson
Affiliation:
The Heart Institute, Arkansas Children’s Hospital, Little Rock, AR, USA
Lawrence Greiten
Affiliation:
Department of Surgery, Division of Pediatric Cardiovascular Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Brian Reemtsen
Affiliation:
Department of Surgery, Division of Pediatric Cardiovascular Surgery, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Elijah Bolin
Affiliation:
Department of Pediatrics, Division of Pediatric Cardiology, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Dala Zakaria
Affiliation:
Department of Pediatrics, Division of Pediatric Cardiology, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Tara L. Johnson*
Affiliation:
Department of Neurology Driscoll Children’s Hospital, Corpus Christi, TX, USA
*
Corresponding author: Tara L. Johnson; Email: [email protected]

Abstract

Introduction:

Medical and surgical advancements have enabled a 95% survival rate for children with CHD. However, these survivors are disproportionately affected by neurodevelopmental disabilities. In particular, they have behavioural problems in toddlerhood. Because there is a known relationship between behavioural problems and early language delay, we hypothesise that children with critical CHD have early detectable language deficits. To test our hypothesis, we performed a retrospective study on a cohort of children with critical CHD to visualise their early language developmental trajectories.

Methods:

We identified a cohort of 27 children with two diagnoses: single ventricle physiology (19) and transposition of the great arteries (8). As part of their routine clinical care, all of these children had serial developmental evaluations with the language subsection of the Capute Scales. We visualised their developmental language trajectories as a function of chronologic age, and we used a univariate linear regression model to calculate diagnosis-specific expected developmental age equivalents.

Results:

In each group, language development is age-appropriate in infancy. Deviation from age-appropriate development is apparent by 18 months. This results in borderline-mild language delay by 30 months.

Discussion:

Using the Capute Scales, our team quantified early language development in infants and toddlers with critical CHD. Our identification of deceleration in skill acquisition reinforces the call for ongoing neurodevelopmental surveillance in these children. Understanding early language development will help clinicians provide informed anticipatory guidance to families of children with critical CHD.

Social Media Synopsis:

Children with single ventricle physiology and transposition of the great arteries have measurable early language delays.

Type
Original Article
Copyright
© The Author(s), 2025. Published by Cambridge University Press

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References

Hasan, AA, Abu Lehyah, NAA, Al Tarawneh, MK, et al. Incidence and types of congenital heart disease at a referral hospital in Jordan: retrospective study from a tertiary center. Front Pediatr 2023; 11: 1261130.Google Scholar
Rao, PS, Agarwal, A. Advances in the diagnosis and management of congenital heart disease in children. Children 2022; 9: 1056. doi: 10.3390/children9071056.CrossRefGoogle ScholarPubMed
Sood, E, Newburger, JW, Anixt, JS, et al. Neurodevelopmental outcomes for individuals with congenital heart disease: updates in Neuroprotection, risk-stratification, evaluation, and management: a scientific statement from the American heart association. Circulation 2024; 149: e997e1022. doi: 10.1161/CIR.0000000000001211.CrossRefGoogle ScholarPubMed
Fourdain, S, Simard, MN, Dagenais, L, et al. Gross motor development of children with congenital heart disease receiving early systematic surveillance and individualized intervention: brief report. Dev Neurorehabil 2021; 24: 5662. doi: 10.1080/17518423.2020.1711541.CrossRefGoogle ScholarPubMed
Finkel, GG, Sun, LS, Jackson, WM. Children with congenital heart disease show increased behavioral problems compared to healthy peers: a systematic review and meta-analysis. Pediatr Cardiol 2023; 44: 116123. doi: 10.1007/s00246-022-02940-x.CrossRefGoogle Scholar
Marino, BS, Lipkin, PH, Newburger, JW, et al. Neurodevelopmental outcomes in children with congenital heart disease: evaluation and management. Circulation 2012; 126: 11431172. doi: 10.1161/cir.0b013e318265ee8a.CrossRefGoogle ScholarPubMed
Robinson, J, Sahai, S, Pennacchio, C, Sharew, B, Chen, L, Karamlou, T. Effects of sociodemographic factors on access to and outcomes in congenital heart disease in the United States. J Cardiovasc Dev Dis 2024; 11: 67. doi: 10.3390/jcdd11020067.Google ScholarPubMed
Bucholz, EM, Sleeper, LA, Goldberg, CS, et al. Socioeconomic status and long-term outcomes in single ventricle heart disease. Pediatrics 2020; 146: e20201240. doi: 10.1542/peds.2020-1240.Google ScholarPubMed
Xiang, L, Su, Z, Liu, Y, et al. Impact of family socioeconomic status on health-related quality of life in children with critical congenital heart disease. J Am Heart Assoc 2019; 8: e010616. doi: 10.1161/JAHA.118.010616.CrossRefGoogle ScholarPubMed
Bayne, J, Garry, J, Albert, MA. Brief review: racial and ethnic disparities in cardiovascular care with a focus on congenital heart disease and precision medicine. Curr Atheroscler Rep 2023; 25: 189195. doi: 10.1007/s11883-023-01093-3.CrossRefGoogle ScholarPubMed
Dumornay, NM, Lebois, LAM, Ressler, KJ, Harnett, NG. Racial disparities in adversity during childhood and the false appearance of race-related differences in brain structure. Am J Psychiatry 2023; 180: 127138. doi: 10.1176/appi.ajp.21090961.CrossRefGoogle ScholarPubMed
Freeman Duncan, A, Watterberg, KL, Nolen, TL, et al. Effect of ethnicity and race on cognitive and language testing at age 18-22 months in extremely preterm infants. J Pediatr 2012; 160: 966971.e2. doi: 10.1016/j.jpeds.2011.12.009.CrossRefGoogle Scholar
Straub, L, Bateman, BT, Hernandez-Diaz, S, et al. Neurodevelopmental disorders among publicly or privately insured children in the United States. Jama Psychiat 2022; 79: 232242. doi: 10.1001/jamapsychiatry.2021.3815.CrossRefGoogle ScholarPubMed
Kumar, TKS. Practical conduct of open heart procedures for congenital heart lesions. J Thorac Dis 2020; 12: 1235. Published online 2020.CrossRefGoogle ScholarPubMed
Shakya, S, Saxena, A, Gulati, S, et al. Neurodevelopmental outcomes in children with cyanotic congenital heart disease following open heart surgery. Ann Pediatr Cardiol 2022; 15: 412.CrossRefGoogle ScholarPubMed
Basgoze, S, Temur, B, Ozcan, ZS, et al. The effect of extracorporeal membrane oxygenation on neurodevelopmental outcomes in children after repair of congenital heart disease: a pilot study from Turkey. Front Pediatr 2023; 11: 1131361.CrossRefGoogle ScholarPubMed
Weyandt, LL, Clarkin, CM, Holding, EZ, et al. Neuroplasticity in children and adolescents in response to treatment intervention: a systematic review of the literature. Clin Transl Neurosci 2020; 4: 2514183X20974231. doi: 10.1177/2514183X20974231.CrossRefGoogle Scholar
Chorna, O, Cioni, G, Guzzetta, A. Chapter 24 - Principles of early intervention. In: Gallagher, A, Bulteau, C, Cohen, D, of Michaud J.L.B.T.H., CN (eds). Neurocognitive Development: Disorders and Disabilities. vol. 174. Elsevier, 2020: 333341. doi: 10.1016/B978-0-444-64148-9.00024-7.CrossRefGoogle Scholar
Rasheed, MA, Kvestad, I, Shaheen, F, Memon, U, Strand, TA. The predictive validity of bayley scales of infant and toddler development-III at 2 years for later general abilities: findings from a rural, disadvantaged cohort in Pakistan. PLOS Glob Public Heal 2023; 3: e0001485. doi: 10.1371/journal.pgph.0001485.CrossRefGoogle ScholarPubMed
Ranjitkar, S, Kvestad, I, Strand, TA, et al. Acceptability and Reliability of the Bayley Scales of Infant and Toddler Development-III Among Children in Bhaktapur, Nepal. Front Psychol 2018; 9: 1265.Google ScholarPubMed
Del Rosario, C, Slevin, M, Molloy, EJ, Quigley, J, Nixon, E. How to use the bayley scales of infant and toddler development. Arch dis child - educ &amp. Pract Ed 2021; 106: 108 LP112. doi: 10.1136/archdischild-2020-319063.Google Scholar
Balasundaram, Palanikumar, Avulakunta, ID. Bayley Scales of Infant and Toddler Development. In: StatPearls, 2022. https://www.ncbi.nlm.nih.gov/books/NBK567715/ Google ScholarPubMed
Accardo Pasquale, J, Capute, A. The Capute Scales. 4th ed. Brookes Publishing, 2005. https://brookespublishing.com/product/the-capute-scales/ Google Scholar
O.’Connor Leppert, ML, Shank, TP, Shapiro, BK, Capute, AJ. The capute scales: CAT/CLAMS - a pediatric assessment tool for the early detection of mental retardation and communicative disorders. Ment Retard Dev Disabil Res Rev 1998; 4: 1419. doi: 10.1002/(SICI)1098-2779(1998)4:13.0.CO;2-X.3.0.CO;2-X>CrossRefGoogle Scholar
Semrud-Clikeman, M. The capute scales. Pediatr Neurol 2006; 34: 7980. doi: 10.1016/j.pediatrneurol.2005.09.012.CrossRefGoogle Scholar
Voigt, RG, Brown, FR, Fraley, JK, et al. Concurrent and predictive validity of the cognitive adaptive test/clinical linguistic and auditory milestone scale (CAT/CLAMS) and the mental developmental index of the bayley scales of infant development. Clin Pediatr (Phila) 2003; 42: 427432. doi: 10.1177/000992280304200507.CrossRefGoogle ScholarPubMed
Allen, KY, Marino, BS. Developmental Delay in Children with Congenital Heart Disease BT - Pediatric Cardiology: Fetal, Pediatric, and Adult Congenital Heart Diseases. In: Abdulla, R id, Berger, S, Backer, C, tal, e, Springer International Publishing, 2020: 111. doi: 10.1007/978-3-030-42937-9_86-1.CrossRefGoogle Scholar
Team, RS. R Studio: Integrated Development for R. RStudio, PBC, Boston, MA, 2000. Published online 2020. http://www.rstudio.com/ Google Scholar
Hampton Gray, W, Sorabella, RA, Moellinger, AB, et al. Standardization of the norwood procedure improves outcomes in a medium-sized volume center. World J pediatr congenit hear surg. World J Pediatr Congenit Hear Surg 2024; 15: 21501351241249110–745. doi: 10.1177/21501351241249112. Published online June 10.Google Scholar
Rogers, SC, Malik, L, Fogel, J, et al. Optimising motor development in the hospitalized infant with CHD: factors contributing to early motor challenges and recommendations for assessment and intervention. Cardiol Young 2023; 33: 18001812. doi: 10.1017/S1047951123003165.Google ScholarPubMed
Leonetti, C, Back, SA, Gallo, V, Ishibashi, N. Cortical dysmaturation in congenital heart disease. Trends Neurosci 2019; 42: 192204. doi: 10.1016/j.tins.2018.12.003.CrossRefGoogle ScholarPubMed
Verrall, CE, Blue, GM, Loughran-Fowlds, A, et al. Big issues, in neurodevelopment for children and adults with congenital heart disease. Open Hear 2019; 6: e000998.CrossRefGoogle ScholarPubMed