Associations Between Age at Arterial Switch Operation, Brain Growth, and Development in Infants With Transposition of the Great Arteries.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
11 06 2019
Historique:
pubmed: 28 5 2019
medline: 17 3 2020
entrez: 29 5 2019
Statut: ppublish

Résumé

Brain injury, impaired brain growth, and long-term neurodevelopmental problems are common in children with transposition of the great arteries. We sought to identify clinical risk factors for brain injury and poor brain growth in infants with transposition of the great arteries undergoing the arterial switch operation, and to examine their relationship with neurodevelopmental outcome. The brains of 45 infants with transposition of the great arteries undergoing surgical repair were imaged pre- and postoperatively using magnetic resonance imaging. Brain weight z scores were calculated based on brain volume and autopsy reference data. Brain injury scores were determined as previously described. Neurodevelopment was assessed at 18 months using the Bayley-III scores of infant development. The relationships between clinical variables, brain injury, perioperative brain growth, and 18-month Bayley-III scores were analyzed. On preoperative imaging, moderate or severe white matter injury was present in 10 of 45 patients, whereas stroke was seen in 4 of 45. A similar prevalence of injury was seen on postoperative imaging, and we were unable to identify any clinical risk factors for brain injury. Brain weight z scores decreased perioperatively in 35 of 45 patients. The presence of a ventricular septal defect ( P=0.009) and older age at surgery ( P=0.007) were associated with impaired perioperative brain growth. When patients were divided into those undergoing surgery during the first 2 weeks of life (32/45) versus those being repaired later (13/45), infants repaired later had significantly worse perioperative brain growth (late repair postoperative brain weight z = -1.0±0.90 versus early repair z = -0.33±0.64; P=0.008). Bayley-III testing scores fell within the normal range for all patients, although age at repair ( P=0.03) and days of open chest ( P=0.03) were associated with a lower composite language score, and length of stay was associated with a lower composite cognitive score ( P=0.02). Surgery beyond 2 weeks of age is associated with impaired brain growth and slower language development in infants with transposition of the great arteries cared for at our center. Although the mechanisms underlying this association are still unclear, extended periods of cyanosis and pulmonary overcirculation may adversely impact brain growth and subsequent neurodevelopment.

Sections du résumé

BACKGROUND
Brain injury, impaired brain growth, and long-term neurodevelopmental problems are common in children with transposition of the great arteries. We sought to identify clinical risk factors for brain injury and poor brain growth in infants with transposition of the great arteries undergoing the arterial switch operation, and to examine their relationship with neurodevelopmental outcome.
METHODS
The brains of 45 infants with transposition of the great arteries undergoing surgical repair were imaged pre- and postoperatively using magnetic resonance imaging. Brain weight z scores were calculated based on brain volume and autopsy reference data. Brain injury scores were determined as previously described. Neurodevelopment was assessed at 18 months using the Bayley-III scores of infant development. The relationships between clinical variables, brain injury, perioperative brain growth, and 18-month Bayley-III scores were analyzed.
RESULTS
On preoperative imaging, moderate or severe white matter injury was present in 10 of 45 patients, whereas stroke was seen in 4 of 45. A similar prevalence of injury was seen on postoperative imaging, and we were unable to identify any clinical risk factors for brain injury. Brain weight z scores decreased perioperatively in 35 of 45 patients. The presence of a ventricular septal defect ( P=0.009) and older age at surgery ( P=0.007) were associated with impaired perioperative brain growth. When patients were divided into those undergoing surgery during the first 2 weeks of life (32/45) versus those being repaired later (13/45), infants repaired later had significantly worse perioperative brain growth (late repair postoperative brain weight z = -1.0±0.90 versus early repair z = -0.33±0.64; P=0.008). Bayley-III testing scores fell within the normal range for all patients, although age at repair ( P=0.03) and days of open chest ( P=0.03) were associated with a lower composite language score, and length of stay was associated with a lower composite cognitive score ( P=0.02).
CONCLUSIONS
Surgery beyond 2 weeks of age is associated with impaired brain growth and slower language development in infants with transposition of the great arteries cared for at our center. Although the mechanisms underlying this association are still unclear, extended periods of cyanosis and pulmonary overcirculation may adversely impact brain growth and subsequent neurodevelopment.

Identifiants

pubmed: 31132861
doi: 10.1161/CIRCULATIONAHA.118.037495
doi:

Types de publication

Comparative Study Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2728-2738

Subventions

Organisme : CIHR
ID : MOP 142204
Pays : Canada

Commentaires et corrections

Type : CommentIn

Auteurs

Jessie Mei Lim (JM)

Department of Physiology (J.M.L.), University of Toronto, Canada.

Prashob Porayette (P)

Division of Cardiology (P.O., D.M., A.S., M. Seed), The Hospital for Sick Children, Toronto, Canada.

Davide Marini (D)

Division of Cardiology (P.O., D.M., A.S., M. Seed), The Hospital for Sick Children, Toronto, Canada.

Vann Chau (V)

Division of Neurology (V.C., S.H.A.-Y., S.P.M.), The Hospital for Sick Children, Toronto, Canada.
Division of Neonatology (V.C., L.G.L.), The Hospital for Sick Children, Toronto, Canada.

Stephanie H Au-Young (SH)

Division of Neurology (V.C., S.H.A.-Y., S.P.M.), The Hospital for Sick Children, Toronto, Canada.
Neurosciences and Mental Health, The Hospital for Sick Children Research Institute, Toronto, Canada (S.H.A.-Y.).

Amandeep Saini (A)

Division of Cardiology (P.O., D.M., A.S., M. Seed), The Hospital for Sick Children, Toronto, Canada.

Linh G Ly (LG)

Division of Neonatology (V.C., L.G.L.), The Hospital for Sick Children, Toronto, Canada.

Susan Blaser (S)

Department of Diagnostic Imaging (S.B., M. Shroff, H.M.B.), The Hospital for Sick Children, Toronto, Canada.

Manohar Shroff (M)

Department of Medical Imaging (M. Shroff), University of Toronto, Canada.
Department of Diagnostic Imaging (S.B., M. Shroff, H.M.B.), The Hospital for Sick Children, Toronto, Canada.

Helen M Branson (HM)

Department of Diagnostic Imaging (S.B., M. Shroff, H.M.B.), The Hospital for Sick Children, Toronto, Canada.

Renee Sananes (R)

Department of Pediatrics (R.S., S.P.M., M. Seed), University of Toronto, Canada.
Labatt Family Heart Centre (R.S.), The Hospital for Sick Children, Toronto, Canada.

Edward J Hickey (EJ)

Division of Cardiovascular Surgery (E.J.H., G.V.A.), The Hospital for Sick Children, Toronto, Canada.

J William Gaynor (JW)

Department of Surgery, Children's Hospital of Philadelphia, PA (J.W.G.).

Glen Van Arsdell (G)

Division of Cardiovascular Surgery (E.J.H., G.V.A.), The Hospital for Sick Children, Toronto, Canada.

Steven P Miller (SP)

Department of Pediatrics (R.S., S.P.M., M. Seed), University of Toronto, Canada.
Division of Neurology (V.C., S.H.A.-Y., S.P.M.), The Hospital for Sick Children, Toronto, Canada.

Mike Seed (M)

Department of Pediatrics (R.S., S.P.M., M. Seed), University of Toronto, Canada.
Division of Cardiology (P.O., D.M., A.S., M. Seed), The Hospital for Sick Children, Toronto, Canada.

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