Sleep and neurocognitive outcome in primary school children with Robin Sequence.
Child
Female
Humans
Male
Anthropometry
Child Behavior
Internal-External Control
Pierre Robin Syndrome
/ complications
Polysomnography
Sleep
/ physiology
Sleep Apnea, Obstructive
/ complications
Surveys and Questionnaires
Wechsler Scales
Infant
Bone Plates
Cross-Sectional Studies
Cognition
Self Report
Checklist
Robin sequence
neurocognitive and behavioral outcome
obstructive sleep apnea
sleep-disordered breathing
upper airway obstruction
Journal
Sleep
ISSN: 1550-9109
Titre abrégé: Sleep
Pays: United States
ID NLM: 7809084
Informations de publication
Date de publication:
10 05 2023
10 05 2023
Historique:
received:
27
07
2022
revised:
16
12
2022
medline:
12
5
2023
pubmed:
26
12
2022
entrez:
25
12
2022
Statut:
ppublish
Résumé
To investigate neurocognitive and behavioral outcomes at primary school age in relation to obstructive sleep apnea (OSA) in children with Robin sequence (RS) treated with the Tuebingen palatal plate in infancy and to assess the impact of OSA in these patients. Forty-two primary school-aged children (n = 21 with RS, n = 21 age- and sex-matched controls) underwent polysomnography, intelligence testing ("Wechsler Intelligence Scale for Children-Fifth Edition" [WISC-V]), and anthropometrics. Families completed a 7-day sleep diary and questionnaires on sleep and behavior (Children's Sleep Habits Questionnaire [CSHQ] and the Child Behavior Checklist [CBCL]). In children with RS (17 non-syndromic, four syndromic; median age 9.7 [8.5-10.8] years), the obstructive apnea-hypopnea index (OAHI) was significantly higher than in controls (1.3 [0.4-2.7]/h vs. 0.4 [0.1-0.6]/h). Two syndromic children with RS were already on nocturnal respiratory support for OSA prior to our study, and one non-syndromic child was diagnosed with severe OSA (OAHI 57/h) despite an unremarkable medical history and questionnaire. The overall intelligence quotient in children with RS was within the normal range and did not differ between children with RS and healthy peers (102 vs. 108, p = .05). However, children with RS had values in the at-risk clinical range for externalizing behavior. These children with RS showed an increased risk of OSA and behavioral problems, suggesting regular screening for OSA throughout childhood. Neurocognitive scores in children with RS were within the normal range after adequate treatment of OSA during infancy.
Identifiants
pubmed: 36566505
pii: 6960708
doi: 10.1093/sleep/zsac317
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© The Author(s) 2022. Published by Oxford University Press on behalf of Sleep Research Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.