Developmental outcome of children with Robin sequence treated with the current Paris protocol
- PMID: 37786287
- DOI: 10.1111/apa.16979
Developmental outcome of children with Robin sequence treated with the current Paris protocol
Abstract
Aim: We aimed to investigate the developmental outcome of children with Robin sequence (RS) for whom continuous positive airway pressure was the main strategy to release upper airway obstruction.
Methods: We included children with isolated RS or RS associated with Stickler syndrome who were aged 15 months to 6 years. We used the French version of the Child Development Inventory and calculated the developmental quotient (DQ) for eight different domains and the global DQ (DQ-global). We searched for determinants of risk of delay.
Results: Of the 87 children, for 71%, the developmental evolution was within the norm (DQ-global ≥86 or ≥-1 SD), 29% were at high risk of delay (DQ-global <86 or <-1 SD), and only 3% were at very high risk of delay (DQ-global <70 or <-2 SD). The DQs for expressive language and language comprehension were lower in our study population than the general population, but an improvement was noticed with the children's growth.
Conclusion: Risk of a developmental delay was not greater for children with the most severe respiratory phenotype than the others. Children whose mothers had low education levels were more at risk than the others.
Keywords: Robin sequence; continuous positive airway pressure; psychomotor development; stickler syndrome; upper airway obstruction.
© 2023 The Authors. Acta Paediatrica published by John Wiley & Sons Ltd on behalf of Foundation Acta Paediatrica.
References
REFERENCES
-
- Breugem CC, Evans KN, Poets CF, et al. Best practices for the diagnosis and evaluation of infants with Robin sequence: a clinical consensus report. JAMA Pediatr. 2016;170(9):894-902. doi:10.1001/jamapediatrics.2016.0796
-
- Fleurance A, Poets C, Chalouhi C, Thouevin B, Abadie V. Developmental outcome of children with Robin sequence:how does the questio arise ? Sem Fetal Nonat Med. 2021;26:101286. doi:10.1016/j.siny.2021.101286
-
- Holder-Espinasse M, Abadie V, Cormier-Daire V, et al. Pierre Robin sequence: a series of 117 consecutive cases. J Pediatr. 2001;139(4):588-590. doi:10.1067/mpd.2001.117784
-
- Varadarajan S, Balaji TM, Raj AT, et al. Genetic mutations associated with Pierre Robin syndrome/sequence: a systematic review. Mol Syndromol. 2021;12(2):69-86.
-
- Malarbi S, Chisholm AK, Gunn-Charlton JK, et al. Intellectual functioning of children with isolated PRS, PRS-plus, and syndromic PRS. Cleft Palate Craniofac J. 10556656221115596. doi:10.1177/10556656221115596
MeSH terms
LinkOut - more resources
Full Text Sources