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Tolerance of polysomnography in children with neurodevelopmental disorders compared to neurotypical peers.
Lanzlinger, Daniela; Kevat, Ajay; Collaro, Andrew; Poh, Siew Hui; Pérez, William Pinzon; Chawla, Jasneek.
Afiliação
  • Lanzlinger D; Child Development Service, Children's Health Queensland, Brisbane, Australia.
  • Kevat A; Department of Respiratory and Sleep Medicine, Queensland Children's Hospital, Brisbane, Australia.
  • Collaro A; Child Health Research Centre, Faculty of Medicine, The University of Queensland, Brisbane, Australia.
  • Poh SH; Department of Respiratory and Sleep Medicine, Queensland Children's Hospital, Brisbane, Australia.
  • Pérez WP; Child Health Research Centre, Faculty of Medicine, The University of Queensland, Brisbane, Australia.
  • Chawla J; Queensland Cyber Infrastructure Foundation, The University of Queensland, Brisbane, Australia.
J Clin Sleep Med ; 19(9): 1625-1631, 2023 09 01.
Article em En | MEDLINE | ID: mdl-37185049
STUDY OBJECTIVES: Diagnostic polysomnography (PSG) is the gold standard test to evaluate sleep-disordered breathing in children. Little is known about how children with neurodevelopmental disorders (NDD) tolerate electrodes and sensors in PSG compared to neurotypical children. METHODS: In this retrospective cohort study of children > 12 months of age who underwent diagnostic PSG at our center from 01/01/2021-30/06/2021, we used sleep technician and physician reports to determine how PSG was tolerated in children with NDD compared to neurotypical children. Subanalyses included tolerance of individual electrodes and sensors and subgroups of NDD (eg, Trisomy 21). RESULTS: A total of 132 children with a NDD and 139 neurotypical children underwent diagnostic PSG. The median age of all children was 8 years, 39% were female, and 50% had a sleep disorder identified on PSG, with no significant differences between NDD and neurotypical groups. The most poorly tolerated sensors for all children were the nasal prongs (poorly tolerated in 30% of all children), followed by thermistor (14%) and electroencephalography electrodes (6%). Children with NDD were > 3 times more likely (odds ratio 3.1, 95% confidence interval 1.8-5.3) to experience problems tolerating any study leads than neurotypical children. Subgroup analysis revealed children with Trisomy 21 had the greatest difficulty tolerating PSG set-up and leads. CONCLUSIONS: This retrospective study demonstrates that children with neurodevelopmental disorders are less likely to tolerate PSG monitoring than neurotypical children and highlights the need to develop alternative measures for evaluation of sleep disorders in this population. CITATION: Lanzlinger D, Kevat A, Collaro A, Poh SH, Pérez WP, Chawla J. Tolerance of polysomnography in children with neurodevelopmental disorders compared to neurotypical peers. J Clin Sleep Med. 2023;19(9):1625-1631.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos do Sono-Vigília / Síndrome de Down / Transtornos do Neurodesenvolvimento Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos do Sono-Vigília / Síndrome de Down / Transtornos do Neurodesenvolvimento Idioma: En Ano de publicação: 2023 Tipo de documento: Article