Measurement of Narcolepsy Symptoms in School-Aged Children and Adolescents: The Pediatric Narcolepsy Severity Scale.


Journal

Neurology
ISSN: 1526-632X
Titre abrégé: Neurology
Pays: United States
ID NLM: 0401060

Informations de publication

Date de publication:
03 08 2021
Historique:
received: 19 01 2021
accepted: 23 04 2021
pubmed: 26 5 2021
medline: 13 8 2021
entrez: 25 5 2021
Statut: ppublish

Résumé

We validated the Narcolepsy Severity Scale (NSS) in adults with narcolepsy type 1 (NT1) to quantify the severity, frequency, and consequences of the 5 key narcolepsy symptoms over the last month, and we now developed the Pediatric NSS (NSS-P); thus, the aims of this study were to assess NSS-P psychometric properties, validity, and reliability, and to evaluate its responsiveness to treatment in a well-characterized sample of children and adolescents with NT1. The NSS was reformulated for children, and the item about driving was removed. The total score of the 14-item NSS-P ranges from 0 to 54, and higher scores reflect more severe disease. Children and adolescents (n = 209, 6-17 years of age) with NT1 diagnosed in 2 Reference Centers for Narcolepsy in France were consecutively asked to fill in the NSS-P. The scale was fully and correctly completed by 160 (10-18 years of age, 68 untreated). Moreover, 65 participants completed it twice (33 before/during treatment, and 32 under the same treatment). The NSS-P psychometric properties, score changes before/during treatment, and convergent validity with other clinical parameters were assessed. The NSS-P showed adequate psychometric properties with significant item-total score correlations. Factor analysis indicated a 4-factor solution with good reliability. The NSS-P score was lower in treated than untreated patients with a mean difference of 3.71 ± 1.45, with a minimum clinically important difference between untreated and treated patients in the longitudinal sample estimated at 4 points. Four severity levels were defined (mild, moderate, severe, very severe) with between-group differences related to treatment. The NSS-P total score was associated with self-reported sleepiness, insomnia, and depressive symptoms. Its temporal stability was satisfactory. We validated a brief instrument to assess NT1 symptom frequency, severity, and consequences in ≥10-year-old children and adolescents with 4 clinically relevant severity score ranges. This scale constitutes a relevant tool to improve and provide guidance for NT1 management in pediatric populations. The ease of administration, its good psychometric properties, and its sensitivity to detect symptom changes after treatment ensure future use of the NSS-P in clinical and research settings.

Identifiants

pubmed: 34031200
pii: WNL.0000000000012272
doi: 10.1212/WNL.0000000000012272
doi:

Types de publication

Journal Article Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e476-e488

Informations de copyright

© 2021 American Academy of Neurology.

Auteurs

Lucie Barateau (L)

From the Sleep-Wake Disorders Unit (L.B., S.C., A.L.R., R.L., Y.D.), Department of Neurology, Gui-de-Chauliac Hospital; National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (L.B., S.C., A.L.R., R.L., C.P., Y.D.); INM (L.B., R.L., I.J., S.B., Y.D.), Université de Montpellier; Pediatric Sleep Centre (M.L.), Hospital Robert-Debré; and National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (M.L.), Paris, France. ydauvilliers@yahoo.fr lucie.barateau@gmail.com.

Michel Lecendreux (M)

From the Sleep-Wake Disorders Unit (L.B., S.C., A.L.R., R.L., Y.D.), Department of Neurology, Gui-de-Chauliac Hospital; National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (L.B., S.C., A.L.R., R.L., C.P., Y.D.); INM (L.B., R.L., I.J., S.B., Y.D.), Université de Montpellier; Pediatric Sleep Centre (M.L.), Hospital Robert-Debré; and National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (M.L.), Paris, France.

Sofiene Chenini (S)

From the Sleep-Wake Disorders Unit (L.B., S.C., A.L.R., R.L., Y.D.), Department of Neurology, Gui-de-Chauliac Hospital; National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (L.B., S.C., A.L.R., R.L., C.P., Y.D.); INM (L.B., R.L., I.J., S.B., Y.D.), Université de Montpellier; Pediatric Sleep Centre (M.L.), Hospital Robert-Debré; and National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (M.L.), Paris, France.

Anna Laura Rassu (AL)

From the Sleep-Wake Disorders Unit (L.B., S.C., A.L.R., R.L., Y.D.), Department of Neurology, Gui-de-Chauliac Hospital; National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (L.B., S.C., A.L.R., R.L., C.P., Y.D.); INM (L.B., R.L., I.J., S.B., Y.D.), Université de Montpellier; Pediatric Sleep Centre (M.L.), Hospital Robert-Debré; and National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (M.L.), Paris, France.

Régis Lopez (R)

From the Sleep-Wake Disorders Unit (L.B., S.C., A.L.R., R.L., Y.D.), Department of Neurology, Gui-de-Chauliac Hospital; National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (L.B., S.C., A.L.R., R.L., C.P., Y.D.); INM (L.B., R.L., I.J., S.B., Y.D.), Université de Montpellier; Pediatric Sleep Centre (M.L.), Hospital Robert-Debré; and National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (M.L.), Paris, France.

Carole Pesenti (C)

From the Sleep-Wake Disorders Unit (L.B., S.C., A.L.R., R.L., Y.D.), Department of Neurology, Gui-de-Chauliac Hospital; National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (L.B., S.C., A.L.R., R.L., C.P., Y.D.); INM (L.B., R.L., I.J., S.B., Y.D.), Université de Montpellier; Pediatric Sleep Centre (M.L.), Hospital Robert-Debré; and National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (M.L.), Paris, France.

Isabelle Jaussent (I)

From the Sleep-Wake Disorders Unit (L.B., S.C., A.L.R., R.L., Y.D.), Department of Neurology, Gui-de-Chauliac Hospital; National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (L.B., S.C., A.L.R., R.L., C.P., Y.D.); INM (L.B., R.L., I.J., S.B., Y.D.), Université de Montpellier; Pediatric Sleep Centre (M.L.), Hospital Robert-Debré; and National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (M.L.), Paris, France.

Séverine Béziat (S)

From the Sleep-Wake Disorders Unit (L.B., S.C., A.L.R., R.L., Y.D.), Department of Neurology, Gui-de-Chauliac Hospital; National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (L.B., S.C., A.L.R., R.L., C.P., Y.D.); INM (L.B., R.L., I.J., S.B., Y.D.), Université de Montpellier; Pediatric Sleep Centre (M.L.), Hospital Robert-Debré; and National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (M.L.), Paris, France.

Yves Dauvilliers (Y)

From the Sleep-Wake Disorders Unit (L.B., S.C., A.L.R., R.L., Y.D.), Department of Neurology, Gui-de-Chauliac Hospital; National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (L.B., S.C., A.L.R., R.L., C.P., Y.D.); INM (L.B., R.L., I.J., S.B., Y.D.), Université de Montpellier; Pediatric Sleep Centre (M.L.), Hospital Robert-Debré; and National Reference Centre for Orphan Diseases, Narcolepsy, Idiopathic Hypersomnia, and Kleine-Levin Syndrome (M.L.), Paris, France. ydauvilliers@yahoo.fr lucie.barateau@gmail.com.

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