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Measurement of Narcolepsy Symptoms in School-Aged Children and Adolescents: The Pediatric Narcolepsy Severity Scale.
Barateau, Lucie; Lecendreux, Michel; Chenini, Sofiene; Rassu, Anna Laura; Lopez, Régis; Pesenti, Carole; Jaussent, Isabelle; Béziat, Séverine; Dauvilliers, Yves.
Afiliación
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
Neurology ; 97(5): e476-e488, 2021 08 03.
Article en En | MEDLINE | ID: mdl-34031200
ABSTRACT

OBJECTIVE:

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.

METHODS:

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.

RESULTS:

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.

DISCUSSION:

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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Narcolepsia Tipo de estudio: Diagnostic_studies / Guideline Límite: Adolescent / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Neurology Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Narcolepsia Tipo de estudio: Diagnostic_studies / Guideline Límite: Adolescent / Child / Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Neurology Año: 2021 Tipo del documento: Article