Your browser doesn't support javascript.
loading
Incidence of pediatric narcolepsy diagnosis and management: evidence from claims data.
Tang, Si Hao; Min, Jungwon; Zhang, Xuemei; Uwah, Eberechukwu; Griffis, Heather M; Cielo, Christopher M; Fiks, Alexander G; Mindell, Jodi A; Tapia, Ignacio E; Williamson, Ariel A.
Afiliação
  • Tang SH; Drexel University College of Medicine, Philadelphia, Pennsylvania.
  • Min J; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Zhang X; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Uwah E; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Griffis HM; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Cielo CM; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Fiks AG; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Mindell JA; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Tapia IE; Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Williamson AA; Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
J Clin Sleep Med ; 20(7): 1141-1151, 2024 Jul 01.
Article em En | MEDLINE | ID: mdl-38450539
ABSTRACT
STUDY

OBJECTIVES:

The purpose of this study was to characterize the incidence of pediatric narcolepsy diagnosis, subsequent care, and potential sociodemographic disparities in a large US claims database.

METHODS:

Merative MarketScan insurance claims (n = 12,394,902) were used to identify youth (6-17 years of age) newly diagnosed with narcolepsy (International Classification of Diseases, 10th revision codes). Narcolepsy diagnosis and care 1 year postdiagnosis included polysomnography with Multiple Sleep Latency Test, pharmacological care, and clinical visits. Potential disparities were examined by insurance coverage and child race and ethnicity (Medicaid-insured only).

RESULTS:

The incidence of narcolepsy diagnosis was 10100,000, primarily type 2 (69.9%). Most diagnoses occurred in adolescents with no sex differences, but higher rates in Black vs White youth with Medicaid. Two thirds had a prior sleep disorder diagnosis and 21-36% had other co-occurring diagnoses. Only half (46.6%) had polysomnography with Multiple Sleep Latency Test (± 1 year postdiagnosis). Specialty care (18.9% pulmonary, 26.9% neurology) and behavioral health visits were rare (34.4%), although half were prescribed stimulant medications (51.0%). Medicaid-insured were 86% less likely than commercially insured youth to have any clinical care and 33% less likely to have polysomnography with Multiple Sleep Latency Test.

CONCLUSIONS:

Narcolepsy diagnoses occurred in 0.01% of youth, primarily during adolescence, and at higher rates for Black vs White children with Medicaid. Only half overall had evidence of a diagnostically required polysomnography with Multiple Sleep Latency Test, underscoring potential misdiagnosis. Many patients had co-occurring conditions, but specialty and behavioral health care were limited. Results suggest misdiagnosis, underdiagnosis, and limited narcolepsy treatment, as well as possible disparities. Results highlight the need to identify determinants of evidence-based pediatric narcolepsy diagnosis and management. CITATION Tang SH, Min J, Zhang X, et al. Incidence of pediatric narcolepsy diagnosis and management evidence from claims data. J Clin Sleep Med. 2024;20(7)1141-1151.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polissonografia / Narcolepsia Limite: Adolescent / Child / Female / Humans / Male País/Região como assunto: America do norte Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polissonografia / Narcolepsia Limite: Adolescent / Child / Female / Humans / Male País/Região como assunto: America do norte Idioma: En Ano de publicação: 2024 Tipo de documento: Article