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Burden and cost of comorbidities in patients with neuromyelitis optica spectrum disorder.
Exuzides, Alex; Sheinson, Daniel; Sidiropoulos, Paris; Magrini, Fabio; Gholizadeh, Shervin; Surinach, Andy; Cook, Lawrence; Meyer, Craig S; Yeaman, Michael.
Afiliação
  • Exuzides A; Genentech, Inc., South San Francisco, CA, USA. Electronic address: exuzides.alex@gene.com.
  • Sheinson D; Genentech, Inc., South San Francisco, CA, USA.
  • Sidiropoulos P; F. Hoffmann-La-Roche Ltd., South San Francisco, CA, USA.
  • Magrini F; Genentech, Inc., South San Francisco, CA, USA.
  • Gholizadeh S; Genentech, Inc., South San Francisco, CA, USA.
  • Surinach A; Genesis Research, Hoboken, NJ, USA.
  • Cook L; Department of Pediatrics, University of Utah, Salt Lake City, UT, USA.
  • Meyer CS; Genentech, Inc., South San Francisco, CA, USA.
  • Yeaman M; University of California, Los Angeles (UCLA), Los Angeles, CA, USA; Division of Molecular Medicine, Harbor-UCLA Medical Center, Torrance, CA, USA; Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
J Neurol Sci ; 427: 117530, 2021 08 15.
Article em En | MEDLINE | ID: mdl-34111762
ABSTRACT

BACKGROUND:

Neuromyelitis optica spectrum disorder (NMOSD) is associated with various comorbidities, including non-autoimmune and autoimmune conditions. The burden and cost of illness for NMOSD are unclear, particularly in the context of comorbidities.

METHODS:

Claims data from IBM MarketScan Commercial and Medicare Supplemental Databases between 2014 and 2018 were analyzed. Patients with NMOSD were specified as having inpatient or outpatient claims for NMOSD diagnosis or specific NMOSD symptoms claims and no subsequent claims for multiple sclerosis (MS) or use of MS disease-modifying therapy (DMT). Continuous enrollment ≥ 6 months before and ≥ 1 year after the first claim (index date) was required for study inclusion. Total costs stratified by comorbidities within 12 months post-index date were calculated per patient and compared 15 with matched non-NMOSD controls.

RESULTS:

A total of 162 patients with NMOSD and 810 non-NMOSD controls were evaluated. A significantly higher proportion of NMOSD patients had comorbidities than non-NMOSD controls (66.7% vs 41.5%; P < 0.001). Concomitant autoimmune disease occurred in 19.1% vs 4.9% (P < 0.001) of patients with NMOSD vs non-NMOSD controls. NMOSD patients incurred significantly higher total median (interquartile range) healthcare costs per patient ($68,386.48 [$23,373.54-$160,862.70]) than matched non-NMOSD controls with autoimmune disease ($17,215.13 [$6715.48-$31,441.93]; P < 0.001) or patients with NMOSD without autoimmune comorbidity ($23,905.42 [$8632.82-$67,251.54]; P = 0.022). Similarly, patients with NMOSD and non-autoimmune comorbidities incurred higher median healthcare costs than matched controls.

CONCLUSIONS:

Patients with NMOSD experience significant disease burden and cost that are amplified by comorbidities. Effective therapies are needed, particularly for patients with concomitant autoimmune disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuromielite Óptica Tipo de estudo: Health_economic_evaluation Limite: Aged / Humans País/Região como assunto: America do norte Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neuromielite Óptica Tipo de estudo: Health_economic_evaluation Limite: Aged / Humans País/Região como assunto: America do norte Idioma: En Ano de publicação: 2021 Tipo de documento: Article