Literature DB >> 31322019

Economic burden of spinal muscular atrophy in the United States: a contemporary assessment.

Marcus Droege1, Douglas Sproule1, Ramesh Arjunji1, Marjolaine Gauthier-Loiselle2, Martin Cloutier2, Omar Dabbous1.   

Abstract

Aims: To estimate healthcare resource utilization (HRU) and costs among patients with spinal muscular atrophy (SMA) type 1 (SMA1) in real-world practice, overall and among patients treated with nusinersen. As a secondary objective, HRU and costs were estimated among patients with other SMA types (i.e. 2, 3, or 4 combined), overall and among patients treated with nusinersen.Materials and methods: Patients with SMA were identified from the Symphony Health's Integrated Dataverse (IDV) open claims database (September 1, 2016-August 31, 2018) and were classified into four cohorts based on SMA type and nusinersen treatment (i.e. SMA1, SMA1 nusinersen, other SMA, and other SMA nusinersen cohorts). The index date was the date of the first SMA diagnosis after December 23, 2016 or, for nusinersen cohorts, the date of nusinersen initiation. The study period spanned from the index date to the earlier among the end of clinical activity or data availability.
Results: Patients in the SMA1 (n = 349) and SMA1 nusinersen (n = 45) cohorts experienced an average of 59.4 and 56.6 days with medical visits per-patient-per-year (PPPY), respectively, including 14.1 and 4.6 inpatient days. Excluding nusinersen-related costs, total mean healthcare costs were $137,627 and $92,618 PPPY in the SMA1 and SMA1 nusinersen cohorts, respectively. Mean nusinersen-related costs were $191,909 per-patient-per-month (PPPM) for the first 3 months post-initiation (i.e. loading phase) and $36,882 PPPM thereafter (i.e. maintenance phase). HRU and costs were also substantial among patients in the other SMA (n = 5,728) and other SMA nusinersen (n = 404) cohorts, with an average of 44.5 and 63.7 days with medical visits PPPY and total mean healthcare costs (excluding nusinersen-related costs) of $49,175 and $76,371 PPPY, respectively.Limitations: The database may contain inaccuracies or omissions in diagnoses, procedures, or costs, and does not capture medical services outside of the IDV network.Conclusions: HRU and healthcare costs were substantial in patients with SMA, including in nusinersen-treated patients.

Entities:  

Keywords:  I00; I10; Spinal muscular atrophy; burden of illness; costs; healthcare resource utilization; nusinersen; real world

Mesh:

Substances:

Year:  2019        PMID: 31322019     DOI: 10.1080/13696998.2019.1646263

Source DB:  PubMed          Journal:  J Med Econ        ISSN: 1369-6998            Impact factor:   2.448


  13 in total

1.  Economic burden of spinal muscular atrophy: an analysis of claims data.

Authors:  Lisa Belter; Rosángel Cruz; Sierra Kulas; Emily McGinnis; Omar Dabbous; Jill Jarecki
Journal:  J Mark Access Health Policy       Date:  2020-11-08

2.  The Burden of Spinal Muscular Atrophy on Informal Caregivers.

Authors:  Isaac Aranda-Reneo; Luz María Peña-Longobardo; Juan Oliva-Moreno; Svenja Litzkendorf; Isabelle Durand-Zaleski; Eduardo F Tizzano; Julio López-Bastida
Journal:  Int J Environ Res Public Health       Date:  2020-12-02       Impact factor: 3.390

3.  Treatment preference among patients with spinal muscular atrophy (SMA): a discrete choice experiment.

Authors:  Alisha Monnette; Er Chen; Dongzhe Hong; Alessandra Bazzano; Stacy Dixon; W David Arnold; Lizheng Shi
Journal:  Orphanet J Rare Dis       Date:  2021-01-20       Impact factor: 4.123

Review 4.  Systematic literature review of the economic burden of spinal muscular atrophy and economic evaluations of treatments.

Authors:  Tamara Dangouloff; Camille Botty; Charlotte Beaudart; Laurent Servais; Mickaël Hiligsmann
Journal:  Orphanet J Rare Dis       Date:  2021-01-23       Impact factor: 4.123

5.  Newborn screening for spinal muscular atrophy in Germany: clinical results after 2 years.

Authors:  Katharina Vill; Oliver Schwartz; Heike Kölbel; Wolfgang Müller-Felber; Astrid Blaschek; Dieter Gläser; Uta Nennstiel; Brunhilde Wirth; Siegfried Burggraf; Wulf Röschinger; Marc Becker; Ludwig Czibere; Jürgen Durner; Katja Eggermann; Bernhard Olgemöller; Erik Harms; Ulrike Schara
Journal:  Orphanet J Rare Dis       Date:  2021-03-31       Impact factor: 4.123

6.  Nusinersen for Spinal Muscular Atrophy in the United States: Findings From a Retrospective Claims Database Analysis.

Authors:  Marjolaine Gauthier-Loiselle; Martin Cloutier; Walter Toro; Anish Patel; Sherry Shi; Mikhail Davidson; Matthias Bischof; Nicole LaMarca; Omar Dabbous
Journal:  Adv Ther       Date:  2021-10-28       Impact factor: 3.845

7.  Quality of life data for individuals affected by spinal muscular atrophy: a baseline dataset from the Cure SMA Community Update Survey.

Authors:  Lisa Belter; Rosángel Cruz; Jill Jarecki
Journal:  Orphanet J Rare Dis       Date:  2020-08-24       Impact factor: 4.123

8.  Characterization of Adult Patients With SMA Treated in US Hospital Settings: A Natural History Study in the Premier Healthcare Database.

Authors:  Nicole B Johnson; Crystal Proud; Christina L Wassel; Jill Dreyfus; Thos Cochrane; Angela D Paradis
Journal:  J Neuromuscul Dis       Date:  2021

9.  Improving Care and Empowering Adults Living with SMA: A Call to Action in the New Treatment Era.

Authors:  Maggie C Walter; Claudia Chiriboga; Tina Duong; Nathalie Goemans; Anna Mayhew; Laëtitia Ouillade; Maryam Oskoui; Ros Quinlivan; Juan F Vázquez-Costa; John Vissing; Laurent Servais
Journal:  J Neuromuscul Dis       Date:  2021

10.  Burden of Spinal Muscular Atrophy (SMA) on Patients and Caregivers in Canada.

Authors:  H J McMillan; B Gerber; T Cowling; W Khuu; M Mayer; J W Wu; B Maturi; K Klein-Panneton; C Cabalteja; H Lochmüller
Journal:  J Neuromuscul Dis       Date:  2021
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