Literature DB >> 27264163

The economic burden of spinal muscular atrophy.

Edward P Armstrong1,2, Daniel C Malone1,2, Wei-Shi Yeh3, Georg J Dahl4, Rees L Lee5, Nicholas Sicignano6.   

Abstract

AIM: To evaluate the economic burden of spinal muscular atrophy (SMA).
MATERIALS AND METHODS: This study used Department of Defense Military Healthcare System (MHS) data from 2003-2012. Healthcare costs were determined for patients with at least one inpatient or three outpatient claims with a diagnosis of SMA before 18 years of age and who had ≥ 6 months of data after first SMA diagnosis or expired within 6 months of initial diagnosis. A comparator cohort was selected using a 3:1 match based on age and gender.
RESULTS: A total of 239 individuals with SMA diagnosis met the inclusion criteria along with 717 matched comparator patients. More patients with SMA had hospitalizations (69.5%) compared to the comparator cohort (17.2%, p < 0.001). Median total expenditures across all years of data for patients with SMA were $83 652 (25-75th percentile = $29 620-228 754) vs the comparator group of $4329 (25-75(th) percentile = $1229-10 062 (p < 0.001)) over an average (SD) of 6.9 ± 3.6 years. The annualized mean costs of total healthcare expenditures were significantly higher for the SMA cases than the comparison cohort, $47 862 ± 88 607 compared to $1861 ± 6374, respectively (p < 0.001). The sub-group of patients with early diagnosis (n = 45) had 4.3 ± 2.9 years of observation with a median cost of $167 921 ($53 349-678 412). Mean age (SD) at first observed SMA diagnosis was 7.5 ± 6.4 years. Mean (SD) duration of follow-up after initial SMA diagnosis was 4.8 ± 3.3 years, with a median post-diagnosis cost of $60 213 ($18 229-192 559). The major costs for all patients were outpatient visits [median = $53 152 ($23 902-136 150)], followed by inpatient costs [median = $11 258 ($0-51 987)] and total prescription costs [median = $3167 ($943-13 283)]. LIMITATIONS: The analysis is limited to the data available and may under-estimate the total cost of SMA.
CONCLUSIONS: Individuals with SMA have a high degree of morbidity, particularly those diagnosed during infancy. SMA patients have significant medical expenditures and high utilization of healthcare services.

Entities:  

Keywords:  Muscle disease; Neuromuscular disease; Spinal muscular atrophy

Mesh:

Year:  2016        PMID: 27264163     DOI: 10.1080/13696998.2016.1198355

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


  12 in total

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Authors:  Ewout J N Groen; Kevin Talbot; Thomas H Gillingwater
Journal:  Nat Rev Neurol       Date:  2018-02-09       Impact factor: 42.937

2.  Healthcare Utilization, Costs of Care, and Mortality Among Psatients With Spinal Muscular Atrophy.

Authors:  Hiangkiat Tan; Tao Gu; Er Chen; Rajeshwari Punekar; Perry B Shieh
Journal:  J Health Econ Outcomes Res       Date:  2019-12-02

3.  Costs of Illness of Spinal Muscular Atrophy: A Systematic Review.

Authors:  Erik Landfeldt; Astrid Pechmann; Hugh J McMillan; Hanns Lochmüller; Thomas Sejersen
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4.  Financial, opportunity and psychosocial costs of spinal muscular atrophy: an exploratory qualitative analysis of Australian carer perspectives.

Authors:  Michelle A Farrar; Kate A Carey; Sarah-Grace Paguinto; Georgina Chambers; Nadine A Kasparian
Journal:  BMJ Open       Date:  2018-05-24       Impact factor: 2.692

5.  Systemic nature of spinal muscular atrophy revealed by studying insurance claims.

Authors:  Scott L Lipnick; Denis M Agniel; Rahul Aggarwal; Nina R Makhortova; Samuel G Finlayson; Alexandra Brocato; Nathan Palmer; Basil T Darras; Isaac Kohane; Lee L Rubin
Journal:  PLoS One       Date:  2019-03-14       Impact factor: 3.240

6.  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

7.  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

8.  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 9.  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

10.  Patient characteristics and hospitalisation costs of spinal muscular atrophy in Spain: a retrospective multicentre database analysis.

Authors:  Josep Darbà; Alicia Marsà
Journal:  BMJ Open       Date:  2019-11-21       Impact factor: 2.692

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