Evidence map›Paper›PMID 42325276›Full record

ArticleClinicoEconomics and outcomes research : CEOR2026

Medical Claim Costs of Facioscapulohumeral Muscular Dystrophy in the United States.

Amanda A Hill, June Kinoshita, Mariefel Nicole Deypalan, Marina Kolocha, Man Hung, Eric Hon, William Sarraille, Wayne Winegarden, Tanyatorn Ghanjanasak, Jamshid Arjomand

Abstract read
In one paragraph

Article in ClinicoEconomics and outcomes research : CEOR, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Amanda A HillFSHD Society, Randolph, MA, USA.ORCID 0009-0009-9392-1717
June KinoshitaFSHD Society, Randolph, MA, USA.ORCID 0000-0001-8952-9434
Mariefel Nicole DeypalanIndependent Researcher, Iligan City, Philippines.ORCID 0000-0002-6809-5873
Marina KolochaIndependent Consultant, Berlin, Germany.ORCID 0009-0004-2413-3622
Man HungAnalytic Galaxy, Salt Lake City, UT, USA.
Eric HonAnalytic Galaxy, Salt Lake City, UT, USA.
William SarrailleFrancis King Carey School of Law, University of Maryland, Baltimore, MD, USA.
Wayne WinegardenCenter for Medical Economics and Innovation, Pacific Research Institute, Sacramento, CA, USA.
Tanyatorn GhanjanasakNext Step Writing, St. Augustine, FL, USA.
Jamshid ArjomandFSHD Society, Randolph, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Facioscapulohumeral muscular dystrophy (FSHD) is a rare, progressive genetic disorder characterized by asymmetric muscle weakness and functional decline. Although it is one of the most common muscular dystrophies, its economic burden in the United States (US) is largely unknown. This study aimed to provide an initial, conservative estimate of annual medical claims costs and identify comorbidities disproportionately affecting individuals with FSHD in the US. Patients and Methods: This retrospective, 1:5 matched case-control study analyzed de-identified claims data from Medicare and commercially insured enrollees from 2018 to 2021. Medical and prescription costs were aggregated and described as means with 95% confidence intervals. Results: The study included 383 individuals with FSHD and 1915 matched controls. The mean annual medical claims cost for the FSHD cohort was $19,370 per person with commercial insurance and $11,704 with Medicare, compared with $5250 among controls. Individuals with FSHD also incurred higher prescription claims costs in commercial and Medicare subgroups without comorbidities. The prevalence of cerebrovascular disease (10.18% vs 4.44%) and ear disorders (8.09% vs. 3.39%) was significantly greater in the FSHD cohort ( Conclusion: This exploratory study provides the first US-based description of the direct medical costs of FSHD, demonstrating a substantially higher healthcare burden than that of matched controls. Because the study design likely underestimates costs, the true economic impact may be even greater. These findings establish a critical foundation for future research into the lifetime medical, nonmedical, and caregiver-related costs of FSHD, and highlight the urgent need for effective therapies and supportive care strategies.

Indexed as

cost of illnessdirect costeconomic burdenFSHDHEORmuscular dystrophy

Identifiers

PMID42325276
PMCPMC13282961

What Socratic holds

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LicenceCC BY-NC
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.