Investigators utilized administrative claims data from IBM MarketScan Medicaid and Commercial Claims and Encounters Research Databases (2013-2018). In this retrospective cohort study, researchers included male patients aged between 1 and 18 years with an International Classification of Diseases (ICD)-9/10 diagnosis code for hereditary progressive muscular dystrophy between January 1, 2013, and December 31, 2017. The patients were stratified into 3 age cohorts:1-6 years (n = 347), 7-12 years (n = 502), and 13-18 years (n = 537). The primary outcome was the rate of annual neurology visits, and the secondary outcomes were annual follow-up rates in other subspecialties and proportion of days covered (PDC) by corticosteroids.
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Top Clinical Takeaways
- Neurology visit rates remain consistently low throughout childhood for patients with DBMD, potentially limiting access to comprehensive care.
- Medicaid insurance is significantly associated with lower likelihoods of annual neurology follow-up among pediatric DBMD patients.
- Despite advancements in therapies like exon-skipping treatments, a substantial portion of patients do not receive optimal care because of infrequent subspecialty follow-up.
“While cardiology and pulmonary follow-up increased with patient age, in parallel with an increased rate of heart and respiratory failure in older patients, overall rates of follow-up with subspecialists were low, with only a quarter of patients regularly accessing annual subspecialty care, “ Matesanz, who also serves as an assistant professor of clinical neurology at University of Pennsylvania Perelman School of Medicine, and colleagues noted.1 “Reasons for low subspecialty follow-up rates are likely multifactorial. The fact that neurology visits do not significantly change over time, whereas other specialty visits like cardiology and pulmonology increase with age and disease severity, may be due to lack of perceived benefit of neurology visits, or the gap between the need for neurologic services and the availability of practicing neurologists.”
Further results revealed that corticosteroid use was low; only 7.1% of person-years (345/4829) had a PDC of at least 80%, and 30% (1452 of4829) had a PDC of at least 20%. Among the cohort of patients aged 1–6 years, 2.8% of person-years (23 of 837) had PDC of at least 80% for corticosteroids, and 24.4% (204 of 837) had a PDC of at least 20%. In the 7–12 and 13–18 years cohorts, 7.9% (153 of1934) and 8.2% (169 of2058) of person-years had PDC of at least 80%, and 35.7% (690 of1934) and 27.1% (558 of 2058) had a PDC of at least 20%, respectively.
Although efforts were made to include only those with a likely DBMD diagnosis, some patients with alternative diagnoses may have been present in the cohort, which could have potentially influenced the observed rates. Authors also noted that the care guidelines primarily apply to DMD, not BMD, so the inclusion of patients with BMD may have also impacted outcomes. The lack of a specific ICD-10 code for DBMD before 2018 and differences in coding practices may have led to missed visits, according to the authors. Additionally, the study could not fully investigate the impact of race and region because of differences in available data between MarketScan Commercial and Medicaid databases. Finally, the databases only contained information for claims submitted, potentially missing some comorbidities and over-the-counter medications.
REFERENCES
1. Matesanz SE, Edelson JB, Iacobellis KA, et al. Subspecialty Health Care Utilization in Pediatric Patients With Muscular Dystrophy in the United States. Neurol Clin Pract. 2024;14(4):e200312. doi:10.1212/CPJ.0000000000200312