(289) Economic burden of macrophage activation syndrome (MAS) in patients with Still’s disease (systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD)): analysis of a US national administrative claims database

Background: : Macrophage activation syndrome (MAS), a form of secondary hemophagocytic lymphohistiocytosis, occurs most frequently in patients with Still’s disease (systemic juvenile idiopathic arthritis (sJIA) or adult-onset Still’s disease (AOSD)). MAS may progress to multiple organ failure and mortality. However, there is currently no FDA approved therapy for MAS and corticosteroids remain the mainstay of treatment.

Objective: : To assess the economic burden of MAS in patients with Still’s disease.

Methods: : A retrospective claims-based analysis (IQVIA PharMetrics Plus) from 2019 to 2024 was used to identify: Patients with Still’s disease ([(ICD-10:M082) including AOSD (ICD-10:M061) and sJIA (ICD-10:M08)]) with ≥6 months of continuous enrolment prior to Still’s diagnosis (index date) and ≥12 months of continuous enrolment post-index without MAS (ICD-10:D76.1); and patients with Still’s disease with ≥6 months of continuous enrolment prior to earliest MAS diagnosis observed in the study period and ≥12 months of continuous enrolment post-MAS diagnosis. Patients were matched (1:1) using a propensity score. All-cause HCRU (inpatient [IP] admission, emergency room [ER] visits, and outpatient [OP] visits) and costs (all-cause and rheumatologic; adjusted to 2024 US dollars) were ascertained in the post-index period.

Results: : After matching, 45 patients with Still’s and 45 patients with Still’s and MAS were included (mean [SD] age, 26.8 [15.1] and 26.8 [16.0] years at Still’s diagnosis, respectively; female, 55.6% and 60.0%, respectively). Mean (SD) Elixhauser Comorbidity Index was 1.6 (1.5) and 2.1 (2.8) and the most common comorbidities were rheumatoid arthritis (48.9% and 42.2%) and cardiac arrythmia (13.3% and 22.2%) in patients with Still’s with and without MAS, respectively. Patients with MAS were significantly more likely to have an ER visit (P=0.04) and/or IP admission (P < 0.001) than patients without MAS in the 12-month post-index period. They also had significantly more frequent IP admissions (P < 0.001), ER visits (P < 0.001), OP visits (P= < 0.001), and longer IP stays (P < 0.001) than patients without MAS. In addition, patients with MAS incurred significantly (P=0.008) higher total all-cause ($318,828 vs $19,233) and rheumatologic-related ($163,099 vs $1,930) healthcare costs (P=0.02) than patients without MAS.

Conclusions: : Patients with Still’s and MAS incurred significantly higher HCRU and costs compared with patients without MAS. Therapies targeting MAS may reduce the overall burden of disease to patients and the healthcare system.

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