Health care resource utilization in the management of patients with Arginase 1 Deficiency in the US: a retrospective,

Aseel Bin Sawad1, John Jackimiec1, Mark Bechter1

  • 1Aeglea BioTherapeutics Inc, Austin, TX, USA.

Insights

Arginase 1 Deficiency (ARG1-D) patients experience higher healthcare use and more comorbidities than those without the condition. This highlights a significant disease burden and the need for better ARG1-D treatments.

Area of Science:

  • Metabolic Disorders
  • Genetics
  • Healthcare Research

Background:

  • Arginase 1 Deficiency (ARG1-D) is a serious inherited metabolic disorder.
  • The full impact of ARG1-D on healthcare resource utilization (HCRU) is not well understood.

Purpose of the Study:

  • To compare HCRU in patients with ARG1-D against a matched cohort without the condition.
  • To identify the specific healthcare needs and burdens associated with ARG1-D.

Main Methods:

  • Utilized professional fee and prescription claims data to identify patients with ARG1-D (≥2 ICD-10-CM codes).
  • Matched ARG1-D patients 1:1 with a control cohort based on age, sex, index year, payer, and region.
  • Analyzed differences in comorbidities, emergency room visits, laboratory tests, and hospitalizations.

Main Results:

  • The ARG1-D cohort (77 patients) showed significantly higher rates of spasticity, developmental delay, intellectual disability, and seizures.
  • Patients with ARG1-D had twice as many ER visits, 1.5 times more lab tests, and 3 times more hospitalizations.
  • Hospital stays for ARG1-D patients were longer (2.4 days vs. 0.3 days).

Conclusions:

  • Patients with ARG1-D exhibit substantially greater HCRU and a more complex comorbidity profile.
  • The findings underscore the high health burden of ARG1-D, indicating current standard care is insufficient.
  • There is a clear need for enhanced treatment strategies for Arginase 1 Deficiency.
Abstract

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