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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.
Background:
Arginase 1 Deficiency (ARG1-D) is an inherited metabolic disease that leads to significant morbidity.
Aims:
Despite the recognized burden of disease, information on health care resource utilization (HCRU) among patients with ARG1-D is lacking. We, therefore, sought to evaluate HCRU in ARG1-D relative to non-ARG1-D cohort.
Materials And Methods:
Patients with ≥2 ICD-10-CM diagnosis codes for ARG1-D were identified (first diagnosis code = index date) using professional fee claims linked with prescription claims. Patients with ARG1-D were matched 1:1 to a comparator cohort of patients with other medical conditions. Matching variables included age, sex, index year, payer type (Medicare, Medicaid, third party) and geographic region.
Results:
A total of 77 patients met the inclusion criteria for the ARG1-D cohort, with a median age of 15 years, 52% <18 years, and 52% male. Several concurrent diagnoses were recorded at a higher frequency in the ARG1-D cohort versus the matched comparator (spasticity 7 times higher; developmental delay ∼2 times higher; intellectual disability 5 times higher; and seizures 8 times higher). Emergency room visits occurred twice as often, laboratory tests were performed 1.5 times more often, hospitalization was required 3 times more often, and mean length of stay was longer for patients with ARG1-D than the comparator cohort (2.4 days vs. 0.3 days).
Limitations:
A relatively short study period while the burden of ARG1-D increases over a lifetime due to disease progression.
Conclusions:
Patients with ARG1-D had significantly greater HCRU compared with those without the disease; they presented with a more extensive comorbidity profile, accessed the health care system more frequently, required more intense monitoring and management, and had more frequent and longer hospitalizations relative to the comparator group. These findings demonstrate a high health burden in ARG1-D that is not mitigated by standard-of-care measures and emphasize the need for improved treatment options.
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