Aeglea BioTherapeutics Inc, Austin, TX, USA.
IQVIA, Inc, Falls Church, VA, USA.
J Med Econ. 2022 Jan-Dec;25(1):848-856. doi: 10.1080/13696998.2022.2089517.
Arginase 1 Deficiency (ARG1-D) is an inherited metabolic disease that leads to significant morbidity.
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.
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.
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).
A relatively short study period while the burden of ARG1-D increases over a lifetime due to disease progression.
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.
精氨酸酶 1 缺乏症(ARG1-D)是一种遗传性代谢疾病,可导致严重的发病率。
尽管该疾病的负担已得到公认,但缺乏关于 ARG1-D 患者医疗保健资源利用(HCRU)的信息。因此,我们旨在评估 ARG1-D 患者的 HCRU 相对于非 ARG1-D 队列。
使用专业费用索赔与处方索赔相关联,通过≥2 个 ARG1-D 的 ICD-10-CM 诊断代码识别患者(第一个诊断代码=索引日期)。将 ARG1-D 患者与患有其他医疗条件的对照组患者 1:1 匹配。匹配变量包括年龄、性别、索引年份、支付方类型(医疗保险、医疗补助、第三方)和地理位置。
共有 77 名患者符合 ARG1-D 队列的纳入标准,中位年龄为 15 岁,52%<18 岁,52%为男性。与匹配的对照组相比,ARG1-D 队列中记录了更高频率的几种并发诊断(痉挛高 7 倍;发育迟缓高 2 倍;智力残疾高 5 倍;癫痫发作高 8 倍)。急诊就诊频率高两倍,实验室检查次数多 1.5 倍,住院需求高 3 倍,ARG1-D 患者的平均住院时间比对照组长(2.4 天比 0.3 天)。
由于疾病进展,ARG1-D 的负担随着时间的推移而增加,而研究时间相对较短。
与没有该疾病的患者相比,ARG1-D 患者的 HCRU 明显更高;他们表现出更广泛的合并症特征,更频繁地使用医疗保健系统,需要更密集的监测和管理,并且与对照组相比,住院频率更高,住院时间更长。这些发现表明 ARG1-D 患者的健康负担很高,标准治疗措施无法缓解,强调需要改善治疗选择。