Glycogen Storage Disease Type Ia: A Retrospective Claims Analysis of Complications, Resource Utilization, and Cost of Care.

IF 2.3 Q2 ECONOMICS Journal of Health Economics and Outcomes Research Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI:10.36469/001c.125886
Eliza Kruger, Justin Nedzesky, Nina Thomas, Jeffrey D Dunn, Andrew A Grimm
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Abstract

Background: Glycogen storage disease type Ia (GSDIa) is a rare inherited disorder resulting in potentially life-threatening hypoglycemia, metabolic abnormalities, and complications often requiring hospitalization. Objective: This retrospective database analysis assessed the complications, resource utilization, and costs in a large cohort of patients with GSDIa. Methods: We conducted a retrospective cohort study of GSDIa patients and matched non-GSDIa comparators utilizing the PharMetrics® Plus database. International Classification of Diseases, Tenth Revision (ICD-10) diagnosis codes in any billing position for inpatient and outpatient claims (January 2016-February 2020) were identified for complications related to GSDIa. Healthcare use and costs were assessed by setting of care (inpatient, outpatient, physician office, emergency department, and pharmacy). Results: Overall, 557 patients with GSDIa and 5570 matched comparators (male, 63%; adults, 67%) were identified. The most frequent complications in patients with GSDIa vs comparators included anemia due to enzyme disorders (odds ratio, 4.0 × 103; 95% confidence interval, 555.9-2.8 × 104), hepatocellular adenoma (305.9; 41.6-2.2 × 104), liver transplantation (164.6; 21.8-1.2 × 103), and gastrostomy (152.2; 61.1-379.2), as well as acidosis (45.5; 29.4-70.3), hepatomegaly (43.6; 29.1-65.3), hyperuricemia (23.6; 11.9-46.9), and hypoglycemia (20.2; 14.3-28.7). Chronic complications (eg, gout, osteoarthritis, chronic kidney disease, and neoplasms) were more common in adults with GSDIa, whereas acute complications (eg, poor growth, gastrostomy, seizure, and hypoglycemia) were more common in children with GSDIa. Patients with GSDIa more often required hospitalization (0.53 vs 0.06 hospitalizations per patient per year) vs comparators, including 2 or more hospitalizations (26.6% vs 2.3%), longer length of stay (3.1 vs 0.4 days), and more annual visits in all care settings, including 4.3 times more visits in the emergency department. Mean annual total healthcare costs were higher for GSDIa patients vs comparators ( 33 910 v s 4410). Discussion: In this large, retrospective database analysis, complications observed among patients with GSDIa were consistent with prior reports and demonstrate the chronic and progressive nature of the disease. Resource utilization was substantial in GSDIa patients, and mean annual total healthcare costs were almost 8 times higher than those of comparators. Conclusions: GSDIa is associated with numerous potentially serious and sometimes fatal complications, extensive resource utilization, and high management costs.

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糖原储存病Ia型:并发症、资源利用和护理费用的回顾性索赔分析。
背景:Ia型糖原储存病(GSDIa)是一种罕见的遗传性疾病,可导致潜在危及生命的低血糖、代谢异常和并发症,通常需要住院治疗。目的:本回顾性数据库分析评估了大队列GSDIa患者的并发症、资源利用和成本。方法:我们利用PharMetrics®Plus数据库对GSDIa患者和匹配的非GSDIa比较者进行了回顾性队列研究。国际疾病分类第十版(ICD-10)诊断代码在住院和门诊索赔的任何计费位置(2016年1月至2020年2月)被确定为与GSDIa相关的并发症。通过护理设置(住院、门诊、医生办公室、急诊科和药房)评估医疗保健使用和成本。结果:总体而言,557例GSDIa患者和5570例匹配的比较者(男性,63%;成人(67%)。与比较组相比,GSDIa患者最常见的并发症包括酶紊乱引起的贫血(优势比,4.0 × 103;95%可信区间,555.9-2.8 × 104),肝细胞腺瘤(305.9;41.6-2.2 × 104),肝移植(164.6;21.8-1.2 × 103),胃造口术(152.2;61.1-379.2),以及酸中毒(45.5;29.4-70.3),肝肿大(43.6;29.1-65.3),高尿酸血症(23.6;11.9-46.9),低血糖(20.2;14.3 - -28.7)。慢性并发症(如痛风、骨关节炎、慢性肾脏疾病和肿瘤)在成人GSDIa患者中更为常见,而急性并发症(如生长不良、胃造口术、癫痫发作和低血糖)在儿童GSDIa患者中更为常见。与比较组相比,GSDIa患者更经常需要住院治疗(每名患者每年0.53次对0.06次住院),包括2次或更多的住院治疗(26.6%对2.3%),更长的住院时间(3.1对0.4天),以及在所有护理机构中更多的年度就诊次数,包括急诊就诊次数的4.3倍。GSDIa患者的平均年总医疗费用高于比较组(33910 vs 4410)。讨论:在这个大型的回顾性数据库分析中,GSDIa患者中观察到的并发症与先前的报道一致,并证明了该疾病的慢性和进行性。GSDIa患者的资源利用率很高,平均年总医疗费用几乎是比较国的8倍。结论:GSDIa与许多潜在的严重甚至致命的并发症、广泛的资源利用和高管理成本有关。
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10 weeks
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