Real-World Clinical and Healthcare Resource Burden Among Burosumab-Naïve Patients With Familial Hypophosphatemia.

IF 3 Q2 ENDOCRINOLOGY & METABOLISM Journal of the Endocrine Society Pub Date : 2024-10-24 eCollection Date: 2024-10-29 DOI:10.1210/jendso/bvae185
Erik A Imel, Zhiyi Li, Heather M Heerssen, Nicole Princic, Hana Schwartz, Yang Zhao, Kathryn M Dahir
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Abstract

Objective: To examine the real-world clinical and healthcare resource burden of familial hypophosphatemia (FH).

Methods: In a retrospective, observational cohort study using MarketScan claims data from 2017 to 2021, clinical characteristics and healthcare resource utilization (HCRU) and costs were compared between burosumab-naïve pediatric and adult patients with ≥ 1 FH diagnosis code and matched controls without FH. Patient characteristics were evaluated at baseline, and disease characteristics, HCRU, and costs were evaluated over a 12-month follow-up period. Outcomes were analyzed descriptively. Costs were additionally analyzed using multivariate regression models.

Results: Overall, 570 patients with FH and 1710 non-FH matched controls were included. Approximately 10% of study participants were aged < 18 years. Patients with FH had 7.8-fold higher mean baseline comorbidity (Charlson Comorbidity Index). The prevalence of morbidities over the 12-month follow-up period was higher in patients with FH than controls, including renal disease (33% vs 3%), arthralgia (25% vs 10%), osteoarthritis (17% vs 6%), and delayed growth/walking difficulty (16% vs 2%; all P < .001). All-cause HCRU was significantly greater for patients with FH than controls over follow-up, including the proportion of patients with at least one inpatient admission (60% vs 4%), outpatient emergency room visit (52% vs 16%), and outpatient pharmacy prescription (96% vs 71%; all P < .001). The mean annual total healthcare cost per patient was also 22.6-fold higher for patients with FH than controls (adjusted cost difference = $129 643; P < .001). Differences were apparent across all age groups.

Conclusion: Compared with non-FH matched controls, burosumab-naïve patients with FH experienced multiple morbidities and had substantially higher HCRU and costs.

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家族性低磷酸盐血症患者中布罗索单抗无效患者的实际临床和医疗资源负担。
目的:研究家族性低磷血症(FH)在现实世界中的临床和医疗资源负担:研究家族性低磷血症(FH)在现实世界中的临床和医疗资源负担:在一项使用 2017 年至 2021 年 MarketScan 索偿数据的回顾性观察队列研究中,对布罗索单抗无效且≥ 1 个 FH 诊断代码的儿童和成人患者与无 FH 的匹配对照组的临床特征、医疗资源利用率(HCRU)和费用进行了比较。基线时评估患者特征,随访 12 个月后评估疾病特征、HCRU 和费用。对结果进行了描述性分析。此外,还使用多变量回归模型对费用进行了分析:总共纳入了 570 名 FH 患者和 1710 名非 FH 匹配对照。约 10% 的研究参与者为老年人(P < .001)。在随访期间,FH 患者的全因 HCRU 明显高于对照组,包括至少有一次住院(60% 对 4%)、门诊急诊就诊(52% 对 16%)和门诊药房处方(96% 对 71%;均 P < .001)的患者比例。FH患者每人每年的平均医疗总费用也比对照组高出22.6倍(调整后的费用差异=129 643美元;P < .001)。所有年龄组的差异都很明显:结论:与非 FH 匹配的对照组相比,布鲁索单抗无效的 FH 患者会出现多种疾病,HCRU 和费用也会大幅增加。
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来源期刊
Journal of the Endocrine Society
Journal of the Endocrine Society Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.50
自引率
0.00%
发文量
2039
审稿时长
9 weeks
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