National Jewish Health, Denver, CO, USA.
Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, USA.
Adv Ther. 2022 Apr;39(4):1794-1809. doi: 10.1007/s12325-022-02066-9. Epub 2022 Feb 23.
We aimed to describe healthcare resource utilization (HCRU) patterns and costs in patients with fibrosing interstitial lung disease (ILD) and those with a progressive phenotype of fibrosing ILD in a US claims database.
Data from the IBM MarketScan databases (1 October 2011-30 September 2015) were used. Diagnosis codes documented on medical claims on two occasions (without any claims during the 12 months prior) identified patients with incident fibrosing ILD. Patients with chronic fibrosing ILD with a progressive phenotype were identified by proxies for progression. Patients aged ≥ 18 years with 365 days of continuous coverage before the index date were eligible for inclusion. Data were analyzed for 12 months prior to identification of fibrosing ILD/progressive phenotype (baseline) and 12 months after (follow-up). Outcomes included treatment patterns, outpatient and inpatient claims, and costs.
We identified 23,577 patients with incident fibrosing ILD and 14,722 with the progressive phenotype. Follow-up data were available for 9986 and 5840 patients, respectively. The most frequent ILD-related medications during baseline were corticosteroids (49.4% and 56.6%). Mean (± standard deviation [SD]) annualized number of outpatient claims was 30.0 (± 26.4) and 34.1 (± 27.7) in the baseline period and 36.2 (± 28.6) and 41.9 (± 30.2) in the follow-up in fibrosing ILD and with a progressive phenotype, respectively. Mean (SD) number of all-cause hospitalizations was 0.5 (± 1.1) and 0.7 (± 1.2) during baseline and 0.6 (± 1.1) and 0.7 (± 1.2) during follow-up. Mean (SD) total costs were $40,907 (± 92,496) and $49,561 (± 98,647) during baseline and $46,157 (± 102,858) and $54,215 (± 116,833) during follow-up. Inpatient mortality during follow-up was 53.50 and 77.44 per 1000 patient-years.
HCRU and costs were high in patients with chronic fibrosing ILD with a progressive phenotype, likely reflecting the disease severity and the need for close monitoring and acute care. Outpatient claims accounted for a substantial proportion of the total costs.
本研究旨在描述美国索赔数据库中纤维化间质性肺病(ILD)患者和具有进行性纤维化 ILD 表型患者的医疗资源利用(HCRU)模式和费用。
使用 IBM MarketScan 数据库(2011 年 10 月 1 日至 2015 年 9 月 30 日)的数据。两次医疗索赔中记录的诊断代码(在 12 个月内没有任何索赔)确定了纤维化 ILD 的新发患者。通过进行性的替代指标来识别患有慢性纤维化 ILD 且具有进行性表型的患者。索引日期前 365 天连续覆盖≥18 岁的患者符合纳入标准。在确定纤维化 ILD/进行性表型前 12 个月(基线)和后 12 个月(随访)分析数据。结果包括治疗模式、门诊和住院费用。
本研究共纳入了 23577 例纤维化 ILD 新发患者和 14722 例具有进行性表型的患者。分别有 9986 例和 5840 例患者有随访数据。基线期最常见的 ILD 相关药物是皮质类固醇(49.4%和 56.6%)。纤维化 ILD 患者和具有进行性表型的患者基线期平均(±标准偏差 [SD])年化门诊就诊次数分别为 30.0(±26.4)和 34.1(±27.7),随访期分别为 36.2(±28.6)和 41.9(±30.2)。全因住院人数的平均(SD)分别为 0.5(±1.1)和 0.7(±1.2),随访期分别为 0.6(±1.1)和 0.7(±1.2)。平均(SD)总费用分别为 40907(±92496)和 49561(±98647),随访期分别为 46157(±102858)和 54215(±116833)。随访期间的住院死亡率为每 1000 患者年 53.50 和 77.44。
具有进行性纤维化 ILD 表型的慢性纤维化 ILD 患者的 HCRU 和费用很高,这可能反映了疾病的严重程度以及对密切监测和急性治疗的需求。门诊就诊占总费用的很大一部分。