Analysis Group Inc., Boston, MA, USA.
Mallinckrodt Pharmaceuticals, Bedminster Township, NJ, USA.
Curr Med Res Opin. 2021 Mar;37(3):431-441. doi: 10.1080/03007995.2021.1872515. Epub 2021 Feb 2.
Repository corticotropin injection (RCI; Acthar Gel) is indicated to induce a diuresis or a remission of proteinuria in nephrotic syndrome (NS) without uremia of the idiopathic type or that due to lupus erythematosus. This study compares patient characteristics and measurable healthcare resource utilization (HCRU) between NS patients who received a prescription for RCI and then were either approved or denied treatment by their insurers.
A retrospective analysis of adults with NS from January 2015 to December 2018 was conducted using a de-identified open-source claims database. Patients were included in the study if they had ≥1diagnosis associated with NS, were age 18+, and had medical claims activity at some point in the year preceding ("baseline") and year following ("follow up") their first approved or denied RCI prescription. Baseline characteristics were reported with p-values indicating the significance of characteristics between cohorts. To assess outcomes, approved and denied patients were matched (1:1) using propensity-matching to account for underlying differences.
Overall, 1,232 patients met inclusion criteria for the study. At baseline, approved patients were older than denied patients (mean age 53.9 vs. 48.4) and had higher rates of comorbidities. A greater proportion of approved patients required inpatient admissions (34.1 vs. 28.0%) and "high" doses of corticosteroids (CS) (26.2 vs. 20.7%) at baseline. Matched outcomes showed directionally more denied patients with inpatient admissions compared to approved (64 vs. 52) and a greater utilization of deep vein thrombosis ultrasound (12.2 vs. 6.6%) and dialysis (10.5 vs. 6.1%). Matched, denied patients had directionally greater CS use during follow-up both in the number of patients receiving CS (104 vs. 95) and the average annualized daily dose (4.1 vs. 3.4 mg).
Patients denied access to RCI treatment had directionally higher HCRU compared to matched, approved counterparts. Thus, the results of this study may aid providers and payers in evaluating scenarios where RCI may be beneficial and improve quality of care for NS patients.
储存促皮质素注射(RCI;Acthar Gel)用于诱导特发性肾病综合征(NS)或狼疮性肾病综合征的利尿或蛋白尿缓解,而无尿毒症。本研究比较了接受 RCI 处方后,保险公司批准或拒绝治疗的 NS 患者的患者特征和可衡量的医疗保健资源利用(HCRU)。
使用去识别的开源索赔数据库,对 2015 年 1 月至 2018 年 12 月的成年人进行了回顾性分析。如果患者有≥1 个与 NS 相关的诊断,年龄≥18 岁,并且在他们首次批准或拒绝 RCI 处方之前(“基线”)和之后(“随访”)的一年中都有医疗索赔活动,则将患者纳入研究。报告了基线特征,并使用 p 值表示特征在队列之间的差异的显著性。为了评估结果,批准和拒绝的患者使用倾向匹配(1:1)进行匹配,以说明潜在差异。
总体而言,1232 名患者符合研究标准。在基线时,批准的患者比拒绝的患者年龄更大(平均年龄 53.9 岁 vs. 48.4 岁),合并症发生率更高。更多批准的患者需要住院治疗(34.1% vs. 28.0%)和基线时接受“高”剂量皮质类固醇(CS)(26.2% vs. 20.7%)。匹配结果显示,与批准的患者相比,更多的拒绝患者住院治疗(64 名 vs. 52 名),并且更多地使用深静脉血栓形成超声(12.2% vs. 6.6%)和透析(10.5% vs. 6.1%)。匹配后,与批准的患者相比,拒绝患者在接受 CS 的患者数量(104 名 vs. 95 名)和平均年化日剂量(4.1 毫克 vs. 3.4 毫克)方面均表现出更高的 CS 使用量。
与匹配的批准患者相比,被拒绝使用 RCI 治疗的患者的 HCRU 方向更高。因此,这项研究的结果可能有助于提供者和付款人评估 RCI 可能有益的情况,并提高 NS 患者的护理质量。