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预先授权延迟了生物制剂的使用,并与哮喘恶化的风险相关。

Prior authorization delays biologic initiation and is associated with a risk of asthma exacerbations.

机构信息

From the Department of Kinesiology, Penn State University, University Park, Pennsylvania; and.

Department of Allergy and Sleep Medicine, Mount Nittany Physician Group, State College, Pennsylvania.

出版信息

Allergy Asthma Proc. 2021 Jan 1;42(1):65-71. doi: 10.2500/aap.2021.42.200101.

Abstract

Biologics are effective treatments for patients with severe allergic disease. Impacts of delays in the prior authorization process on clinical outcomes has not been studied. The objective was to quantify the times for approval and filling of biologics, and whether patients were at risk of exacerbations during this time frame. The times for insurance approval and pharmacy filling of biologics (omalizumab, benralizumab, mepolizumab, dupilumab) in 80 subjects with severe asthma (n = 60) or urticaria (n = 20) from our clinic were reviewed. We compared the impact of clinical features, insurance, specialty pharmacy on fill times, and quantified exacerbations and prednisone use while awaiting biologic initiation. The mean ± standard deviation (SD) time (days) from submission of a prescription to the first dose available for injection was 44.0 ± 23.2 days. This was composed of the mean ± SD time for insurance approval (21.5 ± 19.6 days) and the mean ± SD time for a specialty pharmacy to fill the medication (22.8 ± 14.1 days). There was no significant difference between the times for diagnosis (asthma versus urticaria), specific biologic, or insurance. The "buy and bill" system was faster than filling via a specialty pharmacy (mean ± SD, 7.3 ± 8.5 days versus 23.3 ± 21.3 days, respectively, p < 0.001). Clinical features of patients with fast versus slow approval times was not significantly different. The subjects with asthma were at high risk of exacerbations and need for prednisone while awaiting initiation of the biologics; 28 of 59 patients (47%) required prednisone, with an mean cumulative dose of 483.2 ± 273.7 mg per person. The prior authorization process for biologics was slow, and the subjects were at high risk of exacerbations during this time. The system needs to be improved to expedite approval and initiation of these medications.

摘要

生物制剂是治疗严重过敏疾病患者的有效方法。先前授权过程延迟对临床结果的影响尚未得到研究。目的是量化生物制剂批准和配药的时间,以及在此期间患者是否有恶化的风险。我们回顾了来自我们诊所的 80 名严重哮喘(n = 60)或荨麻疹(n = 20)患者的生物制剂(奥马珠单抗、贝那鲁单抗、美泊利单抗、度普利尤单抗)的保险批准和药房配药时间。我们比较了临床特征、保险、专科药房对配药时间的影响,并量化了在等待生物制剂开始时的恶化和泼尼松使用情况。从提交处方到可注射的第一剂可用的平均(±标准偏差[SD])时间为 44.0 ± 23.2 天。这由保险批准的平均(21.5 ± 19.6 天)和专科药房配药的平均(22.8 ± 14.1 天)组成。诊断(哮喘与荨麻疹)、特定生物制剂或保险之间的时间没有显著差异。“先买后付”系统比通过专科药房配药更快(平均 ± SD,分别为 7.3 ± 8.5 天和 23.3 ± 21.3 天,p <0.001)。快速和慢速审批时间的患者的临床特征没有显著差异。等待生物制剂开始时,哮喘患者有发生恶化和需要泼尼松的高风险;59 名患者中有 28 名(47%)需要泼尼松,每人平均累积剂量为 483.2 ± 273.7mg。生物制剂的先前授权过程缓慢,在此期间患者有发生恶化的高风险。需要改进该系统以加快这些药物的批准和启动。

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