Different Scenarios of Providing Drugs for Patients with Primary Immunodeficiency in Russia: Analysis of Costs and Effectiveness

Tatyana Sergeevna Teptsova, V. K. Fedyaeva, A. V. Nikitina
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Abstract

The only source of financing for immunoglobulin replacement therapy needed by patients with primary immunodeficiencies (PID) in Russian Federation is the compulsory health insurance system: payment is based on diagnosis-related groups (DRG), including the DRG for immunoglobulin treatment at day care and inpatient setting. PID are not included either into regional program for rare diseases, or into federal program of 12 high-cost diseases. This leads to limited coverage of patients with effective drug treatment. Furthermore, currently in Russian Federation there is no neonatal screening for PID, which could facilitate early detection of the disease and timely start of treatment. Goal of the study: to conduct the analysis of cost and effectiveness of different scenarios of drug provision for the patients with PID, which differ in coverage of patients with therapy and by presence/absence of neonatal screening. Materials and methods. The model compared three scenarios of drug provision for patients with PID: a) current practice, when in accordance with available data not all patients get necessary immunoglobulin replacement therapy, b) new scenario 1 – financing of drugs for all registered patients with PID when large-scale neonatal screening for PID is absent; c) new scenario 2 – financing of drugs for all registered patients with PID when large-scale neonatal screening is implemented. In each scenario direct medical costs and number of prevented deaths was calculated. Comparison of scenarios was planned to be made by calculation of additional costs per prevented death due to PID, or by assessment of difference of costs and effectiveness (number of prevented deaths) with identification of a dominant scenario. Results. Both new scenarios including financing of drugs for all registered patients with PID lead to the prevention of significant number of deaths and also to cost savings if compared with current practice. Total costs for current, 1st new and 2nd new scenario for 15 year was^ 2 285,54, 616,49 and 1 318,61 billions of rubles respectively. Also when comparing 1st and 2nd new scenarios with current practice we expect prevention of 243 and 2076 deaths respectively. Conclusion. Most effective approach is the introduction of large-scale neonatal screening for PID combined with the new source of financing: this scenario saves less money, but helps to prevent highest number of deaths compared with current practice. This scenario can prevent deaths of patients who would not have been diagnosed with PID in the absence of screening, and also helps to save healthcare system budget by centralization of government procurement of drugs.
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为俄罗斯原发性免疫缺陷患者提供药物的不同方案:成本和效果分析
俄罗斯联邦原发性免疫缺陷(PID)患者所需的免疫球蛋白替代疗法的唯一资金来源是强制性健康保险制度:支付基于与诊断相关的组(DRG),包括在日托和住院环境中用于免疫球蛋白治疗的DRG。PID既不包括在罕见病的区域计划中,也不包括在12种高成本疾病的联邦计划中。这导致获得有效药物治疗的患者覆盖面有限。此外,目前在俄罗斯联邦没有新生儿PID筛查,这可能有助于早期发现该疾病并及时开始治疗。本研究的目的:分析不同情况下为PID患者提供药物的成本和效果,这些情况在接受治疗的患者覆盖率和是否进行新生儿筛查方面存在差异。材料和方法。该模型比较了为PID患者提供药物的三种情况:a)目前的做法,根据现有数据,并非所有患者都得到了必要的免疫球蛋白替代治疗;b)新的情况1 -在没有大规模新生儿PID筛查的情况下,为所有注册的PID患者提供药物融资;c)新情景2 -在实施大规模新生儿筛查时,为所有登记的PID患者提供药物资助。在每种情况下,都计算了直接医疗费用和预防死亡人数。计划通过计算PID导致的每个预防死亡的额外成本,或通过评估成本和有效性的差异(预防死亡的数量)来进行情景比较,并确定一个主要情景。与目前的做法相比,这两种新方案(包括为所有登记的PID患者提供药物资助)都可以预防大量死亡,并节省成本。当前、第一个新方案和第二个新方案15年的总成本分别为2 285、54、616、49和1 318 610亿卢布。此外,当比较第一和第二种新情况与目前的做法时,我们预计分别预防243和2076人死亡。最有效的方法是引入大规模的新生儿PID筛查,并结合新的资金来源:与目前的做法相比,这种方案节省的资金较少,但有助于防止最高数量的死亡。这种情况可以防止在没有筛查的情况下不会被诊断为PID的患者死亡,也有助于通过集中政府采购药物节省医疗保健系统的预算。
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