Clinical and economic assessment of feasibility of using quadritherapy in patients with reduced ejection fraction chronic heart failure in medical organizations of the Moscow Region

Q3 Medicine
A. D. Ermolaeva, T. N. Ermolaeva, K. A. Kokushkin
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Abstract

Objective: assessment of feasibility of using four-component drug therapy for patients with chronic heart failure with reduced ejection fraction (CHFrEF) in medical organizations of the Moscow Region (MR). Material and methods. Clinical and economic analysis of combined standard therapy with angiotensin-converting enzyme inhibitors, beta-blockers, and mineralocorticoid-receptor antagonists in combination with dapagliflozin (a sodium-glucose cotransporter 2) in the treatment of patients with CHFrEF was carried out. The effectiveness criteria were the number of prevented cardiovascular (CV) deaths and the percentage of the contribution to the achievement of the target indicator to reduce mortality from circulatory diseases within the framework of the regional program “Health care development”. In order to determine the economic feasibility of quadritherapy, direct medical costs for the implemented technology were calculated, the cost of one prevented CV death was determined based on the values of the number needed to treat (NNT) indicator. Budget impact analysis was performed which allowed to build two analytical models. Results . It was shown that the use of quadritherapy can significantly contribute to achieving the target indicator by additionally preventing 512 CV deaths by 2024, which will make it possible to fulfill up to 74.74% of the indicator set by the MR state program “Health care of the Moscow Region” (451.4 persons per 100 thousand population). Using quadruple therapy in 1000 target patients during the first year will prevent 11 CV deaths (NNT 90 persons). The cost of one prevented CV death was 3.860 million rubles. The budget impact analysis made it possible to determine that when CHF patients switch from standard treatment regimens to quadritherapy, including in combination with a drug of the angiotensin/neprilysin receptor inhibitor group (valsartan + sacubitril), this will entail an increase in healthcare system budget costs by 18.8%. Conclusion. The results demonstrate that the standard therapy in combination with the innovative drug dapagliflozin leads to a proven reduction in mortality from circulatory diseases. This technology is a cost-effective approach to organizing medical care for adult patients with CHFrEF on the MR territory.
莫斯科地区医疗机构对射血分数降低的慢性心力衰竭患者使用四疗法可行性的临床和经济评估
目的:评价莫斯科地区(MR)医疗机构使用四组分药物治疗慢性心力衰竭伴射血分数降低(CHFrEF)患者的可行性。材料和方法。对血管紧张素转换酶抑制剂、受体阻滞剂和矿皮质激素受体拮抗剂联合达格列净(钠-葡萄糖共转运蛋白2)治疗CHFrEF患者的联合标准疗法进行了临床和经济分析。有效性标准是预防心血管疾病死亡的人数,以及在区域"保健发展"方案框架内对实现降低循环系统疾病死亡率目标指标的贡献百分比。为了确定四疗法的经济可行性,计算实施技术的直接医疗成本,根据治疗所需人数(NNT)指标的值确定预防1例CV死亡的成本。进行了预算影响分析,从而建立了两个分析模型。结果。结果表明,到2024年,使用四联疗法可以大大有助于实现目标指标,从而额外防止512例CV死亡,这将有可能实现MR国家方案“莫斯科州卫生保健”设定的指标的74.74%(每10万人中有451.4人)。在第一年对1000名目标患者使用四联疗法将预防11例CV死亡(NNT 90人)。预防一例CV死亡的费用为3860万卢布。预算影响分析可以确定,当CHF患者从标准治疗方案转向四联治疗时,包括与血管紧张素/neprilysin受体抑制剂组(缬沙坦+ sacubitril)的药物联合治疗,这将导致医疗保健系统预算成本增加18.8%。结论。结果表明,标准疗法与创新药物达格列净联合使用可降低循环系统疾病的死亡率。这项技术是一种成本效益高的方法,可以为MR地区的成年CHFrEF患者组织医疗保健。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Farmakoekonomika
Farmakoekonomika Medicine-Health Policy
CiteScore
1.70
自引率
0.00%
发文量
43
审稿时长
8 weeks
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