阿哌沙班与其他noac预防意大利房颤患者卒中的预算影响分析

IF 0.3 Q4 HEALTH CARE SCIENCES & SERVICES
L. Pradelli, M. Calandriello, R. D. Virgilio, M. Bellone, M. Tubaro
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引用次数: 0

摘要

目的:本研究旨在对意大利非瓣膜性心房颤动(NVAF)患者使用三种可用的新型口服抗凝剂(NOACs)预防血栓栓塞事件的预算影响进行分析。方法:通过先前发表的终身决策树/马尔可夫模型对意大利患者进行估计,模拟他们使用可用治疗方案的治疗:达比加群两种剂量水平(80岁以上患者110 mg/bid,年轻NVAF患者150 mg/bid),利伐沙班(20 mg/bid)和阿哌沙班(5 mg/bid)。有效性和安全性估计来自以华法林为链接的调整后的间接治疗比较。在模型中考虑的主要临床事件包括缺血性和出血性中风、全体性血栓栓塞、出血(包括大出血和临床相关的小出血)和心血管住院,以及停止治疗。截至2013年的流行病学数据和单位成本收集自意大利公布的资料。预算影响分析通过比较有阿哌沙班和没有阿哌沙班的假设情况下的预期1、2和3年成本来评估引入阿哌沙班的财务影响。意大利非瓣膜性房颤患者群体估计基于官方阿哌沙班报销标准,将试验人群的特征应用于国家流行病学数据。每个方案的患者数量通过预测份额演变来估计。对非实验性非瓣膜性房颤患者进行敏感性分析。结果:在现有的noac中,阿哌沙班预计在估计的364,000名意大利患者中是最便宜的,可在1年、2年和3年分别节省1,180,549欧元、3,841,429欧元和5,368,918欧元。对非实验性非瓣膜性房颤患者的模拟结果得出了可比较的估计。结论:经调整的间接比较显示,三种可用noac的不同安全性和有效性表明,阿哌沙班可以改善医疗保健支出控制,同时维持或增加意大利非瓣膜性房颤人群的治疗适宜性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Budget impact analysis of apixaban versus other NOACs for the prevention of stroke in Italian atrial fibrillation patients
OBJECTIVE: This study aims to perform a budget impact analysis of the use of three available novel oral anticoagulant agents (NOACs) for preventing thromboembolic events in Italian patients with non‑valvular atrial fibrillation (NVAF). METHODS: Estimated Italian population of patients was run through a previously published lifetime decision tree/Markov model simulating their treatment with the available therapeutic options: dabigatran at two dose levels (110 mg/bid for the over 80 years old, 150 mg/bid for younger NVAF patients), rivaroxaban (20 mg/uid), and apixaban (5 mg/bid). Effectiveness and safety estimates derive from an adjusted indirect treatment comparison using warfarin as link. The main clinical events considered in the model are ischemic and hemorrhagic stroke, systemic thromboembolism, bleeds (both major and clinically relevant minor) and cardiovascular hospitalizations, besides treatment discontinuations. Epidemiological data and unit costs, actualized to 2013, are collected from Italian published sources. The budget impact analysis evaluates the financial impact of apixaban introduction by comparing expected 1,2, and 3 years costs in hypothetical scenarios: with and without apixaban. Italian NVAF patient population estimation is based on official apixaban reimbursement criteria, applying the characteristics of the trial population to national epidemiologic data. Numbers of patients for each regimen are estimated by projecting share evolution. Sensitivity analysis is performed on an alternative non‑experimental population of NVAF patients. RESULTS: Among available NOACs, apixaban was expected to be the least expensive in an estimated patient population of 364,000 Italian patients, allowing for savings of € 1,180,549, € 3,841,429 and € 5,368,918 at 1,2, and 3 years, respectively. Results of the simulation run on an alternative non‑experimental population of NVAF patients yields comparable estimates. CONCLUSIONS: The different safety and effectiveness profiles of the three available NOACs emerging from the adjusted indirect comparison indicate that apixaban could improve health care expenditure control while maintaining or increasing therapeutic appropriateness in the Italian NVAF population.
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