Cost-Utility of Venovenous Ecmo Associated with Protective Mechanical Ventilation in the Treatment of Patients with Acute Respiratory Distress Syndrome

C. B. Marta
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Abstract

Introduction: with the emergence of COVID-19 in the world, there was a race against time in the search for studies and scientific information that validated the most appropriate treatment. As a result, when caring for patients with the disease who developed ARDS and progressed to a severe condition with hospitalization in the ICU, the need for scientific evidence to guide care for these patients was even greater. Speculation about the effectiveness of using ECMO for these patients began to emerge, and with it, the need for scientific studies that would show the costs and benefits of acquiring this technology in the SUS. The dissertation that is intended to be defended is whether the use of VV ECMO associated with protective mechanical ventilation in patients with ARDS is more cost-effective compared to exclusive protective mechanical ventilation. General Objective: to analyze the cost-effectiveness of veno-venous ECMO in the treatment of patients with COVID-19 who evolve with severe Acute Respiratory Failure. Specific Objectives: review the scientific literature to summarize the best scientific evidence available on the safety and efficacy of using exclusive mechanical ventilation and venovenous ECMO in patients with acute respiratory failure, and estimate the costs associated with mechanical ventilation and the use of veno-venous ECMO. Method: Rapid systematic review for a complete health economic assessment based on a Markov model to estimate the incremental cost-effectiveness of using venovenous ECMO associated with protective mechanical ventilation in the treatment of patients with ARDS due to COVID-19. Results: Based on the estimated costs in each of the base case scenarios and the probabilities of the clinical effects resulting from the interventions, the study showed that the ECMO + protective IMV intervention offers around 0.295 AAQA compared to 0.2015 AAQA offered by the exclusive protective VMI. The incremental cost of ECMO + protective IMV is BRL 12,519.94 for 0.397 effectiveness compared to 0.215 exclusive protective IMV (incremental effectiveness of 0.182). For each qualityadjusted year of life gained, the amount of R$ 68,902.92 would have to be disbursed. Conclusion: the results showed that both veno-venous ECMO associated with protective mechanical ventilation and exclusive protective mechanical ventilation can be cost-effective alternatives for the treatment of patients with ARDS due to COVID-19 in the SUS, depending on the willingness to pay. However, in terms of effectiveness, ECMO was the most effective alternative, but with the highest cost increase.
静脉-静脉Ecmo联合保护性机械通气治疗急性呼吸窘迫综合征患者的成本-效用
导读:随着COVID-19在世界范围内的出现,人们争分夺秒地寻找验证最适当治疗方法的研究和科学信息。因此,在护理发展为ARDS并发展为重症ICU住院的患者时,更需要科学证据来指导对这些患者的护理。关于这些患者使用ECMO的有效性的猜测开始出现,随之而来的是,需要进行科学研究,以显示在SUS中获得这项技术的成本和收益。论文的目的是捍卫是否使用VV ECMO与保护性机械通气在ARDS患者比单独保护性机械通气更具成本效益。总目的:分析静脉-静脉ECMO治疗新冠肺炎合并严重急性呼吸衰竭患者的成本-效果。具体目的:回顾科学文献,总结急性呼吸衰竭患者使用专用机械通气和静脉-静脉ECMO的安全性和有效性的最佳科学证据,并估计机械通气和使用静脉-静脉ECMO的相关成本。方法:基于Markov模型快速系统回顾完整的健康经济评估,评估静脉静脉ECMO联合保护性机械通气治疗COVID-19所致ARDS患者的增量成本-效果。结果:基于每个基本情况下的估计成本和干预产生的临床效果的概率,研究表明ECMO +保护性IMV干预提供的AAQA约为0.295,而单独保护性VMI提供的AAQA为0.2015。ECMO +保护性IMV的增量成本为12,519.94巴西雷亚尔,有效性为0.397,而单独保护性IMV的增量成本为0.215巴西雷亚尔(增量有效性为0.182)。每增加一个质量调整生命年,必须支付68,902.92雷亚尔。结论:根据患者的支付意愿,静脉-静脉ECMO联合保护性机械通气和单纯保护性机械通气均可作为SUS新型冠状病毒感染急性呼吸窘迫综合征(ARDS)患者的高性价比治疗方案。然而,就有效性而言,ECMO是最有效的替代方案,但成本增加最高。
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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