Wenzel R, Del Favero A, Kibbler C, Rogers T, Rotstein C, Mauskopf J, Morris S, Schlamm H, Troke P, Marciniak A
Department of Internal Medicine, Medical College of Virginia, Virginia Commonwealth University, Old City Hall, 1001 East Broad Street, 4th Floor Suite 405, P.O. Box 980663, Richmond, VA 23298-0663, USA.
J Antimicrob Chemother. 2005 Mar;55(3):352-61. doi: 10.1093/jac/dkh535. Epub 2005 Feb 22.
The objective of this study was to conduct an economic evaluation of voriconazole compared with conventional amphotericin B deoxycholate (CAB) using data from a recently reported randomized comparative trial in patients with various underlying immunosuppressive conditions. This trial demonstrated the superiority of voriconazole in terms of clinical response, survival and safety when used as primary therapy for invasive aspergillosis.
A decision analytic model was designed using an expert panel and populated primarily with efficacy and resource utilization data collected prospectively during the clinical trial. The analysis was carried out from the perspective of the health care system and all costs are reported in 2002 US dollars.
Average total treatment costs per patient were 10% lower in the voriconazole arm ($30 664) than in the CAB arm ($34 144), resulting from reduced consumption of hospital resources and fewer changes in antifungal therapy. In the base case analysis, voriconazole provided an average saving of $3481 per treated patient, resulted in a lower cost per survivor ($43 310 versus $58 971) and a lower cost per successfully treated patient ($58 100 versus $108 124) compared with CAB. Sensitivity analyses demonstrated that the cost savings observed were maintained over a wide range of alternative values for both unit costs and resource utilization, including length of hospital stay, time spent in intensive care units, bed day costs and the cost of lipid formulations of amphotericin B.
Incremental cost-effectiveness analysis indicated the dominance of voriconazole because of both lower costs and greater efficacy.
本研究的目的是利用最近一项针对各种潜在免疫抑制状况患者的随机对照试验数据,对伏立康唑与传统的两性霉素B脱氧胆酸盐(CAB)进行经济学评价。该试验表明,伏立康唑作为侵袭性曲霉病的一线治疗药物,在临床反应、生存率和安全性方面具有优势。
使用专家小组设计了一个决策分析模型,主要填充了临床试验期间前瞻性收集的疗效和资源利用数据。分析从医疗保健系统的角度进行,所有成本均以2002年美元报告。
伏立康唑组每位患者的平均总治疗成本(30664美元)比CAB组(34144美元)低10%,这是由于医院资源消耗减少和抗真菌治疗的变化较少。在基础病例分析中,与CAB相比,伏立康唑为每位接受治疗的患者平均节省3481美元,每位幸存者的成本更低(43310美元对58971美元),每位成功治疗患者的成本更低(58100美元对108124美元)。敏感性分析表明,在所观察到的成本节省在单位成本和资源利用的广泛替代值范围内保持不变,包括住院时间、在重症监护病房的时间、床位日成本和两性霉素B脂质制剂的成本。
增量成本效益分析表明伏立康唑具有优势,因为其成本更低且疗效更高。