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普瑞巴林与度洛西汀治疗痛性糖尿病神经病变的成本-效用分析

A cost-utility analysis of pregabalin versus duloxetine for the treatment of painful diabetic neuropathy.

作者信息

Bellows Brandon K, Dahal Arati, Jiao Tianze, Biskupiak Joseph

机构信息

Pharmacotherapy Outcomes Research Center, University of Utah, Salt Lake City, Utah 84108, USA.

出版信息

J Pain Palliat Care Pharmacother. 2012 Jun;26(2):153-64. doi: 10.3109/15360288.2012.671240. Epub 2012 Apr 18.

Abstract

The objective of the current study was to determine the cost-utility of pregabalin versus duloxetine for treating painful diabetic neuropathy (PDN) using a decision tree analysis. Literature searches identified clinical trials and real-world studies reporting the efficacy, tolerability, safety, adherence, opioid usage, health care utilization, and costs of pregabalin and duloxetine. The proportions of patients reported in the included studies were used to determine probabilities in the decision tree model. The base-case model included the Food and Drug Administration (FDA)-approved doses of pregabalin (300 mg/day) and duloxetine (60 mg/day), whereas "real-world" sensitivity analyses explored the effects over a range of doses (pregabalin 75-600 mg/day, duloxetine 20-120 mg/day). A 6-month time horizon and a US third-party payer perspective were chosen for the study. Outcomes from the model were expressed as cost per quality-adjusted life-year (QALY). In the base-case model, duloxetine cost less and was more effective than pregabalin (incremental cost -$187, incremental effectiveness 0.011 QALYs). Results from two real-world sensitivity analyses indicated that duloxetine cost $16,300 and $20,667 more per additional QALY than pregabalin. Using a decision tree model that incorporated both clinical trial and real-world data, duloxetine was a more cost-effective option than pregabalin in the treatment of PDN from the perspective of third-party payers.

摘要

本研究的目的是通过决策树分析确定普瑞巴林与度洛西汀治疗痛性糖尿病神经病变(PDN)的成本效益。文献检索确定了报告普瑞巴林和度洛西汀的疗效、耐受性、安全性、依从性、阿片类药物使用情况、医疗保健利用情况及成本的临床试验和真实世界研究。纳入研究中报告的患者比例用于确定决策树模型中的概率。基础模型包括美国食品药品监督管理局(FDA)批准的普瑞巴林剂量(300毫克/天)和度洛西汀剂量(60毫克/天),而“真实世界”敏感性分析探讨了一系列剂量(普瑞巴林75 - 600毫克/天,度洛西汀20 - 120毫克/天)的影响。本研究选择了6个月的时间范围和美国第三方支付方的视角。模型结果以每质量调整生命年(QALY)成本表示。在基础模型中,度洛西汀成本更低且比普瑞巴林更有效(增量成本 - 187美元,增量效果0.011 QALY)。两项真实世界敏感性分析结果表明,度洛西汀每增加一个QALY比普瑞巴林成本高16,300美元和20,667美元。从第三方支付方的角度来看,使用结合了临床试验和真实世界数据的决策树模型,度洛西汀在治疗PDN方面比普瑞巴林是更具成本效益的选择。

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