Ulysses S Rosas, Christopher V Almario, Kyung-Sang Yu, Brennan M R Spiegel
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The model compared 3 strategies: (1) usual care (i.e., upfront diagnostic testing with upper endoscopy ± ambulatory pH testing); (2) use of a PPI-adjunctive therapy after positive ambulatory pH testing; and (3) empiric use of a PPI-adjunctive therapy (i.e., diagnostic testing only after failing empiric treatment). The primary outcome was incremental cost per quality-adjusted life year (QALY) gained (third-party payer perspective) over a 10-year time horizon using a willingness to pay threshold of $100,000/QALY.</p><p><strong>Results: </strong>In two-way sensitivity analyses varying the cost and effectiveness of the PPI-adjunctive therapy, most combinations revealed that use of the medication after positive pH testing was the most cost-effective approach. Empiric treatment was the preferred strategy only when the therapy was highly efficacious (≥ 87.5% response rate) and low cost (≤ $109/month). Use of PPI-adjunctive treatments were not cost effective when the cost exceeded $1150/month.</p><p><strong>Conclusion: </strong>Use of PPI-adjunctive therapies in those with persistent GERD symptoms may become cost effective when guided by ambulatory pH tests. 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引用次数: 0
摘要
背景和目的:半数胃食管反流病(GERD)患者在服用质子泵抑制剂(PPI)期间症状持续存在,因此人们努力开发新的辅助疗法来治疗 PPI 难治性胃食管反流病。我们进行了一项经济分析,以确定此类潜在药物在临床实践中的成本和疗效:方法:采用马尔可夫决策模型对美国正在接受 PPI 难治性胃食管反流病评估的假定患者群进行研究。该模型比较了 3 种策略:(1) 常规治疗(即通过上内镜进行前期诊断检测,同时进行非卧床 pH 值检测);(2) 在非卧床 pH 值检测呈阳性后使用 PPI 辅助疗法;(3) 经验性使用 PPI 辅助疗法(即在经验性治疗失败后才进行诊断检测)。主要结果是在 10 年的时间跨度内,每获得一个质量调整生命年(QALY)的增量成本(从第三方支付者的角度),支付意愿阈值为 100,000 美元/QALY:在改变 PPI 辅助疗法成本和有效性的双向敏感性分析中,大多数组合显示,在 pH 值检测呈阳性后使用药物是最具成本效益的方法。只有在疗效高(应答率≥ 87.5%)、成本低(≤ 109 美元/月)的情况下,经验性治疗才是首选策略。当费用超过1150美元/月时,使用PPI辅助治疗就不划算了:结论:在非卧床 pH 值检测的指导下,对有持续性胃食管反流症状的患者使用 PPI 辅助疗法可能具有成本效益。这些数据可以为研究人员、企业和付款人开发、验证和定价 PPI 难治性胃食管反流病的新疗法提供指导。
The Cost Effectiveness of Adjunctive Treatments for Proton Pump Inhibitor-Refractory Gastroesophageal Reflux Disease.
Background and objective: Half of patients with gastroesophageal reflux disease (GERD) experience persistent symptoms while on proton pump inhibitors (PPIs), thus driving efforts to develop novel adjunctive therapies for PPI-refractory GERD. An economic analysis was performed to establish at what cost and efficacy such potential medications are likely to become cost effective in clinical practice.
Methods: A Markov decision model was used to examine a hypothetical cohort of patients being evaluated for PPI-refractory GERD in the USA. The model compared 3 strategies: (1) usual care (i.e., upfront diagnostic testing with upper endoscopy ± ambulatory pH testing); (2) use of a PPI-adjunctive therapy after positive ambulatory pH testing; and (3) empiric use of a PPI-adjunctive therapy (i.e., diagnostic testing only after failing empiric treatment). The primary outcome was incremental cost per quality-adjusted life year (QALY) gained (third-party payer perspective) over a 10-year time horizon using a willingness to pay threshold of $100,000/QALY.
Results: In two-way sensitivity analyses varying the cost and effectiveness of the PPI-adjunctive therapy, most combinations revealed that use of the medication after positive pH testing was the most cost-effective approach. Empiric treatment was the preferred strategy only when the therapy was highly efficacious (≥ 87.5% response rate) and low cost (≤ $109/month). Use of PPI-adjunctive treatments were not cost effective when the cost exceeded $1150/month.
Conclusion: Use of PPI-adjunctive therapies in those with persistent GERD symptoms may become cost effective when guided by ambulatory pH tests. These data can guide investigators, industry, and payers as they develop, validate, and price new treatments for PPI-refractory GERD.
期刊介绍:
Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes:
-Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs.
-Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice.
-Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed.
-Studies focusing on the application of drug delivery technology in healthcare.
-Short communications and case study reports that meet the above criteria will also be considered.
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