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首页> 外文期刊>PharmacoEconomics >Potential Bias Associated with Modeling the Effectiveness of Healthcare Interventions in Reducing Mortality Using an Overall Hazard Ratio
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Potential Bias Associated with Modeling the Effectiveness of Healthcare Interventions in Reducing Mortality Using an Overall Hazard Ratio

机译:与模拟医疗保健干预的有效性使用整体危险比率降低死亡率的潜在偏差

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摘要

Background Clinical trials often report intervention efficacy in terms of the reduction in all-cause mortality between the treatment and control arms (i.e., an overall hazard ratio [oHR]) instead of the reduction in disease-specific mortality (i.e., a disease-specific hazard ratio [dsHR]). Using oHR to reduce all-cause mortality beyond the time horizon of the trial may introduce bias if the relative proportion of other-cause mortality increases with age. We sought to quantify this oHR extrapolation bias and propose a new approach to overcome this bias. Methods We simulated a hypothetical cohort of patients with a generic disease that increased background mortality by a constant additive disease-specific rate. We quantified the bias in terms of the percentage change in life expectancy gains with the intervention under an oHR compared with a dsHR approach as a function of the cohort start age, the disease-specific mortality rate, dsHR, and the duration of the intervention's effect. We then quantified the bias in a cost-effectiveness analysis (CEA) of implantable cardioverter-defibrillators based on efficacy estimates from a clinical trial. Results For a cohort of 50-year-old patients with a disease-specific mortality of 0.05, a dsHR of 0.5, a calculated oHR of 0.55, and a lifetime duration of effect, the bias was 28%. We varied these key parameters over wide ranges and the resulting bias ranged between 3 and 140%. In the CEA, the use of oHR as the intervention's effectiveness overestimated quality-adjusted life expectancy by 9% and costs by 3%, biasing the incremental cost-effectiveness ratio by - 6%. Conclusions The use of an oHR approach to model the intervention's effectiveness beyond the time horizon of the trial overestimates its benefits. In CEAs, this bias could decrease the cost of a QALY, overestimating interventions' cost effectiveness.
机译:背景技术临床试验通常在治疗和控制臂之间的所有导致死亡率降低(即,整体危险比[OCR])而不是降低疾病特异性死亡率(即特异性疾病危险比[DSHR])。使用人权ohR降低全面的死亡率超出试验的时间范围内可能引入偏差,如果其他原因死亡率随着年龄的增长而增加。我们试图量化这种OHR外推偏见,并提出了一种克服这一偏见的新方法。方法采用常规添加剂疾病特异性率提高了仿制性疾病的假设患者假设群体。我们在衡量人权诉讼下的干预率的预期寿命的百分比变化方面量化了偏差,与队列开始年龄,疾病特异性死亡率,DSHR和干预效果的持续时间(DSHR方法)相比,与DSHR方法相比。 。然后,我们基于临床试验的疗效估计量来量化植入心脏病 - 除颤器的成本效益分析(CEA)中的偏差。结果50岁患者的疾病特异性死亡率为0.05,DSHR为0.5,计算的OHR为0.55,寿命持续时间,偏差为28%。我们在宽范围内变化了这些关键参数,并产生的偏差范围为3至140%。在CEA中,使用OHR作为干预的有效性将质量调整的寿命高9%,成本为3%,偏置增量成本效益比偏差 - 6%。结论利用ofR方法模拟干预的效率超出了试验的时间范围内高估了其益处。在CEA中,这种偏差可以降低QALY的成本,过高估计干预措施的成本效益。

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  • 来源
    《PharmacoEconomics》 |2020年第3期|共12页
  • 作者单位

    CONACyT Ctr Res &

    Teaching Econ CIDE Drug Policy Program Circuito Tecnopolo Norte 117;

    Univ Minnesota Sch Publ Hlth Div Hlth Policy &

    Management Minneapolis MN USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药学;
  • 关键词

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