Respiratory Evaluation Sciences Program, Collaboration for Outcomes Research and Evaluation, Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada.
Pharmaceutical Health Services Research at University of Maryland School of Pharmacy, Baltimore, Md.
J Allergy Clin Immunol. 2020 May;145(5):1367-1377.e4. doi: 10.1016/j.jaci.2019.11.038. Epub 2019 Dec 11.
Asthma diagnosis in the community is often made without objective testing.
The aim of this study was to evaluate the cost-effectiveness of implementing a stepwise objective diagnostic verification algorithm among patients with community-diagnosed asthma in the United States.
We developed a probabilistic time-in-state cohort model that compared a stepwise asthma verification algorithm on the basis of spirometry testing and a methacholine challenge test against the current standard of care over 20 years. Model input parameters were informed from the literature and with original data analyses when required. The target population was US adults (≥15 years old) with physician-diagnosed asthma. The final outcomes were costs (in 2018 dollars) and quality-adjusted life years (QALYs), discounted at 3% annually. Deterministic and probabilistic analyses were undertaken to examine the effect of alternative assumptions and uncertainty in model parameters on the results.
In a simulated cohort of 10,000 adults with diagnosed asthma, the stepwise algorithm resulted in removal of the diagnosis of 3,366. This was projected to be associated with savings of $36.26 million in direct costs and a gain of 4,049.28 QALYs over 20 years. Extrapolating these results to the US population indicated an undiscounted potential savings of $56.48 billion over 20 years. The results were robust against alternative assumptions and plausible changes in values of input parameters.
Implementation of a simple diagnostic testing algorithm to verify asthma diagnosis might result in substantial savings and improvement in patients' quality of life.
在社区中,哮喘的诊断通常是在没有客观检测的情况下做出的。
本研究旨在评估在美国,对社区诊断为哮喘的患者实施逐步客观诊断验证算法的成本效益。
我们开发了一个概率状态时间队列模型,该模型比较了基于肺功能测试和乙酰甲胆碱挑战测试的逐步哮喘验证算法与当前 20 年的标准护理。模型输入参数来自文献,并在需要时进行原始数据分析。目标人群是美国成年人(≥15 岁),有医生诊断的哮喘。最终结果是成本(以 2018 年美元计算)和质量调整生命年(QALY),每年贴现 3%。进行了确定性和概率分析,以检查替代假设和模型参数不确定性对结果的影响。
在一个模拟的 10000 名成人哮喘队列中,逐步算法导致 3366 例诊断被取消。这预计将与 20 年内直接成本节省 3626 万美元和 4049.28 个质量调整生命年有关。将这些结果外推到美国人群,20 年内潜在的未经贴现节省额为 564.8 亿美元。结果对替代假设和输入参数值的合理变化具有稳健性。
实施简单的诊断测试算法来验证哮喘诊断可能会带来显著的节省,并改善患者的生活质量。