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药物治疗高危中青年 1 期高血压患者的成本效益分析。

Cost-effectiveness of drug treatment for young and middle-aged stage 1 hypertensive patients with high risk.

机构信息

Department of Social Medicine, School of Public Health, Guangxi Medical University, Nanning, China.

Department of Nephrology, The First People's Hospital of Chenzhou, Chenzhou, China.

出版信息

J Glob Health. 2023 Nov 24;13:04147. doi: 10.7189/jogh.13.04147.

Abstract

BACKGROUND

Drug treatment was recommended for stage 1 hypertensive patients (blood pressure of 130-139 / 80-89 millimetres of mercury (mmHg)) with high cardiovascular disease (CVD) risk in the 2017 Hypertension Clinical Practice Guidelines, 2018 Chinese guidelines and 2021 World Health Organization guidelines, but not in other guidelines. However, evidence on the cost-effectiveness of drug treatment among young and middle-aged patients remains scarce. This study aimed to compare the cost-effectiveness of drug treatment vs. non-drug treatment for stage 1 hypertensive patients aged <60 years with high CVD risk.

METHODS

A microsimulation model projected quality-adjusted life years (QALYs), health care costs, and incremental cost-effectiveness ratios for drug treatment from a societal perspective. Transition probabilities were estimated from the Kailuan study with a sample size of 34 093 patients aged <60 years with high CVD risk. Costs and health utilities were obtained from the Kailuan study, national statistics reports and published literature.

RESULTS

Over a 15-year time horizon, the model predicted that drug treatment generated QALY of 9.36 and was associated with expected costs of 3735 US dollars ($) compared with 9.07 and $3923 produced by non-drug treatment among stage 1 hypertensive patients, resulting in a cost-saving for drug treatment. At a willingness-to-pay threshold of $10439/QALY (one gross domestic product (GDP) per capita in 2020), drug treatment had a 99.99% probability of being cost-effective for 10 000 samples of probabilistic sensitivity analysis. Sensitivity analyses by different values of transition probability, cost, utility and discount rate did not appreciably change the results. Shortening the time horizon to the average follow-up period of eight years resulted in ICER of $189/QALY for drug treatment (<1 × GDP/QALY).

CONCLUSIONS

Our results suggested that drug treatment was a dominant strategy for stage 1 hypertensive patients aged <60 years with high CVD risk in China, which may provide evidence for policymakers and clinicians when weighing the pros and cons of drug treatment for young and middle-aged stage 1 hypertensive patients.

摘要

背景

2017 年高血压临床实践指南、2018 年中国指南和 2021 年世界卫生组织指南建议对 130-139/80-89 毫米汞柱(mmHg)的 1 期高血压患者(伴有高心血管疾病(CVD)风险)进行药物治疗,但其他指南并未推荐。然而,关于年轻和中年患者药物治疗的成本效益证据仍然有限。本研究旨在比较药物治疗与非药物治疗对伴有高 CVD 风险的<60 岁 1 期高血压患者的成本效益。

方法

一项微观模拟模型从社会角度预测了药物治疗的质量调整生命年(QALY)、医疗保健成本和增量成本效益比。转移概率是根据 34093 名伴有高 CVD 风险的<60 岁患者的样本量从开滦研究中估计的。成本和健康效用是从开滦研究、国家统计报告和已发表文献中获得的。

结果

在 15 年的时间内,模型预测药物治疗的 QALY 为 9.36,预期成本为 3735 美元(与非药物治疗相比,1 期高血压患者的预期成本为 9.07 和 3923 美元),药物治疗有成本节约。在支付意愿阈值为 10439 美元/QALY(2020 年人均国内生产总值(GDP))时,药物治疗在 10000 个概率敏感性分析样本中具有 99.99%的成本效益概率。通过不同转移概率、成本、效用和贴现率的值进行敏感性分析并没有明显改变结果。将时间缩短至八年的平均随访期,药物治疗的增量成本效益比为 189 美元/QALY(<1×GDP/QALY)。

结论

我们的研究结果表明,对于伴有高 CVD 风险的<60 岁 1 期高血压患者,药物治疗是一种主导策略,这可能为决策者和临床医生权衡药物治疗年轻和中年 1 期高血压患者的利弊提供证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59a7/10668205/3ef98484d033/jogh-13-04147-F1.jpg

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