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他汀类药物和依折麦布降低慢性肾脏病患者血脂的成本效益。

Cost-effectiveness of lipid lowering with statins and ezetimibe in chronic kidney disease.

机构信息

Health Economics Research Centre, Nuffield Department of Population Health, University of Oxford, UK.

Clinical Trial Service Unit and Epidemiological Studies Unit, Nuffield Department of Population Health, University of Oxford, UK; Medical Research Council Population Health Research Unit, Nuffield Department of Population Health, University of Oxford, UK.

出版信息

Kidney Int. 2019 Jul;96(1):170-179. doi: 10.1016/j.kint.2019.01.028. Epub 2019 Mar 12.

Abstract

Statin-based treatments reduce cardiovascular disease (CVD) risk in patients with non-dialysis chronic kidney disease (CKD), but it is unclear which regimen is the most cost-effective. We used the Study of Heart and Renal Protection (SHARP) CKD-CVD policy model to evaluate the effect of statins and ezetimibe on quality-adjusted life years (QALYs) and health care costs in the United States (US) and the United Kingdom (UK). Net costs below $100,000/QALY (US) or £20,000/QALY (UK) were considered cost-effective. We investigated statin regimens with or without ezetimibe 10 mg. Treatment effects on cardiovascular risk were estimated per 1-mmol/L reduction in low-density lipoprotein (LDL) cholesterol as reported in the Cholesterol Treatment Trialists' Collaboration meta-analysis, and reductions in LDL cholesterol were estimated for each statin/ezetimibe regimen. In the US, atorvastatin 40 mg ($0.103/day as of January 2019) increased life expectancy by 0.23 to 0.31 QALYs in non-dialysis patients with stages 3B to 5 CKD, at a net cost of $20,300 to $78,200/QALY. Adding ezetimibe 10 mg ($0.203/day) increased life expectancy by an additional 0.05 to 0.07 QALYs, at a net cost of $43,600 to $91,500/QALY. The cost-effectiveness findings and policy implications in the UK were similar. In summary, in patients with non-dialysis-dependent CKD, the evidence suggests that statin/ezetimibe combination therapy is a cost-effective treatment to reduce the risk of CVD.

摘要

基于他汀类药物的治疗可降低非透析慢性肾脏病(CKD)患者的心血管疾病(CVD)风险,但哪种治疗方案最具成本效益尚不清楚。我们使用心脏和肾脏保护研究(SHARP)CKD-CVD 政策模型在美国(US)和英国(UK)评估他汀类药物和依折麦布对质量调整生命年(QALY)和医疗保健成本的影响。低于每 QALY(美国)$100,000 或每 QALY(英国)£20,000 的净成本被认为具有成本效益。我们研究了有或没有依折麦布 10 mg 的他汀类药物治疗方案。根据胆固醇治疗试验者协作荟萃分析报告,每降低 1mmol/L 低密度脂蛋白(LDL)胆固醇估计对心血管风险的治疗效果,并且为每种他汀类药物/依折麦布治疗方案估计 LDL 胆固醇的降低。在美国,阿托伐他汀 40 mg(截至 2019 年 1 月每天$0.103)可使 3B 期至 5 期 CKD 非透析患者的预期寿命延长 0.23 至 0.31 QALY,净成本为$20,300 至$78,200/QALY。添加依折麦布 10 mg(每天$0.203)可使预期寿命再延长 0.05 至 0.07 QALY,净成本为$43,600 至$91,500/QALY。英国的成本效益发现和政策影响相似。总之,在非透析依赖型 CKD 患者中,证据表明他汀类药物/依折麦布联合治疗是降低 CVD 风险的一种具有成本效益的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd44/6595178/26dcd61ff86b/fx1.jpg

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