The cost-effectiveness of intensive low-density lipoprotein cholesterol lowering in people with peripheral artery disease

被引:14
|
作者
Nastasi, Domenico R. [1 ]
Moxon, Joseph, V [1 ,2 ]
Norman, Richard [5 ]
Trollope, Alexandra F. [1 ,2 ]
Rowbotham, Sophie [6 ,7 ]
Quigley, Frank [3 ]
Jenkins, Jason [7 ]
Golledge, Jonathan [1 ,2 ,4 ]
机构
[1] James Cook Univ, Queensland Res Ctr Peripheral Vasc Dis, Coll Med & Dent, Townsville, Qld 4811, Australia
[2] James Cook Univ, Ctr Mol Therapeut, Australian Inst Trop Hlth & Med, Townsville, Qld, Australia
[3] Mater Hosp, Dept Vasc & Endovasc Surg, Townsville, Qld, Australia
[4] Townsville Univ Hosp, Dept Vasc & Endovasc Surg, Townsville, Qld, Australia
[5] Curtin Univ, Sch Publ Hlth, Perth, WA, Australia
[6] Univ Queensland, Sch Med, Brisbane, Qld, Australia
[7] Royal Brisbane & Womens Hosp, Dept Vasc & Endovasc Surg, Herston, Qld, Australia
基金
英国医学研究理事会;
关键词
PAD; Cholesterol; PCSK9; inhibitors; Cost-benefit analysis; Cost-effectiveness; HEALTH-CARE COSTS; FAMILIAL HYPERCHOLESTEROLEMIA; LDL-CHOLESTEROL; ADHERENCE; REVASCULARIZATION; EVOLOCUMAB; MORTALITY; CLINICIAN; OUTCOMES; STATINS;
D O I
10.1016/j.jvs.2020.08.129
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: People with peripheral artery disease are at a high risk of major adverse cardiovascular events (MACE) and major adverse limb events (MALE). Randomized controlled trials suggest that intensive lowering of low-density lipoprotein cholesterol (LDL-C) with proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors is an effective strategy to prevent these events. This study estimated the potential benefit and cost-effectiveness of administrating PCSK9 inhibitors to a cohort of participants with peripheral artery disease. Methods: A total of 783 participants with intermittent claudication (IC; n = 582) or chronic limb-threatening ischemia (CLTI; n = 201) were prospectively recruited from three hospitals in Australia. Serum LDL-C was measured at recruitment, and the occurrence of MACE and MALE was recorded over a median (interquartile range) follow-up of 2.2 years (0.3-5.7 years). The potential benefit of administering a PCSK9 inhibitor was estimated by calculating the absolute risk reduction and numbers needed to treat (NNT) based on relative risk reductions reported in published randomized trials. The incremental cost-effectiveness ratio per quality-adjusted life year gained was estimated. Results: Intensive LDL-C lowering was estimated to lead to an absolute risk reduction in MACE of 6.1% (95% confidence interval [CI], 2.0-9.3; NNT, 16) and MALE of 13.7% (95% CI, 4.3-21.5; NNT, 7) in people with CLTI compared with 3.2% (95% CI, 1.1-4.8; NNT, 32) and 5.3% (95% CI, 1.7-8.3; NNT, 19) in people with IC. The estimated incremental cost-effectiveness ratios over a 10-year period were $55,270 USD and $32,800 USD for participants with IC and CLTI, respectively. Conclusions: This analysis suggests that treatment with a PCSK9 inhibitor is likely to be cost-effective in people with CLTI.
引用
收藏
页码:1396 / +
页数:11
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