Lord Sarah J, Howard Kirsten, Allen Felicity, Marinovich Luke, Burgess David C, King Richard, Atherton John J
National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Locked Bag 77, Camperdown, NSW 2050, Australia.
Med J Aust. 2005 Nov 7;183(9):464-71. doi: 10.5694/j.1326-5377.2005.tb07124.x.
To compare the safety, effectiveness and cost-effectiveness of drug-eluting coronary stents used in Australia with bare-metal stents and determine whether the benefits are greater for high-risk subgroups.
MEDLINE, Pre-Medline, EMBASE, Current Contents, CINAHL and the Cochrane Library database were searched to identify eligible randomised controlled trials and systematic reviews published in English between January 1966 and June 2004.
Seven randomised controlled trials that assessed polymer-based paclitaxel- or sirolimus-eluting stents versus bare-metal stents in patients with coronary atherosclerosis and reported on stent thrombosis, mortality, myocardial infarction, coronary artery bypass grafting or target lesion revascularisation.
Two independent reviewers appraised eligible studies and extracted data. Relative risks (RRs) were calculated for each outcome and pooled using the Mantel-Haenszel method.
Rates of stent thrombosis, mortality, myocardial infarction and bypass grafts did not differ by stent type. Drug-eluting stents (DESs) resulted in a 71%-80% lower risk of revascularisation at 12 months (RR 0.29 [95% CI, 0.20-0.43] for paclitaxel-eluting stents [n = 1593 patients]; RR 0.20 [95% CI, 0.13-0.29] for sirolimus-eluting stents [n = 1296 patients]). Similar benefits were seen in several high-risk subgroups of patients: those with diabetes, lesion length > 20 mm and target-vessel diameter < or = 2.5 mm. The benefits of DESs in these high-risk groups over lower-risk groups were inconclusive because of low numbers. The cost per revascularisation avoided by using DESs was 3,750-6,100 Australian dollars, with an estimated cost per quality-adjusted-life-year (QALY) gained of 46,829-76,467 Australian dollars. In sensitivity analyses, estimates varied from DESs being cost-saving to costing an additional 314,385 Australian dollars per QALY gained.
DESs are effective in reducing revascularisation. Estimates of cost-effectiveness are very sensitive to changes in estimates of their true effects in clinical practice, market price and the number of stents used per patient. Decisions to limit DESs to only patients at the highest risk of restenosis may improve their cost-effectiveness but will need to be reassessed when evidence is available to compare absolute benefits between patient groups.
比较澳大利亚使用的药物洗脱冠状动脉支架与裸金属支架的安全性、有效性和成本效益,并确定高危亚组患者使用药物洗脱支架的获益是否更大。
检索MEDLINE、Pre-Medline、EMBASE、《现刊目次》、护理学与健康领域数据库(CINAHL)以及Cochrane图书馆数据库,以识别1966年1月至2004年6月期间发表的符合条件的英文随机对照试验和系统评价。
七项随机对照试验,评估了基于聚合物的紫杉醇或西罗莫司洗脱支架与裸金属支架在冠状动脉粥样硬化患者中的应用,并报告了支架血栓形成、死亡率、心肌梗死、冠状动脉旁路移植术或靶病变血运重建情况。
两名独立的评审员对符合条件的研究进行评估并提取数据。计算每个结局的相对风险(RRs),并使用Mantel-Haenszel方法进行汇总。
支架血栓形成、死亡率、心肌梗死和旁路移植术的发生率在不同类型支架之间无差异。药物洗脱支架(DESs)使12个月时血运重建风险降低71%-80%(紫杉醇洗脱支架[n = 1593例患者]的RR为0.29[95%CI,0.20-0.43];西罗莫司洗脱支架[n = 1296例患者]的RR为0.20[95%CI,0.13-0.29])。在几个高危亚组患者中也观察到类似的获益:糖尿病患者、病变长度>20 mm以及靶血管直径≤2.5 mm的患者。由于病例数较少,DESs在这些高危组中相对于低危组的获益尚无定论。使用DESs避免血运重建的成本为3750-6100澳元,每获得一个质量调整生命年(QALY)的估计成本为46829-76467澳元。在敏感性分析中,估计值的变化范围为DESs节省成本至每获得一个QALY额外花费314385澳元。
DESs在降低血运重建方面有效。成本效益估计对其在临床实践中的真实效果估计、市场价格以及每位患者使用的支架数量的变化非常敏感。将DESs仅限于再狭窄风险最高的患者使用的决策可能会提高其成本效益,但当有证据可比较不同患者组之间的绝对获益时,需要重新评估。