Kuntz K M, Kent K C
Section for Clinical Epidemiology, Brigham and Women's Hospital, Boston, MA 02115, USA.
Circulation. 1996 Nov 1;94(9 Suppl):II194-8.
The North American Symptomatic Carotid Endarterectomy Trial (NASCET) and the Asymptomatic Carotid Atherosclerosis Study (ACAS) showed significant risk reductions for carotid endarterectomy (CE) but did not consider the cost-effectiveness of CE.
We developed Markov models based on NASCET and ACAS to simulate hypothetical cohorts of patients with carotid stenosis and calculated quality-adjusted life expectancies and direct medical costs for those receiving either CE or medical therapy. For symptomatic patients, we used a surgical stroke risk of 5.8%, a 2-year stroke risk of 27.6% for medical patients, and a post-30-day surgical risk reduction of 87% for ipsilateral strokes. For symptom-free patients, we used a surgical stroke risk of 1.7%, a 5-year stroke risk of 17.5% for medical patients, and a post-30-day surgical risk reduction of 74% for ipsilateral strokes. Cost and quality-of-life estimates were estimated from the literature. The incremental cost-effectiveness ratio of CE versus medical therapy was $4100 and $52700 per quality-adjusted life year (QALY) gained for symptomatic and symptom-free patients, respectively. Incremental cost effectiveness ratios were < $50000/QALY gained for symptomatic patients for wide variations in baseline assumptions. For asymptomatic patients, the incremental cost-effectiveness ratio was $100900/QALY gained if the perioperative risk was 4%, $36400/QALY gained if the risk of untreated patients was doubled, and $13500/QALY gained if the cost of CE was halved.
Performance of CE is associated with favorable incremental cost-effectiveness ratios compared with other accepted medical interventions; however, the analysis for symptom-free patients was sensitive to a number of parameters.
北美症状性颈动脉内膜切除术试验(NASCET)和无症状性颈动脉粥样硬化研究(ACAS)显示,颈动脉内膜切除术(CE)可显著降低风险,但未考虑CE的成本效益。
我们基于NASCET和ACAS开发了马尔可夫模型,以模拟颈动脉狭窄患者的假设队列,并计算接受CE或药物治疗患者的质量调整预期寿命和直接医疗成本。对于有症状的患者,我们采用手术卒中风险为5.8%,药物治疗患者的2年卒中风险为27.6%,术后30天同侧卒中手术风险降低87%。对于无症状患者,我们采用手术卒中风险为1.7%,药物治疗患者的5年卒中风险为17.5%,术后30天同侧卒中手术风险降低74%。成本和生活质量估计值来自文献。对于有症状和无症状患者,CE与药物治疗相比的增量成本效益比分别为每获得一个质量调整生命年(QALY)4100美元和52700美元。对于有症状患者,在基线假设存在广泛差异的情况下,增量成本效益比<50000美元/QALY。对于无症状患者,如果围手术期风险为4%,增量成本效益比为100900美元/QALY;如果未治疗患者的风险加倍,增量成本效益比为36400美元/QALY;如果CE成本减半,增量成本效益比为13500美元/QALY。
与其他公认的医学干预措施相比,CE的实施具有良好的增量成本效益比;然而,对无症状患者的分析对一些参数敏感。