From the Department of Neurology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY (A.L.L.).
McCormick School of Engineering and Applied Science, Northwestern University. Evanston, IL (H.-J.C.).
Stroke. 2019 Feb;50(2):463-468. doi: 10.1161/STROKEAHA.118.022857.
Background and Purpose- Differentiating ischemic stroke patients from stroke mimics (SM), nonvascular conditions which simulate stroke, can be challenging in the acute setting. We sought to model the cost-effectiveness of treating suspected acute ischemic stroke patients before a definitive diagnosis could be made. We hypothesized that we would identify threshold proportions of SM among suspected stroke patients arriving to an emergency department above which administration of intravenous thrombolysis was no longer cost-effective. Methods- We constructed a decision-analytic model to examine various emergency department thrombolytic treatment scenarios. The main variables were proportion of SM to true stroke patients, time from symptom onset to treatment, and complication rates. Costs, reimbursement rates, and expected clinical outcomes of ischemic stroke and SM patients were estimated from published data. We report the 90-day incremental cost-effectiveness ratio of administering intravenous thrombolysis compared with no acute treatment from a healthcare sector perspective, as well as the cost-reimbursement ratio from a hospital-level perspective. Cost-effectiveness was defined as a willingness to pay <$100 000 USD per quality adjusted life year gained and high cost-reimbursement ratio was defined as >1.5. Results- There was an increase in incremental cost-effectiveness ratios as the proportion of SM cases increased in the 3-hour time window. The threshold proportion of SM above which the decision to administer thrombolysis was no longer cost-effective was 30%. The threshold proportion of SM above which the decision to administer thrombolysis resulted in high cost-reimbursement ratio was 75%. Results were similar for patients arriving within 0 to 90 minutes of symptom onset as compared with 91 to 180 minutes but were significantly affected by cost of alteplase in sensitivity analyses. Conclusions- We identified thresholds of SM above which thrombolysis was no longer cost-effective from 2 analytic perspectives. Hospitals should monitor SM rates and establish performance metrics to prevent rising acute stroke care costs and avoid potential patient harms.
背景与目的- 在急性发病期,区分缺血性脑卒中患者(中风)和脑卒中模拟症状(SM),即模拟中风的非血管性疾病,可能具有挑战性。我们旨在为疑似急性缺血性脑卒中患者建立一种治疗模型,即在明确诊断之前的治疗决策。我们假设可以确定到达急诊室的疑似中风患者中 SM 的比例阈值,高于该比例,静脉溶栓治疗将不再具有成本效益。方法- 我们构建了一个决策分析模型,以检查各种急诊室溶栓治疗方案。主要变量包括 SM 与真正中风患者的比例、从症状发作到治疗的时间以及并发症发生率。根据已发表的数据,估算了缺血性卒中和 SM 患者的成本、报销率和预期临床结果。我们从医疗保健部门的角度报告了与不进行急性治疗相比,静脉溶栓治疗的 90 天增量成本效益比,以及从医院层面的成本报销比。成本效益的定义是愿意支付每获得 1 个质量调整生命年的费用低于 100000 美元,高成本报销比的定义是大于 1.5。结果- 在 3 小时时间窗内,SM 病例比例增加,增量成本效益比也随之增加。当 SM 比例超过 30%时,决定进行溶栓治疗将不再具有成本效益。当 SM 比例超过 75%时,决定进行溶栓治疗将导致高成本报销比。对于在症状发作后 0 至 90 分钟内到达的患者和在 91 至 180 分钟内到达的患者,结果相似,但在敏感性分析中,阿替普酶的成本对结果有显著影响。结论- 我们从 2 个分析角度确定了溶栓治疗不再具有成本效益的 SM 阈值。医院应监测 SM 发生率并制定绩效指标,以防止急性脑卒中治疗成本上升,并避免潜在的患者伤害。