1 Department of Biostatistics, UTHealth School of Public Health, Houston, USA.
2 Department of Management, Policy and Community Health, UTHealth School of Public Health, Houston, USA.
Int J Stroke. 2018 Apr;13(3):321-327. doi: 10.1177/1747493017711950. Epub 2017 Jun 14.
Rationale Mobile stroke units speed treatment for acute ischemic stroke, thereby possibly improving outcomes. Aim To compare mobile stroke unit and standard management clinical outcomes, healthcare utilization, and cost-effectiveness in tissue plasminogen activator-eligible acute ischemic stroke patients calling 911. Sample size 693. Eighty percent power with 0.05 type I error rate to detect a difference of 0.09 in mean utility-weighted modified Rankin scale between groups. Design Phase III, multicenter, prospective cluster-randomized (mobile stroke unit versus standard management weeks) comparative effectiveness study in tissue plasminogen activator-eligible patients. Outcomes Primary: Ninety-day mean utility-weighted modified Rankin scale. Coprimary: cost-effectiveness based on EQ5D quality of life and one year poststroke costs. Analysis Two-sample t-test and linear regression adjusting for covariates; incremental cost-effectiveness ratio and net benefit regression. Results As of March 2017, 288 tissue plasminogen activator-eligible patients have been enrolled (173 in the mobile stroke unit arm and 115 in the standard management arm). Two new centers start in early 2017 with target end of recruitment September 2019. Conclusion This is the first randomized study to test for disability, healthcare utilization, and cost-effectiveness of a mobile stroke unit. The progress of the study suggests that it is feasible. Management of tissue plasminogen activator eligible acute ischemic stroke patients by a mobile stroke unit could potentially result in less disability and healthcare utilization, and be cost effective. Mobile stroke units are very costly. This trial may determine if the fixed cost can be justified by a reduction in disability and healthcare utilization. Clinical Trial Registration NCT02190500.
背景 移动卒中单元可加快急性缺血性卒中的治疗速度,从而可能改善预后。 目的 比较移动卒中单元与标准治疗在呼叫 911 的组织型纤溶酶原激活剂(tissue plasminogen activator,tPA)治疗适应证的急性缺血性卒中患者中的临床结局、医疗保健利用和成本效益。 样本量 693。80%的功效和 0.05 的Ⅰ类错误率,用以检测两组间平均效用加权改良 Rankin 量表的差异为 0.09。 设计 tPA 治疗适应证的患者中,一项为期 3 年、多中心、前瞻性、集群随机(移动卒中单元与标准治疗组)比较有效性研究。 结局 主要结局:90 天平均效用加权改良 Rankin 量表。 次要结局:基于 EQ5D 生活质量和卒后 1 年成本的成本效益。 分析 两样本 t 检验和线性回归,调整协变量;增量成本效益比和净收益回归。 结果 截至 2017 年 3 月,共纳入 288 例 tPA 治疗适应证患者(移动卒中单元组 173 例,标准治疗组 115 例)。2017 年初新增 2 个中心,目标招募时间截至 2019 年 9 月。 结论 这是首个测试移动卒中单元在残疾、医疗保健利用和成本效益方面的随机研究。研究进展表明其是可行的。移动卒中单元管理 tPA 治疗适应证的急性缺血性卒中患者,可能会导致更少的残疾和医疗保健利用,且具有成本效益。移动卒中单元的成本非常高。本试验可能会确定固定成本是否可通过减少残疾和医疗保健利用来证明其合理性。 临床试验注册 NCT02190500。