Su Yu-Hsiang, Chen Chih-Hung, Lin Huey-Juan, Chen Yu-Wei, Tseng Mei-Chiun, Hsieh Han-Chieh, Chen Chih-Hung, Sung Sheng-Feng
Division of Neurology, Department of Internal Medicine, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi City, Taiwan.
Department of Neurology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Acta Neurol Taiwan. 2017 Mar 15;26(1):3-12.
Only a small percentage of ischemic stroke patients were treated with intravenous thrombolysis in Taiwan, partly because of the narrow reimbursement criteria of the National Health Insurance (NHI). We aimed to assess the safety and effectiveness of intravenous thrombolysis not covered by the NHI.
This is a retrospective analysis of register data from four hospitals. All patients who received intravenous tissue plasminogen activator and fulfilled the American Heart Association/American Stroke Association (AHA/ASA) thrombolysis guidelines between January 2007 and June 2012 were distinguished into two groups: those in accordance (reimbursement group) and those not in accordance (non-reimbursement group) with the NHI reimbursement criteria. Primary outcome was symptomatic intracerebral hemorrhage (SICH). Secondary outcomes were dramatic improvement in the National Institutes of Health Stroke Scale (NIHSS) score at discharge, good functional outcome (modified Rankin Scale ≤2) at discharge, and all-cause in-hospital mortality.
In 569 guideline-eligible patients, 177 (31%) were treated without reimbursement. The reasons for exclusion from reimbursement included age >80 (n=42), baseline NIHSS less than 6 (n=29), baseline NIHSS >25 (n=15), thrombolysis beyond 3 hours (n=49), prior stroke with diabetes (n=28), use of oral anticoagulant (n=2), and more than one contraindication (n=12). Overall, we observed no differences between the reimbursement and non-reimbursement groups in the rate of SICH (7% versus 6%), dramatic improvement (36% versus 36%), good functional outcome (39% versus 37%), and in-hospital mortality (8% versus 6%) Conclusion: In stroke patients treated with intravenous thrombolysis according to the AHA/ASA guidelines, the outcomes were comparable between the reimbursement and non-reimbursement groups.
在台湾,仅有一小部分缺血性中风患者接受了静脉溶栓治疗,部分原因是国民健康保险(NHI)的报销标准狭窄。我们旨在评估未被NHI覆盖的静脉溶栓治疗的安全性和有效性。
这是一项对四家医院登记数据的回顾性分析。2007年1月至2012年6月期间所有接受静脉注射组织型纤溶酶原激活剂并符合美国心脏协会/美国中风协会(AHA/ASA)溶栓指南的患者被分为两组:符合NHI报销标准的患者(报销组)和不符合NHI报销标准的患者(非报销组)。主要结局是症状性脑出血(SICH)。次要结局包括出院时美国国立卫生研究院卒中量表(NIHSS)评分显著改善、出院时良好功能结局(改良Rankin量表≤2)以及全因住院死亡率。
在569例符合指南标准的患者中,177例(31%)接受了无报销的治疗。被排除在报销范围之外的原因包括年龄>80岁(n = 42)、基线NIHSS低于6分(n = 29)、基线NIHSS>25分(n = 15)、溶栓超过3小时(n = 49)、既往中风合并糖尿病(n = 28)、使用口服抗凝剂(n = 2)以及存在不止一项禁忌症(n = 12)。总体而言,我们观察到报销组和非报销组在SICH发生率(7%对6%)、显著改善率(36%对36%)、良好功能结局率(39%对37%)和住院死亡率(8%对6%)方面没有差异。结论:在根据AHA/ASA指南接受静脉溶栓治疗的中风患者中,报销组和非报销组的结局相当。