替奈普酶与阿替普酶治疗急性缺血性脑卒中的比较。

Chen-Chen Tu, Hanqi Kelly Mao, Jennifer L Wessol
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摘要

摘要:背景:急性缺血性脑卒中(AIS)是导致死亡和残疾的主要原因。及时接受溶栓治疗的患者往往有较好的预后。尽管阿替普酶(tPA)是美国食品和药物管理局批准的用于AIS治疗的标准溶栓药物,但最近美国心脏协会的指南建议,替奈普酶(TNK)也可以作为一种替代方案。本项目比较了TNK与tPA治疗AIS的成本效益和临床结果。主要结局包括从门到针的时间、住院时间、美国国立卫生研究院卒中量表评分和出血转化事件的发生率。方法:该项目包括通过太平洋西北地区社区医院具有血栓切除术能力的卒中中心的病历回顾进行回顾性分析。在2022年3月至2023年12月期间,收集了175名接受tPA(82)或TNK(93)治疗的AIS患者的数据。符合溶栓治疗条件的患者在2023年3月15日前接受tPA治疗,此后使用TNK。选择标准遵循美国心脏协会指南和临床医生的判断。结果:虽然门到针的时间相似(P = .20),但排除异常值后显示TNK有显著差异(P = .04)。在人口统计学、美国国立卫生研究院卒中量表评分、住院时间或脑出血后发生率方面,没有观察到显著的组间差异。在项目期间,Tenecteplase的使用节省了4万多美元的药费。结论:Tenecteplase治疗AIS的安全性和有效性与tPA相当,并具有节省成本的额外好处。尽管两种药物之间的临床结果没有显著差异,但TNK的低成本和易于管理使其成为一个有吸引力的选择,特别是在资源有限的环境中。这些结果支持当前的组织治疗方案有利于TNK。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparing Tenecteplase and Alteplase for Acute Ischemic Stroke.

Abstract: BACKGROUND: Acute ischemic stroke (AIS) is a leading cause of mortality and disability. Patients who receive thrombolytic therapy promptly tend to have better outcomes. Although alteplase (tPA) is the standard Food and Drug Administration-approved thrombolytic for AIS treatment, recent American Heart Association guidelines suggest that tenecteplase (TNK) can be used as an alternative. This project compares the cost-effectiveness and clinical outcomes of TNK versus tPA in AIS treatment. Key outcomes include door-to-needle time, length of stay, National Institutes of Health Stroke Scale scores, and the incidence of hemorrhagic conversion events. METHODS: The project involved retrospective analysis through medical chart reviews at a thrombectomy-capable stroke center in a Pacific Northwest community hospital. Data were collected from 175 AIS patients treated with either tPA (82) or TNK (93) between March 2022 and December 2023. Patients eligible for thrombolytic therapy received tPA before March 15, 2023, with TNK used thereafter. Selection criteria adhered to American Heart Association guidelines and clinicians' judgment. RESULTS: Although door-to-needle times were similar (P = .20), excluding outliers revealed a significant difference favoring TNK (P = .04). No significant group differences were observed for demographics, National Institutes of Health Stroke Scale scores, length of stay, or post-intracerebral hemorrhage rates. Tenecteplase use resulted in over $40 000 in medication savings during the project period. CONCLUSION: Tenecteplase offers comparable safety and efficacy to tPA for treating AIS, with the added benefit of cost savings. Although clinical outcomes did not significantly differ between the 2 drugs, TNK's reduced cost and ease of administration make it an attractive option, particularly in resource-limited settings. These results support the current organizational treatment protocol favoring TNK.

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