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阿替普酶溶栓治疗二十五周年:治疗窗的演变

Silver Jubilee of Stroke Thrombolysis With Alteplase: Evolution of the Therapeutic Window.

作者信息

Pan Yuanmei, Shi Guowen

机构信息

Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Front Neurol. 2021 Mar 1;12:593887. doi: 10.3389/fneur.2021.593887. eCollection 2021.

Abstract

In 1995, the results of a landmark clinical trial by National Institute of Neurological Disorders and Stroke (NINDS) made a paradigm shift in managing acute cerebral ischemic stroke (AIS) patients at critical care centers. The study demonstrated the efficacy of tissue-type plasminogen activator (tPA), alteplase in improving neurological and functional outcome in AIS patients when administered within 3 h of stroke onset. After about 12 years of efforts and the results of the ECASS-III trial, it was possible to expand the therapeutic window to 4.5 h, which still represents a major logistic issue, depriving many AIS patients from the benefits of tPA therapy. Constant efforts in this regards are directed toward either speeding up the patient recruitment for tPA therapy or expanding the current tPA window. Efficient protocols to reduce the door-to-needle time and advanced technologies like telestroke services and mobile stroke units are being deployed for early management of AIS patients. Studies have demonstrated benefit of thrombolysis guided by perfusion imaging in AIS patients at up to 9 h of stroke onset, signifying "tissue window." Several promising pharmacological and non-pharmacological approaches are being explored to mitigate the adverse effects of delayed tPA therapy, thus hoping to further expand the current tPA therapeutic window without compromising safety. With accumulation of scientific data, stroke organizations across the world are amending/updating the clinical recommendations of tPA, the only US-FDA approved drug for managing AIS patients. Alteplase has been a part of our neurocritical care and we intend to celebrate its silver jubilee by dedicating this review article discussing its journey so far and possible future evolution.

摘要

1995年,美国国立神经疾病与中风研究所(NINDS)一项具有里程碑意义的临床试验结果,在重症监护中心对急性脑缺血性中风(AIS)患者的管理方面引发了范式转变。该研究证明了组织型纤溶酶原激活剂(tPA)阿替普酶在中风发作3小时内给药时,对改善AIS患者神经功能和功能结局的有效性。经过约12年的努力以及ECASS-III试验的结果,治疗时间窗得以扩大至4.5小时,但这仍然是一个重大的后勤问题,使许多AIS患者无法从tPA治疗中获益。在这方面的持续努力旨在加快tPA治疗的患者招募速度或扩大当前的tPA时间窗。正在部署有效的方案以缩短门到针时间,并采用远程中风服务和移动中风单元等先进技术对AIS患者进行早期管理。研究表明,在中风发作长达9小时的AIS患者中,灌注成像引导的溶栓治疗具有益处,这意味着“组织时间窗”。正在探索几种有前景的药物和非药物方法,以减轻延迟tPA治疗的不良反应,从而希望在不影响安全性的情况下进一步扩大当前的tPA治疗时间窗。随着科学数据的积累,世界各地的中风组织正在修订/更新tPA的临床建议,tPA是唯一获得美国食品药品监督管理局(FDA)批准用于治疗AIS患者的药物。阿替普酶一直是我们神经重症监护的一部分,我们打算通过撰写这篇综述文章来庆祝其问世二十五周年,讨论其迄今为止的历程以及可能的未来发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecc2/7956989/6dbb63c9deb1/fneur-12-593887-g0001.jpg

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