Stroke Research and Mobile Stroke Unit, Memorial Hermann Hospital-Texas Medical Center, Houston, Texas, USA.
Cerebrovasc Dis. 2021;50(6):666-680. doi: 10.1159/000519843. Epub 2021 Oct 14.
It has been 50 years since the first explorations of the physiology of cerebral ischemia by measuring cerebral blood flow (CBF), and 25 years since the approval of tissue plasminogen activator for treating acute ischemic stroke. My personal career began and matured during those eras. Here, I provide my perspective on the evolution of acute stroke research and treatment from 1971 to the present, with some in-depth discussion of the National Institutes of Neurologic Disease and Stroke (NINDS) tissue-type plasminogen activator (tPA) stroke trial and development of mobile stroke units.
Studies of CBF and metabolism in acute stroke patients revealed graded tissue injury that was dependent on the duration of ischemia. Subsequent animal research unraveled the biochemical cascade of events occurring at the cellular level after cerebral ischemia. After a decade of failed translation, the development of a relatively safe thrombolytic allowed us to achieve reperfusion and apply the lessons from earlier research to achieve positive clinical results. The successful conduct of the NINDS tPA stroke study coupled with positive outcomes from companion tPA studies around the world created the specialty of vascular neurology. This was followed by an avalanche of research in imaging, a focus on enhancing reperfusion through thrombectomy, and improving delivery of faster treatment culminating in mobile stroke units. Key Messages: The last half century has seen the birth and evolution of successful acute stroke treatment. More research is needed in developing new drugs and catheters to build on the advances we have already made with reperfusion and also in evolving our systems of care to get more patients treated more quickly in the prehospital setting. The history of stroke treatment over the last 50 years exemplifies that medical "science" is an evolving discipline worth an entire career's dedication. What was impossible 50 years ago is today's standard of care, what we claim as dogma today will be laughed at a decade from now, and what appears currently impossible will be tomorrow's realities.
自首次通过测量脑血流 (CBF) 探索脑缺血生理学以来,已经过去了 50 年,自批准组织型纤溶酶原激活剂治疗急性缺血性中风以来,也已经过去了 25 年。我的个人职业生涯始于那个时代,并在那个时代成熟。在这里,我从 1971 年至今,提供了对急性中风研究和治疗演变的看法,并对国立神经病学与中风研究所 (NINDS) 的组织型纤溶酶原激活剂 (tPA) 中风试验和移动中风单元的发展进行了一些深入讨论。
对急性中风患者的 CBF 和代谢研究揭示了与缺血持续时间相关的分级组织损伤。随后的动物研究揭示了脑缺血后细胞水平发生的生化级联反应。经过十年的翻译失败,相对安全的溶栓药物的开发使我们能够实现再灌注,并将早期研究中的经验教训应用于取得积极的临床结果。NINDS tPA 中风研究的成功进行,加上世界各地伴发的 tPA 研究的积极结果,创建了血管神经病学这一专业。随后,成像研究如雨后春笋般涌现,重点是通过血栓切除术增强再灌注,并加快治疗的输送,最终实现了移动中风单元。
过去的半个世纪见证了成功的急性中风治疗的诞生和发展。在开发新的药物和导管方面,我们需要做更多的研究,以在我们已经在再灌注方面取得的进展的基础上更进一步,还需要改进我们的护理系统,以便在院前环境中更快地治疗更多的患者。过去 50 年中风治疗的历史证明,医学“科学”是一个不断发展的学科,值得投入整个职业生涯。50 年前不可能的事情,现在已经成为了标准的治疗方法;今天我们奉为教条的东西,十年后可能会被嘲笑;而现在看似不可能的事情,将来也会成为现实。