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中风。治疗领域的革命。

Stroke. Revolution in therapy.

作者信息

Gress D R

机构信息

Department of Neurology, University of California, San Francisco, School of Medicine 94143-0114.

出版信息

West J Med. 1994 Sep;161(3):288-91.

Abstract

Stroke remains the third leading cause of death in this country, although recent advances in both clinical and basic science research have revolutionized the concept of stroke. Studies of primary and secondary stroke prevention have now documented the means to prevent thousands of cases of stroke each year. Three distinct strategies are evolving for intervention in the acute stroke process. Evidence is clear that ischemia leads to a toxic accumulation of intracellular calcium, in part mediated by excitatory neurotransmitters such as glutamate. Glutamate antagonists have shown clear benefit in experimental stroke models, and early clinical trials are underway. Acute revascularization to restore perfusion is also feasible and may minimize the extent of infarction. Studies of fibrinolytic agents are promising, with randomized clinical studies being done. While reperfusion is desired, it may be associated with additional neuronal injury. The development of anaerobic metabolism followed by reperfusion and aerobic conditions favors oxidation and free-radical formation. This mechanism of injury can be decreased by agents known to scavenge free radicals, and clinical trials are also testing this. This revolution in the understanding of ischemia, as well as the outpouring of new pharmacologic agents, is making stroke a true neurologic emergency requiring immediate intervention.

摘要

中风仍然是该国第三大死因,尽管临床和基础科学研究的最新进展彻底改变了中风的概念。原发性和继发性中风预防研究现已证明每年可预防数千例中风的方法。目前正在形成三种不同的策略来干预急性中风过程。有证据清楚地表明,缺血会导致细胞内钙的毒性积累,部分是由谷氨酸等兴奋性神经递质介导的。谷氨酸拮抗剂在实验性中风模型中已显示出明显的益处,早期临床试验正在进行中。急性血管重建以恢复灌注也是可行的,并且可以使梗死范围最小化。纤维蛋白溶解剂的研究很有前景,正在进行随机临床研究。虽然需要再灌注,但它可能与额外的神经元损伤有关。无氧代谢后再灌注和有氧条件有利于氧化和自由基形成。已知清除自由基的药物可以减少这种损伤机制,临床试验也在对此进行测试。对缺血理解的这场革命,以及新药物的大量涌现,使中风成为真正需要立即干预的神经急症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c53/1011411/56c816f85985/westjmed00061-0082-a.jpg

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