Tettenborn D, Porto L, Ryman T, Strugo V, Taquoi G, Battye R
Medical Department of Bayer Germany.
Neurosurg Rev. 1987;10(2):77-84. doi: 10.1007/BF01741442.
The present studies show that nimodipine prevents and/or improves permanent ischemic neurological deficits in patients with subarachnoid hemorrhage. This was particularly marked in four double-blind, placebo-controlled studies in which statistically significant reductions in mortality and morbidity as consequence of cerebral vasospasm were found. The drug has been shown to increase cerebral blood flow, to reduce vasoconstriction, although not to fully prevent angiographic vasospasm, and to improve central conduction time. Nimodipine did not increase the rate of rebleeding. Its administration during anesthesia does not result in management problems. In general, nimodipine was well tolerated. Side effects were recorded mainly in open studies using the intravenous formulation and consisted mainly of decreases in blood pressure and headaches. Transient increases in liver enzymes may be due to the organic solvent. Hence, all results indicate that patients with subarachnoid hemorrhage will benefit from preventive or therapeutic nimodipine treatment.
目前的研究表明,尼莫地平可预防和/或改善蛛网膜下腔出血患者的永久性缺血性神经功能缺损。这在四项双盲、安慰剂对照研究中尤为明显,在这些研究中发现,因脑血管痉挛导致的死亡率和发病率有统计学意义的降低。已证明该药物可增加脑血流量、减轻血管收缩,尽管不能完全预防血管造影显示的血管痉挛,并可改善中枢传导时间。尼莫地平不会增加再出血率。在麻醉期间使用该药物不会导致管理问题。总体而言,尼莫地平耐受性良好。副作用主要记录在使用静脉制剂的开放性研究中,主要包括血压下降和头痛。肝酶的短暂升高可能归因于有机溶剂。因此,所有结果表明,蛛网膜下腔出血患者将从预防性或治疗性尼莫地平治疗中获益。