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蛛网膜下腔出血超早期脑池内注射组织型纤溶酶原激活剂后行脑脊液引流的实验研究

Experimental study of intracisternal administration of tissue-type plasminogen activator followed by cerebrospinal fluid drainage in the ultra-early stage of subarachnoid haemorrhage.

作者信息

Kawada S, Kinugasa K, Meguro T, Hirotsune N, Tokunaga K, Kamata I, Nakashima H, Ohmoto T

机构信息

Department of Neurological Surgery, Okayama University Medical School, Japan.

出版信息

Acta Neurochir (Wien). 1999;141(12):1331-8. doi: 10.1007/s007010050438.

Abstract

This experimental study evaluated the effect of intrathecal injection of tissue-type plasminogen activator followed by cisternal drainage in the ultra-early stage of aneurysmal subarachnoid haemorrhage to prevent vasospasm. Twenty Japanese white rabbits were divided into five groups. Either tPA (groups A, B, and E) or saline (groups C and D) was injected intrathecally 1 hour (groups A, B, C, and D) or 21 hours (group E) after the intrathecal injection of blood. Cerebrospinal fluid was drained 2, 4, and 6 hours after the intrathecal injection of blood (groups A, C, and E). On day 4, the angiographic caliber of the basilar artery in each group was as follows (mean +/- SD): A, 85.9 +/- 5.0%; B, 74.6 +/- 5.3%; C, 69.1 +/- 2.7%; D, 64.0 +/- 4.9%; E, 80.2 +/- 2.7% (compared with baseline). In the two groups in which CSF was drained (groups A and C), fibrinolysis with tPA significantly suppressed vasospasm. In the two groups treated with tPA (groups A and B), cisternal drainage significantly suppressed vasospasm. In the two groups treated with saline (groups C and D), however, cisternal drainage did not suppress vasospasm. Examination of the series of CSF samples (groups A and C) showed that fibrinolysis with tPA effectively cleared clots early. In the two groups treated with tPA and CSF drainage (groups A and E), early removal of subarachnoid clots reduced the degree of vasospasm. Early fibrinolysis with tPA and early removal of subarachnoid clots by drainage is effective for preventing vasospasm.

摘要

本实验研究评估了在动脉瘤性蛛网膜下腔出血超早期鞘内注射组织型纤溶酶原激活剂(tPA)后行脑池引流预防血管痉挛的效果。将20只日本白兔分为五组。在鞘内注射血液后1小时(A、B、C和D组)或21小时(E组)鞘内注射tPA(A、B和E组)或生理盐水(C和D组)。在鞘内注射血液后2、4和6小时进行脑脊液引流(A、C和E组)。在第4天,每组基底动脉的血管造影管径如下(平均值±标准差):A组,85.9±5.0%;B组,74.6±5.3%;C组,69.1±2.7%;D组,64.0±4.9%;E组,80.2±2.7%(与基线相比)。在进行脑脊液引流的两组(A和C组)中,tPA介导的纤维蛋白溶解显著抑制了血管痉挛。在接受tPA治疗的两组(A和B组)中,脑池引流显著抑制了血管痉挛。然而,在接受生理盐水治疗的两组(C和D组)中,脑池引流并未抑制血管痉挛。对一系列脑脊液样本(A和C组)的检查表明,tPA介导的纤维蛋白溶解可有效早期清除血凝块。在接受tPA和脑脊液引流治疗的两组(A和E组)中,早期清除蛛网膜下腔血凝块降低了血管痉挛的程度。tPA早期进行纤维蛋白溶解和通过引流早期清除蛛网膜下腔血凝块对预防血管痉挛有效。

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