Mizoi K, Yoshimoto T, Takahashi A, Fujiwara S, Koshu K, Sugawara T
Department of Neurosurgery, Kohnan Hospital, Sendai, Japan.
J Neurosurg. 1993 Mar;78(3):430-7. doi: 10.3171/jns.1993.78.3.0430.
The authors have evaluated the efficacy of postoperative intrathecal injections of tissue-type plasminogen activator (tPA) in preventing cerebral vasospasm in patients with a diffuse thick subarachnoid hemorrhage (SAH). The present study examined 105 patients who underwent direct surgery within 48 hours of SAH and whose computerized tomography (CT) findings were classified as Fisher CT Group 3. Patients showing diffuse thick subarachnoid blood clots on CT with greater than 75 Hounsfield units (HU) were included in the tPA therapy group and those with below 75 HU comprised the control group. The surgical method was the same in both groups, and both groups had cisternal drainage instituted. On the day following the operation, the tPA group was given an intrathecal injection of tPA (2 mg), and this was continued for several days until all of the cisterns exhibited low density on CT scans. Follow-up angiography showed that 26 cases (87%) in the tPA group had no vasospasm, three (10%) had moderate vasospasm, and one (3%) had severe vasospasm. All four patients showing spasm on angiography were asymptomatic, and there were no cases of delayed ischemic neurological deficits (DIND). In contrast, there were 11 cases (15%) with DIND in the control group. In the tPA group, there was one case of SAH caused by drainage catheter removal, one with a small epidural hematoma, and one with subgaleal fluid accumulation; all of these were treated conservatively with favorable results. Overall, there were no infectious complications related to cisternal drainage and intrathecal injection of tPA. These results indicate that multiple intrathecal injections of small doses of tPA are effective and safe in preventing vasospasm. On the basis of this experience, the authors conclude that injection of 2 mg of tPA daily for 5 days (a total of 10 mg) is effective in preventing the development of vasospasm.
作者评估了术后鞘内注射组织型纤溶酶原激活剂(tPA)对弥漫性厚蛛网膜下腔出血(SAH)患者预防脑血管痉挛的疗效。本研究检查了105例在SAH后48小时内接受直接手术且计算机断层扫描(CT)结果分类为Fisher CT 3组的患者。CT显示弥漫性厚蛛网膜下腔血凝块且亨氏单位(HU)大于75的患者被纳入tPA治疗组,HU低于75的患者组成对照组。两组手术方法相同,且两组均进行了脑池引流。术后当天,tPA组接受鞘内注射tPA(2mg),并持续数天,直到所有脑池在CT扫描上显示为低密度。随访血管造影显示,tPA组26例(87%)无血管痉挛,3例(10%)有中度血管痉挛,1例(3%)有重度血管痉挛。血管造影显示有痉挛的4例患者均无症状,且无迟发性缺血性神经功能缺损(DIND)病例。相比之下,对照组有11例(15%)发生DIND。在tPA组,有1例因拔除引流导管导致SAH,1例有小的硬膜外血肿,1例有帽状腱膜下积液;所有这些均经保守治疗,效果良好。总体而言,无与脑池引流和鞘内注射tPA相关的感染并发症。这些结果表明,多次鞘内注射小剂量tPA在预防血管痉挛方面有效且安全。基于这一经验,作者得出结论,每天注射2mg tPA,持续5天(共10mg)可有效预防血管痉挛的发生。