Kiser Tyree H
Associate Professor, Department of Clinical Pharmacy, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, and Critical Care Pharmacy Specialist, University of Colorado Hospital, University of Colorado Anschutz Medical Campus , 12850 E. Montview Boulevard, C238, Aurora, CO 80045 ; phone: 303-724-2883 ; fax: 303-724-0979 ; e-mail:
Hosp Pharm. 2014 Nov;49(10):923-41. doi: 10.1310/hpj4910-923.
The occurrence of cerebral vasospasm after aneurysmal subarachnoid hemorrhage (SAH) is a significant event resulting in decreased cerebral blood flow and oxygen delivery. Prevention and treatment of cerebral vasospasm is vital to avert neurological damage and reduced functional outcomes. A variety of pharmacotherapy interventions for the prevention and treatment of cerebral vasospasm have been evaluated. Unfortunately, very few large randomized trials exist to date, making it difficult to make clear recommendations regarding the efficacy and safety of most pharmacologic interventions. Considerable debate exists regarding the efficacy and safety of hypervolemia, hemodilution, and hypertension (triple-H therapy), and the implementation of each component varies substantially amongst institutions. There is a new focus on euvolemic-induced hypertension as a potentially preferred mechanism of hemodynamic augmentation. Nimodipine is the one pharmacologic intervention that has demonstrated favorable effects on patient outcomes and should be routinely administered unless contraindications are present. Intravenous nicardipine may offer an alternative to oral nimodipine. The addition of high-dose magnesium or statin therapy has shown promise, but results of ongoing large prospective studies are needed before they can be routinely recommended. Tirilazad and clazosentan offer new pharmacologic mechanisms, but clinical outcome results from prospective randomized studies have largely been unfavorable. Locally administered pharmacotherapy provides a targeted approach to the treatment of cerebral vasospasm. However, the paucity of data makes it challenging to determine the most appropriate therapy and implementation strategy. Further studies are needed for most pharmacologic therapies to determine whether meaningful efficacy exists.
动脉瘤性蛛网膜下腔出血(SAH)后发生脑血管痉挛是一个重要事件,会导致脑血流量和氧气输送减少。预防和治疗脑血管痉挛对于避免神经损伤和减少功能预后至关重要。已经评估了多种用于预防和治疗脑血管痉挛的药物治疗干预措施。不幸的是,迄今为止很少有大型随机试验,这使得难以就大多数药物干预措施的疗效和安全性提出明确建议。关于扩容、血液稀释和高血压(三联-H疗法)的疗效和安全性存在相当大的争议,并且各机构在每个组成部分的实施上差异很大。目前新的关注点是等容性高血压作为血流动力学增强的一种潜在优选机制。尼莫地平是一种已证明对患者预后有良好效果的药物干预措施,除非有禁忌症,否则应常规给药。静脉注射尼卡地平可能是口服尼莫地平的一种替代方法。添加高剂量镁或他汀类药物治疗已显示出前景,但在能够常规推荐之前,还需要正在进行的大型前瞻性研究的结果。替拉扎特和氯沙坦提供了新的药理机制,但前瞻性随机研究的临床结局结果大多不理想。局部给药的药物治疗为脑血管痉挛的治疗提供了一种靶向方法。然而,数据的匮乏使得确定最合适的治疗方法和实施策略具有挑战性。对于大多数药物治疗,还需要进一步研究以确定是否存在有意义的疗效。