Intra-arterial nimodipine for the treatment of refractory delayed cerebral ischemia after aneurysmal subarachnoid hemorrhage

医学 尼莫地平 格拉斯哥结局量表 血管痉挛 蛛网膜下腔出血 脑血管痉挛 耐火材料(行星科学) 缺血 麻醉 脑梗塞 梗塞 外科 内科学 格拉斯哥昏迷指数 心肌梗塞 物理 天体生物学
作者
Laura Victoria Vossen,Miriam Weiss,Walid Albanna,Catharina Conzen,Henna Schulze-Steinen,Tobias Rossmann,Tobias Schmidt,Anke Höllig,Martin Wiesmann,Hans Clusmann,Gerrit Alexander Schubert,Michael Veldeman
出处
期刊:Journal of NeuroInterventional Surgery [BMJ]
卷期号:17 (e1): e31-e40 被引量:13
标识
DOI:10.1136/jnis-2023-021151
摘要

Background Delayed cerebral ischemia (DCI) is one of the main contributors to poor clinical outcome after aneurysmal subarachnoid hemorrhage (SAH). Endovascular spasmolysis with intra-arterial nimodipine (IAN) may resolve angiographic vasospasm, but its effect on infarct prevention and clinical outcome is still unclear. We report the effect of IAN on infarction rates and functional outcome in a consecutive series of SAH patients. Methods To assess the effectiveness of IAN, we collected functional outcome data of all SAH patients referred to a single tertiary center since its availability (2011–2020). IAN was primarily reserved as a last tier option for DCI refractory to induced hypertension (iHTN). Functional outcome was assessed after 12 months according to the Glasgow Outcome Scale (GOS, favorable outcome = GOS4-5). Results Out of 376 consecutive SAH patients, 186 (49.5%) developed DCI. Thereof, a total of 96 (25.5%) patients remained unresponsive to iHTN and received IAN. DCI-related infarction was observed in 44 (45.8%) of IAN-treated patients with a median infarct volume of 111.6 mL (Q 1 : 51.6 to Q 3 : 245.7). Clinical outcome was available for 84 IAN-treated patients. Of those, a total of 40 (47.6%) patients reached a favorable outcome after 1 year. Interventional complications were observed in 9 (9.4%) of the IAN-treated patients. Conclusion Intra-arterial spasmolysis using nimodipine infusion was associated with low treatment specific complications. Despite presenting a subgroup of severely affected SAH patients, almost half of IAN-treated patients were able to lead an independent life after 1 year of follow-up. Trial registration number German Clinical Trial Register DRKS00030505.
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