Impact of Carotid Siphon Calcification on the Course and Outcome of Patients With Aneurysmal Subarachnoid Hemorrhage

医学 蛛网膜下腔出血 改良兰金量表 血管痉挛 缺血 阿司匹林 优势比 动脉瘤 内科学 心脏病学 麻醉 外科 缺血性中风
作者
A. Engel,Li Song,Laurèl Rauschenbach,Meltem Gümüs,Alejandro N. Santos,Thiemo Florin Dinger,Marvin Darkwah Oppong,Yan Li,Oliver Gembruch,Yahya Ahmadipour,Philipp Dammann,Ulrich Sure,Ramazan Jabbarli
出处
期刊:Stroke [Ovid Technologies (Wolters Kluwer)]
标识
DOI:10.1161/strokeaha.124.047594
摘要

BACKGROUND: Carotid siphon calcification (CSC) serves as a marker of atherosclerosis and therefore may influence the outcome after subarachnoid hemorrhage (aSAH). We aimed to analyze the impact of CSC on neurological outcomes, ischemia, and vasospasm. METHODS: A total of 716 patients with aSAH were treated between December 2004 and June 2016 in our central European tertiary neurovascular care center in Essen, Germany. CSC was recorded using the Woodcock scale (grades 0–3) on a computed tomography scan. Study end points included an unfavorable outcome at 6 months post-aSAH (modified Rankin Scale score ≥4), vasospasm, and early cerebral ischemia (72 hours) and delayed cerebral ischemia (delayed cerebral ischemia; >72 hours) in the follow-up computed tomography scans. The associations were adjusted for patients’ baseline characteristics and secondary complications. Finally, within a subgroup analysis, patients with and without daily aspirin intake after endovascular aneurysm occlusion were compared. RESULTS: Increasing grades of CSC were associated with lower rates of vasospasm in the anterior circulation. Severe CSC (grade 3) was independently related to the risk of an unfavorable outcome (adjusted odds ratio [aOR], 4.06 [95% CI, 1.98–8.33]; P <0.001) and early cerebral ischemia (aOR, 1.58 [95% CI, 1.03–2.43]; P =0.035) but not delayed cerebral ischemia (aOR, 1.08 [95% CI, 0.67–1.73]; P =0.763). In the aspirin subgroup analysis, the negative effect of severe CSC on functional outcome remained significant only in aSAH cases without aspirin (aOR, 5.47 [95% CI, 2.38–12.54]; P <0.001). In contrast, there was no association between severe CSC and unfavorable outcomes among individuals with daily aspirin intake (aOR, 0.84 [95% CI, 0.59–4.21]; P =0.603). CONCLUSIONS: Our data suggest CSC as a cerebrovascular risk factor resulting in higher rates of early cerebral ischemia and unfavorable outcomes after aSAH. However, by increasing arterial stiffness, CSC might lower the probability of vasospasm, which could explain the missing link between CSC and delayed cerebral ischemia. Additionally, aspirin intake seems to potentially mitigate the negative impact of CSC on aSAH outcome. Further investigations are needed to confirm the observations from the present study.
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