Department of Neurology, Haukeland University Hospital, Bergen, Norway; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
Department of Neurology, Haukeland University Hospital, Bergen, Norway; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
J Stroke Cerebrovasc Dis. 2024 Sep;33(9):107849. doi: 10.1016/j.jstrokecerebrovasdis.2024.107849. Epub 2024 Jul 5.
OBJECTIVES: Cerebral microemboli can be detected by transcranial Doppler monitoring (TCDM) and may elucidate stroke etiology, the effect of preventive therapy, and the risk of stroke recurrence. Microemboli detection is usually performed for up to 60 minutes, but due to temporal variability, microembolization may be missed if the monitoring time is too short. We aimed to assess the time course of microembolization in acute ischemic stroke and explore the utility of prolonged and repeated microemboli detection. MATERIALS AND METHODS: Patients with suspected ischemic stroke and symptom onset within 24 hours were examined with bilateral, stationary TCDM for one hour followed by unilateral, ambulatory TCDM for two hours. Unilateral TCDM was repeated for the following two days and after three months. RESULTS: We included 47 patients, of which 41 had ischemic stroke, five had transient ischemic attack, and one had amaurosis fugax. Microemboli were detected in 60 % of patients. The occurrence was highest within 24 hours after onset and significantly lower at three months. Prolonged and repeated microemboli detection yielded only one additional microemboli-positive patient. Hence, patients who initially were microemboli negative tended to remain negative. We could not demonstrate an association between microemboli occurrence and clinical outcome or stroke recurrence. CONCLUSIONS: Microembolic signals are frequent within 24 hours after ischemic stroke onset, but prolonged and repeated microemboli detection did not increase the yield of MES positive patients. CLINICAL TRIAL REGISTRATION-URL: http://www. CLINICALTRIALS: gov. Unique identifier: NCT03543319.
目的:经颅多普勒监测(TCDM)可检测到脑微栓子,有助于阐明中风病因、预防治疗效果及中风复发风险。微栓子检测通常持续 60 分钟,但由于存在时间变异性,如果监测时间过短,可能会错过微栓塞。我们旨在评估急性缺血性中风中微栓塞的时程,并探讨延长和重复微栓塞检测的效用。
材料和方法:发病 24 小时内疑似缺血性中风的患者接受双侧、固定 TCDM 检查 1 小时,随后进行单侧、移动 TCDM 检查 2 小时。单侧 TCDM 在接下来的两天和三个月后重复进行。
结果:我们纳入了 47 名患者,其中 41 名患者为缺血性中风,5 名患者为短暂性脑缺血发作,1 名患者为一过性黑矇。60%的患者检测到微栓子。微栓子发生的高峰时间为发病后 24 小时内,发病 3 个月时显著降低。延长和重复微栓子检测仅增加了 1 例微栓子阳性患者。因此,最初微栓子阴性的患者倾向于保持阴性。我们未能证明微栓子发生与临床结局或中风复发之间存在关联。
结论:缺血性中风发病后 24 小时内微栓子信号频繁出现,但延长和重复微栓子检测并未增加 MES 阳性患者的检出率。
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