Neurology Department, Hospital del Mar, Passeig Marítim de la Barceloneta 25-29, 08003, Barcelona, Spain.
Neurovascular Research Group, IMIM-Hospital del Mar Medical Research Institute, Carrer del Dr. Aiguader, 88, 08003, Barcelona, Spain.
Neurol Sci. 2023 Jun;44(6):2113-2120. doi: 10.1007/s10072-023-06641-y. Epub 2023 Feb 7.
Migraine with aura (MA) is a frequent stroke simulator that can lead to erroneous diagnosis and subsequent unnecessary acute or secondary prevention treatments. We analyzed clinical and laboratory data of migraine with aura and ischemic stroke patients to detect differences that could help in the diagnosis.
Retrospective analysis of a consecutive register of code strokes between January 2005 and June 2020. Diagnosis of ischemic stroke or MA was collected. Multivariable logistic regression analyses were performed to test associations between clinical and blood data with ischemic stroke.
Of 3140 code strokes, 2424 (77.2%) were ischemic strokes and 34 (1.1%) were MA. Migraine cases were younger, more frequently females and with lower prevalence of vascular risk factors. Initial NIHSS was lower in MA cases, but no differences were seen in fibrinolysis rate (30%). Blood test showed lower levels of glucose, D-dimer, and fibrinogen in MA cases. Multivariable model showed and independent association for ischemic stroke with age [OR, (95%CI): 1.09, (1.07-1.12, p < 0.001], male sex [OR, (95%CI): 4.47, (3.80-5.13), p < 0.001], initial NIHSS [OR, (95%CI): 1.21, (1.07-1.34), p < 0.01], and fibrinogen levels [OR, (95%CI): 1.01, (1.00-1.01), p < 0.05]. A model including sex male OR: 3.55 [2.882; 4.598], p < 0.001, and cutoff points (age > 65, OR: 7.953 [7.256; 8.649], p < 0.001, NIHSS > 6, OR: 3.740 [2.882; 4.598], p < 0.01, and fibrinogen > 400 mg/dL, OR: 2.988 [2.290; 3.686], p < 0.01) showed a good global discrimination capability AUC = 0.89 (95%CI: 0.88-0.94).
In code stroke, a model including age, sex, NIHSS, and fibrinogen showed a good discrimination capability to differentiate between MA and Ischemic stroke. Whether these variables can be implemented in a diagnostic rule should be tested in future studies.
有先兆偏头痛(MA)是一种常见的中风模拟病症,可能导致误诊和随后不必要的急性或二级预防治疗。我们分析了有先兆偏头痛和缺血性中风患者的临床和实验室数据,以发现有助于诊断的差异。
对 2005 年 1 月至 2020 年 6 月连续登记的中风代码进行回顾性分析。收集缺血性中风或 MA 的诊断。进行多变量逻辑回归分析,以测试临床和血液数据与缺血性中风之间的关联。
在 3140 例中风代码中,2424 例(77.2%)为缺血性中风,34 例(1.1%)为 MA。偏头痛患者更年轻,女性更常见,血管危险因素的患病率更低。MA 患者的初始 NIHSS 较低,但纤溶率(30%)无差异。血液检查显示 MA 患者的血糖、D-二聚体和纤维蛋白原水平较低。多变量模型显示,缺血性中风与年龄[OR,(95%CI):1.09,(1.07-1.12,p<0.001]、男性[OR,(95%CI):4.47,(3.80-5.13),p<0.001]、初始 NIHSS[OR,(95%CI):1.21,(1.07-1.34),p<0.01]和纤维蛋白原水平[OR,(95%CI):1.01,(1.00-1.01),p<0.05]之间存在独立关联。包括男性[OR:3.55,(2.882;4.598),p<0.001]和截止点(年龄>65 岁,OR:7.953,(7.256;8.649),p<0.001)、NIHSS>6,OR:3.740,(2.882;4.598),p<0.01)和纤维蛋白原>400mg/dL,OR:2.988,(2.290;3.686),p<0.01)的模型显示出良好的整体判别能力 AUC=0.89(95%CI:0.88-0.94)。
在中风代码中,包括年龄、性别、NIHSS 和纤维蛋白原在内的模型显示出良好的判别能力,可区分 MA 和缺血性中风。这些变量是否可以在诊断规则中实施,应在未来的研究中进行测试。