动脉高血压和动脉粥样硬化背景下慢性脑缺血患者多模式神经保护的可能性

I. Gribacheva, T. Popova, E. Petrova, A. V. Zvonkova
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引用次数: 0

摘要

慢性脑血管病表现为认知、情绪和自主神经障碍的结合。正确及时地评估和准确诊断情绪和自主神经障碍,并及时纠正它们,对于减缓认知缺陷的进展非常重要。目的:探讨以动脉高血压和动脉粥样硬化为背景的中年慢性脑缺血(CCI)患者,经静脉滴注(500 mg 1次/天)给药14 d后,口服药物Mexidol FORTE 250 250 mg 3次/天,连续60 d的疗效和安全性。材料和方法。开放观察项目包括60例年龄在45 - 59岁的CCI患者,经神经心理学和神经影像学检查结果证实。患者首先静脉注射墨西哥idol(14天),然后口服丸剂——墨西哥idol FORTE 250(60天)。患者接受神经心理测试,评估反应性和个人焦虑水平(Spielberger-Khanin量表),植物功能障碍水平(V.L. Golubev修改的A.M. Wayne自主反应量表),一般、精神和身体虚弱的严重程度(MFI-20)和生活质量(MOS SF-36问卷)。结果。治疗的结果使得在使用墨西多的背景下建立衰弱综合征和植物功能障碍的缓解成为可能。与基线及对照组比较,差异均有统计学意义(p<0.05)。使用墨西多后,主诉和主观症状的严重程度有所下降。综合积极效应导致生活质量指标的提高(p<0.05)。这种治疗耐受性良好。结论。CCI患者有明显的情绪、营养和衰弱障碍。使用墨西多可减轻这些疾病的严重程度,因此有理由推荐用于此类患者的治疗。
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Possibilities of multimodal neuroprotection in patients with chronic cerebral ischemia on the background of arterial hypertension and atherosclerosis
hronic cerebrovascular pathology is manifested by a combination of cognitive, emotional and autonomic disorders. Correct and timely assessment and accurate diagnosis of emotional and autonomic disorders and their timely correction are important, among other things, for slowing down the progression of cognitive deficits. Objective: to study the efficacy and safety of Mexidol administered intravenously by drip infusion (500 mg 1 time per day) for 14 days, followed by oral administration of the drug Mexidol FORTE 250 at a dose of 250 mg 3 times a day for 60 days in middle-aged patients with chronic cerebral ischemia (CCI) on the background of arterial hypertension and atherosclerosis. Material and methods. The open observational program included 60 patients aged 45 to 59 years with CCI, confirmed by the results of a neuropsychological and neuroimaging examination. Patients received Mexidol first intravenously (14 days), and then orally in pills – Mexidol FORTE 250 (60 days). Patients underwent neuropsychological testing, assessment of the level of reactive and personal anxiety (Spielberger–Khanin scale), of vegetative disfunction (A.M. Wayne's autonomic response scale modified by V.L. Golubev), of the severity of general, mental and physical asthenia (MFI-20) and quality of life (MOS SF-36 questionnaire). Results. The results of the treatment made it possible to establish relief of asthenic syndrome and vegetative dysfunction on the background of Mexidol use. The differences were statistically significant both when comparing with the baseline and with the comparison group (p<0.05). The use of Mexidol was accompanied by a decrease in the severity of complaints and subjective symptoms. The combination of positive effects led to an increase in indicators of quality of life (p<0.05). The treatment was well tolerated. Conclusion. Patients with CCI have significant emotional, vegetative and asthenic disorders. The use of Mexidol can reduce the severity of these disorders, which gives reason to recommend it for the treatment of such patients.
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