从临床和实验室角度评估脑力药物Actitropil(囟素西坦)治疗气喘综合征的疗效

M. R. Bekuzarova, Amirkhan A. Kumakhov
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引用次数: 0

摘要

背景。气喘是各科医生临床实践中最常见的症状之一。这是因为这种病症的发病率很高:慢性躯体疾病患者的发病率为 45% 至 90%,急性病理过程患者的发病率约为 55%。目前还没有治疗气喘病的统一标准;不过,这种病症的医学矫正基础是促神智药物。研究目的研究促智药物 Actitropil(囟素西坦)对各种类型气喘病患者的临床疗效和安全性。材料和方法。临床观察项目包括50名有气喘症状的患者(平均年龄为43.22±14.60岁)。患者接受的Actitropil(囟素)剂量为每天200毫克,分两次服用。疗程为 30 天,总随访时间为 60 天。疗程前后以及延迟期的治疗效果根据以下量表进行评估:气喘 MFI-20、幸福感、活动、情绪 SAN、焦虑和抑郁 HADS(第 1 部分)、睡眠质量 Spiegel、生活质量 EQoL-5D-3L。患者对治疗的满意度和耐受性也按 5 分制进行评估;记录不良事件,并根据受试者的主观评估计算治疗效果良好、满意和不满意的患者人数。血液参数分析作为实验室评估方法:红细胞、白细胞、网状细胞、血小板、血红蛋白、血细胞比容、血沉、总蛋白、葡萄糖、丙氨酸氨基转移酶、天门冬氨酸氨基转移酶、凝血酶原和凝血酶时间、凝血酶原、国际标准化比率、活化部分凝血活酶时间、纤维蛋白原。结果和结论。研究结果表明,在治疗各种类型的气喘综合征(包括伴有合并症的气喘综合征)时,使用阿昔洛韦具有很高的疗效(98%)和安全性(无不良反应,治疗过程中不良反应水平低,对肝功能、血液凝固和碳水化合物代谢无负面影响)。Actitropil 对气喘的伴随症状有明显的治疗效果:焦虑、睡眠状况和生活质量。该药物的抗气喘作用不因年龄而异,并在延迟期有所增加。
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Clinical and laboratory evaluation of the effectiveness of the nootropic drug Actitropil (fonturacetam) in the treatment of asthenic syndrome
Background. Asthenia is one of the most common symptoms in the clinical practice of a doctor of any specialty. This is due to the high incidence of this pathology: in patients with chronic somatic diseases from 45% to 90%, with an acute pathological process – about 55%. There are no uniform standards for the treatment of asthenic disorder; however, the basis for the medical correction of this pathology is nootropic drugs. Aim. To study the clinical efficacy and safety of the nootropic drug Actitropil (fonturacetam) in patients with various types of asthenic disorder. Materials and methods. The observational clinical program included 50 patients (average age 43.22±14.60) with asthenic symptoms. Patients received Actitropil (fonturacetam) at a dose of 200 mg per day, divided into two doses. The duration of therapy was 30 days, the total duration of follow-up was 60 days. The effectiveness of treatment was evaluated before and after the course of therapy, as well as in the delayed period according to the scales of asthenia MFI-20, well-being, activity, mood SAN, anxiety and depression HADS (part 1), sleep quality Spiegel, quality of life EQoL-5D-3L. Patients' satisfaction with the treatment and tolerability of therapy were also assessed on 5-point scales; adverse events were recorded and the number of patients with good, satisfactory and unsatisfactory treatment results was calculated based on the subjective assessment of the subjects. Blood parameters analysis was used as laboratory assessment methods: erythrocytes, leukocytes, reticulocytes, platelets, hemoglobin, hematocrit, blood sedimentation rate, total protein, glucose, alanine aminotransferase, aspartate aminotransferase, prothrombin and thrombin time, prothrombin, international normalised ratio, activated partial thromboplastin time, fibrinogen. Results and conclusion. The results of the study showed high efficacy (98%) and safety of the use of Actitropil (absence of adverse events, low adverse events level during the course of treatment, no negative effect on liver function, blood coagulation and carbohydrate metabolism) in the treatment of various types of asthenic syndrome, including those associated with comorbid diseases. There is a significant therapeutic effect of Actitropil on concomitant symptoms of asthenia: anxiety, sleep status and quality of life. The antiasthenic effect of the drug does not differ depending on age and increases in the delayed period.
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