Shchepankevich L A, Tanashyan M M, Nikolaev Yu A, Novikova E G, Pinhasov B B, Pervuninskaya M A, Antonova K V
Research Institute of Experimental and Clinical Medicine, Novosibirsk, Russia.
Neurology Research Center, Moscow, Russia.
Zh Nevrol Psikhiatr Im S S Korsakova. 2019;119(5):76-79. doi: 10.17116/jnevro201911905176.
To evaluate the efficacy and safety of cytoflavin as an additional agent in the treatment of painful diabetic polyneuropathy and to analyze changes in the life quality of the patients studied.
An analysis of treatment data was carried out in 61 patients with verified painful diabetic polyneuropathy, who were divided into 2 groups depending on the therapy regimen. Patients of the main group (n=36) at the start of the therapy with gabapentin additionally received cytoflavin: intravenously, slowly, 10 ml diluted in 0.9% NaCl 200 ml for 10 days, followed by switching to per os 2 tablets 2 times a day for 25 days. Patients of the comparison group used gabapentin in comparable doses as an analgesic symptomatic therapy. Clinical neurological and anamnestic methods were used to monitor and assess the condition of patients.
Cytoflavin inclusion in the standard symptomatic treatment of patients with painful diabetic polyneuropathy contributed to a more pronounced decrease in the subjective assessment of pain (VAS scale) by the 10th day (42.8±2.4 mm versus 58.2±2.1 mm in the comparison group) and its maximum level of decline to 21-25 days. The achieved result was maintained by the 35th day (21.4±1.1 mm against 22.4±1.7 mm in the comparison group). At the same time, the quality of life of patients as assessed by SF-36 was significantly increased after treatment. The results obtained, along with the safety of the drug, allow us to recommend its inclusion in the treatment regimens for patients with this pathology.
评估细胞色素复合制剂作为辅助药物治疗疼痛性糖尿病多发性神经病变的疗效和安全性,并分析所研究患者生活质量的变化。
对61例确诊为疼痛性糖尿病多发性神经病变的患者的治疗数据进行分析,根据治疗方案将患者分为2组。主要组(n = 36)在开始使用加巴喷丁治疗时额外接受细胞色素复合制剂:静脉滴注,缓慢滴注,10 ml用200 ml 0.9%氯化钠稀释,持续10天,随后改为口服,每日2次,每次2片,持续25天。对照组患者使用相当剂量的加巴喷丁进行止痛对症治疗。采用临床神经学和既往史方法监测和评估患者状况。
在疼痛性糖尿病多发性神经病变患者的标准对症治疗中加入细胞色素复合制剂,有助于在第10天时更显著地降低疼痛的主观评估(视觉模拟评分法)(42.8±2.4 mm,而对照组为58.2±2.1 mm),且其最大降幅出现在21 - 25天。到第35天时,所取得的结果得以维持(21.4±1.1 mm,而对照组为22.4±1.7 mm)。同时,治疗后通过SF - 36评估的患者生活质量显著提高。所获得的结果以及该药物的安全性,使我们建议将其纳入此类病症患者的治疗方案中。