[Asthenic post-COVID syndrome].

Q3 Medicine
D Kh Khaibullina, Y N Maksimov
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引用次数: 0

Abstract

Objective: To evaluate the efficacy and safety of combination therapy for post-COVID asthenic syndrome with multicomponent bioregulatory drugs Traumeel S, Ubichinon compositum and Coenzyme compositum.

Material and methods: The study included 104 patients (averaged age 39.5 [30.8; 48] years) after COVID-19, clinically recovered from an acute infectious process, with asthenic syndrome lasting from 2 weeks to 6 months; the severity of asthenic syndrome on the asthenia VAS scale was at least 30 points. Before the start of the study, in addition to a physical examination, the patient's condition was assessed using the following questionnaires and scales: VAS for asthenia, subjective scale for assessing asthenia (MFI-20), L.D. Malkova, a questionnaire for the quality of life (EQ-5D), a questionnaire for identifying signs of autonomic disorders (Vayne A.M.). The patient's condition was monitored during follow-up visits 2 weeks, 1 month after the start of treatment and 1 month after the end of treatment. Patients of the main group received combination therapy, which included Traumeel S 1 tablet x 3 times a day, Ubichinone compositum and Coenzyme compositum 2.2 ml intramuscularly, alternating every other day, for 1 month (15 injections of each drug per course of treatment). Patients of the comparison group received eleutherococcus extract 100 mg during 30 days, 2 tablets x 2 times a day before mealsand vitamins B. The effectiveness of therapy was assessed by analysis of the asthenia severity (VAS scale), quality of life (EQ-5D questionnaire), patient satisfaction with treatment on a 5-point scale, which was carried out 1 month after the end of the course of treatment.

Results: As a result of the treatment was positive. The general asthenia severity, low activity and motivation significantly decreased in patients of both groups without significant differences. At the same time, in patients of the comparison group, there was no correlation between the quality of life and physical and mental asthenia, while in the main group there was an inverse correlation with the asthenia severity, which indicates an increase in the quality of life with a decrease in the severity of asthenia. One of the significant differences was the regression of headache and musculoskeletal pain in patients of the main group.

Conclusion: The advantage of combined therapy of post-COVID asthenic syndrome with bioregulation therapy Traumeel S, Ubichinone compositum and Coenzyme compositum was shown in comparison with one of the common treatment regimens, including eleutherococcus extract and combined preparations of B vitamins.

[covid后虚弱综合征]。
目的:评价多组分生物调节药物曲美尔、乌比草素、辅酶复合制剂联合治疗新冠肺炎后虚弱综合征的疗效和安全性。材料和方法:研究纳入104例患者,平均年龄39.5岁[30.8;48]年)后,临床从急性感染过程中恢复,虚弱综合征持续2周到6个月;在衰弱VAS评分中,衰弱综合征的严重程度至少为30分。在研究开始前,除体格检查外,还使用以下问卷和量表对患者的状况进行评估:衰弱VAS评分、衰弱主观评定量表(MFI-20)、L.D. Malkova、生活质量问卷(EQ-5D)、自主神经障碍症状识别问卷(Vayne A.M.)。在治疗开始后2周、1个月和治疗结束后1个月的随访中监测患者的病情。主组患者给予联合治疗:曲美尔S 1片x 3次/ d,联合紫红酮、辅酶复方2.2 ml肌注,隔日交替,疗程1个月(每种药物每疗程15针)。对照组患者在治疗结束1个月后,采用衰弱严重程度(VAS量表)、生活质量(EQ-5D问卷)、患者对治疗的满意度(5分制)进行分析,评价治疗效果。结果:治疗结果为阳性。两组患者全身乏力严重程度、活动量和动力均显著降低,但无显著性差异。同时,对照组患者的生活质量与身心乏力无相关性,而主组患者的生活质量与身心乏力严重程度呈负相关,即随着身心乏力严重程度的减轻,生活质量有所提高。其中一个显著差异是主组患者头痛和肌肉骨骼疼痛的消退。结论:与棘球球菌提取物联合B族维生素制剂等常用治疗方案相比,生物调节疗法曲美美联合紫红酮复合辅酶复合制剂联合治疗新冠肺炎后虚弱综合征具有优势。
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来源期刊
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova Medicine-Psychiatry and Mental Health
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0.80
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