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[新冠后虚弱综合征]

[Asthenic post-COVID syndrome].

作者信息

Khaibullina D Kh, Maksimov Y N

机构信息

Kazan State Medical Academy - branch of the Russian Medical Academy of Continuing Professional Education, Kazan, Russia.

出版信息

Zh Nevrol Psikhiatr Im S S Korsakova. 2023;123(3):61-69. doi: 10.17116/jnevro202312303161.

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.

摘要

目的

评估多组分生物调节药物创伤紫(Traumeel S)、泛癸利酮复方制剂(Ubichinon compositum)和辅酶复方制剂(Coenzyme compositum)联合治疗新冠后虚弱综合征的疗效和安全性。

材料与方法

该研究纳入了104例新冠后患者(平均年龄39.5[30.8;48]岁),这些患者已从急性感染过程中临床康复,虚弱综合征持续2周 至6个月;虚弱综合征在虚弱视觉模拟量表(VAS)上的严重程度至少为30分。在研究开始前,除了体格检查外,还使用以下问卷和量表评估患者的状况:虚弱VAS量表、评估虚弱的主观量表(MFI-20)、L.D.马尔科娃生活质量问卷(EQ-5D)、自主神经功能紊乱体征识别问卷(Vayne A.M.)。在治疗开始后2周、1个月以及治疗结束后1个月的随访中监测患者的状况。主要组患者接受联合治疗,包括创伤紫1片,每日3次,泛癸利酮复方制剂和辅酶复方制剂各2.2 ml,隔日交替肌内注射,共1个月(每个疗程每种药物注射15次)。对照组患者在30天内服用刺五加提取物100 mg,每日2次,每次2片,饭前服用,并服用维生素B。在疗程结束后1个月,通过分析虚弱严重程度(VAS量表)、生活质量(EQ-5D问卷)、患者对治疗的满意度(5分制)来评估治疗效果。

结果

治疗结果呈阳性。两组患者的总体虚弱严重程度、低活动量和低动力均显著降低,无显著差异。同时,对照组患者的生活质量与身心虚弱之间无相关性,而主要组患者的生活质量与虚弱严重程度呈负相关,这表明随着虚弱严重程度的降低,生活质量有所提高。其中一个显著差异是主要组患者的头痛和肌肉骨骼疼痛有所减轻。

结论

与包括刺五加提取物和复合维生素B制剂在内的常见治疗方案之一相比,创伤紫、泛癸利酮复方制剂和辅酶复方制剂联合生物调节疗法治疗新冠后虚弱综合征具有优势。

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