How to optimize the management of patients with post-infectious asthenia who have undergone COVID-19 at the outpatient stage?
- Authors: Zueva I.B1, Kim Y.V2, Suslova M.Y.1
-
Affiliations:
- Saint Petersburg Medico-Social Institute
- Acad. I.P. Pavlov First Saint Petersburg State Medical University of the Ministry of Healthcare of Russia
- Issue: Vol 7, No 6 (2021)
- Pages: 156-162
- Section: Articles
- URL: https://journals.eco-vector.com/2412-4036/article/view/288440
- DOI: https://doi.org/10.18565/therapy.2021.6.156-162
- ID: 288440
Cite item
Abstract
Aim: to study the efficacy and safety of oxyethylammonium methylphenoxyacetate (Trekrezan) in patients with postinfectious asthenia who suffered from COVID-19 on an outpatient basis. Material and methods. The study included 80 people who had COVID-19 on an outpatient basis. Patients were randomized into two groups: main (n=40, mean age 52,14±6,23 years) and control (n=40, mean age 51,62±6,17 years). Patients of the main group received Trekrezan according to the following scheme: on the first day - 3 tablets (600 mg), for the next 7 days - 1 tablet (200 mg) per day. The duration of therapy was 8 days (the total dose of the drug was 2000 mg). Patients in the control group did not receive the drug. Initially and after the study in the main and control groups, testing was carried out using the Asthenic State Scale. Anxiety and depression levels were determined using HADS Scale. Sleep characteristics were scored subjectively. Results. Most of the patients who had COVID-19 presented an average of 7,04±1,06 complaints. In 57 (71,25%) patients included in the study, there were manifestations of moderate asthenia. In the main group of patients, who had a Trekrezan therapy, a distinct positive dynamic was recorded: a decrease in the number of patients with severe asthenia from 8 (20%) to 0 (0%), a decrease in patients with moderate asthenia from 28 (70%) to 0 (0%). At the same time, no such results were observed in the control group: after 8 days of observation, 2 (5%) of 40 patients had signs of severe asthenia, and 16 (40%) of 40 patients had manifestations of moderate asthenia. The drug was well tolerated. There were no side effects. Conclusion. In patients who have suffered from COVID-19 at the outpatient stage, moderate asthenia prevails. Alongside Trekrezan therapy, 80% of patients in the main group have no manifestations of asthenia, while in the control group, half of the patients retain moderate asthenia. Trekrezan can be recommended for the treatment of postinfectious asthenia in patients who have COVID-19.
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About the authors
I. B Zueva
Saint Petersburg Medico-Social Institute
Email: iravit0yandex.ru
195271, Saint Petersburg, 72А Kondratievsky Alley. Tel..: +7 (921) 317-86-94
Yu. V Kim
Acad. I.P. Pavlov First Saint Petersburg State Medical University of the Ministry of Healthcare of Russia197022, Saint Petersburg, 6-8 Lva Tolstogo Str
M. Yu Suslova
Saint Petersburg Medico-Social Institute195271, Saint Petersburg, 72А Kondratievsky Alley
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