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Tytuł pozycji:

Evaluation of the efficiency and safety of combined therapy with a symptomatic sustained-release drug and hyaluronic acid versus monotherapy with hyaluronic acid in patients with knee osteoarthritis

Tytuł:
Evaluation of the efficiency and safety of combined therapy with a symptomatic sustained-release drug and hyaluronic acid versus monotherapy with hyaluronic acid in patients with knee osteoarthritis
Autorzy:
K. A. Berdyugin
I. V. Kadyntsev
O. V. Berdyugina
E. A. Taskina
N. G. Kashevarova
Temat:
остеоартрит
алфлутоп
гиалуроновая кислота
Medicine
Źródło:
Современная ревматология, Vol 14, Iss 3, Pp 63-70 (2020)
Wydawca:
IMA-PRESS LLC, 2020.
Rok publikacji:
2020
Kolekcja:
LCC:Medicine
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
Russian
ISSN:
1996-7012
2310-158X
Relacje:
https://mrj.ima-press.net/mrj/article/view/1048; https://doaj.org/toc/1996-7012; https://doaj.org/toc/2310-158X
DOI:
10.14412/1996-7012-2020-3-63-70
Dostęp URL:
https://doaj.org/article/1ff5cc5c5cbe4202abfea1d651179c79  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.1ff5cc5c5cbe4202abfea1d651179c79
Czasopismo naukowe
Osteoarthritis (OA) is the most common joint disease. Searching for new treatment methods and regimens for OA is relevant.Objective: to evaluate the efficiency and safety of therapy with a symptomatic sustained-release drug (Alflutop) in combination with intra-articular hyaluronic acid (HA) injection versus monotherapy with HA in patients with knee OA in routine clinical practice.Patients and methods. A post-registration open-labeled prospective comparative randomized study was conducted to assess the results of treatment in 76 patients (31 men and 45 women; mean age, 49.3±8.5 years; body mass index, 28.4±0.8 kg/m2 ) in two clinical centers in Yekaterinburg and Perm. The patients were randomized into two equal groups, were homogeneous in terms of gender, the frequency of comorbidities, and vital signs (blood pressure, heart rate, and respiratory rate).Group 1 patients received Alflutop as 1-ml daily intramuscular injections (a total of 20 injections) + 2 ml of 1% intraarticular (IA) HA solution injections three times at 1-week intervals; Group 2 patients were given 2 ml of 1% intraarticular HA solution injections three times at 1-week intervals. As an additional therapy, the use of meloxicam 7.5–15 mg/day was permitted, and, if non-steroidal anti-inflammatory drugs were contraindicated, paracetamol 1–3 g/day might be used.Results and discussion. During treatment, both groups of patients showed improvement (compared to the baseline levels). At the same time, evaluating the intergroup values revealed clear differences: a more pronounced decrease in all WOMAC indicators in Group 1 patients: pain scores, 2 [1; 3] vs. 4 [2; 5] in Group 2 (p

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