Consistent use injectable and oral chondroprotectors in patients with osteoarthritis and lower back pain. Case report
- Authors: Shavlovskaya O.A.1, Romanov I.D.1,2, Bokova I.A.3
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Affiliations:
- International University of Restorative Medicine
- "MD Clinic" LLC
- Sechenov First Moscow State Medical University (Sechenov University)
- Issue: Vol 26, No 11 (2024): NEUROLOGY AND RHEUMATOLOGY
- Pages: 782-787
- Section: Articles
- URL: https://bakhtiniada.ru/2075-1753/article/view/273892
- DOI: https://doi.org/10.26442/20751753.2024.11.203037
- ID: 273892
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Abstract
Osteoarthritis (OA) is a disease of the entire joint, including structural changes in hyaline articular cartilage, subchondral bone, ligaments, capsule, synovial membrane and periarticular muscles. One of the causes of the development of nonspecific chronic lower back pain (LBP) is OA of the facet joints. In the treatment of OA and LBP against the background of OA facet joints, the chondroprotective agents are widely used: chondroitin sulfate (CS), glucosamine sulfate, undenatured type II collagen and their combinations. The aim of the article is to systematize the possibilities of practical application of Chondroguard TRIO® in patients with OA of different phenotypes and different localization. The experience of sequential administration of CS in patients (n=11) with OA and LBP with comorbid diseases is presented. At the initial stage of therapy, CS (Chondroguard®) was prescribed intramuscularly according to the scheme, then CS was prescribed perorally as part of a pharmaconutraceutical (Chondroguard® TRIO). The original pharmaconutraceutical Chondroguard® TRIO contains recommended doses of CS (1200 mg), glucosamine sulfate (1500 mg), undenatured type II collagen (40 mg). Clinical cases of the use of sequential administration of chondroprotectors (stage 1 – intramuscularly Chondroguard®, stage 2 – perorally Chondroguard® TRIO) demonstrate the clinical effectiveness of the proposed treatment regimen in patients of different age groups and OA phenotypes (posttraumatic, metabolic).
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##article.viewOnOriginalSite##About the authors
Olga A. Shavlovskaya
International University of Restorative Medicine
Author for correspondence.
Email: shavlovskaya@1msmu.ru
ORCID iD: 0000-0003-3726-0730
D. Sci. (Med.)
Russian Federation, MoscowIgor D. Romanov
International University of Restorative Medicine; "MD Clinic" LLC
Email: shavlovskaya@1msmu.ru
ORCID iD: 0009-0003-0874-2834
neurologist
Russian Federation, Moscow; MoscowIrina A. Bokova
Sechenov First Moscow State Medical University (Sechenov University)
Email: shavlovskaya@1msmu.ru
ORCID iD: 0000-0002-1640-1605
Cand. Sci. (Med.)
Russian Federation, MoscowReferences
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