Low dose NSAIDs and sysadoas in the management of knee osteoarthritis
- PMID: 41196514
- PMCID: PMC12592241
- DOI: 10.1007/s40520-025-03221-2
Low dose NSAIDs and sysadoas in the management of knee osteoarthritis
Abstract
Introduction: Osteoarthritis (OA) is a chronic, progressive joint disease characterized by the degradation of articular cartilage, subchondral bone remodeling, synovial inflammation, and osteophyte formation. Despite being a leading cause of disability in older people, effective long-term management of OA remains a significant challenge. Current treatment strategies primarily focus on symptom control, with both non-pharmacological and pharmacological interventions.
Materials and methods: A systematic literature review followed by a structured Delphi survey was conducted, involving an international Technical Expert Panel (TEP) of OA specialists. The panel evaluated the efficacy, safety, and clinical utility of combining low dose diclofenac and chondroitin sulfate in OA management.
Results: The analysis of expert consensus indicated that the combination of low dose diclofenac and chondroitin sulfate may be effective in reducing pain and improving joint function in patients with knee OA. Additionally, this combination could reduce the need for higher doses of NSAIDs, thereby minimizing systemic adverse effects.
Conclusion: The combination of low dose diclofenac and chondroitin sulfate represents a promising therapeutic strategy for managing knee OA. Further studies are needed to confirm these findings and optimize therapeutic strategies to improve patient outcomes.
Keywords: Chondroitin sulfate; Diclofenac; Knee osteoarthritis; Low dose diclofenac; NSAIDs; Osteoarthritis.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Competing interests: JYR has received consultancy fees and speaker bureau’s honorarium from IBSA; LS was supported by MHCR 023728; all other authors declare no conflict of interests. Disclosure: JYR has received consultancy fees and speaker bureau’s honorarium from IBSA; LS was supported by MHCR 023728; all other authors declare no conflict of interests.
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