Where Do We Stand in the Management of Rheumatoid Arthritis Ahead of EULAR/ACR 2025?
Abstract
1. Introduction
1.1. Pathophysiology and Causes of Rheumatoid Arthritis
1.2. Clinical Signs and Symptoms
1.3. Diagnosis of Rheumatoid Arthritis
2. Materials and Methods
- Pharmacological interventions, including NSAIDs, corticosteroids, and DMARDs, within a collaborative framework.
- Non-pharmacological strategies, such as physiotherapy, dietary interventions, and psychosocial support.
- The role of a multidisciplinary team in enhancing patient outcomes, including the integration of rheumatologists, general practitioners, psychologists, and rehabilitation specialists.
2.1. Approach to Identifying Relevant Articles
2.2. Eligibility Criteria for Study Selection
2.2.1. Inclusion Criteria
- Pharmacological treatments (NSAIDs, corticosteroids, DMARDs) within a multidisciplinary care framework.
- Monitoring tools, such as inflammatory markers (e.g., CRP, ESR) and imaging techniques (e.g., ultrasound, MRI).
- Non-pharmacological interventions, including physiotherapy, dietary strategies, and psychosocial support.
2.2.2. Exclusion Criteria
- Studies not adhering to PRISMA guidelines, as compliance is critical for methodological rigor.
- Case studies without generalisable findings or lacking a clear interdisciplinary focus.
2.2.3. Selection Process
2.3. Risk of Bias and Evidence Quality Assessment
3. Results
3.1. Overview of Selected Studies
3.2. The Role of NSAIDs in the Management of Rheumatoid Arthritis
3.3. The Role of Corticosteroids in the Management of Rheumatoid Arthritis
3.4. Comparison Between Conventional and Biologic DMARDs in the Treatment of Rheumatoid Arthritis
3.5. Monitoring the Response to Rheumatoid Arthritis Treatment
3.6. The Interdisciplinary Approach in Treatment and Management
4. Discussion
5. Future Perspectives in the Management of Rheumatoid Arthritis
5.1. Expansion of Digital Rehabilitation Platforms
5.2. Virtual and Augmented Reality in Personalised Therapy
5.3. The Role of Artificial Intelligence in Clinical Decision Making
5.4. Integration of Personalised Nutrition into Routine Care
5.5. Towards an Interdisciplinary, Patient-Centred Model
6. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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Aspect | Details | References |
---|---|---|
Primary Objective | Control inflammation, prevent joint destruction, and maintain patient functionality. | [40] |
Role of NSAIDs | Reduce pain and joint stiffness by inhibiting COX-1 and COX-2 enzymes, decreasing the production of prostaglandins involved in inflammation and pain. | [41] |
Clinical Use | Frequently used in the early stages of the disease or during flare-ups. Recommended as symptomatic treatment without impact on disease progression. | [42] |
Choice of NSAID | Depends on the patient’s safety profile, medical history, and individual response. COX-2 selective inhibitors (e.g., celecoxib) pose fewer gastrointestinal risks. | [43] |
Common Side Effects | Gastric ulcers, renal insufficiency, and cardiovascular risks, particularly with long-term use. | [44] |
Monitoring Required | Careful monitoring to prevent complications and integration into a broader therapeutic plan, including DMARDs. | [45] |
Limitations | Do not influence long-term disease progression, being used solely for symptomatic relief. | [46] |
Benefits | Rapid control of inflammatory symptoms and improved quality of life during critical phases of the disease. | [47] |
Importance in Treatment | Part of an integrated therapeutic plan, used judiciously to balance benefits and risks. | [48] |
Aspect | Details | References |
---|---|---|
Mechanism of Action | Mimic the action of glucocorticoids produced by the adrenal glands, exerting anti-inflammatory and immunosuppressive effects. Inhibit the production of inflammatory cytokines and reduce immune cell activity. | [49] |
Clinical Use | Rapidly control inflammation and alleviate acute symptoms, particularly useful during disease flares or as “bridging therapy” before the effects of DMARDs take hold. | [24] |
Benefits | Quickly reduce pain, swelling, and joint stiffness. Slow joint damage progression in early stages and help maintain inflammation control in severe forms. | [50] |
Administration | Low doses for long-term inflammation control or higher doses for short-term intervention during acute crises. | [51] |
Adverse Effects | Osteoporosis, increased blood pressure, steroid-induced diabetes, weight gain, higher infection risk, Cushing’s syndrome, skin fragility, and muscle weakness. | [52] |
Monitoring Required | Dose adjustments to the minimum necessary. Monitor side effects and prevent osteoporosis using calcium, vitamin D supplementation, or anti-resorptive therapy. | [53] |
Limitations | Significant adverse effects limit long-term use. Requires careful management to minimise risks. | [54] |
Role in Treatment | A valuable tool for rapid inflammation control, particularly in severe cases, but should be used responsibly as part of a comprehensive therapeutic plan. | [55] |
Aspect | Conventional DMARDs | Biologic DMARDs | References |
---|---|---|---|
Definition | Conventional drugs that modulate the immune response to reduce inflammation and slow disease progression. | Biologic agents that specifically target molecules or cells involved in the inflammatory immune response. | [56,57] |
Examples | Methotrexate, Sulfasalazine, Hydroxychloroquine, Leflunomide. | Infliximab, Adalimumab, Tocilizumab, Etanercept. | [58,59] |
Mechanism of Action | Inhibit immune cell proliferation and reduce the synthesis of inflammatory cytokines. | Block specific immune targets, such as TNF-α, interleukins, or other inflammatory proteins. | [60,61] |
Efficacy | Gold standard for rheumatoid arthritis treatment (e.g., Methotrexate). Can be used as monotherapy or in combination with other drugs. | Highly effective, particularly for patients unresponsive to conventional DMARDs. | [62,63] |
Route of Administration | Usually, oral. | Typically, injectable or via infusion. Recently, some synthetic biologic therapies (e.g., JAK inhibitors) are available orally. | [64,65] |
Time to Effect | Requires weeks or months to achieve maximum effect. | Faster clinical response compared to conventional DMARDs. | [57,66] |
Risks and Side Effects | Hepatotoxicity, bone marrow suppression, and allergic reactions. Frequent monitoring of liver function and blood counts required. | Increased risk of severe infections, including latent tuberculosis. Injection site or secondary autoimmune reactions may occur. | [67,68,69] |
Costs | Lower costs, accessible in most healthcare systems. | High costs, usually reserved for severe cases or those unresponsive to conventional DMARDs. | [70,71] |
Monitoring | Requires liver function tests and blood counts. | Regular evaluations for infections and adverse reactions needed. | [72,73] |
Benefits | First-line treatment, effective for most patients. | Second-line treatment with high efficacy in refractory cases. | [74,75] |
Limitations | May require combination therapy for optimal response. Slower onset of action. | High costs and increased risk of severe side effects. | [2,76] |
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Vlad, A.L.; Popazu, C.; Lescai, A.-M.; Voinescu, D.C.; Baltă, A.A.Ș. Where Do We Stand in the Management of Rheumatoid Arthritis Ahead of EULAR/ACR 2025? Clin. Pract. 2025, 15, 103. https://doi.org/10.3390/clinpract15060103
Vlad AL, Popazu C, Lescai A-M, Voinescu DC, Baltă AAȘ. Where Do We Stand in the Management of Rheumatoid Arthritis Ahead of EULAR/ACR 2025? Clinics and Practice. 2025; 15(6):103. https://doi.org/10.3390/clinpract15060103
Chicago/Turabian StyleVlad, Adriana Liliana, Corina Popazu, Alina-Maria Lescai, Doina Carina Voinescu, and Alexia Anastasia Ștefania Baltă. 2025. "Where Do We Stand in the Management of Rheumatoid Arthritis Ahead of EULAR/ACR 2025?" Clinics and Practice 15, no. 6: 103. https://doi.org/10.3390/clinpract15060103
APA StyleVlad, A. L., Popazu, C., Lescai, A.-M., Voinescu, D. C., & Baltă, A. A. Ș. (2025). Where Do We Stand in the Management of Rheumatoid Arthritis Ahead of EULAR/ACR 2025? Clinics and Practice, 15(6), 103. https://doi.org/10.3390/clinpract15060103