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It is a prospective case-control study with women diagnosed early rheumatoid arthritis. Three therapeutic failures were considered: failure 1 - to the first Disease-modifying antirheumatic drugs (DMARDs) (methotrexate); failure 2 - to the second DMARDs (leflunomide) and failure 3 - to the first immunobiological drugs (adalimumab). Ultrasound was performed bilaterally on the 2nd and 3rd metacarpophalangeal joints (MCFs), proximal interphalangeal joints (IFPs), and wrists (US10). Ultrasound measurements (qualitative and semi-quantitative) evaluated: 1 - inflammatory: synovial and tenosynovial proliferation in gray scale and power Doppler (0-3); 2 - joint damage: bone erosion (qualitative and semi-quantitative) and cartilage damage (qualitative and semi-quantitative). Clinical and laboratory variables were also assessed blindly at baseline and after 12, 24 e 48 weeks.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Woman with Early Rheumatoid Arthritis |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Drug protocol | Drug | The following drug scheme was carried out: The patients began with methotrexate (MTX) 15 mg / week, which was increased to 25 mg / week until week 12. Subsequent steps for patients with an insufficient response (DAS28 score> 3.2 and the Physician's Global Assessment (PGA)> 4.0 [0-10 cm]) were leflunomide 20mg / day with MTX 15 mg / week from week 12 to week 24 and adalimumab twice a month and MTX 15mg / week from week 24 to week 48. The use of 5mg folic acid was advised once a week during the 48 weeks of the study. Three treatment failures were considered over these 48 weeks:
|
| Measure | Description | Time Frame |
|---|---|---|
| Changes in Synovial blood flow (power doppler) | Measured in ultrasound examination | Baseline, after 4, 12, 24 and 48 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Synovial Proliferation | Measured in ultrasound examination | Baseline, after 4, 12, 24 and 48 weeks |
| Changes in Tenosynovitis | Measured in ultrasound examination |
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Inclusion Criteria:
Exclusion Criteria:
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Woman diagnosed eith early rheumatoid arthritis naive for treatment
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 40023888 | Derived | da Luz KR, Natour J, Pinheiro MM, Petterle GS, Dos Santos MF, Fernandes ADRC, Furtado RNV. Power Doppler in hand joints predicts therapeutic failure in treatment-naive women with early rheumatoid arthritis: A prospective study. Clinics (Sao Paulo). 2025 Mar 1;80:100593. doi: 10.1016/j.clinsp.2025.100593. eCollection 2025. |
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| ID | Term |
|---|---|
| D001172 | Arthritis, Rheumatoid |
| ID | Term |
|---|---|
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
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| ID | Term |
|---|---|
| D004360 | Drug Therapy, Computer-Assisted |
| ID | Term |
|---|---|
| D004358 | Drug Therapy |
| D013812 | Therapeutics |
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|
| Baseline, after 4, 12, 24 and 48 weeks |
| Changes in Joint Damage | Measured in ultrasound examination | Baseline, after 4, 12, 24 and 48 weeks |
| Changes in C-reactive protein level (mg/liter) | Measured in blood test | Baseline, after 4, 12, 24 and 48 weeks |
| Changes in erythrocyte sedimentation rate level (mm/hour) | Measured in blood test | Baseline, after 4, 12, 24 and 48 weeks |
| Changes in function | Measured by Health Assessment Questionnaire | Baseline, after 4, 12, 24 and 48 weeks |
| Changes in upper limb function | Measured by Disabilities of the Arm, Shoulder and Hand Questionnaire | Baseline, after 4, 12, 24 and 48 weeks |
| Changes in disease activity score | Measured by disease activity score 28 | Baseline, after 4, 12, 24 and 48 weeks |
| D003240 |
| Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |