Table 1 |
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|
Treatment protocol |
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|
Follow-up |
DAS28 |
Medication |
|
|
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|
Week 0 |
≥ 2.6 |
Methotrexate 15 mg/wk |
|
Week 8 |
≥ 2.6 |
Methotrexate 25 mg/wk |
|
Week 12 |
≥ 2.6 |
Methotrexate 25 mg/wk + sulfasalazine 2,000 mg/day |
|
Week 20 |
≥ 2.6 |
Methotrexate 25 mg/wk + sulfasalazine 3,000 mg/day |
|
Week 24 |
≥ 3.2† |
Methotrexate 25 mg/wk + adalimumab 40 mg every 2 weeks |
|
Week 36 |
≥ 2.6 and decrease of > 1.2‡ |
Methotrexate 25 mg/wk + adalimumab 40 mg/week |
|
Week 52 |
≥ 3.2† |
Methotrexate 25 mg/wk + etanercept 50 mg/week |
|
1 year + 3 months |
≥ 3.2† |
Methotrexate 25 mg/wk + infliximab 3 mg/kg every 8 weeks (after a loading dose at weeks 0, 2 and 6) |
|
1 year + 6 months |
≥ 2.6 and decrease of > 1.2‡ |
Methotrexate 25 mg/wk + infliximab 3 mg/kg every 4 weeks |
|
|
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The goal of treatment was remission (Disease Activity Score in 28 joints (DAS28) < 2.6). Treatment was intensified when this target was not met. In case of remission, medication was not changed. † Following the guidelines of the Dutch Society of Rheumatology and Dutch reimbursement regulations, anti-tumor necrosis factor α (anti-TNFα) therapy could be prescribed to patients with at least moderate disease activity (DAS28 ≥ 3.2) and in whom treatment with at least two disease-modifying antirheumatic drugs had failed (including methotrexate at 25 mg/week). ‡ Anti-TNFα therapy could be continued only if the DAS28 had decreased by > 1.2 after three months. |
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Vermeer et al. Arthritis Research & Therapy 2012 14:R254 doi:10.1186/ar4099 |
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