| Line | Drug | Monitoring | Key Notes |
|---|---|---|---|
| 1ST LINE | Methotrexate (Trexall) 15โ25 mg PO/SC weekly | CBC, LFTs, Cr q3 months. CXR at baseline (ILD screening). | Cornerstone of RA treatment. Always give with folic acid 1 mg daily (reduces GI/oral side effects). Teratogenic -contraception required. Avoid in liver disease, heavy EtOH. Hold for surgery (infection risk). |
| ADD-ON | Hydroxychloroquine (Plaquenil) 200โ400 mg daily | Annual eye exam (retinal toxicity after 5 years) | Mild disease or combination therapy. Very safe. Also used in SLE. |
| ADD-ON | Sulfasalazine 2โ3g daily | CBC, LFTs | Triple therapy (MTX + HCQ + SSZ) is as effective as many biologics for moderate RA. |
| BIOLOGIC | TNF inhibitors (adalimumab, etanercept, infliximab) | Screen for TB (QuantiFERON), Hep B/C, HIV before starting. Annual TB screening. | Add to MTX if inadequate response. Hold for active infection and peri-operatively. Risk: TB reactivation, serious infections, lymphoma (small increase). |
| BIOLOGIC | IL-6 inhibitor (tocilizumab), JAK inhibitor (tofacitinib, upadacitinib) | CBC, LFTs, lipids. JAKi: screen for VTE risk. | Alternatives if TNFi fails. JAK inhibitors: FDA black box for VTE, MACE, and malignancy in age > 65 ORAL Surveillance, 2022 -use after biologic failure. |
Patient: 56-year-old woman with seropositive RA on methotrexate 20 mg/week ร 2 years, presenting with 1 week of progressive dyspnea, dry cough, and low-grade fever. No sick contacts.
Key findings: CT chest: bilateral ground-glass opacities. PFTs: restrictive pattern with reduced DLCO. BAL: lymphocyte predominance, cultures negative. Mild eosinophilia.
Management:
Teaching point: MTX pneumonitis can occur at any time. It is a hypersensitivity reaction, not dose-related. Acute onset and temporal relationship to MTX distinguishes it from RA-ILD. Never rechallenge.
Patient: 48-year-old man with RA, inadequate response to methotrexate 25 mg/week ร 6 months (DAS28 = 5.1). Rheumatology recommends adalimumab. Pre-biologic screening: QuantiFERON POSITIVE. CXR normal.
Key findings: Latent TB identified. No active disease. HBsAg negative, anti-HBc negative.
Management:
Teaching point: TNF-alpha maintains granuloma integrity. TNF inhibitors โ granuloma breakdown โ disseminated TB. Always screen with QuantiFERON before ANY biologic.
Patient: 63-year-old woman on adalimumab + methotrexate admitted with cellulitis. Also has active RA flare with 6 swollen joints.
Key findings: WBC 14,000, CRP 12. Blood cultures negative. Cellulitis without abscess.
Management:
Teaching point: Holding biologics during infection is mandatory. HCQ is the one DMARD safe to continue through most infections. Do not restart biologics too early, ensure complete clinical resolution.
| Parameter | Frequency | Target / Action |
|---|---|---|
| Vitals | q4h floor, q1โ2h ICU | HR, BP, RR, SpOโ, Temp -notify for significant deviations |
| Labs (BMP, CBC) | Daily AM or as indicated | Trend Cr, Kโบ, WBC, Hgb -adjust treatment based on trajectory |
| Disease-specific markers | Per clinical context | See Overview and Management tabs for condition-specific targets |
| I&Os | Strict if volume-sensitive | UOP โฅ 0.5 mL/kg/hr. Net fluid balance guides diuresis or resuscitation. |
| Telemetry | Continuous if indicated | Arrhythmia detection. Discontinue when no longer indicated (reduces alarm fatigue). |
| Clinical response | Each assessment | Symptom improvement, functional status, appetite, mental status -the exam matters more than labs |
| Drug | Dose | Route | Notes |
|---|---|---|---|
| Conventional DMARDs | |||
| Methotrexate | 15-25 mg/week | PO/SQ | First-line DMARD -anchor drug. Start with folic acid 1 mg daily (reduces GI + oral ulcer side effects). SQ better absorbed at doses > 15 mg. Monitor: CBC, LFTs, Cr q8-12 weeks. Teratogenic (category X) -stop 3 months before conception. |
| Leflunomide | 20 mg daily | PO | Alternative to MTX if intolerant. Pyrimidine synthesis inhibitor. Very long half-life (14 days). Cholestyramine washout if toxicity or pregnancy planned. |
| Sulfasalazine | 1-1.5g BID | PO | Mild RA or combination therapy. Safe in pregnancy (one of few DMARDs). Check G6PD. |
| Hydroxychloroquine | 200-400 mg daily | PO | Mild RA, often combined with MTX. Annual retinal screening after 5 years. |
| Biologic DMARDs -add if inadequate response to MTX at 3 months | |||
| Adalimumab | 40 mg SQ q2 weeks | SQ | TNF inhibitor. Most prescribed biologic. Screen TB/HBV before starting. Risk: serious infections, reactivation TB, lymphoma (rare). |
| Etanercept | 50 mg SQ weekly | SQ | TNF inhibitor (receptor fusion protein). Less TB reactivation risk than monoclonal anti-TNFs. Does NOT work for IBD (unlike other TNFis). |
| Tocilizumab | 162 mg SQ weekly or 8 mg/kg IV monthly | SQ/IV | Anti-IL-6 receptor. Suppresses CRP (can mask infection). Monitor lipids (LDL โ), neutrophils, LFTs. Risk of GI perforation. |
| Abatacept | 125 mg SQ weekly | SQ | T-cell costimulation blocker (CTLA-4 Ig). Generally well tolerated. Good safety profile in elderly. |
| Rituximab | 1000 mg IV ร 2 doses (day 1 + day 15) | IV | Anti-CD20 (B-cell depletion). Usually reserved for refractory RA after TNFi failure. Screen HBV. Monitor immunoglobulins. |
| JAK Inhibitors -oral targeted synthetic DMARDs | |||
| Tofacitinib | 5 mg BID | PO | JAK1/3 inhibitor. FDA boxed warning: increased CV events + malignancy vs TNFi in patients โฅ 50 with CV risk ORAL Surveillance, 2022. Use after TNFi failure. |
| Upadacitinib | 15 mg daily | PO | Selective JAK1 inhibitor. Superior to adalimumab in SELECT-COMPARE. Same FDA boxed warning class. VTE risk. |