Key Clinical Formulas & Scores
DAS28 = 0.56 Γ β(TJC28) + 0.28 Γ β(SJC28) + 0.70 Γ ln(ESR) + 0.014 Γ GH
TJC28 = tender joint count (0-28)
SJC28 = swollen joint count (0-28)
ESR = erythrocyte sedimentation rate
GH = global health assessment (VAS 0-100 mm)
Remission: <2.6 | Low: 2.6-3.2 | Moderate: 3.2-5.1 | High: >5.1
Joint involvement: 1 large=0, 2-10 large=1, 1-3 small=2, 4-10 small=3, >10 joints=5
Serology: RF- AND CCP-=0, RF+ OR CCP+ (low)=2, RF+ OR CCP+ (high)=3
Acute phase reactants: Normal CRP/ESR=0, Elevated CRP or ESR=1
Symptom duration: <6 weeks=0, β₯6 weeks=1
Score β₯6/10 = definite RA
Entry criterion: ANA β₯1:80 (HEp-2) β required
Clinical domains (weighted):
β’ Constitutional: Fever (2)
β’ Hematologic: Leukopenia (3), Thrombocytopenia (4), Autoimmune hemolysis (4)
β’ Neuropsychiatric: Delirium (2), Psychosis (3), Seizure (5)
β’ Mucocutaneous: Non-scarring alopecia (2), Oral ulcers (2), Acute cutaneous lupus (6)
β’ Serosal: Pleural/pericardial effusion (5), Acute pericarditis (6)
β’ Musculoskeletal: Joint involvement (6)
β’ Renal: Proteinuria >0.5 g/24h (4), Class III/V lupus nephritis (8), Class II/IV lupus nephritis (10)
Immunologic domains (weighted):
β’ ANA (entry)
β’ Anti-dsDNA (6), Anti-Smith (6), Antiphospholipid antibodies (2)
β’ Complement C3 or C4 low (3/4)
Score β₯10 = classification as SLE
β₯4 of 17 criteria (at least 1 clinical + 1 immunologic)
Clinical: Acute cutaneous lupus, Chronic cutaneous lupus, Oral/nasal ulcers, Non-scarring alopecia, Synovitis β₯2 joints, Serositis, Neurologic (seizures, psychosis), Hemolytic anemia, Leukopenia (<4,000), Thrombocytopenia (<100,000)
Immunologic: ANA, Anti-dsDNA, Anti-Sm, Antiphospholipid antibodies, Low complement (C3, C4, CH50), Direct Coombs (without hemolytic anemia)
6 questions, VAS 0-10 each:
1. Fatigue 2. Spinal pain 3. Peripheral joint pain 4. Enthesitis
5. Morning stiffness duration 6. Morning stiffness severity
BASDAI = 0.2 Γ (Q1 + Q2 + Q3 + Q4 + 0.5 Γ Q5 + 0.5 Γ Q6)
Score: <4 = inactive, β₯4 = active disease
BASFI (functional index): 10 questions, mean score 0-10
Core Concepts
Rheumatoid Arthritis
Symmetric inflammatory polyarthritis, small joints (MCP, PIP, MTP), morning stiffness >1 hour. Serology: RF (70%), anti-CCP (60-70%, more specific). Radiographic: periarticular osteopenia, joint space narrowing, erosions. Extra-articular: rheumatoid nodules, interstitial lung disease, vasculitis, Felty syndrome. Treatment: methotrexate (first-line DMARD, 15-25 mg/week), hydroxychloroquine, sulfasalazine, leflunomide. Biologics: TNF-Ξ± inhibitors (adalimumab, etanercept, infliximab), IL-6 inhibitors (tocilizumab), JAK inhibitors (tofacitinib, baricitinib), rituximab (anti-CD20). Treat-to-target (DAS28 <2.6 or remission).
Gout
Monosodium urate crystal deposition. Acute monoarthritis (podagra = first MTP, most common). Risk factors: hyperuricemia (purine-rich diet, alcohol, diuretics, CKD, obesity). Diagnosis: joint aspiration β needle-shaped negatively birefringent crystals. Acute treatment: NSAIDs (indomethacin), colchicine, corticosteroids. Chronic: urate-lowering therapy if β₯2 flares/year, tophi, or urate nephropathy. Allopurinol (first-line, start 100 mg daily, titrate to target sUA <6 mg/dL), febuxostat, probenecid. Prophylaxis with colchicine 0.6 mg BID Γ 3-6 months when starting ULT.
Lupus Nephritis
Class I: mesangial (mildest). Class II: mesangial proliferative. Class III: focal (<50% glomeruli). Class IV: diffuse (β₯50%) β most severe. Class V: membranous. Class VI: sclerosing. Class III/IV: high-dose glucocorticoids + mycophenolate mofetil (MMF) or cyclophosphamide (NIH protocol). Class V: MMF or CNIs. Maintenance: MMF or azathioprine for at least 3 years. Biologics: belimumab (anti-BLyS), voclosporin. Monitoring: urinalysis, proteinuria, complement levels, anti-dsDNA.
Clinical Case Studies
Case 1: New Onset Rheumatoid Arthritis
Patient: 45-year-old female, symmetric joint pain and swelling in hands and feet Γ 8 weeks, morning stiffness lasting 2 hours. Exam: swollen MCP2-5 and MTP2-5 bilaterally, warmth, limited ROM. Labs: RF 85, anti-CCP 120, ESR 65, CRP 4.2. X-ray: periarticular osteopenia in MCP joints.
Diagnosis: Rheumatoid Arthritis (ACR/EULAR score = 8/10: 4-10 small joints=3, serology high positive=3, elevated CRP=1, duration β₯6 weeks=1).
Management: Start methotrexate 15 mg/week with folic acid 1 mg daily (except MTX day). Prednisone 10 mg daily as bridge therapy (taper over 3 months). Hydroxychloroquine 400 mg daily added. Tuberculosis screening before biologics. Follow-up DAS28 in 3 months. Target: DAS28 <2.6 or clinical remission. If inadequate response at 6 months: add TNF-Ξ± inhibitor (adalimumab 40 mg SC every 2 weeks).
Case 2: Acute Gout Flare
Patient: 52-year-old male, excruciating pain in right first MTP Γ 2 days, red, hot, swollen, unable to bear weight. PMH: HTN, BMI 35, drinks beer daily. Tophus on right ear helix. Serum uric acid 9.2 mg/dL. Joint aspiration: needle-shaped negatively birefringent crystals in polarized light.
Diagnosis: Acute gouty arthritis (podagra).
Management: Acute: indomethacin 50 mg TID Γ 5 days (or colchicine 1.2 mg then 0.6 mg 1 hour later). Ice packs. Once flare resolves: initiate allopurinol 100 mg daily, titrate every 2-5 weeks to target sUA <6 mg/dL. Colchicine 0.6 mg BID prophylaxis for 3-6 months when starting ULT. Lifestyle: reduce alcohol, purine-rich foods, weight loss. Avoid starting ULT during acute flare if patient already on ULT (continue current dose).
Case 3: Lupus Nephritis (Class IV)
Patient: 28-year-old female, malar rash, photosensitivity, joint pain Γ 3 months. New onset facial edema, foamy urine. Labs: ANA 1:640 (homogeneous), anti-dsDNA 350, C3 35 (low), C4 <10 (low), proteinuria 3.8 g/24h, hematuria with cellular casts. Renal biopsy: Class IV-G (A/C) diffuse proliferative glomerulonephritis with crescents.
Diagnosis: Systemic Lupus Erythematosus with Class IV lupus nephritis (ACR/EULAR score >10).
Management: Induction: IV methylprednisolone 1 g daily Γ 3 days, then prednisone 1 mg/kg/day. Mycophenolate mofetil 1 g BID (or cyclophosphamide IV monthly Γ 6 months if crescents/severe). ACE inhibitor for proteinuria. Hydroxychloroquine 400 mg daily for all SLE patients. Maintenance: MMF 1-1.5 g BID or azathioprine 2 mg/kg daily for β₯3 years. Nephrology follow-up, renal function monitoring.
Practice Questions
A: DAS28 = 0.56 Γ β8 + 0.28 Γ β6 + 0.70 Γ ln(45) + 0.014 Γ 60 = 0.56Γ2.83 + 0.28Γ2.45 + 0.70Γ3.81 + 0.84 = 1.58 + 0.69 + 2.67 + 0.84 = 5.78. High disease activity (>5.1).
A: Anti-cyclic citrullinated peptide (anti-CCP) antibodies β specificity >95% (compared to RF ~85%). High titers predict erosive disease.
A: ANA entry (0), Acute cutaneous (6) + Joint (6) + Leukopenia (3) + Anti-dsDNA (6) + Low complement (4) = 25 points. Score β₯10 = classification as SLE.
A: Allopurinol (xanthine oxidase inhibitor) β start 100 mg daily, titrate every 2-5 weeks to target serum uric acid <6 mg/dL. Febuxostat is alternative if allopurinol contraindicated.
A: High-dose glucocorticoids + mycophenolate mofetil (MMF) 1-1.5 g BID, or IV cyclophosphamide (NIH protocol: 0.5-1 g/mΒ² monthly Γ 6 months). MMF has comparable efficacy to cyclophosphamide with better safety profile.