How to Diagnose Psoriatic Arthritis
Diagnose psoriatic arthritis using the CASPAR criteria, which requires established inflammatory articular disease plus at least 3 points from specific clinical features, with current psoriasis weighted most heavily at 2 points. 1, 2, 3
Diagnostic Criteria: CASPAR Classification
The CASPAR criteria demonstrate 98.7% specificity and 91.4% sensitivity and should be applied systematically 3:
Required: Established inflammatory articular disease (joint, spine, or entheseal) with erythema, warmth, swelling, and prominent morning/rest stiffness 1
Plus ≥3 points from:
- Current psoriasis (2 points) 3
- Personal history of psoriasis (1 point) 3
- Family history of psoriasis (1 point) 3
- Nail dystrophy (pitting, onycholysis, hyperkeratosis) (1 point) 3
- Negative rheumatoid factor (1 point) 3
- Dactylitis (current or history) (1 point) 3
- Radiographic evidence of juxta-articular new bone formation (1 point) 3
Clinical Assessment Algorithm
Step 1: Identify Inflammatory Features
Look for these specific patterns that distinguish PsA from mechanical joint disease 1, 4:
- Morning stiffness lasting >30 minutes that improves with activity 4
- Dactylitis ("sausage digit"): entire digit swelling from combined enthesitis and synovitis 2
- Enthesitis: tenderness at lateral epicondyle of humerus, medial femoral condyle, Achilles tendon insertion, or plantar fascia 2, 4
- Distal interphalangeal (DIP) joint involvement: uncommon in other arthritides, strongly suggests PsA when present 1, 5
- Asymmetric oligoarthritis: affects 60% in early disease 5
Step 2: Examine for Psoriasis
Ideally confirm psoriasis with dermatology consultation 1:
- Check scalp, intergluteal/perianal areas, and nails (these sites associate with higher PsA risk) 5
- Note that 20% develop arthritis before skin manifestations, sometimes years earlier 4
- Family history of psoriasis counts toward CASPAR criteria even without personal skin disease 3
Step 3: Perform Comprehensive Joint Examination
Conduct a 68/66 joint assessment (68 for tenderness, 66 for swelling), specifically including DIP joints of hands and both proximal interphalangeal and DIP joints of feet 1, 2, 3
Laboratory Testing
Order these specific tests 2, 3:
- ESR and CRP: assess inflammation severity (elevated ESR indicates poor prognosis) 1, 2, 3
- Rheumatoid factor and anti-CCP antibodies: typically negative in PsA (seronegative arthritis), but order to exclude rheumatoid arthritis, especially in symmetric polyarticular presentations 2, 3, 4
Critical pitfall: Presence of RF or anti-CCP does not automatically exclude PsA but demands careful diagnostic scrutiny 4
Imaging Studies
Baseline Radiography
Obtain X-rays of hands and feet at baseline for all suspected inflammatory arthritis 4:
- Look for juxta-articular new bone formation (counts toward CASPAR criteria) 3
- Erosions present in ~50% at 10 years of disease 5
- Use for prognostic assessment and monitoring structural damage 1
Advanced Imaging When Indicated
Consider MRI or ultrasound when 6, 7, 8:
- Isolated enthesitis without obvious joint swelling 6
- Inflammatory spinal pain suspected 6
- Early disease detection needed before radiographic changes 7, 8
- Clinical examination and blood tests are inconclusive 7
Mandatory Baseline Assessment Domains
Once diagnosis is established, document these OMERACT 8 consensus domains 1, 2:
- Pain: visual analogue or category rating scale 1, 2
- Patient global assessment of disease activity 1, 2
- Physical function: Health Assessment Questionnaire (HAQ) 1, 2
- Quality of life: SF-36 or PsA-specific PsAQoL 1, 2
- Fatigue: patient self-report or FACIT instrument 1, 2
Differential Diagnosis Considerations
Distinguish from Rheumatoid Arthritis
PsA differs by 1:
- Less tender/swollen joints, asymmetric distribution 1
- Presence of dactylitis, enthesitis, DIP involvement (uncommon in RA) 1
- Absence of rheumatoid nodules and extra-articular RA features 1
- Negative RF (though 20% of PsA patients, especially women, have symmetric polyarthritis resembling RA) 1
Distinguish from Osteoarthritis
Key differences 1:
- PsA has inflammatory DIP involvement vs. Heberden's nodes (bone spurs) in OA 1
- Morning stiffness in PsA vs. stiffness with activity in OA 1
Distinguish from Ankylosing Spondylitis
When axial disease present 1:
- PsA has asymmetric, less symptomatic sacroiliitis 1
- "Skip" pattern spinal involvement vs. continuous in AS 1
- Presence of psoriatic skin/nail changes 1
- Less progression to ankylosis 1
Prognostic Factors Requiring Documentation
Identify these poor prognosis indicators at baseline (they trigger earlier aggressive therapy) 1, 2, 3:
- Polyarticular disease (high number of actively inflamed joints) 1, 2
- Elevated ESR at presentation 1, 2
- Previous medication failures 1, 2
- Existing structural damage (clinical or radiographic) 1, 2
- Diminished quality of life on standardized measures 1, 2
Comorbidity Screening
Assess these associated conditions that impact treatment decisions 1, 2:
- Cardiovascular risk factors (hypertension, hyperlipidemia, diabetes) 1, 2
- Metabolic syndrome 1, 2
- Inflammatory bowel disease 1, 2
- Depression and anxiety 1
- Non-alcoholic fatty liver disease 1
- Osteoporosis 1
Referral Timing
Refer urgently to rheumatology any patient with suspected inflammatory arthritis and ≥6 weeks of painful, swollen joints 4. Early diagnosis and treatment substantially improve long-term prognosis, as PsA patients have 60% higher premature mortality risk and ~3 years shorter life expectancy than general population 4.
Ideally involve both dermatology (to confirm psoriasis) and rheumatology (to confirm inflammatory musculoskeletal disease) 1, 2.