Gout and pseudogout Flashcards
What are some risk factors for gout?
- Non-modifiable: male, age >50yrs, Fx of gout
- Modifiable: obesity, hypertension, diuretic use, alcohol, foods high in purines (seafood, red meats)
What is the pathology of gout?
- prolonged hyperuricemia leads to the formation of monosodium urate crystals
- these deposit in the synovium, connective tissues, and kidneys
- (uric acid crystal deposition in the kidneys can cause interstitial nephritis, renal stones, and acute tubular damage)
What are the clinical features of acute gout?
- sudden, severe pain in affected joint, joint swelling/erythema/warmth
- first MTP joint most commonly affected
- (acute gout attacks often subside after days or weeks)
Extensive bone erosive destruction of the digits with soft tissue calcified tophi on plain radiograph…
- tophi = crystal deposition in soft tissues
What investigations should be done for suspected gout?
- Joint aspiration and synovial fluid analysis under polarised light: negatively birefringent needle-shaped monosodium urate crystals
- Bloods: serum uric acid, ESR, CRP, WBC
- X-ray: normal joint space, soft tissue swelling, periarticular erosions
Monosodium urate (MSU) crystals VS calcium pyrophosphate dihydrate (CPPD) crystals under polarised light…
What condition (presents similar to gout) should be ruled out if suspected?
- septic arthritis
- urgent gram stain and culture
- (look for other features of sepsis: high temp., tachycardia, high resp. rate, low BP)
- (if in doubt, treat patients with antibiotics)
What is the management for an acute gout attack?
- NSAIDs, or colchicine (if patient cannot take NSAIDs)
- intra-articular corticosteroid injections
- lifestyle: modifiable risk factors (lower alcohol, diet etc.)
What prophylactic therapy should be given to manage chronic gout?
- Allopurinol (reduces uric acid production by inhibiting the enzyme xanthine oxidase)
- note: Febuxostat (another xanthine oxidase inhibitor)
What is pseudogout (CPPD disease)?
- Calcium pyrophosphate dihydrate (CPPD) disease
- CPPD disease is an arthropathy associated with the deposition of CPPD crystals
What are the clinical features of CPPD disease?
- more common in elderly
- Acute synovitis (pseudogout): pain, swelling, stiffness, erythema (most commonly affects wrists and knees)
What investigations should be done for suspected CPPD disease?
- Joint aspiration and synovial fluid analysis under polarised light: weakly positively birefringent rhomboid (or rod) shaped CPPD crystals
- Radiology: similar to OA, with associated chondrocalcinosis
What is the management for CPPD disease?
- NSAIDs or colchicine (if NSAIDs cannot be used)
- oral corticosteroids or intra-articular steroid injections (if NSAIDs and colchicine are contra-indicated)