RHEUMATOLOGY

Reactive arthritis (Reiter’s syndrome)

a term for arthritis following an infection (e.g. rheumatic fever, Reiter’s syndrome)

Epidemiology:

  • Relatively rare, with incidence rates varying between 0.6 to 27 per 100,000.
  • 90% patients are male between 20-40 years

Aetiology:

  • Symptoms manifest days to weeks post-infection, often after the resolution of initial infection symptoms.
  • Infectious episode involving either the GI or GU tract
    • GI: Shigella, salmonella, campylobacter, Yersinia
    • GU: Chlamydia, Mycoplasma
  • Acute pattern of clinical course:
    • 1-4 weeks post-infection
    • Lasts weeks to years (with 1/3 chronic)
    • Often recurring
    • Spinal involvement persists

Clinical features

  • Often characterized by a triad. though not all patients present with this classic triad:
    • arthritis
    • urethritis
    • conjunctivitis
  • fever
  • Peripheral arthritis, asymmetric pattern 
  • Axial arthritis
  • enthesitis (inflammation where tendons insert into bone)- plantar fasciitis, Achilles tendonitis,
  • dactylitis/sausage digits (swelling of an entire finger or toe) – characteristic of reactive and psoriatic arthritis
  • conjunctivitis and iritis 
  • oral ulcers
  • diarrhoea
  • Keratoderma blennorrhagica (hyperkeratotic skin lesions on palms and soles)
  • balanitis circinata (small, shallow, painless ulcers of glans penis) are diagnostic 

Diagnosis:

  • Clinical
  • There is no specific test for diagnosing ReA.
  • Lab findings – normocytic, normochromic anaemia and leukocytosis
  • Cultures are sterile

Treatment:

  • Appropriate antibiotics if there is infection
  • Treatment is aimed at symptomatic relief and preventing or halting further joint damage 
  • NSAIDS, physical therapy, home exercise
  • Local therapy – joint protection, intra-articular steroid injection, topical steroid for ocular involvement
  • Systemic therapy – corticosteroids, sulfasalazine, methotrexate 

Prognosis

  • Generally self-limited, with symptoms resolving within 3 to 5 months.
  • Approximately 30% to 50% of patients will go on to develop some form of chronic ReA.

Complications

  • Potential for recurrent or chronic arthritis, sacroiliitis, urethral stricture, aortic root necrosis, cataracts, and cystoid macular edema

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