Ankylosing Spondylitis Flashcards

1
Q

What is the epidemiology of AS?

A

Peak onset between 20-30yrs

M>F:

  • 3:1
  • Women have it more mild or a sublcinical disease

0.1-2% of the population

Most common in people form northern Europe

Underdiagnosed - especially mild types

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2
Q

What is the aetiology and pathophysiology of AS?

A

Genetics:

  • > 90% of the risk is familial
  • Strong association with HLA-B27 (1-2% of people with this, rising to 15-20% if they also have a 1st degree relative)
  • Major histocompatability complex (MHC) = cell surface molecule encoded by a large gene family which mediates actions of leukocytes - accounts of nearly 1/2 of disease susceptibility

Other disorders:

  • Crohn’s + UC
  • Psoriasis

Chronic, seronegative spondyloarthropathy:

  • Primarily the axial skeleton (so sacroilitis and spondylitis)
  • Inflammation around enthesis (ligament-bone junction) > sclerosis of underlying bone > possible fusion of vertebral bodies > loss of function
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3
Q

How does AS present?

A

Inflammatory back pain:

  • Often improves with moderate physical activity
  • Unlike mechanical back pain = stiffness + pain worse in early morning (may awaken person; stiffness >30mins)
  • Starts in sacroiliac joints bilaterally and felt as a non-specific buttock pain
  • Tenderness of SI joints or limited range of spinal motion

Peripheral enthesitis:

  • 1/3 patients
  • Commonly - Achilles tendonitis, plantar fasciitis and tibial tuberosity
  • Tend to be painful in the morning
  • Possible swelling of tendon or ligament insertion

Peripheral arthritis;

  • 1/3 patients
  • Usually asymmetric involving hips, shoulder girdle, chest wall and symphysis pubis; sometimes TMJ

Systemic features:

  • Fever + weight loss may occur during active disease
  • Also fatigue

Insidious:
- Subtle/mild early stage, progressing over months-years, usually before 30yrs

Most have mild chronic disease or intermittent flares with periods of remission

Advanced:
- Loss of lumbar lordosis, buttock atrophy and exaggerated thoracic kyphosis with a stooped neck = question mark posture

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4
Q

How do you examine someone for AS?

A

Measure:

  • Chest expansion
  • Lateral and forward lumber flexion including Schober’s test

Palpate SI joints

Examine peripheral joints for signs of synovitis or enthesitis

Look for extra-articular manifestations of AS (up to 40% of patients)

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5
Q

What are the extra-articular manifestations in AS?

A

Eyes:

  • Acute anterior uveitis in 20-30% of patients
  • Of all patients presenting with AAU, 33-50% will go on to develop AS
  • Acute painful red eye + severe photophobia - needs emergency treatment

Less common (mostly in severe and long standing disease):

Cardiovascular:

  • Aortitis +/- aortic regurgitation
  • Fibrosis of conduction system may cause arrhythmias or blocks
  • <10%

Pulmonary:

  • Restrictive lung disease secondary to costobertebral/sternal involvement limiting expansion
  • Pulmonary fibrosis of upper lobes

Renal:
- Amyloidosis = rare

Neuro:

  • Usually secondary to fractures of a fused spine
  • Also cauda equina

Metabolic bone disease:
- Osteopaenia/porosis

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6
Q

What are the clinical criteria required for Dx of AS?

A

Radiological features of sacroiliitis on XR AND at least one of the following:

  • Low back pain for >3/12, improved by exercise and not relieved by rest
  • Limitation of lumbar spine motion in both sagittal and frontal planes
  • Limitation of chest expansion relative to normal values for age/sex
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7
Q

What tests might be useful to aid diagnosis?

A

Bloods:

  • Possible normochromic normocytic anaemia of chronic disease
  • Alk phos often raised
  • ESR/CRP may correlate with disease activity but are less useful for monitoring

XR:

  • SI joints and spine
  • Useful to fulfil criteria but may be normal in early disease
  • Sacroiliitis shows as blurring in lower part of joint then bony erosions or sclerosis and widening or eventual fusion of joint
  • Spinal osteopaenia = common

Spinal MRI - more sensitive in early stages

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8
Q

How do initially/conservatively manage AS?

A

No cure - aim for good symptom control + maximised function

Referral of all new suspected cases to rheumatologists + complications to relevant specialists e.g. ophthalmology

Physio:

  • For functioning
  • Supervised > home exercise
  • Spinal extension and deep breathing exercises to maintain mobility, encourage correct posture and promote chest expansion
  • Hydrotherapy + swimming
  • Firm mattress and thin pillow
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9
Q

What medications can you use to treat AS?

A

NSAIDs (or COX-2 inhibitors):

  • To improve symptoms
  • Possible PPI prescription
  • Paracetamol +/- codeine if not tolerated

Other pain relief:

  • Amitriptyline - for pain affecting sleep
  • Local corticosteroid injections - for symptomatic sacroiliitis, peripheral enthesitis and arthritis
  • PO corticosteroids short term

Cytokine modulators:

  • TNF-alpha inhibitors
  • Effective in disease poorly controlled with NSAIDs
  • Rheumatology care only
  • Etanercept and adalimumab chosen drugs
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10
Q

When is surgery indicated in AS?

A

Used occasionally to correct spinal deformity or repair damaged peripheral joints

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11
Q

What is the prognosis of AS?

A

Variable:

  • Pattern of symptoms in first 10yrs correlates with long term degree of disabiltiy - Minority develop significant disability from spinal fusion and other joint arthritis etc
  • Poor prognostic indicators = male sex, peripheral joint involvement, intractable iritis, young age of onset, elevated ESR and poor response to NSAIDs
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