Rhuematoid arthritis Flashcards

1
Q

Definition

A

Chronic systemic inflammatory disease characterised by a symmetrical deforming peripheral polyarthritis mainly affecting the small peripheral joints

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2
Q

Epidemiology

A
  • 1% of population
  • women> men 3:1 BEFORE MENOPAUSE
  • typically 30-50 years
  • higher prevalence in caucasians
  • lifetime risk of 4% for women adn 3% for men
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3
Q

Aetiology

A
  • Multi-factorial
  • genetic predisposition
    • HLA-DRB1
    • shared epitope
  • environmental
    • smoking
    • infectious trigger
  • Specific antigen - anti-CCP
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4
Q

Pathogenesis

A
  • Innate and acquired immune response
  • B lymphocytes – RF, immune complexes
  • T lymphocytes – cell mediated, cytokines
  • Macrophage derived cytokines – TNFα, IL-6, IL-1
  • Synovial fibroblasts
  • Chronic inflammatory response in synovium – “synovitis” –>pannus
  • Inflammatory changes not confined to joints
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5
Q

American college of rhuemtology criteria

A

Test those with >1 joint with definitive swelling which is not better explained by another disease. Add total A-D score >6/10 are diagnostic

A- joint involvement

  • 1 large = 0
  • 2-10 large =1
  • 1-3 small =2
  • 4-10 small =3
  • >10 joints =5

Serology (at least 1 test result)

  • Negative RF and negatie anti-CCP = 0
  • Low +ve RF or low +ve anti- CCP=2
  • High RF or high +ve anti CCPT = 3

Acute phase reactants

  • normal CRP and normal ESR = 0
  • abnormal CRP or abnormal ESR =1

Duration of symptoms

  • <6 weeks = 0
  • >6 or equal to = 1
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6
Q

Presentation

A
  • symmetrically swollen
  • Pain and swelling
    • Small joints of hands, feet and wrists
    • often symmetrical
    • response to anti-inflammatory
    • large joints may be involved
  • Joint stiffness
    • worse in the morning
    • >30 minutes
    • diurnal variation
  • insidious onset
  • sytemic illnes with extra-articular symptoms
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7
Q

Name the hand joints

A
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8
Q

Examination

A
  • swelling - boggy synovitis
  • warmth
  • joint line tenderness
  • deformity
    • swan neck
    • boutonniere
    • ulnar deviation of metacarpals
    • radial deviation of wrist
  • muscle wasting
  • extra-articular e.g nodules, iritis, anaemia
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9
Q

Name the bones of the hand

A
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10
Q

Joints affected in RA

A

Symmetrical polyarthroapthy

  • MCP (metacarpal phalangeal joint) - 90%
  • PIP (proximal interphalangeal joint) - 90%
  • MTP (metatarsal joints) - 90%
  • Wrists 80%
  • Knees 80%
  • Ankle/subtalar- 80%
  • Shoulder -60%
  • Hip 50%
  • Elbow 50%
  • Cervical spine -40%
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11
Q

Features of rhuematoid hand

A
  • Prominent ulnar styloid
  • z-shaped deformition of the thumb
  • Ulnar deviation of the fingers at the MCP joints
  • palmar subluxation at the MCP joints
  • Boggy, welling, erythema and heat at the MCP, PIP joints
  • Swan neck- deformity
  • Boutonniere deformity
  • Fixed flexion contracture
  • palmar erythema
  • wasting of the thenar eminemce related to carpal tunnel syndrom
  • Rhuematoid nodules are most commonly found on bony prominences
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12
Q

What does this show?

A

Prominent ulnar styloid due to subluxation at MCP joints

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13
Q

What does this show?

A

Z-shaped deformity of the thumb -

The thumb flexes at the metacarpophalangeal joint and hyperextends at the interphalangeal joint below your thumb nai

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14
Q

What does this show?

A

Ulnar deviation of the fingers at the MCP joint

Ulnar deviation, also known as ulnar drift, is a hand deformity in which the swelling of the metacarpophalangeal joints (the big knuckles at the base of the fingers) causes the fingers to become displaced, tending towards the little finger.

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15
Q

what does this show?

A

Palmar subluxation at the MCP joints -

If the collateral ligaments become stretched and the fibers of the extensor tendon are damaged by synovial swelling, the strong flexor muscles will pull the base of the proximal phalanx in a palmar direction, so causing palmar subluxation.

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16
Q

What does this show?

A

Swan neck deformitiy - PIP hyperextension and DIP flexion

17
Q

What does this card show?

A

Boutonniere deformity- PIP flexion and DIP hyperextension

18
Q

Extra-articular features of Rhuematoid arthritis

A
  • General - Malaise, fever, weight loss
  • Skin- Subcuatenous nodles (20-30%), elbows, fingers, achilles
  • Vasculitis - small vessel inflamm leads to infarct in peri-ungal area, fingers and toes
  • Haematological - anaemia of chroic disease maybe B12 or folic acid
  • Felty’s syndrome- lymphadenopathy, splenomegaly, leukopenia
  • Cardiac- pericarditis
  • Pulmonary - asymptomatic involvement, pleural effusion
  • Occular- secondary sjogrens
  • Neuro- vasculitis of vasa nervorum - peripheral neuropathy
  • Renal invlovment and amyloidosis
19
Q

Risk factors

A
  • Genetics - HLA B27
  • Female
    • nullparity
    • just gave birth
    • post-menopause
  • increasing age
20
Q

What is rhuematoid factor?

A
  • Circulating antibodies – have Fc portion of IgG as their antigen
  • Usually IgM but also IgG and IgA
  • Self aggregate into immune complexes -activate complement system
  • Transient production normal
  • In RA:
    • Persistent production
    • Higher affinity
    • Produced in joints
21
Q

Investigations

A

Haematology

FBC

  • Hb -low
  • WCC- norm
  • Pt- Norm
  • ESR raised

blood film

  • normochromic, normocytic anaemia of CD

LFTS

  • ALP increased, Gamma GT raised

Immunology

Autoantibodies

  • ANA- negative
  • RF +ve (70% in all cases, 100% with extra-articular involvement)

Complement studies

  • normal (to exclude lupus)

Immunoglobulins

  • increased total IgG and IgA norm IGM

Acute phase protein

  • CRP high

Xray, CT, MRI

22
Q

X-ray features

A
  • soft tisue swelling
  • loss of joint space due to erosion of articular cartlage
  • juxta-articular osteoporosis
  • marginal bone erosions
  • joint deformities
23
Q

Ultrasound and MRI

A

Shows synovitis more accurately and have greater sensitivity in detecting bone erosions than conventional X-rays

24
Q

Management

A

Referal early to a rhuematologist to prevent early destruction

  • early use of DMARDs and biological agents improves long term outcomes
  • steroids rapidly reduce symptoms and inflammation. Useful for treating exacerbations. Intra-articular steroids have a rapid but short term effect
  • NSAIDS good for symptom relief but have no effect on disease progression
  • offer specialist physi and occupational therapy
25
Q

Symptom modifying drugs

A
  • Analgesiacs
  • NSAIDS
26
Q

DMARDs (disease modifying anti-rhuematic drugs)

A

Most sufferers can get appropriate pain control

  • methotrexate
  • sulfasalzine
  • ciclosporin
  • gold
  • azathiprine
  • Pencillamine
  • HydroxyChloroquine

Slow acting (2-3 month), side effects (nausea, headache, vomitting), regular bloods needed

27
Q

How to give DMARDs

A

1st - Methotrexate

2nd - methotracate + sulfasalazine + hydroxychloroquine

3rd - MTX + biologics

All +/- steroids

28
Q

Biological therapy

A

Anti-TNFα- infliximab

  • Reduce signs & symptoms
  • Preserve function
  • Reduce radiological progression
  • Improve quality of life

Anti B cell (rituximab)

Anti-IL-6 receptor antibody (tocilizumab)

CTLA-4 immunoglobulin(abatacept)

29
Q

Monitoring response

A
  • tender joint count
  • swollen joint count
  • ESR
  • Global health score
      • 2.6-3.1 - mildly active disease
    • 3.2-5.1 - moderaly active disease
    • >5.1 - severly active disease
30
Q

Surgical options

A

Ostetomy

  • realignment
  • change mechanial axis of joint to relieve weight

Arthrodesis

  • artifical injuction of joint ossification

Joint replacmeent

  • established disease