2+ Rheumatoid Arthritis Flashcards

1
Q

What is rheumatoid arthritis?

A

A chronic, auto-immune inflammatory joint condition characterised by symmetrical synovitis of the small joints

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2
Q

What is the epidemiology of rheumatoid arthritis?

A

F>M
Age 40-60

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3
Q

What is the aetiology of rheumatoid arthritis?

A

Interplay between genetic, environmental and host factors

Genetic: HLA-DR4, PTPN22, PADI-4

Environmental: smoking, vitamin D, infection (EBV, HHV8)

Host: female, 12 months post-partum

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4
Q

What is the pathophysiology of rheumatoid arthritis?

A

Inflammatory-mediated attack on the synovium of the joint
- Self-reactive T cells, MAC and fibroblast
- IL-1, TNFalpha

Hyperplasia/hypertrophy of the synovium –> panus

Destruction of the internal joint structures: erodes bone, cartilage, joint capsule, ligaments

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5
Q

What is the textbook presentation of rheumatoid arthritis?

A

Synovitis (inflammation, tenderness, erythema) of the peripheral, small joints. Symmetrical

= Symmetric polyarthritis of small joints of hands and feet

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6
Q

What is the history of rheumatoid arthritis?

A

Systemic: fatigue, malaise, depression

  • Morning stiffness, eased with activity
  • Pain, swelling, redness of joints
  • Insidious/sub-acute onset (>6 weeks)
  • Symmetrical, peripheral, small joints of hands and feet
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7
Q

Inflammatory vs mechanical joint pain:

A

Inflammatory: sub-acute, morning stiffness, eases with activity

Mechanical: chronic, progressive, worse with activity, better at rest

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8
Q

What are the signs on examination of rheumatoid arthritis?

A

Synovitis:
- Swelling
- Tenderness
- Bogginess

Joint effusion:
- Reduced ROM
- Erythema
- Warmth

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9
Q

What are the late signs on examination of rheumatoid arthritis?

A
  • Swan neck deformity: flex DIP, hyper-ext PIP
  • Boutonniere deformity: hyper-ext DIP, flex PIP
  • Z-thumb deformity: flex MCP, hyper-ext IP
  • Ulnar deviation
  • Hammer toe
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10
Q

What are the extra-articular features of rheumatoid arthritis?

A
  • Rheumatoid nodules
  • Cutaneous: pyoderma gangrenosum, palmar erythema
  • Lung: pleuritis, pleural effusion, alveolitis
  • Cardiac: pericarditis, valvular heart disease, pericardial effusion
  • Ocular: scleritis, episcleritis, keratoconjunctivitis sicca
  • Neuro: peripheral neuropathy, nerve entrapment
  • Haematology: neutropenia/splenomegaly (Fenty’s), anaemia of chronic disease
  • Vasculitis: nailfold, systemic
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11
Q

What are the ACR criteria for RA?

A
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12
Q

What lab Ix do you do for RA?

A

Auto-antibodies:
- RF
- Anti-CCP (98% specific for RA)

Disease activity:
- CRP
- ESR
- Plts (thrombocytosis)

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13
Q

What imaging Ix do you do for RA?

A

X-Ray
- Early= soft tissue swelling
- Late = erosions, joint deformity, ankylosis

USS and MRI increasingly used:
- Show bony erosions, synovitis and soft tissue swelling that is otherwise not seen on plain radiologic film

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14
Q

What is the non-pharmacological management of RA?

A
  • Physiotherapy/OT
  • Psychological support
  • Quit smoking
  • Reduce alcohol intake
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15
Q

What is the goal of RA treatment?

A

To get remission
- No active inflammation, no erosion, no functional disturbance

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16
Q

What is the early treatment of RA?

A

Low dose prednisolone + DMARD

+ NSAID for symptomatic

17
Q

What is the escalating treatment of RA?

A
  1. Add an additional DMARD/change DMARD
  2. Biologic
18
Q

What are the traditional DMARDs?

A

MTX
Hydroxychloroquine
Leflunomide
Sulfasalazine

19
Q

What are the biologic DMARDs?

A

TNFalpha inhibitiors: infliximab, adalimumab
IL-6 inhibitors: tocilizumab
Cell adhesion molecule inhibitors: abatacept
B cell inhibitors: rituximab

20
Q

What are the complications of RA treatment?

A

Cytopenias
Increased infection risk
GIT disturbance
Liver function: cirrhosis
Malignancy risk?