Rheumatoid arthritis Flashcards

1
Q

What is rheumatoid arthritis

A

A chronic systemic inflammatory disease characterised by a symmetrical deforming peripheral polyarthritis

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2
Q

What does RA increase the risk of?

A

Cardio and cerebro vascular disease

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3
Q

Who does RA typically affect

A

Women
Age 50-60
Smokers

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4
Q

Name the genetic link to increased severity of RA

A

HLA-DR4/DR1

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5
Q

Describe the typical symptoms of RA

A

Symmetrical, stiff, swollen, painful small joints of hands and feet
Worse in morning
Can fluctuate and larger joints may be involved
Can have less common presentation with widespread arthritis, recurring polyarthritis (palindromic), persistent monoarthritis or systemic illness (extra-articular features)

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6
Q

What are some signs of RA?

A

Swollen MCP, PIP, wrist or MTP joints
Look for tenosynovitis or bursitis
Ulnar deviation and subluxation of the wrists
Boutonnière and swan neck deformity of the fingers and Z deformity of the thumb
Foot changes are similar
Atlanto-axial subluxation is rare but can threaten the spinal cord

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7
Q

List the extra-articular manifestations of RA

A
Nodules on elbows, lungs, cardiac and CNS
Vasculitis
Lymphadenopathy 
Pleural disease, interstitial fibrosis, bronchiolitis obliterans, organising pneumonia
IHD, pericarditis, pericardial effusion 
Carpal tunnel syndrome
Peripheral neuropathy 
Feltys syndrome 
Episcleritis, keratoconjunctivitis sicca
Osteoporosis
Amyloidosis (rare)
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8
Q

What is feltys syndrome

A

Splenomegaly
RA
Neutropenia

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9
Q

What are the investigations for RA

A

Rheumatoid factor - positive in 70% and high levels associated with poorer outcomes
Anti-CCP - highly specific for RA and predict progression
Anaemia of chronic disease, increased platelets, increased ESR/CRP
Xrays - soft tissue swelling, bony erosion, subluxation and complete carpal destruction

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10
Q

What is needed for diagnosis of RA

A

Clinical suspicion - those with > 1 swollen joint and suggestive clinical history not explained by another disease. Scores greater than 6
A - joint involvement (5 for >10 joints)
B- serology (3 for high positive RF or anti-CCP)
C- acute phase reactants (1 for abnormal CRP/ESR)
D - duration of symptoms (1 for >6weeks)

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11
Q

How is RA managed

A

Rheum referral
Disease activity - DAS28 score - treat to target
Early DMARDs and biologics
IM steroids for flares
NSAIDs for symptomatic relief - do not alter progression
OT and physio referral
Lifestyle - CVD RF adjustment
Surgery - relieve pain, improve function and reduce deformity

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12
Q

Name the 4 types of biological and give examples

A

TNF alpha inhibitors - infliximab, etanercept, adalimumab
B cell depletion - rituximab
IL-1 and IL-6 inhibition - tociluluzimab
Inhibition of T cell co-stimulation - abatacept

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13
Q

How long does methotrexate take to work?

A

6-12 weeks

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14
Q

When should DMARDs ideally be started?

A

Within 3 months of persistent symptoms

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15
Q

What are the SEs of methotrexate

A

Pneumonitis, oral ulcers, hepatotoxicity, teratogenic

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16
Q

What are the SEs of sulfalazine

A

rash, decreased sperm count, oral ulcers, GI upset

17
Q

What are the SEs of lefulomide

A

Teratogenicity, oral ulcers, hypertension, hepatotoxicity

18
Q

What are the SEs of hydroxychloroquine

A

Retinopathy

19
Q

What is the fatal SE of DMARDs and biologics?

A

Immunosuppression - pancytopenia and neutropenic sepsis

20
Q

What is required before starting biologics and DMARDs?

A

TB, HIV, HepB/C screen and CXR