Rheumatoid Arthritis Flashcards

1
Q

What type of swelling occurs in inflammatory arthritis?

A

Boggy swelling - similar to when squashing a grape, this is suggestive of synovitis.

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2
Q

Which joints are involved in rheumatoid arthritis?

A
  • Wrists
  • Metacarpophalangeal (MCP)
  • Proximal interphalangeal (PIPJ)
  • Involvement is usually symmetrical
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3
Q

Which joints are involved in osteoarthritis?

A
  • PIPJ
  • DIPJ
  • Carpometacarpal phalangeal (CMPJ) - base of thumb
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4
Q

What deformities can RA patients develop?

A
  • Swan neck deformities: hyperextension of the PIPJ and flexion of DIPJ
  • Boutonniere deformity: flexion of PIPJ and hyperextension of DIPJ
  • Guttering: muscle wasting seen over dorsum of the hand
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5
Q

What do you do if you suspect RA?

A
  • Prescribe analgesia for symptomatic relief
  • Refer them urgently to rheumatology
  • Rapid and aggressive suppression of inflammation improves long-term outcome by reducing joint damage, maintaining function and quality of life
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6
Q

What investigations do you do for RA?

A
  • Baseline - FBC, LFTs, U+Es
  • Inflammatory markers to check levels of inflammation
  • Immunology: RF and anti-CCP antibody, also anti-nuclear antibody may indicate CTD
  • X-rays of swollen/painful joints
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7
Q

Why is RF not diagnostic for RA?

A

RF is an immunoglobulin directed against the patient’s Fc portion of self IgG. It can present in the normal population, Sjorgren’s syndrome, other rheumatic conditions, certain malignancies and chronic infections.

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8
Q

What is the best test for the diagnosis of RA?

A

Anti-CCP antibodies have high sensitivity and specificity for RA.

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9
Q

What x-ray changes can occur in established RA disease?

A
  • Periarticular erosions (juxta-articular)
  • Osteopenia
  • Joint space narrowing (usually uniform)
  • Deformity
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10
Q

Why could the FBC be abnormal in RA?

A
  • Anaemia of chronic disease
  • IDA secondary to use of non-steroidals or other causes
  • Felty’s syndrome: anaemia, leucopenia and enlarged spleen
  • Pernicious anaemia: autoimmune diseases are more likely to have a 2nd one
  • Autoimmune haemolytic anaemia
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11
Q

What other abnormalities could show up in baseline tests for RA?

A
  • Platelet count can go up due to inflammatory process
  • Raised LFTs
  • Raised ferritin
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12
Q

What are the target populations for testing for RA?

A
  1. Have at least 1 joint with definite clinical synovitis (swelling)
  2. With the synovitis, not better explained by another disease
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13
Q

How is the DAS28 score calculated?

A

Calculated from a composite of a joint tenderness score, no. of swollen joints, patient global assessment of disease activity and a measure of acute phase response (ESR or CRP).

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14
Q

What is the DAS28 score figures?

A

Remission <2.6
Low 2.6-3.2
Moderate 3.2-5.1
Severe >5.1

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15
Q

What are the extra-articular features of RA?

A
  • Carpal tunnel syndrome, peripheral neuropathy (mononeuritis multiplex), atlanto-axial subluxation (misalignment of 1st/2nd cervical vertebrae)
  • Palmar erythema, nail fold infarcts, ulceration
  • Pleural effusion, pleuritis
  • Pericardial effusion, pericarditis, nodules, ILD, PF
  • Vasculitis
  • Lymphadenopathy
  • Splenomegaly
  • Felty’s syndrome
  • Episcleritis, scleritis, scleromalacia perforans (corneal melt)
  • Keratoconjunctivits sicca (dry eyes and mouth)
  • Normochromic normocytic anaemia, leukopenia, pancytopenia
  • Amyloidosis
  • Fatigue, low grade fever, weight loss
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16
Q

What is the first line treatment of RA?

A

DMARD monotherapy +/- a short course of bridging prednisolone. Monitor with CRP and DAS28 to assess response to treatment.

17
Q

What is the treatment for flares of RA?

A

Oral or intramuscular corticosteroids

18
Q

What DMARDs are used in RA?

A

Methotrexate is most common - monitor FBC and LFTs due to risk of myelo-suppression, liver cirrhosis and pneumonitis.
Also, there is sulfasalazine, leflunomide, hydroxychloroquine

19
Q

When are TNF-inhibitors used instead of DMARDs?

A

Inadequate response to at least 2 DMARDs including methotrexate. For example, etanercept, infliximab or adalimumab.

20
Q

What is synovitis?

A

The synovium becomes inflamed and thickened and proliferative synovitis (pannus) can be seen. Angiogenesis occurs so leucocytes accumulate, along with inflammatory cells e.g. macrophages, T cells etc. The synovial fluid becomes fibrinous inflammatory exudate, containing many neutrophils. Local release of matrix-degrading enzymes and inflammatory mediators can damage adjacent cartilage to form erosions.

21
Q

What is the presentation of RA?

A
  • Swollen, painful joints in hands and feet
  • Stiffness worse in the morning
  • Gradually gets worse with larger joints becoming involved
  • Presentation usually insidiously develops over a few months
  • Positive ‘squeeze test’ - discomfort on squeezing across the metacarpal or metatarsal joints
22
Q

What is the classification criteria for RA?

A

Score of >/= 6/10 in categories A to D

23
Q

What is the A group of symptoms for classifying RA?

A

Joint movement

  1. 1 large joint
  2. 2-10 large joints
  3. 1-3 small joints (*with or without involvement of large joints)
  4. 4-10 small joints (*)
  5. > 10 joints (at least 1 small joint)
24
Q

What is the B group of symptoms for classifying RA?

A

Serology (at least 1 test result needed for classification)

  1. Negative RF and ACPA
  2. Low-positive RF or low-positive ACPA
  3. High-positive RF or high-positive ACPA
25
Q

What is the C group of symptoms for classifying RA?

A

Acute-phase reactants (at least 1 needed for classification)

  1. Normal CRP and normal ESR
  2. Abnormal CRP or abnormal ESR
26
Q

What is the D group of symptoms for classifying RA?

A

Duration of symptoms

  1. <6 weeks
  2. > /= 6 weeks
27
Q

How would Felty’s syndrome present?

A

Splenomegaly causing neutropenia/pancytopenia