Rheumatoid Arthritis - workbook ONLY (lecture in intro) Flashcards
1
Q
What is RA?
A
- Autoimmune disease associated with antibodies to the Fc portion of IgG (rheumatoid factor) and anti citrullinated cyclic peptide
2
Q
Pathogenesis of RA
A
- Citrullination of self antigens which are then recognised by T and B cells
- These then produce antibodies (RF and anti-CCP)
- Stimulated macrophages and fibroblasts release TNF-a
- Inflammatory cascade = proliferation of synoviocytes (=boggy joint swelling)
- These grow over cartilage = restriction of nutrients and cartilage is damage
- Macrophages stimulate osteoclast differentiation –> bone damage
3
Q
Typical history of RA
A
- Female
- 3-50yrs old
- Progressive, peripheral, symmetrical arthiritis
- History more than 6 weeks
- Morning stiffness lasts more than 30 minutes
- Fatigue and malaise
4
Q
Which joint does RA often affect?
A
- MCPs
- PIPs
- MTPs
- SPARES DIPs (unlike OA)
- Can affect any joint though inc hips, knees, shoulders, c-spine
5
Q
Examination findings RA
A
- Soft tissue swelling and tenderness
- Ulnar deviation/palmar subluxation of MCPs
- Swan neck and Boutonierre deformity to digits
- Rheumatoid nodules - most common at elbow
- Check median nerve - carpal tunnel association
6
Q
Investigations findings of RA
A
- RF and anti-CCP
- FBC - normocytic anaemia (chronic disease)
- Do WCC if concerned septic arthiritis
- Inflammatory markers - elevated
- X-ray changes apparent in established disease - USS/MRI more sensitive in early disease
- Others guided by history and exam eg may need PFTs and HRCT if lungs involved
7
Q
Treatment for RA
A
- Initially DMARD monotherapy - usually MTX
- Consider combination of DMARDs eg leflunomide, hydroxychloroquine, sulfasalazine
- Steroids - acute PO/IM or intra-articular
- Symptom control with NSAIDs (+PPI cover) as long as no contraindication
- If still severe –> biologics eg etanercept anti-TNF)
- Non drug - OT/PT, podiatry, psychological
8
Q
3 C’s associated with RA
A
- Carpal tunnel
- Elevated Cardiac risk
- Cord compression - due to atlantoaxial subluxation
9
Q
3 A’s associated with RA
A
- Anaemia - normocytic and normochromic
- Amyloidosis - very rare now due to good treatment but can cause nephrotic syndrome and CKD
- Arteritis - rarer now as better treatment but can cause nail fold infarcts, cutaneous vasculitis, mononeuritis multiplex
10
Q
3 P’s associated with RA
A
- Pericarditis (uncommmon)
- Pleural disease (common)
- Pulmonary disease eg bronchiectasis, bronchiolotis obliterans, fibrosis (common)
11
Q
3 S’s associated with RA
A
- Sjogrens - common
- Scleritis/episcleritis - uncommon
- Splenic enlargement (if + neutropenia = Feltys syndrome = rare
12
Q
X-ray features of RA
A
- Loss of joint space
- Erosions- periarticualr
- Soft tissue swelling
- Subluxation
LESS
13
Q
Monitoring required with DMARDs
A
- Liver function tests
- FBC
- U&E
- Eye assessement
Every 2 weeks blood tests until stable/for 6 weeks
Then every 12 weeks
If dose increases restart process
14
Q
Features distinguishing RA from other arthropathies
A
- Symmetrical
- Affects small joints - spares DIPs
- Multisystem effects
- Specific deformities - Swan neck, Boutonierre, Ulnar deviation
15
Q
A