Rheumatology Flashcards

1
Q

Describe typical presentation of rheumatoid arthritis

A

Female, 30 – 50 years old
Symmetrical, affecting MCPs, PIPs, MTPs and typically spares DIPs (can affect any other joint)
History > 6 weeks
Morning stiffness > 30 minutes duration

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2
Q

List investigations to do for suspected RA

A

RF and anti-CCP
FBC
Inflammatory markers
X-ray (changes more apparent in established disease, USS/MRI in early disease)

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3
Q

Describe treatment for RA

A

Initially DMARD monotherapy – methotrexate
Steroids (acutely) – PO/IM or intra-articular
Symptom control with NSAIDs (PPI cover) if no contraindication
If disease still severe after combination DMARDs – biologics (anti-TNFs)
OT/PT, podiatry, psychological

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4
Q

List the extra-articular manifestations of RA

A

3Cs – carpal tunnel syndrome, increased cardiac risk, cord compression
3As – anaemia, amyloidosis, arteritis
3Ps – pericarditis, pleural disease, pulmonary disease
3Ss – Sjogrens, scleritis, splenic enlargement

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5
Q

List x-ray features of RA

A

Loss of joint space
Erosions (periarticular)
Soft tissue swelling
Subluxation

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6
Q

Describe polymyalgia rheumatica

A

Clinical syndrome characterised by pain and stiffness of the shoulder, hip girdles and neck
Average age of onset is 70 years & is associated with GCA

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7
Q

Describe the typical presentation of polymyalgia rheumatica

A

Elderly patients with new sudden onset of proximal limb pain and stiffness (neck, shoulders, hips)
Difficulty rising from chair/combing hair (proximal muscle involvement)
Night time pain
Systemic symptoms – fatigue, weight loss, low grade fever

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8
Q

List investigations done for suspected polymyalgia rheumatica

A

Typical history & examinations
Inflammatory markers – ESR/PV, CRP
Consider temporal artery biopsy if symptoms of GCA

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9
Q

Describe the treatment for polymyalgia rheumatica

A

Dramatic response within 5 days of starting prednisolone (15mg daily)
Has to be tapered very slowly; rapid taper is associated with symptom relapse
Methotrexate can be steroid-sparing in relapsing patients

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10
Q

Describe ankylosing spondylitis

A

Inflammatory disorder of the spine
Radiographic changes at the sacroiliac joints are present

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11
Q

Describe the typical presentation of ankylosing spondylitis

A

Young men (teens – mid-thirties)
Bilateral buttock pain, chest wall & thoracic pain
Prolonged morning stiffness in the lower back and buttocks
Pain and stiffness improve with exercise but not with rest
Progressive loss of spinal movement

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12
Q

Describe examination findings for ankylosing spondylitis

A

Often normal
Later:
1) Loss of lumbar lordosis & exaggerated thoracic kyphosis
2) Schober’s test (mark skin 10cm above and 5cm below PSIS, bend forward with straight legs, distance increase to >20cm is normal)
3) Reduced chest expansion

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13
Q

List investigations for suspected ankylosing spondylitis

A

CRP may be raised but often normal
MRI spine & SI joints

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14
Q

List treatment options for ankylosing spondylitis

A

NSAIDs
Physio
TNF inhibitors
IL-17 inhibitors

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15
Q

List extra-articular manifestations of ankylosing spondylitis

A

Anterior uveitis
Aortic incompetence
AV block
Apical lung fibrosis
Amyloidosis

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16
Q

Describe SLE

A

Multisystemic autoimmune disease
Autoantibodies are made against a variety of autoantigens which form immune complexes
Inadequate clearance of immune complexes results in a host of immune responses which cause tissue inflammation & damage

17
Q

List common signs and symptoms of SLE

A

Serositis
Oral ulcers
Arthritis
Photosensitivity – malar/discoid rash
Blood disorders
Renal involvement
Autoantibodies – ANA positive in > 90% cases
Immunologic tests
Neurologic disorder – seizures or psychosis

18
Q

List investigations for suspected SLE

A

Raised ESR or plasma viscosity
Anaemia & leukopenia are common
Anti-Ro, anti-La, anti-dsDNA, antiphospholipid antibodies
C3 and C4 fall with disease activity
Urinalysis – detecting renal disease
Skin biopsy
Renal biopsy

19
Q

Describe the treatment for SLE

A

Sun protection
Healthy lifestyle – increased CVS risk
Hydroxychloroquine – helpful for rash and arthralgia
Mycophenolate mofetil, azathioprine and rituximab
Prednisolone – for flares

20
Q

Describe the management for osteoarthritis

A

Non-drug therapy: strengthening & range of movement exercises, weight loss, walking stick
Pharmacological therapy: regular paracetamol, NSAIDs short term, intra-articular corticosteroids can be offered
Surgery: if nothing else has worked, surgery can be considered

21
Q

Describe fibromyalgia

A

Common disorder if central pain processing characterised by chronic widespread pain in all 4 quadrants of the body
Allodynia, a heightened and painful response to innocuous stimuli is often present

22
Q

List symptoms and signs of fibromyalgia

A

Pain
Joint/muscle stiffness
Profound fatigue
Unrefreshed sleep
Numbness
Headaches
IBS
Depression & anxiety

23
Q

List treatment options for fibromyalgia

A

Should be specifically tailored based on pain intensity, function and associated features
Low dose amitriptyline
Pregabalin may be effective
Opiates NOT recommended
CBT

24
Q

Describe osteoporosis

A

Characterised by low bone mass, deterioration of bone tissue & disruption of bone architecture -> compromised bone strength & increased risk of fracture

25
Q

List investigations for suspected osteoporosis

A

Dual energy x-ray absorptiometry (DEXA) of lumbar spine and hip = gold standard
T-score (number of SDs from the mean bone density of persons of same gender at age of peak density): minus 2.5 or less

26
Q

Describe the treatment for osteoporosis

A

Vitamin D +/- calcium supplementation plus:
1st line – oral bisphosphonates/IV if oral not tolerated
2nd line – denosumab or teriparatide

27
Q

Describe the pathogenesis of gout

A

Inflammatory arthritis related to hyperuricaemia
Deposition of monosodium urate crystals -> accumulate in joints and soft tissues, result in acute and chronic arthritis, soft-tissue masses (tophi), urate nephropathy & uric acid nephrolithiasis

28
Q

List risk factors for gout

A

Non-modifiable: age > 40 years, male gender
Modifiable: increased purine uptake, alcohol intake, high fructose intake, obesity, CCF

29
Q

Describe the treatment for gout

A

General prevention – maintain optimal weight, regular exercise, diet modification
First line treatment in acute gout – NSAIDs, oral/IM steroids, colchicine
Chronic cases – urate lowering therapy: allopurinol & febuxostat

30
Q

Describe osteomalacia

A

Normal amount of bone but decreased mineral content
Occurs after fusion of the epiphyses (rickets if this process occurs during the period of bone growth)

31
Q

List signs and symptoms of osteomalacia

A

Bone pain and tenderness
Fractures (esp. femoral neck)
Proximal myopathy due to decreased phosphate & vit D deficiency

32
Q

List investigations for suspected osteomalacia

A

Calcium, phosphate, ALP, PTH, 25(OH)-vitamin D
Bone biopsy – shows incomplete mineralisation
X-ray – loss of cortical bone

33
Q

List treatment options for osteomalacia

A

Vitamin D
Vitamin D2/calcitriol (malabsorption or hepatic disease)
Alfacalcidol/calcitriol (renal disease or vitamin D resistance)
Monitor plasma Ca2+, initially weekly, and if nausea/vomiting