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Gout Flashcards

(33 cards)

1
Q

What causes gout?

A

Deposition of monosodium urate crystals in joints due to hyperuricaemia.

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2
Q

What triggers the inflammation and pain in gout?

A

The immune system attacks urate crystals deposited in joints.

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3
Q

Which joints are most commonly affected by gout?

A

Distal joints—especially the 1st MTP (toe), knees, ankles, and fingers.

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4
Q

What is the primary risk factor for gout?

A

Hyperuricaemia.

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5
Q

Name three dietary factors that increase gout risk.

A

Alcohol, sugary drinks, red meat, and seafood.

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6
Q

List three medical conditions associated with increased gout risk.

A

CKD, hypertension, diabetes.

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7
Q

Which medications are associated with gout?

A

Diuretics, low-dose aspirin, ciclosporin.

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8
Q

What lab test supports a gout diagnosis?

A

Serum urate ≥360 µmol/L.

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9
Q

What is a tophus?

A

A chalky urate crystal deposit under the skin.

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10
Q

What are the first-line treatments for acute gout?

A

NSAIDs, colchicine, or oral corticosteroids.

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11
Q

Why use colchicine with caution?

A

It has a narrow therapeutic range and risk of toxicity.

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12
Q

Can ULT be started during a flare?

A

Yes, especially if flares are frequent, but generally started after a flare settles.

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13
Q

When should urate-lowering therapy (ULT) be offered?

A

≥2 flares/year, CKD (stage 3–5), on diuretics, presence of tophi or chronic gout.

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14
Q

What is the urate level target in chronic gout management?

A

<360 µmol/L; <300 µmol/L if tophi/chronic symptoms.

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15
Q

Name two first-line ULT medications.

A

Allopurinol and febuxostat.

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16
Q

What can be used as prophylaxis during ULT initiation?

A

Colchicine, low-dose NSAID, or corticosteroid.

17
Q

What is the usual dose of colchicine for acute gout?

A

500 micrograms 2–4 times a day (maximum 2 mg per day), for up to 3 days.

17
Q

What is the minimum interval between colchicine courses?

A

At least 3 days (BNF requirement to reduce toxicity risk).

18
Q

What are two key contraindications for colchicine use?

A

Blood disorders, severe renal/hepatic impairment.

18
Q

What are the main side effects of colchicine?

A

GI upset (diarrhoea, nausea, vomiting), myopathy, bone marrow suppression (rare).

18
Q

What is a major drug interaction of colchicine?

A

Strong CYP3A4 or P-gp inhibitors (e.g., clarithromycin, ciclosporin) ↑ risk of toxicity.

19
Q

What is important counselling advice for colchicine?

A

Stop treatment and seek advice if nausea, vomiting, or diarrhoea occur.

20
Q

What is the mechanism of action of allopurinol?

A

Xanthine oxidase inhibitor – reduces uric acid production.

21
Q

When should allopurinol be started in gout?

A

At least 2–4 weeks after a flare has settled (unless frequent flares).

22
What is the main adverse effect to monitor for with allopurinol?
Severe skin rash (can signal Stevens-Johnson Syndrome).
23
Drug class of allopurinol and febuxostat?
Xanthine oxidase inhibitors.
24
Should allopurinol be continued during a gout flare?
Yes – continue and treat the flare separately.
25
What is a key interaction with allopurinol?
Azathioprine or mercaptopurine – risk of severe toxicity (reduce dose significantly or avoid).
26
What is the mechanism of action of febuxostat?
Xanthine oxidase inhibitor – lowers uric acid levels.
27
What is the initial dose of febuxostat?
80 mg once daily, can increase to 120 mg if target urate not achieved.
28
What are the main contraindications for febuxostat?
Ischaemic heart disease, congestive heart failure.
29
What are the common side effects of febuxostat?
Liver function abnormalities, diarrhoea, rash, headache.
30
What is a serious but rare cardiovascular warning with febuxostat?
Risk of cardiovascular death – caution in patients with CVD history.