Gout Flashcards

1
Q

2 main strategies for the treatment of gout:

A
  1. Management of acute attacks of gouty arthritis
  2. Long-term management of chronic gout.
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2
Q

AGENTS THAT SUPPRESS LEUKOCYTE RECRUITMENT AND ACTIVATION

A
  • NSAIDs
  • COLCHICINE
  • GLUCOCORTICOIDS
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3
Q

NSAIDs for Gout Rx

A
  • First-line drugs for acute gout.
  • Indomethacin is the most popular.
  • Other NSAIDs are also effective.
  • Aspirin is contraindicated, because it competes with uric acid for the organic acid secretion mechanism in the proximal tubule of the kidney.

Adverse

  • Bleeding, salt and water retention, and renal insufficiency.
  • COX-2 selective inhibitors may decrease the risk of GI bleeding, but concerns about adverse CV effects limit their long-term use.
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4
Q

AGENTS THAT LOWER PLASMA URATE CONCENTRATION

A

AGENTS THAT DECREASE URIC ACID SYNTHESIS: ALLOPURINOL

AGENTS THAT ENHANCE URIC ACID EXCRETION (URICOSURIC AGENTS)

  • PROBENECID
  • SULFINPYRAZONE

AGENTS THAT ENHANCE URIC ACID METABOLISM: RASBURICASE

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5
Q
A
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6
Q

ALLOPURINOL

A
  • Purine analog.
  • Inhibits xanthine oxidase.
  • An NSAID or colchicine is coadministered during the first 4-6 months of allopurinol therapy to reduce the chance of an acute attack of gout.

Adverse

  • Well tolerated by most patients.
  • Hypersensitivity reactions, especially skin rashes, are the most common adverse reactions.
  • In rare instances the rash may progress to
  • Steven-Johnson syndrome.
  • All patients who develop a cutaneous reaction to allopurinol should discontinue the drug.

Drug interactions

  • anticancer drug mercaptopurine and the immunosuppressant azathioprine are purine analogues which are metabolized by xanthine oxidase.
  • Inhibition of xanthine oxidase by allopurinol can result in toxic levels of coadministered mercaptopurine or azathioprine.
  • Therefore, a dose reduction of these drugs is required.
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7
Q

URICOSURIC AGENTS

A
  • Urate is filtered, secreted, and reabsorbed by the kidneys.
  • Reabsorption predominates: the amount excreted is 10% of that filtered.
  • This process is mediated by a specific transporter.
  • The transporter exchanges urate for an anion.
  • Uricosuric drugs compete with urate for the
  • transporter, thereby inhibiting its reabsorption.
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8
Q

PROBENECID

A
  • Colchicine or NSAIDs are given early in the therapy to avoid precipitating an attack of gout.
  • Probenecid should not be used in gouty patients with nephrolithiasis or with overproduction of uric acid.

Adverse

  • Mild GI irritation.
  • Hypersensitivity reactions; usually mild. Serious hypersensitivity is extremely rare.
  • A liberal fluid intake should be maintained to minimize risk of renal stones.
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9
Q

SULFINPYRAZONE: ADVERSE EFFECTS

A
  • GI irritation.
  • Hypersensitivity reactions, usually a rash with fever, occur less frequently than with probenecid.
  • Depression of hematopoiesis.
  • Should not be used by patients with underlying blood dyscrasias.
  • A liberal fluid intake should be maintained to minimize the risk of renal stones.

Drug Interactions

  • Sulfinpyrazone inhibits warfarin metabolism.
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10
Q

RASBURICASE

A
  • AGENTS THAT ENHANCE URIC ACID METABOLISM
  • Most mammals other than humans express the enzyme uricase.
  • This enzyme oxidizes uric acid to allantoin, a soluble compound that is easily excreted by the kidney.
  • In cancer chemotherapy, the rapid lysis of tumor cells can release free nucleotides and increase plasma urate levels.
  • This can lead to massive renal injury.
  • Exogenous uricase can reduce plasma urate levels and prevent renal damage.
  • Allopurinol can also be used to prevent this component of tumor lysis syndrome.
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