Few arthritides are as painful, incapacitating, and stressful as a severe attack of acute gout, pseudogout, or calcific periarthritis. Successful treatment of these acute microcrystalline events depends on early use of an effective and safe anti-inflammatory drug in full dosage. The sooner such treatment is started the more rapid and complete the response. Treatment options include colchicine, non-steroidal anti-inflammatory drugs (NSAIDs), and corticosteroids including adrenocorticotrophic hormone. 1 Although colchicine is traditionally rooted in the treatment of acute gout, in recent years its use has declined steadily. 1 Its drawbacks include slow onset of action, narrow ratio of benefit to toxicity, and reduced efficacy when used more than 24 hours after the an attack begins. Colchicine (0.6 mg orally every 2 hours, up to 4-6 mg/day) is now reserved for patients without renal, hepatic, or bone marrow disease, in whom the more effective NSAIDs are contraindicated or poorly tolerated. Intravenous colchicine is best avoided given its potential for serious toxicity, which potentially can result in myelosuppression, hepatic necrosis, renal failure, hypotension, seizures, and death. Intra-articular corticosteroids (for example, methylprednisolone acetate 5-25 mg per joint), systemic corticosteroids (oral prednisone 20 mg/day tapered off over 4-10 days, or intramuscular triamcinolone hexacetonide 60 mg/day, repeated in 1-4 days), and corticotrophin (40-80 IU every 6-24 hours) are valuable, highly effective, and relatively safe alternatives in patients with acute microcrystalline synovitis in whom neither NSAIDs nor colchicine are recommended. Such patients include elderly people and those with renal insufficiency, hepatic dysfunction, cardiac failure, peptic ulcer disease, and hypersensitivity to NSAIDs. 1 The duration of treatment is usually short, and side effects due to steroids are rare. 1 Non-salicylate NSAIDs are the drugs of choice in the treatment of acute crystal induced arthritis. 1 Although no comparative studies have been conducted, NSAIDs are generally better tolerated and have more predictable therapeutic effects than colchicine.

The patient is usually supplied with the appropriate NSAIDs (preferably carried with the person, for all too often gout strikes when the patient is far from home) and instructions to how to self treat the acute episode at the first “twinge” of an attack. No clear advantage is known of any one NSAID over another, but large initial doses are recommended: indomethacin 150-200 mg/day, naproxen 1000 mg/day, or diclofenac sodium 150 mg/day. 1 Although adverse reactions may occur, the duration of treatment with NSAIDs is generally short (4-8 days), and serious toxicity leading to drug withdrawal (such as gastrointestinal bleeding) is rare. Conventional NSAIDs exert their antiinflammatory effects mainly through inhibition of the enzyme cyclo-oxygenase, which catalyses the conversion of arachidonic acid to proinflammatory prostaglandins, particularly prostaglandin E2. These play a major part in both experimental and clinical crystal induced inflammation, and act synergistically with other mediators (for example, bradykinin, leukotriene B4) to enhance capillary dilatation, pain sensitivity, and neutrophil chemotaxis. 2 Cyclo-oxygenase exists in two isoforms: cyclo-oxygenase-1 and cyclo-oxygenase-2. 3 4 Cyclo-oxygenase-1 is constitutively expressed in most tissues and is relatively unaffected by inflammatory mediators. It supports biosynthesis of prostanoids required for normal homeostatic “housekeeping” functions such as renal blood flow and maintaining the integrity of gastric mucosa. By contrast, cyclooxygenase-2 is constitutively expressed in a …