1. IF a gout patient is receiving an initial prescription for allopurinol and has significant renal impairment (defined as a serum creatinine level ≥ 2 mg/dl or measured/estimated creatinine clearance ≤ 50 ml/min), THEN the initial daily allopurinol dose should be < 300 mg/day.
2. IF a patient with tophaceous gout is given an initial prescription for a urate-lowering medication and lacks both 1) significant renal impairment (a serum creatinine level ≥ 2 mg/dl or measured/ estimated creatinine clearance ≤ 50 ml/min and 2) peptic ulcer disease, THEN a prophylactic agent (colchicine or NSAID) should be given concomitantly.
3. IF a gout patient has either 1) a history of nephrolithiasis or 2) significant renal insufficiency (defined as a serum creatinine level ≥ 2 mg/dl or measured/estimated creatinine clearance ≤ 50 ml/min) THEN a xanthine oxidase inhibitor should be started as the initial urate-lowering medication rather than a uricosuric agent.
4. IF a patient has hyperuricemia and gouty arthritis characterized by any of the following clinical characteristics 1) tophaceous deposits, 2) gouty erosive changes on radiographs, or 3) gout attack of twice or more per year, THEN the patient should be offered therapy with a urate lowering drug unless contraindicated.
1. IF a patient is newly prescribed any of the following drugs: NSAIDs (selective or non-selective), DMARDs, glucocorticoids or narcotics, THEN a discussion with the patient about the risks of the chosen therapy should be documented.
2. IF a patient is treated with 1) a non-selective NSAID or 2) a COX-2 selective NSAID plus aspirin, AND the patient has risk factors for upper gastrointestinal bleeding, THEN the patient should be treated concomitantly with either misoprostol or a proton pump inhibitor unless patient refuses.
3. IF a patient is treated with daily NSAIDs (selective or non-selective) and the patient has risk factors for gastrointestinal bleeding, THEN a hemoglobin or hematocrit should be performed at baseline and during the first year after initiating therapy.
4. IF a patient is treated with daily NSAIDs (selective or non-selective) AND the patient has risk factors for developing renal insufficiency** THEN a serum creatinine should be assessed at baseline, within the first 3 months, and then at least annually thereafter.
6. IF a patient has established treatment with a DMARD or glucocorticoids, THEN monitoring for drug toxicity should be performed. (SEE Table 2)