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Biochemical effectiveness of allopurinol and allopurinol-probenecid in previously benzbromarone-treated gout patients

机译:别嘌呤醇和别嘌呤醇-前苯丙酮酸在先前苯溴马隆治疗的痛风患者中的生化有效性

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摘要

In 2003, the uricosuric drug benzbromarone was withdrawn from the market. The first alternative drug of choice was the xanthine oxidase inhibitor allopurinol. The purpose was to (1) investigate the efficacy of allopurinol (standard dosage) compared with previous treatment with benzbromarone; and (2) investigate the combination therapy allopurinol - probenecid as an effective alternative treatment compared with previous benzbromarone treatment. A prospective, open study was carried out in a cohort of 51 gout patients who discontinued benzbromarone therapy because of market withdrawal. Patients were given 200-300 mg allopurinol (stage 1). When allopurinol failed to attain the target serum urate (sUr) levels
机译:2003年,尿酸排泄药物苯溴马隆被撤出市场。选择的第一种替代药物是黄嘌呤氧化酶抑制剂别嘌醇。目的是(1)研究别嘌呤醇(标准剂量)与先前使用苯溴马隆治疗的疗效; (2)与以前的苯溴马隆治疗相比,研究了别嘌醇-丙磺舒联合治疗是有效的替代治疗。一项针对51名痛风患者的前瞻性开放研究因市场退出而中断了苯溴马隆治疗。给予患者200-300 mg别嘌醇(1期)。当别嘌呤醇未能达到目标血清尿酸盐(sUr)水平时

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