Harris M, Bryant L R, Danaher P, Alloway J
Department of Rheumatology and Medicine, San Antonio 78236-5300, USA.
J Rheumatol. 2000 Dec;27(12):2873-6.
To determine if low dose daily enteric coated aspirin significantly affects the therapeutic actions of probenecid with respect to serum urate levels or urinary urate excretion.
Patients with gouty arthritis taking a stable dose of probenecid for at least 3 months were enrolled in a prospective crossover study. Twenty-four hour urinary and serum uric acid levels were measured after 14 days in patients crossed over to receive probenecid alone; probenecid and aspirin 325 mg taken concomitantly; and probenecid followed by aspirin 325 mg at 6 hours.
Eleven patients completed the crossover study. The addition of aspirin to a stable dose of probenecid had no significant effect upon serum urate levels or 24 h urinary urate excretion (p > 0.05, paired t test).
Low dose daily enteric coated aspirin does not significantly interfere with the uricosuric effects of probenecid in patients with gouty arthritis.
确定每日低剂量肠溶阿司匹林是否会显著影响丙磺舒在血清尿酸水平或尿尿酸排泄方面的治疗作用。
将服用稳定剂量丙磺舒至少3个月的痛风性关节炎患者纳入一项前瞻性交叉研究。在交叉接受单独丙磺舒治疗、丙磺舒与325毫克阿司匹林同时服用、丙磺舒服用后6小时服用325毫克阿司匹林的患者中,14天后测量24小时尿尿酸和血清尿酸水平。
11名患者完成了交叉研究。在稳定剂量的丙磺舒中添加阿司匹林对血清尿酸水平或24小时尿尿酸排泄没有显著影响(配对t检验,p>0.05)。
每日低剂量肠溶阿司匹林不会显著干扰痛风性关节炎患者中丙磺舒的促尿酸排泄作用。