别嘌呤醇
医学
痛风
肾脏疾病
肾功能
加药
内科学
尿酸
高尿酸血症
泌尿科
肾
胃肠病学
外科
内分泌学
作者
Michael Toprover,Daria B. Crittenden,Dodji Modjinou,Cheongeun Oh,Svetlana Krasnokutsky,Mark Fisher,Robert T. Keenan,Michael H. Pillinger
出处
期刊:PubMed
日期:2019-03-01
卷期号:77 (2): 87-91
被引量:4
摘要
Gout patients with chronic kidney disease (CKD) accumulate the active allopurinol metabolite oxypurinol, suggesting that allopurinol may promote greater serum urate (sU) lowering in CKD patients.We identified all patientswith gout diagnoses on either 100 mg or 300 mg of allopurinol daily, with available pre- and on-treatment sU levels, in our system in a 1-year period. Mean sU decrement by dosing per CKD groups was determined by CKD stage.Of 1,288 subjects with gout, 180 met entry criteria, with 83 subjects receiving 100 mg and 97 receiving 300 mg allopurinol. Subjects with CKD stage 1 experienced less sU lowering with 100 mg than 300 mg of allopurinol. Subjects with stage 4 and 5 CKD had equivalent sU decreases across the 100 mg and 300 mg allopurinol groups. However, the 100 mg group started at a higher pre-treatment sU and ended at a higher final sU than the 300 mg group.The strategy of titrating allopurinol to sU in patients with kidney impairment may result in greater sU lowering at lower doses than in patients without CKD but may also pose a treatment challenge from a possible drug ceiling effect.
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