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[接受别嘌醇治疗患者的血清氧嘌呤醇浓度和肾功能研究]

[A study of serum oxipurinol concentration and renal function in patients administered allopurinol].

作者信息

Saji M

机构信息

Department of Internal Medicine (II), Jikei University School of Medicine, Tokyo, Japan.

出版信息

Nihon Jinzo Gakkai Shi. 1996 Dec;38(12):640-50.

PMID:9014485
Abstract

Allopurinol is used frequently to treat patients with gout and hyperuricemia. However, adverse effects associated with this agent have been reported occasionally, especially among patients with hyperuricemia complicated with renal diseases. A rise in the blood concentration of oxipurinol, the chief active metabolite of allopurinol, has been noted in patients with renal dysfunctions, pointing to an implication of oxipurinol toxicity. It has been reported that monitoring the serum oxipurinol concentration to maintain in level below 15.2 micrograms/ml (= 100 mumol/l: recommended level) is helpful in avoiding toxicity. At Jikei University Hospital, a survey was conducted on 148 hyperuricemic patients who had been treated with allopurinol at the dosages of 50, 100, 200 and 300 mg daily or 100 mg on alternate days for more than one month. Because oxipurinol is an uricosuric substance, the steady-state serum oxipurinol concentration was determined by HPLC; and creatinine clearance (CCr) was calculated for each patient. 1. In the group composed of patients with normal kidney function (CCr > or = 80 ml/min), increase in the dosage of allopurinol was associated with a linear increase in the serum concentration of oxipurinol. 2. Among the patients with varying renal function who were receiving 100 mg of allopurinol daily, the oxipurinol level increased logarithmically as the creatinine clearance decreased. In some of the patients with renal insufficiency (CCr < 30 ml/min), daily administration of 100 mg of allopurinol resulted in a serum concentration of oxipurinol over 15.2 micrograms/ml. 3. For patients with renal insufficiency (CCr < 30 ml/min), administration of allopurinol at the dosage of 50 mg/day is considered adequate to avoid the accumulation of serum oxipurinol.

摘要

别嘌醇常用于治疗痛风和高尿酸血症患者。然而,该药物相关的不良反应偶有报道,尤其是在合并肾脏疾病的高尿酸血症患者中。肾功能不全患者体内已观察到别嘌醇的主要活性代谢产物氧嘌呤醇血药浓度升高,提示存在氧嘌呤醇毒性。据报道,监测血清氧嘌呤醇浓度并维持在15.2微克/毫升以下(=100微摩尔/升:推荐水平)有助于避免毒性。在东京慈惠会医科大学医院,对148例高尿酸血症患者进行了调查,这些患者接受了每日50、100、200和300毫克或隔日100毫克的别嘌醇治疗,疗程超过一个月。由于氧嘌呤醇是一种促尿酸排泄物质,采用高效液相色谱法测定稳态血清氧嘌呤醇浓度;并计算每位患者的肌酐清除率(CCr)。1. 在肾功能正常(CCr≥80毫升/分钟)的患者组中,别嘌醇剂量增加与氧嘌呤醇血清浓度呈线性增加相关。2. 在每日接受100毫克别嘌醇治疗的肾功能不同的患者中,随着肌酐清除率降低,氧嘌呤醇水平呈对数增加。在一些肾功能不全(CCr<30毫升/分钟)的患者中,每日服用100毫克别嘌醇导致血清氧嘌呤醇浓度超过15.2微克/毫升。3. 对于肾功能不全(CCr<30毫升/分钟)的患者,认为每日50毫克的别嘌醇剂量足以避免血清氧嘌呤醇蓄积。

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