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头孢克洛在正常志愿者和肾衰竭患者中的药理学。

Pharmacology of cefaclor in normal volunteers and patients with renal failure.

作者信息

Santoro J, Agarwal B N, Martinelli R, Wenger N, Levison M E

出版信息

Antimicrob Agents Chemother. 1978 Jun;13(6):951-4. doi: 10.1128/AAC.13.6.951.

Abstract

After a 500-mg dose of cefaclor, the mean peak plasma level was 12.4 mug/ml and after a 250-mg dose it was 5 mug/ml in normal volunteers. Food intake significantly reduced absorption. Probenecid prolonged plasma levels. Mean plasma half-life in normal volunteers was 0.8 h. Only about 50% of the dose was excreted in the urine within 4 h in normal volunteers. Plasma half-life in patients with renal insufficiency was only about 3 h, which suggests that cefaclor may be eliminated by nonrenal mechanisms in humans. Urinary levels of cefaclor were adequate to inhibit susceptible pathogens even in patients with moderately severe renal failure. Plasma half-life during hemodialysis was 2.1 h and rose to 2.8 h after dialysis.

摘要

在正常志愿者中,服用500毫克头孢克洛剂量后,平均血浆峰值水平为12.4微克/毫升,服用250毫克剂量后为5微克/毫升。食物摄入显著降低吸收。丙磺舒延长血浆水平。正常志愿者的平均血浆半衰期为0.8小时。在正常志愿者中,仅约50%的剂量在4小时内随尿液排出。肾功能不全患者的血浆半衰期仅约为3小时,这表明头孢克洛在人体内可能通过非肾脏机制消除。即使在中度严重肾衰竭患者中,头孢克洛的尿液水平也足以抑制易感病原体。血液透析期间的血浆半衰期为2.1小时,透析后升至2.8小时。

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