首页> 美国卫生研究院文献>British Journal of Clinical Pharmacology >Pharmacokinetics of ornidazole in patients with renal insufficiency; influence of haemodialysis and peritoneal dialysis.
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Pharmacokinetics of ornidazole in patients with renal insufficiency; influence of haemodialysis and peritoneal dialysis.

机译:奥硝唑在肾功能不全患者中的药代动力学;血液透析和腹膜透析的影响。

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摘要

The pharmacokinetics of ornidazole (Tiberal) was studied after intravenous administration of a single 500 mg dose in eight patients with advanced chronic renal failure (ACRF) (creatinine clearance 2-16 ml/min), in seven patients treated by haemodialysis (residual renal creatinine clearance 0-5 ml/min) and in five patients treated by continuous ambulatory peritoneal dialysis (CAPD) (residual renal creatinine clearance 0-6 ml/min). In ACRF patients, the half-life of ornidazole was 10.8 +/- 1.4 h, the total plasma clearance 46.3 +/- 2.3 ml/min and the volume of distribution 0.73 +/- 0.06 l/kg. During haemodialysis, ornidazole was partly removed: the dialyser extraction ratio was 42 +/- 5% and the dialysis clearance 64 +/- 7 ml/min. During CAPD, peritoneal excretion was low: the dialysis clearance was 3.0 +/- 0.4 ml/min and in 48 h 6.0 +/- 1.1% of the administered dose was found in the peritoneal fluids. In these patients, the half-life of ornidazole was 11.8 +/- 0.8 h and total plasma clearance was 48.3 +/- 5.5 ml/min, values which were close to those determined in non dialysed patients. In patients with end-stage renal disease, the half-life of ornidazole is comparable to that of subjects with normal renal function. This is due to the predominantly extra-renal elimination of the drug. Therefore, there is no need to modify the usual dosage of ornidazole for these patients. Because of the large elimination of the drug during haemodialysis it is necessary to administer the drug after the dialysis session.
机译:在八名患有晚期慢性肾衰竭(ACRF)(肌酐清除率2-16 ml / min)的患者中,静脉注射奥硝唑(Tiberal)的药代动力学后,对七名接受血液透析治疗的患者(残余肾肌酐)进行静脉内研究清除0-5毫升/分钟)和5例接受连续门诊腹膜透析(CAPD)治疗的患者(残余肾肌酐清除率0-6毫升/分钟)。在ACRF患者中,奥硝唑的半衰期为10.8 +/- 1.4 h,总血浆清除率为46.3 +/- 2.3 ml / min,分布体积为0.73 +/- 0.06 l / kg。在血液透析过程中,奥硝唑被部分除去:透析液提取率为42 +/- 5%,透析清除率为64 +/- 7 ml / min。在CAPD期间,腹膜排泄很低:透析清除率是3.0 +/- 0.4 ml / min,并且在48小时内腹膜液中发现了6.0 +/- 1.1%的给药剂量。在这些患者中,奥硝唑的半衰期为11.8 +/- 0.8 h,总血浆清除率为48.3 +/- 5.5 ml / min,接近于非透析患者的测定值。在患有晚期肾脏疾病的患者中,奥硝唑的半衰期与肾功能正常的受试者相当。这是由于主要在肾脏外清除了药物。因此,对于这些患者,无需修改奥硝唑的常规剂量。由于在血液透析期间大量清除了药物,因此有必要在透析后再使用药物。

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