Braun J, Sörgel F, Engelmaier F, Gluth W P, Gessler U
Eur J Clin Pharmacol. 1985;28(6):665-70. doi: 10.1007/BF00607912.
The plasma levels of tocainide have been followed after oral administration of 600 mg p.o. to 20 patients with renal failure due to various causes, and to 8 healthy controls. The peak plasma concentrations in the patients with pyelonephritis (3.80 micrograms/ml) and interstitial nephritis (3.74 micrograms/ml) but not in those with glomerulonephritis (3.17 micrograms/ml) differed from that in healthy volunteers (3.24 micrograms/ml). The renal clearance of tocainide was well correlated with the endogenous creatinine clearance and was dependent on urine pH. No difference in renal clearance was observed between the patients groups. It is suggested that the changes in plasma levels are a consequence of decreased renal clearance. Creatinine clearance was shown to be a poor estimator of tocainide clearance, which suggests that extrarenal clearance plays an important role in the handling of the drug in the body. The findings are used to suggest a safe dosage regimen.
对20例因各种原因导致肾衰竭的患者及8名健康对照者口服600毫克托卡胺后,跟踪观察了其血浆水平。肾盂肾炎患者(3.80微克/毫升)和间质性肾炎患者(3.74微克/毫升)的血浆峰值浓度与健康志愿者(3.24微克/毫升)不同,但肾小球肾炎患者(3.17微克/毫升)的血浆峰值浓度与健康志愿者无差异。托卡胺的肾清除率与内生肌酐清除率密切相关,并取决于尿液pH值。各患者组之间未观察到肾清除率有差异。提示血浆水平的变化是肾清除率降低的结果。肌酐清除率被证明是托卡胺清除率的一个较差的估计指标,这表明肾外清除在药物在体内的处置中起重要作用。这些研究结果用于提出一个安全的给药方案。