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呋塞米在肾病综合征患儿中的临床药代动力学

Clinical pharmacokinetics of furosemide in children with nephrotic syndrome.

作者信息

González-Martín G, Bravo I, Ibarra N, Arancibia A

出版信息

Int J Clin Pharmacol Ther Toxicol. 1983 Dec;21(12):598-601.

PMID:6668097
Abstract

The pharmacokinetic disposition of furosemide has been investigated in seven children with nephrotic syndrome and in eight control children. Furosemide in plasma was analyzed by spectrofluorometry. After a single intravenous dose of furosemide (1 mg/kg body wt.) the nephrotic children showed lower initial plasma concentrations because of the larger volume of distribution. The mean half-life of furosemide in nephrotic children (38.5 +/- 7.8 min) was significantly longer than in the control group (28.0 +/- 7.7 min). The two groups did not differ in the body clearance of total furosemide. The average serum clearance was 4.95 +/- 1.7 ml/min/kg body wt. in the control group and 5.10 +/- 1.4 ml/min/kg body wt. in the nephrotic children. There was a significant reduction in urine sodium and distribution volume, whereas potassium excretion remained unchanged.

摘要

已经在7名肾病综合征患儿和8名对照儿童中研究了呋塞米的药代动力学特征。采用荧光分光光度法分析血浆中的呋塞米。单次静脉注射呋塞米(1mg/kg体重)后,由于分布容积较大,肾病患儿的初始血浆浓度较低。呋塞米在肾病患儿中的平均半衰期(38.5±7.8分钟)明显长于对照组(28.0±7.7分钟)。两组在总呋塞米的体内清除率方面没有差异。对照组的平均血清清除率为4.95±1.7ml/分钟/千克体重,肾病患儿为5.10±1.4ml/分钟/千克体重。尿钠和分布容积显著降低,而钾排泄保持不变。

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