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[去纤苷在接受血液透析的尿毒症患者中的药代动力学]

[Pharmacokinetics of defibrotide in uremic patients undergoing hemodialysis].

作者信息

Rossi R, Farma A, Maggi G C, Marelli A

机构信息

Divisione di Nefrologia e Dialisi, Ospedale S. Anna, Como.

出版信息

Minerva Med. 1991 Dec;82(12):853-7.

PMID:1780093
Abstract

Defibrotide pharmacokinetics were studied in 6 voluntary healthy subjects and in 10 uremic patients undergoing dialysis during which (instead of heparin) defibrotide was administered to prevent fibrino-formation in the circuit. Blood concentrations of the drug were assessed (expressed with reference to the residual glycidic deoxyribose) during a standard dialysis using defibrotide, 3.5, 15, 30, 45, 60 and 90 minutes after the defibrotide bolus (200 mg) had been injected into the arterial channel. The half-lives of the alpha and beta plasmatic phases were found to be equal at 3.79 and 41.4 min in dialysed subjects and at 1.13 and 16.54 in healthy volunteers. These results indicate that in uremic patients undergoing dialysis at intervals using defibrotide, a longer time is required to eliminate the drug from the circulation. This variation does not however appear to be significant in terms of the therapeutic use of the drug during dialysis.

摘要

在6名健康志愿者和10名接受透析的尿毒症患者中研究了去纤苷的药代动力学,在透析过程中(而非肝素)给予去纤苷以防止回路中形成纤维蛋白。在使用去纤苷进行标准透析期间,在将去纤苷推注(200mg)注入动脉通道后3.5、15、30、45、60和90分钟评估药物的血药浓度(以残留的糖基化脱氧核糖为参照表示)。在接受透析的受试者中,α和β血浆相的半衰期分别为3.79分钟和41.4分钟,在健康志愿者中分别为1.13分钟和16.54分钟。这些结果表明,在间歇性使用去纤苷进行透析的尿毒症患者中,药物从循环中消除需要更长时间。然而,就透析期间药物的治疗用途而言,这种差异似乎并不显著。

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