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庆大霉素在人体中的腹膜药代动力学。

Peritoneal pharmacokinetics of gentamicin in man.

作者信息

de Paepe M, Lameire N, Belpaire F, Bogaert M

出版信息

Clin Nephrol. 1983 Mar;19(3):107-9.

PMID:6839558
Abstract

The peritoneal pharmacokinetics of gentamicin were investigated in patients on continuous ambulatory peritoneal dialysis. Gentamicin was added to the dialyzate, and gentamicin concentrations were measured repeatedly in serum and dialyzate. After administration of a single dose of gentamicin, equilibrium between serum and dialyzate levels is achieved within 24 hours; dialyzate levels of gentamicin are lower and mass transfer coefficients higher in patients with peritonitis. With chronic intraperitoneal gentamicin treatment for peritonitis, steady state serum levels around 4 to 5 mg/l are achieved and otovestibular toxicity should be feared.

摘要

在持续非卧床腹膜透析患者中研究了庆大霉素的腹膜药代动力学。将庆大霉素加入透析液中,并反复测定血清和透析液中的庆大霉素浓度。单次给予庆大霉素后,血清和透析液水平在24小时内达到平衡;腹膜炎患者的透析液中庆大霉素水平较低,而传质系数较高。对于腹膜炎采用慢性腹腔内庆大霉素治疗时,血清稳态水平可达4至5mg/l左右,应警惕耳前庭毒性。

相似文献

1
Peritoneal pharmacokinetics of gentamicin in man.庆大霉素在人体中的腹膜药代动力学。
Clin Nephrol. 1983 Mar;19(3):107-9.
2
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引用本文的文献

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2
ISPD Peritonitis Recommendations: 2016 Update on Prevention and Treatment.国际腹膜透析学会腹膜炎推荐意见:2016年预防与治疗更新版
Perit Dial Int. 2016 Sep 10;36(5):481-508. doi: 10.3747/pdi.2016.00078. Epub 2016 Jun 9.
3
Pharmacokinetics of intraperitoneal gentamicin in peritoneal dialysis patients with peritonitis (GIPD study).
腹腔内注射庆大霉素在腹膜炎患者腹膜透析中的药代动力学(GIPD 研究)。
Clin J Am Soc Nephrol. 2012 Aug;7(8):1249-56. doi: 10.2215/CJN.12211211. Epub 2012 Jun 14.
4
Optimising intraperitoneal gentamicin dosing in peritoneal dialysis patients with peritonitis (GIPD) study.优化腹膜炎患者腹腔内庆大霉素剂量(GIPD)研究。
BMC Nephrol. 2009 Dec 16;10:42. doi: 10.1186/1471-2369-10-42.
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Pharmacokinetic aspects during continuous ambulatory peritoneal dialysis: a literature review.持续非卧床腹膜透析的药代动力学研究进展:文献综述
Pharm Weekbl Sci. 1984 Dec 14;6(6):229-36. doi: 10.1007/BF01954550.
6
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Eur J Clin Pharmacol. 1985;28(2):187-91. doi: 10.1007/BF00609690.
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Clin Pharmacokinet. 1985 Sep-Oct;10(5):404-25. doi: 10.2165/00003088-198510050-00003.
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