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甲硝唑在感染性休克患者肌肉组织中的分布及其体外抗脆弱拟杆菌的效果。

Distribution of metronidazole in muscle tissue of patients with septic shock and its efficacy against Bacteroides fragilis in vitro.

作者信息

Karjagin Juri, Pähkla Rein, Karki Tõnis, Starkopf Joel

机构信息

Anaesthesiology and Intensive Care Clinic, University of Tartu, 8 L. Puusepa Street, Tartu, Estonia.

出版信息

J Antimicrob Chemother. 2005 Mar;55(3):341-6. doi: 10.1093/jac/dkh544. Epub 2005 Feb 22.

Abstract

OBJECTIVES

Studies investigating the target site concentration of antibiotics, such as beta-lactams and fluoroquinolones, have demonstrated differences between the drug concentrations in healthy volunteers and septic patients. The aims of this study were (i) to evaluate the muscle tissue concentration of metronidazole in patients with septic shock and (ii) to test the efficacy of metronidazole in an in vitro pharmacodynamic model at different single doses.

MATERIALS AND METHODS

Six patients admitted to the ICU of Tartu University Clinics with a diagnosis of septic shock were studied. Patients receiving metronidazole treatment within 48 h before the study or with a BMI > 35 were excluded. Metronidazole muscle tissue concentration was assessed by a microdialysis technique. Based on the microdialysis data, similar kinetics were simulated in in vitro experiments using Bacillus fragilis strains with MIC(90)s of 0.125 mg/L (BF125) and 1.0 mg/L (BF1).

RESULTS

Metronidazole concentrations in plasma achieved a mean (s.d.) value of 11.4+/-2.0 mg/L at 30 min after administration of a single 500 mg intravenous dose, while in the muscle tissue, maximum concentrations of 8.2+/-4.5 mg/L were achieved at 140+/-92.3 min after the dose. When this metronidazole time course was simulated in vitro, the time to 99.9% kill ranged from 1.0 to 1.4 h for BF125 and from 1.8 to 3.5 h for BF1, while the eradication time ranged from 1.7 to 2.5 h and from 3.4 to 6.5 h, respectively. No regrowth was detected.

CONCLUSION

Pharmacokinetic-pharmacodynamic simulation of metronidazole interstitial concentrations shows a high efficacy of the drug in septic patients.

摘要

目的

研究β-内酰胺类和氟喹诺酮类等抗生素的靶位浓度,已证明健康志愿者和脓毒症患者的药物浓度存在差异。本研究的目的是:(i)评估脓毒症休克患者肌肉组织中甲硝唑的浓度;(ii)在体外药效学模型中测试不同单剂量甲硝唑的疗效。

材料与方法

对塔尔图大学临床医院重症监护病房收治的6例诊断为脓毒症休克的患者进行研究。排除在研究前48小时内接受甲硝唑治疗或BMI>35的患者。采用微透析技术评估甲硝唑肌肉组织浓度。基于微透析数据,在体外实验中使用脆弱拟杆菌菌株进行类似动力学模拟,其MIC(90)分别为0.125mg/L(BF125)和1.0mg/L(BF1)。

结果

单次静脉注射500mg后30分钟,血浆中甲硝唑浓度平均(标准差)达到11.4±2.0mg/L,而在肌肉组织中,给药后140±92.3分钟达到最大浓度8.2±4.5mg/L。在体外模拟该甲硝唑时间过程时,BF125达到99.9%杀灭的时间为1.0至1.4小时,BF1为1.8至3.5小时,而根除时间分别为1.7至2.5小时和3.4至6.5小时。未检测到再生长。

结论

甲硝唑组织间液浓度的药代动力学-药效学模拟显示该药物在脓毒症患者中具有高效性。

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