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治疗多重耐药革兰阳性感染患者时,达到泰利霉素治疗谷血浆浓度所需的负荷剂量。

Loading dose required to achieve rapid therapeutic teicoplanin trough plasma concentration in patients with multidrug-resistant gram-positive infections.

机构信息

Division of Infectious Diseases, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

Basic Clin Pharmacol Toxicol. 2012 May;110(5):416-20. doi: 10.1111/j.1742-7843.2012.00862.x. Epub 2012 Feb 28.

DOI:10.1111/j.1742-7843.2012.00862.x
PMID:22309355
Abstract

Teicoplanin is an antibiotic drug prescribed for the treatment of multidrug-resistant Gram-positive infections. However, there is currently no consensus as to the optimal teicoplanin loading dose. The objective of this study was to compare plasma concentrations of teicoplanin in patients with multidrug-resistant Gram-positive infections after the administration of two different loading doses. Two groups of patients were infused intravenously with four loading doses of 6 mg/kg body-weight (group A, n = 12) or 12 mg/kg body-weight (group B, n = 11). The first three loading doses were administered at 12-hr intervals, and the fourth was given 24 hr after the third dose. Maintenance doses of 6 mg/kg were administered every day, every other day or every third day depending on the individual's creatinine clearance, and teicoplanin trough plasma concentrations were monitored. Only samples obtained on the same day for both groups were compared statistically. A higher percentage of group B patients achieved the desired therapeutic concentration of teicoplanin (C(min.)  ≥ 10 mg/L) on days 2 and 3 (90.0% and 100%, respectively) compared with patients in group A (18.2% and 16.7%, respectively) (p < 0.001). In addition, more patients in group B achieved therapeutic concentrations from days 2 through 12. In conclusion, despite limitations in drawing definitive conclusions because of a relatively small sample size and variability in renal impairment among patients, our findings suggest that a teicoplanin loading dose of 12 mg/kg body-weight results in a safe and rapid attainment of therapeutic trough plasma concentrations. This regimen may enhance treatment efficacy.

摘要

替考拉宁是一种抗生素药物,用于治疗多种耐药革兰阳性感染。然而,目前对于替考拉宁的最佳负荷剂量尚未达成共识。本研究的目的是比较两种不同负荷剂量给药后多重耐药革兰阳性感染患者的替考拉宁血药浓度。两组患者分别静脉输注 4 个负荷剂量的 6mg/kg 体重(A 组,n=12)或 12mg/kg 体重(B 组,n=11)。前三个负荷剂量每 12 小时给药一次,第四个负荷剂量在第三个剂量后 24 小时给予。维持剂量为 6mg/kg,根据个体的肌酐清除率,每天、每隔一天或每三天给药一次,并监测替考拉宁谷浓度。仅对两组在相同日期获得的样本进行统计学比较。与 A 组患者(分别为 18.2%和 16.7%)相比,B 组患者在第 2 天和第 3 天达到替考拉宁所需治疗浓度(C(min.)≥10mg/L)的比例更高(分别为 90.0%和 100%)(p<0.001)。此外,B 组患者在第 2 天至第 12 天有更多患者达到治疗浓度。总之,尽管由于患者肾功能损害的个体差异和样本量相对较小,限制了得出明确结论,但我们的研究结果表明,替考拉宁负荷剂量为 12mg/kg 体重可安全、快速地达到治疗谷浓度。这种方案可能会提高治疗效果。

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