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儿童初始血清万古霉素谷浓度评估及其与基于体重的初始经验性万古霉素给药和肾毒性发生的关联:一项多中心回顾性研究。

Assessment of initial serum vancomycin trough concentrations and their association with initial empirical weight-based vancomycin dosing and development of nephrotoxicity in children: a multicenter retrospective study.

作者信息

Matson Kelly L, Shaffer Christopher L, Beck Gary L, Simonsen Kari A

机构信息

Department of Pharmacy Practice, University of Rhode Island, Kingston, Rhode Island.

出版信息

Pharmacotherapy. 2015 Mar;35(3):337-43. doi: 10.1002/phar.1552. Epub 2015 Mar 10.

Abstract

STUDY OBJECTIVES

To determine whether a relationship exists between initial serum vancomycin trough concentrations and initial empirical vancomycin dose, patient weight, and patient age, and to determine the risks for vancomycin-associated nephrotoxicity in pediatric patients stratified by hospital setting.

DESIGN

Stepwise linear and multinomial logistic regression analysis of retrospectively collected data.

SETTING

Two geographically distinct children's tertiary care medical centers.

PATIENTS

A total of 316 pediatric patients without preexisting renal dysfunction who were managed outside of the neonatal intensive care unit and were treated with at least 3 doses of vancomycin for gram-positive bacterial infections and had at least one serum vancomycin trough concentration between January 1, 2008, and July 31, 2010.

MEASUREMENTS AND MAIN RESULTS

Elevated vancomycin trough concentrations had no statistically significant relationship with initial empirical vancomycin dosing across all hospital settings. Serum vancomycin trough concentrations (lower than 15 mg/L or 15-20 mg/L) were not associated with increased risk of nephrotoxicity. Concomitant nephrotoxic agents, however, including loop diuretics, vasopressors, angiotensin-converting enzyme (ACE) inhibitors, and nonsteroidal antiinflammatory drugs (NSAIDs) were significantly associated with the development of nephrotoxicity in medical-surgical and intensive care patients. Based on this analysis, use of loop diuretics and vasopressors increased the odds of developing nephrotoxicity (odds ratio [OR] 42.8 [p=0.001] and 18.4 [p=0.02], respectively). Use of NSAIDS and ACE inhibitors also increased the odds of developing nephrotoxicity (OR 18.6 [p=0.02] and 4.7 [p=0.03], respectively).

CONCLUSION

No significant associations were found between initial empirical weight-based vancomycin dosing or elevated serum trough concentrations and development of nephrotoxicity in children; rather, nephrotoxicity was associated with combination therapy with vancomycin and other potentially nephrotoxic agents.

摘要

研究目的

确定初始血清万古霉素谷浓度与初始经验性万古霉素剂量、患者体重和患者年龄之间是否存在关联,并确定按医院环境分层的儿科患者发生万古霉素相关肾毒性的风险。

设计

对回顾性收集的数据进行逐步线性和多项逻辑回归分析。

地点

两个地理位置不同的儿童三级医疗中心。

患者

共有316例无既往肾功能不全的儿科患者,这些患者在新生儿重症监护病房以外接受治疗,因革兰氏阳性细菌感染接受至少3剂万古霉素治疗,且在2008年1月1日至2010年7月31日期间至少有一次血清万古霉素谷浓度。

测量和主要结果

在所有医院环境中,升高的万古霉素谷浓度与初始经验性万古霉素给药无统计学显著关联。血清万古霉素谷浓度(低于15mg/L或15 - 20mg/L)与肾毒性风险增加无关。然而,包括袢利尿剂、血管加压药、血管紧张素转换酶(ACE)抑制剂和非甾体抗炎药(NSAIDs)在内的伴随肾毒性药物与内科 - 外科和重症监护患者的肾毒性发生显著相关。基于此分析,使用袢利尿剂和血管加压药增加了发生肾毒性的几率(优势比[OR]分别为42.8[p = 0.001]和18.4[p = 0.02])。使用NSAIDs和ACE抑制剂也增加了发生肾毒性的几率(OR分别为18.6[p = 0.02]和4.7[p = 0.03])。

结论

在儿童中,初始经验性基于体重的万古霉素给药或升高的血清谷浓度与肾毒性发生之间未发现显著关联;相反,肾毒性与万古霉素和其他潜在肾毒性药物的联合治疗有关。

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