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肾功能亢进患者万古霉素血药浓度监测与临床疗效分析
引用本文:唐莲,严晓薇,彭秋菊,薛盛敏,赵富丽,庄智伟,尚尔宁.肾功能亢进患者万古霉素血药浓度监测与临床疗效分析[J].中国医院药学杂志,2018,38(15):1629-1632.
作者姓名:唐莲  严晓薇  彭秋菊  薛盛敏  赵富丽  庄智伟  尚尔宁
作者单位:1. 南京医科大学附属苏州医院药学部, 江苏 苏州 215002; 2. 南京医科大学药学院, 江苏 南京 211166; 3. 广东药科大学药学院, 广东 广州 510006; 4. 南京医科大学附属苏州医院重症监护室, 江苏 苏州 215002
基金项目:苏州市科技计划项目(编号:SYSD2016152);江苏省药学会奥赛康基金项目(编号:A201613)
摘    要:目的:调查分析肾功能亢进(augmented renal clearance, ARC)患者使用万古霉素的用药剂量、谷浓度及临床疗效。方法:回顾性研究2013年7月-2017年3月在某院住院期间使用过万古霉素并进行了血药浓度监测的67例ARC患者和142例肾功能正常患者病历资料,比较2组万古霉素给药方案、谷浓度及临床疗效。结果:ARC组与肾功能正常组初始给药的日剂量分别为(2.0±0.3) g和(1.8±0.4) g,具有显著性差异(P=0.041)。ARC组初始给药方案下谷浓度均值(8.3±5.2) mg·L-1明显低于肾功能正常组的谷浓度均值(14.3±8.4) mg·L-1,有显著性差异(P=0.000)。ARC患者的初始给药方案谷浓度达标率为20.6%,肾功能正常组为40.1%,具有显著性差异(P=0.007)。ARC组万古霉素的临床总有效率和革兰阳性菌清除率分别为69.1%和67.6%,肾功能正常组为76.7%和81.6%,均无显著性差异(P=0.286;P=0.143)。结论:多数ARC患者初始方案万古霉素用药剂量不足,谷浓度达标率较肾功能正常患者更低。

关 键 词:肾功能亢进  肾功能正常  万古霉素  血药浓度监测  
收稿时间:2017-08-02

Analysis of therapeutic drug monitoring and clinical efficacy of vancomycin in patients with augmented renal clearance
TANG Lian,YAN Xiao-wei,PENG Qiu-ju,XUE Sheng-min,ZHAO Fu-li,ZHUANG Zhi-wei,SHANG Er-ning.Analysis of therapeutic drug monitoring and clinical efficacy of vancomycin in patients with augmented renal clearance[J].Chinese Journal of Hospital Pharmacy,2018,38(15):1629-1632.
Authors:TANG Lian  YAN Xiao-wei  PENG Qiu-ju  XUE Sheng-min  ZHAO Fu-li  ZHUANG Zhi-wei  SHANG Er-ning
Institution:1. Department of Pharmacy, The Affiliated Suzhou Hospital of Nanjing Medical University, Jiangsu Suzhou 215002, China; 2. College of Pharmacy, Nanjing Medical University, Jiangsu Nanjing 211166, China; 3. College of Pharmacy, Guangdong Pharmaceutical University, Guangdong Guangzhou 510006, China; 4. Intensive Care Unit, The Affiliated Suzhou Hospital of Nanjing Medical University, Jiangsu Suzhou 215002, China
Abstract:OBJECTIVE To analyze the dosage regimen, trough concentration and clinical effect of vancomycin treatment in patients with augmented renal clearance (ARC).METHODS This retrospective study recorded the clinical data of adult inpatients treated with vancomycin and had therapeutic drug monitored from July 2013 to March 2017 in a Hospital, involving 67 cases of ARC and 142 cases of normal renal function. The dosage regimen, trough concentration and clinical effect were compared between ARC and normal renal function groups.RESULTS The daily doses of vancomycin in initial dosage regimen were (2.0±0.3) g and (1.8±0.4) g in ARC and normal renal function groups (P=0.041). Trough concentration of initial dosage regimen in ARC group was much lower than that of normal renal function group(8.3±5.2) mg·L-1 vs. (14.3±8.4) mg·L-1, P=0.000)]. The rate of the high trough concentration standards was only 20.6%, with statistical difference when compared to normal renal function group (20.6% vs. 40.1%, P=0.007). The clinical total effective rate and bacterial clearance rate had no statistical difference between ARC and normal renal function groups (69.1% vs. 76.7%, P=0.286; 67.6% vs. 81.6%, P=0.143).CONCLUSION The daily doses of initial and adjusted dosage regimens of most ARC patients in a hospital were inadequate, and most trough concentrations were below 10-20 mg·L-1.
Keywords:augmented renal clearance  normal renal function  vancomycin  therapeutic drug monitoring  
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