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万古霉素治疗药物监测对患者护理的影响。

Impact of vancomycin therapeutic drug monitoring on patient care.

作者信息

Welty T E, Copa A K

机构信息

Department of Pharmaceutical Support Services, Methodist Hospital of Indiana, Indianapolis.

出版信息

Ann Pharmacother. 1994 Dec;28(12):1335-9. doi: 10.1177/106002809402801201.

Abstract

OBJECTIVE

To document differences in the outcome of vancomycin therapy in patients managed through a therapeutic drug monitoring (TDM) service and patients managed empirically, without the participation of a TDM service.

DESIGN

Prospective, cohort study.

SETTING

An 1100-bed, tertiary-care, teaching hospital.

PATIENTS

Those who received vancomycin for more than four days, were at least 18 years old, had an estimated creatinine clearance of more than 0.33 mL/s (20 mL/min), were not neutropenic at the start of vancomycin therapy, and were not treated in a critical care unit were enrolled in the study. A total of 116 patients (61 TDM; 55 non-TDM) were monitored prospectively from June 1990 through March 1991.

INTERVENTIONS

Patients in the TDM group had vancomycin drug therapy monitored daily by a pharmacist and vancomycin dosages adjusted following a pharmacokinetic analysis of vancomycin serum concentrations. For patients in the non-TDM group, the pharmacist only completed a data collection form. The patients and physicians were unaware of the monitoring.

MAIN OUTCOME MEASURES

Duration of therapy, total vancomycin dosage, infection site, concomitant antibiotics, body temperature, and white blood cell counts were compared between the two groups. Length of stay data were also compared. Nephrotoxicity was evaluated by comparing serum creatinine concentration and estimated creatinine clearance.

RESULTS

TDM of vancomycin appeared to reduce the incidence of vancomycin-related renal insufficiency (TDM 7 percent; non-TDM 24 percent). Patients managed through the TDM service received an average of 5 g less of vancomycin than did the patients in the non-TDM group. The duration of vancomycin therapy was an average of 2 days less for patients in the TDM group. Mean length of stay was 38.0 days for the TDM group and 44.5 days for the non-TDM group. Other measures of efficacy, infection site, and concomitant antibiotics were the same for both groups.

CONCLUSIONS

TDM of vancomycin was associated with fewer cases of vancomycin-related renal insufficiency. Vancomycin efficacy was not compromised by TDM. Provision of TDM for vancomycin therapy aided in patient management.

摘要

目的

记录通过治疗药物监测(TDM)服务管理的患者与未经TDM服务参与而凭经验管理的患者在万古霉素治疗结果上的差异。

设计

前瞻性队列研究。

地点

一家拥有1100张床位的三级护理教学医院。

患者

纳入那些接受万古霉素治疗超过四天、年龄至少18岁、估计肌酐清除率超过0.33 mL/s(20 mL/min)、在万古霉素治疗开始时非中性粒细胞减少且未在重症监护病房接受治疗的患者。从1990年6月至1991年3月,共前瞻性监测了116例患者(61例TDM组;55例非TDM组)。

干预措施

TDM组患者的万古霉素药物治疗由药剂师每日监测,并根据万古霉素血清浓度的药代动力学分析调整万古霉素剂量。对于非TDM组患者,药剂师仅填写一份数据收集表。患者和医生并不知晓监测情况。

主要观察指标

比较两组患者的治疗持续时间、万古霉素总剂量、感染部位、联用抗生素、体温及白细胞计数。还比较了住院时间数据。通过比较血清肌酐浓度和估计肌酐清除率评估肾毒性。

结果

万古霉素的TDM似乎降低了万古霉素相关肾功能不全的发生率(TDM组7%;非TDM组24%)。通过TDM服务管理的患者比非TDM组患者平均少接受5 g万古霉素。TDM组患者的万古霉素治疗持续时间平均少2天。TDM组的平均住院时间为38.0天,非TDM组为44.5天。两组的其他疗效指标、感染部位及联用抗生素情况相同。

结论

万古霉素的TDM与较少的万古霉素相关肾功能不全病例相关。TDM未损害万古霉素疗效。为万古霉素治疗提供TDM有助于患者管理。

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