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药剂师与医生协作实践模式改善重症监护病房万古霉素给药剂量

Pharmacist and Physician Collaborative Practice Model Improves Vancomycin Dosing in an Intensive Care Unit.

作者信息

Levin Dimitriy, Glasheen Jeffrey J, Kiser Tyree H

机构信息

Department of Medicine, University of Colorado, Aurora, Colorado, USA.

University of Colorado Hospital Medicine Group, Aurora, Colorado, USA.

出版信息

Int J Clin Med. 2016 Oct;7(10):675-684. doi: 10.4236/ijcm.2016.710073. Epub 2016 Oct 25.

DOI:10.4236/ijcm.2016.710073
PMID:32211212
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7093063/
Abstract

OBJECTIVE

A pharmacist and physician collaborative practice intervention to improve the initial dosing of vancomycin was implemented with the goal of decreasing the number of subtherapeutic first troughs and increasing the number of therapeutic troughs.

METHODS

Using the best available evidence, a nomogram was created to determine the initial vancomycin dose. The nomogram utilized actual bodyweight and glomerular filtration rate (eGFR) estimated with the MDRD4 equation. The dose was based on the 2009 ASHP/IDSA/SIDP guidelines, which recommended 15-20 mg/kg every 8-12 hours. Providers ordered "vancomycin IV dosed per pharmacy".

RESULTS

The pre- (n = 75) and post-intervention (n = 108) cohorts had similar age, gender distribution, weight, and eGFR. The median total daily vancomycin dose was similar in pre- and post-intervention groups (2000 mg), although the median first trough was higher following the intervention (13.0 vs. 14.8 mcg/ml, p = 0.03). Following the intervention, the proportion of first troughs under 10 mcg/ml decreased (32% to 13%, = 0.003), while the proportion of troughs in the 10 - 20 mcg/ml therapeutic range increased (50.7% vs. 69.4%, = 0.01). There was no difference in the proportion of troughs over 20 mcg/ml (17.3% vs. 17.6%, = 0.96).

CONCLUSIONS

A multi-disciplinary intervention utilizing a nomogram-based pharmacy collaborative practice model significantly improves the proportion of therapeutic initial vancomycin troughs and decreases the number of subtherapeutic troughs by half.

摘要

目的

实施一项药剂师与医生的协作实践干预措施,以改善万古霉素的初始给药剂量,目标是减少次治疗性首次谷浓度的数量并增加治疗性谷浓度的数量。

方法

利用现有最佳证据创建了一个列线图,以确定万古霉素的初始剂量。该列线图使用实际体重和用MDRD4方程估算的肾小球滤过率(eGFR)。剂量基于2009年美国卫生系统药师协会/美国感染病学会/美国传染病药师协会指南,该指南推荐每8 - 12小时给予15 - 20mg/kg。医护人员开具“万古霉素静脉滴注,由药房给药”的医嘱。

结果

干预前(n = 75)和干预后(n = 108)队列在年龄、性别分布、体重和eGFR方面相似。干预前和干预后组的万古霉素每日总剂量中位数相似(2000mg),尽管干预后首次谷浓度中位数更高(13.0对14.8mcg/ml,p = 0.03)。干预后,低于10mcg/ml的首次谷浓度比例下降(32%至13%, = 0.003),而在10 - 20mcg/ml治疗范围内的谷浓度比例增加(50.7%对69.4%, = 0.01)。超过20mcg/ml的谷浓度比例没有差异(17.3%对17.6%, = 0.96)。

结论

采用基于列线图的药房协作实践模式的多学科干预措施可显著提高治疗性初始万古霉素谷浓度的比例,并将次治疗性谷浓度数量减半。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a00d/7093063/1d19f56cc369/nihms-1564996-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a00d/7093063/1d19f56cc369/nihms-1564996-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a00d/7093063/1d19f56cc369/nihms-1564996-f0001.jpg

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