Expansion of a Pharmacist-Led Culture Follow-Up Program to Real-Time Notification of Multidrug-Resistant Microbiology Results in the Emergency Department.

IF 0.8 Q4 PHARMACOLOGY & PHARMACY
Hospital Pharmacy Pub Date : 2023-08-01 Epub Date: 2023-02-27 DOI:10.1177/00185787231155833
Justin Andrade, James Truong, Christine Ciaramella
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引用次数: 0

Abstract

Introduction: There are currently limited published data for a pharmacist-led multidrug-resistant (MDR) culture follow-up program through a collaborative drug therapy management (CDTM) agreement in the emergency department (ED). Objective: The objective of this study was to assess the impact of a pharmacist-led culture follow-up program for MDR microbiology results on ED revisit rate. Methods: A single-center quasi-experimental retrospective study was conducted comparing the outcomes before (December 2017 to March 2019) and after (April 2019 to July 2020) implementation of the ED MDR Culture program. Patients 18 years of age or older; with confirmed positive microbiology culture of extended-spectrum beta-lactamases (ESBL), methicillin-resistant Staphylococcus aureus (MRSA), and vancomycin-resistant Enterococcus (VRE) at any site; and discharged from the ED were included. The primary outcome was to evaluate ED revisit within 30 days due to antimicrobial treatment failure, defined as lack of resolution or worsening of infection. A statistical analysis was performed for categorical data using Fisher's exact test, and for continuous data using unpaired t test or Mann-Whitney U Test, when applicable. Results: A total of 130 patients were included in the analysis. Patients in the post-implementation group (n = 70) had a significant reduction in ED revisits compared to the pre-implementation group (n = 60); 9 [12.9%] versus 17 [28.3%], respectively; P = .046. Conclusion: Implementation of an ED MDR culture program was associated with significantly less ED revisits within 30 days due to antimicrobial treatment failure, thus demonstrating the expanded role of ED pharmacists in antimicrobial stewardship in the outpatient setting.

将药剂师主导的培养随访计划扩展为在急诊科实时通知耐多药微生物学结果。
简介:目前,关于在急诊科(ED)通过药物治疗管理协作协议(CDTM)开展药剂师主导的耐多药(MDR)培养跟踪项目的公开数据十分有限。研究目的本研究旨在评估由药剂师主导的 MDR 微生物培养结果随访计划对急诊科复诊率的影响。研究方法:进行了一项单中心准实验性回顾研究,比较了 ED MDR 培养计划实施前(2017 年 12 月至 2019 年 3 月)和实施后(2019 年 4 月至 2020 年 7 月)的结果。研究对象包括年龄在 18 周岁或以上;任何部位的广谱β-内酰胺酶 (ESBL)、耐甲氧西林金黄色葡萄球菌 (MRSA) 和耐万古霉素肠球菌 (VRE) 微生物培养阳性;从急诊室出院的患者。主要结果是评估急诊室在 30 天内因抗菌治疗失败而再次就诊的情况,抗菌治疗失败的定义是感染未缓解或恶化。对分类数据采用费舍尔精确检验进行统计分析,对连续数据采用非配对 t 检验或 Mann-Whitney U 检验(如适用)进行统计分析。结果共有 130 名患者参与了分析。与实施前(n = 60)相比,实施后组(n = 70)患者的 ED 复诊率显著下降;分别为 9 [12.9%] 对 17 [28.3%];P = .046。结论:实施急诊室 MDR 培养计划后,因抗菌药物治疗失败而在 30 天内再次就诊的急诊室患者明显减少,这表明急诊室药剂师在门诊抗菌药物管理中的作用得到了扩大。
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来源期刊
Hospital Pharmacy
Hospital Pharmacy PHARMACOLOGY & PHARMACY-
CiteScore
1.70
自引率
0.00%
发文量
63
期刊介绍: Hospital Pharmacy is a monthly peer-reviewed journal that is read by pharmacists and other providers practicing in the inpatient and outpatient setting within hospitals, long-term care facilities, home care, and other health-system settings The Hospital Pharmacy Assistant Editor, Michael R. Cohen, RPh, MS, DSc, FASHP, is author of a Medication Error Report Analysis and founder of The Institute for Safe Medication Practices (ISMP), a nonprofit organization that provides education about adverse drug events and their prevention.
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