Evaluation of the Impact of Antimicrobial Stewardship Program (ASP) on Unrestricted Use of Meropenem at an Academic Medical Center

Priyam Mithawala, Edo-abasi McGee
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Abstract

Objective The primary objectives were to evaluate the prescriber acceptance rate of Antimicrobial Stewardship Program (ASP) pharmacist recommendation to de-escalate/discontinue meropenem, and estimate the difference in duration of meropenem therapy. The secondary objective was to determine incidence of adverse events in the two groups. Methods It was a retrospective study. All patients admitted to Gwinnett Medical Center and receiving meropenem from January–November 2015 were included in the study. Exclusion criteria were: patients admitted to intensive care unit, one-time dose, infectious disease consultation, and age <18 years. Electronic medical records were reviewed for data collection. The control group consisted of patients from January–July 2015 when there was no ASP pharmacist. The intervention group consisted of patients from August–November 2015 during which period the ASP pharmacist recommended de-escalation/discontinuation of meropenem based on culture and sensitivity results. Results A total of 41 patients were studied, 21 in the control group and 20 in the intervention group. There was no significant difference in baseline characteristics in the two groups and in terms of prior hospitalization or antibiotic use (within 90 days) and documented or suspected MDRO infection at the time of admission. De-escalation/discontinuation was suggested in 16/20 patients in the intervention group (80%), and intervention was accepted in 68%. The mean duration of therapy was significantly decreased in the intervention group (5.6 days vs. 8.1 days, p =0.0175). Two patients had thrombocytopenia (unrelated to meropenem), and none of the patients had seizure. Conclusion Targeted antibiotic review is an effective ASP strategy, which significantly decreases the duration of meropenem therapy.
学术医疗中心抗菌药物管理计划(ASP)对美罗培南无限制使用的影响评估
目的评价抗菌药物管理计划(ASP)药师推荐美罗培南降级/停药的处方接受率,并评估美罗培南治疗持续时间的差异。次要目的是确定两组不良事件的发生率。方法回顾性研究。所有2015年1月至11月入住Gwinnett医疗中心并接受美罗培南治疗的患者均纳入本研究。排除标准为:入住重症监护室、一次性给药、传染病就诊、年龄<18岁的患者。审查电子病历以收集数据。对照组为2015年1 - 7月无ASP药师的患者。干预组由2015年8月至11月的患者组成,在此期间,ASP药剂师根据培养和敏感性结果建议美罗培南降级/停药。结果共41例患者,对照组21例,干预组20例。两组患者的基线特征、既往住院或抗生素使用(90天内)以及入院时记录或疑似MDRO感染方面均无显著差异。干预组有16/20(80%)的患者建议降低/停药,68%的患者接受干预。干预组的平均治疗时间显著缩短(5.6天比8.1天,p =0.0175)。2例患者有血小板减少症(与美罗培南无关),无癫痫发作。结论靶向抗生素审查是一种有效的ASP策略,可显著缩短美罗培南治疗的持续时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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