Safety of Extended Infusion Piperacillin-Tazobactam plus Vancomycin versus Standard Infusion Piperacillin-Tazobactam plus Vancomycin in General Medicine Patients with a diagnosis of Healthcare associated Pneumonia

Kati J Khouri, Joseph Levato, Rolla T. Sweis
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Abstract

Objective: The primary safety objective is Acute Kidney Injury (AKI), defined as an increase in serum creatinine of at least 0.5 mg/dL or a 50% increase in serum creatinine from baseline at any time during antibiotic therapy. The objective of this study is to assess safety of Extended Infusion Piperacillin-tazobactam (EIPT) and vancomycin therapy versus Standard Infusion Piperacillin-tazobactam (SIPT) and vancomycin in general medicine patients, and to evaluate if one treatment modality predisposes patients to a greater risk of nephrotoxicity. Setting: Data from a large academic medical center was analyzed over a 3 month period pre and post implementation of extended infusion piperacillin-tazobactam protocol. Design: A retrospective analysis was conducted comparing patients admitted to the hospital with a diagnosis of Healthcare Associated Pneumonia (HCAP) who received EIPT plus vancomycin versus SIPT plus vancomycin. Patients: Adult hospitalized patients on combination therapy with two or more Serum Creatinine (SCr) measurements were included. Patients were excluded if they are less than 18 years of age, are pregnant, or if they are on any form of dialysis including continuous renal replacement therapy. Conclusion: A total of 241 patients were evaluated for AKI. Safety outcomes were compared between the two treatment groups and contributing factors for developing AKI were also assessed. The incidence of AKI was significantly higher in the SIPT and vancomycin group (20.0%) compared with the EIPT and vancomycin group (10.0%) in the analysis (p=0.033). There were no significant differences in the baseline characteristics between the groups with the exception of a higher percentage of patients with a diagnosis of hypertension in the EIPT and vancomycin group (p<0.05).
延长输注哌拉西林-他唑巴坦加万古霉素与标准输注哌拉西林-他唑巴坦加万古霉素在诊断为医疗保健相关性肺炎的普通内科患者中的安全性
目的:主要的安全性目标是急性肾损伤(AKI),定义为在抗生素治疗期间的任何时间血清肌酐增加至少0.5 mg/dL或血清肌酐从基线增加50%。本研究的目的是评估延长输注哌拉西林-他唑巴坦(EIPT)和万古霉素治疗与标准输注哌拉西林-他唑巴坦(SIPT)和万古霉素治疗在普通医学患者中的安全性,并评估一种治疗方式是否使患者有更大的肾毒性风险。背景:来自一家大型学术医疗中心的数据分析了延长输注哌拉西林-他唑巴坦方案实施前后3个月的时间。设计:对诊断为医疗保健相关性肺炎(HCAP)的住院患者进行回顾性分析,比较接受EIPT加万古霉素与SIPT加万古霉素的患者。患者:接受两种或两种以上血清肌酐(SCr)测量的联合治疗的成年住院患者。年龄小于18岁、怀孕或正在进行任何形式的透析(包括持续肾替代治疗)的患者被排除在外。结论:共评估了241例AKI患者。比较两个治疗组之间的安全性结果,并评估发生AKI的因素。SIPT +万古霉素组AKI发生率(20.0%)明显高于EIPT +万古霉素组(10.0%)(p=0.033)。两组之间的基线特征无显著差异,除了EIPT和万古霉素组诊断为高血压的患者比例较高(p<0.05)。
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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