The Emperor’s New Clothes: PRospective Observational Evaluation of the Association Between Initial VancomycIn Exposure and Failure Rates Among ADult HospitalizEd Patients With Methicillin-resistant Staphylococcus aureus Bloodstream Infections (PROVIDE)

医学 万古霉素 观察研究 金黄色葡萄球菌 耐甲氧西林金黄色葡萄球菌 前瞻性队列研究 血流感染 内科学 重症监护医学 细菌 遗传学 生物
作者
Thomas P. Lodise,Susan L. Rosenkranz,Matthew Finnemeyer,Scott Evans,Matthew Sims,Marcus Zervos,C. Buddy Creech,Pratish C Patel,Michael C. Keefer,Paul Riska,Fernanda P. Silveira,Marc H. Scheetz,Richard G. Wunderink,Martín Rodríguez,John Schrank,Susan C Bleasdale,Sara Schultz,Michelle Barron,Ann E. Stapleton,Dannah Wray
出处
期刊:Clinical Infectious Diseases [Oxford University Press]
卷期号:70 (8): 1536-1545 被引量:135
标识
DOI:10.1093/cid/ciz460
摘要

Abstract Background Vancomycin is the most commonly administered antibiotic in hospitalized patients, but optimal exposure targets remain controversial. To clarify the therapeutic exposure range, this study evaluated the association between vancomycin exposure and outcomes in patients with methicillin-resistant Staphylococcus aureus (MRSA) bacteremia. Methods This was a prospective, multicenter (n = 14), observational study of 265 hospitalized adults with MRSA bacteremia treated with vancomycin. The primary outcome was treatment failure (TF), defined as 30-day mortality or persistent bacteremia ≥7 days. Secondary outcomes included acute kidney injury (AKI). The study was powered to compare TF between patients who achieved or did not achieve day 2 area under the curve to minimum inhibitory concentration (AUC/MIC) thresholds previously found to be associated with lower incidences of TF. The thresholds, analyzed separately as co-primary endpoints, were AUC/MIC by broth microdilution ≥650 and AUC/MIC by Etest ≥320. Results Treatment failure and AKI occurred in 18% and 26% of patients, respectively. Achievement of the prespecified day 2 AUC/MIC thresholds was not associated with less TF. Alternative day 2 AUC/MIC thresholds associated with lower TF risks were not identified. A relationship between the day 2 AUC and AKI was observed. Patients with day 2 AUC ≤515 experienced the best global outcomes (no TF and no AKI). Conclusions Higher vancomycin exposures did not confer a lower TF risk but were associated with more AKI. The findings suggest that vancomycin dosing should be guided by the AUC and day 2 AUCs should be ≤515. As few patients had day 2 AUCs <400, further study is needed to define the lower bound of the therapeutic range.
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