Is Early Monitoring Better? Impact of Early Vancomycin Exposure on Treatment Outcomes and Nephrotoxicity in Patients with Methicillin-Resistant Staphylococcus aureus Infections

被引:14
作者
Chattaweelarp, Thanawat [1 ,2 ]
Changpradub, Dhitiwat [3 ]
Punyawudho, Baralee [4 ]
Thunyaharn, Sudaluck [5 ]
Santimaleeworagun, Wichai [6 ,7 ]
机构
[1] Coll Pharmacotherapy Thailand, Nonthaburi 11000, Thailand
[2] Payap Univ, Fac Pharm, Dept Pharm Practice, Chiang Mai 50000, Thailand
[3] Phramongkutklao Hosp, Dept Med, Div Infect Dis, Bangkok 10400, Thailand
[4] Chiang Mai Univ, Fac Pharm, Dept Pharmaceut Care, Chiang Mai 50200, Thailand
[5] Nakhonratchasima Coll, Fac Med Technol, Nakhon Ratchasima 30000, Thailand
[6] Silpakorn Univ, Fac Pharm, Dept Pharm, Nakhon Pathom 73000, Thailand
[7] Pharmaceut Initiat Resistant Bacteria & Infect Di, Nakhon Pathom 73000, Thailand
来源
ANTIBIOTICS-BASEL | 2020年 / 9卷 / 10期
关键词
area under the curve; mortality; MRSA; nephrotoxicity; vancomycin; HEALTH-SYSTEM PHARMACISTS; CRITICALLY-ILL PATIENTS; AMERICAN SOCIETY; DISEASES SOCIETY; RATIO; BACTEREMIA; GUIDELINES; MORTALITY;
D O I
10.3390/antibiotics9100672
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Optimal early vancomycin target exposure remains controversial. To clarify the therapeutic exposure range, we investigated the association between vancomycin exposure and treatment outcomes or nephrotoxicity in patients with methicillin-resistant Staphylococcus aureus (MRSA) infection. This retrospective study reviewed clinical data obtained from 131 patients with MRSA infections between January 2017 and September 2019. Clinical outcomes included treatment failure, 30-day mortality, microbiological failure, and acute kidney injury. We measured serum vancomycin levels after the first dose to 48 h and estimated vancomycin exposure using the Bayesian theorem. The minimum inhibitory concentration (MIC) of antimicrobial agents was determined using the broth microdilution method. Classification and Regression Tree analyses identified day 1 and 2 exposure thresholds associated with an increased risk of failure and nephrotoxicity. Treatment failure (27.9% vs. 33.3%) and 30-day mortality (26.6% vs. 31.74%) were numerically but not significantly reduced in patients with the area under the curve (AUC)(24-48h)/MICBMD >= 698. Patients with AUC(ss)/MICBMD >= 679 exhibited a significantly increased risk of acute kidney injury (27.9% vs. 10.9%, p = 0.041). These findings indicate that AUC(ss)/MICBMD ratios > 600 may cause nephrotoxicity. AUC/MICBMD at days 1 and 2 do not appear to be significantly associated with particular clinical outcomes, but further studies are needed.
引用
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页码:1 / 10
页数:10
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