Impact of the First Twenty-Four-Hour Area Under the Concentration-Time Curve/Minimum Inhibitory Concentration of Vancomycin on Treatment Outcomes in Patients With Methicillin-Resistant Staphylococcus aureus Bacteremia

被引:0
|
作者
Higashi, Mika [1 ]
Nakano, Takafumi [1 ,2 ,5 ]
Sato, Keisuke [1 ]
Eguchi, Yukiomi [1 ]
Moriwaki, Norihiro [1 ]
Kamada, Mitsuhiro [1 ]
Ikeuchi, Tadahiro [1 ]
Kaneshige, Susumu [1 ]
Uchiyama, Masanobu [1 ]
Hayashi, Toshinobu [3 ]
Togawa, Atsushi [4 ]
Matsuo, Koichi [1 ]
Kamimura, Hidetoshi [1 ]
机构
[1] Fukuoka Univ Hosp, Dept Pharm, Jonan Ku, Fukuoka 8140133, Japan
[2] Fukuoka Univ, Fac Pharmaceut Sci, Dept Oncol & Infect Dis Pharm, Jonan Ku, Fukuoka 8140180, Japan
[3] Fukuoka Univ, Fac Pharmaceut Sci, Dept Emergency & Disaster Med Pharm, Jonan Ku, Fukuoka 8140180, Japan
[4] Fukuoka Univ, Fac Med, Dept Med Oncol Hematol & Infect Dis, Jonan Ku, Fukuoka, Japan
[5] Fukuoka Univ Hosp, Dept Pharm, Jonan Ku, Fukuoka 8140133, Japan
来源
关键词
First; 24-hAUC/MIC; Vancomycin; Methicillin-resistant Staphylococcus aureus; Bacteremia; INFECTIOUS-DISEASES SOCIETY; PRACTICE GUIDELINES; AUREUS BACTEREMIA; PHARMACOKINETICS; DAPTOMYCIN; CLEARANCE; MORTALITY; AMERICA;
D O I
10.14740/jocmr5238
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Vancomycin regimens are designed to achieve an area under the concentration-time curve/minimum inhibitory concentration (AUC/MIC) ratio ranging between 400 and 600 mu g<middle dot>h/mL in the steady state. However, in cases of critical infections such as bacteremia requiring an early treatment approach, the clinical course may be affected by the AUC/MIC before reaching the steady state, that is, the AUC/MIC values 24 h after the first dose (first 24-h AUC/MIC). This study evaluated the relationship between the first 24-h AUC/MIC and the clinical course of methicillin-resistant Staphylococcus aureus (MRSA) infection. Methods: We retrospectively reviewed the records of patients with MRSA bacteremia in a university hospital between 2015 and 2022. The first 24-h AUC/MIC cutoff was set at 300 mu g<middle dot>h/mL based on the results of early response, and eligible patients were divided into groups with a first 24-h AUC/MIC either < 300 <mu>g<middle dot>h/mL (< 300 group, n = 32) or >= 300 <mu>g<middle dot>h/mL (>= 300 group, n = 38). The primary endpoint was the rate of treatment efficacy, and the secondary endpoints were time to clinical and bacteriological improvement and 30-day survival rate. Results: Treatment efficacy and 30-day survival rates were not significantly different between the two groups (78.1% vs. 79.0%, P = 0.933 and 83.9% vs. 87.2%, P = 0.674, respectively). Among patients who showed treatment efficacy, the median time to clinical and bacteriological improvement was 11.5 days and 8.0 days in the < 300 and >= 300 groups, respectively; compared to the >= 300 group, the < 300 group had a significantly longer time to improvement (P = 0.001). Conclusions: The first 24-h AUC/MIC had no effect on the treatment efficacy and 30-day survival rates. However, the time to clinical and bacteriological improvement was significantly prolonged in the < 300 group, indicating that the first 24-h AUC/MIC does not affect the rate of therapeutic efficacy but may affect the treatment period.
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页码:325 / 334
页数:10
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