Optimal exposure targets for vancomycin in the treatment of neonatal coagulase-negative Staphylococcus infection: A retrospective study based on electronic medical records

被引:12
作者
Chen, Quanyao [1 ]
Wan, Jun [1 ]
Shen, Wei [1 ]
Lin, Wanlong [1 ]
Lin, Xiuxian [1 ]
Huang, Zhiyi [1 ]
Lin, Min [1 ]
Chen, Yao [1 ]
机构
[1] Xiamen Univ, Women & Childrens Hosp, Sch Med, Xiamen, Fujian, Peoples R China
关键词
area under the curve; clinical effect; nephrotoxicity; vancomycin; REVISED CONSENSUS GUIDELINE; HEALTH-SYSTEM PHARMACISTS; AUREUS INFECTIONS; DISEASES SOCIETY; AMERICAN SOCIETY; GLOBAL BURDEN; 195; COUNTRIES; TERRITORIES;
D O I
10.1016/j.pedneo.2021.11.010
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: The currently advocated ratio of area under the curve (AUC) over 24 h to minimum inhibitory concentration (AUC/MIC) > 400 and AUC < 600 mg h/L as the therapeutic drug monitoring (TDM) target of vancomycin is based on data from multiple observational studies in adult patients with methicillin-resistant Staphylococcus aureus (MRSA) infection. It may not be applicable to newborns with coagulase-negative Staphylococcus (CoNS) infection. We conducted a retrospective study to identify the optimal exposure targets for vancomycin in the treatment of neonatal CoNS infection. Methods: Based on the inclusion and exclusion criteria, serum vancomycin concentration, demographics, clinical data, and related laboratory data of newborns who received vancomycin intravenous infusion from June 1, 2016 to February 1, 2021 were collected retrospectively. The AUC was calculated using the maximum a posteriori Bayesian (MAPB) method. The vancomycin exposure threshold of AUC/MIC for efficacy and AUC for toxicity (acute kidney injury, AKI) were determined based on receiver operating characteristic (ROC) curve analysis. The correlation between vancomycin exposure and both clinical effect and nephrotoxicity was analyzed using logistic multivariate regression. Results: In total, 153 patients and 245 vancomycin concentrations (160 trough and 85 peak concentrations) were included. The ROC curve analysis showed that the exposure thresholds of AUC/MIC for clinical efficacy and AUC for nephrotoxicity were 281 and 602 mg h/L, respectively. The multivariate regression analysis showed that AUC/MIC > 280 was a predictor of efficacy (OR: 13.960, 95% CI: 1.891-103.078, P < 0.05) and AUC > 600 mg h/L was associated with AKI (OR: 9.008, 95% CI: 2.706-29.983, P < 0.05). The vancomycin AUC/MIC threshold for treating neonatal CoNS infection with vancomycin is lower than the currently advocated AUC/ MIC >400. Conclusion: The optimal exposure targets for vancomycin in neonatal CoNS infection were AUC/MIC > 280 , AUC < 600 mg h/L. Copyright 2022, Taiwan Pediatric Association. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/ by-nc-nd/4.0/).
引用
收藏
页码:247 / 254
页数:8
相关论文
共 40 条
[1]   The Predictive Factors for Poor Outcomes in Preterm Infants with Coagulase-Negative Staphylococci Infection [J].
Al-Matary, Abdulrahman ;
Huseynova, Roya ;
Qaraqe, Mostafa ;
Aldandan, Faisal K. .
JOURNAL OF CLINICAL NEONATOLOGY, 2021, 10 (01) :19-23
[2]   Pharmacokinetic modelling and Bayesian estimation-assisted decision tools to optimize vancomycin dosage in neonates: only one piece of the puzzle [J].
Allegaert, Karel ;
Flint, Robert ;
Smits, Anne .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2019, 15 (09) :735-749
[3]   Towards precision dosing of vancomycin: a systematic evaluation of pharmacometric models for Bayesian forecasting [J].
Broeker, A. ;
Nardecchia, M. ;
Klinker, K. P. ;
Derendorf, H. ;
Day, R. O. ;
Marriott, D. J. ;
Carland, J. E. ;
Stocker, S. L. ;
Wicha, S. G. .
CLINICAL MICROBIOLOGY AND INFECTION, 2019, 25 (10) :1286.e1-1286.e7
[4]   A Moving Target-Vancomycin Therapeutic Monitoring [J].
Burns, Alaina N. ;
Goldman, Jennifer L. .
JOURNAL OF THE PEDIATRIC INFECTIOUS DISEASES SOCIETY, 2020, 9 (04) :474-478
[5]   Prevalence of early-onset neonatal infection among newborns of mothers with bacterial infection or colonization: a systematic review and meta-analysis [J].
Chan, Grace J. ;
Lee, Anne C. C. ;
Baqui, Abdullah H. ;
Tan, Jingwen ;
Black, Robert E. .
BMC INFECTIOUS DISEASES, 2015, 15
[6]  
Chavada R, 2017, ANTIMICROB AGENTS CH, V61, DOI [10.1128/AAC.02535-16, 10.1128/aac.02535-16]
[7]   Precision and accuracy of commercial assays for vancomycin therapeutic drug monitoring: evaluation based on external quality assessment scheme [J].
Chen, Chao-Yang ;
Li, Meng-Ya ;
Ma, Ling-Yun ;
Zhai, Xing-Yu ;
Luo, Dao-Huang ;
Zhou, Ying ;
Liu, Zhen-Ming ;
Cui, Yi-Min .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2020, 75 (08) :2110-2119
[8]   Survey of infections due to Staphylococcus species:: Frequency of occurrence and antimicrobial susceptibility of isolates collected in the United States, Canada, Latin America, Europe, and the Western Pacific region for the SENTRY Antimicrobial Surveillance Program, 1997-1999 [J].
Diekema, DJ ;
Pfaller, MA ;
Schmitz, FJ ;
Smayevsky, J ;
Bell, J ;
Jones, RN ;
Beach, M .
CLINICAL INFECTIOUS DISEASES, 2001, 32 :S114-S132
[9]   Vancomycin Advanced Therapeutic Drug Monitoring: Exercise in Futility or Virtuous Endeavor to Improve Drug Efficacy and Safety? [J].
Dilworth, Thomas J. ;
Schulz, Lucas T. ;
Rose, Warren E. .
CLINICAL INFECTIOUS DISEASES, 2021, 72 (10) :E675-E681
[10]   The dosing and monitoring of vancomycin: what is the best way forward? [J].
Drennan, Philip G. ;
Begg, Evan J. ;
Gardiner, Sharon J. ;
Kirkpatrick, Carl M. J. ;
Chambers, Steve T. .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2019, 53 (04) :401-407