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1
Use of vancomycin pharmacokinetic-pharmacodynamic properties in the treatment of MRSA infections.万古霉素药代动力学-药效学特性在治疗耐甲氧西林金黄色葡萄球菌感染中的应用。
Expert Rev Anti Infect Ther. 2010 Jan;8(1):95-106. doi: 10.1586/eri.09.123.
2
Impact of initial vancomycin pharmacokinetic/pharmacodynamic parameters on the clinical and microbiological outcomes of methicillin-resistant Staphylococcus aureus bacteremia in children.初始万古霉素药代动力学/药效学参数对儿童耐甲氧西林金黄色葡萄球菌菌血症的临床和微生物学结局的影响。
PLoS One. 2021 Apr 1;16(4):e0247714. doi: 10.1371/journal.pone.0247714. eCollection 2021.
3
Pharmacokinetic/Pharmacodynamic Target Attainment of Vancomycin, at Three Reported Infusion Modes, for Methicillin-Resistant (MRSA) Bloodstream Infections in Critically Ill Patients: Focus on Novel Infusion Mode.三种报告的输注模式下,治疗重症耐甲氧西林金黄色葡萄球菌(MRSA)血流感染时,万古霉素的药代动力学/药效学目标达成情况:新型输注模式重点关注。
Front Cell Infect Microbiol. 2022 Jul 7;12:874401. doi: 10.3389/fcimb.2022.874401. eCollection 2022.
4
Prediction of vancomycin pharmacodynamics in children with invasive methicillin-resistant Staphylococcus aureus infections: a Monte Carlo simulation.儿童侵袭性耐甲氧西林金黄色葡萄球菌感染的万古霉素药效学预测:蒙特卡罗模拟。
Clin Ther. 2010 Mar;32(3):534-42. doi: 10.1016/j.clinthera.2010.03.005.
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Evaluation of ceftaroline, vancomycin, daptomycin, or ceftaroline plus daptomycin against daptomycin-nonsusceptible methicillin-resistant Staphylococcus aureus in an in vitro pharmacokinetic/pharmacodynamic model of simulated endocardial vegetations.在模拟心内膜赘生物的体外药代动力学/药效学模型中,评价头孢洛林、万古霉素、达托霉素或头孢洛林联合达托霉素对达托霉素不敏感的耐甲氧西林金黄色葡萄球菌的作用。
Antimicrob Agents Chemother. 2014 Jun;58(6):3177-81. doi: 10.1128/AAC.00088-14. Epub 2014 Mar 24.
6
Pharmacodynamic activity of ceftobiprole compared with vancomycin versus methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-intermediate Staphylococcus aureus (VISA) and vancomycin-resistant Staphylococcus aureus (VRSA) using an in vitro model.使用体外模型比较头孢比普与万古霉素对耐甲氧西林金黄色葡萄球菌(MRSA)、万古霉素中介金黄色葡萄球菌(VISA)和耐万古霉素金黄色葡萄球菌(VRSA)的药效学活性。
J Antimicrob Chemother. 2009 Aug;64(2):364-9. doi: 10.1093/jac/dkp176. Epub 2009 May 19.
7
Pharmacodynamics of vancomycin at simulated epithelial lining fluid concentrations against methicillin-resistant Staphylococcus aureus (MRSA): implications for dosing in MRSA pneumonia.万古霉素在模拟上皮衬液浓度下对耐甲氧西林金黄色葡萄球菌(MRSA)的药效学:对MRSA肺炎给药的启示
Antimicrob Agents Chemother. 2009 Sep;53(9):3894-901. doi: 10.1128/AAC.01585-08. Epub 2009 Jul 13.
8
Evaluation of clinical outcome in children and adolescents receiving vancomycin for invasive infections due to methicillin-resistant Staphylococcus aureus: impact of increasing vancomycin MICs.对因耐甲氧西林金黄色葡萄球菌侵袭性感染而接受万古霉素治疗的儿童和青少年的临床结局评估:万古霉素最低抑菌浓度升高的影响。
Minerva Pediatr. 2018 Jun;70(3):207-211. doi: 10.23736/S0026-4946.16.04688-0. Epub 2016 Dec 22.
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Current recommended dosing of vancomycin for children with invasive methicillin-resistant Staphylococcus aureus infections is inadequate.目前推荐用于侵袭性耐甲氧西林金黄色葡萄球菌感染儿童的万古霉素剂量不足。
Pediatr Infect Dis J. 2009 May;28(5):398-402. doi: 10.1097/INF.0b013e3181906e40.
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Population Pharmacokinetics and Dosing Optimization of Norvancomycin for Chinese Patients with Community-Acquired Pneumonia.中国社区获得性肺炎患者去甲万古霉素的群体药代动力学及给药方案优化
Infect Drug Resist. 2024 Dec 27;17:5881-5893. doi: 10.2147/IDR.S496776. eCollection 2024.
2
Development of an on-site therapeutic drug monitoring method using a portable spectrometer.开发一种使用便携式分光光度计的现场治疗药物监测方法。
Anal Sci. 2024 May;40(5):863-869. doi: 10.1007/s44211-024-00513-x. Epub 2024 Feb 15.
3
Population pharmacokinetics of vancomycin in patients with diabetic foot infection: a comparison of five models.糖尿病足感染患者万古霉素的群体药代动力学:五种模型的比较
J Diabetes Metab Disord. 2023 Jul 10;22(2):1385-1390. doi: 10.1007/s40200-023-01259-5. eCollection 2023 Dec.
4
Antimicrobial-loaded biodegradable nanoemulsions for efficient clearance of intracellular pathogens in bacterial peritonitis.载抗菌剂的可生物降解纳米乳剂用于有效清除细菌性腹膜炎中的细胞内病原体。
Biomaterials. 2023 Nov;302:122344. doi: 10.1016/j.biomaterials.2023.122344. Epub 2023 Oct 10.
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Model-informed precision dosing of vancomycin for rapid achievement of target area under the concentration-time curve: A simulation study.基于模型的万古霉素精准给药以快速达到浓度-时间曲线下目标面积:一项模拟研究。
Clin Transl Sci. 2023 Nov;16(11):2265-2275. doi: 10.1111/cts.13626. Epub 2023 Sep 22.
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Discrepancy between perceptions and acceptance of clinical decision support Systems: implementation of artificial intelligence for vancomycin dosing.临床决策支持系统认知与接受度的差异:万古霉素剂量人工智能的实施。
BMC Med Inform Decis Mak. 2023 Aug 11;23(1):157. doi: 10.1186/s12911-023-02254-9.
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A study to explore the appropriateness of dosing regimen of vancomycin in critically ill patients in a tertiary care unit of India.一项在印度一家三级医疗机构中探索危重症患者万古霉素给药方案适宜性的研究。
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Clinical Practice Guidelines for Therapeutic Drug Monitoring of Vancomycin in the Framework of Model-Informed Precision Dosing: A Consensus Review by the Japanese Society of Chemotherapy and the Japanese Society of Therapeutic Drug Monitoring.基于模型的精准给药框架下万古霉素治疗药物监测临床实践指南:日本化疗学会和日本治疗药物监测学会的共识性综述
Pharmaceutics. 2022 Feb 23;14(3):489. doi: 10.3390/pharmaceutics14030489.

本文引用的文献

1
Relationship between initial vancomycin concentration-time profile and nephrotoxicity among hospitalized patients.住院患者初始万古霉素浓度-时间曲线与肾毒性之间的关系。
Clin Infect Dis. 2009 Aug 15;49(4):507-14. doi: 10.1086/600884.
2
Nine-hospital study comparing broth microdilution and Etest method results for vancomycin and daptomycin against methicillin-resistant Staphylococcus aureus.一项针对九家医院的研究,比较肉汤微量稀释法和Etest法检测万古霉素及达托霉素对耐甲氧西林金黄色葡萄球菌的结果。
Antimicrob Agents Chemother. 2009 Jul;53(7):3162-5. doi: 10.1128/AAC.00093-09. Epub 2009 Apr 27.
3
Endocarditis caused by Staphylococcus aureus: A reappraisal of the epidemiologic, clinical, and pathologic manifestations with analysis of factors determining outcome.金黄色葡萄球菌引起的感染性心内膜炎:对流行病学、临床及病理表现的重新评估并分析决定预后的因素。
Medicine (Baltimore). 2009 Jan;88(1):1-22. doi: 10.1097/MD.0b013e318194da65.
4
Therapeutic monitoring of vancomycin in adult patients: a consensus review of the American Society of Health-System Pharmacists, the Infectious Diseases Society of America, and the Society of Infectious Diseases Pharmacists.成人患者万古霉素的治疗监测:美国卫生系统药师协会、美国传染病学会和传染病药师协会的共识综述
Am J Health Syst Pharm. 2009 Jan 1;66(1):82-98. doi: 10.2146/ajhp080434.
5
Impact of inoculum size and heterogeneous vancomycin-intermediate Staphylococcus aureus (hVISA) on vancomycin activity and emergence of VISA in an in vitro pharmacodynamic model.接种量和异质性万古霉素中介金黄色葡萄球菌(hVISA)对体外药效学模型中万古霉素活性及万古霉素中介金黄色葡萄球菌(VISA)出现的影响
Antimicrob Agents Chemother. 2009 Feb;53(2):805-7. doi: 10.1128/AAC.01009-08. Epub 2008 Nov 17.
6
Vancomycin ototoxicity: a reevaluation in an era of increasing doses.万古霉素耳毒性:在剂量不断增加时代的重新评估。
Antimicrob Agents Chemother. 2009 Feb;53(2):483-6. doi: 10.1128/AAC.01088-08. Epub 2008 Nov 10.
7
Vancomycin MICs for methicillin-resistant Staphylococcus aureus isolates differ based upon the susceptibility test method used.耐甲氧西林金黄色葡萄球菌分离株的万古霉素最低抑菌浓度(MIC)因所采用的药敏试验方法而异。
Antimicrob Agents Chemother. 2008 Dec;52(12):4528. doi: 10.1128/AAC.00904-08. Epub 2008 Oct 6.
8
Comparison of method-specific vancomycin minimum inhibitory concentration values and their predictability for treatment outcome of meticillin-resistant Staphylococcus aureus (MRSA) infections.特定方法的万古霉素最低抑菌浓度值比较及其对耐甲氧西林金黄色葡萄球菌(MRSA)感染治疗结果的预测性
Int J Antimicrob Agents. 2008 Nov;32(5):378-85. doi: 10.1016/j.ijantimicag.2008.05.007. Epub 2008 Aug 12.
9
Predictors of high vancomycin MIC values among patients with methicillin-resistant Staphylococcus aureus bacteraemia.耐甲氧西林金黄色葡萄球菌菌血症患者中万古霉素高 MIC 值的预测因素
J Antimicrob Chemother. 2008 Nov;62(5):1138-41. doi: 10.1093/jac/dkn329. Epub 2008 Aug 11.
10
Relationship between vancomycin MIC and failure among patients with methicillin-resistant Staphylococcus aureus bacteremia treated with vancomycin.万古霉素最低抑菌浓度(MIC)与接受万古霉素治疗的耐甲氧西林金黄色葡萄球菌血症患者治疗失败之间的关系。
Antimicrob Agents Chemother. 2008 Sep;52(9):3315-20. doi: 10.1128/AAC.00113-08. Epub 2008 Jun 30.

万古霉素药代动力学-药效学特性在治疗耐甲氧西林金黄色葡萄球菌感染中的应用。

Use of vancomycin pharmacokinetic-pharmacodynamic properties in the treatment of MRSA infections.

机构信息

Texas Tech University Health Sciences Center, 1300 Coulter, Suite 203, Amarillo, TX 79106, USA.

出版信息

Expert Rev Anti Infect Ther. 2010 Jan;8(1):95-106. doi: 10.1586/eri.09.123.

DOI:10.1586/eri.09.123
PMID:20014904
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2877625/
Abstract

Vancomycin is a commonly used antimicrobial in patients with methicillin-resistant Staphylococcus aureus (MRSA) infections. Increasing vancomycin MIC values in MRSA clinical isolates makes the optimization of vancomycin dosing pivotal to its continued use. Unfortunately, limited data exist regarding the optimal pharmacokinetic-pharmacodynamic (PK-PD) goal to improve bacterial killing and clinical outcomes with vancomycin. The hallmark study in this area suggests that achieving an AUC to MIC ratio of over 400 improves the likelihood of achieving these outcomes. Challenges in the implementation of PK-PD-based dosing for vancomycin include current methodologies utilized in microbiology laboratories, as well as intra- and interpatient pharmacokinetic variability. Individualized dosing based on MIC and specific patient factors is important to achieve optimal outcomes from vancomycin therapy.

摘要

万古霉素是耐甲氧西林金黄色葡萄球菌 (MRSA) 感染患者常用的抗菌药物。MRSA 临床分离株中万古霉素 MIC 值的增加使得优化万古霉素剂量对于其持续使用至关重要。不幸的是,关于优化药代动力学-药效学 (PK-PD) 目标以提高万古霉素杀菌效果和临床结局的数据有限。该领域的标志性研究表明,达到 AUC/MIC 比值超过 400 可提高实现这些结局的可能性。万古霉素基于 PK-PD 的给药实施面临的挑战包括微生物学实验室目前使用的方法,以及患者内在和个体间的药代动力学变异性。基于 MIC 和特定患者因素的个体化给药对于实现万古霉素治疗的最佳结局非常重要。