Critical assessment of the revised guidelines for vancomycin therapeutic drug monitoring

被引:7
作者
Aljutayli, Abdullah [1 ,2 ,3 ,7 ]
Thirion, Daniel J. G. [2 ,4 ]
Nekka, Fahima [2 ,5 ,6 ]
机构
[1] Qassim Univ, Fac Pharm, Dept Pharmaceut, Buraydah, Saudi Arabia
[2] Univ Montreal, Fac Pharm, Montreal, PQ, Canada
[3] Qassim Univ, Fac Pharm, Buraydah, Saudi Arabia
[4] McGill Univ, Dept Pharm, Hlth Ctr, Montreal, PQ, Canada
[5] Univ Montreal, Fac Pharm, Lab Pharmacometrie, Montreal, PQ, Canada
[6] Univ Montreal, Ctr Rech Math, Montreal, PQ, Canada
[7] Univ Montreal, Fac Pharm, Pavillon Jean Coutu, 2940 Chemin Polytech, Montreal, PQ H3T 1J4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Area under curve (AUC); Trough monitoring; Drug monitoring humans; Methicillin-resistant Staphylococcus aureus*; Vancomycin; therapeutic use; POPULATION PHARMACOKINETIC ANALYSIS; STAPHYLOCOCCUS-AUREUS INFECTIONS; HEALTH-SYSTEM PHARMACISTS; CONCENTRATION-TIME CURVE; UNDER-THE-CURVE; TROUGH CONCENTRATION; CONSENSUS GUIDELINE; CONTINUOUS-INFUSION; AMERICAN SOCIETY; DISEASES SOCIETY;
D O I
10.1016/j.biopha.2022.113777
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: The revised vancomycin guidelines recommend replacing trough-only with trough or peak/trough Bayesian and first-order equations monitoring, citing their better AUC predictions and poor AUC-trough R2. Yet, evidence suggesting good AUC-trough correlation has been overlooked, and the optimality of peak/trough samples has been doubted. The guidelines recommend Bayesian programs implement richly-sampled PopPK priors despite their scarcity. Therefore, whether complex Bayesian and sample-demanding first-order equations can bring significant advantages to the practice over simple trough-only monitoring is worth weighing.Objectives: The primary aim is to compare the predictive performance of the AUC monitoring methods. Then, we investigate the impact of not adhering to trough sampling on the Bayesian-based predictions. Moreover, we report the nature of PopPK priors used in Bayesian programs to assess the applicability of the guideline recommendations.Methods: We calculated the predictive performance of the monitoring methods using a standard PopPK modeling and simulation approach. We thoroughly explored the prior PK models implemented in Bayesian programs. Results: Predictive performances of the monitoring methods were comparable at steady-state relative to the number of samples. Contrary to the recommendation, Bayesian trough monitoring did not result in better pre-dictive performances compared to using random levels. Very few programs implemented richly-sampled priors.Conclusion: All the monitoring methods can be, relatively, reliable at steady-state, if properly implemented. Although only Bayesian-based monitoring can be used pre-steady-state, its predictive performance can be modest. Trough-only monitoring is the simplest approach. Constraints regarding trough sampling times could be relaxed. The scarcity of richly-sampled Bayesian priors questions the applicability of the revised guidelines recommendation.
引用
收藏
页数:10
相关论文
共 94 条
[1]   Evaluation of the Effectiveness of Dose Individualization to Achieve Therapeutic Vancomycin Concentrations [J].
Abulfathi, Ahmed A. ;
Chirehwa, Maxwell ;
Rosenkranz, Bernd ;
Decloedt, Eric H. .
JOURNAL OF CLINICAL PHARMACOLOGY, 2018, 58 (09) :1134-1139
[2]   Pharmacokinetics of Vancomycin in Extremely Obese Patients with Suspected or Confirmed Staphylococcus aureus Infections [J].
Adane, Eyob D. ;
Herald, Michael ;
Koura, Firas .
PHARMACOTHERAPY, 2015, 35 (02) :127-139
[3]  
Aljutayli, 2022, PHARMACOKINETIC EQUA
[4]   Pharmacokinetic equations versus Bayesian guided vancomycin monitoring: Pharmacokinetic model and model-informed precision dosing trial simulations [J].
Aljutayli, Abdullah ;
Thirion, Daniel J. G. ;
Bonnefois, Guillaume ;
Nekka, Fahima .
CTS-CLINICAL AND TRANSLATIONAL SCIENCE, 2022, 15 (04) :942-953
[5]   An Update on Population Pharmacokinetic Analyses of Vancomycin, Part I: In Adults [J].
Aljutayli, Abdullah ;
Marsot, Amelie ;
Nekka, Fahima .
CLINICAL PHARMACOKINETICS, 2020, 59 (06) :671-698
[6]   Renal drug clearance in preterm neonates: Relation to prenatal growth [J].
Allegaert, Karel ;
Anderson, Brian J. ;
van den Anker, John N. ;
Vanhaesebrouck, Sophie ;
de Zegher, Francis .
THERAPEUTIC DRUG MONITORING, 2007, 29 (03) :284-291
[7]   AUC- vs. Trough-Guided Monitoring of Vancomycin in Infants [J].
Alsultan, Abdullah ;
Abouelkheir, Manal ;
Albassam, Ahmad ;
Alharbi, Emad ;
Assiri, Ahmed ;
Alqahtani, Saeed .
INDIAN JOURNAL OF PEDIATRICS, 2020, 87 (05) :359-364
[8]   Vancomycin pharmacokinetics in preterm neonates and the prediction of adult clearance [J].
Anderson, Brian J. ;
Allegaert, Karel ;
Van den Anker, John N. ;
Cossey, Veerle ;
Holford, Nicholas H. G. .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2007, 63 (01) :75-84
[9]   Comment on: AUCs and 123s: a critical appraisal of vancomycin therapeutic drug monitoring in paediatrics [J].
Avedissian, Sean N. ;
Le, Jennifer ;
Neely, Michael N. ;
Cortes-Penfield, Nicolas ;
Bradley, John ;
Rybak, Michael J. ;
Rhodes, Nathaniel J. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2021, 76 (09) :2486-2488
[10]   Evaluation of Vancomycin Use in Late-Onset Neonatal Sepsis Using the Area Under the Concentration-Time Curve to the Minimum Inhibitory Concentration ≥400 Target [J].
Bhongsatiern, Jiraganya ;
Stockmann, Chris ;
Roberts, Jessica K. ;
Yu, Tian ;
Korgenski, Kent E. ;
Spigarelli, Michael G. ;
Desai, Pankaj B. ;
Sherwin, Catherine M. T. .
THERAPEUTIC DRUG MONITORING, 2015, 37 (06) :756-765