Optimizing Antibiotic Drug Therapy in Pediatrics: Current State and Future Needs

被引:41
作者
Le, Jennifer [1 ]
Bradley, John S. [2 ,3 ]
机构
[1] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, 9500 Gilman Dr,MC 0714, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pediat, Div Infect Dis, La Jolla, CA 92093 USA
[3] Rady Childrens Hosp San Diego, San Diego, CA USA
关键词
Pharmacokinetic; pharmacodynamic; pediatrics; neonates; antimicrobials; vancomycin; Monte Carlo simulation; beta-lactams; aminoglycosides; antibiotics; Bayesian methods; opportunistic study; ceftaroline; STAPHYLOCOCCUS-AUREUS BACTEREMIA; MONTE-CARLO-SIMULATION; SINGLE-DOSE PHARMACOKINETICS; UNDER-THE-CURVE; POPULATION PHARMACOKINETICS; PSEUDOMONAS-AERUGINOSA; CYSTIC-FIBROSIS; CONTINUOUS-INFUSION; DEVELOPMENTAL PHARMACOKINETICS; MEROPENEM PHARMACOKINETICS;
D O I
10.1002/jcph.1128
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The selection of the right antibiotic and right dose necessitates clinicians understand the contribution of pharmacokinetic variability stemming from age-related physiologic maturation and the pharmacodynamics to optimize drug exposure for clinical response. The complexity of selecting the right dose arises from the multiplicity of pediatric age groups, from premature neonates to adolescents. Body size and age (which relate to organ function) must be incorporated to optimize antibiotic dosing in this vulnerable population. In the effort to optimize and individualize drug dosing regimens, clinical pharmacometrics that incorporate population-based pharmacokinetic modeling, Bayesian estimation, and Monte Carlo simulations are utilized as a quantitative approach to understanding and predicting the pharmacology and clinical and microbiologic efficacy of antibiotics. In addition, opportunistic study designs and alternative blood sampling strategies can serve as practical approaches to ensure successful conduct of pediatric studies. This review article examines relevant literature on optimization of antibiotic pharmacotherapy in pediatric populations published within the last decade. Specific pediatric antibiotic data, including beta-lactam antibiotics, aminoglycosides, and vancomycin, are critically evaluated.
引用
收藏
页码:S108 / S122
页数:15
相关论文
共 102 条
[1]   Mechanism-based concepts of size and maturity in pharmacokinetics [J].
Anderson, B. J. ;
Holford, N. H. G. .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2008, 48 :303-332
[2]   Understanding dosing: children are small adults, neonates are immature children [J].
Anderson, Brian J. ;
Holford, Nick H. G. .
ARCHIVES OF DISEASE IN CHILDHOOD, 2013, 98 (09) :737-744
[3]   Increasing resistance of the Liverpool Epidemic Strain (LES) of Pseudomonas aeruginosa (Psa) to antibiotics in cystic fibrosis (CF)-A cause for concern? [J].
Ashish, Abdul ;
Shaw, Matthew ;
Winstanley, C. ;
Ledson, Martin J. ;
Walshaw, Martin J. .
JOURNAL OF CYSTIC FIBROSIS, 2012, 11 (03) :173-179
[4]   Pharmacokinetics and Pharmacodynamics of Antifungals in Children: Clinical Implications [J].
Autmizguine, Julie ;
Guptill, Jeffrey T. ;
Cohen-Wolkowiez, Michael ;
Benjamin, Daniel K., Jr. ;
Capparelli, Edmund V. .
DRUGS, 2014, 74 (08) :891-909
[5]   Antibiotic dosing in children in Europe: can we grade the evidence from pharmacokinetic/pharmacodynamic studies - and when is enough data enough? [J].
Barker, Charlotte I. S. ;
Standing, Joseph F. ;
Turner, Mark A. ;
McElnay, James C. ;
Sharland, Mike .
CURRENT OPINION IN INFECTIOUS DISEASES, 2012, 25 (03) :235-242
[6]   INCIDENCE OF AMIKACIN OTOTOXICITY - A SIGMOID FUNCTION OF TOTAL DRUG EXPOSURE INDEPENDENT OF PLASMA-LEVELS [J].
BEAUBIEN, AR ;
DESJARDINS, S ;
ORMSBY, E ;
BAYNE, A ;
CARRIER, K ;
CAUCHY, MJ ;
HENRI, R ;
HODGEN, M ;
SALLEY, J ;
ENG, B ;
STPIERRE, A .
AMERICAN JOURNAL OF OTOLARYNGOLOGY, 1989, 10 (04) :234-243
[7]   Meropenem pharmacokinetics, pharmacodynamics, and Monte Carlo simulation in the neonate [J].
Bradley, John S. ;
Sauberan, Jason B. ;
Ambrose, Paul G. ;
Bhavnani, Sitjata M. ;
Rasmussen, Maynard R. ;
Capparelli, Edmund V. .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2008, 27 (09) :794-799
[8]   Pharmacokinetics, Pharmacodynamics, and Monte Carlo Simulation Selecting the Best Antimicrobial Dose to Treat an Infection [J].
Bradley, John S. ;
Garonzik, Samira Merali ;
Forrest, Alan ;
Bhavnani, Sujata M. .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2010, 29 (11) :1043-1046
[9]   Population Pharmacokinetic Comparison and Pharmacodynamic Breakpoints of Ceftazidime in Cystic Fibrosis Patients and Healthy Volunteers [J].
Bulitta, J. B. ;
Landersdorfer, C. B. ;
Huettner, S. J. ;
Drusano, G. L. ;
Kinzig, M. ;
Holzgrabe, U. ;
Stephan, U. ;
Soergel, F. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (03) :1275-1282
[10]   Population Pharmacokinetics of Piperacillin/Tazobactam in Critically Ill Young Children [J].
Cies, Jeffrey J. ;
Shankar, Venkat ;
Schlichting, Christine ;
Kuti, Joseph L. .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2014, 33 (02) :168-173