Individualized vancomycin dosing in infants: prospective evaluation of an online dose calculator

被引:2
|
作者
Wilkins, Amanda L. [1 ,2 ,3 ,26 ]
Lai, Tony [4 ,5 ]
Zhu, Xiao [6 ]
Bolisetty, Srinivas [7 ]
Chiletti, Roberto [8 ,9 ,10 ]
Cranswick, Noel [1 ,2 ,11 ,12 ]
Gardiner, Kaya [3 ,13 ]
Hunt, Rodney [14 ,15 ,16 ]
Malhotra, Atul [14 ,15 ]
McMullan, Brendan [17 ,18 ]
Mehta, Bhavesh [19 ,20 ]
Michalowski, Joanna [7 ]
Popat, Himanshu [19 ,21 ,22 ]
Ward, Meredith [7 ,23 ]
Duffull, Stephen [24 ]
Curtis, Nigel [2 ,3 ,25 ]
Gwee, Amanda [2 ,3 ,25 ]
机构
[1] Royal Childrens Hosp Melbourne, Dept Gen Med, Parkville, Vic, Australia
[2] Univ Melbourne, Dept Paediat, Parkville, Vic, Australia
[3] Murdoch Childrens Res Inst, Infect Dis Grp, Parkville, Vic, Australia
[4] Childrens Hosp Westmead, Pharm Dept, Westmead, NSW, Australia
[5] Univ Sydney, Sch Pharm, Camperdown, NSW, Australia
[6] Fudan Univ, Sch Pharm, Dept Clin Pharm & Pharm Adm, Shanghai, Peoples R China
[7] Royal Hosp Women, Dept Newborn Care, Randwick, NSW, Australia
[8] Royal Childrens Hosp Melbourne, Dept Intens Care, Parkville, Vic, Australia
[9] Murdoch Childrens Res Inst, Paediat Intens Care Res Grp, Melbourne, Vic, Australia
[10] Univ Melbourne, Dept Crit Care, Melbourne, Vic, Australia
[11] Royal Childrens Hosp Melbourne, Clin Pharmacol Unit, Parkville, Vic, Australia
[12] Murdoch Childrens Res Inst, Melbourne Childrens Trials Ctr, Parkville, Vic, Australia
[13] Royal Childrens Hosp Melbourne, Res Operat, Parkville, Vic, Australia
[14] Monash Childrens Hosp, Monash Newborn, Clayton, Vic, Australia
[15] Monash Univ, Dept Paediat, Clayton, Vic, Australia
[16] Murdoch Childrens Res Inst, Clin Sci Theme, Parkville, Vic, Australia
[17] Univ New South Wales, Fac Med, Sydney, NSW, Australia
[18] Sydney Childrens Hosp, Dept Immunol & Infect Dis, Randwick, NSW, Australia
[19] Childrens Hosp Westmead, Grace Ctr Newborn Intens Care, Westmead, NSW, Australia
[20] Univ Sydney, Sydney Med Sch, Discipline Paediat & Child Hlth, Sydney, NSW, Australia
[21] NHMRC Clin Trial Ctr, Camperdown, NSW, Australia
[22] Univ Sydney, Sydney Childrens Hosp, Westmead Clin Sch, Camperdown, NSW, Australia
[23] Univ New South Wales, Sch Womens & Childrens Hlth, Randwick, NSW, Australia
[24] Univ Otago, Sch Pharm, Dunedin, New Zealand
[25] Royal Childrens Hosp Melbourne, Dept Infect Dis, Parkville, Vic, Australia
[26] Univ Melbourne, Royal Childrens Hosp Melbourne, Dept Paediat, 50 Flemington Rd, Parkville, Vic 3052, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
vancomycin; individualized dosing; pharmacokinetics; infants; neonates; INFECTIOUS-DISEASES SOCIETY; HEALTH-SYSTEM PHARMACISTS; AMERICAN SOCIETY;
D O I
10.1016/j.ijantimicag.2023.106728
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Empiric vancomycin dosing regimens fail to achieve recommended target trough concentra-tions of 10-20 mg/L in the majority of infants. This study assessed the performance of a model-based dosing calculator (Vanc App) in achieving target vancomycin concentrations at first steady-state level.Methods: This was a multicenter prospective study in four tertiary pediatric hospitals over an 18-month period. Infants aged 0-90 days with suspected Gram-positive sepsis requiring empiric vancomycin treat-ment were included if they did not meet any of the exclusion criteria: post-menstrual age (PMA) < 25 weeks, weight < 500 g, glycopeptide allergy, receiving extracorporeal membrane oxygenation, vancomycin use within the previous 72 h, and renal impairment. The Vanc App used a published population pharma-cokinetic model to generate a dose based on the infant's PMA, weight, creatinine, and target vancomycin concentration.Results: A total of 40 infants were included; 40% were female, median (range) weight was 2505 (700-4460) g and median (range) PMA was 37.4 (25.7-49.0) weeks. The median (range) vancomycin dose was 45 (24-79) mg/kg/day. All infants had trough vancomycin concentrations measured at steady-state (24-< 48 hours) and 30 (75%) infants achieved target concentrations. Five infants had supratherapeutic (me-dian 25, range 21-38 mg/L) and five had subtherapeutic (median 6, range < 5-9 mg/L) concentrations. An area under the concentration-time curve (AUC0-24) of 400-650 mg/L.h was achieved in 33 (83%) infants. There were no infusion-related reactions or nephrotoxicity.Conclusion: Individualized intermittent vancomycin dosing using a model-based online calculator resulted in 75% and 83% of infants achieving target trough and AUC0-24, respectively, at first steady-state level.There were no vancomycin-related nephrotoxicity or infusion-related reactions.(c) 2023 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.
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页数:7
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