Metronidazole Population Pharmacokinetics in Preterm Neonates Using Dried Blood-Spot Sampling

被引:53
作者
Suyagh, Maysa [1 ]
Collier, Paul S. [1 ]
Millership, Jeffrey S. [1 ]
Iheagwaram, Godwill [1 ]
Millar, Muriel [2 ]
Halliday, Henry L. [2 ]
McElnay, James C. [1 ]
机构
[1] Queens Univ Belfast, Clin & Practice Res Grp, Sch Pharm, Dept Child Hlth, Belfast BT9 7BL, Antrim, North Ireland
[2] Queens Univ Belfast, Royal Matern Hosp, Reg Neonatal Unit, Dept Child Hlth, Belfast BT9 7BL, Antrim, North Ireland
关键词
metronidazole; preterm neonates; population pharmacokinetics; dried blood spots; necrotizing enterocolitis; NECROTIZING ENTEROCOLITIS; PART I; INFANTS; PREMATURE; GROWTH; MODELS; ASSAY; SIZE;
D O I
10.1542/peds.2010-0807
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVES: To characterize the population pharmacokinetics of metronidazole in preterm neonates. PATIENTS AND METHODS: Data were collected prospectively from 32 preterm neonates who received intravenous metronidazole for the treatment of or prophylaxis against necrotizing enterocolitis. Dried blood spots (n = 203) on filter paper were analyzed by high-performance liquid chromatography, and the data were subjected to pharmacokinetic analysis performed by using nonlinear mixed-effect modeling. RESULTS: A 1-compartment model best described the data. Significant covariates were weight (WT) and postmenstrual age (PMA). The final population models for metronidazole clearance (CL) and volume of distribution (V) were: CL = 0.0247 x (WT/1.00)(0.75) x (1 + 0.107 x [PMA - 30]) and V = 0.726 x WT, where CL is in liters per hour, WT is in kilograms, PMA is in weeks, and V is in liters. This model predicts that the half-life of metronidazole decreases rapidly from similar to 40 hours at 25 weeks' PMA to 19 hours at 32 weeks' PMA, after which it starts to plateau. This decrease in half-life is the result of a 5-fold increase in CL compared with only a 2.5-fold increase in V during the same period. CONCLUSIONS: Currently, there are no specific dose recommendations for metronidazole in preterm neonates. However, a dosing scheme for preterm neonates that takes into consideration both the weight and PMA has been suggested and should avoid administration of doses that are excessive or more frequent than necessary. Pediatrics 2011;127:e367-e374
引用
收藏
页码:E367 / E374
页数:8
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