Dexmedetomidine pharmacokinetics in pediatric intensive care - a pooled analysis

被引:131
|
作者
Potts, Amanda L. [1 ]
Anderson, Brian J. [1 ]
Warman, Guy R. [1 ]
Lerman, Jerrold [2 ,3 ]
Diaz, Susan M. [4 ,5 ]
Vilo, Sanna [6 ]
机构
[1] Univ Auckland, Dept Anaesthesiol, Auckland 1, New Zealand
[2] SUNY Buffalo, Women & Childrens Hosp Buffalo, Buffalo, NY 14260 USA
[3] Univ Rochester, Strong Mem Hosp, Rochester, NY 14642 USA
[4] Rady Childrens Hosp & Hlth Ctr, Albuquerque, NM USA
[5] Presbyterian Healthcare Serv, Albuquerque, NM USA
[6] Turku Univ Hosp, Dept Anaesthesiol Intens Care Emergency Care & Pa, FIN-20520 Turku, Finland
关键词
dexmedetomidine; pharmacokinetics; children; allometrics; DOSE DEXMEDETOMIDINE; CHILDREN; SEDATION; INFUSION; SIZE; PHARMACODYNAMICS; INFANTS; RAT; BUPIVACAINE; VOLUNTEERS;
D O I
10.1111/j.1460-9592.2009.03133.x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
P>Background: Published dexmedetomidine pharmacokinetic studies in children are limited by participant numbers and restricted pathology. Pooling the available studies allows investigation of covariate effects. Methods: Data from four studies investigating dexmedetomidine pharmacokinetics after i.v. administration (n = 95) were combined to undertake a population pharmacokinetic analysis of dexmedetomidine time-concentration profiles (730 observations) using nonlinear mixed effects modeling (NONMEM). Estimates were standardized to a 70-kg adult using allometric size models. Results: Children had a mean age of 3.8 (median 3 years, range 1 week-14 years) and weight of 16.0 kg (median 13.3 kg, range 3.1-58.9 kg). Population parameter estimates (between subject variability) for a two-compartment model were clearance (CL) 42.1 (CV 30.9%) l center dot h-1 center dot 70 kg-1, central volume of distribution (V1) 56.3 (61.3%) l center dot 70 kg-1, inter-compartment clearance (Q) 78.3 (37.0%) l center dot h-1 center dot 70 kg-1 and peripheral volume of distribution (V2) 69.0 (47.0%) l center dot 70 kg-1. Clearance maturation with age was described using the Hill equation. Clearance increases from 18.2 l center dot h-1 center dot 70 kg-1 at birth in a term neonate to reach 84.5% of the mature value by 1 year of age. Children given infusion after cardiac surgery had 27% reduced clearance compared to a population given bolus dose. Simulation of published infusion rates that provide adequate sedation for intensive care patients found a target therapeutic concentration of between 0.4 and 0.8 mu g center dot l-1. Conclusions: The sedation target concentration is similar to that described for adults. Immature clearance in the first year of life and a higher clearance (when expressed as l center dot h-1 center dot kg-1) in small children dictate infusion rates that change with age. Extrapolation of dose from children given infusion in intensive care after cardiac surgery may not be applicable to those sedated for noninvasive procedures out of intensive care.
引用
收藏
页码:1119 / 1129
页数:11
相关论文
共 50 条
  • [31] Dexmedetomidine Applications in Pediatric Critical Care: Closer but There Is Still Work to Do
    Berkenbosch, John W.
    PEDIATRIC CRITICAL CARE MEDICINE, 2020, 21 (07) : 683 - 684
  • [32] Highly variable pharmacokinetics of dexmedetomidine during intensive care: A case report
    Iirola T.
    Laitio R.
    Kentala E.
    Aantaa R.
    Kurvinen J.-P.
    Scheinin M.
    Olkkola K.T.
    Journal of Medical Case Reports, 4 (1)
  • [33] Research in Pediatric Intensive Care
    Prout, Andrew
    Meert, Kathleen L.
    PEDIATRIC CLINICS OF NORTH AMERICA, 2022, 69 (03) : 607 - 620
  • [34] The use of dexmedetomidine in intensive care sedation
    Antonelli, Massimo
    Conti, Giorgio
    Belisari, Andrea
    D'Angiolella, Lucia S.
    Mantovani, LorenzoG.
    Montella, Sabato
    Piacentini, Patrizio
    Ranieri, Marco
    FARMECONOMIA-HEALTH ECONOMICS AND THERAPEUTIC PATHWAYS, 2013, 14 : 3 - 28
  • [35] Sedation with dexmedetomidine in the intensive care setting
    Gerlach, Anthony T.
    Murphy, Claire V.
    OPEN ACCESS EMERGENCY MEDICINE, 2011, 3 : 77 - 85
  • [36] Pharmacokinetics of intravenous dexmedetomidine in children under 11 yr of age
    Vilo, S.
    Rautiainen, P.
    Kaisti, K.
    Aantaa, R.
    Scheinin, M.
    Manner, T.
    Olkkola, K. T.
    BRITISH JOURNAL OF ANAESTHESIA, 2008, 100 (05) : 697 - 700
  • [37] Pharmacokinetics and pharmacodynamics of dexmedetomidine-induced vasoconstriction in healthy volunteers
    Talke, Pekka
    Anderson, Brian J.
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2018, 84 (06) : 1364 - 1372
  • [38] The Pharmacokinetics of Beta-Lactam Antibiotics Using Scavenged Samples in Pediatric Intensive Care Patients: The EXPAT Kids Study Protocol
    Schouwenburg, Stef
    Wildschut, Enno D.
    de Hoog, M.
    Koch, Birgit C. P.
    Abdulla, Alan
    FRONTIERS IN PHARMACOLOGY, 2021, 12
  • [39] Pain Assessment Practices in the Pediatric Intensive Care Unit
    Laures, Elyse
    LaFond, Cynthia
    Hanrahan, Kirsten
    Pierce, Nicole
    Min, Haeyoung
    McCarthy, Ann Marie
    JOURNAL OF PEDIATRIC NURSING-NURSING CARE OF CHILDREN & FAMILIES, 2019, 48 : 55 - 62
  • [40] Growing up with Midazolam in the Neonatal and Pediatric Intensive Care
    Swart, Eleonora L.
    Slort, Pauline R.
    Plotz, Frans B.
    CURRENT DRUG METABOLISM, 2012, 13 (06) : 760 - 766