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
  • [21] Impact of Dexmedetomidine on Pediatric Agitation in the Postanesthesia Care Unit
    Li, Hongyan
    Zhang, Longming
    Shi, Min
    Yang, Shengqiang
    Li, Shengde
    Gao, Shenqiang
    JOURNAL OF PERIANESTHESIA NURSING, 2018, 33 (01) : 53 - 57
  • [22] Comparison of dexmedetomidine with chloral hydrate as sedatives for pediatric patients A systematic review and meta-analysis
    Lian, Xianghong
    Lin, Yunzhu
    Luo, Ting
    Yuan, Hongbo
    Chen, Yuan
    MEDICINE, 2020, 99 (31) : E21008
  • [23] Prolonged use of dexmedetomidine in the paediatric cardiothoracic intensive care unit
    Bejian, Sharon
    Valasek, Cassie
    Nigro, John J.
    Cleveland, David C.
    Willis, Brigham C.
    CARDIOLOGY IN THE YOUNG, 2009, 19 (01) : 98 - 104
  • [24] Pharmacokinetics and pharmacodynamics of dexmedetomidine
    Li, Aiwei
    Yuen, Vivian Man Ying
    Goulay-Dufay, Sophie
    Kwok, Philip Chi Lip
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2016, 42 (12) : 1917 - 1927
  • [25] An unintentional overdose of dexmedetomidine in the pediatric intensive care unit
    Sud, Payal
    Choi, Andrew
    Nogar, Joshua
    CLINICAL TOXICOLOGY, 2013, 51 (07) : 600 - 600
  • [26] Safety of dexmedetomidine in the cardiac intensive care unit
    Adie, Sarah K.
    Farina, Nicholas
    Abdul-Aziz, Ahmad A.
    Lee, Ran
    Thomas, Michael P.
    Konerman, Matthew C.
    EUROPEAN HEART JOURNAL-ACUTE CARDIOVASCULAR CARE, 2021, 10 (04) : 422 - 426
  • [27] Adverse cardiovascular events are common during dexmedetomidine administration in neonates and infants during intensive care
    Tervonen, Miikka
    Cajanus, Johanna
    Kallio, Merja
    Huhtamaki, Heikki
    Pokka, Tytti
    Peltoniemi, Outi
    ACTA PAEDIATRICA, 2023, 112 (11) : 2338 - 2345
  • [28] Efficacy of sedation regimens to facilitate mechanical ventilation in the pediatric intensive care unit: A systematic review
    Hartman, Mary E.
    McCrory, Douglas C.
    Schulman, Scott R.
    PEDIATRIC CRITICAL CARE MEDICINE, 2009, 10 (02) : 246 - 255
  • [29] Dexmedetomidine. Pharmacokinetics and pharmacodynamics
    Ihmsen, H.
    Saari, T. I.
    ANAESTHESIST, 2012, 61 (12): : 1059 - +
  • [30] Evaluation of drug formularies for pediatric intensive care
    Ceelie, Ilse
    van der Starre, Cynthia
    Tibboel, Dick
    Stol, Kim
    Koren, Gideon
    de Wildt, Saskia N.
    PEDIATRIC CRITICAL CARE MEDICINE, 2011, 12 (01) : E14 - E19