Pharmacotherapy during pediatric extracorporeal membrane oxygenation: a review

被引:19
|
作者
Himebauch, Adam S. [1 ,2 ]
Kilbaugh, Todd J. [1 ]
Zuppa, Athena F. [1 ,2 ]
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Dept Anesthesiol & Crit Care Med, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Ctr Clin Pharmacol, Philadelphia, PA 19104 USA
关键词
ECMO; pharmacokinetics; pharmacodynamics; pediatric; MECHANICAL CIRCULATORY SUPPORT; CRITICALLY-ILL CHILDREN; IN-VITRO CLEARANCE; LIFE-SUPPORT; POPULATION PHARMACOKINETICS; MORPHINE PHARMACOKINETICS; GENTAMICIN PHARMACOKINETICS; VANCOMYCIN PHARMACOKINETICS; CONTINUOUS-INFUSION; DRUG DISPOSITION;
D O I
10.1080/17425255.2016.1201066
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Pediatric critical illness and associated alterations in organ function can change drug pharmacokinetics (PK). Extracorporeal membrane oxygenation (ECMO), a life-saving therapy for severe cardiac and/or respiratory failure, causes additional PK alterations that affect drug disposition. Areas covered: The purposes of this review are to discuss the PK changes that occur during ECMO, the associated therapeutic implications, and to review PK literature relevant to pediatric ECMO. We discuss various classes of drugs commonly used for pediatric patients on ECMO, including sedatives, analgesics, antimicrobials and cardiovascular drugs. Finally, we discuss future areas of research and recommend strategies for future pediatric ECMO pharmacologic investigations. Expert opinion: Clinicians caring for pediatric patients treated with ECMO must have an understanding of PK alterations that could lead to either therapeutic failures or increased drug toxicity during this life-saving therapy. Limited data currently exist for optimal drug dosing in pediatric populations who are treated with ECMO. While there are clear challenges to conducting and analyzing data associated with clinical pharmacokinetic-pharmacodynamic studies of children on ECMO, we present techniques to address these challenges. Improved understanding of the physiology and drug disposition during ECMO combined with PK-PD modeling will allow for more adaptable and individualized dosing schemes.
引用
收藏
页码:1133 / 1142
页数:10
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