Pediatric Cardiovascular Drug Dosing in Critically Ill Children and Extracorporeal Membrane Oxygenation

被引:29
作者
Watt, Kevin [1 ]
Li, Jennifer S. [1 ]
Benjamin, Daniel K., Jr. [1 ]
Cohen-Wolkowiez, Michael [1 ]
机构
[1] Duke Univ, Duke Clin Res Inst, Dept Pediat, Durham, NC 27710 USA
关键词
cardiovascular agents; extracorporeal membrane oxygenation; pharmacology; pharmacokinetics; CONTINUOUS INTRAVENOUS FUROSEMIDE; JUNCTIONAL ECTOPIC TACHYCARDIA; CONGESTIVE-HEART-FAILURE; CLINICAL PHARMACOKINETICS; PULMONARY-HYPERTENSION; ORAL SILDENAFIL; GENTAMICIN PHARMACOKINETICS; VANCOMYCIN PHARMACOKINETICS; CONTINUOUS-INFUSION; INFANTS;
D O I
10.1097/FJC.0b013e318213aac2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiovascular disease in children is common and results in significant morbidity and mortality. The sickest children with cardiovascular disease may require support with extracorporeal membrane oxygenation (ECMO), which provides life-saving assistance for children with refractory cardiorespiratory failure. Many classes of cardiovascular drugs are used in children, but very few of these agents have been well studied in children. The knowledge gap is even more pronounced in children supported by ECMO. Pharmacokinetic (PK) data collected to date (primarily from antibiotics and sedatives) suggest that the ECMO circuit has the potential to significantly alter the PK of drugs including changes in clearance and volume of distribution. Of all cardiovascular drugs administered to children supported by ECMO, only 11 have been partially studied and reported in the medical literature. Esmolol, amiodarone, nesiritide, bumetanide, sildenafil, and prostaglandin E-1 seem to require dosing modifications in children supported by ECMO, whereas it seems that hydralazine, nicardipine, furosemide, epinephrine, and dopamine can be dosed similarly to children not supported by ECMO. However, trials evaluating the PK of these drugs in patients supported by ECMO are extremely limited (ie, case reports), and therefore, definitive dosing recommendations are not plausible. Research efforts should focus on evaluating the PK of drugs in patients on ECMO to avoid therapeutic failures or unnecessary toxicities.
引用
收藏
页码:126 / 132
页数:7
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