Department of Pediatrics Duke University, Durham, NC, USA.
J Cardiovasc Pharmacol. 2011 Aug;58(2):126-32. doi: 10.1097/FJC.0b013e318213aac2.
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 E1 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.
儿童心血管疾病很常见,会导致严重的发病率和死亡率。病情最严重的心血管疾病患儿可能需要体外膜肺氧合(ECMO)支持,这可为难治性心肺衰竭患儿提供救生援助。许多类别的心血管药物都可用于儿童,但只有少数药物在儿童中进行了充分研究。在接受 ECMO 支持的儿童中,这种知识差距更为明显。迄今为止收集的药代动力学(PK)数据(主要来自抗生素和镇静剂)表明,ECMO 回路有可能显著改变药物的 PK,包括清除率和分布容积的变化。在所有接受 ECMO 支持的儿童中,只有 11 种心血管药物部分进行了研究,并在医学文献中报告过。艾司洛尔、胺碘酮、奈西立肽、布美他尼、西地那非和前列腺素 E1 似乎需要在接受 ECMO 支持的儿童中调整剂量,而似乎肼屈嗪、尼卡地平、呋塞米、肾上腺素和多巴胺可以以与未接受 ECMO 支持的儿童相似的剂量给药。然而,评估这些药物在接受 ECMO 支持的患者中的 PK 的临床试验非常有限(即病例报告),因此,无法确定明确的剂量建议。研究工作应集中在评估 ECMO 患者的药物 PK 上,以避免治疗失败或不必要的毒性。