Liviskie Caren J, DeAvilla Kathryn M, Zeller Brandy N, Najaf Tasnim, McPherson Christopher C
Department of Pharmacy, St. Louis Children's Hospital One Children's Place, St. Louis, MO, 63110, USA.
Southern Illinois University in Edwardsville School of Pharmacy, 200 University Park Dr, Edwardsville, IL, 62025, USA.
Pediatr Cardiol. 2019 Jun;40(5):1041-1045. doi: 10.1007/s00246-019-02113-3. Epub 2019 May 7.
Extracorporeal membrane oxygenation (ECMO) is one of the primary reasons systemic hypertension is experienced in hospitalized neonates. Commonly used antihypertensive agents have resulted in significant adverse effects in neonatal and pediatric populations. Nicardipine is a desirable option because of its rapid and titratable antihypertensive properties and low incidence of adverse effects. However, data for use in neonatal ECMO are limited. We conducted a retrospective review of patients less than 44 weeks post-menstrual age who received a nicardipine infusion for first-line treatment of systemic hypertension while on ECMO at our institution between 2010 and 2016. Systolic (SBP), diastolic (DBP), and mean arterial (MAP) blood pressures were evaluated for 48-h after nicardipine initiation. Eight neonates received a nicardipine infusion while on ECMO during the study period. Nicardipine was initiated at a mean dose of 0.52 ( ± 0.22) mcg/kg/min and titrated to a maximum dose of 1.1 ( ± 0.85) mcg/kg/min. The median duration of nicardipine use was 51 (range 4-227) hours. Significant decreases in SBP, DBP, and MAP occurred within one hour of initiation of nicardipine and were sustained through the majority of the 48-h evaluation period. No patients experienced hypotension. Prospective studies are warranted to evaluate the optimal dose, safety, and efficacy of nicardipine in neonates who require ECMO.
体外膜肺氧合(ECMO)是住院新生儿发生全身性高血压的主要原因之一。常用的抗高血压药物在新生儿和儿科人群中会产生显著的不良反应。尼卡地平是一个理想的选择,因为它具有快速且可滴定的降压特性以及较低的不良反应发生率。然而,用于新生儿ECMO的数据有限。我们对2010年至2016年间在我院接受尼卡地平输注作为全身性高血压一线治疗的胎龄小于44周的患者进行了回顾性研究。在开始使用尼卡地平后48小时内评估收缩压(SBP)、舒张压(DBP)和平均动脉压(MAP)。在研究期间,有8名新生儿在接受ECMO治疗时接受了尼卡地平输注。尼卡地平起始平均剂量为0.52(±0.22)微克/千克/分钟,滴定至最大剂量1.1(±0.85)微克/千克/分钟。尼卡地平使用的中位持续时间为51(范围4 - 227)小时。在开始使用尼卡地平后1小时内,SBP、DBP和MAP显著下降,并在48小时评估期的大部分时间内持续下降。没有患者出现低血压。有必要进行前瞻性研究以评估尼卡地平在需要ECMO的新生儿中的最佳剂量、安全性和疗效。