Rausa Jacqueline, Loomba Rohit S, Dorsey Vincent, Chandra Priya, Penk Jamie S, Flores Saul, Villarreal Enrique G, Goldstein Stuart L
Division of Pediatric Critical Care, Advocate Children's Hospital/Chicago Medical School, Chicago, Illinois, United States.
Division of Critical Care Medicine, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, United States.
J Pediatr Intensive Care. 2021 Feb 19;11(4):294-299. doi: 10.1055/s-0041-1724095. eCollection 2022 Dec.
This retrospective study aimed to determine if fenoldopam is associated with a decrease in fluid balance and to define the factors that may promote this in children with a history of congenital heart disease at the cardiac intensive care unit (CICU). Patients cared from January 2014 to December 2018 in the CICU were reviewed, and those on fenoldopam infusion were identified. Patient cohort data included demographics, clinical information, laboratory results, hemodynamic and urine output measurements, and information regarding fenoldopam infusion were compared between those with and without decrease in fluid balance. Forty-six patients were identified. Patients received a starting dose of fenoldopam of 0.2 mcg/kg/h, a maximum dose of 0.3 mcg/kg/h, and duration of 64 hours. Over the 4-hour study period, statistically significant change was noted in systolic pressure (decrease of 5.4%; < 0.001), diastolic pressure (decrease of 3.5%; = 0.01), fluid balance, and urine output (decrease of 1.3%; = 0.027). In the cohort, 34 patients (74%) had a decrease in fluid balance, 18 (39%) had an increase in urine output, and 25 (54%) had a decrease in fluid input after the initiation of fenoldopam. Patients that had a decrease in fluid balance tended to have a higher blood urea nitrogen level at the time of fenoldopam initiation. Fenoldopam was associated with decrease in fluid balance and fluid input, but not associated with an increase in urine output. The identification of factors that can decrease fluid balance may help identify those patients who can be benefited with this treatment.
这项回顾性研究旨在确定非诺多泮是否与液体平衡的减少有关,并确定在心脏重症监护病房(CICU)中可能促进先天性心脏病患儿出现这种情况的因素。对2014年1月至2018年12月在CICU接受治疗的患者进行了回顾,并确定了接受非诺多泮输注的患者。比较了有和没有液体平衡减少的患者队列数据,包括人口统计学、临床信息、实验室结果、血流动力学和尿量测量以及关于非诺多泮输注的信息。共确定了46例患者。患者接受的非诺多泮起始剂量为0.2 mcg/kg/h,最大剂量为0.3 mcg/kg/h,持续时间为64小时。在4小时的研究期间,收缩压(下降5.4%;P<0.001)、舒张压(下降