Moffett Brady S, Mott Antonio R, Nelson David P, Goldstein Stuart L, Jefferies John Lynn
Texas Children's Hospital, Department of Pharmacy, Houston, TX, USA.
Pediatr Crit Care Med. 2008 Jul;9(4):403-6. doi: 10.1097/PCC.0b013e3181728c25.
Published data describe the use of fenoldopam in adults for treatment of oliguria/anuria and for renal perfusion and protection, but pediatric data are scant. We assessed the effects of fenoldopam on urine output and potential deleterious changes in hemodynamics or serum creatinine in children.
Retrospective analysis.
Academic institution.
: All patients <or=18 yrs old at our institution who received >or=24 hrs of fenoldopam therapy. Exclusion criteria included mechanical circulatory support, initiation of fenoldopam in the operating room, and age >18 yrs.
None.
Demographics, renal function, fenoldopam dosing, concomitant inotropes, and inotrope score data were collected and analyzed. Thirteen patients (age 0.3-18.7 yrs, median 5.5 yrs) received a mean infusion dose of 0.07 +/- 0.08 microg/kg/min (range 0.01-0.26 microg/kg/min) over the first 24 hrs of therapy. Eight patients received fenoldopam to augment urine output, and five patients received fenoldopam to increase renal perfusion. Nine (69%) patients received dopamine concurrently. Mean inotrope score at the beginning of therapy was 11.3 +/- 7.6 and did not change during therapy. Mean urine output increased from 1.82 +/- 1.5 mL/kg/hr to 2.74 +/- 1.4 mL/kg/hr (p = .009) in the first 24 hrs of fenoldopam therapy. No change in serum creatinine occurred (p not significant). Blood urea nitrogen was significantly different from baseline (41.7 +/- 18.7 vs. 49.0 +/- 19.8 mg/dL, p = .02). Patients with lower baseline urine output had a greater increase in urine output with fenoldopam. One patient experienced clinically significant hypotension while receiving fenoldopam, which was thought to be due to a concurrent nitroprusside infusion.
Fenoldopam increases urine output in select critically ill pediatric patients without requiring escalation of inotropic support. There were no adverse hemodynamic effects or alterations in serum creatinine. Further prospective pediatric studies to define the role of fenoldopam in children are warranted.
已发表的数据描述了非诺多泮在成人中用于治疗少尿/无尿以及肾脏灌注和保护,但儿科数据很少。我们评估了非诺多泮对儿童尿量以及血流动力学或血清肌酐潜在有害变化的影响。
回顾性分析。
学术机构。
我们机构中所有年龄≤18岁且接受非诺多泮治疗≥24小时的患者。排除标准包括机械循环支持、在手术室开始使用非诺多泮以及年龄>18岁。
无。
收集并分析人口统计学、肾功能、非诺多泮剂量、同时使用的血管活性药物以及血管活性药物评分数据。13例患者(年龄0.3 - 18.7岁,中位数5.5岁)在治疗的最初24小时内接受的平均输注剂量为0.07±0.08微克/千克/分钟(范围0.01 - 0.26微克/千克/分钟)。8例患者使用非诺多泮以增加尿量,5例患者使用非诺多泮以增加肾脏灌注。9例(69%)患者同时使用多巴胺。治疗开始时的平均血管活性药物评分为11.3±7.6,治疗期间未发生变化。在非诺多泮治疗的最初24小时内,平均尿量从1.82±1.5毫升/千克/小时增加至2.74±1.4毫升/千克/小时(p = 0.009)。血清肌酐未发生变化(p无统计学意义)。血尿素氮与基线相比有显著差异(41.7±18.7对49.0±19.8毫克/分升,p = 0.02)。基线尿量较低的患者使用非诺多泮后尿量增加幅度更大。1例患者在接受非诺多泮治疗时出现临床上显著的低血压,认为这是由于同时输注硝普钠所致。
非诺多泮可增加部分危重症儿科患者的尿量,而无需增加血管活性药物支持。未观察到不良血流动力学效应或血清肌酐改变。有必要进行进一步的前瞻性儿科研究以明确非诺多泮在儿童中的作用。