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甲磺酸酚妥拉明在儿科患者血压控制中的药代动力学和药效学。

Pharmacokinetics And Pharmacodynamics Of Fenoldopam Mesylate For Blood Pressure Control In Pediatric Patients.

机构信息

Departments of Anesthesia and Pediatrics, Stanford University School of Medicine, Stanford, USA.

出版信息

BMC Anesthesiol. 2008 Oct 6;8:6. doi: 10.1186/1471-2253-8-6.

Abstract

BACKGROUND

Fenoldopam mesylate, a selective dopamine1-receptor agonist, is used by intravenous infusion to treat hypertension in adults. Fenoldopam is not approved by the FDA for use in children; reports describing its use in pediatrics are limited. In a multi-institutional, placebo controlled, double-blind, multi-dose trial we determined the pharmacokinetic (PK) and pharmacodynamic (PD) characteristics and side-effect profile of fenoldopam in children.

METHODS

Seventy seven (77) children from 3 weeks to 12 years of age scheduled for surgery in which deliberate hypotension would be induced were enrolled. Patients were randomly assigned to one of five, blinded treatment groups (placebo or fenoldopam 0.05, 0.2, 0.8, or 3.2 mcg/kg/min iv) for a 30-minute interval after stabilization of anesthesia and placement of vascular catheters. Following the 30-minute blinded interval, investigators adjusted the fenoldopam dose to achieve a target mean arterial pressure in the open-label period until deliberate hypotension was no longer indicated (e.g., muscle-layer closure). Mean arterial pressure and heart rate were continuously monitored and were the primary endpoints.

RESULTS

Seventy-six children completed the trial. Fenoldopam at doses of 0.8 and 3.2 mcg/kg/min significantly reduced blood pressure (p < 0.05) during the blinded interval, and doses of 1.0-1.2 mcg/kg/min resulted in continued control of blood pressure during the open-label interval. Doses greater than 1.2 mcg/kg/min during the open-label period resulted in increasing heart rate without additional reduction in blood pressure. Fenoldopam was well-tolerated; side effects occurred in a minority of patients. The PK/PD relationship of fenoldopam in children was determined.

CONCLUSION

Fenoldopam is a rapid-acting, effective agent for intravenous control of blood pressure in children. The effective dose range is significantly higher in children undergoing anesthesia and surgery (0.8-1.2 mcg/kg/min) than as labeled for adults (0.05-0.3 mcg/kg/min). The PK and side-effect profiles for children and adults are similar.

摘要

背景

甲磺酸酚妥拉明,一种选择性多巴胺 1 受体激动剂,通过静脉输注用于治疗成人高血压。美国食品和药物管理局 (FDA) 尚未批准将其用于儿童;有关其在儿科中应用的报告有限。在一项多机构、安慰剂对照、双盲、多剂量试验中,我们确定了甲磺酸酚妥拉明在儿童中的药代动力学(PK)和药效学(PD)特征和副作用特征。

方法

从 3 周至 12 岁计划接受手术的 77 名儿童被纳入研究。患者被随机分配到五个盲法治疗组之一(安慰剂或甲磺酸酚妥拉明 0.05、0.2、0.8 或 3.2 mcg/kg/min 静脉),在麻醉稳定和放置血管导管后 30 分钟间隔内。在 30 分钟盲法间隔后,研究人员在开放标签期调整甲磺酸酚妥拉明剂量,以达到目标平均动脉压,直至不再需要故意低血压(例如,肌肉层闭合)。连续监测平均动脉压和心率,作为主要终点。

结果

76 名儿童完成了试验。在盲法间隔期间,0.8 和 3.2 mcg/kg/min 的甲磺酸酚妥拉明剂量显著降低血压(p < 0.05),而 1.0-1.2 mcg/kg/min 的剂量导致开放标签间隔期间血压持续控制。在开放标签期间,剂量大于 1.2 mcg/kg/min 会导致心率增加而血压无进一步降低。甲磺酸酚妥拉明耐受良好;少数患者出现副作用。确定了儿童中甲磺酸酚妥拉明的 PK/PD 关系。

结论

甲磺酸酚妥拉明是一种快速作用、有效的儿童静脉内血压控制药物。在接受麻醉和手术的儿童中,有效剂量范围明显高于成人(0.8-1.2 mcg/kg/min)的标签剂量(0.05-0.3 mcg/kg/min)。儿童和成人的 PK 和副作用特征相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d75/2576052/164aeff9ead4/1471-2253-8-6-1.jpg

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