Efficacy and safety of fenoldopam for the treatment of hypertensive crises in children with kidney disease: a retrospective study.

IF 2.6 3区 医学 Q1 PEDIATRICS Pediatric Nephrology Pub Date : 2025-01-01 Epub Date: 2024-09-09 DOI:10.1007/s00467-024-06490-7
Nicola Bertazza Partigiani, Serena Vigezzi, Davide Meneghesso, Matteo Tinnirello, Alessandra Rosalba Brazzale, Marco Daverio, Enrico Vidal
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Abstract

Background: Hypertensive crises in children represent critical medical situations characterized by severe hypertension and potential organ damage. Fenoldopam, a dopaminergic medication, offers a viable therapeutic option for managing such clinical scenarios. We aimed to evaluate efficacy and safety of fenoldopam in the management of hypertensive urgencies and emergencies.

Methods: This retrospective analysis focused on pediatric patients affected by acute or chronic kidney disease, aged 1 month-18 years, admitted to the Pediatric Nephrology and the Pediatric Intensive Care Unit at University-Hospital of Padua, Italy, who presented with a hypertensive crisis treated with fenoldopam between March 2010 and December 2022.

Results: The study included 74 patients with median age 10 years (interquartile range [IQR] 4-15 years) who received 102 fenoldopam infusions. Seventy-two percent were already receiving antihypertensive treatment before admission. In all cases, fenoldopam was associated with a reduction of blood pressure (BP) after 8 h of treatment, but in 87% of patients reduction of the initial mean arterial pressure (MAP) was higher than 25% of calculated drop pressure. MAP normalized in 26% of cases after 24 h and in 35% after 48 h. Occurrence of hypotension was 7%, while hypokalemia was observed in 13% of cases. Patients who presented a MAP reduction not exceeding 25% of calculated drop pressure received a lower median fenoldopam dose (0.2 mcg/kg/min; IQR 0.1-0.2) compared with patients having a MAP reduction > 25% of calculated drop pressure (0.4 mcg/kg/min; IQR 0.2-0.6; p = 0.002).

Conclusions: Fenoldopam seems effective and safe for the treatment of hypertensive crises in children with kidney disease, at a starting dose of 0.2 mcg/kg/min. Strict BP monitoring is required to identify possible excessive drop pressure in the first hours of infusion.

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非诺多泮治疗肾病儿童高血压危象的有效性和安全性:一项回顾性研究。
背景:儿童高血压危象是以严重高血压和潜在器官损伤为特征的危急医疗状况。非诺多泮是一种多巴胺能药物,为处理此类临床情况提供了一种可行的治疗方案。我们旨在评估非诺多泮治疗高血压急症和紧急情况的有效性和安全性:这项回顾性分析主要针对 2010 年 3 月至 2022 年 12 月期间,意大利帕多瓦大学医院小儿肾脏内科和小儿重症监护室收治的急性或慢性肾脏病儿科患者,他们的年龄在 1 个月至 18 岁之间,都曾出现过高血压危象,并接受了非诺多泮治疗:研究共纳入74名患者,中位年龄为10岁(四分位距[IQR] 4-15岁),接受了102次非诺多泮输注。72%的患者在入院前已经接受了降压治疗。在所有病例中,非诺多泮都能在治疗 8 小时后降低血压(BP),但 87% 患者的初始平均动脉压(MAP)降幅高于计算降压的 25%。低血压发生率为 7%,低钾血症发生率为 13%。MAP 下降不超过计算降压值 25% 的患者接受的非诺多泮剂量中位数(0.2 mcg/kg/min;IQR 0.1-0.2)低于 MAP 下降超过计算降压值 25% 的患者(0.4 mcg/kg/min;IQR 0.2-0.6;P = 0.002):结论:非诺多泮治疗肾病儿童高血压危象既有效又安全,起始剂量为0.2微克/千克/分钟。需要严格监测血压,以确定在输注的最初几小时内血压可能过度下降。
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来源期刊
Pediatric Nephrology
Pediatric Nephrology 医学-泌尿学与肾脏学
CiteScore
4.70
自引率
20.00%
发文量
465
审稿时长
1 months
期刊介绍: International Pediatric Nephrology Association Pediatric Nephrology publishes original clinical research related to acute and chronic diseases that affect renal function, blood pressure, and fluid and electrolyte disorders in children. Studies may involve medical, surgical, nutritional, physiologic, biochemical, genetic, pathologic or immunologic aspects of disease, imaging techniques or consequences of acute or chronic kidney disease. There are 12 issues per year that contain Editorial Commentaries, Reviews, Educational Reviews, Original Articles, Brief Reports, Rapid Communications, Clinical Quizzes, and Letters to the Editors.
期刊最新文献
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