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儿科患者对慢性间歇性呋塞米治疗的耐受性发展

Development of Tolerance to Chronic Intermittent Furosemide Therapy in Pediatric Patients.

作者信息

Kim Gloria J, Capparelli Edmund, Romanowski Gale, Proudfoot James A, Tremoulet Adriana H

机构信息

Department of Clinical Pharmacy (GJK, GR, AHT), Rady Children's Hospital San Diego, California, Department of Pediatrics (EC, AHT), University of California, San Diego, Clinical and Translational Research Institute (JAP), University of California, San Diego.

出版信息

J Pediatr Pharmacol Ther. 2017 Nov-Dec;22(6):394-398. doi: 10.5863/1551-6776-22.6.394.

Abstract

OBJECTIVES

The purpose of this study is to describe whether tolerance develops in pediatric patients receiving chronic intermittent furosemide therapy, to characterize when it occurs and whether age-related variations exist. The effects of increasing total daily dose of furosemide and concurrent diuretics and vasopressors were assessed as secondary aims.

METHODS

Charts from patients receiving intravenous or oral furosemide for at least 3 consecutive days of therapy between June 1, 2013, and December 31, 2013, were reviewed retrospectively. Daily net fluid balance was used as the objective marker for development of tolerance. Net fluid balance (mL/kg/mg) was defined as the difference in a patient's daily intake and urine output (mL), normalized by weight (kg) and total daily dose of furosemide (mg).

RESULTS

Sixty-one patients, aged 2 days to 20 years (median 3 years), were included in this study. Median daily dose of furosemide was 1.96 mg/kg/day (range, 0-13.7 mg/kg/day). Average net fluid balance for all patients on the first day and last day of therapy was 6.83 and 26.66 mL/kg/mg, respectively (p = 0.011). Linear regression and Spearman's correlation found no significant relationship between age and difference in net fluid balance between the first and last day. Linear mixed-effects model for net fluid balance with day as covariate found that net fluid balance increases over time (p = 0.002).

CONCLUSIONS

Pediatric patients appear to develop tolerance to chronic intermittent furosemide therapy.

摘要

目的

本研究旨在描述接受慢性间歇性呋塞米治疗的儿科患者是否会产生耐受性,确定耐受性何时出现以及是否存在与年龄相关的差异。评估增加呋塞米每日总剂量以及同时使用利尿剂和血管加压药的效果作为次要目的。

方法

回顾性分析2013年6月1日至2013年12月31日期间接受静脉或口服呋塞米治疗至少连续3天的患者病历。每日净液体平衡用作耐受性发展的客观指标。净液体平衡(mL/kg/mg)定义为患者每日摄入量与尿量(mL)之差,按体重(kg)和呋塞米每日总剂量(mg)进行标准化。

结果

本研究纳入了61例年龄在2天至20岁(中位数3岁)的患者。呋塞米的中位数每日剂量为1.96 mg/kg/天(范围为0 - 13.7 mg/kg/天)。所有患者在治疗第一天和最后一天的平均净液体平衡分别为6.83和26.66 mL/kg/mg(p = 0.011)。线性回归和Spearman相关性分析发现年龄与第一天和最后一天净液体平衡差异之间无显著关系。以天数为协变量的净液体平衡线性混合效应模型发现净液体平衡随时间增加(p = 0.002)。

结论

儿科患者似乎会对慢性间歇性呋塞米治疗产生耐受性。

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