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高剂量速尿用于急性肾衰竭儿童:一项初步回顾性研究

High doses of furosemide in children with acute renal failure. A preliminary retrospective study.

作者信息

Prandota J

机构信息

Department of Nephrology, J. Korczak Memorial Children's Hospital, Wrocław, Poland.

出版信息

Int Urol Nephrol. 1991;23(4):383-92. doi: 10.1007/BF02549611.

Abstract

The diuretic effect of high doses of furosemide alone and furosemide plus mannitol was analysed retrospectively in 30 children with acute renal failure. In 10 children (Group 1) renal failure developed mainly during glomerulonephritis, and in 20 children (Group 2) the cause was gastroenteritis. The diuretic effects of furosemide and furosemide plus mannitol were evaluated measuring the 24-hour urine volume at the time of anuria, oliguria or normal diuresis. The highest mean single intravenous doses of furosemide were 6.5 and 14 mg/kg in Groups 1 and 2, respectively; the highest average daily doses were 10.1 and 25.5 mg/kg, respectively. A broad relationship was observed between single i.v. dose and diuretic response following administration of furosemide (1.2 to 30.8 mg/kg). In both groups of patients a statistically significant negative linear correlation was found between the daily intravenous dose of furosemide and the 24-hour urine volume. Calculations based on the obtained regression equations showed that the expected 24-hour urine volumes corresponding to daily diuresis normal for age could be obtained after administration of daily 2.8 to 1.4 mg/kg furosemide in Group 1 and 9.3 to 2.3 in Group 2. It is therefore suggested that the total daily dose of furosemide should not exceed 100 mg in children with acute renal failure. Administration of furosemide plus mannitol did not result in higher daily diuresis as compared to 24-hour urine volume obtained when furosemide was given alone. Furosemide was well tolerated. Electrolyte disturbances, especially in Group 2, were the most frequent side effects due to high doses of furosemide.

摘要

对30例急性肾衰竭患儿回顾性分析了大剂量呋塞米单独使用及呋塞米联合甘露醇的利尿效果。10例患儿(第1组)肾衰竭主要在肾小球肾炎期间发生,20例患儿(第2组)病因是胃肠炎。通过在无尿、少尿或正常利尿时测量24小时尿量来评估呋塞米及呋塞米联合甘露醇的利尿效果。第1组和第2组呋塞米的最高平均单次静脉剂量分别为6.5和14mg/kg;最高平均每日剂量分别为10.1和25.5mg/kg。静脉注射呋塞米(1.2至30.8mg/kg)后,单次静脉剂量与利尿反应之间观察到广泛的关系。两组患者中,呋塞米每日静脉剂量与24小时尿量之间均发现有统计学意义的负线性相关性。根据所得回归方程计算表明,第1组每日给予2.8至1.4mg/kg呋塞米、第2组每日给予9.3至2.3mg/kg呋塞米后,可获得与年龄正常的每日利尿相对应的预期24小时尿量。因此建议急性肾衰竭患儿呋塞米的每日总剂量不应超过100mg。与单独给予呋塞米时获得的24小时尿量相比,给予呋塞米联合甘露醇并未导致更高的每日尿量。呋塞米耐受性良好。电解质紊乱,尤其是在第2组中,是大剂量呋塞米最常见的副作用。

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