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对接受芬太尼持续输注的危重症儿童戒断现象的前瞻性研究。

Prospective study on the occurrence of withdrawal in critically ill children who receive fentanyl by continuous infusion.

作者信息

Katz R, Kelly H W, Hsi A

机构信息

Department of Pediatrics, College of Pharmacy and School of Medicine, University of New Mexico, Albuquerque 87107.

出版信息

Crit Care Med. 1994 May;22(5):763-7. doi: 10.1097/00003246-199405000-00009.

Abstract

OBJECTIVE

To determine the occurrence of narcotic withdrawal in critically ill children who receive continuous infusions of fentanyl.

DESIGN

Prospective case series.

SETTING

A university hospital pediatric intensive care unit.

PATIENTS

Twenty-three children, aged 1 wk to 22 months (mean 6 months), who required assisted mechanical ventilation and who received continuous infusions of fentanyl for > 24 hrs.

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

Total fentanyl dose received, length of infusion, and peak infusion rate were recorded. Patients were evaluated for narcotic withdrawal by the Neonatal Abstinence Scoring System of Finnegan. Children with scores of > or = 8 were considered to have narcotic withdrawal. Withdrawal was observed in 13 (57%) of 23 infants. Total fentanyl dose (2.96 +/- 4.10 vs. 0.53 +/- 0.37 mg/kg, p < .005) and length of fentanyl infusion (13.1 +/- 11.3 vs. 3.8 +/- 1.5 days, p < .0001) were significantly greater in those infants with narcotic withdrawal than in those infants with no withdrawal, respectively. Peak fentanyl infusion rate (9.9 +/- 7.8 vs. 9.2 +/- 4.4 micrograms/kg/hr) did not differ significantly between the two groups. A total fentanyl dose of > 2.5 mg/kg or a duration of infusion of > 9 days was 100% predictive of withdrawal.

CONCLUSIONS

Continuous infusions of fentanyl produce a high occurrence rate of narcotic withdrawal when administered to critically ill children. This effect is both dose- and duration-dependent.

摘要

目的

确定接受芬太尼持续输注的危重症儿童中麻醉剂戒断的发生率。

设计

前瞻性病例系列研究。

地点

一所大学医院的儿科重症监护病房。

患者

23名年龄在1周龄至22个月(平均6个月)之间、需要辅助机械通气且接受芬太尼持续输注超过24小时的儿童。

干预措施

无。

测量指标及主要结果

记录芬太尼总剂量、输注时间及峰值输注速率。采用芬尼根新生儿戒断评分系统对患者进行麻醉剂戒断评估。评分≥8分的儿童被视为出现麻醉剂戒断。23名婴儿中有13名(57%)出现戒断。出现麻醉剂戒断的婴儿的芬太尼总剂量(2.96±4.10 vs. 0.53±0.37 mg/kg,p<0.005)和芬太尼输注时间(13.1±11.3 vs. 3.8±1.5天,p<0.0001)分别显著高于未出现戒断的婴儿。两组间芬太尼峰值输注速率(9.9±7.8 vs. 9.2±4.4微克/千克/小时)差异无统计学意义。芬太尼总剂量>2.5 mg/kg或输注持续时间>9天对戒断的预测准确率为100%。

结论

对危重症儿童持续输注芬太尼时,麻醉剂戒断的发生率较高。这种效应与剂量和持续时间均相关。

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