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儿科急诊科急性躁动的肌内注射齐拉西酮给药:一项观察性研究。

Intramuscular Ziprasidone Dosing for Acute Agitation in the Pediatric Emergency Department: An Observational Study.

作者信息

Nguyen Tammy, Stanton Jillian, Foster Robin

机构信息

1 Department of Pharmacy, Virginia Commonwealth University Medical Center, Richmond, VA, USA.

2 Department of Emergency Medicine, Virginia Commonwealth University Medical Center, Richmond, VA, USA.

出版信息

J Pharm Pract. 2018 Feb;31(1):18-21. doi: 10.1177/0897190017692922. Epub 2017 Feb 16.

Abstract

BACKGROUND

Intramuscular (IM) ziprasidone is often used to manage acute agitation. Limited data exist on the pediatric dosing of ziprasidone in the emergency department (ED).

OBJECTIVE

To characterize the mg/kg dosing differences between pediatric ED patients who respond to an initial dose of ziprasidone versus patients who do not.

METHODS

This was a retrospective, observational study of 5- to 18-year-old patients who were treated with IM ziprasidone in the pediatric ED from 2007 to 2015. Medical records were reviewed to determine demographic and clinical information. Patients were deemed responders to ziprasidone if they required no additional rescue medication for acute agitation within 30 minutes of the initial dose.

RESULTS

Forty children received 50 doses of IM ziprasidone. Twenty-seven (68%) patients responded to the initial ziprasidone dose, requiring no further medication intervention for their acute agitation. Responders were given a mean initial dose of 0.19 ± 0.1 mg/kg, while nonresponders were given an initial mean dose of 0.13 ± 0.06 mg/kg ( P = .03).

CONCLUSION

A significant dose difference exists between patients who required only one initial dose of ziprasidone compared to those who required additional medication. As a result, an initial dose of 0.2 mg/kg of IM ziprasidone may be considered when managing acutely agitated pediatric patients in the ED.

摘要

背景

肌内注射齐拉西酮常用于处理急性激越状态。关于急诊科(ED)小儿齐拉西酮给药剂量的数据有限。

目的

描述对初始剂量齐拉西酮有反应的小儿急诊科患者与无反应患者之间每千克体重给药剂量的差异。

方法

这是一项对2007年至2015年在小儿急诊科接受肌内注射齐拉西酮治疗的5至18岁患者进行的回顾性观察研究。查阅病历以确定人口统计学和临床信息。如果患者在初始剂量后30分钟内无需额外的抢救药物来处理急性激越状态,则被视为对齐拉西酮有反应。

结果

40名儿童接受了50次肌内注射齐拉西酮。27名(68%)患者对初始齐拉西酮剂量有反应,其急性激越状态无需进一步药物干预。有反应者的平均初始剂量为0.19±0.1毫克/千克,而无反应者的初始平均剂量为0.13±0.06毫克/千克(P = 0.03)。

结论

仅需一剂初始齐拉西酮的患者与需要额外药物的患者之间存在显著的剂量差异。因此,在急诊科处理急性激越的小儿患者时,可考虑肌内注射齐拉西酮的初始剂量为0.2毫克/千克。

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