与儿童外周血管活性输液相关的局部不良事件:用元分析进行系统性审查
Jun Takeshita1, Atsushi Kawaguchi2, Tatsuya Kawasaki3
1Department of Anesthesiology, Osaka Prefectural Hospital Organization, Osaka Women's and Children's Hospital, Osaka, Japan.
Journal of cardiothoracic and vascular anesthesia
|September 3, 2024
概括
周围输注的血管活性剂如上腺素和上腺素在儿童中具有较低的局部不良事件的发生率. 这一系统性审查支持在必要时对重症儿科患者进行考虑.
科学领域:
- 儿科重症监护医学 儿科重症监护医学
- 药理学 药理学是指药理学的学科.
- 基于证据的医学基于证据的医学.
背景情况:
- 之前的研究表明,在儿童接受外周血管活性剂输液时,局部不良事件很少发生.
- 然而,之前的分析包括了有限的患者数量,主要集中在多巴胺上.
研究的目的:
- 系统地审查和分析输注血管活性剂 (上腺素,北上腺素) 的安全性,通过外周静脉或骨内接入,在重症儿童中.
- 为了确定局部不良事件的发生率,如外流或透.
主要方法:
- 更新了MEDLINE (PubMed) 和柯克兰控制试验中央注册表的系统审查和元分析.
- 包括12项观察性研究和1项随机对照试验.
主要成果:
- 对于外周静脉或骨内通道的局部不良事件的综合发病率: 2.1% (95% CI: 0.8%-3.9%).
- 仅对外围静脉导管的综合发病率:2.3% (95% CI:1.0%-4.0%).
- 仅用于骨内接入的综合发病率: 1.1% (95% CI: 0.0%-9.8%).
结论:
- 与临界血管活性输注相关的局部不良事件发生率在重症儿童中很低.
- 周围输注血管活性剂,包括上腺素和上腺素,在临床上适用时是可行的选择.
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