Effects of avoidance versus use of neuromuscular blocking agents for facilitation of tracheal intubation in children and infants

被引:1
作者
Christensen, Michelle Icka [1 ]
Vested, Matias [1 ,2 ]
Creutzburg, Andreas [1 ]
Norskov, Anders Kehlet [3 ]
Lundstrom, Lars Hyldborg [2 ,3 ]
Afshari, Arash [2 ,4 ]
机构
[1] Copenhagen Univ Hosp, Rigshosp, Ctr Head & Orthoped, Operat & Trauma Ctr,Dept Anesthesiol, Copenhagen, Denmark
[2] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[3] Copenhagen Univ Hosp, Nordsjaellands Hosp, Dept Anesthesiol, Hillerod, Denmark
[4] Copenhagen Univ Hosp, Rigshospitalet, Juliane Marie Ctr, Dept Anesthesiol & Operat, Copenhagen, Denmark
关键词
difficult laryngoscopy; difficult tracheal intubation; failed intubation; protocol; systematic review; upper airway injury; AIRWAY MANAGEMENT; DIFFICULT AIRWAY; ANESTHESIA; COMPLICATIONS; METAANALYSIS; AUDIT;
D O I
10.1111/aas.14429
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: The European Society of Anesthesiology and Intensive Care recommends the use of neuromuscular blocking agents (NMBA) in adults, to facilitate tracheal intubation and reduce its associated complications. Children who under got racheal intubation may suffer some of the same complications, however, no consensus exists regarding the use of NMBA for tracheal intubation in the pediatric population. We will explore the existing evidence assessing the effects of avoidance versus the use of NMBA for the facilitation of tracheal intubation in children and infants. Methods: This protocol follows the preferred reporting items for systematic reviewsand meta-analyses protocols recommendations. We will include all randomized con-trolled clinical trials assessing the effects of avoidance versus the use of NMBA for facilitation of tracheal intubation (oral or nasal) using direct laryngoscopy or video laryngoscopy in pediatric participants (<18 years). Our primary outcome is incidence of difficult tracheal intubation. Secondary outcomes include incidence of seriou adverse events, failed intubation, events of upper airway discomfort or injury, and difficult laryngoscopy. We will conduct a thorough database search to identify relevant trials, including CEN-TRAL, MEDLINE, EMBASE, BIOSIS, Web of Science, CINAHL, and trial registries. Two review authors will independently handle the screening of literature and datextraction. Each trial will be evaluated for major sources of bias with the "classic risk of bias tool" used in the Cochrane Collaboration tool from 2011. We will use Review manager (RevMan) or R with the meta package to perform the meta-analysis. We wil perform a trial sequential analysis on the meta-analysis of our primary outcome, pro-viding an estimate of statistical reliability. Two review authors will independently assess the quality of the body of evidence using the grading of recommendations assessment, development, and evaluation(GRADE) approach. We will use GRADE pro software to conduct the GRADE assessments and to create "Summary of the findings "tables.
引用
收藏
页码:1094 / 1100
页数:7
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