Video laryngoscopy versus direct laryngoscopy for pediatric emergency tracheal intubation: a systematic review and meta-analysis
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Updated: Oct 31, 2026

Guidelines for Elective Pediatric Fiberoptic Intubation
Published on: January 17, 2011
Thomaz Bittencourt Couto1,2, Jason Acworth3,4, Leandra Rech5
1Emergency Department, Instituto da Criança e do Adolescente do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, Brazil.
Aim:
To compare video laryngoscopy with direct laryngoscopy for pediatric intubation during cardiac arrest and peri-arrest scenarios.
Methods:
This systematic review (PROSPERO CRD420251081694) searched MEDLINE, Embase, and Cochrane from inception to May 1, 2026. Two authors independently screened studies; data were extracted by one and independently verified by a second reviewer. Eligible studies compared video versus direct laryngoscopy in pediatric acute care; emergency department, intensive care, and prehospital settings. Risk of bias was assessed using ROBINS-I and RoB2. Critical outcomes were survival to hospital discharge, first-pass intubation success, overall intubation success, and severe tracheal intubation-associated events. Additional data included study design, setting, age, operator type, and device. Meta-analyses used random-effects Mantel-Haenszel models reporting risk ratios (RR) with 95% confidence intervals. Certainty of evidence was assessed using GRADE.
Results:
Eighteen studies (17 observational, 1 RCT). First-pass success was higher with video laryngoscopy (72.2% vs 69.0%; RR 1.11, 95% CI 1.06-1.16; very low certainty). Severe adverse events were less frequent with video laryngoscopy (7.7% vs 11.8%; RR 0.76, 95% CI 0.62-0.93; very low certainty). Overall success (RR 1.00, 95% CI 0.99-1.01) and desaturation (RR 0.88, 95% CI 0.77-1.01) were similar. No studies reported survival outcomes or data specific to cardiac arrest.
Conclusion:
Among children undergoing emergency tracheal intubation, video laryngoscopy may be associated with improved first-pass success and fewer adverse events, although the certainty of evidence is very low and causal inferences are limited. No data were available for survival outcomes and cardiac arrest.
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