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Updated: Jan 28, 2026

Guidelines for Elective Pediatric Fiberoptic Intubation
Published on: January 17, 2011
Transnasal Humidified Rapid Insufflation Ventilatory Exchange in children requiring emergent intubation (Kids
Shane George1,2,3,4,5, Susan Humphreys3, Tara Williams3
1Children's Critical Care Service, Gold Coast University Hospital, Southport, Queensland, Australia.
Insights
Transnasal Humidified Rapid Insufflation Ventilatory Exchange (THRIVE) may reduce adverse events during pediatric emergency intubations. This trial investigates THRIVE
Area of Science:
- Pediatric Emergency Medicine
- Critical Care
- Respiratory Physiology
Background:
- Emergency intubation in children is high-risk, with frequent adverse events like hypoxemia.
- Current preoxygenation methods aim to maximize oxygen reserves but may be insufficient.
- Transnasal Humidified Rapid Insufflation Ventilatory Exchange (THRIVE) has shown promise in elective settings.
Purpose of the Study:
- To test if THRIVE reduces adverse and hypoxemic events during emergency pediatric intubations.
- To evaluate the cost-effectiveness of THRIVE compared to standard care in this population.
Main Methods:
- Multicenter randomized controlled trial (Kids THRIVE trial) in emergency departments and PICUs.
- 960 children (0-16 years) requiring emergency intubation randomized 1:1 to THRIVE or control.
- Primary outcomes: hypoxemic events (SpO2 <90%) and first-attempt intubation success without hypoxemia.
Main Results:
- Data analysis is ongoing; results will be published upon completion.
- The trial aims to provide definitive evidence on THRIVE's efficacy and safety.
Conclusions:
- The study is expected to determine if THRIVE offers a significant benefit over standard care.
- Findings will inform clinical practice guidelines for emergency airway management in children.
Introduction:
Emergency intubation of children with abnormal respiratory or cardiac physiology is a high-risk procedure and associated with a high incidence of adverse events including hypoxemia. Successful emergency intubation is dependent on inter-related patient and operator factors. Preoxygenation has been used to maximise oxygen reserves in the patient and to prolong the safe apnoeic time during the intubation phase. Transnasal Humidified Rapid Insufflation Ventilatory Exchange (THRIVE) prolongs the safe apnoeic window for a safe intubation during elective intubation. We designed a clinical trial to test the hypothesis that THRIVE reduces the frequency of adverse and hypoxemic events during emergency intubation in children and to test the hypothesis that this treatment is cost-effective compared with standard care.
Methods And Analysis:
The Kids THRIVE trial is a multicentre randomised controlled trial performed in participating emergency departments and paediatric intensive care units. 960 infants and children aged 0-16 years requiring emergency intubation for all reasons will be enrolled and allocated to THRIVE or control in a 1:1 allocation with stratification by site, age (<1, 1-7 and >7 years) and operator (junior and senior). Children allocated to THRIVE will receive weight appropriate transnasal flow rates with 100% oxygen, whereas children in the control arm will not receive any transnasal oxygen insufflation. The primary outcomes are defined as follows: (1) hypoxemic event during the intubation phase defined as SpO2 <90% (patient-dependent variable) and (2) first intubation attempt success without hypoxemia (operator-dependent variable). Analyses will be conducted on an intention-to-treat basis.
Ethics And Dissemination:
Ethics approval for the protocol and consent process has been obtained (HREC/16/QRCH/81). The trial has been actively recruiting since May 2017. The study findings will be submitted for publication in a peer-reviewed journal.
Trial Registration Number:
ACTRN12617000147381.
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