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Apnoeic Oxygenation by Nasal Cannula During Airway Management in Children Undergoing General Anaesthesia.

U

University of Birmingham

Status

Completed

Conditions

Apnoeic Oxygenation

Treatments

Device: Apnoeic oxygenation

Study type

Interventional

Funder types

Other

Identifiers

NCT03271827
SP15/134

Details and patient eligibility

About

Airway management is a core clinical skill in anaesthesia. Pre-oxygenation prior to induction of anaesthesia is standard practice to prevent desaturation. Apnoeic oxygenation in adults is effective and prolongs the time to desaturation. The effectiveness of apnoeic oxygenation in the adult is well document, however evidence in the paediatric is lacking. Therefore, the aim of this study was to investigate the effectiveness of apnoeic oxygenation during airway management in children.

This was a pilot randomised controlled trial. Patients were randomised to either receive apnoeic oxygenation or standard care during the induction of anaesthesia. The primary outcome was the duration of safe apnoea, defined as a composite of the time to first event, either time for SpO2 to drop to 92% or time to successfully secure the airway, and the lowest SpO2 observed during airway management. Secondary outcomes were number of patients whose SpO2 dropped below 95% and number of patients whose SpO2 dropped below 92%.

Enrollment

30 patients

Sex

All

Ages

1 to 8 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients were included who were scheduled for elective surgery under general anaesthesia.
  • Age: one eight years old.
  • ASA I and II only.
  • Patients with normal cardiorespiratory function.

Exclusion criteria

  • Children undergoing dental surgeries in which nasal intubation is needed.
  • Patients who suffered from quick drops in oxygen saturation more rapidly than healthy children due to different reasons such as: respiratory and pulmonary diseases, active or recent upper respiratory tract infection, syndromes with cardiopulmonary pathologies, cardiac anomalies, anaemia, depressed respiratory effort, ventilation/perfusion imbalance, Obstructive Sleep Apnoea (OSA), and airway obstruction.
  • Patients reported with nasal obstruction.
  • Patients with grades of laryngoscopic view (Cormack Lahane) greater than II, which indicates upper airway obstruction.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Apnoeic oxygenation group
Experimental group
Description:
Standard airway management + 3 L/min of oxygen by nasal cannula
Treatment:
Device: Apnoeic oxygenation
Standard care group
No Intervention group
Description:
Standard airway management

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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