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Effect of Head Position on MACEI of Sevoflurane in Children With Obstructive Airway

Effect of Head Position on Minimum Alveolar Concentration of Endotracheal Intubation(MACEI)of Sevoflurane in Children With Obstructive Airway

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03522402
Acronym
MACEI
Enrollment
38
Registered
2018-05-11
Start date
2018-01-01
Completion date
2018-10-31
Last updated
2018-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endotracheal Intubation, Sevoflurane

Keywords

head position, obstructive airway, minimum alveolar concentration(MACendotracheal intubation), sevoflurane concentration

Brief summary

Children scheduled for tonsillectomy surgery were recruited into the study. General anesthesia was induced with 8% sevoflurane inhaled with 8 l.min-1 of oxygen via mask, followed by adjustment of inspired sevoflurane to the target concentration based on the result in previous patient at which laryngoscopy and tracheal intubation were attempted and maintained for 12 min. All responses to tracheal intubation were assessed. At the end of the procedure, sevoflurane was titrated to the target concentration, which was kept constant for 12 min before a standard stimulus was applied to determine whether the children was awake. The Dixon's 'up and down'method was used to determine progression of subsequent concentrations.The aim of this study was to determine whether the minimum alveolar concentration of endotracheal intubation(MACEI)of sevoflurane in children with obstructive airway are different from that observed in normal children.

Detailed description

38 patients American Society of Anesthesiologists (ASA) class I or II aged 2-8 years undergoing tonsillectomy surgery were randomized to either the patient's head in the neutral position or 30 degree rotated lateral position. All patients were preoxygenated using 100% oxygen with a normal tidal volumen for 3 min. The circuit was primed with sevoflurane 8% at a fresh gas flow of 8 Litre/min (L/min) for 1 min. Anaesthesia was induced with inhaled sevoflurane up to 5% in oxygen via facemask with fresh gas flow at 6 L/min.After loss of consciousness, the inspired concentration of sevoflurane was maintained 10-12min a predetermined end-tidal concentration. A single experienced anaesthetist in the use of endotracheal devices inserted the devices according to the manufacturer's recommendations. Neuromuscular blocking agents and other intravenous anesthetics were not given. One nurse, who was blinded to the anaesthetic concentration, classified responses by the patient to tracheal intubation as either movement or not movement. Assesment was made for jaw relaxation and graded with intubation score. The sum of intubation scores \>4 was defined as a failure of insertion. The end-tidal (ET) sevoflurane concentration used for each patient was determined using the Dixon's up-and-down method. The ratio of the end-tidal to predetermined end-tidal concentrations was maintained at 0.95-1.0 for at least 10 minutes to establish equilibration before device insertion was attempted. The first patient received a 5.0% sevoflurane concentration and the step size of increase/decrease was 0.5%. If the endotracheal device insertion was successful, sevoflurane concentration for the next patient was decrease by 0.5%. If not, sevoflurane concentration was increased by the same amount for the next patient. For their comfort, patients experiencing movement received a 2 mg/kg bolus dose of propofol,fentanyl 2.0ug/kg and rocuronium 0.6mg/kg.If the endotracheal device insertion was successful,fentanyl 2.0ug/kg and rocuronium 0.6mg/kg was also administered.

Interventions

DRUGSevoflurane

38 patients American Society of Anesthesiologists (ASA) class I or II aged 2-8 years undergoing tonsillectomy surgery were randomized to either the patient's head in the neutral position or 30 degree rotated lateral position. The end-tidal (ET) sevoflurane concentration used for each patient was determined using the Dixon's up-and-down method. The ratio of the end-tidal to predetermined end-tidal concentrations was maintained at 0.95-1.0 for at least 10 minutes to establish equilibration before device insertion was attempted. The first patient received a 5.0% sevoflurane concentration and the step size of increase/decrease was 0.5%.

Sponsors

Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
2 Years to 8 Years
Healthy volunteers
No

Inclusion criteria

* class I or II * children aged 2-8 years * children with obstruction airway under general anesthesia undergoing tonsillectomy surgery * signed informed consent

Exclusion criteria

* Patients with a history of adverse reactions to sevoflurane * Patients with a potentially difficult airway (Mallampati III or IV, a limited mouth opening and/or cervical spine disease) * Patients with reactive airway disease * Signs of upper respiratory infection * Violate experimental scheme * refused to participate

Design outcomes

Primary

MeasureTime frameDescription
minimum alveolar anesthetic concentration of endotracheal intubationThe sevoflurane concentration is obtained when tracheal intubated immediately.To compare the minimum alveolar anesthetic concentration of endotracheal intubation required for different head position in children with obstructive airway.

Secondary

MeasureTime frameDescription
intubation scoreThe intubation score is obtained when tracheal intubation was inserted immediately.One nurse, who was blinded to the anaesthetic concentration, classified responses by the patient to tracheal intubation as either movement or not movement. Assesment was made for jaw relaxation and graded with intubation score. The sum of intubation scores \>4 was defined as a failure of insertion.
blood pressure include systolic and diastolic in mmHgBaseline and every 1 minutes until 10 minutes after insertion of the endotracheal intubation.To compare the evolution of blood pressure include systolic and diastolic during different head position group.
heart rate in bpmBaseline and every 1 minutes until 10 minutes after insertion of the endotracheal intubation.To compare the evolution of heart rate during different head position group.
bispectral index(BIS), number from 100 (awake) to 40-60(anesthetic status)Baseline and every 1 minutes until 10 minutes after insertion of the endotracheal intubation.To compare the evolution of of bispectral index values during different head position group.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026