MedPath

Sellick Interest in Rapid Sequence Induction

Phase 3
Completed
Conditions
Rapid Sequence Induction of General Anesthesia
Acid Aspiration Syndrome
Aspiration Pneumonia
Lung Aspiration
Sellick Maneuver
Interventions
Other: effective sellick maneuver
Other: sham sellick maneuver
Registration Number
NCT02080754
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

Lung aspiration can occur when a rapid sequence induction of anesthesia is performed (emergency and/or presence of at least one risk factor for regurgitation of stomach contents).

The aim of this study is to assess the Sellick maneuver, which is recommended for patient at high risk of aspiration of gastric content during induction of general anesthesia, despite the lack of solid evidence of its efficacy and possible adverse effects The primary outcome of this non inferiority study is the incidence of lung aspiration whether this maneuver is effectively applied or sham.

Detailed Description

Introduction:

Lung aspiration is an inherent complication of the loss of protective upper airway reflexes during general anesthesia. Its incidence is low in elective surgery, when preoperative fasting rules have been complied and in absence of risk factors for regurgitation of gastric contents. In emergency conditions, non-compliance with preoperative fasting rules and delayed gastric emptying increase the risk of regurgitation and therefore lung aspiration of gastric contents. In this context, a rapid sequence induction of anaesthesia is recommended to minimize the risk of regurgitation which combines the use of short delay and short duration of action anesthetics agents associated with the application of a Sellick maneuver. The goal of this maneuver is to collapse the esophagus by compressing it between the cricoid cartilage and the fifth cervical vertebra. Because of the low level of evidence supporting the Sellick maneuver in the literature, this maneuver, remains controversial although recommended.

Hypothesis: The aim of this study is to assess the Sellick maneuver during rapid sequence induction in adults (pregnant women excluded) by comparing the incidence of lung aspiration whether this maneuver is applied or sham, in a noninferiority trial.

Primary endpoint: Incidence of lung aspiration

Secondary endpoints: Cormack and Lehane Grade , frequency of difficult intubation, frequency of impossible intubation, effect of releasing the Sellick maneuver on these three criteria, frequency of aspiration pneumonia within 24 hours, frequency of complications due to the Sellick maneuver (esophageal rupture and cricoid cartilage fracture rates) and mortality at day 28 or at hospital discharge.

Methods: This is a multicenter, randomized, double-blind, non-inferiority trial. We compare a group of patients benefiting from a rapid sequence induction without achieving the Sellick maneuver, where the movement is fake (sham group) with a group of patients undergoing a rapid sequence induction with effective execution of this maneuver (Sellick group). The two patient groups differ only by the effective or sham application of the Sellick maneuver .

In both arms, the Sellick maneuver , whether real or fake , can be released at the request of the person performing orotracheal intubation in particular to improve intubating conditions or in case of active vomiting. However, it should be kept in case of need for ventilation facemask.

Number of patients: The number of patients is estimated at 1 750 patients per group and so 3500 patients.

Inclusion criteria: patients older than 18 yr undergoing general anesthesia requiring rapid sequence induction (full stomach or presence of at least one risk factor for regurgitation of stomach content) are eligible.

Exclusion criteria: patients non consenting, pregnancy, contraindication to Sellick maneuver or succinylcholine, patients with predictive signs of bronchopneumonia during the preanesthetic consultation, patients with pulmonary contusion, upper respiratory tract abnormalities, laryngeal trauma, patients requiring an alternative to direct laryngoscopy, patients with troubles of consciousness, use of plastic single used laryngoscopic blade, use of rocuronium as neuromuscular blockade agent.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3472
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
sellick armeffective sellick maneuvereffective sellick maneuver
sham armsham sellick maneuversham sellick maneuver
Primary Outcome Measures
NameTimeMethod
Incidence of lung aspirationWithin 1 hour

in the operating room presence of gastric fluid on the vocal cords at the orotracheal intubation or in endotracheal suction when performed immediately after intubation

Secondary Outcome Measures
NameTimeMethod
Cormack and Lehane GradeWithin 1 hour

During orotracheal intubation

Number of times the Sellick maneuver should be discontinuedWithin 1 hour

In the operating room, if the person who realize the intubation requires a loosening of the Sellick manoeuver, whether real or feigned (difficult intubation, vomiting)

Incidence of difficult and impossible intubationWithin 1 hour

difficult intubation is defined by more than two attempts or the need for an alternative technique. Impossible intubation is defined by the need to awake the patient or perform a tracheotomy or cricothyrotomy rescue.

Incidence of aspiration pneumoniawithin the 24 hours

Aspiration pneumonia is defined by the association of a lung aspiration recorded in the operating room during the induction of anesthesia and the presence of a non-existent preoperative radiological infiltrate

Incidence of oesophageal ruptureday 28

This complication is extremely rare and clinically very telling. No further review is planned to diagnose it

Incidence of cricoid cartilage fractureday 28

This complication is extremely rare and clinically very telling. No further review is planned to diagnose it.

Effects of releasing the Sellick maneuver on the conditions of tracheal intubation assessed by Cormack and Lehane gradeWithin 1 hour

During orotracheal intubation

Frequency of use of a mask ventilationWithin 1 hour

In the operating room, if needed, the mask ventilation will be recorded

MortalityHospital discharge Hospital discharge if anterior at day 28

Trial Locations

Locations (1)

Groupe Hospitalier Pitié Salpetriere

🇫🇷

Paris, France

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