Our study aimed to compare the manual placement, direct laryngoscopy and video laryngoscopy assisted placement techniques of LMA Proseal, a new generation laryngeal mask (LMA), and to find an effective placement technique that does not allow airway leakage in one go.
LMA is an airway device frequently used in pediatric anesthesia. It is preferred for short interventions because it is less invasive compared to intubation. However, problems such as not being fully seated, slipping, and leakage can be encountered during placement. Multiple attempts after unsuccessful placement may cause undesirable results such as edema and sore throat. The aim in this study is to reveal the most accurate placement technique and to transfer this method to clinical applications. Our research is a prospective, randomized controlled method study. Patients will be divided into 3 groups. Group 1:(Standard technique) Group 2:(Placement with direct laryngoscopy) Group 3:(Placement with the aid of video laryngoscopy) After LMA Proseal placement, airway sealing pressures will be measured with appropriate technique. Airway tightness pressure measurement will be made with the technique accepted in the literature through the sensors in the anesthesia machine.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Enrollment
150
The LMA Proseal will be inserted directly by hand, without the use of any laryngoscope, as recommended in the instruction manual. The cuff will be gently guided along the hard palate where it is pushed into the hypopharynx and increased resistance is felt, and the cuff will be placed towards the hypopharynx.
Appropriately sized laryngoscope blade will be used and after the location of the epiglottis is determined, the tongue and epiglottis will be lifted forward. Then, LMA Proseal will be placed at the point where resistance is felt at a level where the proximal edge of the mask can be seen.
After the video laryngoscope is placed with an appropriately sized blade, the location of the epiglottis and vocal cords will be determined and the LMA Proseal will be placed at the point where slight resistance is encountered after the epiglottis is lifted. proximal aspect of LMA
Ondokuz Mayis University
Samsun, Turkey (Türkiye)
Oropharyngeal leak pressure
Oropharyngeal leak pressure (OLP) will be measured by closing the adjustable pressure limiting valve on the anesthesia machine. The fresh gas flow was adjusted to 3 L/min. When the APL (Adjustable pressure limiting) valve was closed and manually ventilated. The leak sound that occurs during ventilation will be auscultated. The first peak airway pressure at which the leak occurs will be recorded as the oropharyngeal leak pressure. After successful insertion, lma proseal location will be evaluated with fiberoptic imaging.
Time frame: within 2-3 minutes after laryngeal mask insertion before start of surgery
Blood pressure
Measure blood pressure in millimeter of mercury by non-invasive blood pressure.
Time frame: Preoperatively, one minute after the induction, fifth minute and before removed laryngeal mask.
İnsertion time
LMA insertion time (time from LMA handling to first wave formation in capnography)
Time frame: intraoperative period
Number of placement attempts
The number of attempts for optimal placement will be recorded
Time frame: intraoperative period
Need for optimization maneuvers
It will be recorded whether additional maneuvering is performed for optimal placement. LMA rotation, jaw thrust, head extension, and flexion will be use as optimization maneuvers.
Time frame: intraoperative period
Complications
İnvestigate the existence of complications that may be encountered in the routine after LMA placement and removal.
Time frame: intraoperative and postoperative day 1.
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Heart rate
Measure heart rate in beats per minute by electrocardiography monitor.
Time frame: Preoperatively, one minute after the induction, fifth minute and before removed laryngeal mask.
Peripheral oxygen saturation
Measure peripheral oxygen saturation per minute by pulse oximeter.
Time frame: Preoperatively, one minute after the induction, fifth minute and before removed laryngeal mask.