Clinical Study

Postoperative Pharyngolaryngeal Adverse Events with Laryngeal Mask Airway (LMA Supreme) in Laparoscopic Surgical Procedures with Cuff Pressure Limiting 25 : Prospective, Blind, and Randomised Study

Table 1

Demographic data.

L groupH group

Gender (M/F)18/3118/311.00
Age (yrs) 0.828
Height (cm) 0.468
Weight (kg) 0.592
Operation0.686
 Appendectomy69
 Cholecystectomy3434
 Gynecological96
CO2 pr (mmHg)1212
Time (min)
 Anesthesia 0.962
 Operation 0.767
LMA size0.299
 Size 373
 Size 43639
 Size 567
Attempt number0.399
 14745
 224
 300
Insertion failure
 Into airway00
 Air leak00
 Ineffective V00
Blood on LMA340.698
Sevoflurane
 Min (%) 0.76
 Max (%) 0.63
Op site pain
 POD 1 0.86
 POD 2 0.30
Ketorolac (mg)
 ~POD 1 0.88
 POD 1~POD 2 0.80

Values are expressed as number of patients or mean ± standard deviation.
L group: laryngeal mask airway (LMA) cuff pressure limiting 25 cmH2O group; H group: LMA cuff pressure at 60 cmH2O group; M: male; F: female; CO2 pr: insufflated carbon dioxide pressure for pneumoperitoneum, time, attempt number, and attempt number for successful LMA insertion; Into airway: failure into airway; Air leak: persistent air leak; Ineffective V: ineffective ventilation; Blood stained LMA: the presence of visible blood inside or outside of LMA; Min (%): minimal end expiratory concentrations of sevoflurane concentration (%); Max (%): maximal end expiratory concentration of sevoflurane (%); Op; operation; POD 1: postoperative day 1 (discharge from postanaesthetic care unit (PACU)); POD 2: postoperative day 2 (24 hours after discharge from PACU); ~POD 1: from end of surgery to discharge from PACU; POD 1~POD 2: from POD 1 to POD 2.