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Indian Journal of Clinical Anaesthesia
Year : 2018, Volume : 5, Issue : 3
First page : ( 431) Last page : ( 436)
Print ISSN : 2394-4781. Online ISSN : 2394-4994.
Article DOI : 10.18231/2394-4994.2018.0080

Comparison of clinical performance of laryngeal mask airway supremeTM and I-gelTM in patients undergoing elective non-laparoscopic surgeries

Gogia Smita1,*, Singh Ishwar2, Gupta Monica3

1Senior Resident, Dept. of Anaesthesia, Rajiv Gandhi Super Speciality Hospital, New Delhi

2HOD, Dept. of Anaesthesia, Jaipur Golden Hospital, New Delhi, India

3Associate Consultant, Dept. of Anaesthesia, Jaipur Golden Hospital, New Delhi, India

*Corresponding Author: Email: smitagogia@gmail.com

Online published on 3 January, 2019.

Abstract

Supraglottic airway devices have a special niche for themselves with regards to airway management in modern anaesthesia practice. They have become a very good alternative to mask ventilation and tracheal intubation in elective surgeries and have an important place in the emergency settings. The single-use supraglottic airway devices I-gel™ and LMA-Supreme™ have been developed with the aim to overcome the limitations and improve the efficacy of currently available supraglottic airway devices like there airway sealing pressure, ease of placement but with discordant results with regards to airway sealing pressure, ease and success of placement and airway morbidity. The aim of this prospective, randomized trial was to evaluate these two airway devices in routine clinical practice.

Materials and Methods

80 patients (ASA grade1-2) were randomly allocated to two groups; Group I (I-gelTM; n=40) and Group S (LMA-SupremeTM; n=40). A size 3 or 4 (I-gelTM and LMA-SupremeTM) was used in patients and inserted by experienced anaesthesiologists who had 3 years’ experience and had performed 20 successful insertions with each device. First attempt success rate, time for insertion and airway sealing pressure of each device was measured. Airway sealing pressure with LMA-SupremeTM was measured at an intracuff pressure of 60cmH2O. Patients were enquired after surgery for the presence of any dysphagia, sore-throat or hoarseness of voice. Data were analyzed statistically using unpaired ‘t’ test and Chi-square test. A p value of < 0.05 was considered to be statistically significant.

Results

The first attempt success rate for I-gelTM was 92.5% and for LMA-SupremeTM was 87.5%. Ventilation was established in 19.7 seconds (range 14–24 seconds) in the I-gelTM group and in 24.2 seconds (range 19-29seconds) in LMA-SupremeTM group (p<0.001). There was no failure in either of the groups. Mean airway sealing pressure was comparable between both the devices (I-gelTM 23.2 cmH2O; LMA-SupremeTM 22.4 cmH2O; p>0.001).

Conclusion

Both I-gelTM and LMA SupremeTM are disposable, latex-free devices which do not need any digital or introducer tool for insertion. They have good airway sealing pressures, ease of insertion and low airway morbidity especially with I-gel, so they can be a good choice in patients undergoing elective surgeries.

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Keywords

I-gel, LMA supreme, Airway sealing pressure.

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