دورية أكاديمية
Comparison of incidence of sore throat with laryngeal mask airway Protector and laryngeal mask airway ProSeal: A randomised clinical trial
| العنوان: | Comparison of incidence of sore throat with laryngeal mask airway Protector and laryngeal mask airway ProSeal: A randomised clinical trial |
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| المؤلفون: | Vidya Mohan, Priya Rudingwa, Sakthirajan Panneerselvam, Aswini Kuberan, Gnanasekaran Srinivasan, Santhosh Arulprakasam |
| المصدر: | Indian Journal of Anaesthesia, Vol 68, Iss 7, Pp 637-643 (2024) |
| بيانات النشر: | Wolters Kluwer Medknow Publications, 2024. |
| سنة النشر: | 2024 |
| المجموعة: | LCC:Anesthesiology |
| مصطلحات موضوعية: | laryngeal masks, lma® proseal, lma® protector, pharyngitis, post, postoperative, postoperative sore throat, risk factors, supraglottic airway device, Anesthesiology, RD78.3-87.3 |
| الوصف: | Background and Aims: Postoperative sore throat (POST) can be as high as 42% in supraglottic devices. LMA® Protector™ is a novel second-generation laryngeal mask airway (LMA) with Cuff Pilot™ technology that allows continuous cuff pressure monitoring. Elevated cuff pressure is a risk factor for POST in supraglottic devices, so we conducted this study to determine whether continuous cuff pressure monitoring can alleviate POST. Methods: This randomised double-blinded clinical trial compared the incidence of sore throat between LMA® Protector™ and LMA® ProSeal™ and was conducted in 118 patients scheduled for elective short surgical procedures. They were randomised to either LMA® Protector™ (Group PT) or LMA® ProSeal™ (Group P). The airway was secured with either of the two devices. The primary outcome was the incidence of sore throat at 1, 6, and 24 hours postoperatively and compared using the Chi-square test along with other parameters like first attempt success rate and blood staining of the device. The time taken for insertion and oropharyngeal seal pressure were compared using an independent t-test. Results: The incidence of POST was low with Group PT (12%) compared to Group P (28.8%) (P = 0.005). The mean oropharyngeal seal pressure was significantly higher in Group PT than in Group P [33.72 (3.07) versus 27.72 (3.88) cm of H2O], P < 0.005. The first attempt success rate was 81.2% and 100% in LMA® Protector™ versus LMA® ProSeal™. Conclusion: LMA® Protector™ had a reduced incidence of POST compared to LMA ProSeal. However, a longer insertion time and difficult placement may be a concern. |
| نوع الوثيقة: | article |
| وصف الملف: | electronic resource |
| اللغة: | English |
| تدمد: | 0019-5049 0976-2817 36343501 |
| Relation: | https://journals.lww.com/10.4103/ija.ija_1068_23; https://doaj.org/toc/0019-5049; https://doaj.org/toc/0976-2817 |
| DOI: | 10.4103/ija.ija_1068_23 |
| URL الوصول: | https://doaj.org/article/363435014fb34563adbf2318546d47d1 |
| رقم الأكسشن: | edsdoj.363435014fb34563adbf2318546d47d1 |
| قاعدة البيانات: | Directory of Open Access Journals |
Full Text Finder | تدمد: | 00195049 09762817 36343501 |
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| DOI: | 10.4103/ija.ija_1068_23 |