Effect of Use of Endotracheal Tube With Subglottic Suction in Rhinoplasty
Keywords
Abstract
Description
Suction Above Cuff Endotracheal Tube (SACETT) has a dorsal port above the cuff designed to allow continuous or intermittent suctioning of secretions from the subglottic space. Thus, it facilitates suctioning of excessive secretions around the mouth and the cuff. In this study, the investigators aimed to investigate the effect of the use of SACETT on laryngospasm and postoperative complications in rhinoplasty operations.
This randomized controlled clinical trial was conducted in 132 patients undergoing rhinoplasty. The patients were randomly divided into 2 groups: Suction Above Cuff Endotracheal Tube (n:66) (Group SA) and classic endotracheal tube (n:66) (Group C). Complications following general anesthesia were statistically analyzed among the two groups.
55 male patients and 77 female patients were included in the study. The incidences of postoperative laryngospasm and respiratory complications were found to be lower in Group SA compared to Group C. In addition, the incidences of agitation, postoperative nausea and vomiting (PONV), swallowing difficulty, and sore throat were found to be lower in Group SA compared to Group C. However, the incidences of cough, hypotension, and tachycardia were similar in both groups. No PONV, swallowing difficulty, and hypotension were observed in Group SA. The blood volume accumulated in the suction chamber was found to be greater in Group SA compared to Group C.
The investigators believe that the use of SACETT in rhinoplasty operations reduces the incidences of laryngospasm, emergence agitation, sore throat, swallowing difficulty, and PONV when compared with classic endotracheal tube.
Dates
| Last Verified: | 11/30/2018 |
| First Submitted: | 06/18/2018 |
| Estimated Enrollment Submitted: | 06/27/2018 |
| First Posted: | 07/11/2018 |
| Last Update Submitted: | 11/30/2018 |
| Last Update Posted: | 12/03/2018 |
| Actual Study Start Date: | 05/31/2018 |
| Estimated Primary Completion Date: | 10/29/2018 |
| Estimated Study Completion Date: | 10/29/2018 |
Condition or disease
Intervention/treatment
Other: Group SA
Phase
Arm Groups
| Arm | Intervention/treatment |
|---|---|
| Active Comparator: Group SA Group SA intubated with Suction Above Cuff Endotracheal Tube | Other: Group SA Suction Above Cuff Endotracheal Tube (SACETT) has a dorsal port above the cuff designed to allow continuous or intermittent suctioning of secretions from the subglottic space |
| No Intervention: Group C Group C intubated with classic endotracheal tube |
Eligibility Criteria
| Ages Eligible for Study | 18 Years To 18 Years |
| Sexes Eligible for Study | All |
| Accepts Healthy Volunteers | Yes |
| Criteria | Inclusion Criteria: - Patients who will undergo rhinoplasty surgery, - American Society of Anesthesiologists (ASA) I-II patients, - Aged 18-65 years Exclusion Criteria: - Patients who had upper or lower respiratory tract infections, - asthma, - a history of allergy, - who received isoflurane and desflurane for maintenance of anesthesia, - who were the ASA class III-IV, - and who had a long uvula, - gastroesophageal reflux or sleep apnea, - electrolyte disturbances such as hypomagnesemia and hypocalcemia, - a BMI (body mass index) over 30 were excluded from the study. |
Outcome
Primary Outcome Measures
1. Incidence of laryngospasm [1 mounth]
Secondary Outcome Measures
1. emergence agitation [1 mounth]
