Effect of Use of Endotracheal Tube With Subglottic Suction in Rhinoplasty

Yuzuncu Yıl University

Status: Completed

Conditions: Rhinoplasty

Treatments: Other: Suction Above Cuff Endotracheal Tube

Study type: Interventional

Funder types: Other

Identifiers

NCT03584503

SACETT

Details and patient eligibility

About

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, we 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 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.

Full 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.

Enrollment: 132 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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132 participants in 2 patient groups

Group SA

Active Comparator group

Description:

Group SA intubated with Suction Above Cuff Endotracheal Tube

Treatment:

Other: Suction Above Cuff Endotracheal Tube

Group C

No Intervention group

Description:

Group C intubated with classic endotracheal tube