Pressure Over Nasotracheal Intubation Related Nasal Alar Injury
Keywords
Abstract
Description
While assisting ventilation during general anesthesia or other reasons, patients are often intubated with endotracheal tube to secure airway. Endotracheal tube can be placed trans-orally or trans-nasally according to surgical conditions, anatomical considerations and nursing needs. Except inadequate cuff pressure related complication, nasotracheal intubation can cause dysfunction of nasal mucosal cilia, injury and hemorrhage of nasal mucosa, turbinate avulsion, obstruction of nasal airway, sinusitis and compression and injury of nasal alar, resulting in local erythema, ischemia, pressure sore, necrosis, tissue damage and may affect appearance.
Previous studies focus on the process of nasal tracheal intubation, aim to reduce mucosal injury and hemorrhage via specific intubation tool, special endotracheal tube design, lubricant and so on. However, evidences in preventing nasal alar injury are limited, in which injuries are mostly prevented by self-made special endotracheal tube and artificial leather. In general, the etiology of tissue damage is compression pressure exceeding local capillary perfusion pressure, resulting in reduced perfusion, ischemia and necrosis. Clinically, health providers prevent the injury by standardized endotracheal tube fixation and/or artificial leather at sites with potential compression. But the extend of the effect of endotracheal tube to trachea mucosa varies, range of pressure affecting capillary perfusion pressure are not yet defined, and no routine monitoring for dermis compression. Thus, endotracheal tube related skin damage is an important clinical issue without best standard operating procedure.
In this study, the investigators will place a pressure sensor at the angle of nasotracheal tube, measure the actual pressure, define the sites of compression and its pressure, analyze the relationship of clinical signs and symptoms, pressure, and duration of nasotracheal intubation, and build up optimal clinical routines.
Dates
Last Verified: | 05/31/2020 |
First Submitted: | 11/05/2018 |
Estimated Enrollment Submitted: | 11/05/2018 |
First Posted: | 11/07/2018 |
Last Update Submitted: | 06/02/2020 |
Last Update Posted: | 06/04/2020 |
Actual Study Start Date: | 04/30/2020 |
Estimated Primary Completion Date: | 03/31/2023 |
Estimated Study Completion Date: | 12/30/2023 |
Condition or disease
Intervention/treatment
Device: Nasal intubation with pressure sensor
Phase
Arm Groups
Arm | Intervention/treatment |
---|---|
Nasal intubation with pressure sensor anesthetized patient with nasotracheal intubation | Device: Nasal intubation with pressure sensor Pressure sensor at the angle of intratracheal tube and nasal alar |
Eligibility Criteria
Ages Eligible for Study | 18 Years To 18 Years |
Sexes Eligible for Study | All |
Sampling method | Probability Sample |
Accepts Healthy Volunteers | Yes |
Criteria | Inclusion Criteria: - American Society of Anesthesiologists (ASA) Physical classification I & II - patients undergo general anesthesia and receive intratracheal intubation through nose - elective surgery Exclusion Criteria: - with known nasal injury - already intubation before induction - surgery on the nose - emergent operation |
Outcome
Primary Outcome Measures
1. appearance of nose [from induction to one day after surgery]
2. VAS [from induction to one day after surgery]
3. pressure between nose and intratracheal tube [during intubation]
4. NPUAP classification [from induction to one day after surgery]