Video vs. Direct Laryngoscopy in Pediatric Nasal Intubation
Клучни зборови
Апстракт
Опис
The objective of this study is to compare the need for the use of standard Magill forceps when performing a nasal intubation with either conventional DL or VL with a C-Mac. Secondarily the investigators will also examine the time to intubate (TTI) for both methods as well.
Once the patient is recruited, the patient will then be randomized to either intubation using DL or VL with a C-Mac. Once the patient is under anesthesia, the intubation will be performed by an attending pediatric anesthesiologist or experience pediatric CRNA who has experience both DL and with the C-Mac and will attempt to intubate the patient with or without Magill forceps as needed.
The investigators will record the time to intubation (TTI) from the time the laryngoscope or C-Mac is placed in the mouth to the first appearance of end tidal carbon dioxide (ETCO2). the investigators will record the presence or absence of nasal bleeding, and the grade of laryngeal view. The investigators will also record any general narrative comments about the ease or difficulty of intubation in both groups.
The study will be performed at Wake Forest Baptist Medical Center.
Patients between the ages of 3 and 14 scheduled for comprehensive dental treatment under general anesthesia will be included.
Normal appearing airway upon pre-operative assessment. The investigators have calculated a sample size of 35 patients in each group to be able to detect a significant difference in the rate of use of Magill forceps to place a nasal RAE ETT in this patient population.
Датуми
Последен пат проверено: | 06/30/2018 |
Прво доставено: | 01/11/2017 |
Поднесено е проценето запишување: | 01/22/2017 |
Прво објавено: | 01/25/2017 |
Последното ажурирање е доставено: | 07/09/2018 |
Последно ажурирање објавено: | 08/07/2018 |
Датум на први доставени резултати: | 06/13/2018 |
Датум на први доставени резултати за КК: | 06/13/2018 |
Датум на објавување на првите резултати: | 07/10/2018 |
Крај на датумот на започнување на студијата: | 02/29/2016 |
Проценет датум на примарно завршување: | 08/06/2017 |
Проценет датум на завршување на студијата: | 08/06/2017 |
Состојба или болест
Интервенција / третман
Device: Video Laryngoscopy
Device: Direct Laryngoscopy
Фаза
Групи за раце
Рака | Интервенција / третман |
---|---|
Active Comparator: Direct Laryngoscopy These patients will be nasally intubated for their procedure via direct laryngoscopy. We will observe and record incidence of Magill forcep use, presence or absence of nasal bleeding, and the grade of laryngeal view. We will also record any general narrative comments from the provider about the ease or difficulty of intubation. | Device: Direct Laryngoscopy These patients will be nasally intubated for their procedure via direct laryngoscopy |
Experimental: Video Laryngoscopy These patients will undergo Video Laryngoscopy for nasal intubation. We will observe and record incidence of Magill forcep use, presence or absence of nasal bleeding, and the grade of laryngeal view. We will also record any general narrative comments from the provider about the ease or difficulty of intubation. | Device: Video Laryngoscopy The anesthesia provider will use a video laryngoscope to facilitate the nasal intubation for the procedure. |
Критериуми за подобност
Возраст подобни за студии | 3 Years До 3 Years |
Полови квалификувани за студии | All |
Прифаќа здрави волонтери | Да |
Критериуми | Inclusion Criteria: - Patients between the ages of 3 and 14 scheduled for comprehensive dental treatment under general anesthesia - Normal appearing airway upon pre-operative assessment Exclusion Criteria: - Patient with a history of difficult airway/intubation - Patients suspected to have a difficult airway - History of cleft palate and/or cleft palate repair - Pregnancy - Emergency status of surgery - Any patient with a contra-indication to nasal tube placement - Any patient with a potentially increased risk of nasal bleeding from nasal placement of the ETT i.e. patients on aspirin or other anticoagulants, patient's with hemophilia |
Исход
Мерки на примарниот исход
1. Number of Participants Requiring Use of Magill Forceps for Nasal Intubations [1 day]
Секундарни мерки на исходот
1. Time to Intubation [1 day]
2. Grade of Larynx View [1 day]
3. Presence of Nasal Bleeding [1 day]
4. Incidence of Failed Nasal Intubation [1 day]