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Anticipation of the Difficult Airway: the Preoperative Airway Assessment Form

Anticipation of the Difficult Airway: the Preoperative Airway Assessment Form as an Educational and Quality Improvement Tool

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01037374
Enrollment
89
Registered
2009-12-23
Start date
2008-08-31
Completion date
2012-12-31
Last updated
2014-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endotracheal Intubation Risk Assessment

Keywords

risk, assessment, difficult, endotracheal, intubation

Brief summary

The purpose of this study is to see if our experimental preoperative airway assessment form is a better indicator of difficult airway as compared to the anesthesia record that is presently used.

Detailed description

Predicting difficult airway continues to be problematic for even the most seasoned of anesthesiologists. In our study, the resident class will be our sample population. The residents will be randomly assigned into two groups: the experimental group will be utilizing the new preoperative airway assessment form and the control group will be utilizing the standard anesthesia record. Simultaneously, a subset of our anesthesia experts will also be assessing patients preoperatively. The five areas of difficult airway management will be considered: difficult mask ventilation, difficult supraglottic airway, difficult laryngoscopy, difficult intubation, and difficult surgical airway. According to the American Society of Anesthesiologists, the incidence of intubation has remained stable throughout the 1980s and 1990s despite attempts to predict its occurrence. Many of these cases were considered to be preventable; therefore, a better prediction of and preparation for difficult airway management may lead to a reduction in adverse events.

Interventions

OTHERPreoperative assessment form

(based on the american society of anesthesiologists)components of the form include: neck measurements; neck mobility; mallampati; wilson's test; pre-existing conditions; and predictions of difficult mask ventilation, supraglottic airway, laryngoscopy, intubation, and surgical airway.

Sponsors

Foundation for Anesthesia Education and Research
CollaboratorOTHER
The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* CA-1, CA-2, and CA-3 anesthesiology residents starting from July 2008-July 2010

Exclusion criteria

* the same anesthesiology residents who are working with patients 17 and younger, patients who are already intubated, and patients undergoing emergent surgery.

Design outcomes

Primary

MeasureTime frame
Use of an experimental preoperative assessment form by residents will result in more complete documentation of important airway features compared to use of the current formsinterim analysis will be assessed after 1 year

Secondary

MeasureTime frame
use of the experimental preoperative assessment form will result in greater resident recognition of patients at high risk for a difficult airway as judged independently by one of 3 senior faculty investigators.interim analyses will be assessed after 1 year
the percentage of patients intubated using an awake method will be greater among residents using the new form than those using the current forminterim analysis will be assessed after 1 year
the percentage of patients requiring multiple intubation attempts or use of invasive airway techniques will be lower among residents using the new form.interim analysis will be assessed after 1 year
spontaneous knowledge of important airway features will be more complete among residents using the new form at 18 months of training.interim analysis will be assessed after 1 year
observations made during this study will allow refinement of the new form to augment the identification of patients with difficult airway.interim analysis will be assessed after 1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026