Acute Respiratory Failure
Conditions
Keywords
Critical Illness, Emergency Airway Management, Tracheal intubation, Video laryngoscope, Direct laryngoscope
Brief summary
Clinicians perform rapid sequence induction, laryngoscopy, and tracheal intubation for more than 5 million critically ill adults as a part of clinical care each year in the United States. Failure to intubate the trachea on the first attempt occurs in more than 10% of all tracheal intubation procedures performed in the emergency department (ED) and intensive care unit (ICU). Improving clinicians rate of intubation on the first attempt could reduce the risk of serious procedural complications. In current clinical practice, two classes of laryngoscopes are commonly used to help clinicians view the larynx while intubating the trachea: a video laryngoscope (equipped with a camera and a video screen) and a direct laryngoscope (not equipped with a camera or video screen). For nearly all laryngoscopy and intubation procedures performed in current clinical practice, clinicians use either a video or a direct laryngoscope. Prior research has shown that use of a video laryngoscope improves the operator's view of the larynx compared to a direct laryngoscope. Whether use of a video laryngoscope increases the likelihood of successful intubation on the first attempt remains uncertain. A better understanding of the comparative effectiveness of these two common, standard-of-care approaches to laryngoscopy and intubation could improve the care clinicians deliver and patient outcomes.
Detailed description
Clinicians frequently perform tracheal intubation of critically ill patients in the emergency department (ED) or intensive care unit (ICU). In 10-20% of emergency tracheal intubations, clinicians are unable to intubate the trachea on the first attempt, which increases the risk of peri-intubation complications. Successful laryngoscopy and tracheal intubation requires using a laryngoscope to \[1\] visualize the larynx and vocal cords and \[2\] create a pathway through which an endotracheal tube can be advanced through the oropharynx and larynx and into the trachea. In current clinical practice, two classes of laryngoscopes are commonly used by clinicians to view the larynx while intubating the trachea: a video laryngoscope (equipped with a camera and a video screen) and a direct laryngoscope (not equipped with a camera or video screen). Clinicians use either a video laryngoscope or a direct laryngoscope as standard of care for every laryngoscopy and intubation procedure performed in current clinical practice. Direct Laryngoscope: The Macintosh direct laryngoscope consists of a battery-containing handle and a blade with a light source. The operator achieves a direct line of sight -from the operator's eye through the mouth to the larynx and trachea - by using the laryngoscope blade to displace the tongue and elevate the epiglottis. Video Laryngoscope: Video laryngoscopes consist of a fiberoptic camera and light source near the tip of the laryngoscope blade, which transmits images to a video screen. The position of the camera near the tip of the laryngoscope blade facilitates visualization of the larynx and trachea. Use of a video laryngoscope and use of a direct laryngoscope are both common, standard-of-care approaches the clinicians use to perform tracheal intubation in the ED and ICU in current clinical care. Currently, it is unknown whether use of a video laryngoscope or use of a direct laryngoscope has any effect on successful intubation on the first attempt or any other outcome. Some prior research has raised the hypothesis that using a video laryngoscope would increase clinicians' rate of successful intubation on the first attempt by facilitating the view of the larynx. Some prior research has raised the hypothesis that using a direct laryngoscope would increase clinicians' rate of successful intubation on the first attempt by facilitating a clear pathway for placement of the tube through the mouth into the trachea. To date, 8 small single-center randomized trials and one 371-patient multicenter randomized clinical trial have been conducted under waiver of or alteration of informed consent to compare use of a video vs a direct laryngoscope in the setting of emergency tracheal intubation in the ED or ICU. Two of these trials provide the most direct preliminary data for this proposal. The Facilitating EndotracheaL intubation by Laryngoscopy technique and apneic Oxygenation Within the ICU (FELLOW) randomized clinical trial, conducted under waiver of informed consent, compared these two standard-of-care approaches during 150 emergency tracheal intubations at Vanderbilt University Medical Center, finding no difference in the rate of successful intubation on the first attempt between use of a video and use of a direct laryngoscope. The McGrath Mac Videolaryngoscope Versus Macintosh Laryngoscope for Orotracheal Intubation in the Critical Care Unit (MACMAN) randomized clinical trial among 371 critically ill adults found no difference between use of a video vs direct laryngoscope in the rate of successful intubation on the first attempt. However, a hypothesis-forming post-hoc exploratory analysis of peri-intubation complications suggested that use of a video laryngoscope may be associated with a higher rate of complications than direct laryngoscope (9.5% vs 2.8%, respectively, p=0.01). These trials were underpowered to rule out small but clinically significant differences in first pass success, and were limited to intubations performed by inexperienced trainees in one practice setting (intensive care units), but they demonstrated hypothesis-generating findings requiring validation in larger trials that reflect the full spectrum of settings, operator specialties, and operator experience levels in which emergency tracheal intubation is routinely performed. Because of the imperative to optimize emergency tracheal intubation in clinical care, the common use of both video and direct laryngoscopes in current clinical practice, and the lack of definitive data from randomized trials to definitively inform whether use of a video laryngoscope or a direct laryngoscope effects the rate of successful intubation on the first attempt, examining whether one approach increases the odds of successful intubation on the first attempt represents an urgent research priority. To address this knowledge gap, the investigators propose to conduct a large, multicenter, randomized clinical trial comparing use of a video laryngoscope versus use of a direct laryngoscope with regard to successful intubation on the first attempt among critically ill adults undergoing tracheal intubation in the ED or ICU.
Interventions
Laryngoscope with a camera and a video screen
Laryngoscope without a camera or a video screen
Sponsors
Study design
Eligibility
Inclusion criteria
* Patient is located in a participating unit. * Planned procedure is orotracheal intubation using a laryngoscope. * Planned operator is a clinician expected to routinely perform tracheal intubation in the participating unit.
Exclusion criteria
* Patient is known to be less than 18 years old. * Patient is known to be pregnant. * Patient is known to be a prisoner. * Immediate need for tracheal intubation precludes safe performance of study procedures. * Operator has determined that use of a video laryngoscope or use of a direct laryngoscope is required or contraindicated for the optimal care of the patient.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Intubations With Successful Intubation on the First Attempt | Duration of procedure (minutes) | The primary outcome is defined as placement of an endotracheal tube in the trachea with a single insertion of a laryngoscope blade into the mouth and EITHER a single insertion of an endotracheal tube into the mouth OR a single insertion of a bougie into the mouth followed by a single insertion of an endotracheal tube over the bougie into the mouth. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Severe Complications of Tracheal Intubation | from induction to 2 minutes following tracheal intubation | The secondary outcome is defined as the number of patients who experienced one or more of the following occurring between induction and 2 minutes after successful intubation: * Severe hypoxemia (lowest oxygen saturation measured by pulse oximetry \< 80%); * Severe hypotension (systolic blood pressure \< 65 mm Hg or new or increased vasopressor administration); * Cardiac arrest not resulting in death within 1 hour of intubation; or * Cardiac arrest resulting in death within 1 hour of induction |
Other
| Measure | Time frame | Description |
|---|---|---|
| Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Duration of procedure (minutes) | — |
| Successful Intubation on the First Attempt Without a Severe Complication | from induction to 2 minutes following tracheal intubation | This outcome reports the number of participants that experienced successful intubation on the first attempt without experiencing complications, a composite of two independent outcomes: successful intubation on the first attempt (the primary outcome of the trial) and severe complication (the secondary outcome of the trial). |
| Reason for Failure to Intubate on the First Attempt | Duration of procedure (minutes) | Providers could give more than one reason for failure to intubate on the first attempt for each intubation (not mutually exclusive). In addition, data on the reason for failure to intubate on the first attempt was missing for 23 patients in the video laryngoscope group and 40 patients in the direct laryngoscope group. Reason for failure among those who did not meet the primary outcome (successful intubation on the first attempt): * Inadequate view of the larynx * Inability to intubate the trachea with an endotracheal tube * Inability to cannulate the trachea with a bougie * Attempt aborted due to change in patient condition (e.g., worsening hypoxemia, hypotension, bradycardia, vomiting, bleeding) * Technical failure of the laryngoscope (e.g., battery, light source, camera, screen) * Other * Not Reported |
| Operator-reported Aspiration | from induction to 2 minutes following tracheal intubation | — |
| Duration of Laryngoscopy and Tracheal Intubation | Duration of procedure (minutes) | The interval (in seconds) between the first insertion of a laryngoscope blade into the mouth and the final placement of an endotracheal tube or tracheostomy tube in the trachea. |
| Injury to the Teeth | from induction to 2 minutes following tracheal intubation | — |
| ICU-free Days in the First 28 Days | 28 days | — |
| Ventilator Free Days in the First 28 Days | 28 days | — |
| All-cause In-hospital Mortality | 28 days | — |
| Esophageal Intubation | from induction to 2 minutes following tracheal intubation | — |
| Number of Laryngoscopy Attempts | Duration of procedure (minutes) | — |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Video Laryngoscope Group For patients assigned to the video laryngoscope group, the operator will use a video laryngoscope on the first laryngoscopy attempt. A video laryngoscope will be defined as a laryngoscope with a camera and a video screen. Trial protocol will not dictate the brand of video laryngoscope.
Video Laryngoscope: Laryngoscope with a camera and a video screen | 705 |
| Direct Laryngoscope Group For patients assigned to the direct laryngoscope group, the operator will use a direct laryngoscope on the first laryngoscopy attempt. A direct laryngoscope will be defined as a laryngoscope without a camera or a video screen. Trial protocol will not dictate the brand of direct laryngoscope or the blade shape.
Direct Laryngoscope: Laryngoscope without a camera or a video screen | 712 |
| Total | 1,417 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | After enrollment, discovered to be a person experiencing incarceration. | 2 | 1 |
Baseline characteristics
| Characteristic | Video Laryngoscope Group | Direct Laryngoscope Group | Total |
|---|---|---|---|
| Age, Continuous | 54 years | 55 years | 55 years |
| Race/Ethnicity, Customized Race or ethnic group Hispanic | 101 Participants | 94 Participants | 195 Participants |
| Race/Ethnicity, Customized Race or ethnic group Non-Hispanic Black | 166 Participants | 167 Participants | 333 Participants |
| Race/Ethnicity, Customized Race or ethnic group Non-Hispanic White | 360 Participants | 346 Participants | 706 Participants |
| Race/Ethnicity, Customized Race or ethnic group Not reported | 17 Participants | 21 Participants | 38 Participants |
| Race/Ethnicity, Customized Race or ethnic group Other | 61 Participants | 84 Participants | 145 Participants |
| Region of Enrollment United States | 705 participants | 712 participants | 1417 participants |
| Sex: Female, Male Female | 240 Participants | 258 Participants | 498 Participants |
| Sex: Female, Male Male | 465 Participants | 454 Participants | 919 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 184 / 705 | 191 / 712 |
| other Total, other adverse events | 0 / 705 | 0 / 712 |
| serious Total, serious adverse events | 0 / 705 | 0 / 712 |
Outcome results
Number of Intubations With Successful Intubation on the First Attempt
The primary outcome is defined as placement of an endotracheal tube in the trachea with a single insertion of a laryngoscope blade into the mouth and EITHER a single insertion of an endotracheal tube into the mouth OR a single insertion of a bougie into the mouth followed by a single insertion of an endotracheal tube over the bougie into the mouth.
Time frame: Duration of procedure (minutes)
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Video Laryngoscope Group | Number of Intubations With Successful Intubation on the First Attempt | 600 Participants |
| Direct Laryngoscope Group | Number of Intubations With Successful Intubation on the First Attempt | 504 Participants |
Number of Participants With Severe Complications of Tracheal Intubation
The secondary outcome is defined as the number of patients who experienced one or more of the following occurring between induction and 2 minutes after successful intubation: * Severe hypoxemia (lowest oxygen saturation measured by pulse oximetry \< 80%); * Severe hypotension (systolic blood pressure \< 65 mm Hg or new or increased vasopressor administration); * Cardiac arrest not resulting in death within 1 hour of intubation; or * Cardiac arrest resulting in death within 1 hour of induction
Time frame: from induction to 2 minutes following tracheal intubation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Video Laryngoscope Group | Number of Participants With Severe Complications of Tracheal Intubation | 151 Participants |
| Direct Laryngoscope Group | Number of Participants With Severe Complications of Tracheal Intubation | 149 Participants |
All-cause In-hospital Mortality
Time frame: 28 days
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Video Laryngoscope Group | All-cause In-hospital Mortality | 184 Participants |
| Direct Laryngoscope Group | All-cause In-hospital Mortality | 191 Participants |
Duration of Laryngoscopy and Tracheal Intubation
The interval (in seconds) between the first insertion of a laryngoscope blade into the mouth and the final placement of an endotracheal tube or tracheostomy tube in the trachea.
Time frame: Duration of procedure (minutes)
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Video Laryngoscope Group | Duration of Laryngoscopy and Tracheal Intubation | 38 Seconds |
| Direct Laryngoscope Group | Duration of Laryngoscopy and Tracheal Intubation | 46 Seconds |
Esophageal Intubation
Time frame: from induction to 2 minutes following tracheal intubation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Video Laryngoscope Group | Esophageal Intubation | 6 Participants |
| Direct Laryngoscope Group | Esophageal Intubation | 9 Participants |
ICU-free Days in the First 28 Days
Time frame: 28 days
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Video Laryngoscope Group | ICU-free Days in the First 28 Days | 20 days |
| Direct Laryngoscope Group | ICU-free Days in the First 28 Days | 19 days |
Injury to the Teeth
Time frame: from induction to 2 minutes following tracheal intubation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Video Laryngoscope Group | Injury to the Teeth | 3 Participants |
| Direct Laryngoscope Group | Injury to the Teeth | 2 Participants |
Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube
Time frame: Duration of procedure (minutes)
Population: Data was not available for entire patient population.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Video Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Endotracheal Tube - 3+ | 15 number of events |
| Video Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Bougie - 1 | 316 number of events |
| Video Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Endotracheal Tube - 2 | 43 number of events |
| Video Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Bougie - 2 | 19 number of events |
| Video Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Bougie - 0 | 364 number of events |
| Video Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Bougie - 3+ | 6 number of events |
| Video Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Endotracheal Tube - 1 | 646 number of events |
| Direct Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Bougie - 3+ | 27 number of events |
| Direct Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Endotracheal Tube - 1 | 620 number of events |
| Direct Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Endotracheal Tube - 2 | 66 number of events |
| Direct Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Endotracheal Tube - 3+ | 19 number of events |
| Direct Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Bougie - 0 | 330 number of events |
| Direct Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Bougie - 1 | 317 number of events |
| Direct Laryngoscope Group | Number of Attempts to Cannulate the Trachea With a Bougie or an Endotracheal Tube | Bougie - 2 | 33 number of events |
Number of Laryngoscopy Attempts
Time frame: Duration of procedure (minutes)
Population: A subset of patients were missing this data variable.
| Arm | Measure | Category | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Video Laryngoscope Group | Number of Laryngoscopy Attempts | Number of times a laryngoscope entered the patient's mouth (reported by observer) - 1 | 636 Participants |
| Video Laryngoscope Group | Number of Laryngoscopy Attempts | Number of times a laryngoscope entered the patient's mouth (reported by observer) - 2 | 54 Participants |
| Video Laryngoscope Group | Number of Laryngoscopy Attempts | Number of times a laryngoscope entered the patient's mouth (reported by observer) - 3+ | 14 Participants |
| Direct Laryngoscope Group | Number of Laryngoscopy Attempts | Number of times a laryngoscope entered the patient's mouth (reported by observer) - 1 | 546 Participants |
| Direct Laryngoscope Group | Number of Laryngoscopy Attempts | Number of times a laryngoscope entered the patient's mouth (reported by observer) - 2 | 127 Participants |
| Direct Laryngoscope Group | Number of Laryngoscopy Attempts | Number of times a laryngoscope entered the patient's mouth (reported by observer) - 3+ | 33 Participants |
Operator-reported Aspiration
Time frame: from induction to 2 minutes following tracheal intubation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Video Laryngoscope Group | Operator-reported Aspiration | 7 Participants |
| Direct Laryngoscope Group | Operator-reported Aspiration | 12 Participants |
Reason for Failure to Intubate on the First Attempt
Providers could give more than one reason for failure to intubate on the first attempt for each intubation (not mutually exclusive). In addition, data on the reason for failure to intubate on the first attempt was missing for 23 patients in the video laryngoscope group and 40 patients in the direct laryngoscope group. Reason for failure among those who did not meet the primary outcome (successful intubation on the first attempt): * Inadequate view of the larynx * Inability to intubate the trachea with an endotracheal tube * Inability to cannulate the trachea with a bougie * Attempt aborted due to change in patient condition (e.g., worsening hypoxemia, hypotension, bradycardia, vomiting, bleeding) * Technical failure of the laryngoscope (e.g., battery, light source, camera, screen) * Other * Not Reported
Time frame: Duration of procedure (minutes)
| Arm | Measure | Group | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|---|
| Video Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Inability to cannulate the trachea with a bougie | 7 Participants |
| Video Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Technical failure of the laryngoscope (e.g., battery, light source, camera, screen) | 2 Participants |
| Video Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Inability to intubate the trachea with an endotracheal tube | 44 Participants |
| Video Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Other | 13 Participants |
| Video Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Attempt aborted due to change in patient condition | 2 Participants |
| Video Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Not Reported | 23 Participants |
| Video Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Inadequate view of the larynx | 26 Participants |
| Direct Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Not Reported | 40 Participants |
| Direct Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Inadequate view of the larynx | 123 Participants |
| Direct Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Inability to intubate the trachea with an endotracheal tube | 32 Participants |
| Direct Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Inability to cannulate the trachea with a bougie | 19 Participants |
| Direct Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Attempt aborted due to change in patient condition | 14 Participants |
| Direct Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Technical failure of the laryngoscope (e.g., battery, light source, camera, screen) | 4 Participants |
| Direct Laryngoscope Group | Reason for Failure to Intubate on the First Attempt | Other | 10 Participants |
Successful Intubation on the First Attempt Without a Severe Complication
This outcome reports the number of participants that experienced successful intubation on the first attempt without experiencing complications, a composite of two independent outcomes: successful intubation on the first attempt (the primary outcome of the trial) and severe complication (the secondary outcome of the trial).
Time frame: from induction to 2 minutes following tracheal intubation
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Video Laryngoscope Group | Successful Intubation on the First Attempt Without a Severe Complication | 484 Participants |
| Direct Laryngoscope Group | Successful Intubation on the First Attempt Without a Severe Complication | 420 Participants |
Ventilator Free Days in the First 28 Days
Time frame: 28 days
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Video Laryngoscope Group | Ventilator Free Days in the First 28 Days | 24 days |
| Direct Laryngoscope Group | Ventilator Free Days in the First 28 Days | 23 days |