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The New GlideRite DLT Stylet®: An Observational Study

The New GlideRite DLT Stylet®: An Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01308918
Enrollment
50
Registered
2011-03-04
Start date
2010-05-31
Completion date
2011-01-31
Last updated
2012-03-26

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

Conditions

Double Lumen Tube Intubation

Keywords

Thoracic surgery, Double lumen tube intubation, GlideScope, Stylet

Brief summary

Thoracic surgeries usually require lung isolation techniques. Double-lumen tube (DLT), either right or left sided, is the most frequent tool used to realize this technique. In front of difficult airways, the use of videolaryngoscopy (GllideScope®) (GS) may advantageous. Hypothesis: We will test the hypothesis that under GS, the use of a specific semi-rigid stylet is efficacious to insert a DLT, and also safe. The increased rigidity of the GlideRite DLT Stylet for double-lumen tubes will enable the DLT to keep its form while it is railroaded into superior airways. This new stylet combined to Glidescope® utilization will increase the rate of successful intubation, especially in patients with difficult airways. This technique will allow us to directly intubate with a DLT using the GlideScope®, avoiding a beforehand SLT intubation and airway exchange catheter use. Consequently, its use could reduce risks associated to blind insertion of DLT with airway exchange catheter (airway traumatism and pulmonary aspiration). Primary objective: To determine the GlideRite DLT Stylet efficiency for double-lumen tubes orotracheal intubation under videolaryngoscopy (GllideScope®). Secondary objectives: to time successful intubation, to count the number of intubation attempt, to verify the influence of difficult intubation score (DIS) on successful intubation, and to log complications associated to its use. Exclusion criterion are: previous history of difficult intubation, anticipated difficult mask ventilation, and anticipated difficult intubation. Conclusion: The aim of using the GlideRite DLT Stylet for an orotracheal intubation under videolaryngoscopy is to allow the primary intubation with a DLT in patients with abnormal superior airways. These anomalies are more and more frequent. Alternative airway management implies more manipulations, leading to an increased risk of oxygen desaturation, lung aspiration, and airway lesions. Moreover, these alternatives take more time than using a Glidescope, which can be compare to direct laryngoscopy. The development of a semi-rigid stylet, such as the GlideRite DLT Stylet, is a great advancement in the management of primary intubation with DLT, mainly in face of difficult airways.

Detailed description

INTRODUCTION Anesthesia in thoracic surgery (non cardiac) often requires pulmonary isolation techniques in order to facilitate the surgery, to protect a healthy lung, and to control the ventilation. The double lumen tube (DLT), in right and left version, is the technique of choice to obtain lung isolation, whereas the bronchial blocker can also be used. Double-lumen tube One-lung ventilation is required in most of thoracic surgeries. Many strategies can be used to achieve lung isolation: 1) use of endobronchial tube, 2) use of a single-lumen tube (SLT) and a bronchial blocker (BB),or 3) use of a double-lumen tube (DLT). There is many advantages of using a DLT: easier to position, shorter time of lung collapsing and re-expansion than BB, each lung can be suctioned/ventilated separately, and less subject to displacement than BB. Since no medical instrument is perfect, DLT has also some inconvenient: DLT are larger, and less compliant than a SLT. They also have two cuffs, one bronchial and another one tracheal. The latter is causing problem when intubating patients with teeth at the superior jaw. Precautions have to be taken to avoid rupturing the tracheal cuff. These characteristics are exaggerated when anesthesiologist faces a patient with a difficult airway. These cases are usually managed by first proceeding to a standard intubation with a SLT, second, use an airway exchange catheter (AEC) to withdraw the SLT, and then, advance the DLT into the proper position. Thereafter, the gold standard is to confirm the DLT position with a fiberoptic bronchoscope (FOB). If direct laryngoscopy provides poor glottis visualization, another option is to proceed to a FOB-assisted DLT intubation. Video laryngoscopes Over the last decade, video laryngoscopes have been developed to handle difficult airway management. They have the advantage of improving Cormack-Lehane (CL) grade over direct laryncoscopy. Many manufacturers distribute video laryngoscopes: the Storz® C-MAC™, the McGrath® Series-5™, and the GlideScope® Video Laryngoscope™ (GVL) are few examples. This latter is frequently used in our centre to allow tracheal intubation with a SLT in numerous situations where conventional laryngoscopy is not possible. The GVL requires the same technique than a direct laryngoscopy without a line of sight, turning CL Grade III or IV into CL Grade I or II. Stylet To facilitate the endotracheal tube (ETT) insertion using the GVL, either a semi-rigid or a malleable stylet must be used. There is also a lot of discussion about the best stylet configuration allowing the tip of the ETT to be positioned at the glottis opening and advancing the tube into the trachea, but no consensus has been obtained yet. Difficult airway management may be optimized by shaping the SLT using a malleable stylet, directing the ETT through vocal cords. The main problem of malleable stylet is that it loses its initial shape when the ETT goes through narrow airways. It is why many clinicians prefer the semi-rigid stylet when using the GlideScope®. Double-lumen tubes are already supplied with a malleable aluminum stylet in order for them to maintain their initial shape, and some authors found that accuracy of placement have improved when it is retained into a left-DLT for the entire intubation procedure. New semi-rigid stylet Video laryngoscopes have been designed to be mostly used with SLT, but recent publications have suggested using a GlideScope® for primary DLT placement in difficult airways, as described by Hernandez, A et al. in 2005 and Chen, A et al. in 2008. Even if DLT are provided with a stylet, the technique of intubation with the GVL remains difficult, mainly because the aluminum stylet is too malleable. Verathon Inc. has marketed the GlideRite® rigid stylet, especially design to use with the GlideScope®. Its length fits most of SLT, its shape is adapted to the GVL's curvature, and the curvature can be modified to accommodate a difficult airway only with intentional movement. In collaboration with Verathon Inc., we have designed a new semi-rigid intubating stylet that can be use for primary DLT intubation with the Glidescope® Videolaryngoscope, the GlideRite DLT Stylet®. This improved intubating tool is sharing the same curve but is longer than the GlideRite® rigid stylet. It present a specific handle to fit with the DLT and to orient the distal extremity into the right or left bronchus. The new stylet fits 35 to 41 French, left of right-sided DLTs. Anticipated benefits of this new design are a shorter time required to position the DLT, less intubating attempt, lower risk of trauma to the airway, lower risk of desaturation and, lower risk of tracheal cuff' rupture, resulting in a one-step lung isolation. HYPOTHESIS We believe that, under video laryngoscopy, the use of the semi-rigid GlideRite DLT Stylet® for primary insertion of DLT is possible. The gain of rigidity that we have developed for the GlideRite DLT Stylet® imposes its shape to the DLT, and conserves it while the tube is guided through the superior airway. We hope that the combination of both the GlideScope® and the new semi-rigid stylet will increase the number of successful primary intubation with a double lumen tube. Furthermore, its utilization could drastically decrease associated risks of blind DLT intubation with an AEC. These risks are oxygen desaturation, pulmonary aspiration, and superior airway trauma. OBJECTIVES The primary objective of this observational study is to determine the GlideRite DLT Stylet® efficiency during endotracheal intubation with a double lumen tube under video laryngoscopy (GlideScope®). The secondary objectives are: 1. To time the intubating process. 2. To count the number of attempt to obtain a successful intubation. 3. To verify the correlation between the difficult intubation score and a successful intubation. 4. To note all complications associated to the GlideRite DLT Stylet® utilization. METHODS After obtaining local REB approval, 50 patients having a thoracic surgery (non cardiac) via either thoracoscopy or thoracostomy, were enrolled to this observational study between May 14th 2010 and January 17th 2011. Intraoperative proceeding Before anesthesia was induced, patients were pre-oxygenated in order to obtain an inspired-expired O2 gradient ≤10%. Anesthesia was performed in conformity with local practice standards. Curarization was achieved by injecting a dose of ≥1.0 mg/kg (ideal body weight) of rocuronium (Zémuron®, Merck & Co., Whitehouse Station, NJ, USA). If mask ventilation was proven to be difficult, the patient was excluded from the study. The malleable stylet was removed from the DLT (Broncho-Cath R- or L-DLT, 35 to 41Fr, Mallinckrodt Inc, St-Louis, MO, USA) and replaced with a GlideRite DLT Stylet® (Verathon Medical ULC, Burnaby, BC, Canada). Before proceeding to the intubation, curarization level was verified with a neuromuscular stimulator, absence of thumb movement when a train-of-four was applied allowed us to begin the protocol. The timer was started when either the GlideScope® blade (Verathon Medical ULC, Burnaby, BC, Canada) was inserted between the lips and stopped when the tracheal cuff was passed through the vocal cords. In case of patients presenting with upper teeth, the timer was started when the DLT was inserted between the lips. Immediately after intubation, intratracheal position was confirmed with FOB. When a patient had teeth at the superior jaw, the DLT was inserted first into the mouth in order to avoid rupturing the tracheal cuff. External larynx manipulations were allowed at all time. If after one (1) minute, the intubation was not successful, the anesthesiologist could then modify the stylet shape. If after two (2) minutes, the intubation was still not achieved, the DLT and GVL blade were withdrawn, and mask ventilation was started again. At that time, the anesthesiologist could use the intubation technique of his choice. The position of the DLT was confirmed by the visualization of the trachea through the FOB. Throughout this process, if oxygen saturation dropped below 94%, mask ventilation was started to increase saturation up to 98% or more before another intubation could be attempted. If oxygen saturation dropped below 90%, mask ventilation was started to increase saturation up to 98% or more, the patient was then excluded from the study, and the anesthesiologist could use the intubation technique of his choice. Statistical analysis Data obtained during the preoperative period will be correlated with the success rate, the time to achieve a successful intubation and, the number of attempt.

Interventions

None listed

Sponsors

Laval University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* 18 years old * Elective thoracic surgery (non cardiac)

Exclusion criteria

* history of a difficult intubation in the past * anticipated difficult mask ventilation * anticipated difficult intubation according to the anesthesiologist's evaluation

Design outcomes

Primary

MeasureTime frameDescription
Number of Successfull Primary Placement of the Double Lumen Tube.1 hour (Post intubation)To evaluate the number of participants where GlideRite DLT Stylet® associated to the video laryngoscopy (GlideScope®)allowed the primary placement of the double lumen tube into their trachea.

Secondary

MeasureTime frameDescription
Duration of the Intubating Process1 hour (Post intubation)The timer was started when the GLS blade was inserted between the lips and stopped when the proximal part of the tracheal cuff was passed through the vocal cords. When a patient had teeth at the superior jaw, the DLT was first inserted into the mouth prior to the insertion of the GLS blade in order to avoid rupturing the tracheal cuff. For these cases, the timer was started when the DLT was inserted between the lips.
Number of Attempt to Obtain a Successful Intubation1 hour (Post intubation)
Correlation Between the Difficult Intubation Score and a Successful Intubation1 hour (Post intubation)
Number of Complications Associated to the GlideRite DLT Stylet® Utilization1 hour (Post intubation)Complications defined either as oxygen desaturation below 95%, oxygen desaturation below 90%, minor bleeding, anatomic lesion.

Countries

Canada

Participant flow

Recruitment details

Between May 14th 2010 and January 17th 2011, 50 patients were enrolled in the study at the end of their pre-operative visit to the thoracic surgery department.

Pre-assignment details

No enrolled participant were excluded from the study. All participants were included into the same group.

Participants by arm

ArmCount
GlideScope DLT Intubation
Patients having a thoracic surgery (non cardiac) via either thoracoscopy or thoracostomy. Patients were all 18 years old or over, and have read, understood and signed an informed consent at the preoperative evaluation or on surgery morning.
50
Total50

Baseline characteristics

CharacteristicGlideScope DLT Intubation
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
22 Participants
Age, Categorical
Between 18 and 65 years
28 Participants
Age Continuous58.7 years
STANDARD_DEVIATION 14.3
Body mass index26.8 kg/m2
STANDARD_DEVIATION 4.8
Region of Enrollment
Canada
50 participants
Sex: Female, Male
Female
23 Participants
Sex: Female, Male
Male
27 Participants
Weight74.3 kg
STANDARD_DEVIATION 14.5

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 50
serious
Total, serious adverse events
0 / 50

Outcome results

Primary

Number of Successfull Primary Placement of the Double Lumen Tube.

To evaluate the number of participants where GlideRite DLT Stylet® associated to the video laryngoscopy (GlideScope®)allowed the primary placement of the double lumen tube into their trachea.

Time frame: 1 hour (Post intubation)

ArmMeasureValue (NUMBER)
GlideScope DLT IntubationNumber of Successfull Primary Placement of the Double Lumen Tube.49 Participants
Secondary

Correlation Between the Difficult Intubation Score and a Successful Intubation

Time frame: 1 hour (Post intubation)

Secondary

Duration of the Intubating Process

The timer was started when the GLS blade was inserted between the lips and stopped when the proximal part of the tracheal cuff was passed through the vocal cords. When a patient had teeth at the superior jaw, the DLT was first inserted into the mouth prior to the insertion of the GLS blade in order to avoid rupturing the tracheal cuff. For these cases, the timer was started when the DLT was inserted between the lips.

Time frame: 1 hour (Post intubation)

ArmMeasureValue (MEAN)Dispersion
GlideScope DLT IntubationDuration of the Intubating Process46.3 SecondsStandard Deviation 32.3
Secondary

Number of Attempt to Obtain a Successful Intubation

Time frame: 1 hour (Post intubation)

ArmMeasureGroupValue (NUMBER)
GlideScope DLT IntubationNumber of Attempt to Obtain a Successful IntubationOne (1) attempt37 Attempts
GlideScope DLT IntubationNumber of Attempt to Obtain a Successful IntubationTwo (2) attempts11 Attempts
GlideScope DLT IntubationNumber of Attempt to Obtain a Successful IntubationThree (3) attempts1 Attempts
GlideScope DLT IntubationNumber of Attempt to Obtain a Successful IntubationFailure1 Attempts
Secondary

Number of Complications Associated to the GlideRite DLT Stylet® Utilization

Complications defined either as oxygen desaturation below 95%, oxygen desaturation below 90%, minor bleeding, anatomic lesion.

Time frame: 1 hour (Post intubation)

ArmMeasureValue (NUMBER)
GlideScope DLT IntubationNumber of Complications Associated to the GlideRite DLT Stylet® Utilization3 Participants

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