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ORIGINAL ARTICLE
Year : 2021 | Volume
: 37
| Issue : 2 | Page : 266-271
A randomized control led study comparing CMAC video laryngoscope and Macintosh laryngoscope for insertion of double lumen tube in patients undergoing elective thoracotomy
Amit Mathew1, Jacob Chandy1, Joseph Punnoose1, Birla Roy Gnanamuthu2, L Jeyseelan3, Raj Sahajanandan1
1 Department of Anaesthesia, Christian Medical College, Vellore, Tamil Nadu, India
2 Department of CTVS, Christian Medical College, Vellore, Tamil Nadu, India
3 Department of Biostatistics, Christian Medical College, Vellore, Tamil Nadu, India
Correspondence Address:
Dr. Raj Sahajanandan
Department of Anaesthesia, Ida Scudder Road Christian Medical College, Vellore - 632 002, Tamil Nadu
India
Source of Support: None, Conflict of Interest: None
CheckDOI: 10.4103/joacp.JOACP_79_20
Background and Aims: Double lumen tube (DLT) insertion for isolation of lung during thoracic surgery is challenging and is associated with considerable airway trauma. The advent of video laryngoscopy has revolutionized the management of difficult airway. Use of video laryngoscopy may reduce the time to intubate for DLTs even in patients with normal airway.
Material and Methods: A total of 87 ASA 1–3 adults, scheduled to undergo elective thoracotomy, requiring a DLT were randomly allocated to videolaryngoscope (CMAC) arm or Macintosh laryngoscope arm. It was on open label study, and only the patient was blinded. The primary objective of this study was to compare the mean time taken for DLT intubation with CMAC (Mac 3) and Macintosh laryngoscope blade and the secondary objectives included the hemodynamic response to intubation, the level of difficulty using the intubation difficulty scale (IDS), and complications associated with intubation.Data was analysed using the statistical software SPSS (version 18.0).
Results: The time taken for intubation was not significantly different (42.8 ± 14.8 s for CMAC and 42.5 ± 11.5 s for Macintosh laryngoscope P -0.908). The CMAC video laryngoscope was associated with an improved laryngoscopy grade (Grade I in 81.8% with CMAC and in 46.5% with Macintosh), less pressure applied on the tongue, and less external laryngeal pressure required. Hemodynamic responses to intubation were similar in both groups.
Conclusion: Macintosh blade is as good as CMAC (mac 3) blade to facilitate DLT intubation in adult patients with no anticipated airway difficulty, however CMAC was superior as it offers better laryngoscopic view, needed less force, and fewer external laryngeal manipulations.
Keywords: Anesthesia, CMAC video laryngoscope, double lumen tube, intubation difficulty scale (IDS), Macintosh
Thoracic surgery requires the collapse and isolation of the lung and ventilation of the other lung to be operated. Double lumen tube (DLT), the most common method by which lung isolation is achieved, is considered the gold standard for lung isolation.[1] A double lumen tube is longer, more rigid, and has a larger external diameter as compared to a single lumen tube. This difficulty is compounded if it is done by an occasional thoracic anesthetist or if the patient has a difficult airway.[2],[3]
Video laryngoscopes are a part of most of the widely accepted airway guidelines such as Difficult Airway Society (DAS) and American Society of Anesthesiologists (ASA) for endotracheal intubation in case of a difficult airway. Video laryngoscopes have been studied for the ease of intubation of DLT but with varied success. CMAC, a videolaryngoscope introduced by Karl Storz in 2009 is widely used for insertion of endotracheal tubes especially in difficult airway scenarios.[4]
We hypothesized that CMAC video laryngoscope is superior to Macintosh laryngoscope for insertion of DLTs in patients undergoing thoracotomy. The primary objective of this study was to compare the mean time taken for DLT intubation with CMAC (Mac 3) and Macintosh laryngoscope blade.
The secondary objectives were to assess the hemodynamic response to intubation with either scopes, the level of difficulty using the intubation difficulty scale (IDS) and the complications associated with intubation.[5]
Material and MethodsAfter approval from the Institutional Review Board and obtaining written informed consent, a randomized controlled trial was conducted in 87 patients. They were randomized to CMAC group or Macintosh group. The study was done in thoracic surgery operating rooms of our hospital. All patients were posted for surgeries requiring lung isolation.
Patients between the ages of 18 to 70 years were included in the study. Pregnant patients, patients with anticipated difficult airway – limited neck extension, thyromental distance less than 6.5 cm, height <150 cm, BMI greater than 30, Mallampatti 4, ASA IV patients, and patients at risk of aspiration were not recruited. Patients in whom there was a failure to intubate after three attempts were excluded from the study.
Sample size was calculated using G*Power (Version 3.2.1, Kiel, Germany) to show a minimum difference of about 10 s in the mean intubation time. This is considered clinically important when using CMAC as compared to Macintosh based on previously published studies.[6],[7] The calculated sample size was 47 in each group, with 80% power and 5% level of significance.
Anesthetists who had the experience of inserting more than 10 DLTs and who had used both scopes more than 10 times on an intubating mannequin and 5 times in patients were allowed to participate in the study.
Patients who met the eligibility criteria were enrolled by the primary investigator the day before the surgery and patient information sheet was discussed with the patient.
Permuted block randomization of size 2, 4, or 6 was used to generate the random sequence using SAS 9.1.3 software. This computer generated randomization was put in serially numbered opaque sealed envelopes and kept in the operating room. The sealed envelopes were given to the anesthetist just before the induction of anesthesia. During intubation, the method provided in the envelope was administered by the anesthetist.
The study was not blinded as we could not hide the laryngoscope from the study participants, but it was blinded from the patient and the author doing the outcome analysis.
The anesthesia protocol was standardized. All patients received ASA standard monitoring with invasive blood pressure monitoring. The patients were preoxygenated (ETO2 > 90%), anesthesia was induced with propofol (1.5 mg/kg) and fentanyl (2-3 mcg/kg). Additional propofol boluses (maximum upto 3 mg/kg) were titrated till loss of verbal response. After checking for adequacy of mask ventilation, rocuronium (1 mg/kg) was administered. Adequacy of muscle relaxation was ensured by a TOF ratio of zero on ulnar nerve stimulation of adductor pollicis longus using a TOF watch. 35 or 37 F DLT was used for female patients depending on whether their height was less or more than 160 cm. Male patients received 39 or 41 F DLT (Mallinckrodt Medical, Athlone, Ireland) depending on whether their height was less or more than 170 cm. Left main bronchus diameter of >12 mm, 12 mm, 11 mm, and 10 mm were also looked at for selection of 41,39,37, and 35 DLT.[8] After glottic visualization, DLT with stylet curved to match the laryngoscope was introduced with distal concavity facing anteriorly.[1] Once the blue cuff was beyond the vocal cords, the stylet was removed and the tube was rotated 90° counter clockwise and inserted till mild resistance was perceived. If the Cormack & Lehane grade was more than 2, backward, upward and right-sided pressure (BURP) manoeuvre was applied to improve the view.
The time taken for intubation was defined as the time from introduction of the scope till three complete capnographic cycles. The position of the tube was confirmed with a fibre optic bronchoscope. An independent observer, who was familiar with the protocol, measured the time taken for successful intubation using the timer set on Philips MP 70 monitor. The observer also documented the use of external laryngeal manipulations.
We looked at complications like postoperative hoarseness, sore throat, esophageal intubation, blood on the laryngoscope blade, and for any obvious lacerations after intubation. Hemodynamic response (HR, blood pressure. and mean arterial pressure (MAP) to intubation was monitored at zero (baseline), one min, three min, and five min. Postoperatively, an independent observer looked for hoarseness and sore throat. We did not have any changes in methodology or outcome variables after the trial commenced.
We computed mean and standard deviation for normally distributed continuous variables and frequencies and percentages for categorical variables. We used Shapiro Wilk's test to check for normality and then median with inter quartile range was reported for those continuous variables, which were not normally distributed. Student's t-test and ANOVA were used for normally distributed continuous variables. We used Mann Whitney U test to compare between groups for non-normally distributed continuous variables. Chi-square tests were used for categorical variables. We used SPSS version 18 for all analyses. We used P < 0.05 as the criterion for statistical significance.
ResultsA total of 101 patients were screened, of which 14 patients were excluded from the study as they did not meet the inclusion criteria or did not consent to participate in the study.
Recruitment was done between May 2015 and August 2016. Recruitment was completed when the sample size was attained. Our final sample size was 87, with 44 assigned randomly to the CMAC group and 43 to the Macintosh group. The flow of participants is shown in the Consort diagram [Figure 1].
Figure 1: Participant flow [on the basis of guidelines for randomized controlled trails of the CONSORT (consolidated standards of reporting trails) statement]Both groups were comparable in terms of demographic parameters like age, sex, height, BMI, and airway characteristics [Table 1]. Four consultants and three senior trainees did all the intubations. During lung isolation, left DLTs were preferred due to an increased margin of safety.
The mean time taken to intubate with CMAC laryngoscope was similar to that with Macintosh laryngoscope [Table 2] and [Table 3]. The hemodyanamic response to intubation with the two scopes at baseline, intubation, and 1, 3 and 5 min after intubation is shown in [Figure 2] and [Figure 3].
The IDS for the CMAC video laryngoscope (2.6) was significantly less than that, for the Macintosh laryngoscope (4.0) (P < 0.001).
None of the subjects in our study developed postoperative hoarseness. One patient in the Macintosh group had mild airway injury during intubation, which was indicated by blood on the blade of the scope. One patient in the CMAC group had a small laceration near the anterior tonsillar pillar. There was no significant difference between two groups when it came to mucosal injuries None of the patients had esophageal intubations, while one patient in the Macintosh group had intubation on the wrong side. The DLT cuff was torn in two patients in the CMAC group.
DiscussionThere was no significant difference in time taken for DLT intubation using CMAC and Macintosh blades in our study. The average time taken in our study was comparable to similar studies published by the likes of Hsu et al., Russel et al.[6],[9] Hsu et al. in their study comparing Glidescope (videolaryngoscope) and Macintosh laryngoscope had only two anesthetists intubating all cases and both of them had done more than 300 intubations with video laryngoscope. The time taken to intubate was 45.6 ± 10.7 s with Glidescope and 62 ± 29.7 s with Macintosh.[6] As most of the intubations in our study were done by regular thoracic anesthetists, the timings recorded were slightly better in both the groups. Another study done by Russel et al. had 30 junior anesthetists intubating with the same two scopes, where Glidescope took significantly longer (32 s for Macintosh vs 70 s for Glidescope).[9]
The subgroup analysis of the consultant's average time and shortest time taken for intubation with CMAC was comparable to Hsu et al.(2013). This brings out an important issue about training and the learning curve.[3] We had a heterogeneous group consisting of consultants and trainees performing the intubations rather than one or two experienced anesthetists (Russel et al). Thus, our results could be extrapolated to the wider anesthetist pool who may need to perform a DLT intubation. We feel that the learning curve for video laryngoscopic intubation of DLT may be more than 15 intubations. Inexperienced operators tend to use the video laryngoscope similar to the Macintosh laryngoscope by keeping the tip of the blade in the vallecula, resulting in difficulty in intubation despite a better glottic view. Consultants who were regularly posted in the cardiothoracic theatres were able to visualize the cords and intubate much faster as compared to the trainees, irrespective of the type of scope. Macintosh is commonly used for all DLT insertion and this familiarity may be one reason for similar intubation times. Our study was conducted in patients with no anticipated difficult airway where CMAC blade improved the view but not intubation times.
When used by the trainees, the amount of lifting force required and laryngeal pressure applied was however lesser with the CMAC blade, which is significant. However, this did not translate to faster intubation.
Unlike Hsu et al., we used height as a criterion and tried to use the largest DLT, which could be introduced. We also used three complete ETCO2 traces for confirmation. Despite this, our intubation times were comparable with the more experienced operators in Hsu's study.[6]
Unlike the Glidescope and Mcgrath series 5, CMAC MAC3 is not an angulated blade, which necessitates curving the DLT to match its shape. This can result in a rigid tube, getting impinged at subglottis. This may explain the intubation difficulties in some of the studies using Glidescope (Russel, Yao).[9],[10] With CMAC MAC 3, we curve the bronchial lumen about 10 cm from the tip to match a normal ET tube.
We removed the stylet immediately after the bronchial cuff negotiated the vocal cords, which made the tube less rigid and probably reduced trauma and the incidence of sore throat. Further, the incidence of first attempt failures and malpositions were less in our study.
We noticed that the time taken to intubate improved during the course of the study for the primary investigator and other trainees. This observation was similar to El Thahan et al.[11] and could be due to the steeper learning curve to learn DLT insertion with video laryngoscope.
The hemodynamic response to intubation was not significantly different between the groups due to the comparable time taken for intubation. The subjective feeling of force exerted on the tongue is significantly less with CMAC blade, which may make it a good option for individuals in whom hypertension and tachycardia may be detrimental.
The difference in IDS score for Macintosh and CMAC was significant, implying a subjective ease for DLT insertion with CMAC scope as compared to the Macintosh scope. CMAC offered a significantly better laryngoscopy grade and significant reduction in external laryngeal manipulations to facilitate intubation.
The better view of the laryngeal inlet with CMAC did not translate to faster intubation, probably because a good view on the video laryngoscopy does not require the alignment of the airway axes.[12] Also, the new DLT, when unpacked, has a well defined oropharyngeal curve and a small bronchial curve, which needs to be curved to match the shape of the laryngoscope. This is especially important when angled blades like Glidescope or CMAC D blades are being used.
Our results were different from Shah et al.[1] who had only 55% of tube insertions in the first attempt and a much higher incidence of bleeding and trauma with the Macintosh scope. This significant difference could be attributed to Shah et al. including patients with difficulty airway, while such patients were excluded from our study and all our operators had experience in intubating with DLT and also using the CMAC video laryngoscope.
Videolaryngoscopy offers an advantage over traditional laryngoscopy when it comes to teaching residents on how to intubate with DLT as they can observe the manipulations done by an experienced anesthetist. However, this did not translate to a faster intubation time.[13] The limitations of this study were, firstly, that the study was not blinded as it was difficult to hide the scope, which is used to intubate.
Secondly, we did not include patients with difficult airway in our study. Hence, our results cannot be extrapolated to patients with difficult airway. Thirdly, the difficulty level was assessed using an intubation difficulty scale and subjective feel of lifting force required or the need for external laryngeal manipulations, which were all operator dependent and not objectively measured variables. Finally, we did not measure the time to visualize the cords with either scope, which may have been less with CMAC due to camera optics.
We had two cases of torn tracheal cuff in the CMAC group. Clinicians are advised to look into the mouth during the introduction of video laryngoscope, then obtain the desired view on screen and look in for initial introduction of the tube[14] A videolaryngoscope has lesser flange height of 1.6 cm as compared to 2.5 cm in case of a Macintosh laryngoscope. A reduced space as well as the wrong technique of looking only at the screen resulted in the two instances of cuff tears.
ConclusionCMAC video laryngoscopes can be a useful alternative to traditional Macintosh laryngoscope for the insertion of DLT in patients with uncomplicated airway. There is an improved laryngoscopy grade, lesser pressure is applied on the tongue, and lesser external laryngeal pressure is required while using CMAC video laryngoscope. However, the time taken and hemodynamic response to intubation are similar to those with Macintosh laryngoscope.
Acknowledgements
Dr. Sajan Philip George, former Head of the Department of Anesthesia, Christian Medical College Vellore for constant support and guidance. 2. The Department of Anesthesia technical staff for helping with the cases. 3. The Research Office and Institutional Review Board for guidance and access to the internal fluid research fund. 4. CTRI - The trial was registered with CTRI (CTRI/2019/04/018521).
Financial support and sponsorship
Study was funded by the research fund of our medical college – Christian Medical College, Vellore.
Conflicts of interest
There are no conflicts of interest.
References
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