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Videolaryngoscopy vs. Fibreoptic Bronchoscopy For Awake Tracheal Intubation - A Systematic Review and Meta-Analysis
Videolaryngoscopy vs. Fibreoptic Bronchoscopy For Awake Tracheal Intubation - A Systematic Review and Meta-Analysis
14299
Review Article
Videolaryngoscopy vs. fibreoptic bronchoscopy for awake tracheal
intubation: a systematic review and meta-analysis
M. Alhomary,1 E. Ramadan,2 E. Curran3 and S. R. Walsh4
Summary
Awake fibreoptic intubation is often considered the technique of choice when a difficult airway is anticipated. How-
ever, videolaryngoscopes are being used more commonly. We searched the current literature and performed a meta-
analysis to compare the use of videolaryngoscopy and fibreoptic bronchoscopy for awake tracheal intubation. Our
primary outcome was the time needed to intubate the patient’s trachea. Secondary outcomes included: failed intuba-
tion; the rate of successful intubation at the first attempt; patient-reported satisfaction with the technique; and any
complications resulting from intubation. Eight studies examining 429 patients were included in this review. The intu-
bation time was shorter when videolaryngoscopy was used instead of fibreoptic bronchoscopy (seven trials, 408 par-
ticipants, mean difference (95%CI) 45.7 ( 66.0 to 25.4) s, p < 0.0001, low-quality evidence). There was no
significant difference between the two techniques in the failure rate (six studies, 355 participants, risk ratio (95%CI)
1.01 (0.24–4.35), p = 0.99, low-quality evidence) or the first-attempt success rate (six studies, 391 participants, risk
ratio (95%CI) 1.01 (0.95–1.06), p = 0.8, moderate quality evidence). The level of patient satisfaction was similar
between both groups. No difference was found in two reported adverse events: hoarseness/sore throat (three studies,
167 participants, risk ratio (95%CI) 1.07 (0.62–1.85), p = 0.81, low-quality evidence), and low oxygen saturation (five
studies, 337 participants, risk ratio (95%CI) 0.49 (0.22–1.12), p = 0.09, low-quality evidence). In summary, video-
laryngoscopy for awake tracheal intubation is associated with a shorter intubation time. It also seems to have a suc-
cess rate and safety profile comparable to fibreoptic bronchoscopy.
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Correspondence to: M. Alhomary
Email: mohamed.alhomary@gmail.com
Accepted: 2 March 2018
Keywords: airway management; awake tracheal intubation; systematic review; videolaryngoscopy
In a recent prospective study, awake fibreoptic intu- Register of Controlled Trials (CENTRAL); MEDLINE;
bation was performed in 1.71% of patients presenting and Embase. The details of our search strategy can be
for surgery under general anaesthesia [6]. The success found in the Supporting Information (Appendix S1).
rate reported was 99%, and the overall complication The reference lists of all eligible papers were hand-
rate was 11%. In addition, this study demonstrated a searched for additional potential studies. We did not
significant negative correlation between the number of restrict our search by language of publication. We dealt
previous awake fibreoptic intubations performed by the with incomplete data by contacting the principal authors,
anaesthetist and the incidence of complications. This when possible, to ask for missing or unclear information.
underlines how continued training in awake fibreoptic Two reviewers (MA and EC or ER) independently
intubation is essential to maintaining the safety of this screened the articles by title and abstract according to
technique. the predetermined inclusion criteria and excluded any
Videolaryngoscopes, on the other hand, are irrelevant or duplicate studies. Two authors then
increasing in popularity and are slowly becoming the examined the full texts of all potential trials to further
preferred tool for the management of the difficult air- assess their eligibility for inclusion in this review. Any
way. They seem to be easier to use and quicker to learn. disagreement between the authors was resolved by dis-
Heidegger et al. described that anaesthetists need cussion or by consulting a fourth author (SW) to make
around 25 intubations to be competent with fibreoptic a final decision if consensus was not achieved.
intubation [3], whereas only one to six intubations are We included only randomised controlled trials
needed to reach the same level of competence with comparing videolaryngoscopy with fibreoptic bron-
videolaryngoscopy [7, 8]. choscopy in patients requiring awake tracheal intuba-
There are some potential advantages of videolaryngo- tion. We excluded case reports, observational studies
scopes over fibreoptic bronchoscopes. First, they provide and cross-over trials. Mannikin studies were not con-
a wider view of the airway, which results in a better view sidered in this review, and we only accepted trials if
of nearby structures [9]. Second, there is no limitation on they reported intubation time as one of their out-
the tracheal tube diameter which may be used, in contrast comes. Studies were included if they compared the use
to fibreoptic bronchoscopes, when smaller size tracheal of videolaryngoscopes of any model with the use of
tubes cannot be used. Finally, it is easier to change the fibreoptic flexible bronchoscopes. Participants were
size of the tracheal tube if required while maintaining the patients of any age and sex who needed awake tracheal
airway view. This differs from the fibreoptic technique, intubation either via the nasal or oral route, regardless
which requires the removal of the fibrescope from the of the indication and the surgical procedure.
patient’s airway in order to make this change. Our primary outcome was the time needed to
However, the use of videolaryngoscopes for awake intubate the trachea. Our secondary outcomes were:
intubation is a relatively new technique. It is unclear failed intubation; the rate of successful intubation at
whether they truly provide advantages over fibreoptic the first attempts; patient-reported satisfaction; and
intubation. With the aim of summarising the available any complications or adverse events resulting from
literature, we conducted this systematic review and intubation.
meta-analysis to compare videolaryngoscopy and The potential risk of bias in each included study
fibreoptic bronchoscopy for awake intubation. was assessed independently by two authors (MA and
EC or ER). We used the Cochrane Collaboration’s tool
Methods [11] to evaluate the quality of each study design, con-
This systematic review and meta-analysis were con- sidering the following possible sources of bias: random
ducted in accordance with the PRISMA guidelines sequence generation; allocation concealment; blinding
[10]. All authors agreed on the study protocol before of participants, personnel and outcome assessors;
commencing the review. incomplete outcome data; and selective outcome
We carried out a search until June 2017 in the reporting. We also assessed the risk of bias that can
following electronic databases: the Cochrane Central result from the level of experience of the anaesthetist
with the device used for tracheal intubation, as we felt After removal of duplicates, we screened 165 articles
this could be an important confounding factor. by title and abstract for eligibility. From these studies,
We used Review Manager (RevMan 5.3; Copen- we only included nine trials for full-text evaluation.
hagen: The Nordic Cochrane Centre, The Cochrane We excluded one additional article due to irrelevant
Collaboration, 2014) for data analysis. For dichotomous methodology (Fig. 1) [17].
outcomes (e.g. failure rate, first-attempt success), we Eight studies were eventually included in our
calculated risk ratios (RR) with 95%CI, and for contin- review [18–25]. We excluded one study from the
uous outcomes (e.g. intubation time), we used the meta-analysis due to incomplete data reporting [23].
mean difference (MD). When the continuous outcome Table 1 presents the characteristics of included studies,
was reported in some studies as median, range and and Table S1 summarises the baseline characteristics
interquartile range, we estimated means and standard of participants.
deviations using the formula described by Hozo [12]. A total number of 429 participants were included
Risk ratios were calculated with the Mantel–Haen- in the eight studies. All participants were adult patients
szel method using the random-effects model as we with ASA physical status 1–3. None of the studies
expected clinical and methodological heterogeneity investigated patients who required emergency intuba-
between the studies. We evaluated the heterogeneity by tions. Two studies included only obese patients sched-
using the I2 statistic, with I2 levels of 25%, 50% and 75% uled for bariatric surgery [18, 23]. All intubations were
implying low, moderate and high degrees of heterogene- performed in operating theatres by anaesthetists with
ity, respectively. We carried out sub-group analyses for variable expertise in both videolaryngoscopy and fibre-
the route of intubation and the design of videolaryngo- optic techniques.
scope to investigate the causes of significant heterogene- Five different types of videolaryngoscopes were
ity. In addition, we undertook a post-hoc sensitivity used: GlideScope™ in four studies [18, 21, 23, 25]; Bul-
analysis by omitting certain studies from the data syn- lard™ laryngoscope [19]; McGrath series 5™ [24]; C-
thesis to further explore the robustness of our results. MAC D-blade™ [20] and Pentax AWS™ [22] (each in
Visual inspection of funnel plots is often used to one study). Two types of fibreoptic bronchoscopes
assess for publication bias, as evidence of this can be were used; the Karl Storz fibrescope in two studies [20,
indicated by the presence of asymmetry in the scatter 21] and the Olympus fibrescope in four studies [18,
plot. However, publication bias is only one reason for 19, 22, 25]. Two studies did not specify the type of
funnel plot asymmetry, and other factors can con- fibreoptic bronchoscope used [23, 24]. In most of the
tribute to this asymmetry [13]. When funnel plot included studies, intubations were performed via the
asymmetry exists, this should further be determined oral route. Only in two studies was the nasal route
using statistically relevant analyses [14]. We intended used for intubation [20, 21].
to investigate publication bias using the funnel plot According to our assessment, the majority of the
technique, with Egger’s regression when appropriate. studies had a low risk of selection, attrition and selec-
Finally, we applied the Grades of Recommenda- tive reporting biases. Blinding of participants, person-
tion, Assessment, Development, and Evaluation nel and outcome assessors was not possible due to the
(GRADE) system [15] using GRADEpro software nature of the intervention. Most of the studies
(https://gradepro.org) to rate the quality of evidence reported in detail the number of previous intubations
for each of our primary and secondary outcomes, tak- performed with each device, so we rated these studies
ing into account risk of bias, inconsistency, impreci- as being at low risk of bias. The anaesthetists studied
sion and indirectness [16]. by Cohn et al. [19] had performed at least 10 previous
intubations with videolaryngoscopy and fibreoptic
Results bronchoscopy; we felt that this number would favour
In our initial electronic search, we identified 239 the videolaryngoscopy group. A summary of the risk
potential articles. No additional studies were detected of bias for each included study is shown in Figure 2.
through manual scrutiny of reference lists of studies. Publication bias was not assessed because the number
Studies included in
qualitative synthesis
(n = 8)
Included
Studies included in
quantitative synthesis (meta-
analysis)
(n = 7)
of included studies was insufficient to explore a funnel between the studies (I2 = 94%). This significant
plot or use more advanced regression-based assess- heterogeneity did not improve when we performed
ments appropriately. sub-group analyses by the type of videolaryngoscope
All studies reported intubation times. However, used or the route of tracheal intubation. We were able
one study reported only the adjusted difference in only to combine the trials that used the GlideScope, as
mean time for intubation between the two groups with each of the remaining studies investigated a different
no further details [23], and for this reason, we could videolaryngoscope design. To further explore potential
not include this study in the meta-analysis. Our analy- causes of this high heterogeneity, we performed a sen-
sis of the remaining seven studies showed that video- sitivity analysis by omitting two studies from our
laryngoscopy resulted in a shorter intubation time pooled data synthesis [22, 25]. The results of this anal-
compared with fibreoptic bronchoscopy (Fig. 3). How- ysis demonstrated a shorter intubation time in the
ever, we detected a marked degree of heterogeneity videolaryngoscopy group compared with the fibreoptic
Study Device Participants (n) Inclusion criteria Exclusion criteria Interventions Outcomes
Cohn et al. Bullard VL: 8 Adults; ASA 1–3; risk No details Oral intubation; fentanyl, Time to glottic
[19] FB: 9 of neurological injury midazolam and droperidol visualisation; time to
Surgical (radicular symptoms, for sedation; topical intubate the trachea;
correction of request for awake anaesthesia with lidocaine failure rate
cervical spine intubation by
problem neurosurgeon)
Rosenstock McGrath VL: 48 Adults; ASA 1, 2, Age less than 18; Oral intubation; Intubation time;
et al. [24] FB: 45 3; modified SARI ASA 4, 5; mouth premedication with first-attempt success
Elective score ≥ 4; requiring opening less than glycopyrrolate; rate; number of
gynaecology, oral intubation for GA 15 mm; poor remifentanil infusion intubation attempts;
urology, ENT and dentition; surgeon’s and a bolus of glottic view; ease of
abdominal surgery request for nasal remifentanil or propofol; the technique
intubation; target Ramsay score of (VAS 0–10);
contraindication to 2–4; topical anaesthesia complications;
(continued)
5
Anaesthesia 2018
6
Table 1 (continued)
Study Device Participants (n) Inclusion criteria Exclusion criteria Interventions Outcomes
Kramer et al. C-MAC VL: 50 Surgical procedure Dental abscess; ASA ≥ 4 Nasal intubation; Intubation time; best
[20] D-blade FB: 50 requiring nasal midazolam and glottic view;
Anaesthesia 2018
EGRI, El-Ganzouri risk index; FB, fibreoptic bronchoscopy; GA, general anaesthesia; MILS, manual in-line stabilisation; SARI, simplified airway risk index; TCI, target-con-
trolled infusion; VAS, visual analogue scale; VL, videolaryngoscopy.
Alhomary et al. | Videolaryngoscopy vs. fibreoptic bronchoscopy for awake tracheal intubation
Figure 3 Forest plot for the comparison of intubation time between videolaryngoscopy and fibreoptic bronchoscopy
groups. FB, fibreoptic bronchoscopy; IV, inverse variance; VL, videolaryngoscopy.
Figure 4 Forest plot for the comparison of failed intubation between videolaryngoscopy and fibreoptic bronchoscopy
groups. FB, fibreoptic bronchoscopy; M-H, Mantel–Haenszel; VL, videolaryngoscopy.
Figure 5 Forest plot for the comparison of first-attempt success between videolaryngoscopy and fibreoptic bron-
choscopy groups. FB, fibreoptic bronchoscopy; M-H, Mantel–Haenszel; VL, videolaryngoscopy.
The intubation time was our primary outcome heterogeneity was detected between the studies. Sub-
investigated; the pooled data analysis demonstrated group analysis by the type of videolaryngoscope or
that the use of videolaryngoscopy is probably associ- the route of intubation did not explain this hetero-
ated with a shorter intubation time compared with geneity. We found no significant difference between
fibreoptic bronchoscopy. However, a high degree of the two techniques with regard to our secondary
Figure 6 Forest plot for the comparison of sore throat/hoarseness between videolaryngoscopy and fibreoptic bron-
choscopy groups. FB, fibreoptic bronchoscopy; M-H, Mantel–Haenszel; VL, videolaryngoscopy.
Figure 7 Forest plot for the comparison of oxygen saturation less than 90% between videolaryngoscopy and fibreop-
tic bronchoscopy groups. FB, fibreoptic bronchoscopy; M-H, Mantel–Haenszel; VL, videolaryngoscopy.
outcomes of failed intubation, first-attempt success the definition of intubation time was different between
rate, patient satisfaction or complications related to studies and various points of time were used to assess
intubation. this outcome.
Several possible factors may explain the high level In our sensitivity analysis, we omitted the study by
of heterogeneity detected. First, although all studies Wahba et al. as they did not include patients with
recruited participants with known or predicted difficult apparent airway difficulty in their research [25].
airway, the criteria used to assess this varied consider- Although cervical spine immobility can make intuba-
ably in different studies. For example, Cohn et al. and tion more challenging, it has been shown that video-
Wahba et al. included patients with cervical spine dis- laryngoscopes are associated with less cervical spine
ease and traumatic cervical spine injury, respectively movement [26–28]. These participants may have had
(which indicates a requirement to maintain neutral relatively easier airways and this may have accounted
cervical spine position during intubation) [19, 25]. for the shorter intubation times found in this study.
This is in contrast to the more robust criterion (sim- We also removed the trial by Mendonca et al. due to
plified airway risk index) used by Abdellatif et al., different methodology [22]. The authors described a
Moore et al. and Rosenstock et al. [18, 23, 24], which ‘spray as you go’ technique for providing topical
takes into consideration multiple factors such as anaesthesia to the airway. This may explain why intu-
mouth opening, neck movement, weight, thyromental bation times noted in this trial were significantly
distance and a previous history of difficulty in intuba- longer than those in the remaining studies. Further-
tion. Second, our review included patients of different more, their sample size was not calculated to detect a
populations in different clinical settings, from obese difference in intubation time, as their primary outcome
patients for bariatric surgery to patients with oropha- was the total procedure time (sedation time and intu-
ryngeal cancer requiring maxillofacial procedures. bation time). The degree of inconsistency improved
However, this diversity of types of patient potentially following this sensitivity analysis and the results
contributes to the generalisability of the results. Finally, demonstrated an effect estimate comparable to our
primary analysis. However, as this was a post-hoc should be interpreted with caution for two possible
analysis, we did not consider these findings in our reasons. First, these studies were not powered to detect
assessment of the quality of evidence. a difference in patient satisfaction between the two
A major limitation of our study is that we carried groups. Second, the awake intubation described in
out a meta-analysis on an outcome with high hetero- these trials involved the use of various sedative agents
geneity (intubation time). We believe that this hetero- to facilitate the procedure; this can affect the ability of
geneity may have resulted from the different patients to recall the procedure and to measure this
methodologies and clinical factors within the studies, outcome reliably.
but we acknowledged this limitation, and we down- Our assessment demonstrated a low risk of bias in
graded the quality of the evidence accordingly. most domains among the majority of the included
Another limiting factor is the variation in the types of studies. However, the blinding of intubators and out-
videolaryngoscope used in different studies and our come assessors was not possible, and this could be an
inability to perform sufficient sub-group analysis. The area of concern regarding our results. Another factor
GlideScope was the only scope used in more than one was the experience of the anaesthetist who performed
trial; the remaining studies used different models of the intubation. As most of the trials clearly quantified
videolaryngoscope. This probably contributed to the the previous experience of the intubators with each
substantial heterogeneity between the studies, but simi- device, we believe this potential source of bias did not
larly, added to the generalisability of our results, as affect the quality of evidence from this review.
various institutions and practitioners will choose to Most studies in our review did not include
use different types of videolaryngoscope in their rou- patients with limited mouth opening due to the poten-
tine practice. tial difficulty in inserting the videolaryngoscope blade
Intubation times, particularly when they are short, into the airway in these patients [32, 33]. This makes
may not be of clinical importance. However, if intuba- applying the results of our review to this group of
tion time is prolonged due to patient factors or the patients more difficult, although fibreoptic bron-
anaesthetist’s level of experience, a further increase in choscopy might be more appropriate in this setting. In
time can be critical, especially in anxious patients with addition, all intubations were performed in elective
respiratory compromise and who are at increased risk patients, and this precludes the generalisability of the
of loss of airway patency. Furthermore, intubation time results to emergency intubations when anaesthetists
may also provide information about the ease of the and patients can be under psychological and time
technique, although this is debatable. Finally, we can pressures.
argue that decreasing intubation time in awake, albeit To our knowledge, this is the first systematic
sedated, patients may be associated with less patient review to provide data on the use of videolaryngoscopy
discomfort, as it shortens the duration of a potentially for awake tracheal intubation. We did not find previ-
stressful procedure. ous similar reports that we can compare for agreement
Patient satisfaction is an important outcome and disagreement with our results. It highlights the
because awake intubation can be uncomfortable and value of videolaryngoscopy as an alternative to awake
requires an adequate level of sedation and topical fibreoptic intubation in carefully selected patients.
anaesthesia to be tolerated. However, patient satisfac- Videolaryngoscopes appear to be safe for awake intu-
tion can be difficult to define and is often influenced bation, and can achieve overall and first-attempt suc-
by cultural, social and cognitive factors [29]. Examples cess rates comparable to fibreoptic bronchoscopy.
of attributes of care that have been shown to improve Furthermore, there is lower quality evidence that the
patient satisfaction include shared decision making, use of videolaryngoscopes can result in faster tracheal
effective communication, information and respect [30, intubations. Future research should focus on evaluating
31]. Although a significant difference in patient satis- awake videolaryngoscopy in non-elective environments
faction was not found between the videolaryngoscopy and explore patient satisfaction with awake videolaryn-
and the fibreoptic bronchoscopy groups, these results goscopy in more detail.
33. Aziz MF, Bayman EO, van Tienderen MM, Todd MM, StAGE Table S1. Baseline characteristics of participants in
Investigator Group, Brambrink AM. Predictors of difficult vide-
olaryngoscopy with GlideScope(R) or C-MAC(R) with D-blade:
the included studies. Values are mean SD, median
secondary analysis from a large comparative videolaryn- [range] or number, n.
goscopy trial. British Journal of Anaesthesia 2016; 117: 118– Table S2. Summary of findings for videolaryn-
23.
goscopy compared with fibreoptic bronchoscopy for
awake tracheal intubation.
Supporting Information
Appendix S1. Search strategy for electronic data-
Additional Supporting Information may be found in
bases.
the online version of this article: