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Comparison of different Methods. of ventilation via cannula cricothyroidotomy in a trachea-lung model
Article in BJA British Journal of Anaesthesia · September 2009
DOI: 10.1093/bja/aep264 · Source: PubMed
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Comparison of different methods of ventilation via cannula cricothyroidotomy in a trachea – lung model
†
N. J. Flint1*, W. C. Russell1 and J. P. Thompson2
1 Department of Anaesthesia, Critical Care and Pain Management, University Hospitals of Leicester NHS
Trust, Leicester Royal Infirmary, Leicester LE1 5WW, UK. 2 Department of Cardiovascular Sciences, Clinical
Division of Anaesthesia, Critical Care and Pain Management, University of Leicester and University
Hospitals of Leicester NHS Trust, Leicester Royal Infirmary, Leicester LE1 5WW, UK
*Corresponding author. E-mail: [email protected]
Background. Cannula cricothyroidotomy is recommended in recent guidelines as a rescue
intervention in the ‘cannot-intubate cannot-ventilate’ scenario. Several methods of providing
ventilation via a cannula cricothyroidotomy have been described, but there are no data compar-
ing these methods and using cannulae of differing diameters.
Methods. Using a bench-top trachea – lung model (comprising a Siemens test lung attached to
commercially available breathing system tubing), we compared delivered minute volumes (MVs)
for five methods of ventilation administered through cannulae of diameters 20, 16, 14, and
13 G. The ventilation methods were: an ENK oxygen flow modulator, a Manujet, a self-inflating
resuscitation bag, the oxygen flush of an anaesthetic machine, and oxygen from a wall-mounted
flow meter attached via a three-way tap to the cannula. All experiments were performed
with and without a proximal 2.5 mm diameter constriction to simulate partial upper airway
obstruction.
Results. MVs increased with increasing cannula diameter. In the absence of a proximal constric-
tion, MVs delivered via a 20 G cannula were ,1 litre min21 with all devices; only the Manujet
delivered MVs .2 litre min21, at cannula sizes of �16 G. MVs were greater in the presence of a proximal constriction, but did not exceed 4 litre min
21 using the low-pressure devices.
Conclusions. Extrapolated to the clinical situation, these data suggest that low-pressure devices
will not deliver adequate MVs via a cannula cricothroidotomy and should no longer be advocated.
Purpose-made devices should be available in all areas where anaesthesia is administered or
airway interventions are performed.
Br J Anaesth 2009; 103: 891–5
Keywords: airway, obstruction; equipment, breathing systems; ventilation, transtracheal
Accepted for publication: August 10, 2009
Failure to intubate and to ventilate a patient’s lungs with
oxygen [the cannot-intubate cannot-ventilate (CICV) scen-
ario] can have devastating consequences. This situation is
fortunately rare (with a quoted incidence of 1 in 10 000
general anaesthetics) 1
but is life threatening, and rapid
action is required to prevent hypoxic brain injury, cardiac
arrest, or death. This has led to the publication of guidelines
for the management of the CICV situation. 2 3
The United
Kingdom Difficult Airway Society (DAS) recommends two
options: the use of cannula cricothyroidotomy or surgical
cricothyroidotomy. 3
Surgical cricothyroidotomy has been
advocated as the procedure of choice in pre-hospital care; 4
however, many anaesthetists prefer transtracheal cannula
techniques with which they may be more familiar. 5
There is
little consensus as to the optimal cannula size, although the
DAS guidelines suggest that a ‘large’ cannula should be
used. 3
Previous investigators have commonly used a 14 G
cannula, 6 7
but there are few comparative published data on
which to base recommendations.
In addition to siting a cannula cricothyroidotomy, a
means of ventilation is required. Several purpose-
† Presented in part to the Anaesthetic Research Society Meeting,
Loughborough, UK, November 2005.
# The Author [2009]. Published by Oxford University Press on behalf of the British Journal of Anaesthesia. All rights reserved.
For Permissions, please email: [email protected]
British Journal of Anaesthesia 103 (6): 891–5 (2009)
doi:10.1093/bja/aep264 Advance Access publication September 29, 2009
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manufactured devices are now available, but several other
improvised systems have been described and rec-
ommended 8 – 11
and included in resuscitation manuals. 10
The DAS recommend the use of ‘a high-pressure device
capable of delivering a high minute volume’ (MV); though
they do not state what this MV should be. 3
There are few
data directly comparing the different available systems.
The primary aim of this study was to assess the minute
ventilation delivered by different systems described for ven-
tilation through a cannula cricothyroidotomy using cannulae
of different diameters. Upper airway obstruction is a
common contributor to the CICV scenario and so a second-
ary aim was to assess minute ventilation in the presence or
absence of a simulated proximal airway constriction.
Methods
A simple physical model (Fig. 1) was used, based on the
one previously described. 12
This comprised a 210 mm
length of corrugated plastic anaesthetic breathing system
tubing (22 mm internal diameter), connected to a test lung
(Siemens test lung 190, Siemens Medical Solutions,
Bracknell, UK) which had a static compliance of 24 ml
kPa 21
. The proximal end of the ‘trachea’ was open to
atmosphere via a tracheal tube connector. During each
experiment, an i.v. cannula of varying size (13 – 20 G) was
inserted up to its hub through the wall of the hollow tube
60 mm from the proximal end and secured in place. The
i.v. cannulae were 20, 16, and 14 G (Abbocath Ireland
Ltd, Sligo, Ireland) and 13 G (Ravussin cannula, VBM
Medical, Sultz, Germany); the lengths of these cannulae
were 32, 51, 51, and 63 mm, respectively. MV was deter-
mined using a Wright respirometer connected in series at
the junction of the model trachea and test lung. The respi-
rometer was calibrated before the study against an industry
standard Biotek VT plus gas flow analyser (Biotek
Instruments, Winooski, VT, USA).
Five devices were compared. These were two purpose-
manufactured commercially available devices: the ENK
oxygen flow modulator (Cook, Bjaeverskov, Denmark)
and the Manujet (VBM Medical), and three systems
which are ‘improvised’ but have been described
previously. 8 – 10
The ENK (Fig. 2) and Manujet both
connect to the piped oxygen supply at 4 bar. The ENK
allows the oxygen flow to be controlled manually (by
occlusion of a number of its five side openings); it was
connected to the cannula using the ‘Luer lock’ tubing sup-
plied with the device. The Manujet is a high-pressure gas
injecting device (similar to a Sanders injector) but in
addition the driving pressure can be altered; in this study,
the Manujet was connected to piped oxygen at 4 bar, its
pressure reducing valve set to maximum pressure and con-
nected to the device via the luer lock tubing provided. The
‘improvised’ systems were:
(i) A self-inflating resuscitation bag (Laerdal Medical
Ltd, Orpington, UK) connected to the cannula via a 5
mm tracheal tube connector and connected to wall
oxygen via a flow regulator set at 15 litre min 21
(Fig. 2).
(ii) The oxygen flush from a Blease Frontline 560 anaes-
thetic machine (Blease UK, Chesham, UK) connected
to the cannula via oxygen tubing.
(iii) An improvised three-way tap device (Fig. 2) con-
nected to the cannula via oxygen tubing and con-
nected to wall oxygen via a flow regulator set at 15
litre min 21
, as described in the UK Resuscitation
Council Advanced Life Support Course manual. 10
Oxygen pipeline pressures and delivered flow rates were
measured by the Medical Physics Department using a
Biotek VT plus gas flow analyser. Ventilation was deliv-
ered via all devices at a rate of 20 min 21
with an inspira-
tory time of 1 s. In each case, ventilation was administered
for at least 20 s and the system allowed to stabilize before
measurements of MV were made. MV was recorded six
times in random order for each combination of device and
cannula. All measurements were made over a duration of
60 s and the Wright respirometer dial was concealed from
the investigator throughout each experiment. The diameter
Adjustable restriction (8 or 2.5 mm)
Flow monitor (Wright respirometer)
Test lung22 mm
Cannula (13–20 G)
210 mm10 mm
Fig 1 The trachea – lung model.
Fig 2 From left to right, ENK flow modulator, self-inflating bag, and
three-way tap connections.
Flint et al.
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of the proximal trachea tube connector was 8 mm and in
order to investigate the effect of an upper airway stenosis
on delivered MV, all experiments were repeated after sub-
stituting this for a tracheal tube connector of 2.5 mm
diameter.
Results
Recorded MVs varied significantly according to the type
of device, the size of cannula, and the presence or absence
of a constriction proximal to the cannula. MV increased
with increasing cannula size with all devices, although
there were large differences between devices in delivered
MV at a given cannula size. MV was generally increased
in the presence of a proximal constriction.
At an airway diameter of 8 mm (no constriction) MV
was low, with only the Manujet producing MV .2 litre
min 21
, and at a cannula diameter �20 G (Table 1). The ENK and three-way tap device produced no measurable
MV with either of the two smallest cannulae and achieved
above 1 litre min 21
only with the 13 G cannula. Neither
of the two low-pressure devices (oxygen flush and self-
inflating bag) were able to generate a measurable MV
regardless of cannula size.
Measurements of delivered pipeline pressures confirmed
a mean pressure of 406 kPa (data not shown) except the
machine O2 flush, which was 47 kPa.
In the presence of a simulated proximal airway constric-
tion (2.5 mm diameter), delivered MV was greater
(Table 2): MV .2 litre min 21
was recorded with all
devices via the 13 G cannula. However, at a cannula diam-
eter ,13 G, the self-inflating bag recorded no minute ven-
tilation, and the oxygen flush produced minimal or no
ventilation at a cannula diameter �14 G. The Manujet pro- duced MV .10 litre min
21 for all but the smallest
cannula, and both the Manujet and three-way tap produced
MV .2 litre min 21
at all cannula diameters.
Discussion
In this bench-top model, we found large differences
between delivered MV with different ventilation devices.
As expected, increasing cannula size was associated with
substantial increases in MV for a given device. At an
upper airway diameter of 8 mm, simulating a clear airway,
only the high-pressure devices delivered any recordable
MV; only the Manujet delivered an MV .2 litre min 21
and required a cannula size of �16 G to achieve this. The presence of a proximal constriction in the model to simu-
late upper airway obstruction also increased the delivered
MV, which is consistent with previous work using high-
frequency jet ventilation in a similar model. 13
However,
MV was negligible at an upper airway diameter of 2.5 mm
using the oxygen flush or self-inflating bag with cannula
sizes of ,14 or 13 G, respectively. Irrespective of upper
airway diameter, no device produced above 3 litre min 21
with the 20 G cannula.
These results compare broadly with previous investi-
gations which have found flow rates of 2.5 – 6.0 litre
min 21
using a 14 G cannula delivered via a ‘transtracheal’
model similar to the one used here. 6 7
Precise comparisons
are difficult because the studies differed in the gas delivery
systems, the precise method and configuration of the venti-
lating device and cannulae, and the presence or absence of
a test-lung. Previous studies have investigated different
individual devices and routes of ventilation, although this
is the first comparative study of available devices. Marr
and Yamamoto 9
found no difference in ventilation
volumes between catheters of different size when venti-
lation was delivered using a self-inflating bag. This study
had several limitations including that no lung-tracheal
model was incorporated, and the authors inferred gas
delivery from the displacement of water. Nevertheless,
they concluded and recommended that transtracheal venti-
lation is feasible using a self-inflating bag. Our data con-
tradict this and are consistent with the more sophisticated
models previously described.
Previous authors have commented on constriction of the
upper airway in the CICV scenario and concluded that
there is a critical diameter below which obstruction to
expiration occurs 12 14
and that passive expiration is likely
to occur despite a seemingly obstructed upper airway. 15 16
Our data suggest that upper airway obstruction is likely to
increase delivered MV when delivered manually via a cri-
cothyroid cannula. This is consistent with previous work
showing that distal airway pressures increase during
high-frequency jet ventilation delivered below a small
constriction of the proximal airway, 12 17
because of
Table 1 Mean (SD) MVs (litre min 21
) for each device across the range of
cannula sizes with a proximal airway diameter of 8 mm (‘no constriction’)
20 G 16 G 14 G 13 G
Manujet 0.89 (0.1) 2.43 (0.2) 3.38 (0.2) 10.55 (0.7)
Three-way tap 0.00 0.00 0.80 (0.1) 1.67 (0.5)
ENK 0.00 0.00 0.39 (0.1) 1.14 (0.2)
Oxygen flush 0.00 0.00 0.00 0.00
Self-inflating
bag
0.00 0.00 0.00 0.00
Table 2 Mean (SD) MVs (litre min 21
) for each device across the range of
cannula sizes with a proximal airway diameter of 2.5 mm (‘upper airway
constriction’)
20 G 16 G 14 G 13 G
Manujet 2.12 (0.1) 10.28 (0.2) 12.55 (0.2) 15.73 (0.2)
Three-way tap 2.93 (0.2) 3.72 (0.4) 5.25 (0.3) 6.07 (0.8)
ENK 1.15 (0.3) 2.00 (0.3) 3.12 (0.4) 6.08 (0.7)
Oxygen flush 0.00 0.70 (0.0) 3.10 (0.1) 3.90 (0.1)
Self-inflating
bag
0.00 0.00 0.00 2.17 (0.3)
Comparison of devices for cannula ventilation
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impedance to expiratory gas flow. To assess this risk, we
measured the peak (112 mbar) and mean (46 mbar) pressures
generated using the Manujet via a 13 G cannula with a 2.5
mm constriction. The effects of an immobile, rigid stenosis
as used in this model may be greater than those of a flaccid,
mobile, or semi-rigid upper airway obstruction, which is a
more likely scenario in clinical practice. Practitioners should
be aware of the potential for pulmonary barotrauma when
using this technique and specifically the importance of
allowing time for expiration, to prevent breath stacking.
Clearly, extrapolation of the precise values obtained
from this model to clinical practice should be made with
caution. Gas flow through the tracheobronchial tree in
humans during artificial ventilation depends on many
factors, including lung and thoracic compliance, airway
resistance, pressure and flow characteristics of the venti-
lation device and its airway conduit, route of delivery of
ventilation, pharmacological factors, and anatomical
abnormalities of the respiratory tract. However, this
trachea – lung model was of similar dimensions and the
test lung of similar compliance to that of an adult human.
It should be noted that the cannulae were of differing
lengths and different diameter. According to the Hagen –
Poiseuille equation, flow rates decrease with increased
catheter length, but this cannot be avoided in the clinical
situation; other authors have considered cannula length to
be insignificant in practice. 9
Furthermore, the primary aim
of the study was to compare the performance of the
devices in a stable laboratory situation. The Wright respi-
rometer has a tendency to underread at low volumes due
to inertia; however, the absolute values obtained using the
Wright respirometer were consistent, reproducible, and
were compared before the series of experiments against
the Biotek, an industry-standard gas flow analyser. On the
basis of previous data showing optimal I:E ratios for low-
and high-pressure systems, 18
we used a ventilatory rate of
20 min 21
and inspiratory time of 1 s, which would also be
appropriate in clinical practice. Our choice of cannula size
was determined partly by the range commonly available,
and which are likely to be accessible in the emergency
situation. We included a small (20 G) cannula for com-
parison as these are often used to instil local anaesthetics
and are readily available. We limited our study to devices
well described in the literature, resuscitation guidelines, in
the DAS guidelines, or both. Other available devices not
advocated in the DAS guidelines [e.g. the Quicktrach
(VBM Medical)] were not studied.
It is important to remember that the MV required for
effective ventilation and resuscitation in a CICV situation
is not clearly established. The primary aim during a CICV
situation is to deliver oxygen to the lungs (rather than
striving to achieve normal minute ventilation); however, a
greater MV will lead to a more rapid reversal of hypoxia.
Equally, since this scenario is likely to be associated with
a variable degree of hypercapnia, acidaemia, and hypoxaemia,
MVs in excess of basal physiological values may be
required. ‘Adequate’ MV has been defined as 7 19
or 4 litre
min 21
in the short term, if metabolic requirements are
low; 18
Zornow and colleagues 20
demonstrated that it was
possible to reverse hypoxia and hypercarbia in 22 kg
swine within 1 min with an MV of 7.8 litre min 21
.
Notwithstanding the limitations of our model, there were
clear differences between different devices and cannula
sizes. Only the Manujet in conjunction with a larger bore
cannula was able to consistently deliver MV that might be
considered adequate. In the presence of a proximal con-
striction of 2.5 mm diameter, MVs were greater, but absol-
ute values were still dependent on the device used and
cannula size. In general, only the high-pressure devices
(Manujet, ENK, and three-way tap) are likely to be able to
produce adequate ventilation.
In conclusion, these data suggest that in the absence of a
significant upper airway obstruction or stenosis, the Manujet
is the only device of those tested likely to deliver adequate
minute ventilation, and this depends on using as large a diam-
eter cannula as possible. In the presence of significant upper
airway obstruction, distal effective ventilation is augmented
and clinicians should be aware of the potential for pulmonary
barotrauma and hence the requirement for an appropriate
expiration time. Of the ad hoc devices, the simple three-way
tap and oxygen tubing performed best. In all cases, a cannula
of �14 G is recommended. Although the oxygen flush and self-inflating bag should be immediately available at every
location where anaesthesia is administered, they failed to
produce any effective ventilation. In the emergency situation,
hypoxia (and to a lesser extent hypercarbia) must be reversed
as rapidly as possible; therefore, low-pressure devices should
no longer be advocated. Furthermore, we suggest that
although ad hoc devices may be useful in the emergency situ-
ation, purpose-made devices that use a high-pressure oxygen
supply should be available in all areas where anaesthesia or
airway interventions are performed.
Funding
No external funding.
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