Position-dependent distribution of lung ventilation
– A feasability study
Waldmann A, Ortolá C, Martinez M, Vidal A, Santos A, Manuel
Márquez M, Róka P, Böhm S, Sipmann F, Sensors Applications
Symposium, Zadar, Croatia, 2015
Position-dependent distribution of lung ventilation
– A feasability study
Andreas D. Waldmann1
, Carlos Ferrando Ortolá2
, Manuel Muñoz Martinez3
, Anxela Vidal4
, Arnoldo Santos
4
, Manuel
Perez Márquez4
, Péter L. Róka1
, Stephan H. Bohm1
, Fernando Suarez-Sipmann5
1
Swisstom AG, Landquart, Switzerland,
2
Department of Anesthesia and Critical Care. Hospital Clínico Universitario, Valencia, Spain.
3
Departement of Anesthesiology, Hospital Universitario de la Princesa, Madrid, Spain.
4
Department of Critical Care. Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Madrid, Spain,
5
Department of Surgical Sciences, Hedenstierna Laboratory, Uppsala University, Uppsala, Sweden
Abstract—The aim of this feasibility study was to determine
whether the measurement setup and study protocol were able to
show the effect that lung disease, body position and different
levels of positive end expiratory pressure (PEEP) have on lung
function. By means of a motorized rotation table and gravity
sensors six pigs were rotated in steps of 30° from left to right
lateral position. Regional ventilation distributions, measured by
electrical impedance tomography (EIT), oxygenation and
compliance measurements were performed at each position.
Both, experimental and measurement setup as well as the
parameters chosen to characterize lung function appear suitable
for analyzing the effects of PEEP and rotation in healthy and
injured lungs. The initial results show that the distribution of
regional ventilation was highly gravity-dependent especially in
sick lungs. Furthermore lateral rotation showed significant
recruitment effects on previously collapsed lung tissue as
witnessed by the increases in oxygenation at all PEEPs.
Keywords—EIT, electrical impedance tomography, lung
function mechanical ventilation, oxygenation, PEEP, positive end
expiratory pressure, rotation, recruitment, sensors.
I. INTRODUCTION
The therapeutic role of lateral rotation and prone
positioning during mechanical ventilator support of patients
with severe lung injury has been a matter of much debate [1].
Although most clinical trials have failed to show a clear
beneficial effect of prone positioning on outcomes [2]–[4], a
recent study in patients with severe lung injury showed that an
early application of prolonged prone-positioning sessions
significantly decreased 28-day and 90-day mortality [5].
However, the pathophysiologic and therapeutic mechanisms
behind the effectiveness of position therapy remain unclear.
Most parameters such as lung mechanics and blood gases used
in clinical practice describe lung function only globally, but do
not allow insights at a regional level.
Electrical impedance tomography (EIT) is a novel method
to investigate and monitor regional lung function and heart
activity. For this purpose, 32 sensors are placed around the
thorax. Weak alternating currents are applied via two of these
sensors and the resulting potentials are measured at the
remaining sensors. From the measured voltages, sequences of
real-time images are calculated which show the distribution of
electrical impedance within the body [6] representing organ
function rather than structure. It has been shown that intra-
thoracic impedance changes with ventilation [7]–[10] and the
cardiac cycle [11]. The signals caused by the breathing lungs
are about 10 times stronger than that caused by the beating
heart. Therefore, EIT has been proposed for measuring regional
ventilation rather than cardiac function within the human
thorax. Unlike traditional medical imaging methods such as
computer tomography, EIT imaging is non-invasive and can
thus be employed continuously right at the bedside.
The distribution of ventilation depends on the lung´s
condition, body position [12], [13] and on the positive end
expiratory pressure (PEEP) [14]–[17] applied. Turning from
the supine to the right lateral and the left lateral position,
Riedel et al. [13] showed in 10 healthy subjects that the
regional distribution of ventilation changes significantly with
body position. They also showed that the gravity-dependent
lower part of the lung is ventilated more than the non-
dependent upper lung. Blankman et al. [17] showed in patients
after cardiac surgery that ventilation moves towards the non-
dependent lung when decreasing PEEP from 15 cmH2O to
0 cmH2O.
The aim of this feasibility study performed in six pigs, three
with healthy lungs and three with acute lung injury, was to
determine whether the measurement setup and study protocol
were able to show the effect that lung disease, body position
and different levels of PEEP have on global lung function and
particularly on the fraction of ventilation delivered to either
lung.
II. METHODS
A. Study design
The study protocol was approved by the Ethic Committee of
Fundación Jiménez Díaz research institute. Acute lung
damage was induced by repeated saline lung lavage for
surfactant depletion and subsequent 2 hours of injurious
mechanical ventilation to establish a two-hit ventilator induced
lung injury model. All pigs were placed in the supine position
at 0°, and were then rotated in steps of 30° in a clockwise
direction until +90° and back to 0°, the same procedure was
978-1-4799-6117-7/15/$31.00 ©2015 IEEE
This full text paper was peer-reviewed at the direction of IEEE Instrumentation and Measurement Society prior to the acceptance and publication.
429
Fig. 1. Protocol: pigs were rotated in 30°-steps from the supine to the right
and then to the left lateral position and back to 0°. The numbers from 1 to 13
indicate the measurements taken in sequence.
then repeated in a counter-clockwise direction until -90° and
back to 0° (for details see Fig. 1). The exact rotation of the
subject was measured with an accelerometer positioned on the
subject´s sternum. To ensure stable recording conditions no
data were obtained during the first 2 of 3 minutes at a given
angle. Baseline ventilation was performed with a tidal volume
of 6 ml/kg in a volume controlled mode, at a respiratory rate
of 30 breaths per min, an inspiratory to expiratory ratio of 1:2
and a PEEP of 5 cmH2O. The fraction of inspiratory oxygen
(FIO2) was set to 0.4 for the healthy model and 1 for the lung
injury model. An entire measurement sequence consisting of a
total of 13 EIT recordings and arterial and mixed venous
blood gas analyses was performed at each angle studied and at
each of the following PEEP levels: 5, 10 and 15 cmH2O. The
order in which PEEP levels were applied was randomized. To
avoid carry over effects baseline ventilation conditions were
applied for 5 minutes before changing to the next level of
PEEP.
B. Motorized rotation table
We used a costum-built motorized table (Guido Kübler
GmbH, Bobingen, Germany) to rotate the animal to the
predefined angles (Fig. 2c). The table has two linear actuators
(MAX30-A200415C510F, SKF Group, Gothenburg, Sweden)
and one DC motor (403.957, Valco, Germany). In contrast to
tables with only one motor, our table rotates the animal
concentrically around its longitudinal axis without changing
the z-direction of the table or its lateral extension. Rotation of
the table was controlled by a laptop via a serial
communication protocol. Before starting the experiment the
table was calibrated by the electronic inclinometer Incli Tronic
plus (BMI, Hersbruck, Germany) with an accuracy of ± 0.1° at
0° and 90° and of ± 0.3° between 1° and 89°. A vacuum
mattress and two belts were used to tightly fix the animals
during the rotation, see Fig. 2a.
C. EIT device
EIT measurements were performed with the Pioneer-Set
(Swisstom AG, Landquart, Switzerland). This device consists
of a custom-built pig interface, the SensorBelt (SB) and a
SensorBeltConnector (SBC) to drive the SB, see Fig. 2b. The
special pig interface was made of an elastic tube (Silcolatex
7x10, Tefelex Medical, Germany) carrying 32 contact pads
made of stainless steel tubing. A standard electrically non-
conductive ultrasonic gel was used to reduce the impedance
between these pads and the skin.
(a) Pig placement (b) SensorBelt
(c) Motorized table
Fig. 2. (a) Measurement set-up, consisting of a vacuum matress, flow and
pressure sensors and the SensorBelt, (b) SensorBelt, consicting of gravity
sensor, pig interface and plug for SensorBeltConnector. (c) Motorized table,
consisting of a wooden table top, two linear motors and one DC motor. The
table can be moved vertically from 84 cm to 90 cm and rotated concentrically
from -90 to +90° at a maximum speed of 1° per second using serial
commands.
Each of these pads was connected via a cable to the SB.
The SB contained 32 active sensors, which were switched
between a current injecting and a voltage measurement
function. In order to reduce the complexity of the belt bus
within the SB the 32 sensors are arranged in daisy chain
architecture. Digital commands, sent by the SBC, are then used
to sequentially read out all sensors. The measured analog
voltages are converted into digital signals using a 14 bit analog
to digital converter. The SBC is plugged into the SB equipped
with an integrated 3-axis accelerometer (ADXL343, Analog
Devices, Boston, MA; USA) to measure the subject´s exact
body position. Gravity and the respective other accelerations
were measured at 30 Hz and converted into a longitudinal and
a transversal angle, to describe the rotation angle of the subject.
An electrical drive current with peak-to-peak amplitude of
3 mA and a frequency of 144 kHz was used in all
measurements. 30 tomographic differential images were
recorded per second. EIT-based moving images of regional
ventilation were generated from the collected potential
differences and the known excitation currents using a
derivative of the publically available GREIT image
reconstruction algorithm [18]. More information about the EIT
device can be found in [19], [20].
D. EIT data analysis
During each one of the predefined study angles EIT movies
were created from 20 consecutive breaths. During post hoc
analysis for each pixel the impedance difference between
inspiration and the preceding end-expiration was calculated
which delivered the so-called tidal EIT images. From these 20
tidal images the fraction of ventilation delivered to the right
and left lung was determined simply splitting the image into a
right and left hemithorax.
430
E. Dynamic complicance
Dynamic compliance was calculated on a breath-by-breath
basis using the internal flow and pressure sensors of the Open
Lung Tool (Servo-i Maquet Critical Care, Solna, Sweden).
III. RESULTS
During the experiments neither technical nor medical
difficulties were encountered. All devices and sensors
delivered the expected data. Fig. 3 and 4 depict the percentage
of ventilation delivered to the right lung, dynamic compliance
and oxygenation index for the healthy and for the lung injury
model. Right at the start and during the study the lungs of the
supposedly “healthy” pigs presented with a wide range of
mechanical and gas exchange properties ranging from fully
healthy to rather sick.
A. EIT data / Ventilation distribution
At PEEP 5 cmH2O the healthy right lung received 55% of
the tidal volume and the left lung received 45%, see Fig.3. A
slight asymmetry remained at all angles returning to almost
50% after a complete rotation sequence. At PEEP 10 cmH2O
and 15 cmH2O ventilation to the right lung increased to 70% in
the right lateral positions, whereas rotation to the left side
decreased right lung ventilation to 60 and 50%, respectively.
In contrast, the injured lung showed a higher rotation-
dependency, see Fig.4. Whereas in the supine position
ventilation was rather equally distributed between the right
(52%) and the left lung (48%), in the left lateral positions 78%
of the ventilation shifted to the non-dependent upper right lung
reaching as much as 73% when back in the supine position.
Even the slightest rotation by 30° to the right side inverted this
distribution abruptly with the right lower lung now receiving
less than 50%. Increasing and decreasing the rotation angle did
not change this ventilation pattern. The distribution of
ventilation between the lungs at PEEP 10 and 15 cmH2O
resembled that of the healthy lungs at PEEP 5 and 10 cmH2O,
but showing a slightly larger angle-dependent hysteresis in the
sick lung at PEEP 10 cmH2O.
B. Dynamic compliance
The dynamic compliance in the healthy pig ventilated at PEEP
5 cmH2O remained unchanged during the entire rotation
sequence but its overall level increased with PEEP 10 cmH2O
from around 15 to 20 ml/cmH2O without showing a major
hysteresis, see Fig. 3. During the initial leftward rotation at
PEEP 15 cmH2O a marked gain in compliance was noticed
which stabilized between 20 and 25 ml/cmH2O for the
remainder of the study. The sick lungs showed a similar
behavior however at compliance values approximately 5
ml/cmH2O lower than their healthy counterparts see Fig. 4.
C. Blood gas PaO2/FiO2 ratio
At PEEP 5 cmH2O the oxygenation index PaO2/FIO2
remained between 250 and 350 mmHg in the healthy lung,
reached values around 250 mmHg at PEEP 10 cmH2O and did
not change with the rotation angle. At PEEP 15 cmH2O
PaO2/FIO2 remain between 300 and 350 mmHg and did not
change with the rotation angle.
The PaO2/FIO2 of about 120 mmHg at 0° corresponded to a
very sick lung. At PEEP 5 cmH2O, oxygenation improved with
lateral rotations to both sides reaching maximum values
between 250 and 300 mmHg. Rotation at PEEP 10 cmH2O
opened collapsed lung units and stabilized PaO2/FIO2 value
above 350 mmHg showing the same behavior also at PEEP 15
cmH2O, see Fig. 4.
IV. DISCUSSION
These initial results show that the distribution of regional
ventilation was highly gravity-dependent especially in sick
lungs.
The function of the healthy lung at PEEP 5 cmH2O was
normal and appeared rotation-independent. With higher PEEPs
a clear dependency on the rotation angle was revealed which
reached its maximal expression at ± 60° and ± 90° and together
with the upward-convex shape of the compliance curve can be
interpreted as the beginning (10 cmH2O) of overt (15 cmH2O)
overdistension of the respective non-dependent healthy upper
lung. Thus, high PEEP in conjunction with a high rotation
angle increased the heterogeneity of ventilation in the healthy
lungs.
Starting from low oxygenation levels lateral rotation
showed significant recruitment effects on previously collapsed
lung tissue as witnessed by the increases in oxygenation at all
PEEPs. PEEP 5 cmH2O, however, was not able to maintain
this recruitment. Once PEEP reached 10 cmH2O it was high
enough to keep the newly recruited lung units open shifting
oxygenation and compliance into the normal range. Increasing
PEEP further to 15 cmH2O created a lung situation similar to
the one seen in the healthy lung at 10 cmH2O reflecting a
stable but slightly overdistended upper lung.
V. CONCLUSION
The distribution of regional ventilation was gravity-
dependent and the combined effects of PEEP and rotation
angle were different in health and disease. Both, experimental
and measurement setup as well as the parameters chosen to
characterize lung function appear suitable for analyzing the
effects of PEEP and rotation in healthy and injured lungs.
VI. OUTLOOK
In this feasibility study in six subjects we calculated the
distribution of ventilation between the right and left lung, only.
In the future we should also analyze the distribution of
ventilation between the gravity dependent and the non-
dependent lung by dividing the lung at each angle by a
horizontal line perpendicular to the gravity vector. This way,
the true gravity- dependency of lung function and a correlation
with parameters of global lung function should become more
obvious. Furthermore it would be interesting to study the local
matching of ventilation and perfusion, as suggested by [21],
[22], under different rotation and PEEP conditions. Therefore,
regional perfusion measurements should be included in the
next study protocol. Once data analysis and study protocol
have been refined in the above way they should be applied in
431
more pigs to reveal the underlying mechanisms of gravity- and
PEEP-dependency of lung function.
ACKNOWLEDGMENT
This project was funded by the “Fondo de Investigaciones
Sanitarias FIS, PI10/01885.
REFERENCES
[1] C. Guérin, “Prone ventilation in acute respiratory distress
syndrome.,” Eur. Respir. Rev., vol. 23, no. 132, pp. 249–57, Jun.
2014.
[2] L. Gattinoni, G. Tognoni, A. Pesenti, P. Taccone, D. Mascheroni, V.
Labarta, R. Malacrida, P. Di Giulio, R. Fumagalli, P. Pelosi, L.
Brazzi, and R. Latini, “Effect of prone positioning on the survival of
patients with acute respiratory failure.,” N. Engl. J. Med., vol. 345,
no. 8, pp. 568–73, Aug. 2001.
[3] J. Mancebo, R. Fernández, L. Blanch, G. Rialp, F. Gordo, M. Ferrer,
F. Rodríguez, P. Garro, P. Ricart, I. Vallverdú, I. Gich, J. Castaño,
P. Saura, G. Domínguez, A. Bonet, and R. K. Albert, “A multicenter
trial of prolonged prone ventilation in severe acute respiratory
distress syndrome.,” Am. J. Respir. Crit. Care Med., vol. 173, no.
11, pp. 1233–9, Jun. 2006.
[4] P. Taccone, A. Pesenti, R. Latini, F. Polli, F. Vagginelli, C. Mietto,
and L. Caspani, “Prone Positioning in Patients With Moderate and
Severe Acute Respiratory Distress Syndrome,” vol. 302, no. 18, pp.
1977–1984, 2009.
[5] C. Guérin, J. Reignier, J.-C. Richard, P. Beuret, A. Gacouin, T.
Boulain, E. Mercier, M. Badet, A. Mercat, O. Baudin, M. Clavel, D.
Chatellier, S. Jaber, S. Rosselli, J. Mancebo, M. Sirodot, G. Hilbert,
C. Bengler, J. Richecoeur, M. Gainnier, F. Bayle, G. Bourdin, V.
Leray, R. Girard, L. Baboi, and L. Ayzac, “Prone positioning in
severe acute respiratory distress syndrome.,” N. Engl. J. Med., vol.
368, no. 23, pp. 2159–68, Jun. 2013.
[6] E. L. Costa, R. G. Lima, and M. B. Amato, “Electrical impedance
tomography,” Curr. Opin. Crit. Care, vol. 15, no. 1, pp. 18–24, Feb.
2009.
[7] J. A. Victorino, J. B. Borges, V. N. Okamoto, G. F. J. Matos, M. R.
Tucci, M. P. R. Caramez, H. Tanaka, F. S. Sipmann, D. C. B.
Santos, C. S. V Barbas, C. R. R. Carvalho, and M. B. P. Amato,
“Imbalances in regional lung ventilation: a validation study on
electrical impedance tomography.,” Am. J. Respir. Crit. Care Med.,
vol. 169, no. 7, pp. 791–800, Apr. 2004.
[8] B. Vogt, S. Pulletz, G. Elke, Z. Zhao, P. Zabel, N. Weiler, and I.
Frerichs, “Spatial and temporal heterogeneity of regional lung
ventilation determined by electrical impedance tomography during
pulmonary function testing.,” J. Appl. Physiol., vol. 113, no. 7, pp.
1154–61, Oct. 2012.
[9] I. Frerichs, P. A. Dargaville, H. van Genderingen, D. R. Morel, and
P. C. Rimensberger, “Lung volume recruitment after surfactant
administration modifies spatial distribution of ventilation.,” Am. J.
Respir. Crit. Care Med., vol. 174, no. 7, pp. 772–9, Oct. 2006.
[10] G. K. Wolf, C. Gómez-Laberge, J. S. Rettig, S. O. Vargas, C. D.
Smallwood, S. P. Prabhu, S. H. Vitali, D. Zurakowski, and J. H.
Arnold, “Mechanical ventilation guided by electrical impedance
tomography in experimental acute lung injury.,” Crit. Care Med.,
vol. 41, no. 5, pp. 1296–304, May 2013.
[11] I. Frerichs, J. Hinz, P. Herrmann, G. Weisser, G. Hahn, M. Quintel,
and G. Hellige, “Regional lung perfusion as determined by electrical
impedance tomography in comparison with electron beam CT
imaging.,” IEEE Trans. Med. Imaging, vol. 21, no. 6, pp. 646–52,
Jun. 2002.
[12] I. Frerichs, G. Hahn, and G. Hellige, “Gravity-dependent
phenomena in lung ventilation determined by functional EIT.,”
Physiol. Meas., vol. 17 Suppl 4, pp. A149–57, Nov. 1996.
[13] T. Riedel, T. Richards, and A. Schibler, “The value of electrical
impedance tomography in assessing the effect of body position and
positive airway pressures on regional lung ventilation in
spontaneously breathing subjects.,” Intensive Care Med., vol. 31,
no. 11, pp. 1522–8, Nov. 2005.
[14] I. Frerichs, P. Braun, T. Dudykevych, G. Hahn, D. Genée, and G.
Hellige, “Distribution of ventilation in young and elderly adults
determined by electrical impedance tomography.,” Respir. Physiol.
Neurobiol., vol. 143, no. 1, pp. 63–75, Oct. 2004.
[15] F. Reifferscheid, G. Elke, S. Pulletz, B. Gawelczyk, I.
Lautenschläger, M. Steinfath, N. Weiler, and I. Frerichs, “Regional
ventilation distribution determined by electrical impedance
tomography: reproducibility and effects of posture and chest
plane.,” Respirology, vol. 16, no. 3, pp. 523–31, Apr. 2011.
[16] G. Zick, G. Elke, T. Becher, D. Schädler, S. Pulletz, S. Freitag-
Wolf, N. Weiler, and I. Frerichs, “Effect of PEEP and tidal volume
on ventilation distribution and end-expiratory lung volume: a
prospective experimental animal and pilot clinical study.,” PLoS
One, vol. 8, no. 8, p. e72675, Jan. 2013.
[17] P. Blankman, D. Hasan, E. Groot Jebbink, and D. Gommers,
“Detection of ‘best’ positive end-expiratory pressure derived from
electrical impedance tomography parameters during a decremental
positive end-expiratory pressure trial.,” Crit. Care, vol. 18, no. 3, p.
R95, May 2014.
[18] A. Adler, J. H. Arnold, R. Bayford, A. Borsic, B. Brown, P. Dixon,
T. J. C. Faes, I. Frerichs, H. Gagnon, Y. Gärber, B. Grychtol, G.
Hahn, W. R. B. Lionheart, A. Malik, R. P. Patterson, J. Stocks, A.
Tizzard, N. Weiler, and G. K. Wolf, “GREIT: a unified approach to
2D linear EIT reconstruction of lung images.,” Physiol. Meas., vol.
30, no. 6, pp. S35–55, Jun. 2009.
[19] P. O. Gaggero, A. Adler, J. Brunner, and P. Seitz, “Electrical
impedance tomography system based on active electrodes.,”
Physiol. Meas., vol. 33, no. 5, pp. 831–47, May 2012.
[20] P. O. Gaggero, “Miniaturization and Distinguishability Limits of
Electrical Impedance Tomography for Biomedical Application By,”
no. June, 2011.
[21] Y. Li, E. Tesselaar, J. B. Borges, S. H. Böhm, F. Sjöberg, and B.
Janerot-Sjöberg, “Hyperoxia affects the regional pulmonary
ventilation/perfusion ratio: an electrical impedance tomography
study.,” Acta Anaesthesiol. Scand., vol. 58, no. 6, pp. 716–25, Jul.
2014.
[22] J. B. Borges, F. Suarez-Sipmann, S. H. Bohm, G. Tusman, A. Melo,
E. Maripuu, M. Sandström, M. Park, E. L. V Costa, G.
Hedenstierna, and M. Amato, “Regional lung perfusion estimated
by electrical impedance tomography in a piglet model of lung
collapse.,” J. Appl. Physiol., vol. 112, no. 1, pp. 225–36, Jan. 2012.
432
0° 30° 60° 90°-30°-60°-90°
PEEP 5
PEEP 10
0° 30° 60° 90°-30°-60°-90°
R
R
R
R
R
R
R
R
R
R
R
R
R
R
PEEP 15
30° 60° 90°-30°-60°-90° 0°
R
R
R
R
R
R
R
Fig. 3. Healthy lung: Percentage of ventilation delivered to the right lung, dynamic compliance and oxygenation index PaO2/FIO2 are plotted for different body
positions and PEEP level. Small arrows indicate the measurement sequence. Representative sequence of tidal EIT images during roation from the left (+90°) to the
right (-90°) lateral position show regional ventilation where bright pixels depict a large and dark ones a low ventilation amplitude. Data are plotted for each
condition for three pigs. The thin lines show the data of the individual pigs, the thick violet line represents the mean value.
433
PEEP 5
PEEP 10
PEEP 15
0° 30° 60° 90°-30°-60°-90°
0° 30° 60° 90°-30°-60°-90°
0° 30° 60° 90°-30°-60°-90°
R
R
R
R
R
R
R
R
R
R
R
R
R
R
R
R
R
R
R
R
R
Fig. 4. Sick lung: Percentage of ventilation delivered to the right lung, dynamic compliance and oxygenation index PaO2/FIO2 are plotted for different body
positions and PEEP level. Small arrows indicate the measurement sequence. Representative sequence of tidal EIT images during roation from the left (+90°) to the
right (-90°) lateral position show regional ventilation where bright pixels depict a large and dark ones a low ventilation amplitude. Data are plotted for each
condition for three pigs. The thin lines show the data of the individual pigs, the thick violet line represents the mean value.
434
SWI SSTO M SCIE NT IFIC LIBRARY 2 015
Content:Dr.StephanBöhm;Concept&Design:ZweizeitBrandDevelopment
Made in Switzerland
electrical
impedance
tomography
Real-time tomographic images for organ
function monitoring and diagnosis
Contact us!
call: + 41 (0) 81 330 09 72
mail: info@swisstom.com
visit: www.swisstom.com
Swisstom AG
Schulstrasse 1, CH-7302
Landquart, Switzerland
Swisstom AG
Swisstom AG, located in Landquart, Switzerland,
develops and manufactures innovative medical devices.
Our new lung function monitor enables life-saving
treatments for patients in intensive care and during
general anesthesia.
Unlike traditional tomography, Swisstom´s bedside
imaging is based on non-radiating principles: Electrical
Impedance Tomography (EIT). To date, no comparable
devices can show such regional organ function
continuously and in real-time at the patient’s bedside.
Swisstom creates its competitive edge by passionate
leadership in non-invasive tomography with the goal
to improve individual lives and therapies.
© Swisstom AG 2015

Waldmann A. et al.: Position-dependent distribution of lung Ventilation – A feasability study.

  • 1.
    Position-dependent distribution oflung ventilation – A feasability study Waldmann A, Ortolá C, Martinez M, Vidal A, Santos A, Manuel Márquez M, Róka P, Böhm S, Sipmann F, Sensors Applications Symposium, Zadar, Croatia, 2015
  • 2.
    Position-dependent distribution oflung ventilation – A feasability study Andreas D. Waldmann1 , Carlos Ferrando Ortolá2 , Manuel Muñoz Martinez3 , Anxela Vidal4 , Arnoldo Santos 4 , Manuel Perez Márquez4 , Péter L. Róka1 , Stephan H. Bohm1 , Fernando Suarez-Sipmann5 1 Swisstom AG, Landquart, Switzerland, 2 Department of Anesthesia and Critical Care. Hospital Clínico Universitario, Valencia, Spain. 3 Departement of Anesthesiology, Hospital Universitario de la Princesa, Madrid, Spain. 4 Department of Critical Care. Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Madrid, Spain, 5 Department of Surgical Sciences, Hedenstierna Laboratory, Uppsala University, Uppsala, Sweden Abstract—The aim of this feasibility study was to determine whether the measurement setup and study protocol were able to show the effect that lung disease, body position and different levels of positive end expiratory pressure (PEEP) have on lung function. By means of a motorized rotation table and gravity sensors six pigs were rotated in steps of 30° from left to right lateral position. Regional ventilation distributions, measured by electrical impedance tomography (EIT), oxygenation and compliance measurements were performed at each position. Both, experimental and measurement setup as well as the parameters chosen to characterize lung function appear suitable for analyzing the effects of PEEP and rotation in healthy and injured lungs. The initial results show that the distribution of regional ventilation was highly gravity-dependent especially in sick lungs. Furthermore lateral rotation showed significant recruitment effects on previously collapsed lung tissue as witnessed by the increases in oxygenation at all PEEPs. Keywords—EIT, electrical impedance tomography, lung function mechanical ventilation, oxygenation, PEEP, positive end expiratory pressure, rotation, recruitment, sensors. I. INTRODUCTION The therapeutic role of lateral rotation and prone positioning during mechanical ventilator support of patients with severe lung injury has been a matter of much debate [1]. Although most clinical trials have failed to show a clear beneficial effect of prone positioning on outcomes [2]–[4], a recent study in patients with severe lung injury showed that an early application of prolonged prone-positioning sessions significantly decreased 28-day and 90-day mortality [5]. However, the pathophysiologic and therapeutic mechanisms behind the effectiveness of position therapy remain unclear. Most parameters such as lung mechanics and blood gases used in clinical practice describe lung function only globally, but do not allow insights at a regional level. Electrical impedance tomography (EIT) is a novel method to investigate and monitor regional lung function and heart activity. For this purpose, 32 sensors are placed around the thorax. Weak alternating currents are applied via two of these sensors and the resulting potentials are measured at the remaining sensors. From the measured voltages, sequences of real-time images are calculated which show the distribution of electrical impedance within the body [6] representing organ function rather than structure. It has been shown that intra- thoracic impedance changes with ventilation [7]–[10] and the cardiac cycle [11]. The signals caused by the breathing lungs are about 10 times stronger than that caused by the beating heart. Therefore, EIT has been proposed for measuring regional ventilation rather than cardiac function within the human thorax. Unlike traditional medical imaging methods such as computer tomography, EIT imaging is non-invasive and can thus be employed continuously right at the bedside. The distribution of ventilation depends on the lung´s condition, body position [12], [13] and on the positive end expiratory pressure (PEEP) [14]–[17] applied. Turning from the supine to the right lateral and the left lateral position, Riedel et al. [13] showed in 10 healthy subjects that the regional distribution of ventilation changes significantly with body position. They also showed that the gravity-dependent lower part of the lung is ventilated more than the non- dependent upper lung. Blankman et al. [17] showed in patients after cardiac surgery that ventilation moves towards the non- dependent lung when decreasing PEEP from 15 cmH2O to 0 cmH2O. The aim of this feasibility study performed in six pigs, three with healthy lungs and three with acute lung injury, was to determine whether the measurement setup and study protocol were able to show the effect that lung disease, body position and different levels of PEEP have on global lung function and particularly on the fraction of ventilation delivered to either lung. II. METHODS A. Study design The study protocol was approved by the Ethic Committee of Fundación Jiménez Díaz research institute. Acute lung damage was induced by repeated saline lung lavage for surfactant depletion and subsequent 2 hours of injurious mechanical ventilation to establish a two-hit ventilator induced lung injury model. All pigs were placed in the supine position at 0°, and were then rotated in steps of 30° in a clockwise direction until +90° and back to 0°, the same procedure was 978-1-4799-6117-7/15/$31.00 ©2015 IEEE This full text paper was peer-reviewed at the direction of IEEE Instrumentation and Measurement Society prior to the acceptance and publication. 429
  • 3.
    Fig. 1. Protocol:pigs were rotated in 30°-steps from the supine to the right and then to the left lateral position and back to 0°. The numbers from 1 to 13 indicate the measurements taken in sequence. then repeated in a counter-clockwise direction until -90° and back to 0° (for details see Fig. 1). The exact rotation of the subject was measured with an accelerometer positioned on the subject´s sternum. To ensure stable recording conditions no data were obtained during the first 2 of 3 minutes at a given angle. Baseline ventilation was performed with a tidal volume of 6 ml/kg in a volume controlled mode, at a respiratory rate of 30 breaths per min, an inspiratory to expiratory ratio of 1:2 and a PEEP of 5 cmH2O. The fraction of inspiratory oxygen (FIO2) was set to 0.4 for the healthy model and 1 for the lung injury model. An entire measurement sequence consisting of a total of 13 EIT recordings and arterial and mixed venous blood gas analyses was performed at each angle studied and at each of the following PEEP levels: 5, 10 and 15 cmH2O. The order in which PEEP levels were applied was randomized. To avoid carry over effects baseline ventilation conditions were applied for 5 minutes before changing to the next level of PEEP. B. Motorized rotation table We used a costum-built motorized table (Guido Kübler GmbH, Bobingen, Germany) to rotate the animal to the predefined angles (Fig. 2c). The table has two linear actuators (MAX30-A200415C510F, SKF Group, Gothenburg, Sweden) and one DC motor (403.957, Valco, Germany). In contrast to tables with only one motor, our table rotates the animal concentrically around its longitudinal axis without changing the z-direction of the table or its lateral extension. Rotation of the table was controlled by a laptop via a serial communication protocol. Before starting the experiment the table was calibrated by the electronic inclinometer Incli Tronic plus (BMI, Hersbruck, Germany) with an accuracy of ± 0.1° at 0° and 90° and of ± 0.3° between 1° and 89°. A vacuum mattress and two belts were used to tightly fix the animals during the rotation, see Fig. 2a. C. EIT device EIT measurements were performed with the Pioneer-Set (Swisstom AG, Landquart, Switzerland). This device consists of a custom-built pig interface, the SensorBelt (SB) and a SensorBeltConnector (SBC) to drive the SB, see Fig. 2b. The special pig interface was made of an elastic tube (Silcolatex 7x10, Tefelex Medical, Germany) carrying 32 contact pads made of stainless steel tubing. A standard electrically non- conductive ultrasonic gel was used to reduce the impedance between these pads and the skin. (a) Pig placement (b) SensorBelt (c) Motorized table Fig. 2. (a) Measurement set-up, consisting of a vacuum matress, flow and pressure sensors and the SensorBelt, (b) SensorBelt, consicting of gravity sensor, pig interface and plug for SensorBeltConnector. (c) Motorized table, consisting of a wooden table top, two linear motors and one DC motor. The table can be moved vertically from 84 cm to 90 cm and rotated concentrically from -90 to +90° at a maximum speed of 1° per second using serial commands. Each of these pads was connected via a cable to the SB. The SB contained 32 active sensors, which were switched between a current injecting and a voltage measurement function. In order to reduce the complexity of the belt bus within the SB the 32 sensors are arranged in daisy chain architecture. Digital commands, sent by the SBC, are then used to sequentially read out all sensors. The measured analog voltages are converted into digital signals using a 14 bit analog to digital converter. The SBC is plugged into the SB equipped with an integrated 3-axis accelerometer (ADXL343, Analog Devices, Boston, MA; USA) to measure the subject´s exact body position. Gravity and the respective other accelerations were measured at 30 Hz and converted into a longitudinal and a transversal angle, to describe the rotation angle of the subject. An electrical drive current with peak-to-peak amplitude of 3 mA and a frequency of 144 kHz was used in all measurements. 30 tomographic differential images were recorded per second. EIT-based moving images of regional ventilation were generated from the collected potential differences and the known excitation currents using a derivative of the publically available GREIT image reconstruction algorithm [18]. More information about the EIT device can be found in [19], [20]. D. EIT data analysis During each one of the predefined study angles EIT movies were created from 20 consecutive breaths. During post hoc analysis for each pixel the impedance difference between inspiration and the preceding end-expiration was calculated which delivered the so-called tidal EIT images. From these 20 tidal images the fraction of ventilation delivered to the right and left lung was determined simply splitting the image into a right and left hemithorax. 430
  • 4.
    E. Dynamic complicance Dynamiccompliance was calculated on a breath-by-breath basis using the internal flow and pressure sensors of the Open Lung Tool (Servo-i Maquet Critical Care, Solna, Sweden). III. RESULTS During the experiments neither technical nor medical difficulties were encountered. All devices and sensors delivered the expected data. Fig. 3 and 4 depict the percentage of ventilation delivered to the right lung, dynamic compliance and oxygenation index for the healthy and for the lung injury model. Right at the start and during the study the lungs of the supposedly “healthy” pigs presented with a wide range of mechanical and gas exchange properties ranging from fully healthy to rather sick. A. EIT data / Ventilation distribution At PEEP 5 cmH2O the healthy right lung received 55% of the tidal volume and the left lung received 45%, see Fig.3. A slight asymmetry remained at all angles returning to almost 50% after a complete rotation sequence. At PEEP 10 cmH2O and 15 cmH2O ventilation to the right lung increased to 70% in the right lateral positions, whereas rotation to the left side decreased right lung ventilation to 60 and 50%, respectively. In contrast, the injured lung showed a higher rotation- dependency, see Fig.4. Whereas in the supine position ventilation was rather equally distributed between the right (52%) and the left lung (48%), in the left lateral positions 78% of the ventilation shifted to the non-dependent upper right lung reaching as much as 73% when back in the supine position. Even the slightest rotation by 30° to the right side inverted this distribution abruptly with the right lower lung now receiving less than 50%. Increasing and decreasing the rotation angle did not change this ventilation pattern. The distribution of ventilation between the lungs at PEEP 10 and 15 cmH2O resembled that of the healthy lungs at PEEP 5 and 10 cmH2O, but showing a slightly larger angle-dependent hysteresis in the sick lung at PEEP 10 cmH2O. B. Dynamic compliance The dynamic compliance in the healthy pig ventilated at PEEP 5 cmH2O remained unchanged during the entire rotation sequence but its overall level increased with PEEP 10 cmH2O from around 15 to 20 ml/cmH2O without showing a major hysteresis, see Fig. 3. During the initial leftward rotation at PEEP 15 cmH2O a marked gain in compliance was noticed which stabilized between 20 and 25 ml/cmH2O for the remainder of the study. The sick lungs showed a similar behavior however at compliance values approximately 5 ml/cmH2O lower than their healthy counterparts see Fig. 4. C. Blood gas PaO2/FiO2 ratio At PEEP 5 cmH2O the oxygenation index PaO2/FIO2 remained between 250 and 350 mmHg in the healthy lung, reached values around 250 mmHg at PEEP 10 cmH2O and did not change with the rotation angle. At PEEP 15 cmH2O PaO2/FIO2 remain between 300 and 350 mmHg and did not change with the rotation angle. The PaO2/FIO2 of about 120 mmHg at 0° corresponded to a very sick lung. At PEEP 5 cmH2O, oxygenation improved with lateral rotations to both sides reaching maximum values between 250 and 300 mmHg. Rotation at PEEP 10 cmH2O opened collapsed lung units and stabilized PaO2/FIO2 value above 350 mmHg showing the same behavior also at PEEP 15 cmH2O, see Fig. 4. IV. DISCUSSION These initial results show that the distribution of regional ventilation was highly gravity-dependent especially in sick lungs. The function of the healthy lung at PEEP 5 cmH2O was normal and appeared rotation-independent. With higher PEEPs a clear dependency on the rotation angle was revealed which reached its maximal expression at ± 60° and ± 90° and together with the upward-convex shape of the compliance curve can be interpreted as the beginning (10 cmH2O) of overt (15 cmH2O) overdistension of the respective non-dependent healthy upper lung. Thus, high PEEP in conjunction with a high rotation angle increased the heterogeneity of ventilation in the healthy lungs. Starting from low oxygenation levels lateral rotation showed significant recruitment effects on previously collapsed lung tissue as witnessed by the increases in oxygenation at all PEEPs. PEEP 5 cmH2O, however, was not able to maintain this recruitment. Once PEEP reached 10 cmH2O it was high enough to keep the newly recruited lung units open shifting oxygenation and compliance into the normal range. Increasing PEEP further to 15 cmH2O created a lung situation similar to the one seen in the healthy lung at 10 cmH2O reflecting a stable but slightly overdistended upper lung. V. CONCLUSION The distribution of regional ventilation was gravity- dependent and the combined effects of PEEP and rotation angle were different in health and disease. Both, experimental and measurement setup as well as the parameters chosen to characterize lung function appear suitable for analyzing the effects of PEEP and rotation in healthy and injured lungs. VI. OUTLOOK In this feasibility study in six subjects we calculated the distribution of ventilation between the right and left lung, only. In the future we should also analyze the distribution of ventilation between the gravity dependent and the non- dependent lung by dividing the lung at each angle by a horizontal line perpendicular to the gravity vector. This way, the true gravity- dependency of lung function and a correlation with parameters of global lung function should become more obvious. Furthermore it would be interesting to study the local matching of ventilation and perfusion, as suggested by [21], [22], under different rotation and PEEP conditions. Therefore, regional perfusion measurements should be included in the next study protocol. Once data analysis and study protocol have been refined in the above way they should be applied in 431
  • 5.
    more pigs toreveal the underlying mechanisms of gravity- and PEEP-dependency of lung function. ACKNOWLEDGMENT This project was funded by the “Fondo de Investigaciones Sanitarias FIS, PI10/01885. REFERENCES [1] C. Guérin, “Prone ventilation in acute respiratory distress syndrome.,” Eur. Respir. Rev., vol. 23, no. 132, pp. 249–57, Jun. 2014. [2] L. Gattinoni, G. Tognoni, A. Pesenti, P. Taccone, D. Mascheroni, V. Labarta, R. Malacrida, P. Di Giulio, R. Fumagalli, P. Pelosi, L. Brazzi, and R. Latini, “Effect of prone positioning on the survival of patients with acute respiratory failure.,” N. Engl. J. Med., vol. 345, no. 8, pp. 568–73, Aug. 2001. [3] J. Mancebo, R. Fernández, L. Blanch, G. Rialp, F. Gordo, M. Ferrer, F. Rodríguez, P. Garro, P. Ricart, I. Vallverdú, I. Gich, J. Castaño, P. Saura, G. Domínguez, A. Bonet, and R. K. Albert, “A multicenter trial of prolonged prone ventilation in severe acute respiratory distress syndrome.,” Am. J. Respir. Crit. Care Med., vol. 173, no. 11, pp. 1233–9, Jun. 2006. [4] P. Taccone, A. Pesenti, R. Latini, F. Polli, F. Vagginelli, C. Mietto, and L. Caspani, “Prone Positioning in Patients With Moderate and Severe Acute Respiratory Distress Syndrome,” vol. 302, no. 18, pp. 1977–1984, 2009. [5] C. Guérin, J. Reignier, J.-C. Richard, P. Beuret, A. Gacouin, T. Boulain, E. Mercier, M. Badet, A. Mercat, O. Baudin, M. Clavel, D. Chatellier, S. Jaber, S. Rosselli, J. Mancebo, M. Sirodot, G. Hilbert, C. Bengler, J. Richecoeur, M. Gainnier, F. Bayle, G. Bourdin, V. Leray, R. Girard, L. Baboi, and L. Ayzac, “Prone positioning in severe acute respiratory distress syndrome.,” N. Engl. J. Med., vol. 368, no. 23, pp. 2159–68, Jun. 2013. [6] E. L. Costa, R. G. Lima, and M. B. Amato, “Electrical impedance tomography,” Curr. Opin. Crit. Care, vol. 15, no. 1, pp. 18–24, Feb. 2009. [7] J. A. Victorino, J. B. Borges, V. N. Okamoto, G. F. J. Matos, M. R. Tucci, M. P. R. Caramez, H. Tanaka, F. S. Sipmann, D. C. B. Santos, C. S. V Barbas, C. R. R. Carvalho, and M. B. P. Amato, “Imbalances in regional lung ventilation: a validation study on electrical impedance tomography.,” Am. J. Respir. Crit. Care Med., vol. 169, no. 7, pp. 791–800, Apr. 2004. [8] B. Vogt, S. Pulletz, G. Elke, Z. Zhao, P. Zabel, N. Weiler, and I. Frerichs, “Spatial and temporal heterogeneity of regional lung ventilation determined by electrical impedance tomography during pulmonary function testing.,” J. Appl. Physiol., vol. 113, no. 7, pp. 1154–61, Oct. 2012. [9] I. Frerichs, P. A. Dargaville, H. van Genderingen, D. R. Morel, and P. C. Rimensberger, “Lung volume recruitment after surfactant administration modifies spatial distribution of ventilation.,” Am. J. Respir. Crit. Care Med., vol. 174, no. 7, pp. 772–9, Oct. 2006. [10] G. K. Wolf, C. Gómez-Laberge, J. S. Rettig, S. O. Vargas, C. D. Smallwood, S. P. Prabhu, S. H. Vitali, D. Zurakowski, and J. H. Arnold, “Mechanical ventilation guided by electrical impedance tomography in experimental acute lung injury.,” Crit. Care Med., vol. 41, no. 5, pp. 1296–304, May 2013. [11] I. Frerichs, J. Hinz, P. Herrmann, G. Weisser, G. Hahn, M. Quintel, and G. Hellige, “Regional lung perfusion as determined by electrical impedance tomography in comparison with electron beam CT imaging.,” IEEE Trans. Med. Imaging, vol. 21, no. 6, pp. 646–52, Jun. 2002. [12] I. Frerichs, G. Hahn, and G. Hellige, “Gravity-dependent phenomena in lung ventilation determined by functional EIT.,” Physiol. Meas., vol. 17 Suppl 4, pp. A149–57, Nov. 1996. [13] T. Riedel, T. Richards, and A. Schibler, “The value of electrical impedance tomography in assessing the effect of body position and positive airway pressures on regional lung ventilation in spontaneously breathing subjects.,” Intensive Care Med., vol. 31, no. 11, pp. 1522–8, Nov. 2005. [14] I. Frerichs, P. Braun, T. Dudykevych, G. Hahn, D. Genée, and G. Hellige, “Distribution of ventilation in young and elderly adults determined by electrical impedance tomography.,” Respir. Physiol. Neurobiol., vol. 143, no. 1, pp. 63–75, Oct. 2004. [15] F. Reifferscheid, G. Elke, S. Pulletz, B. Gawelczyk, I. Lautenschläger, M. Steinfath, N. Weiler, and I. Frerichs, “Regional ventilation distribution determined by electrical impedance tomography: reproducibility and effects of posture and chest plane.,” Respirology, vol. 16, no. 3, pp. 523–31, Apr. 2011. [16] G. Zick, G. Elke, T. Becher, D. Schädler, S. Pulletz, S. Freitag- Wolf, N. Weiler, and I. Frerichs, “Effect of PEEP and tidal volume on ventilation distribution and end-expiratory lung volume: a prospective experimental animal and pilot clinical study.,” PLoS One, vol. 8, no. 8, p. e72675, Jan. 2013. [17] P. Blankman, D. Hasan, E. Groot Jebbink, and D. Gommers, “Detection of ‘best’ positive end-expiratory pressure derived from electrical impedance tomography parameters during a decremental positive end-expiratory pressure trial.,” Crit. Care, vol. 18, no. 3, p. R95, May 2014. [18] A. Adler, J. H. Arnold, R. Bayford, A. Borsic, B. Brown, P. Dixon, T. J. C. Faes, I. Frerichs, H. Gagnon, Y. Gärber, B. Grychtol, G. Hahn, W. R. B. Lionheart, A. Malik, R. P. Patterson, J. Stocks, A. Tizzard, N. Weiler, and G. K. Wolf, “GREIT: a unified approach to 2D linear EIT reconstruction of lung images.,” Physiol. Meas., vol. 30, no. 6, pp. S35–55, Jun. 2009. [19] P. O. Gaggero, A. Adler, J. Brunner, and P. Seitz, “Electrical impedance tomography system based on active electrodes.,” Physiol. Meas., vol. 33, no. 5, pp. 831–47, May 2012. [20] P. O. Gaggero, “Miniaturization and Distinguishability Limits of Electrical Impedance Tomography for Biomedical Application By,” no. June, 2011. [21] Y. Li, E. Tesselaar, J. B. Borges, S. H. Böhm, F. Sjöberg, and B. Janerot-Sjöberg, “Hyperoxia affects the regional pulmonary ventilation/perfusion ratio: an electrical impedance tomography study.,” Acta Anaesthesiol. Scand., vol. 58, no. 6, pp. 716–25, Jul. 2014. [22] J. B. Borges, F. Suarez-Sipmann, S. H. Bohm, G. Tusman, A. Melo, E. Maripuu, M. Sandström, M. Park, E. L. V Costa, G. Hedenstierna, and M. Amato, “Regional lung perfusion estimated by electrical impedance tomography in a piglet model of lung collapse.,” J. Appl. Physiol., vol. 112, no. 1, pp. 225–36, Jan. 2012. 432
  • 6.
    0° 30° 60°90°-30°-60°-90° PEEP 5 PEEP 10 0° 30° 60° 90°-30°-60°-90° R R R R R R R R R R R R R R PEEP 15 30° 60° 90°-30°-60°-90° 0° R R R R R R R Fig. 3. Healthy lung: Percentage of ventilation delivered to the right lung, dynamic compliance and oxygenation index PaO2/FIO2 are plotted for different body positions and PEEP level. Small arrows indicate the measurement sequence. Representative sequence of tidal EIT images during roation from the left (+90°) to the right (-90°) lateral position show regional ventilation where bright pixels depict a large and dark ones a low ventilation amplitude. Data are plotted for each condition for three pigs. The thin lines show the data of the individual pigs, the thick violet line represents the mean value. 433
  • 7.
    PEEP 5 PEEP 10 PEEP15 0° 30° 60° 90°-30°-60°-90° 0° 30° 60° 90°-30°-60°-90° 0° 30° 60° 90°-30°-60°-90° R R R R R R R R R R R R R R R R R R R R R Fig. 4. Sick lung: Percentage of ventilation delivered to the right lung, dynamic compliance and oxygenation index PaO2/FIO2 are plotted for different body positions and PEEP level. Small arrows indicate the measurement sequence. Representative sequence of tidal EIT images during roation from the left (+90°) to the right (-90°) lateral position show regional ventilation where bright pixels depict a large and dark ones a low ventilation amplitude. Data are plotted for each condition for three pigs. The thin lines show the data of the individual pigs, the thick violet line represents the mean value. 434
  • 8.
    SWI SSTO MSCIE NT IFIC LIBRARY 2 015 Content:Dr.StephanBöhm;Concept&Design:ZweizeitBrandDevelopment Made in Switzerland electrical impedance tomography Real-time tomographic images for organ function monitoring and diagnosis Contact us! call: + 41 (0) 81 330 09 72 mail: info@swisstom.com visit: www.swisstom.com Swisstom AG Schulstrasse 1, CH-7302 Landquart, Switzerland Swisstom AG Swisstom AG, located in Landquart, Switzerland, develops and manufactures innovative medical devices. Our new lung function monitor enables life-saving treatments for patients in intensive care and during general anesthesia. Unlike traditional tomography, Swisstom´s bedside imaging is based on non-radiating principles: Electrical Impedance Tomography (EIT). To date, no comparable devices can show such regional organ function continuously and in real-time at the patient’s bedside. Swisstom creates its competitive edge by passionate leadership in non-invasive tomography with the goal to improve individual lives and therapies. © Swisstom AG 2015