Top Banner
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
8

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

Aug 18, 2015

Download

Healthcare

Hauke Sann
Welcome message from author
This document is posted to help you gain knowledge. Please leave a comment to let me know what you think about it! Share it to your friends and learn new things together.
Transcript
Page 1: Waldmann A. et al.: Position-dependent distribution of lung Ventilation – A feasability study.

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

Page 2: Waldmann A. et al.: Position-dependent distribution of lung Ventilation – A feasability study.

Position-dependent distribution of lung ventilation

– A feasability study Andreas D. Waldmann

1, Carlos Ferrando Ortolá

2, Manuel Muñoz Martinez

3, Anxela Vidal

4, Arnoldo Santos

4, Manuel

Perez Márquez4, Péter L. Róka

1, Stephan H. Bohm

1, Fernando Suarez-Sipmann

5

1Swisstom AG, Landquart, Switzerland,

2 Department of Anesthesia and Critical Care. Hospital Clínico Universitario, Valencia, Spain.

3Departement of Anesthesiology, Hospital Universitario de la Princesa, Madrid, Spain.

4 Department of Critical Care. Instituto de Investigación Sanitaria Fundación Jiménez Díaz, Madrid, Spain,

5Department 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

Page 3: Waldmann A. et al.: Position-dependent distribution of lung Ventilation – A feasability study.

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

Page 4: Waldmann A. et al.: Position-dependent distribution of lung Ventilation – A feasability study.

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

Page 5: Waldmann A. et al.: Position-dependent distribution of lung Ventilation – A feasability study.

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

Page 6: Waldmann A. et al.: Position-dependent distribution of lung Ventilation – A feasability study.

0° 30° 60° 90°-30°-60°-90°

PEEP 5

PEEP 10

0° 30° 60° 90°-30°-60°-90°

R

R

R

R

R

R RR

R

R

R

R

R R

PEEP 1530° 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

Page 7: Waldmann A. et al.: Position-dependent distribution of lung Ventilation – A feasability study.

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 RR

R

R

R

R

R R

R

RR

RR

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

Page 8: Waldmann A. et al.: Position-dependent distribution of lung Ventilation – A feasability study.

S W I S S T O M S C I E N T I F I C L I B R A RY 2 0 1 5

Co

nte

nt:

Dr.

Ste

ph

an

hm

; C

on

cep

t &

Desi

gn

: Zw

eiz

eit

Bra

nd

Deve

lop

men

t

Made in Switzerland

electricalimpedancetomography

Real-time tomographic images for organ function monitoring and diagnosis

Contact us!

call: + 41 (0) 81 330 09 72 mail: [email protected]: www.swisstom.com

Swisstom AGSchulstrasse 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