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The EIT-based global inhomogeneity index is highly correlated with regional lung opening in patients with acute respiratory distress syndrome

BMC Research Notes volume 7, Article number: 82 (2014) Cite this article

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Abstract

Background

The electrical impedance tomography (EIT)-based global inhomogeneity (GI) index was introduced to quantify tidal volume distribution within the lung. Up to now, the GI index was evaluated for plausibility but the analysis of how it is influenced by various physiological factors is still missing. The aim of our study was to evaluate the influence of proportion of open lung regions measured by EIT on the GI index.

Methods

A constant low-flow inflation maneuver was performed in 18 acute respiratory distress syndrome (ARDS) patients (58 ± 14 years, mean age ± SD) and 8 lung-healthy patients (41 ± 12 years) under controlled mechanical ventilation. EIT raw data were acquired at 25 scans/s and reconstructed offline. Recruited lung regions were identified as those image pixels of the lung regions within the EIT scans where local impedance amplitudes exceeded 10% of the maximum amplitude during the maneuver. A series of GI indices was calculated during mechanical lung inflation, based on the differential images obtained between different time points. Respiratory system elastance (Ers) values were calculated at 10 lung volume levels during low-flow maneuver.

Results

The GI index decreased during low-flow inflation, while the percentage of open lung regions increased. The values correlated highly in both ARDS (r2 = 0.88 ± 0.08, p < 0.01) and lung-healthy patients (r2 = 0.92 ± 0.05, p < 0.01). Ers and GI index were also significantly correlated in 16 out of 18 ARDS (r2 = 0.84 ± 0.13, p < 0.01) and in 6 out of 8 lung-healthy patients (r2 = 0.84 ± 0.07, p < 0.01). Significant differences were found in GI values between two groups (0.52 ± 0.21 for ARDS and 0.41 ± 0.04 for lung-healthy patients, p < 0.05) as well in Ers values (0.017 ± 0.008 cmH2O/ml for ARDS and 0.009 ± 0.001 cmH2O/ml for lung-healthy patients, p < 0.01).

Conclusions

We conclude that the GI index is a reliable measure of ventilation heterogeneity highly correlated with lung recruitability measured with EIT. The GI index may prove to be a useful EIT-based index to guide ventilation therapy.

Background

Ventilation distribution in patients under mechanical ventilation is often inhomogeneous [1]. Cyclic opening and closing of alveoli in patients with acute respiratory distress syndrome (ARDS) increases ventilation heterogeneity and the risk for ventilator-induced lung injury (VILI) [2]. Regional inhomogeneities of the damaged lung should be taken into consideration to develop improved ventilation strategies [3]. Unfortunately, hardly any established clinical tools possess the ability to assess regional ventilation in patients with ARDS except computed tomography (CT). However, CT is not suitable for bedside monitoring of patients with ARDS due to the radiation exposure and hazardous patient transport to the radiological examination site.

Electrical impedance tomography (EIT) is a non-invasive, radiation-free imaging technique. It measures regional lung ventilation and aeration distribution by means of changes in electrical potentials at the skin surface of the chest wall during breathing cycles [4]. The physical principle is that changes in lung ventilation and blood content in the thorax modify the electrical impedance of lung tissue [5, 6]. Although EIT has a relatively low spatial resolution (typically an image with 32 × 32 pixels for EIT vs. 512 × 512 pixels for CT), it achieves a much higher temporal resolution than CT (typically 20–50 Hz for EIT vs. 0.3-1 Hz for CT) which is an important prerequisite for bedside monitoring. The reliability of EIT has already been confirmed by comparison with different established methods [7–9]. Applications of EIT have been reported in subjects with [10–13] and without [14–16] lung disease. However, EIT is still not widely accepted in the clinical environment due to the difficult interpretation of the results [17–20]. Understandable and clinically relevant analysis methods and EIT parameters are still warrant to improve the acceptance of EIT. There exist multiple approaches for defining such parameters: Wrigge et al., Hinz et al. and Frerichs et al. considered the delay and the curvature of regional impedance-time curve as representing local lung mechanics [15, 21, 22]; Lowhagen et al. and Dargaville et al. analyzed regional pressure-volume curves to assess potentially recruitable lung volume and regional lung compliance [23, 24]. Grant et al. used the regional filling characteristics to indicate tidal hyperinflation or recruitment [25]. However, these parameters summarizing the dynamic information obtained by EIT restrict to the time changes of regions of interest (ROIs), i.e. impedance pattern associated with different ROIs will not be described by these parameters.

Recently, the so-called global inhomogeneity (GI) index has been proposed and used to quantify tidal volume distribution within the lung [26]. The GI index represents an uncomplicated and efficient approach to summarize the complex pulmonary impedance distribution pattern by one number [16, 27–29]. Up to now, the GI index has been evaluated for plausibility but an analysis of how it is affected by physiological factors is still missing. Since opening and closing of alveoli strongly influence ventilation distribution, we evaluated the influence of proportion of open lung regions measured by EIT on the GI index.

Methods

Patients and protocol

A total of 18 ARDS patients (12 male, 6 female; age 58 ± 14 years; height 177 ± 9 cm; weight 80 ± 11 kg (mean ± SD)) and 8 lung-healthy patients (5 male, 3 female; age 41 ± 12 years; height 177 ± 8 cm; weight 76 ± 8 kg) were analyzed retrospectively. Exclusion criteria were: age <18 years, pregnancy and lactation period, and any contraindication to the use of EIT (pacemaker, automatic implantable cardioverter defibrillator, and implantable pumps). The study was approved by the Ethics Committee of the Medical Faculty of the Christian Albrechts University in Kiel, Germany. Written informed consent was obtained from all patients or their legal representatives prior to the study.

The characteristics of the patients and the study protocol applied in the patients were previously described in detail [30]. The patients were sedated, paralyzed, and mechanically ventilated under pressure-controlled mode in supine position. Low-flow inflation was performed (Evita XL; Dräger, Lübeck, Germany) with a constant gas flow of 4 L/min starting at a zero end-expiratory pressure up to a tidal volume of 2 L or until a maximum airway pressure of 35 cmH2O was reached. Airway flow, pressure and volume were measured by the ventilator with a sampling rate of 126 Hz. EIT examinations were performed with the Goe-MF II EIT device (CareFusion, Höchberg, Germany). Sixteen ECG electrodes were attached on the chest circumference at the level of the fifth intercostal space. Alternating electrical currents (50 kHz, 5 mA peak-to-peak) were applied through adjacent pairs of electrodes in a sequential rotating process. The resulting potential differences were measured by the remaining electrode pairs. EIT raw data were acquired at 25 Hz and reconstructed offline with the Graz Consensus Reconstruction Algorithm for EIT, GREIT [31]. The reconstructed data were smoothed by a low-pass filter with 1 Hz cut-off frequency to suppress the influence of cardiac activity.

Data analysis - recruitable lung regions

The lung regions in EIT images were defined during low-flow maneuver based on functional EIT scans (fEIT), which show the spatial distribution of the pixel linear regression coefficients [32]. Large positive values of linear regression coefficients indicate that the trends of the local (pixel) and total relative impedance curves are highly correlated. Regions with regression coefficients (Rpixel) higher than 20% of the maximum value of all pixels (0.2 × max(Rimage)) in the corresponding fEIT images were considered to be lung regions. Thereafter, the maximum impedance amplitude during the low-flow inflation maneuver was determined in every pixel of the lung regions (max(Zpixel, t1:tn), where t1:tn was the time period of low-flow inflation). Lung region was defined as open (recruited) when, in the corresponding time course, the pixel amplitude exceeded 10% of the maximum amplitude, i.e. Zpixel, tk > 0.1 × max(Zpixel, t1:tn) [30]. The remaining lung regions at that time point were recruitable. The percentage of recruitable lung regions was defined as 100% minus the number of recruited pixels divided by the total number of pixels in the lung regions.

Data analysis - the GI index

The calculation of GI index has been described in previous studies [16, 26]. In the present study, we modified the original GI index to adapt to the low-flow inflation. In brief, a differential image is first generated using EIT scans at two selected time points (not necessary to be end points of inspiration and expiration as defined in previous studies). Then the median impedance value within the predefined lung regions is calculated. The sum of the absolute difference between median value and every pixel value is considered to indicate the variation of ventilation distribution. Subsequently, it is normalized to the sum of the impedance values within the lung regions, in order to make the GI index universal and inter-patient comparable (Eq. 1).

GI = ∑ x , y ∈ lung D I xy - Median D I lung ∑ x , y ∈ lung D I xy
(1)

where DI is the value of the differential impedance in differential images; DI xy denotes the DI of pixel xy in the identified lung regions; DI lung are DI of all pixels in the lung regions under observation. In the present study, we modified the GI index slightly. Since the sampling rate of EIT scans was 25 Hz, the calculation of the GI index began one second after the onset of inflation. A series of GI indices was calculated during the inflation based on the differential images between time points t26 to t1, t27 to t1, t28 to t1, …, tn to t1 (t1, the first EIT scan during inflation; tn, the n th EIT scan, n = 26, 27, …, until the end of inflation). The percentages of recruitable lung regions at corresponding time points were calculated and compared with GI index values using linear regression. To check for the effect of cardiac related changes in electrical impedance, the GI indices were calculated using both the low-pass filtered and unfiltered EIT data.

Data analysis - respiratory system elastance

During low flow inflation, inspiratory volume was equally divided into 10 slices. Since the airway flow rate was constant during the maneuver, the respiratory system elastance (Ers) was calculated within each slice with the modified first order equation of motion:

P aw , i = E rs , i × V i + k i
(2)

where P aw,i and V i represent the airway pressure and volume within slice i (i = 1, 2, … 10). k is a constant, containing the resistive part of pressure drop. The volume level at the middle of each slice was identified and matched with the time point in the EIT measurements. Ten GI index values were determined at the corresponding time points.

Statistical analysis

Data analysis was performed using MATLAB 7.2 (The MathWorks Inc., Natick, MA, USA). The Lilliefors test was used for normality testing. For normally distributed data, results were expressed as mean values ± standard deviations. Otherwise, data were presented as median and quartiles. The correlations between GI index and the percentages of recruitable lung regions, between GI index and Ers, between GI index and airway pressure, between GI index and lung volume were examined. Mediation analysis was performed to confirm that percentage of recruitable lung regions was a mediator variable for the observed relationship between GI index and airway pressure, between GI index and lung volume. Median GI values and median Ers values of patients in ARDS group were compared to that in lung-healthy group with Mann–Whitney U test. A P value < 0.05 was considered to be significant.

Results

Figure 1 shows differential images and regional lung opening maps during low-flow inflation in one ARDS patient. The calculation of the GI index was based on these differential images. At low level of inflation, only a small proportion of all lung regions was recruited and, thus, ventilation distribution was inhomogeneous. While the number of open lung regions increased (percentages of recruitable lung regions decreased), ventilation distribution became more homogeneous, as indicated by the decrease of the GI index. Although the individual regression coefficients varied among different patients (the lower, median and upper quartile were 0.65, 0.74 and 1.04 respectively; Figure 2), the GI index and percentages of recruitable lung regions were highly correlated (r2= 0.88 ± 0.08, p < 0.01). Similar results were obtained for lung-healthy patients (r2= 0.92 ± 0.05, p < 0.01).

Figure 1
figure1

Differential images (D) and the regional lung opening maps (O) during low-flow inflation. Differential images show the impedance differences of lung region pixels between the EIT scans acquired at time points highlighted on the total relative impedance curve (left top) with red open circles and the EIT scan at the beginning of the inflation maneuver highlighted by a red asterisk. At the corresponding time points, open lung regions are shown in white in the regional lung opening maps. The highlighted time points from left to right are: the beginning of the low-flow inflation, 85%, 50%, 0% of the recruitable lung regions, and the end of inflation. Color bars indicate the magnitude of relative impedance values in each pixel.

Full size image
Figure 2
figure2

Correlation of the GI indices and percentages of recruitable lung regions. The aggregate trend of the GI indices and percentages of recruitable lung regions are summarized from all 18 ARDS patients during low-flow inflation. The line in the middle and the dashed lines above and below represent the median, upper and lower quartile respectively.

Full size image

Figure 3 presents a comparison of the GI index values with and without low-pass filtering of cardiac related signals. The period of cardiac activity in this ARDS patient could be identified in the curve as 0.6 second. Ers of the same patient at different ventilation levels were also shown in Figure 3. Ers and sampled GI index values were highly correlated in 16 out of 18 ARDS patients (r2= 0.84 ± 0.13, p < 0.01). Comparable results were found in 6 out of 8 lung-healthy patients (r2= 0.84 ± 0.07, p < 0.01).

Figure 3
figure3

Comparison of GI index values and respiratory system elastance. The values of respiratory system elastance (Ers) are indicated with red circles. The GI index values with (blue solid line) and without (blue dashed line) low-pass filtering of cardiac related signals are plotted. Periodic cardiac activities can be recognized. The same patient as in Figure 1 is shown.

Full size image

The GI index values were also significantly correlated with other parameters such as airway pressure and lung volume (p < 0.01). It was confirmed with mediation analysis that percentages of recruitable lung regions mediated the relation between airway pressure and GI index, between lung volume and GI index (regression coefficient decreased significantly, p < 0.01).

Median GI values and median Ers values were calculated for every patient in both ARDS and lung-healthy groups during low-flow maneuver (Figure 4). Significant differences were found in GI (0.41 ± 0.04 for lung-healthy and 0.52 ± 0.21 for ARDS, p < 0.05) and Ers values (0.009 ± 0.001 cmH2O/ml for lung-healthy and 0.017 ± 0.008 cmH2O/ml for ARDS, p < 0.01) between the two study groups.

Figure 4
figure4

Comparison of GI index values and respiratory system elastance in lung-healthy and ARDS groups. H_G, A_G: median of GI index values in both lung-healthy (H) and ARDS (A) groups; H_E, A_E: median of respiratory system elastance (Ers) in both lung-healthy (H) and ARDS (A) groups. The boxes mark the quartiles while the whiskers extend from the box out to the most extreme data value within 1.5*the interquartile range of the sample. *, p < 0.05; **, p < 0.01.

Full size image

Discussion

In the present study, we examined the effect of heart-beat, lung inflation and the degree of lung opening on GI index during a low-flow inflation maneuver and confirmed that the GI index was strongly influenced by the fraction of open lung areas in mechanically ventilated patients. We also confirmed that GI index values in lung-healthy and ARDS patients were significantly different.

The GI index has been proposed to monitor ventilation distribution [27, 28], progression of obstructive lung disease [29], and to guide ventilator therapy [16]. Previously observed differences in the GI index between healthy volunteers and patients with various lung diseases [16, 26, 29] may be partly explained by the findings of the present study. In particular, lung regions of healthy volunteers open at low airway pressures (or even do not collapse at all) so that the GI index reaches a lower value during tidal ventilation. In patients, atelectatic lung regions may not be completely recruited during tidal ventilation so that the patients exhibit higher GI index values.

The GI index was originally calculated for tidal ventilation using differential EIT images between end-inspiration and end-expiration [26]. In a previous [29] and the present study, we found that a modified GI index can be used to assess the inhomogeneity at different lung volume levels. In the present study, the GI index was further modified to a quasi-continuous calculation. This enables us to closely monitor ventilation during prolonged inspiration and expiration. The same lung regions were used for GI calculation during whole low-flow inflation so that the values were intra-patient comparable. A limitation of the presented calculation compared to the original one is that regional overdistension cannot be captured in the serial differential images. Referencing to the baseline image, overdistended regions are considered to be “ventilated”. In the experimental setup, the low-flow inflation was terminated when a maximum airway pressure of 35 cm H2O was reached, to minimize the risk of VILI. Ers values didn’t increase during low-flow maneuver (Figure 3), which indicated that the used threshold pressure was not sufficient to induce significant overdistension that was not identified by the lung mechanics measurement. Therefore, the influence of regional overdistension on the presenting calculation was minimum. Although a previous study [16] indicated that the GI index may be influenced by regional overdistension, their correlation should be systematically investigated with recruitment maneuvers and titration of positive end-expiratory pressure in further studies.

We selected ARDS patients since their lungs are heterogeneously affected and their alveoli tend to collapse at low end-expiratory airway pressures [33]. With a low-flow inflation maneuver, the relation between the GI index and the fraction of open lung regions (Figure 2), and between the GI index and Ers (Figure 3) can be easily observed. The originate of GI index and open lung regions are different, although they are both derived from EIT images: the GI index depicts the relationship among pixels at certain time point; for open lung region calculation, impedance change of every single pixel in the lung region against time is traced.

We included also lung-healthy patients as control group. We found a similar trend to ARDS group that GI index decreased as ventilated regions increased. However, since recruitable lung regions occurred to a lesser degree in lung-healthy than in ARDS patients, both GI index and Ers values were significantly lower in lung-healthy than in ARDS patients (Figure 4).

Continuous calculation of ventilation inhomogeneity is contaminated by cardiac-related signals in EIT data (Figure 3). This problem is solved by applying an adequate low-pass filter to the data to eliminate the signal component related to the heart beat, so that the resulting GI index is more plausible and comparable to Ers.

The correlations of the GI index and Ers were not significant in two ARDS and two lung-healthy patients. The reason may be the limited number of Ers estimates during the low-flow inflation in each patient, and sensitivity of the correlation to noise. However, because of the respiratory signal quality delivered by the ventilator, it was not possible to calculate more Ers estimates.

One limitation of the study is that the gold-standard of identifying collapsed lung regions, namely CT scans, was missing. Due to radiation, CT is not a suitable bedside tool and indeed, there is no well established tool available for measuring recruitment/derecruitment dynamically. Besides CT scanning for study purposes would not be ethically justifiable. We used lung mechanics and the area of open lung measured in EIT to estimate the degree of recruitment. We confirmed that airway pressure increased the area of open lung, which influenced the GI index value. Further, we were not certain if all collapsed lung regions were recruited at a pressure level of 35 cm H2O [34]. These non-aerated regions would not be recognized as lung regions in fEIT and not be included into analysis. Identification of non-aerated lung regions in EIT measurements remains an important research topic and deserves further investigation. Nevertheless, patients with higher percentage of potential recruitable lung have higher mortality [34]. Thus, we focused on recruitable lung regions in the present study.

As discussed in our previous study [30], the identification of open lung regions with a threshold of 10% of the maximum local pixel amplitude of relative impedance change may slightly underestimate the true percentage of regional lung opening. This may influence the values of regression coefficients but not the conclusion that the GI index highly correlates with regional lung recruitment. Since it is not a well accepted method to estimate the recruitable regions, we also compared the GI index with respiratory system elastance and obtained a similar conclusion. The values of regression coefficients varied in different patients (Figure 2) indicating that individual therapeutic strategies should be developed to optimize the mechanical ventilation treatment. In practice, given the character of the GI curves presented in Figure 2, a simplified low-flow maneuver with half of duration or scanning at 3–4 different PEEP levels is sufficient to depict the GI index-recruitable regions curves, which may be helpful for development of individual therapeutic strategies.

Conclusions

We conclude that the GI index is a reliable measure of ventilation heterogeneity highly correlated with lung recruitability measured with EIT. The GI index may prove to be a useful EIT-based index to guide ventilation therapy.

References

  1. 1.

    Gattinoni L, D’Andrea L, Pelosi P, Vitale G, Pesenti A, Fumagalli R: Regional effects and mechanism of positive end-expiratory pressure in early adult respiratory distress syndrome. JAMA. 1993, 269 (16): 2122-2127. 10.1001/jama.1993.03500160092039.

  2. 2.

    The Acute Respiratory Distress Syndrome Network: Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Engl J Med. 2000, 342 (18): 1301-1308.

  3. 3.

    Rouby JJ, Lu Q, Goldstein I: Selecting the right level of positive end-expiratory pressure in patients with acute respiratory distress syndrome. Am J Respir Crit Care Med. 2002, 165 (8): 1182-1186. 10.1164/ajrccm.165.8.2105122.

  4. 4.

    Frerichs I, Dargaville PA, Dudykevych T, Rimensberger PC: Electrical impedance tomography: a method for monitoring regional lung aeration and tidal volume distribution?. Intensive Care Med. 2003, 29 (12): 2312-2316. 10.1007/s00134-003-2029-z.

  5. 5.

    Brown BH, Barber DC, Morice AH, Leathard AD: Cardiac and respiratory related electrical impedance changes in the human thorax. IEEE Trans Biomed Eng. 1994, 41 (8): 729-734. 10.1109/10.310088.

  6. 6.

    Nopp P, Rapp E, Pfutzner H, Nakesch H, Ruhsam C: Dielectric properties of lung tissue as a function of air content. Phys Med Biol. 1993, 38 (6): 699-716. 10.1088/0031-9155/38/6/005.

  7. 7.

    Frerichs I, Hinz J, Herrmann P, Weisser G, Hahn G, Quintel M, Hellige G: Regional lung perfusion as determined by electrical impedance tomography in comparison with electron beam CT imaging. IEEE Trans Med Imaging. 2002, 21 (6): 646-652. 10.1109/TMI.2002.800585.

  8. 8.

    Hinz J, Neumann P, Dudykevych T, Andersson LG, Wrigge H, Burchardi H, Hedenstierna G: Regional ventilation by electrical impedance tomography: a comparison with ventilation scintigraphy in pigs. Chest. 2003, 124 (1): 314-322. 10.1378/chest.124.1.314.

  9. 9.

    Marquis F, Coulombe N, Costa R, Gagnon H, Guardo R, Skrobik Y: Electrical impedance tomography’s correlation to lung volume is not influenced by anthropometric parameters. J Clin Monit Comput. 2006, 20 (3): 201-207. 10.1007/s10877-006-9021-4.

  10. 10.

    Eyuboglu BM, Oner AF, Baysal U, Biber C, Keyf AI, Yilmaz U, Erdogan Y: Application of electrical impedance tomography in diagnosis of emphysema--a clinical study. Physiol Meas. 1995, 16 (3 Suppl A): A191-A211.

  11. 11.

    Lowhagen K, Lundin S, Stenqvist O: Regional intratidal gas distribution in acute lung injury and acute respiratory distress syndrome–assessed by electric impedance tomography. Minerva Anestesiol. 2010, 76 (12): 1024-1035.

  12. 12.

    Miedema M, Frerichs I, de Jongh FH, van Veenendaal MB, van Kaam AH: Pneumothorax in a preterm infant monitored by electrical impedance tomography: a case report. Neonatology. 2011, 99 (1): 10-13. 10.1159/000292626.

  13. 13.

    Victorino JA, Borges JB, Okamoto VN, Matos GF, Tucci MR, Caramez MP, Tanaka H, Sipmann FS, Santos DC, Barbas CS, Carvalho CR, Amato MB: Imbalances in regional lung ventilation: a validation study on electrical impedance tomography. Am J Respir Crit Care Med. 2004, 169 (7): 791-800. 10.1164/rccm.200301-133OC.

  14. 14.

    Frerichs I, Braun P, Dudykevych T, Hahn G, Genee D, Hellige G: Distribution of ventilation in young and elderly adults determined by electrical impedance tomography. Respir Physiol Neurobiol. 2004, 143 (1): 63-75. 10.1016/j.resp.2004.07.014.

  15. 15.

    Frerichs I, Dudykevych T, Hinz J, Bodenstein M, Hahn G, Hellige G: Gravity effects on regional lung ventilation determined by functional EIT during parabolic flights. J Appl Physiol. 2001, 91 (1): 39-50.

  16. 16.

    Zhao Z, Steinmann D, Frerichs I, Guttmann J, Möller K: PEEP titration guided by ventilation homogeneity: a feasibility study using electrical impedance tomography. Crit Care. 2010, 14 (1): R8-10.1186/cc8860.

  17. 17.

    Adler A, Amato MB, Arnold JH, Bayford R, Bodenstein M, Bohm SH, Brown BH, Frerichs I, Stenqvist O, Weiler N, et al: Whither lung EIT: Where are we, where do we want to go and what do we need to get there?. Physiol Meas. 2012, 33 (5): 679-694. 10.1088/0967-3334/33/5/679.

  18. 18.

    Frerichs I, Pulletz S, Elke G, Gawelczyk B, Frerichs A, Weiler N: Patient examinations using electrical impedance tomography–sources of interference in the intensive care unit. Physiol Meas. 2011, 32 (12): L1-L10. 10.1088/0967-3334/32/12/F01.

  19. 19.

    Lundin S, Stenqvist O: Electrical impedance tomography: potentials and pitfalls. Curr Opin Crit Care. 2012, 18 (1): 35-41. 10.1097/MCC.0b013e32834eb462.

  20. 20.

    Moerer O, Hahn G, Quintel M: Lung impedance measurements to monitor alveolar ventilation. Curr Opin Crit Care. 2011, 17 (3): 260-267. 10.1097/MCC.0b013e3283463c9c.

  21. 21.

    Hinz J, Gehoff A, Moerer O, Frerichs I, Hahn G, Hellige G, Quintel M: Regional filling characteristics of the lungs in mechanically ventilated patients with acute lung injury. Eur J Anaesthesiol. 2007, 24 (5): 414-424. 10.1017/S0265021506001517.

  22. 22.

    Wrigge H, Zinserling J, Muders T, Varelmann D, Gunther U, von der Groeben C, Magnusson A, Hedenstierna G, Putensen C: Electrical impedance tomography compared with thoracic computed tomography during a slow inflation maneuver in experimental models of lung injury. Crit Care Med. 2008, 36 (3): 903-909. 10.1097/CCM.0B013E3181652EDD.

  23. 23.

    Dargaville PA, Rimensberger PC, Frerichs I: Regional tidal ventilation and compliance during a stepwise vital capacity manoeuvre. Intensive Care Med. 2010, 36 (11): 1953-1961. 10.1007/s00134-010-1995-1.

  24. 24.

    Lowhagen K, Lindgren S, Odenstedt H, Stenqvist O, Lundin S: A new non-radiological method to assess potential lung recruitability: a pilot study in ALI patients. Acta Anaesthesiol Scand. 2011, 55 (2): 165-174. 10.1111/j.1399-6576.2010.02331.x.

  25. 25.

    Grant CA, Fraser JF, Dunster KR, Schibler A: The assessment of regional lung mechanics with electrical impedance tomography: a pilot study during recruitment manoeuvres. Intensive Care Med. 2009, 35 (1): 166-170. 10.1007/s00134-008-1324-0.

  26. 26.

    Zhao Z, Möller K, Steinmann D, Frerichs I, Guttmann J: Evaluation of an electrical impedance tomography-based global inhomogeneity index for pulmonary ventilation distribution. Intensive Care Med. 2009, 35 (11): 1900-1906. 10.1007/s00134-009-1589-y.

  27. 27.

    Hough JL, Johnston L, Brauer SG, Woodgate PG, Pham TM, Schibler A: Effect of body position on ventilation distribution in preterm infants on continuous positive airway pressure. Pediatr Crit Care Med. 2012, 13 (4): 446-451. 10.1097/PCC.0b013e31822f18d9.

  28. 28.

    Humphreys S, Pham TM, Stocker C, Schibler A: The effect of induction of anesthesia and intubation on end-expiratory lung level and regional ventilation distribution in cardiac children. Paediatr Anaesth. 2011, 21 (8): 887-893. 10.1111/j.1460-9592.2011.03547.x.

  29. 29.

    Zhao Z, Fischer R, Frerichs I, Müller-Lisse U, Möller K: Regional ventilation in cystic fibrosis measured by electrical impedance tomography. J Cyst Fibros. 2012, 11 (5): 412-418. 10.1016/j.jcf.2012.03.011.

  30. 30.

    Pulletz S, Adler A, Kott M, Elke G, Gawelczyk B, Schadler D, Zick G, Weiler N, Frerichs I: Regional lung opening and closing pressures in patients with acute lung injury. J Crit Care. 2012, 27 (3): 323-e311-328

  31. 31.

    Adler A, Arnold JH, Bayford R, Borsic A, Brown B, Dixon P, Faes TJ, Frerichs I, Gagnon H, Garber Y, et al: GREIT: a unified approach to 2D linear EIT reconstruction of lung images. Physiol Meas. 2009, 30 (6): S35-S55. 10.1088/0967-3334/30/6/S03.

  32. 32.

    Pulletz S, van Genderingen HR, Schmitz G, Zick G, Schadler D, Scholz J, Weiler N, Frerichs I: Comparison of different methods to define regions of interest for evaluation of regional lung ventilation by EIT. Physiol Meas. 2006, 27 (5): S115-S127. 10.1088/0967-3334/27/5/S10.

  33. 33.

    Barbas CS, de Matos GF, Pincelli MP, da Rosa Borges E, Antunes T, de Barros JM, Okamoto V, Borges JB, Amato MB, de Carvalho CR: Mechanical ventilation in acute respiratory failure: recruitment and high positive end-expiratory pressure are necessary. Curr Opin Crit Care. 2005, 11 (1): 18-28. 10.1097/00075198-200502000-00004.

  34. 34.

    Gattinoni L, Caironi P, Cressoni M, Chiumello D, Ranieri VM, Quintel M, Russo S, Patroniti N, Cornejo R, Bugedo G: Lung recruitment in patients with the acute respiratory distress syndrome. N Engl J Med. 2006, 354 (17): 1775-1786. 10.1056/NEJMoa052052.

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Acknowledgements

This work was partially supported by the FP7-PIRSES 318943 (eTime), PulMoDS (BMBF FKZ 01DR12095) and BMBF 03FH038I3 (MOSES).

The results of this study have been presented in part at the 13th International Conference on Electrical Impedance Tomography (EIT 2012) in Tianjin, China (23–25, May).

Author information

Affiliations

  1. Institute of Technical Medicine, Furtwangen University, Jakob-Kienzle Straße 17, D-78054, VS-Schwenningen, Germany
    • Zhanqi Zhao
    •  & Knut Möller
  2. Department of Anaesthesiology and Intensive Care Medicine, Medical Center Osnabrück, Osnabrück, Germany
    • Sven Pulletz
  3. Department of Anaesthesiology and Intensive Care Medicine, University Medical Center Schleswig-Holstein, Kiel, Germany
    • Inéz Frerichs
  4. Department of Radiology, University of Munich, Munich, Germany
    • Zhanqi Zhao
    •  & Ullrich Müller-Lisse
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Corresponding author

Correspondence to Zhanqi Zhao.

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Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

ZZ designed the study, analyzed the data and drafted the manuscript. SP carried out the data measurement. IF contributed to study design and revised the manuscript critically. UML gave valuable advices and contributed to writing. KM contributed to study design, data analysis and writing. All authors read and approved the final manuscript.

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This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.

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Zhao, Z., Pulletz, S., Frerichs, I. et al. The EIT-based global inhomogeneity index is highly correlated with regional lung opening in patients with acute respiratory distress syndrome. BMC Res Notes 7, 82 (2014) doi:10.1186/1756-0500-7-82

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Keywords

  • Electrical impedance tomography
  • Acute lung injury
  • Global inhomogeneity index
  • Regional lung opening
  • Lung mechanics

BMC Research Notes

ISSN: 1756-0500

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