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Structural-functional lung imaging using a combined CT-EIT and a Discrete Cosine Transformation reconstruction method


Lung EIT is a functional imaging method that utilizes electrical currents to reconstruct images of conductivity changes inside the thorax. This technique is radiation free and applicable at the bedside, but lacks of spatial resolution compared to morphological imaging methods such as X-ray computed tomography (CT). In this article we describe an approach for EIT image reconstruction using morphologic information obtained from other structural imaging modalities. This leads to recon- structed images of lung ventilation that can easily be superimposed with structural CT or MRI images, which facilitates image interpretation. The approach is based on a Discrete Cosine Transformation (DCT) of an image of the considered transversal thorax slice. The use of DCT enables reduction of the dimensionality of the reconstruction and ensures that only conductivity changes of the lungs are reconstructed and displayed. The DCT based approach is well suited to fuse morphological image information with functional lung imaging at low computational costs. Results on simulated data indicate that this approach preserves the morphological structures of the lungs and avoids blurring of the solution. Images from patient measurements reveal the capabilities of the method and demonstrate benefits in possible applications.


Electrical Impedance Tomography (EIT) is used to visualize the internal conductivity distribution of a domain from voltage measurements on the surface of the domain. In clinical context EIT is most often used to visualize regional ventilation of the lungs which has proven useful to reduce ventilator induced lung injury (VILI)1,2 and guide clinicians to set adequate PEEP levels for mechanically ventilated patients in the intensive care unit (ICU)3. In lung EIT an array of electrodes is attached around the patient’s chest. The electrodes are used to inject small alternating currents into the body and simultaneously measure the resulting voltages between pairs of electrodes. Usually the electrodes are attached equidistantly in a plane around the 5th intercostal space (ICS5), which seems to be less influenced by lung tissue shifts than more cranial or caudal positions for the electrodes4.

Compared to morphological imaging methods, such as X-ray computed tomography (CT) or magnetic resonance imaging (MRI), the spatial resolution of EIT is much lower (about 2–3 cm)5, whereas the temporal resolution is very high (up to 50 frames/s in commercially available devices). In comparison to established methods for functional imaging of the lungs, such as single photon emission computed tomography (SPECT) or positron emission tomography (PET), EIT is very cheap. Additionally it is non-invasive, radiation free and currently the only technique capable for real-time and long-term bedside monitoring of regional lung ventilation6,7.

Besides the application in the ICU, EIT has recently been used in spontaneously breathing patients, suffering from asthma bronchiole8, cystic fibrosis (CF)9 or chronic obstructive pulmonary disease (COPD)10. It has been shown in these studies, that EIT is capable to identify functional abnormalities in obstructive lung diseases. However, in order to obtain a comprehensive insight into the pulmonary pathophysiology it is necessary to combine structural and functional data11, such as it is done in SPECT-CT or PET-CT.

Such combined imaging modalities simplify image interpretation; e.g. image fusion of PET and CT data substitutes error-prone cognitive allocation of anomalies and therefore improves diagnostics12. Additionally, it is common to use information obtained from one method to improve the reconstruction or the interpretability of the respectively other. E.g. the attenuation correction for PET imaging is derived from CT data13 and vice versa the detailed anatomic information from CT imaging is used to localize accumulation of the radiotracer14.

EIT has already been validated against CT15,16, SPECT17 and PET18, confirming that it is able to measure regional ventilation. Basic geometric relations between organs are preserved in EIT and images roughly correspond to the anatomy19.

The objective of this work is to fuse morphological and functional information to improve interpretability of EIT images. We propose a novel approach to include detailed prior information about the contour of the thorax as well as the shape of the lungs in the image reconstruction process. This can be regarded as ‘patient specific EIT imaging’, where resulting images can easily be superimposed with CT data and thus improve readability for clinicians. Morphological changes can be directly correlated with changes in ventilation distribution or other functional images derived from EIT. It is demonstrated in simulations and measurements on patients how advantages of both imaging modalities (CT and EIT) can be combined to improve the potential utility of functional lung image in clinical applications.


Classical approach for image reconstruction

The EIT reconstruction problem is ill-posed, arbitrarily small perturbation in the boundary voltages may create arbitrarily large perturbations of the solution, i.e. the conductivity distribution20. Therefore, to obtain useful estimates of conductivity distribution a regularization scheme is needed21. Additionally the EIT problem is non-linear, which means that boundary voltages are non-linearly related to internal conductivities22.

Several reconstruction methods for EIT imaging have been developed, all showing one or the other advantage. Most of them have been developed for special purposes, e.g. absolute EIT imaging23, compensation of motion artifacts24, compensation for faulty electrodes25, 3D imaging26, methods considering temporal correlation to reduce image noise27 or utilizing Kalman filter approaches to track fast changes in conductivity distribution28. Other algorithms are based on expert defined figures of merit29 or on eigenimages from CT data as training sets30. Blurring of reconstructed images is prevented in approaches using the level set method31 or Total Variation Regularization32. Constantly increasing computational power and parallel computing allow fast reconstruction of nonlinear EIT33 and direct methods, such as the d-bar algorithm34.

The below described one-step Gauss-Newton method represents a broad group of structurally similar algorithms for image reconstruction, that have been widely applied in EIT29,35. We therefore use this ‘classical’ approach for both: a) to demonstrate the benefits of the overall approach of direct structure integration into EIT reconstruction and b) to relate the outcome to generally accepted standard EIT modalities.

A common method to estimate the conductivity from voltage measurements on the boundary is to discretize the domain into a finite element model (FEM) of nelem piecewise constant regions. Rather constructing absolute values of conductivity most of the clinical EIT research uses time-difference EIT, where the change in conductivity distribution x = σ − σbaseline between two times is calculated from voltage changes y = v − vbaseline. The vectors σbaseline and vbaseline denote the conductivity and boundary voltage at an appropriately chosen baseline; vectors σ and v contain the conductivity and voltages at another time. In practice it is common to set the baseline at functional residual capacity (FRC) or for mechanically ventilated patients at positive end-expiratory pressure (PEEP). Since this conductivity distribution is usually not known it is common to set σbaseline = 1, which may lead to significant errors. It is recommended to consider the conductivity distribution obtained e.g. from CT or MRI images to improve image quality36. In normalized time-difference EIT the difference in measured voltage y is normalized, such that , where the index i denotes the i-th element of the vectors, respectively. In the remainder of this paper we use normalized values for voltage change.

The classical approach for reconstruction of conductivity distribution in difference EIT is

where is the reconstructed conductivity change. The non-linear forward model F(x) maps changes in conductivity distribution to voltage changes at the electrodes. For small changes in conductivity the change in boundary voltage can be approximated by a linear mapping such that which leads to

where n is the noise of the measurement system and J is the Jacobian. Each element of J relates a small voltage change at the i-th position on the measurement vector y to a conductivity change of the j-th FEM element and is calculated as:

The Jacobian J is depending on the linearization point σbaseline. To avoid errors caused by an assumed homogeneous distribution σbaseline we considered different conductivities for lung tissue and remaining tissue, throughout this paper. This is described in more detail below. The Jacobian J does as well depend on the current stimulation pattern. In this paper we use the adjacent current stimulation pattern, which applies current and measures voltages between neighboring pairs of electrodes. For nelec electrodes this results in nmeas = nelec · (nelec − 3) voltage measurements (of which are independent) for every frame and thus .

Thus, the linearized problem is formulated as:

The first term is often called the ‘data fidelity term’, the second term is called ‘regularization term’ and adds, depending on the choice of R, penalties to reconstructed conductivity distributions. The level of regularization is controlled with the scalar value λ. The norm of the regularization term is specified with j. Mathematically the ‘regularization term’ is used to replace the ill-posed problem by a nearby well-posed37.

There are numerous publications about the choice of R, which can be regarded as a way of implementing prior knowledge into the solution. Most of these approaches penalize the solution such that a given structure of the solution is obtained. This leads to small, smooth or slowly changing solutions 38. In this paper we either use the Tikhonov prior RTik = I, which leads to solutions with smaller norms, or the Laplace prior RLP39, to penalizes non-smooth solutions.

If the l2-norm is used for the regularization term of equation (4) the estimated change in conductivity can be calculated in a closed form

Matrix B is called ‘reconstruction matrix’ which maps voltage changes y to changes in conductivity distribution . In real-time systems B is usually pre-calculated, e.g. during startup of the device. The reconstruction of is thus realized as a trivial matrix multiplication, which is one of the reasons for real-time capability of EIT.

Introduction to Discrete Cosine Transformation (DCT)

The Discrete Cosine Transformation (DCT) is an established method in image processing. A popular application is the JPEG image compression, where images are converted to a frequency-domain representation. The idea of DCT is to represent a signal as a weighted sum of basis functions, whereas the basis functions are cosine functions with different frequencies p and q in x-direction and y-direction, respectively. For a two dimensional image A with M rows and N columns the DCT is defined as follows:



The resulting matrix V contains the DCT coefficients. A lossy compression of the image A can be reconstructed using only a subset of the DCT coefficients.

where is a matrix of the same size as V but contains only few nonzero elements (e.g. the k-largest elements of V).

Figure 1 is an example of a DCT with a relatively high compression ratio of 96%. Figure 1 (left) shows the original image (256 × 256 pixels), Fig. 1 (right) is a reconstruction with the 50 lowest frequency components in each direction, which means that contains zero values for row and column indices greater than 50.

Figure 1
figure 1

Left: Original image with 256 × 256 pixels. Right: Reconstruction using only the 50 lowest frequency components.

Dimensionality reduction using DCT and implementation of prior knowledge

The idea of this paper is to represent the solution of the inverse problem in terms of cosine basis functions. Only a subset of DCT coefficients is considered for reconstruction, which reduces the dimensionality of the problem. We only need to solve for the coefficients of cosine basis functions instead of all elements in the FEM mesh. This reduction of dimensionality is achieved by multiplying the Jacobian by a matrix , where nDCT is the number of DCT coefficients used for reconstruction and nDCTnelem. In this paper we use the same number of frequencies for the x-direction nX_DCT and y-direction nY_DCT such that , which means that only nDCT = 225 DCT coefficients are reconstructed. This is substantially less than the number of elements in typical FEM meshes.

The above formulation of the DCT is expressed as:

with D(p, q) being the cosine function at frequencies p and q. To introduce prior knowledge about the shape of the lungs and thus the possible conductivity distribution we generate the matrices C(p, q), which are

with being a binary image of the lungs with

The binary image of the lungs can be obtained e.g. by separating the lungs from CT data. If no CT data is available it might be suitable to define lung-shaped regions of possible conductivity change. Each column kj of K is created as follows

where is the map assigning each pixel in the matrix to the finite element which covers the corresponding pixel. The values of the index depend on as follows:

Please note that the number of FEM elements representing the lung tissue might be smaller than the number of pixels categorized as lung tissue in the matrix C(p, q). Although this means that not all elements of C(p, q) are used, the columns of K are still linearly independent, which means that K is a valid basis of the selected low frequency subspace of the DCT representation.

For better understanding the exemplarily illustration of the result of the element-wise multiplication of a cosine function and a binary lung image according to equation (9) is depicted in Fig. 2 (left), according to equation (10) the matrix C(p, q) is mapped to the elements of the FEM model, which is represented by a column of matrix K (Fig. 2 (right)).

Figure 2
figure 2

Left: Representation of the matrix C with p = 0 and q = 1. Right: Visualization of the corresponding column k16 of K with the FEM model of the thorax.

Each column jj of the Jacobian J describes how change in conductivity of the j-th FEM element influences the measured changes in boundary voltages. Hence the image reconstruction algorithm calculates a linear combination of the columns of J that best fits the measured voltage change y. Generating a new Jacobian JDCT = J · K, where leads to a different interpretation of the columns. In this case each column jDCT, j describes how a certain distribution of conductivity change kj influences the measured changes in boundary voltage. This results in a new formulation of equation (5) such that:

where can be interpreted as reconstruction of DCT coefficients. In other words the j-th element of the vector explains to what extend the relative voltage change y is induced by the j-th column of K. Accordingly, the reconstruction matrix BDCT maps voltage changes y to DCT coefficients.

Prior knowledge about the DCT coefficients can be incorporated in RDCT. By setting , the solution of equation (11) is drawn towards an expected solution with h being the DCT coefficients of the expected solution, which might be obtained from CT or MRI data. Throughout this paper we set RDCT = I, which is the identity matrix and thus the classical approach for Tikhonov regularization40.

The result can now be used to reconstruct an image with the same resolution as the lung shape obtained from the original CT image. Therefore the matrices C(p, q) have to be multiplied with the corresponding values of and summed element by element:

where the subscript j of corresponds to the values of p and q as already described below equation (10).

The image H contains information about the lung shape. It is therefore a method to incorporate information of ventilation distribution obtained from boundary voltage measurements of an EIT device with patient specific physiological information about the lung shape. The cognitive allocation of ventilation distribution to lung areas in CT images can be replaced with the described approach and resulting images can directly be superimposed with CT images.

In order to be able to compare different approaches for image reconstruction we used the noise figure (NF) calculation41 to find values for the hyperparameter λ.

where the function S is used to map changes in voltage y or noise n to conductivity change. Depending on the approach used for reconstruction S is realized either as described in equation (4) or as in equation (11) and (12) if images are reconstructed with the DCT approach. A bisection search technique was used to find the corresponding values for λ to obtain a noise figure of NF = 0.5 for all reconstructions in this article.

Data generation

Data of the boundary voltage were simulated using MATLAB R2015a (Mathworks, Natick, MA) and the EIDORS toolbox42. FEM meshes were generated with NETGEN43. To test the above described approach on artificial data we used a CT dataset of a subject (male, 68 years) to simulate boundary voltages. We used the adjacent current stimulation pattern because the used hardware in the subsequent part of this article also runs with the adjacent current stimulation pattern, although this method for current injection and voltage measurement is not optimal44. The thorax shape at 5th intercostal space was derived from CT data as well as the shape of the lungs. Subsequently the thorax shape was used to generate a FEM mesh with 3570 elements. The conductivity of the elements belonging to the lungs was set to σ = 0.5, remaining elements were set to σ = 1. The corresponding voltage vbaseline of this conductivity distribution was simulated. Different distributions of ventilation were simulated by changing the conductivity of selected elements to σ = 0.25. Again boundary voltages v were simulated, leading to the normalized change in voltage y. The procedure of generating different ventilation patterns is depicted in Fig. 3.

Figure 3
figure 3

Procedure of voltage simulation for different configurations of the lungs: Thorax shape and lung shape were derived from CT data and used to create FEM models to simulate boundary voltages. Different ventilation patterns were simulated by setting selected FEM elements to σ = 0.5 for non-ventilated lung-tissue and σ = 0.25 for ventilated lung-tissue.

Four different ventilation patterns were created: a) homogeneous ventilation of complete lung, b) no ventilation in dorsal right lung, c) no ventilation in the most ventral and most dorsal parts of both lungs and d) no ventilation in ventral left lung and dorsal right lung. Pattern a) is used to evaluate the behavior of the algorithm on lung-healthy subjects whereas b) describes a typical pattern e.g. of patients under general anesthesia when the dorsal parts of the lungs collapse and lead to atelectasis. Pattern c) represents the simultaneous occurrence of alveolar hyperinflation in the most ventral parts and atelectasis in the most dorsal parts of the lung which may occur at the same time in critically-ill patients45. Pattern d) is rarely seen in real patients and is used to demonstrate the capability of the described algorithm. Figure 4 (upper) shows all used ventilation patterns.

Figure 4
figure 4

Upper row: Patterns of conductivity change used for simulation of boundary voltages (ground truth). Middle row: Reconstruction of the conductivity change from simulated voltages. Lower row: Reconstructed conductivity changes with 25% Gaussian noise on the simulated voltages.

Besides the four ventilation patterns different states of atelectasis of the dorsal lungs were simulated. Overall 25 datasets were generated, starting at 0% until 50% of the lungs in anterior-posterior direction were considered as collapsed. Elements belonging to collapsed lung regions were assigned to σ = 0.5, ventilated elements to σ = 0.25.

Another FEM mesh was used for the reconstruction of conductivity change to avoid the ‘inverse crime’46.

Patient data

In order to evaluate the performance of the described method we also used real measured retrospective EIT data covering a clinical context. EIT data were recorded for different clinical studies on 5 patients (male, 66y ± 3) with different types of diseases. Informed consent was obtained from all subjects, the methods were carried out in accordance with the approved guidelines and regulations. The studies were approved by the local ethics committee of Kiel University and LMU Munich. The patients were either spontaneously breathing or connected to a mechanical ventilator while a PEEP step was performed. The Goe-MF II device (Viasys Healthcare, Höchberg, Germany) or the PulmoVista500 (Dräger Medical, Lübeck, Germany) were used to measure the boundary voltages. Data were collected at ICS5. For all patients an actual CT dataset was available which was used to determine the contour of the thorax and the shape of the lungs at the position of the electrodes. Table 1 provides an overview of the patient’s diseases and the used EIT device.

Table 1 Patient overview.

Evaluation of image quality

For the simulated ventilation patterns the pixel values of the considered ventilation patterns and the pixel values of the reconstructed images were compared. Since we are most interested in conductivity decrease we define that pixels Hm, n in the reconstructed image H with a lower value than a heuristically defined threshold are classified as ‘decrease in conductivity’ (pixel set to 1). Other pixels are classified as ‘no change in conductivity’ (pixel set to 0). The threshold is defined with a parameter α as described below:

With this classification we are able to distinguish the fraction of pixels which correctly depict the underlying conductivity change and quantify the amount of correctly and incorrectly reconstructed data. The pixels are clustered in four groups, where G1 and G4 correspond to correct conductivity reconstruction; G2 and G3 correspond to incorrect reconstruction.

  • G1 = Pixel correctly depicts decrease in conductivity

  • G2 = Pixel wrongly depicts decrease in conductivity

  • G3 = Pixel wrongly depicts no change in conductivity

  • G4 = Pixel correctly depicts no change in conductivity


DCT image reconstruction for different ventilation patterns

The performance of the DCT-approach with four different patterns of ventilation is depicted in Fig. 4. The upper row depicts the conductivity change used in the simulation of boundary voltages (ground truth). No change in conductivity is shown in black. Tissue with a change in conductivity from σ = 0.5 to σ = 0.25, as described above, is shown in light blue. The middle row and lower row represent reconstructions using the DCT approach without noise and with 25% Gaussian noise added, respectively.

The fraction of correctly (clusters G1 and G4) or wrongly (clusters G2 and G3) classified pixels is visualized in Fig. 5. Threshold parameter was set to α = 0.65. The fraction of correctly classified pixels for the four considered patterns without noise is: (a) 0.91; (b) 0.99; (c) 0.91; (d) 0.96. With 25% of artificial noise these values change to: (a) 0.90; (b) 0.96; (c) 0.91; (d) 0.96.

Figure 5
figure 5

Fraction of pixels that are correctly classified as conductivity change (G1) or no change in conductivity (G4). Classes G2 and G3 respectively show the amount of pixels wrongly depicting changes in conductivity although there is none and pixels that show no changes in conductivity although the conductivity has changed. Threshold parameter α = 0.65. Upper graph is calculated with no noise, in the lower graph 25% Gaussian noise is added.

Simulation of atelectasis

Figure 6 shows the difference between the DCT-approach for image reconstruction compared with the classical solution using the Laplace prior for three ventilation patterns, representing 0%, 25% and 50% of atelectasis of the dorsal lungs.

Figure 6
figure 6

Left column: Atelectasis patterns used for voltage simulations (ground truth conductivity change). Middle column: Reconstruction of conductivity changes using the DCT-approach. Right column: Reconstruction of conductivity change using the classical approach and Laplace prior.

The Laplace prior in Fig. 6 (right) smoothes the reconstructed values of conductivity change, which causes a loss of morphological structures of the lungs. In contrast the DCT-approach in Fig. 6 (middle) utilizes the morphological information form CT data and reconstructs the conductivity change onto these structures.

Computing the l1-norm of the difference of reconstructed image to the ground truth data confirms this observation, as depicted in Fig. 7. Using the DCT reconstruction results in a reduced l1-norm of image difference compared to the classical approach using Tikhonov prior or Laplace prior.

Figure 7
figure 7

l1-norm of difference of reconstructed images and true conductivity distribution for different amounts of simulated atelectasis. Blue circle: DCT reconstruction, red x-marker: classical approach with Tikhonov prior, yellow plus-marker: classical approach with Laplace prior.

Patient data

Reconstructed images of conductivity change for the 5 subjects are shown in Fig. 8. The pixels belonging to the lung were extracted from CT values as well as the thorax shape of the considered slice.

Figure 8
figure 8

Upper row: Lung and thorax shape of the patients used for reconstruction. Lower row: Reconstructed images of conductivity change based on the DCT approach.

The images use the same color scheme as in the simulations above, where white color depicts large negative changes in conductivity, light blue color depicts small negative changes in conductivity. Positive changes in conductivity are depicted in purple, but are rarely seen during inspiration. For the purpose of illustration we do not depict the color scale in Fig. 8, which is different for every patient (Fig. 9).

Figure 9
figure 9

Superposition of changes in conductivity distribution obtained by the described DCT approach and CT images in a patient with emphysema in the ventral lungs (left) and atelectasis in dorsal lungs (right).

Although we do not know the correct distribution of conductivity change, the results of Fig. 8 seem to be reasonable. Patient 1 did not show any abnormalities in the lung CT; hence we expect to obtain homogeneous ventilation distribution. The reconstructed data confirm this. Patient 2 shows areas of pulmonary emphysema in both ventral lungs. We therefore expect lower values of ventilation, which is confirmed by the EIT data. Patient 3 has atelectasis in the dorsal left lung regions determined from lung CT. This can as well be seen on the reconstructed EIT data. Also Patient 4 has atelectasis, which can be recognized in both lungs from CT images and EIT reconstructions. Patient 5 has pulmonary emphysema in the dorsal right lung while the left lung is hyperinflated. Ventilation distribution obtained with EIT confirms lower ventilation of the left lung and reveals that the upper left lobe shows almost no ventilation.

A superposition of conductivity change reconstructed with the proposed DCT algorithm and a CT image is depicted in Fig. 9 for patients 2 and 4. It can be seen in Fig. 9 (left) that both ventral lungs show no change in conductivity. Figure 9 (right) reveals that the most dorsal regions of both lungs show no change in conductivity, which strengthens the diagnosis of atelectasis.


In this paper we present a method to incorporate patient specific structural information (e.g. CT data) in the reconstruction process of EIT imaging. It is demonstrated in simulations and as well in real patient data that the morphological structure of the lungs is preserved in the reconstructions. Blurring of the solution into non-lung regions is prevented and resulting images can easily be superimposed with high-resolution morphological data, as it is done already in combined imaging methods, such as SPECT-CT or PET-CT. This facilitates a comprehensive insight into the pathophysiology of lungs, since regional information about the functional status can directly be correlated with the morphology of the lungs. Furthermore, the use of DCT reduces the dimensionality of the problem, which is computationally beneficial for large scale problems (e.g. dense mesh 3D EIT) or iterative reconstruction methods47.

Other approaches have been proposed earlier that use detailed and patient specific anatomical information in the image reconstruction. As demonstrated on simulation models it is possible to enhance the sharpness of the images using structural prior information, incorporating anisotropic smoothness constraints in the regularization48 or Gaussian anisotropic filters49, relaxing the smoothness in direction of expected change. Compared to our approach there is no explicit reduction of the dimensionality of the problem. Other approaches using a small number of simple fixed conductivity sets to model the physiology of the considered domain, to reduce dimensionality have been described50,51. These studies use the shape of the lungs and the contour of the thorax, derived from CT or MRI data, to group FEM elements and assigning them the same electrical properties. The results of these methods for reduction of dimensionality are strongly biased52 and, contrary to our approach, inhomogeneities of the lungs cannot be visualized. In other articles21,53 nine different states of the lungs and the heart are used to generate orthonormal basis functions. However, in these methods the underlying truncated basis for the reconstructed conductivity is not capable to visualize more complex distributions of lung ventilation. The feasibility of reduced-order models using orthogonal decomposition of conductivity and potential distributions has been demonstrated in simulations and tank measurements47, but no individual structural information is embedded in the reconstruction. An approach that shows the capabilities of image fusion of CT and EIT data utilizing a coregistration algorithm is described for measurements on a phantom54. However, neither structural information is directly used in the EIT reconstruction nor is the dimensionality of the problem reduced.

The stability and low computational costs of linear reconstruction algorithms are reasons for their important role in clinical applications30. The presented DCT approach is based on the simple, but probably most often used35 reconstruction method, which is the one-step Gauss-Newton solver. Thus it is not directly applicable to all of the above mentioned algorithms, e.g. the d-bar method34 or Total Variation Regularization32. However, we are confident that the DCT approach can be combined with some of the existing linear methods. As an example temporal one-step solvers27 could be adapted to reconstruct DCT coefficients instead of conductivity changes for every FEM element. In a similar way Kalman filter approaches28 could be extended to benefit from the advantages of the proposed approach. Furthermore, the DCT approach could easily be extended to 3D-EIT, where the reduction of dimensionality might facilitate real-time reconstruction with sufficient resolution.

Its radiation free operation is often mentioned as an advantage of EIT compared to other imaging techniques. However, in combination with structural imaging described in this paper we utilize morphological information of the lungs, which is usually acquired with CT. The described imaging approach is therefore not radiation-free per se, but need not necessarily expose patients to extra radiation dose if CTs were taken for different clinical purpose anyway.

As a limitation of the approach it should be mentioned that morphological changes, occurring between CT examination and EIT measurement, will act as a wrong prior and may lead to corrupted reconstruction. Shape deformations during breathing are as well a known and often addressed problem in EIT, whose errors are currently accepted in all routinely applied reconstruction methods. Though a real thorax shape is unlikely to be more error prone than a static circle in reconstruction, the sensitivity of the approach to the mismatch between assumed lung shapes and actual form needs to be examined in future research. A further limitation of our study was a heuristical determination of the number of DCT coefficients. Additional examinations are necessary to define an optimal number of DCT coefficients, considering e.g. the inherently low resolution of EIT. Furthermore we only considered the lung shapes of a single slice; this has to be extended in future studies to investigate whether a 3D model of the lungs leads to better results. Additional studies with more patients are necessary to further evaluate the approach and to demonstrate the performance in combination with morphological data.

Although the images obtained with this method look quite attractive we want to point out that we have no evidence that the general resolution is improved, however it is proven that using the actual thorax contour for image reconstruction leads to better results7. Nevertheless we are confident that the approach described in this paper simplifies superposition of CT or MRI images with data obtained from EIT and therefore might help clinicians in image interpretation and diagnosis in a similar way as it is already done in the combination of PET or SPECT images and CT data.


In conclusion, anomalies in ventilation distribution can be correlated with underlying morphological information and vice versa the impact of pathological changes in lung tissue on ventilation distribution can be examined if the described approach is used for image reconstruction. We want to emphasize that EIT data might as well be used to generate functional images, e.g. regional time constant maps, which is only possible due to the high frame rate of EIT. Correlation of morphological images with EIT data might especially be useful for spontaneously breathing patients, suffering e.g. from asthma bronchiole, CF or COPD. For these patients we do not expect large changes in lung shape as it might happen in a ventilated patient e.g. during a recruitment maneuver. This means that for EIT the described method might be a step out of the intensive care unit, towards radiology and pulmonology, where merged CT-EIT images might be used to improve diagnostic accuracy and as a result patient outcome.

Additional Information

How to cite this article: Schullcke, B. et al. Structural-functional lung imaging using a combined CT-EIT and a Discrete Cosine Transformation reconstruction method. Sci. Rep. 6, 25951; doi: 10.1038/srep25951 (2016).


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This work is partially supported by the Federal Ministry of Education and Research (BMBF) under grant no. 03FH038I3 (MOSES). Thanks to S.Pulletz for providing some of the clinical data.

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B.S. conceived the approach and wrote the paper. B.G. and S.K. assisted during aquisition of EIT data. M.S. and K.M. gave valuable advice. U.M.-L. provided CT patient data. All authors reviewed the manuscript.

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Schullcke, B., Gong, B., Krueger-Ziolek, S. et al. Structural-functional lung imaging using a combined CT-EIT and a Discrete Cosine Transformation reconstruction method. Sci Rep 6, 25951 (2016).

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