Current investigation techniques (Rhinomanometry, Endoscopy, e.g.) of the nasal cavity are not always able to diagnose a successful surgery outcome to relieve breathing. The presented approach uses medical imaging datasets (i.e. cone beam Computer Tomography) to simulate the flow through the nasal cavity with a Laser Doppler Anemometry (LDA) validated lattice Boltzmann (LB) simulation. In order to find potential surgically relevant points (SRP), the determination of the patient’s LB-simulated pressure drop is used for comparison with a critical pressure drop found by a sensitivity analysis (3 patients with nasal septum deviation, 1 person without breathing problems). Based on SRPs a developed optimizer shapes the nasal cavity. All locations of SRPs in postoperative CT datasets show an increase of the crosssection of the nasal cavity. The difference of cross-section between pre- and optimized nasal cavity in the postoperative CT is smaller than 15%. The optimization result shows good and this method will be validated in a future clinical trial.
Michael Verius, Ralf Huttary, Florian Koppelstaetter, C. Siedentopf, Thomas Fiegele, Wolfgang Recheis, S. Golaszewski, Stephan Felber, Wilhelm Eisner, Dieter Zur Nedden
Content of this study is the verification whether the direct cortical stimulation agrees with the results of fMRI
and to determine of what size the deviations are. It is primary to say that neuron populations, which lead to
an involuntary movement with the anesthetized and awake patient over synapses, are excited during an
electric direct cortical stimulation. With fMRI (similarly like in positron emission tomography), the circulation
alteration after an activation of brain areas by arbitrary, active movement or spontaneous cerebral activation
by sensory stimulation is represented in sectional images. With intraoperative electrophysiology individual
muscles or muscle groups can be activated directly. The exact correlation of these two methods has the goal
to replace ICS in future by preoperative fMRI. Numerous authors pointed out that fMRI can play an important
part in preoperative functional mapping [39]. Indeed these studies don't comprise any direct comparison with
intraoperative cortical stimulation, the gold standard of intraoperative functional localisation.
Aim of this study therefore was the development of a three-dimensional registration system for the transfer of
preoperative functional MR-data on intraoperative electro-physiological stimulation points with high precision
and to install in the neuro-surgical operating room. The preoperative neuro-functional diagnostics should be
integrated directly in the neuro-surgical operation planning and the correlation of the functional localisation
should be examined.
Micro-CT will have a profound influence on the accumulation of anatomical and physiological phenotypic changes in natural and transgenetic mouse models. Longitudinal studies will be greatly facilitated, allowing for a more complete and accurate description of events if in-vivo studies are accomplished. The purpose of the ongoing project is to establish a feasible and reproducible setup for in-vivo mouse lung micro-computed tomography (μCT). We seek to use in-vivo respiratory-gated μCT to follow mouse models of lung disease with subsequent recovery of the mouse. Methodologies for optimizing scanning parameters and gating for the in-vivo mouse lung are presented. A Scireq flexiVent ventilated the gas-anesthetized mice at 60 breaths/minute, 30 cm H20 PEEP, 30 ml/kg tidal volume and provided a respiratory signal to gate a Skyscan 1076 μCT. Physiologic monitoring allowed the control of vital functions and quality of anesthesia, e.g. via ECG monitoring. In contrary to longer exposure times with ex-vivo scans, scan times for in-vivo were reduced using 35μm pixel size, 158ms exposure time and 18μm pixel size, 316ms exposure time to reduce motion artifacts. Gating via spontaneous breathing was also tested. Optimal contrast resolution was achieved at 50kVp, 200μA, applying an aluminum filter (0.5mm). There were minimal non-cardiac related motion artifacts. Both 35μm and 1μm voxel size images were suitable for evaluation of the airway lumen and parenchymal density. Total scan times were 30 and 65 minutes respectively. The mice recovered following scanning protocols. In-vivo lung scanning with recovery of the mouse delivered reasonable image quality for longitudinal studies, e.g. mouse asthma models. After examining 10 mice, we conclude μCT is a feasible tool evaluating mouse models of lung pathology in longitudinal studies with increasing anatomic detail available for evaluation as one moves from in-vivo to ex-vivo studies. Further developments include automated bronchial tree segmentation and airway wall thickness measurement tools. Improvements in Hounsfield unit calibration have to be performed when the interest of the study lies in determining and quantifying parenchymal changes and rely on estimating partial volume contributions of underlying structures to voxel densities.
Mouse models are important for pulmonary research to gain insight into structure and function in normal and diseased states, thereby extending knowledge of human disease conditions. The flexibility of human disease induction into mice, due to their similar genome, along with their short gestation cycle makes mouse models highly suitable as investigative tools. Advancements in non-invasive imaging technology, with the development of micro-computed tomography (μ-CT), have aided representation of disease states in these small pulmonary system models. The generation ofμCT 3D airway reconstructions has to date provided a means to examine structural changes associated with disease. The degree of accuracy ofμCT is uncertain. Consequently, the reliability of quantitative measurements is questionable. We have developed a method of sectioning and imaging the whole mouse lung using the Large Image Microscope Array (LIMA) as the gold standard for comparison. Fixed normal mouse lungs were embedded in agarose and 250μm sections of tissue were removed while the remaining tissue block was imaged with a stereomicroscope. A complete dataset of the mouse lung was acquired in this fashion. Following planar image registration, the airways were manually segmented using an in-house built software program PASS. Amira was then used render the 3D isosurface from the segmentations. The resulting 3D model of the normal mouse airway tree developed from pathology images was then quantitatively assessed and used as the standard to compare the accuracy of structural measurements obtained from μ-CT.
This study investigates the instationary flow field in human femoarl arteries. The flow fiel is measured before and after the implantaion of five different metal stent implants in elastic and scaled silicone models of femoral arteries. The pulsating flow field is investigated under physiological conditions within the silicone vessel. For the simulation of the physilogical hemodynamics a computer controlled pump for the reproducible generation of flow patterns and a fluid with flow properties similar to human blood is used. At significant positions distal, proximal and inside the stent dopplersonographic measurements are performed with stationary and pulsatile flow. Via fast fourier analysis the sampled doppler audio signal, gained from the ultrasound stereo output, is converted into velocity profiles and displayed as color coded 3D spectrograms. By subtracting the spectra of the unstented model of the stented models differential spectra are obtained and compared. These differential spectra are used for a semiquantitative analysis of the flow field change caused by stents and are easy to interpret for the examining physician.
Wolfgang Recheis, Leo Pallwein, Peter Soegner, Ralph Faschingbauer, Georg Schmidbauer, Axel Kleinsasser, Alexander Loeckinger, Christoph Hoermann, Dieter zur Nedden
The purpsoe was to evaluate the influence of a right-sided pleural effusion on the lung aeration dynamics in the respiratory cycle during pressure controlled ventilation. Pleural effusion was simulated by infusion of 3% gelatin into the pleural cavity in steps of 300ml totaling 1200ml in four anesthetized pigs. After each step, volume scans and respirator gated 50ms scans at a constant table position (carina niveau) were taken. The dynamic changes of the previously defined air-tissue ratios (in steps of 100HU) were evaluated in three separate regions of left and right lung: a ventral, an intermediate and a dorsal area. The affected side revealed dramatic alveolar collapse. There was a shift of the lung density to higher air-tissue ratios (+200HU) but showing the same air-tissue ratio dynamics. A slight lateral shift of 32mm (±14mm) the mediastinum was measured. The unaffected side showed no increase in the air-tissue ratios caused by hyperinflation but an increase of density due to mediastinal shift. Air-tissue ratio dynamics remained unchanged on the unaffected side compared to baseline measurements. We visualized the ventilation mismatch caused by pleural effusion. The contra-lateral lung is not affected by unilateral pleural effusion. Pressure controlled ventilation prevents hyper-inflation of non-dependent lung areas.
There are open questions concerning the hemodynamics during cardiopulmonary resuscitation (CPR). The purpose was to evaluate a model of the blood flow during CPR in specified anatomic regions. After cardiac arrest, one intubated swine under full intensive care supervision was scanned during CPR using an automated resuscitation device. CT scans were performed with an EBCT in the 50ms modus at eight levels, therefore covering most of the heart and pulmonary vessels. 50ml contrast agent was administered with 10ml/sec and a delay of five seconds to visualize the contrast agent passage through the heart and pulmonary circulation. The gray-value changes in previously specified ROIs were directly correlated with the resuscitation device position in respect to the thorax. The effects of CPR on the blood flow could be visualized dynamically by quantifying the contrast enhancement. The increase of gray values could be estimated with different delays, depending on the anatomical situation. The inflow and outflow dependent on thumper dynamics could be estimated. At the onset of contrast medium inflow, turbulence could be visualized in the right ventricle, which are caused by the inhomogeneous contrast medium distribution. Triggered EBCT during CPR offers the opportunity to study regional blood flow depending on chest compression.
The purpose was to evaluate changes of the air-tissue ratio (ATR) in previously defined regions of interest after cardiopulmonary resuscitation (CPR) in porcine model. Eight anesthetized and ventilated pigs we scanned in supine position before and 30 minutes after CPR at two different constant PEEP levels (5 cm H2O, 15 cm H2O). Volume scans were obtained using 6 mm slices. The gray values of the lung were divided into steps of 100 HU in order to get access to the changes of ATR. ATR was evaluated in ventral, intermediate and dorsal regions of the lung. CPR for 9 minutes led to an uneven distribution of ventilation. In the ventral region, areas with high ATR increased. Areas with normal ATR decreased. In contrast the dorsal regions with low ATR increased. ATR in the intermediate regions remained almost unchanged. Using the higher PEEP level, areas with normal ATR showed a marked increase accompanied by a decrease of areas with low ATR. After CPR, an uneven distribution of lung aeration was detected. According to the impaired hemodynamics, areas with normal ATR decreased and areas with high and low ATR increased. Using higher PEEP levels improved lung aeration.
The purpose was to evaluate differences in dynamic changes of the lung aeration (air-tissue ratio) between augmented modes of ventilation (AMV) and controlled mechanical ventilation (CMV) in normal subjects. 4 volunteers, ventilated with the different respirator protocols via face mask, were scanned using the EBCT in the 50 ms mode. A software analyzed the respirator's digitized pressure and volume signals of two subsequent ventilation phases. Using these values it was possible to calculate the onset of inspiration or expiration of the next respiratory phase. The calculated starting point was then used to trigger the EBCT. The dynamic changes of air- tissue ratios were evaluated in three separate regions: a ventral, an intermediate and a dorsal area. AMV results in increase of air-tissue ratio in the dorsal lung area due to the active contraction of the diaphragm, whereas CMV results in a more pronounced increase in air-tissue ratio of the ventral lung area. This study gives further insight into the dynamic changes of the lung's biomechanics by comparing augmented ventilation and controlled mechanical ventilation in the healthy proband.
The purpose of this project is to evaluate the dynamic changes during expiration at different levels of positive end- expiratory pressure (PEEP) in the ventilated patient. We wanted to discriminate between normal lung function and acute respiratory distress syndrome (ARDS). After approval by the local Ethic Committee we studied two ventilated patients: (1) with normal lung function; (2) ARDS). We used the 50 ms scan mode of the EBCT. The beam was positioned 1 cm above the diaphragm. The table position remained unchanged. An electronic trigger was developed, that utilizes the respirators synchronizing signal to start the EBCT at the onset of expiration. During controlled mechanical expiration at two levels of PEEP (0 and 15 cm H2O), pulmonary aeration was rated as: well-aerated (-900HU/-500HU), poorly- aerated (-500HU/-100HU) and non-aerated (-100HU/+100HU). Pathological and normal lung function showed different dynamic changes (FIG.4-12). The different PEEP levels resulted in a significant change of pulmonary aeration in the same patient. Although we studied only a very limited number of patients, respirator triggered EBCT may be accurate in discriminating pathological changes due to the abnormal lung function in the mechanically ventilated patient.
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