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  • HEALTHY-VOLUNTEERS  (6)
  • RESOLUTION  (6)
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  • 1
    Keywords: measurement ; tumor ; Germany ; LUNG ; CT ; IMAGES ; DISEASE ; NEW-YORK ; TUMORS ; PATIENT ; REDUCTION ; CONTRAST ; MRI ; CYCLE ; SEQUENCE ; NO ; DIFFERENCE ; REGION ; LOCALIZATION ; LENGTH ; COMPUTED-TOMOGRAPHY ; CURVES ; 3-DIMENSIONAL RECONSTRUCTION ; MOTION ; HEALTHY ; ORIENTATION ; LOCATION ; dynamic MRI ; ADULT ; ADULTS ; STRENGTH ; TRUEFISP ; HEALTHY-VOLUNTEERS ; PULMONARY-FUNCTION ; HEART-FAILURE ; EXPIRATION ; LUNG-VOLUMES ; breathing cycle ; diaphragmatic function
    Abstract: The purpose of this study was to assess diaphragmatic length and shortening during the breathing cycle in healthy volunteers and patients with a lung tumor using dynamic MRI (dMRI). In 15 healthy volunteers and 28 patients with a solitary lung tumor, diaphragmatic motion and length were measured during the breathing cycle using a trueFISP sequence (three images per second in the coronal and sagittal plane). Time-distance curves and maximal length reduction (= shortening) of the diaphragm were calculated. The influence of tumor localization on diaphragmatic shortening was examined. In healthy volunteers maximal diaphragmatic shortening was 30% in the coronal and 34% in the sagittal orientation, with no difference between both hemithoraces. Tumors of the upper and middle lung region did not affect diaphragmatic shortening. In contrast, tumors of the lower lung region changed shortening significantly (P〈0.05). In hemithoraces with a tumor in the lower region, shortening was 18% in the coronal and 19% in the sagittal plane. The ratio of diaphragmatic length change from inspiration to expiration changed significantly from healthy subjects (inspiration length &MGT; expiratory length, P〈0.05) to patients with a tumor in the lower lung region (inspiratory length = expiratory length). dMRI is a simple, non-invasive method to evaluate diaphragmatic motion and shortening in volunteers and patients during the breathing cycle. Tumors of the lower lung region have a significant influence on shortening of the diaphragm
    Type of Publication: Journal article published
    PubMed ID: 15127220
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  • 2
    Keywords: BLOOD ; Germany ; LUNG ; PERFUSION ; imaging ; QUANTIFICATION ; VOLUME ; TIME ; BLOOD-FLOW ; blood flow ; FLOW ; HIGH-RESOLUTION MEASUREMENT ; MRI ; TRACER BOLUS PASSAGES ; MAGNETIC-RESONANCE ; magnetic resonance imaging ; AGE ; PARAMETERS ; SCINTIGRAPHY ; CONTRAST-ENHANCED MRI ; magnetic resonance imaging (MRI) ; QUANTITATIVE-ANALYSIS ; HEALTHY ; LUNG PERFUSION ; TRANSIT-TIME ; HEALTHY-VOLUNTEERS ; ARTERIAL ; INFLATION ; contrast-enhanced
    Abstract: Rationale and Objectives: The effect of breathholding on pulmonary perfusion remains largely unknown. The aim of this study was to assess the effect of inspiratory and expiratory breathhold on pulmonary perfusion using quantitative pulmonary perfusion magnetic resonance imaging (MRI). Methods and Results: Nine healthy volunteers (median age, 28 years; range, 20-45 years) were examined with contrast-enhanced time-resolved 3-dimensional pulmonary perfusion MRI (FLASH 313, TR/TE: 1.9/0.8 ms; flip angle: 40degrees; GRAPPA) during end-inspiratory and expiratory breathholds. The perfusion parameters pulmonary blood flow (PBF), pulmonary blood volume (PBV), and mean transit time (MTT) were calculated using the indicator dilution theory. As a reference method, end-inspiratory and expiratory phase-contrast (PC) MRI of the pulmonary arterial blood flow (PABF) was performed. Results: There was a statistically significant increase of the PBF (Delta = 182 mL/100mL/min), PBV (Delta = 12 mL/100 mL), and PABF (Delta = 0.5 L/min) between inspiratory and expiratory breathhold measurements (P 〈 0.0001). Also, the MTT was significantly shorter (Delta = -0.5 sec) at expiratory breathhold (P = 0.03). Inspiratory PBF and PBV showed a moderate correlation (r = 0.72 and 0.61, P less than or equal to0.008) with inspiratory PABF. Conclusion: Pulmonary perfusion during breathhold depends on the inspiratory level. Higher perfusion is observed at expiratory breathhold
    Type of Publication: Journal article published
    PubMed ID: 15654250
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  • 3
    Keywords: BLOOD ; Germany ; LUNG ; QUANTIFICATION ; TIME ; BLOOD-FLOW ; blood flow ; FLOW ; MRI ; PATTERNS ; PARAMETERS ; HYPERTENSION ; BLOOD-FLOW MEASUREMENTS ; BREATH-HOLD ; ENCODED CINE MRI ; HEMODYNAMICS ; RE ; HEALTHY-VOLUNTEERS ; phase-contrast MRI ; pulmonary circulation ; systemic circulation ; VENTRICULAR STROKE VOLUME
    Abstract: OBJECTIVE. The purpose of this study was to use phase-contrast MRI to evaluate the influence of various breathing maneuvers on the hemodynamics of the pulmonary and systemic arterial circulation. SUBJECTS AND METHODS. Twenty-five volunteers were examined with phase-contrast MRI. Flow measurements were acquired in the aorta, pulmonary trunk, and left and right pulmonary arteries during deep, large-volume inspiratory breath-hold, expiratory breath-hold, and smooth respiration (no breath-hold). Parameters assessed were peak velocity, blood flow, velocity gradient, and acceleration time. RESULTS. Pulmonary blood flow and peak velocity were significantly reduced during inspiratory breath-hold and expiratory breath-hold compared with no breath-hold (p 〈 0.01). Pulmonary velocity gradient in inspiratory breath-hold was significantly (p:! 0.01) lower than in expiratory breath-hold and no breath-hold. There was no difference in velocity gradient between expiratory breath-hold and no breath-hold. Peak velocity in the aorta was lowest with no breath-hold. Velocity gradient was highest in expiratory breath-hold, and no breath-hold had the smallest SD. Acceleration time in the pulmonary trunk showed no difference between inspiratory breath-hold, expiratory breath-hold, and no breath-hold. Blood flow distribution to the left (45-47%) and to the right (53-55%) lung was not influenced by breathing maneuver. CONCLUSION. Measurements during smooth respiration showed the smallest SD. Therefore, no-breath-hold measurements should be considered for assessment of hemodynamics in clinical practice
    Type of Publication: Journal article published
    PubMed ID: 16861549
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  • 4
    Keywords: CANCER ; tumor ; carcinoma ; Germany ; LUNG ; imaging ; lung cancer ; LUNG-CANCER ; VOLUME ; TUMORS ; RESOLUTION ; PATIENT ; MRI ; SEQUENCE ; MAGNETIC-RESONANCE ; magnetic resonance imaging ; REGION ; LOCALIZATION ; LENGTH ; PARAMETERS ; FUNCTION TESTS ; 3-DIMENSIONAL RECONSTRUCTION ; MOTION ; HEALTHY ; COMPLICATIONS ; dynamic MRI ; STAGE-I ; HEALTHY-VOLUNTEERS ; PULMONARY-FUNCTION ; HUMAN DIAPHRAGM SHAPE ; breathing cycle ; HEALTHY-SUBJECTS ; SPIROMETRY ; parallel imaging ; TEMPORAL RESOLUTION ; IA ; FEV1 /VC ; INTRATHORACIC TUMOR
    Abstract: Purpose: To assess relative forced expiratory volume in one second (FEV1/vital capacity (VQ in healthy subjects and patients with a lung tumor using dynamic magnetic resonance imaging (dMRI) parameters. Materials and Methods: In 15 healthy volunteers and 31 patients with a non-small-cell lung carcinoma stage I (NSCLC 1), diaphragmatic length change (LEI) and craniocaudal (CC) intrathoracic distance change within one second; from maximal inspiration (DEI) were divided by total length change (LEtotal, DEtotal) as a surrogate of spirometric FEV 1 /VC using a true fast imaging with steady-state precession (trueFISP) sequence TE/TR = 1.7/37.3 msec, temporal resolution = 3 images/second). Influence of tumor localization was examined. Results: In healthy volunteers FEV I /VC showed a highly significant correlation with LE1/LEtotal and DE1/DEtotal (r 〉 0.9. P 〈 0.01). In stage IB tumor patients, comparing tumor-bearing with the non-tumor-bearing hemithorax, there,was a significant difference in tumors of the middle (LE1 /LEtotal= 0.63 +/- 0.05 vs. 0. 73 +/- 0.04, DE1/DEtotal= 0.66 +/- 0.05 vs. 0.72 +/- 0.04; P 〈 0.05) and lower (P 〈 0.05) lung region. Stage IA tumor patients showed no significant differences with regard to healthy subjects. Conclusion: dMRI is a simple noninvasive method to locally determine LE1 /LEtotal and DE1 /DEtotal as a surrogate of FEV1/VC in volunteers and patients. Tumors of the middle and lower lung regions have a significant influence on these MRI parameters
    Type of Publication: Journal article published
    PubMed ID: 15723381
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  • 5
    Keywords: Germany ; LUNG ; chest ; CT ; DIAGNOSIS ; FOLLOW-UP ; imaging ; DISEASE ; EXPOSURE ; RESOLUTION ; radiation ; PATIENT ; IMPACT ; prognosis ; MRI ; MAGNETIC-RESONANCE ; magnetic resonance imaging ; MORPHOLOGY ; COMPUTED-TOMOGRAPHY ; FUNCTION TESTS ; magnetic resonance imaging (MRI) ; CHILDREN ; HRCT ; fibrosis ; ADULTS ; LIFE ; CYSTIC-FIBROSIS ; TESTS ; technique ; function ; cystic fibrosis ; RADIATION EXPOSURE ; lungs ; improvement of ; gold ; mucoviscidosis
    Abstract: Cystic fibrosis (CF) is a multi-systemic disease with major impact on the lungs. Pulmonary manifestation is crucial for the prognosis and life expectancy of patients. Imaging modalities and lung function tests reflect the pulmonary status in these patients. The standard imaging modality for diagnosis and follow-up of pulmonary changes is chest x-ray. The gold standard for the detection of parenchymal lung changes remains high resolution computed tomography (HRCT), but this is not used routinely for CF-patients due to radiation exposure. Magnetic resonance imaging (MRI) used to be of no importance in monitoring cystic fibrosis lung disease, as shown in studies from the 1980s and early 1990s. The continuing improvement of MRI techniques, however, has allowed for an adequate application of this non-radiation method in diagnosing the major pulmonary findings in CF, in addition to the assessment of lung function
    Type of Publication: Journal article published
    PubMed ID: 16437239
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  • 6
    Keywords: Germany ; LUNG ; DIAGNOSIS ; segmentation ; DISEASE ; RESOLUTION ; TRANSPLANTATION ; MRI ; MAGNETIC-RESONANCE ; magnetic resonance imaging ; prevention ; MOTION ; dynamic MRI ; MANAGEMENT ; MOVEMENT ; SCIENCE ; breathing cycle ; HEALTHY-SUBJECTS ; SPIROMETRY ; volumetry ; RESPIRATORY MOTION ; MR-compatible spirometry ; respiratory mechanics ; GLOBAL STRATEGY
    Abstract: Rationale and Objectives: Most lung disease is inhomogeneously distributed but diagnosed by global spirometry. Regional lung function might allow for earlier diagnosis. Dynamic two-dimensional magnetic resonance imaging (2D-MRI) can depict lung motion with high temporal resolution. We evaluated whether measurement of lung area on dynamic 2D-MRI has sufficient agreement with spirometry to allow for lung function testing of single lungs. Material and Methods: Ten healthy volunteers were examined in a 1.5 T MRI scanner with a Flash 2D-sequence (8.5 images per second, sagittal and coronal orientation) with simultaneous spirometry. The lung area was segmented semiautomatically and the area changes were compared with spirometric volume changes. Results: Segmentation of one time series took 191 seconds on average. Volume-time and flow-volume curves from MRI data were almost congruent with spirometric curves. Pearson correlation of MRI area with spirometry was very high (mean correlation coefficients 〉0.97). Bland-Altman plots showed good agreement of lung area with spirometry (95% limits of agreement below 11% in each direction). Differences between lung area and spirometry were significantly smaller for sagittal measurement of the right lung than sagittal measurement of the left lung and coronal measurement. The relative forced expiratory volume in the first second differed less than 5% between MRI and spirometry in all but one volunteer. Conclusions: Measurement of lung area on 2D-MRI allows for functional measurement of single lungs with good agreement to spirometry. Postprocessing is fast enough for application in a clinical context and possibly provides increased sensitivity for lung functional measurement of inhomogeneously distributed lung disease
    Type of Publication: Journal article published
    PubMed ID: 20138554
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  • 7
    Keywords: Germany ; LUNG ; PERFUSION ; CT ; DIAGNOSIS ; IMAGES ; VISUALIZATION ; DISEASE ; DIFFERENTIATION ; RESOLUTION ; TIME ; PATIENT ; MR ; MRI ; MAGNETIC-RESONANCE ; arteries ; EMBOLISM ; MR-ANGIOGRAPHY ; magnetic resonance angiography ; pathology ; ANGIOGRAPHY ; HYPERTENSION ; contrast media ; MANAGEMENT ; PULMONARY ; PH ; ARTERIAL-HYPERTENSION ; ARTERIAL ; LEVEL ; IMAGE QUALITY ; CONSENSUS ; PULMONARY-ARTERIES ; TEMPORAL RESOLUTION ; HIGH-SPATIAL-RESOLUTION ; CTEPH ; IPAH
    Abstract: Differentiation between different forms of pulmonary hypertension (PH) is essential for correct disease management. The goal of this study was to elucidate the clinical impact of high spatial resolution MR angiography (SR-MRA) and time-resolved MRA (TR-MRA) to differentiate between patients with chronic thromboembolic PH (CTEPH) and idiopathic pulmonary arterial hypertension (IPAH). Ten PH patients and five volunteers were examined. Twenty TR-MRA data sets (TA 1.5 s) and SR-MRA (TA 23 s) were acquired. TR-MRA data sets were subtracted as angiography and perfusion images. Evaluation comprised analysis of vascular pathologies on a segmental basis, detection of perfusion defects, and bronchial arteries by two readers in consensus. Technical evaluation comprised evaluation of image quality, signal-to-noise ratio (SNR) measurements, and contrast-media passage time. Visualization of the pulmonary arteries was possible down to a subsegmental (SR-MRA) and to a segmental (TR-MRA) level. SR-MRA outperformed TR-MRA in direct visualization of intravascular changes. Patients with IPAH predominantly showed tortuous pulmonary arteries while in CTEPH wall irregularities and abnormal proximal-to-distal tapering was found. Perfusion images showed a diffuse pattern in IPAH and focal defects in CTEPH. TR-MRA and SR-MRA resulted in the same final diagnosis. Both MRA techniques allowed for differentiation between IPAH and CTEPH. Therefore, TR-MRA can be used in the clinical setting, especially in dyspneic patients
    Type of Publication: Journal article published
    PubMed ID: 16041529
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  • 8
    Keywords: BLOOD ; Germany ; LUNG ; SPIRAL CT ; VOLUME ; DISEASE ; POPULATION ; HEART ; TIME ; PATIENT ; BLOOD-FLOW ; blood flow ; FLOW ; MRI ; MAGNETIC-RESONANCE ; magnetic resonance imaging ; AGE ; arteries ; PARAMETERS ; HYPERTENSION ; HEALTHY ; PULMONARY ; VELOCITY ; fibrosis ; PH ; HEALTHY-VOLUNTEERS ; CHRONIC THROMBOEMBOLISM ; CYSTIC-FIBROSIS ; ARTERIAL ; PULMONARY-ARTERIES ; early development ; bronchosystemic shunt ; cystic fibrosis
    Abstract: Cystic fibrosis (CF) leads to disabling lung disease and pulmonary hypertension (PH). The goal of this study was to assess the hemodynamics in the systemic and pulmonary arterial circulation of patients with CF using MRI. Ten patients with CF and 15 healthy volunteers were examined (1.5-T MRI). Phase-contrast flow measurements were assessed in the ascending aorta, pulmonary trunc, and the left and right pulmonary arteries (PA), resulting in the following parameters: peak velocity (PV) (centimeters per second) velocity rise gradient (VRG), time to PV (milliseconds), and the average area (centimeters squared). The blood flow ratio between the right and left lungs and the bronchosystemic shunt were calculated. For the ascending aorta and pulmonary trunc no parameter was significantly different between both populations. In the right PA a significantly lower PV (p=0.001) and VRG (p=0.02) was found. In the left PA there was a significantly (p=0.007) lower PV but no significant (p=0.07) difference between the VRG. The areas of the right (p=0.08) and left (p=0.5) PA were not significantly enlarged. For the volunteers a linear increase of PV in both PA was found with age, while it decreased in patients with CF. The blood flow distribution (right/left lung) showed no significant (p=0.7) difference between the groups. There was a significantly (p 〈 0.001) higher bronchosystemic shunt volume in patients with CF (1.3 l/min) than in volunteers (0.1 l/min). Magnetic resonance based flow measurements in the right and left PA showed first indications for early development of PH. The significant increase in bronchosystemic shunt volume might be indicative fo the extent of parenchymal changes
    Type of Publication: Journal article published
    PubMed ID: 15761712
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  • 9
    Keywords: COMBINATION ; Germany ; LUNG ; MODEL ; PERFUSION ; EMPHYSEMA ; IMAGES ; imaging ; TOOL ; VOLUME ; DISEASE ; MRI ; CYCLE ; SEQUENCE ; MAGNETIC-RESONANCE ; magnetic resonance imaging ; REGION ; COMPUTED-TOMOGRAPHY ; MOTION ; HEALTHY ; RE ; HEALTHY-VOLUNTEERS ; CHEST-WALL ; PULMONARY-FUNCTION TESTS ; HUMAN DIAPHRAGM SHAPE ; breathing cycle ; HEALTHY-SUBJECTS ; lung motion ; SPIROMETRY ; view sharing ; volumetry ; dynamic 3D MRI ; respiration
    Abstract: Rationale and Objectives: We sought to investigate lung volume and surface measurements during the breathing cycle using dynamic three-dimensional magnetic resonance imaging (3D MRI). Materials and Methods: Breathing cycles of 20 healthy volunteers were examined using a 2D trueFISP sequence (3 images/second) in combination with a model and segmented 3D FLASH sequence (1 image/second) MR images using view sharing. Segmentation was performed semiautomatically using an interactive region growing technique. Vital capacity (VC) was calculated from MRI using the model (2D) and counting the voxels (3D) and was compared with spirometry. Results: VC from spirometry was 4.9 +/- 0.9 L, 4.4 +/- 1.2 L from 2D MRI measurement, and 4.7 +/- 0.9 L for 3D MRI. Using the 3D technique, correlation to spirometry was higher than using the 2D technique (r 〉 0.95 vs. r 〉 0.83). Using the 3D technique, split lung volumes and lung surface could be calculated. There was a significant difference between the left and right lung volume in expiration (P 〈 0.05). Conclusions: Dynamic 3D MRI is a noninvasive tool to evaluate split lung volumes and lung surfaces during the breathing cycle with a high correlation to spirometry
    Type of Publication: Journal article published
    PubMed ID: 15714092
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  • 10
    Keywords: Germany ; LUNG ; chest ; CT ; FOLLOW-UP ; imaging ; INFORMATION ; SYSTEM ; TOOL ; DEATH ; POPULATION ; computed tomography ; RESOLUTION ; PATIENT ; IMPACT ; CONTRAST ; MRI ; MAGNETIC-RESONANCE ; magnetic resonance imaging ; COMPUTED-TOMOGRAPHY ; CHILDREN ; LUNG PERFUSION ; ADULTS ; PHASE ; cystic fibrosis
    Abstract: Cystic fibrosis (CF) is the most frequent inherited disorder leading to premature death in the Caucasian population. As life expectancy is limited by pulmonary complications, repeated imaging [chest X-ray, multislice high-resolution computed tomography (MS-HRCT)] is required in the follow-up. Magnetic resonance imaging (MRI) of the lung parenchyma is a promising new diagnostic tool. Its value for imaging lung changes caused by CF compared with CT is demonstrated. MRI performs well when compared with CT, which serves as the gold standard. Its lack in spatial resolution is obvious, but advantages in contrast and functional assessment compensate for this limitation. Thus, MRI is a reasonable alternative for imaging the CF lung and should be introduced as a radiation-free modality for follow-up studies in CF patients. For further evaluation of the impact of MRI, systematic studies comparing MRI and conventional imaging modalities are necessary. Furthermore, the value of the additional functional MRI (fMRI) information has to be studied, and a scoring system for the morphological and functional aspect of MRI has to be established
    Type of Publication: Journal article published
    PubMed ID: 16941092
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