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      Correlation of positron emission tomography ventilation-perfusion matching with CT densitometry in severe emphysema

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          Abstract

          Background

          Emphysema severity is frequently measured on CT via densitometry. Correlation with scintigraphic and spirometric functional measures of ventilation or perfusion varies widely, and no prior study has evaluated correlation between densitometry and lobar ventilation/perfusion in patients with severe emphysema. The aim of this study was to evaluate the utility and findings of gallium-68 ( 68Ga) ventilation/perfusion positron emission tomography-CT ( 68Ga-VQ/PET-CT) in severe emphysema assessment.

          Methods

          Fourteen consecutive patients undergoing evaluation for bronchoscopic lung volume reduction between March 2015 and March 2018 underwent 68Ga-VQ/PET-CT assessment for lobar functional lung mapping, in addition to CT densitometry. Correlations between CT densitometry and 68Ga-VQ/PET-CT parameters for individual lobar lung function were sought.

          Results

          CT densitometry assessment of emphysema correlated only weakly ( R 2 = 0.13) with lobar perfusion and was not correlated with ventilation ( R 2 = 0.04). Densitometry was moderately ( R 2 = 0.67) correlated with V/Q units in upper lobes, though poorly reflected physiological function in lower lobes ( R 2 = 0.19). Emphysema severity, as measured by CT densitometry, was moderately correlated with proportion of normal V/Q units and matched V/Q defects in individual lobes.

          Conclusions

          Assessment of lobar pulmonary function by 68Ga-VQ/PET-CT provides physiologic information not evident on CT densitometry such as ventilation and perfusion specifics and matched defects. Further research is needed to see if the discordant findings on 68Ga-VQ/PET-CT provide prognostic information or can be used to modify patient management and improve outcomes.

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          Most cited references27

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          Pulmonary Microvascular Blood Flow in Mild Chronic Obstructive Pulmonary Disease and Emphysema. The MESA COPD Study.

          Smoking-related microvascular loss causes end-organ damage in the kidneys, heart, and brain. Basic research suggests a similar process in the lungs, but no large studies have assessed pulmonary microvascular blood flow (PMBF) in early chronic lung disease.
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            Automatic lung segmentation from thoracic computed tomography scans using a hybrid approach with error detection.

            Lung segmentation is a prerequisite for automated analysis of chest CT scans. Conventional lung segmentation methods rely on large attenuation differences between lung parenchyma and surrounding tissue. These methods fail in scans where dense abnormalities are present, which often occurs in clinical data. Some methods to handle these situations have been proposed, but they are too time consuming or too specialized to be used in clinical practice. In this article, a new hybrid lung segmentation method is presented that automatically detects failures of a conventional algorithm and, when needed, resorts to a more complex algorithm, which is expected to produce better results in abnormal cases. In a large quantitative evaluation on a database of 150 scans from different sources, the hybrid method is shown to perform substantially better than a conventional approach at a relatively low increase in computational cost.
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              Endobronchial Valves for Endoscopic Lung Volume Reduction: Best Practice Recommendations from Expert Panel on Endoscopic Lung Volume Reduction.

              Endoscopic lung volume reduction (ELVR) is being adopted as a treatment option for carefully selected patients suffering from severe emphysema. ELVR with the one-way endobronchial Zephyr valves (EBV) has been demonstrated to improve pulmonary function, exercise capacity, and quality of life in patients with both heterogeneous and homogenous emphysema without collateral ventilation. In this "expert best practices" review, we will highlight the practical aspects of this therapy. Key selection criteria for ELVR are hyperinflation with a residual volume >175% of predicted, forced expiratory volume 100 m. Patients with repeated infectious complications, severe bronchiectasis, and those with unstable cardiovascular comorbidities should be excluded from EBV treatment. The procedure may be performed with either conscious sedation or general anesthesia and positive pressure mechanical ventilation using a flexible endotracheal tube or a rigid bronchoscope. Chartis and EBV placement should be performed in 1 procedure when possible. The sequence of valve placement should be orchestrated to avoid obstruction and delivery of subsequent valves. If atelectasis has not occurred by 1 month after procedure, evaluate valve position on CT and consider replacing the valves that are not optimally positioned. Pneumothorax is a common complication and typically occurs in the first 2 days following treatment. A management algorithm for pneumothorax has been previously published. Long-term sequelae from EBV therapy do occur but are easily manageable.
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                Author and article information

                Contributors
                daniel.steinfort@unimelb.edu.au
                Journal
                EJNMMI Res
                EJNMMI Res
                EJNMMI Research
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                2191-219X
                28 July 2020
                28 July 2020
                2020
                : 10
                : 86
                Affiliations
                [1 ]GRID grid.416153.4, ISNI 0000 0004 0624 1200, Department of Respiratory Medicine, , Royal Melbourne Hospital, ; Parkville, Victoria Australia
                [2 ]GRID grid.1008.9, ISNI 0000 0001 2179 088X, Department of Medicine, , University of Melbourne, ; Parkville, Victoria Australia
                [3 ]GRID grid.1055.1, ISNI 0000000403978434, Department of Radiation Oncology, , Sir Peter MacCallum Cancer Centre, ; Melbourne, Victoria Australia
                [4 ]GRID grid.1055.1, ISNI 0000000403978434, Department of Molecular Imaging and Therapeutic Nuclear Medicine, , Sir Peter MacCallum Cancer Centre, ; Melbourne, Victoria Australia
                [5 ]GRID grid.411766.3, ISNI 0000 0004 0472 3249, Nuclear Medicine Department, , University Hospital and EA3878 (GETBO) IFR 148, ; Brest, France
                [6 ]GRID grid.416153.4, ISNI 0000 0004 0624 1200, Department of Radiology, , Royal Melbourne Hospital, ; Parkville, Victoria Australia
                Article
                672
                10.1186/s13550-020-00672-8
                7387398
                32725552
                340ff0bf-fd6b-4fbc-92a3-1cae7a9220ee
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 14 April 2020
                : 14 July 2020
                Categories
                Original Research
                Custom metadata
                © The Author(s) 2020

                Radiology & Imaging
                ventilation,perfusion,pet,emphysema,bronchoscopy
                Radiology & Imaging
                ventilation, perfusion, pet, emphysema, bronchoscopy

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