Les 120 martyrs de Chine: canonisés le 1er octobre 2000
In: Études et documents 12
In: Églises d'Asie
In: Série Histoire
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In: Études et documents 12
In: Églises d'Asie
In: Série Histoire
In: Collection Rolf Heyne
BACKGROUND: Exposure to inhalational hazards during post-9/11 deployment to Southwest Asia and Afghanistan puts military personnel at risk for respiratory symptoms and disease. Pulmonary function and qualitative chest high resolution computed tomography (HRCT) are often normal in "deployers" with persistent respiratory symptoms. We explored the utility of quantitative HRCT imaging markers of large and small airways abnormalities, including airway wall thickness, emphysema, and air trapping, in symptomatic deployers with clinically-confirmed lung disease compared to controls. METHODS: Chest HRCT images from 45 healthy controls and 82 symptomatic deployers with asthma, distal lung disease or both were analyzed using Thirona Lung quantification software to calculate airway wall thickness (by Pi10), emphysema (by percentage of lung volume with attenuation < -950 Hounsfield units [LAA%-950]), and three parameters of air trapping (expiratory/inspiratory total lung volume and mean lung density ratios, and LAA%-856). SAS v.9.4 was used to compare demographic and clinical characteristics between deployers and controls using Chi-Square, Fisher Exact or t-tests. Linear regression was used to assess relationships between pulmonary function and quantitative imaging findings. RESULTS: Gender and smoking status were not statistically significantly different between groups, but deployers were significantly younger than controls (42 vs 58 years, p < 0.0001), had higher body mass index (31 vs 28 kg/m(2), p = 0.01), and had fewer total smoking pack-years (8 vs. 26, p = 0.007). Spirometric measures were not statistically significantly different between groups. Pi10 and LAA%-950 were significantly elevated in deployers compared to controls in unadjusted analyses, with the emphysema measure remaining significantly higher in deployers after adjustment for age, sex, smoking, BMI, and expiratory total lung volume. Air trapping parameters were more common in control images, likely due to differences in age and smoking between ...
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Removing the bias and variance of multicentre data has always been a challenge in large scale digital healthcare studies, which requires the ability to integrate clinical features extracted from data acquired by different scanners and protocols to improve stability and robustness. Previous studies have described various computational approaches to fuse single modality multicentre datasets. However, these surveys rarely focused on evaluation metrics and lacked a checklist for computational data harmonisation studies. In this systematic review, we summarise the computational data harmonisation approaches for multi-modality data in the digital healthcare field, including harmonisation strategies and evaluation metrics based on different theories. In addition, a comprehensive checklist that summarises common practices for data harmonisation studies is proposed to guide researchers to report their research findings more effectively. Last but not least, flowcharts presenting possible ways for methodology and metric selection are proposed and the limitations of different methods have been surveyed for future research. ; This study was supported in part by the European Research Council Innovative Medicines Initiative (DRAGON#, H2020-JTI-IMI2 101005122), the AI for Health Imaging Award (CHAIMELEON##, H2020-SC1-FA-DTS-2019–1 952172), the UK Research and Innovation Future Leaders Fellowship (MR/V023799/1), the British Hear Foundation (Project Number: TG/18/5/34111, PG/16/78/32402), the SABRE project supported by Boehringer Ingelheim Ltd, the European Union's Horizon 2020 research and innovation programme (ICOVID, 101016131), the Euskampus Foundation (COVID19 Resilience, Ref. COnfVID19), and the Basque Government (consolidated research group MATHMODE, Ref. IT1294–19, and 3KIA project from the ELKARTEK funding program, Ref. KK-2020/00049)
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