In-vivo X-ray Dark-Field Chest Radiography of a Pig

Lukas B. Gromann(Technical University of Munich), Fabio De Marco(Technical University of Munich), Konstantin Willer(Technical University of Munich), Peter B. Noël(TUM Klinikum), K. Scherer(Technical University of Munich), Bernhard Renger(TUM Klinikum), Bernhard Gleich(Technical University of Munich), Klaus Achterhold(Technical University of Munich), Alexander A. Fingerle(TUM Klinikum), Daniela Muenzel(TUM Klinikum), Sigrid Auweter(Ludwig-Maximilians-Universität München), Katharina Hellbach(Ludwig-Maximilians-Universität München), Maximilian F. Reiser(Ludwig-Maximilians-Universität München), Andrea Baehr(Institute of Bioinformatics and Systems Biology), Michaela Dmochewitz(Institute of Bioinformatics and Systems Biology), Tobias J. Schroeter(Karlsruhe Institute of Technology), Frieder Koch(Karlsruhe Institute of Technology), Pascal Meyer(Karlsruhe Institute of Technology), N. Kunka(Karlsruhe Institute of Technology), J. Mohr(Karlsruhe Institute of Technology), Andre Yaroshenko(Philips (Germany)), Hanns-Ingo Maack(Philips (Germany)), Thomas Pralow(Philips (Germany)), Hendrik van der Heijden(Philips (Germany)), Roland Proksa(Philips (Germany)), Thomas Koehler(Institute for Advanced Study), Nataly Wieberneit(Philips (Germany)), Karsten Rindt(Philips (Germany)), Ernst J. Rummeny(TUM Klinikum), Franz Pfeiffer(TUM Klinikum), Julia Herzen(Technical University of Munich)
Scientific Reports
June 30, 2017
Cited by 102Open Access
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Abstract

Abstract X-ray chest radiography is an inexpensive and broadly available tool for initial assessment of the lung in clinical routine, but typically lacks diagnostic sensitivity for detection of pulmonary diseases in their early stages. Recent X-ray dark-field (XDF) imaging studies on mice have shown significant improvements in imaging-based lung diagnostics. Especially in the case of early diagnosis of chronic obstructive pulmonary disease (COPD), XDF imaging clearly outperforms conventional radiography. However, a translation of this technique towards the investigation of larger mammals and finally humans has not yet been achieved. In this letter, we present the first in - vivo XDF full-field chest radiographs (32 × 35 cm 2 ) of a living pig, acquired with clinically compatible parameters (40 s scan time, approx. 80 µSv dose). For imaging, we developed a novel high-energy XDF system that overcomes the limitations of currently established setups. Our XDF radiographs yield sufficiently high image quality to enable radiographic evaluation of the lungs. We consider this a milestone in the bench-to-bedside translation of XDF imaging and expect XDF imaging to become an invaluable tool in clinical practice, both as a general chest X-ray modality and as a dedicated tool for high-risk patients affected by smoking, industrial work and indoor cooking.


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