In vitro studies have demonstrated that densitometric quantification of coronary artery stenoses is superior to geometric methods to assess non-circular lumens. However, in patients, several authors have reported significant discrepancies between area reduction percentages obtained densitometrically from two different imaging projections. Some of the factors causing the discrepancies can be reduced by simple precautions taken during image acquisition. Some others may be compensated for during analysis. Nevertheless, two factors remain problematic. The first is the inadequate spatial orientation of the vessel axes at the stenotic and reference cross sections with respect to the x-rays. The second is the difficulty in identifying the same vessel cross section in both planes at the time of analysis. We have designed a new densitometric technique that eliminates the error contributions of these two factors. The technique requires simultaneously acquired biplane coronary angiograms and biplane images of a translucent cube bearing steel markers acquired in exactly the same biplane geometry. Using the two projection matrices calculated from the images of the cube, the centerlines and the edges of the coronary arteries can be reconstructed in space from the biplane angiograms. The angles between the vessel axes and the x-ray beams can be determined and the densitometric cross sections can be corrected accordingly. Moreover, the 3D reconstruction allows the identification of the same cross section in the two planes for the determination of the area reduction percentages. Validation measurements were performed on a Perspex phantom and in patients, before and after angioplasty. In both types of measurement, the interplane discrepancies could be roughly halved. The densitometric technique presented can be incorporated into routine angiography and could become a strong alternative to the geometric approach that is presently dominating this field.
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http://dx.doi.org/10.1088/0967-3334/18/4/002 | DOI Listing |
Anim Reprod Sci
December 2024
Faculty of Veterinary Medicine, University Antonio Nariño, Popayán, Colombia. Electronic address:
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View Article and Find Full Text PDFBMC Chem
November 2024
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr Al-Aini Street, Cairo, 11562, Egypt.
Parkinson's disease (PD) emerges as a notable health concern among the elderly population. Safinamide mesylate (SAF) is a novel and emerging add-on therapy in PD treatment. The stability of innovative drug formulations and the development of appropriate stability-indicating methods are of great importance to modern pharmaceutical analysis.
View Article and Find Full Text PDFSci Rep
November 2024
Pharm R&D Lab and Department of Medicinal Chemistry, School of Pharmacy, Muhimbili University of Health and Allied Sciences, P. O. Box 65545, Dar es Salaam, Tanzania.
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September 2024
Université Paris Cité, Innovative Thérapies in Haemostasis, INSERM UMR-S1140, F-75006 Paris, France, AP-HP, Hôpital européen Georges Pompidou, Service d'Hématologie biologique, F-75015 Paris, France.
Phytochem Anal
January 2025
Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai Campus, Songkhla, Thailand.
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