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Gender based lung cancer risks for symptomatic coronary artery disease patients undergone cardiac CT

We estimate the lifetime attributable risk (LAR) of lung cancer incidence in symptomatic Coronary Artery Disease (CAD) patients receiving enhanced Coronary Computed Tomography Angiography (CCTA) and the unenhanced Computed Tomography Calcium Scoring (CTCS) examination. Retrospective analysis has bee...

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Autores principales: Dalah, Entesar Zawam, Obaideen, Abdulmunhem, Anam, Sabaa, Alzimami, Khalid, Jambi, Layal Khalid, Bradley, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000096/
https://www.ncbi.nlm.nih.gov/pubmed/35404962
http://dx.doi.org/10.1371/journal.pone.0265609
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author Dalah, Entesar Zawam
Obaideen, Abdulmunhem
Anam, Sabaa
Alzimami, Khalid
Jambi, Layal Khalid
Bradley, David A.
author_facet Dalah, Entesar Zawam
Obaideen, Abdulmunhem
Anam, Sabaa
Alzimami, Khalid
Jambi, Layal Khalid
Bradley, David A.
author_sort Dalah, Entesar Zawam
collection PubMed
description We estimate the lifetime attributable risk (LAR) of lung cancer incidence in symptomatic Coronary Artery Disease (CAD) patients receiving enhanced Coronary Computed Tomography Angiography (CCTA) and the unenhanced Computed Tomography Calcium Scoring (CTCS) examination. Retrospective analysis has been made of CCTA and CTCS data collected for 87 confirmed CAD adult patients. Patient effective dose (E) and organ doses (ODs) were calculated using CT-EXPO. Statistical correlation and the differences between E and ODs in enhanced CCTA and unenhanced CTCS were calculated using the Pearson coefficient and Wilcoxon unpaired t-test. Following BEIR VII report guidance, organ-specific LARs for the cohort were estimated using the organ-equivalent dose-to-risk conversion factor for numbers of cases per 100,000 patients exposed to low doses of 0.1 Gy. Significant statistical difference (p<0.0001) is found between E obtained for CTCS and that of CCTA. The scan length was found to be greater in CCTA (17.5 ± 2.9 cm) compared to that for CTCS (15 ± 2 cm). More elevated values of dose were noted for the esophagus (4.2 ± 2.15 mSv) and thymus (9.6 ± 2.54 mSv) for both CTCS and CCTA. CTCS organ doses were lower than that of CCTA. Per 100,000 patients, female cumulative doses are seen to give rise to greater lung cancer LARs compared to that for males, albeit with risk varying significantly, noticeably greater for females, younger patients and combined CCTA and CTCS scans. While scan parameters and tube-modulation methods clearly contribute to patient dose, mAs offers by far the greater contribution.
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spelling pubmed-90000962022-04-12 Gender based lung cancer risks for symptomatic coronary artery disease patients undergone cardiac CT Dalah, Entesar Zawam Obaideen, Abdulmunhem Anam, Sabaa Alzimami, Khalid Jambi, Layal Khalid Bradley, David A. PLoS One Research Article We estimate the lifetime attributable risk (LAR) of lung cancer incidence in symptomatic Coronary Artery Disease (CAD) patients receiving enhanced Coronary Computed Tomography Angiography (CCTA) and the unenhanced Computed Tomography Calcium Scoring (CTCS) examination. Retrospective analysis has been made of CCTA and CTCS data collected for 87 confirmed CAD adult patients. Patient effective dose (E) and organ doses (ODs) were calculated using CT-EXPO. Statistical correlation and the differences between E and ODs in enhanced CCTA and unenhanced CTCS were calculated using the Pearson coefficient and Wilcoxon unpaired t-test. Following BEIR VII report guidance, organ-specific LARs for the cohort were estimated using the organ-equivalent dose-to-risk conversion factor for numbers of cases per 100,000 patients exposed to low doses of 0.1 Gy. Significant statistical difference (p<0.0001) is found between E obtained for CTCS and that of CCTA. The scan length was found to be greater in CCTA (17.5 ± 2.9 cm) compared to that for CTCS (15 ± 2 cm). More elevated values of dose were noted for the esophagus (4.2 ± 2.15 mSv) and thymus (9.6 ± 2.54 mSv) for both CTCS and CCTA. CTCS organ doses were lower than that of CCTA. Per 100,000 patients, female cumulative doses are seen to give rise to greater lung cancer LARs compared to that for males, albeit with risk varying significantly, noticeably greater for females, younger patients and combined CCTA and CTCS scans. While scan parameters and tube-modulation methods clearly contribute to patient dose, mAs offers by far the greater contribution. Public Library of Science 2022-04-11 /pmc/articles/PMC9000096/ /pubmed/35404962 http://dx.doi.org/10.1371/journal.pone.0265609 Text en © 2022 Dalah et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dalah, Entesar Zawam
Obaideen, Abdulmunhem
Anam, Sabaa
Alzimami, Khalid
Jambi, Layal Khalid
Bradley, David A.
Gender based lung cancer risks for symptomatic coronary artery disease patients undergone cardiac CT
title Gender based lung cancer risks for symptomatic coronary artery disease patients undergone cardiac CT
title_full Gender based lung cancer risks for symptomatic coronary artery disease patients undergone cardiac CT
title_fullStr Gender based lung cancer risks for symptomatic coronary artery disease patients undergone cardiac CT
title_full_unstemmed Gender based lung cancer risks for symptomatic coronary artery disease patients undergone cardiac CT
title_short Gender based lung cancer risks for symptomatic coronary artery disease patients undergone cardiac CT
title_sort gender based lung cancer risks for symptomatic coronary artery disease patients undergone cardiac ct
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000096/
https://www.ncbi.nlm.nih.gov/pubmed/35404962
http://dx.doi.org/10.1371/journal.pone.0265609
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