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Sub-milliSievert ultralow-dose CT colonography with iterative model reconstruction technique

Purpose. The purpose of this study was to evaluate the technical and diagnostic performance of sub-milliSievert ultralow-dose (ULD) CT colonograpy (CTC) in the detection of colonic and extracolonic lesions. Materials and Methods. CTC with standard dose (SD) and ULD acquisitions of 64 matched patient...

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Autores principales: Lambert, Lukas, Ourednicek, Petr, Briza, Jan, Giepmans, Walter, Jahoda, Jiri, Hruska, Lukas, Danes, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824919/
https://www.ncbi.nlm.nih.gov/pubmed/27069813
http://dx.doi.org/10.7717/peerj.1883
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author Lambert, Lukas
Ourednicek, Petr
Briza, Jan
Giepmans, Walter
Jahoda, Jiri
Hruska, Lukas
Danes, Jan
author_facet Lambert, Lukas
Ourednicek, Petr
Briza, Jan
Giepmans, Walter
Jahoda, Jiri
Hruska, Lukas
Danes, Jan
author_sort Lambert, Lukas
collection PubMed
description Purpose. The purpose of this study was to evaluate the technical and diagnostic performance of sub-milliSievert ultralow-dose (ULD) CT colonograpy (CTC) in the detection of colonic and extracolonic lesions. Materials and Methods. CTC with standard dose (SD) and ULD acquisitions of 64 matched patients, half of them with colonic findings, were reconstructed with filtered back projection (FBP), hybrid (HIR) and iterative model reconstruction techniques (IMR). Image noise in six colonic segments, in the left psoas muscle and aorta were measured. Image quality of the left adrenal gland and of the colon in the endoscopic and 2D view was rated on a five point Likert scale by two observers, who also completed the reading of CTC for colonic and extracolonic findings. Results. The mean radiation dose estimate was 4.1 ± 1.4 mSv for SD and 0.86 ± 0.17 mSv for ULD for both positions (p < 0.0001). In ULD-IMR, SD-IMR and SD-HIR, the endoluminal noise was decreased in all colonic segments compared to SD-FBP (p < 0.001). There were 27 small (6–9 mm) and 17 large (≥10 mm) colonic lesions that were classified as sessile polyps (n = 38), flat lesions (n = 3), or as a mass (n = 3). Per patient sensitivity and specificity were 0.82 and 0.93 for ULD-FBP, 0.97 and 0.97 for ULD-HIR, 0.97 and 1.0 for ULD-IMR. Per polyp sensitivity was 0.84 for ULD-FBP, 0.98 for ULD-HIR, 0.98 for ULD-IMR. Significantly less extracolonic findings were detected in ULD-FBP and ULD-HIR, but in the E4 category by C-RADS (potentially important findings), the detection was similar. Conclusion. Both HIR and IMR are suitable for sub-milliSievert ULD CTC without sacrificing diagnostic performance of the study.
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spelling pubmed-48249192016-04-11 Sub-milliSievert ultralow-dose CT colonography with iterative model reconstruction technique Lambert, Lukas Ourednicek, Petr Briza, Jan Giepmans, Walter Jahoda, Jiri Hruska, Lukas Danes, Jan PeerJ Gastroenterology and Hepatology Purpose. The purpose of this study was to evaluate the technical and diagnostic performance of sub-milliSievert ultralow-dose (ULD) CT colonograpy (CTC) in the detection of colonic and extracolonic lesions. Materials and Methods. CTC with standard dose (SD) and ULD acquisitions of 64 matched patients, half of them with colonic findings, were reconstructed with filtered back projection (FBP), hybrid (HIR) and iterative model reconstruction techniques (IMR). Image noise in six colonic segments, in the left psoas muscle and aorta were measured. Image quality of the left adrenal gland and of the colon in the endoscopic and 2D view was rated on a five point Likert scale by two observers, who also completed the reading of CTC for colonic and extracolonic findings. Results. The mean radiation dose estimate was 4.1 ± 1.4 mSv for SD and 0.86 ± 0.17 mSv for ULD for both positions (p < 0.0001). In ULD-IMR, SD-IMR and SD-HIR, the endoluminal noise was decreased in all colonic segments compared to SD-FBP (p < 0.001). There were 27 small (6–9 mm) and 17 large (≥10 mm) colonic lesions that were classified as sessile polyps (n = 38), flat lesions (n = 3), or as a mass (n = 3). Per patient sensitivity and specificity were 0.82 and 0.93 for ULD-FBP, 0.97 and 0.97 for ULD-HIR, 0.97 and 1.0 for ULD-IMR. Per polyp sensitivity was 0.84 for ULD-FBP, 0.98 for ULD-HIR, 0.98 for ULD-IMR. Significantly less extracolonic findings were detected in ULD-FBP and ULD-HIR, but in the E4 category by C-RADS (potentially important findings), the detection was similar. Conclusion. Both HIR and IMR are suitable for sub-milliSievert ULD CTC without sacrificing diagnostic performance of the study. PeerJ Inc. 2016-03-31 /pmc/articles/PMC4824919/ /pubmed/27069813 http://dx.doi.org/10.7717/peerj.1883 Text en ©2016 Lambert et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Gastroenterology and Hepatology
Lambert, Lukas
Ourednicek, Petr
Briza, Jan
Giepmans, Walter
Jahoda, Jiri
Hruska, Lukas
Danes, Jan
Sub-milliSievert ultralow-dose CT colonography with iterative model reconstruction technique
title Sub-milliSievert ultralow-dose CT colonography with iterative model reconstruction technique
title_full Sub-milliSievert ultralow-dose CT colonography with iterative model reconstruction technique
title_fullStr Sub-milliSievert ultralow-dose CT colonography with iterative model reconstruction technique
title_full_unstemmed Sub-milliSievert ultralow-dose CT colonography with iterative model reconstruction technique
title_short Sub-milliSievert ultralow-dose CT colonography with iterative model reconstruction technique
title_sort sub-millisievert ultralow-dose ct colonography with iterative model reconstruction technique
topic Gastroenterology and Hepatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824919/
https://www.ncbi.nlm.nih.gov/pubmed/27069813
http://dx.doi.org/10.7717/peerj.1883
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