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Optimal timing of contrast-enhanced computed tomography in an evaluation of severe acute pancreatitis-associated complications

Dynamic contrast-enhanced computed tomography (CECT) has been used previously to evaluate severe acute pancreatitis (SAP)-associated complications. However, optimal time points of CECT have not yet been established. The present study aimed to determine optimal timings for CECT to be undertaken for p...

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Autores principales: Huang, Huali, Chen, Wenjing, Tang, Guodu, Liang, Zhihai, Qin, Mengbin, Qin, Minzhen, Tang, Yongfeng, Qin, Heping, Chang, Renjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614731/
https://www.ncbi.nlm.nih.gov/pubmed/31363364
http://dx.doi.org/10.3892/etm.2019.7700
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author Huang, Huali
Chen, Wenjing
Tang, Guodu
Liang, Zhihai
Qin, Mengbin
Qin, Minzhen
Tang, Yongfeng
Qin, Heping
Chang, Renjie
author_facet Huang, Huali
Chen, Wenjing
Tang, Guodu
Liang, Zhihai
Qin, Mengbin
Qin, Minzhen
Tang, Yongfeng
Qin, Heping
Chang, Renjie
author_sort Huang, Huali
collection PubMed
description Dynamic contrast-enhanced computed tomography (CECT) has been used previously to evaluate severe acute pancreatitis (SAP)-associated complications. However, optimal time points of CECT have not yet been established. The present study aimed to determine optimal timings for CECT to be undertaken for patients with SAP. The results of CECT from 309 patients with SAP, who were classified into either infected or non-infected SAP groups, were retrospectively analyzed. The severity and alterations in the periods within 72 h to >4 weeks of SAP onset were also assessed. In the analysis of the disease severity and changes, acute peripancreatic fluid collection was detected, where the number of areas increased within 1 week of SAP onset but decreased within 4 weeks and longer. However, no significant differences were observed between the infected and non-infected groups. The acute necrotic collection (ANC) areas were ≤30% of the area of the pancreas, with significantly more ANC areas and pancreatic necrosis in the infected SAP group compared with the non-infected SAP group at a time interval of >4 weeks. The exudation of pleural effusion (PE) was elevated within 1 week, but decreased within 2 weeks and longer. The difference in the alteration of the exudation of PE was not statistically different between the two groups. In conclusion, the results suggest that the period between 72 h and 1 week of SAP onset is optimal timing of CECT to assess SAP-associated complications, particularly for infected SAP patients.
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spelling pubmed-66147312019-07-30 Optimal timing of contrast-enhanced computed tomography in an evaluation of severe acute pancreatitis-associated complications Huang, Huali Chen, Wenjing Tang, Guodu Liang, Zhihai Qin, Mengbin Qin, Minzhen Tang, Yongfeng Qin, Heping Chang, Renjie Exp Ther Med Articles Dynamic contrast-enhanced computed tomography (CECT) has been used previously to evaluate severe acute pancreatitis (SAP)-associated complications. However, optimal time points of CECT have not yet been established. The present study aimed to determine optimal timings for CECT to be undertaken for patients with SAP. The results of CECT from 309 patients with SAP, who were classified into either infected or non-infected SAP groups, were retrospectively analyzed. The severity and alterations in the periods within 72 h to >4 weeks of SAP onset were also assessed. In the analysis of the disease severity and changes, acute peripancreatic fluid collection was detected, where the number of areas increased within 1 week of SAP onset but decreased within 4 weeks and longer. However, no significant differences were observed between the infected and non-infected groups. The acute necrotic collection (ANC) areas were ≤30% of the area of the pancreas, with significantly more ANC areas and pancreatic necrosis in the infected SAP group compared with the non-infected SAP group at a time interval of >4 weeks. The exudation of pleural effusion (PE) was elevated within 1 week, but decreased within 2 weeks and longer. The difference in the alteration of the exudation of PE was not statistically different between the two groups. In conclusion, the results suggest that the period between 72 h and 1 week of SAP onset is optimal timing of CECT to assess SAP-associated complications, particularly for infected SAP patients. D.A. Spandidos 2019-08 2019-06-21 /pmc/articles/PMC6614731/ /pubmed/31363364 http://dx.doi.org/10.3892/etm.2019.7700 Text en Copyright: © Huang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Huang, Huali
Chen, Wenjing
Tang, Guodu
Liang, Zhihai
Qin, Mengbin
Qin, Minzhen
Tang, Yongfeng
Qin, Heping
Chang, Renjie
Optimal timing of contrast-enhanced computed tomography in an evaluation of severe acute pancreatitis-associated complications
title Optimal timing of contrast-enhanced computed tomography in an evaluation of severe acute pancreatitis-associated complications
title_full Optimal timing of contrast-enhanced computed tomography in an evaluation of severe acute pancreatitis-associated complications
title_fullStr Optimal timing of contrast-enhanced computed tomography in an evaluation of severe acute pancreatitis-associated complications
title_full_unstemmed Optimal timing of contrast-enhanced computed tomography in an evaluation of severe acute pancreatitis-associated complications
title_short Optimal timing of contrast-enhanced computed tomography in an evaluation of severe acute pancreatitis-associated complications
title_sort optimal timing of contrast-enhanced computed tomography in an evaluation of severe acute pancreatitis-associated complications
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614731/
https://www.ncbi.nlm.nih.gov/pubmed/31363364
http://dx.doi.org/10.3892/etm.2019.7700
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