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Immune thrombocytopenic purpura increased risk of subsequent pancreatitis: A Nationwide population cohort study
Immune thrombocytopenic purpura (ITP) is characterized by thrombocytopenia and bleeding diathesis. Pancreatitis is a very rare complication but may be fatal. We analyzed data of newly diagnosed ITP patients, excluding those with a history of splenectomy, unknown sex or date of birth, or preexisting...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858306/ https://www.ncbi.nlm.nih.gov/pubmed/31729447 http://dx.doi.org/10.1038/s41598-019-53165-7 |
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author | Wu, Shih-Chi Lin, Sheng-fung Fang, Chu-Wen Tsai, I-Ju Yang, Wen-Chi |
author_facet | Wu, Shih-Chi Lin, Sheng-fung Fang, Chu-Wen Tsai, I-Ju Yang, Wen-Chi |
author_sort | Wu, Shih-Chi |
collection | PubMed |
description | Immune thrombocytopenic purpura (ITP) is characterized by thrombocytopenia and bleeding diathesis. Pancreatitis is a very rare complication but may be fatal. We analyzed data of newly diagnosed ITP patients, excluding those with a history of splenectomy, unknown sex or date of birth, or preexisting pancreatitis at the time of ITP diagnosis, and compared these with selected age-, gender-, and index-year-matched controls, using the Taiwan National Health Insurance Research Database from 1996 to 2013. The study enrolled 100,177 ITP patients and 100,177 controls. We found that pancreatitis risk was higher in secondary ITP patients, regardless of age group, gender, baseline Charlson comorbidity index (CCI) score, history of biliary stone, hyperlipidemia, or alcoholism, than in the control population. Primary ITP patients with CCI score 1 and without biliary tract stone history also showed a higher pancreatitis risk than the controls. The incidence rate and cumulative incidence of pancreatitis were increased in primary, secondary, and unspecified ITP cases. These phenomena may be related to the presence of autoantibodies against glycoprotein IIb/IIIa, or to IgG4, microparticle obstruction, or sclerosis. We noted a direct association between ITP and the development of pancreatitis in Taiwan population. |
format | Online Article Text |
id | pubmed-6858306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68583062019-11-27 Immune thrombocytopenic purpura increased risk of subsequent pancreatitis: A Nationwide population cohort study Wu, Shih-Chi Lin, Sheng-fung Fang, Chu-Wen Tsai, I-Ju Yang, Wen-Chi Sci Rep Article Immune thrombocytopenic purpura (ITP) is characterized by thrombocytopenia and bleeding diathesis. Pancreatitis is a very rare complication but may be fatal. We analyzed data of newly diagnosed ITP patients, excluding those with a history of splenectomy, unknown sex or date of birth, or preexisting pancreatitis at the time of ITP diagnosis, and compared these with selected age-, gender-, and index-year-matched controls, using the Taiwan National Health Insurance Research Database from 1996 to 2013. The study enrolled 100,177 ITP patients and 100,177 controls. We found that pancreatitis risk was higher in secondary ITP patients, regardless of age group, gender, baseline Charlson comorbidity index (CCI) score, history of biliary stone, hyperlipidemia, or alcoholism, than in the control population. Primary ITP patients with CCI score 1 and without biliary tract stone history also showed a higher pancreatitis risk than the controls. The incidence rate and cumulative incidence of pancreatitis were increased in primary, secondary, and unspecified ITP cases. These phenomena may be related to the presence of autoantibodies against glycoprotein IIb/IIIa, or to IgG4, microparticle obstruction, or sclerosis. We noted a direct association between ITP and the development of pancreatitis in Taiwan population. Nature Publishing Group UK 2019-11-15 /pmc/articles/PMC6858306/ /pubmed/31729447 http://dx.doi.org/10.1038/s41598-019-53165-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wu, Shih-Chi Lin, Sheng-fung Fang, Chu-Wen Tsai, I-Ju Yang, Wen-Chi Immune thrombocytopenic purpura increased risk of subsequent pancreatitis: A Nationwide population cohort study |
title | Immune thrombocytopenic purpura increased risk of subsequent pancreatitis: A Nationwide population cohort study |
title_full | Immune thrombocytopenic purpura increased risk of subsequent pancreatitis: A Nationwide population cohort study |
title_fullStr | Immune thrombocytopenic purpura increased risk of subsequent pancreatitis: A Nationwide population cohort study |
title_full_unstemmed | Immune thrombocytopenic purpura increased risk of subsequent pancreatitis: A Nationwide population cohort study |
title_short | Immune thrombocytopenic purpura increased risk of subsequent pancreatitis: A Nationwide population cohort study |
title_sort | immune thrombocytopenic purpura increased risk of subsequent pancreatitis: a nationwide population cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858306/ https://www.ncbi.nlm.nih.gov/pubmed/31729447 http://dx.doi.org/10.1038/s41598-019-53165-7 |
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