Drug-induced acute pancreatitis due to medications used for inflammatory bowel disease: A VigiBase pharmacovigilance database study
Nearly all medications used for inflammatory bowel disease (IBD) have been reported as causes of acute pancreatitis (AP), with the thiopurines being among the most frequently described. However, with the development of newer medications, thiopurine monotherapy has largely been replaced by newer immu...
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Veröffentlicht in: | Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2023-09, Vol.23 (6), p.569-573 |
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container_title | Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] |
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creator | Lee, Alice A. Gupta, Sanchit Labban, Muhieddine Cao, Frank T. Trinh, Quoc-Dien McNabb-Baltar, Julia |
description | Nearly all medications used for inflammatory bowel disease (IBD) have been reported as causes of acute pancreatitis (AP), with the thiopurines being among the most frequently described. However, with the development of newer medications, thiopurine monotherapy has largely been replaced by newer immunosuppressive drugs. There are few data on the association between AP and biologic/small molecule agents.
VigiBase, the World Health Organization's Global Individual Case Safety Report database, was used to assess the association between AP and common IBD medications. A case/non-case disproportionality analysis was performed and disproportionality signals were reported as a reporting odds ratio (ROR) with 95% confidence intervals (CIs).
A total of 4,223 AP episodes were identified for common IBD medications. Azathioprine (ROR 19.18, 95% CI 18.21–20.20), 6-mercaptopurine (ROR 13.30, 95% CI 11.73–15.07), and 5-aminosalicylic acid (ROR 17.44, 95% CI 16.24–18.72) all had strong associations with AP, while the biologic/small molecule agents showed weaker or no disproportionality. The association with AP was much higher for thiopurines when used for Crohn's disease (ROR 34.61, 95% CI 30.95–38.70) compared to ulcerative colitis (ROR 8.94, 95% CI 7.47–10.71) or rheumatologic conditions (ROR 18.87, 95% CI 14.72–24.19).
We report the largest real-world database study investigating the association between common IBD medications and AP. Among commonly used IBD medications including biologic/small molecule agents, only thiopurines and 5-aminosalicylic acid are strongly associated with AP. The association between thiopurines and AP is much stronger when the drug is used for Crohn's disease compared to ulcerative colitis and rheumatologic conditions. |
doi_str_mv | 10.1016/j.pan.2023.06.003 |
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VigiBase, the World Health Organization's Global Individual Case Safety Report database, was used to assess the association between AP and common IBD medications. A case/non-case disproportionality analysis was performed and disproportionality signals were reported as a reporting odds ratio (ROR) with 95% confidence intervals (CIs).
A total of 4,223 AP episodes were identified for common IBD medications. Azathioprine (ROR 19.18, 95% CI 18.21–20.20), 6-mercaptopurine (ROR 13.30, 95% CI 11.73–15.07), and 5-aminosalicylic acid (ROR 17.44, 95% CI 16.24–18.72) all had strong associations with AP, while the biologic/small molecule agents showed weaker or no disproportionality. The association with AP was much higher for thiopurines when used for Crohn's disease (ROR 34.61, 95% CI 30.95–38.70) compared to ulcerative colitis (ROR 8.94, 95% CI 7.47–10.71) or rheumatologic conditions (ROR 18.87, 95% CI 14.72–24.19).
We report the largest real-world database study investigating the association between common IBD medications and AP. Among commonly used IBD medications including biologic/small molecule agents, only thiopurines and 5-aminosalicylic acid are strongly associated with AP. The association between thiopurines and AP is much stronger when the drug is used for Crohn's disease compared to ulcerative colitis and rheumatologic conditions.</description><identifier>ISSN: 1424-3903</identifier><identifier>EISSN: 1424-3911</identifier><identifier>DOI: 10.1016/j.pan.2023.06.003</identifier><identifier>PMID: 37302896</identifier><language>eng</language><publisher>Switzerland: Elsevier B.V</publisher><subject>Drug-induced acute pancreatitis ; Inflammatory bowel disease ; Pharmacovigilance ; Vigibase</subject><ispartof>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2023-09, Vol.23 (6), p.569-573</ispartof><rights>2023 IAP and EPC</rights><rights>Copyright © 2023 IAP and EPC. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-ad921cd3a050ff3fe8b675b1f7985584b88b765e1a0659ea3d7f3d15085b77e03</citedby><cites>FETCH-LOGICAL-c353t-ad921cd3a050ff3fe8b675b1f7985584b88b765e1a0659ea3d7f3d15085b77e03</cites><orcidid>0000-0003-2035-284X ; 0000-0002-4580-1915 ; 0000-0002-5241-1878 ; 0000-0003-4112-7908 ; 0000-0003-4824-455X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37302896$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Alice A.</creatorcontrib><creatorcontrib>Gupta, Sanchit</creatorcontrib><creatorcontrib>Labban, Muhieddine</creatorcontrib><creatorcontrib>Cao, Frank T.</creatorcontrib><creatorcontrib>Trinh, Quoc-Dien</creatorcontrib><creatorcontrib>McNabb-Baltar, Julia</creatorcontrib><title>Drug-induced acute pancreatitis due to medications used for inflammatory bowel disease: A VigiBase pharmacovigilance database study</title><title>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]</title><addtitle>Pancreatology</addtitle><description>Nearly all medications used for inflammatory bowel disease (IBD) have been reported as causes of acute pancreatitis (AP), with the thiopurines being among the most frequently described. However, with the development of newer medications, thiopurine monotherapy has largely been replaced by newer immunosuppressive drugs. There are few data on the association between AP and biologic/small molecule agents.
VigiBase, the World Health Organization's Global Individual Case Safety Report database, was used to assess the association between AP and common IBD medications. A case/non-case disproportionality analysis was performed and disproportionality signals were reported as a reporting odds ratio (ROR) with 95% confidence intervals (CIs).
A total of 4,223 AP episodes were identified for common IBD medications. Azathioprine (ROR 19.18, 95% CI 18.21–20.20), 6-mercaptopurine (ROR 13.30, 95% CI 11.73–15.07), and 5-aminosalicylic acid (ROR 17.44, 95% CI 16.24–18.72) all had strong associations with AP, while the biologic/small molecule agents showed weaker or no disproportionality. The association with AP was much higher for thiopurines when used for Crohn's disease (ROR 34.61, 95% CI 30.95–38.70) compared to ulcerative colitis (ROR 8.94, 95% CI 7.47–10.71) or rheumatologic conditions (ROR 18.87, 95% CI 14.72–24.19).
We report the largest real-world database study investigating the association between common IBD medications and AP. Among commonly used IBD medications including biologic/small molecule agents, only thiopurines and 5-aminosalicylic acid are strongly associated with AP. The association between thiopurines and AP is much stronger when the drug is used for Crohn's disease compared to ulcerative colitis and rheumatologic conditions.</description><subject>Drug-induced acute pancreatitis</subject><subject>Inflammatory bowel disease</subject><subject>Pharmacovigilance</subject><subject>Vigibase</subject><issn>1424-3903</issn><issn>1424-3911</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kD1vFDEQhq2IKAkhPyANckmzy9g-7wdUSQgQKRIN0Fpeexx82j0f_gi6mj8eny6kpJrRzDOv7IeQSwYtA9a9X7dbvWk5cNFC1wKII3LGVnzViJGxVy89iFPyOqU1AOeMjSfkVPQC-DB2Z-Tvp1geGr-xxaCl2pSMtIaaiDr77BO1BWkOdEHrTR2FTaIlVdSFSP3GzXpZdA5xR6fwB2dqfUKd8AO9oj_9g7-uPd3-0nHRJjzWwVyzkVqd9bRfpVzs7g05dnpOePFcz8mPz7ffb74299--3N1c3TdGSJEbbUfOjBUaJDgnHA5T18uJuX4cpBxW0zBMfSeRaejkiFrY3gnLJAxy6nsEcU7eHXK3MfwumLJafDI41zdhKEnxgUsm-25cVZQdUBNDShGd2ka_6LhTDNTevVqrqknt3SvoVHVfb94-x5ep6nq5-Ce7Ah8PANZPPnqMKhmP1Yf1EU1WNvj_xD8BvV-WsA</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Lee, Alice A.</creator><creator>Gupta, Sanchit</creator><creator>Labban, Muhieddine</creator><creator>Cao, Frank T.</creator><creator>Trinh, Quoc-Dien</creator><creator>McNabb-Baltar, Julia</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2035-284X</orcidid><orcidid>https://orcid.org/0000-0002-4580-1915</orcidid><orcidid>https://orcid.org/0000-0002-5241-1878</orcidid><orcidid>https://orcid.org/0000-0003-4112-7908</orcidid><orcidid>https://orcid.org/0000-0003-4824-455X</orcidid></search><sort><creationdate>20230901</creationdate><title>Drug-induced acute pancreatitis due to medications used for inflammatory bowel disease: A VigiBase pharmacovigilance database study</title><author>Lee, Alice A. ; Gupta, Sanchit ; Labban, Muhieddine ; Cao, Frank T. ; Trinh, Quoc-Dien ; McNabb-Baltar, Julia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-ad921cd3a050ff3fe8b675b1f7985584b88b765e1a0659ea3d7f3d15085b77e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Drug-induced acute pancreatitis</topic><topic>Inflammatory bowel disease</topic><topic>Pharmacovigilance</topic><topic>Vigibase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Alice A.</creatorcontrib><creatorcontrib>Gupta, Sanchit</creatorcontrib><creatorcontrib>Labban, Muhieddine</creatorcontrib><creatorcontrib>Cao, Frank T.</creatorcontrib><creatorcontrib>Trinh, Quoc-Dien</creatorcontrib><creatorcontrib>McNabb-Baltar, Julia</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Alice A.</au><au>Gupta, Sanchit</au><au>Labban, Muhieddine</au><au>Cao, Frank T.</au><au>Trinh, Quoc-Dien</au><au>McNabb-Baltar, Julia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Drug-induced acute pancreatitis due to medications used for inflammatory bowel disease: A VigiBase pharmacovigilance database study</atitle><jtitle>Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]</jtitle><addtitle>Pancreatology</addtitle><date>2023-09-01</date><risdate>2023</risdate><volume>23</volume><issue>6</issue><spage>569</spage><epage>573</epage><pages>569-573</pages><issn>1424-3903</issn><eissn>1424-3911</eissn><abstract>Nearly all medications used for inflammatory bowel disease (IBD) have been reported as causes of acute pancreatitis (AP), with the thiopurines being among the most frequently described. However, with the development of newer medications, thiopurine monotherapy has largely been replaced by newer immunosuppressive drugs. There are few data on the association between AP and biologic/small molecule agents.
VigiBase, the World Health Organization's Global Individual Case Safety Report database, was used to assess the association between AP and common IBD medications. A case/non-case disproportionality analysis was performed and disproportionality signals were reported as a reporting odds ratio (ROR) with 95% confidence intervals (CIs).
A total of 4,223 AP episodes were identified for common IBD medications. Azathioprine (ROR 19.18, 95% CI 18.21–20.20), 6-mercaptopurine (ROR 13.30, 95% CI 11.73–15.07), and 5-aminosalicylic acid (ROR 17.44, 95% CI 16.24–18.72) all had strong associations with AP, while the biologic/small molecule agents showed weaker or no disproportionality. The association with AP was much higher for thiopurines when used for Crohn's disease (ROR 34.61, 95% CI 30.95–38.70) compared to ulcerative colitis (ROR 8.94, 95% CI 7.47–10.71) or rheumatologic conditions (ROR 18.87, 95% CI 14.72–24.19).
We report the largest real-world database study investigating the association between common IBD medications and AP. Among commonly used IBD medications including biologic/small molecule agents, only thiopurines and 5-aminosalicylic acid are strongly associated with AP. The association between thiopurines and AP is much stronger when the drug is used for Crohn's disease compared to ulcerative colitis and rheumatologic conditions.</abstract><cop>Switzerland</cop><pub>Elsevier B.V</pub><pmid>37302896</pmid><doi>10.1016/j.pan.2023.06.003</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-2035-284X</orcidid><orcidid>https://orcid.org/0000-0002-4580-1915</orcidid><orcidid>https://orcid.org/0000-0002-5241-1878</orcidid><orcidid>https://orcid.org/0000-0003-4112-7908</orcidid><orcidid>https://orcid.org/0000-0003-4824-455X</orcidid></addata></record> |
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subjects | Drug-induced acute pancreatitis Inflammatory bowel disease Pharmacovigilance Vigibase |
title | Drug-induced acute pancreatitis due to medications used for inflammatory bowel disease: A VigiBase pharmacovigilance database study |
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