The Association of Medications and Vaccination with Risk of Pneumonia in Inflammatory Bowel Disease

Abstract Background Patients with inflammatory bowel disease (IBD) are at increased risk for pneumonia, and corticosteroids are reported to amplify this risk. Less is known about the impact of corticosteroid-sparing IBD therapies on pneumonia risk or the efficacy of pneumococcal vaccination in reduc...

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Veröffentlicht in:Inflammatory bowel diseases 2020-05, Vol.26 (6), p.919-925
Hauptverfasser: Gregory, Martin H, Ciorba, Matthew A, Wiitala, Wyndy L, Stidham, Ryan W, Higgins, Peter, Morley, S Celeste, Hou, Jason K, Feagins, Linda A, Govani, Shail M, Cohen-Mekelburg, Shirley A, Waljee, Akbar K
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container_end_page 925
container_issue 6
container_start_page 919
container_title Inflammatory bowel diseases
container_volume 26
creator Gregory, Martin H
Ciorba, Matthew A
Wiitala, Wyndy L
Stidham, Ryan W
Higgins, Peter
Morley, S Celeste
Hou, Jason K
Feagins, Linda A
Govani, Shail M
Cohen-Mekelburg, Shirley A
Waljee, Akbar K
description Abstract Background Patients with inflammatory bowel disease (IBD) are at increased risk for pneumonia, and corticosteroids are reported to amplify this risk. Less is known about the impact of corticosteroid-sparing IBD therapies on pneumonia risk or the efficacy of pneumococcal vaccination in reducing all-cause pneumonia in real-world IBD cohorts. Methods We performed a population-based study using an established Veterans Health Administration cohort of 29,957 IBD patients. We identified all patients who developed bacterial pneumonia. Cox survival analysis was used to determine the association of corticosteroids at study entry and as a time-varying covariate, corticosteroid-sparing agents (immunomodulators and antitumor necrosis-alpha [TNF] inhibitors), and pneumococcal vaccination with the development of all-cause pneumonia. Results Patients with IBD who received corticosteroids had a greater risk of pneumonia when controlling for age, gender, and comorbidities (hazard ratio [HR] 2.21; 95% confidence interval [CI], 1.90–2.57 for prior use; HR = 3.42; 95% CI, 2.92–4.01 for use during follow-up). Anti-TNF inhibitors (HR 1.52; 95% CI, 1.02–2.26), but not immunomodulators (HR 0.91; 95% CI, 0.77–1.07), were associated with a small increase in pneumonia. A history of pneumonia was strongly associated with subsequent pneumonia (HR = 4.41; 95% CI, 3.70–5.27). Less than 15% of patients were vaccinated against pneumococcus, and this was not associated with a reduced risk of pneumonia (HR = 1.02; 95% CI, 0.80–1.30) in this cohort. Conclusion In a large US cohort, corticosteroids were confirmed to increase pneumonia risk. Tumor necrosis-alpha inhibitors were associated with a smaller increase in the risk of pneumonia. Surprisingly, pneumococcal vaccination did not reduce all-cause pneumonia in this population, though few patients were vaccinated.
doi_str_mv 10.1093/ibd/izz189
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Less is known about the impact of corticosteroid-sparing IBD therapies on pneumonia risk or the efficacy of pneumococcal vaccination in reducing all-cause pneumonia in real-world IBD cohorts. Methods We performed a population-based study using an established Veterans Health Administration cohort of 29,957 IBD patients. We identified all patients who developed bacterial pneumonia. Cox survival analysis was used to determine the association of corticosteroids at study entry and as a time-varying covariate, corticosteroid-sparing agents (immunomodulators and antitumor necrosis-alpha [TNF] inhibitors), and pneumococcal vaccination with the development of all-cause pneumonia. Results Patients with IBD who received corticosteroids had a greater risk of pneumonia when controlling for age, gender, and comorbidities (hazard ratio [HR] 2.21; 95% confidence interval [CI], 1.90–2.57 for prior use; HR = 3.42; 95% CI, 2.92–4.01 for use during follow-up). Anti-TNF inhibitors (HR 1.52; 95% CI, 1.02–2.26), but not immunomodulators (HR 0.91; 95% CI, 0.77–1.07), were associated with a small increase in pneumonia. A history of pneumonia was strongly associated with subsequent pneumonia (HR = 4.41; 95% CI, 3.70–5.27). Less than 15% of patients were vaccinated against pneumococcus, and this was not associated with a reduced risk of pneumonia (HR = 1.02; 95% CI, 0.80–1.30) in this cohort. Conclusion In a large US cohort, corticosteroids were confirmed to increase pneumonia risk. Tumor necrosis-alpha inhibitors were associated with a smaller increase in the risk of pneumonia. Surprisingly, pneumococcal vaccination did not reduce all-cause pneumonia in this population, though few patients were vaccinated.</description><identifier>ISSN: 1078-0998</identifier><identifier>EISSN: 1536-4844</identifier><identifier>DOI: 10.1093/ibd/izz189</identifier><identifier>PMID: 31504531</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Bacterial pneumonia ; Clinical Research ; Comorbidity ; Complications and side effects ; Corticosteroids ; Development and progression ; Drug therapy ; Gastrointestinal diseases ; Pneumonia ; Risk factors ; Tumor necrosis factor ; Vaccination</subject><ispartof>Inflammatory bowel diseases, 2020-05, Vol.26 (6), p.919-925</ispartof><rights>2019 Crohn’s &amp; Colitis Foundation. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 2019</rights><rights>2019 Crohn’s &amp; Colitis Foundation. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>COPYRIGHT 2020 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-202d352ef93c196ed18a4947fa39e1fa31e82d2064ce8fb9aa61f2dc17ec9ecd3</citedby><cites>FETCH-LOGICAL-c475t-202d352ef93c196ed18a4947fa39e1fa31e82d2064ce8fb9aa61f2dc17ec9ecd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,778,782,883,1581,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31504531$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gregory, Martin H</creatorcontrib><creatorcontrib>Ciorba, Matthew A</creatorcontrib><creatorcontrib>Wiitala, Wyndy L</creatorcontrib><creatorcontrib>Stidham, Ryan W</creatorcontrib><creatorcontrib>Higgins, Peter</creatorcontrib><creatorcontrib>Morley, S Celeste</creatorcontrib><creatorcontrib>Hou, Jason K</creatorcontrib><creatorcontrib>Feagins, Linda A</creatorcontrib><creatorcontrib>Govani, Shail M</creatorcontrib><creatorcontrib>Cohen-Mekelburg, Shirley A</creatorcontrib><creatorcontrib>Waljee, Akbar K</creatorcontrib><title>The Association of Medications and Vaccination with Risk of Pneumonia in Inflammatory Bowel Disease</title><title>Inflammatory bowel diseases</title><addtitle>Inflamm Bowel Dis</addtitle><description>Abstract Background Patients with inflammatory bowel disease (IBD) are at increased risk for pneumonia, and corticosteroids are reported to amplify this risk. Less is known about the impact of corticosteroid-sparing IBD therapies on pneumonia risk or the efficacy of pneumococcal vaccination in reducing all-cause pneumonia in real-world IBD cohorts. Methods We performed a population-based study using an established Veterans Health Administration cohort of 29,957 IBD patients. We identified all patients who developed bacterial pneumonia. Cox survival analysis was used to determine the association of corticosteroids at study entry and as a time-varying covariate, corticosteroid-sparing agents (immunomodulators and antitumor necrosis-alpha [TNF] inhibitors), and pneumococcal vaccination with the development of all-cause pneumonia. Results Patients with IBD who received corticosteroids had a greater risk of pneumonia when controlling for age, gender, and comorbidities (hazard ratio [HR] 2.21; 95% confidence interval [CI], 1.90–2.57 for prior use; HR = 3.42; 95% CI, 2.92–4.01 for use during follow-up). Anti-TNF inhibitors (HR 1.52; 95% CI, 1.02–2.26), but not immunomodulators (HR 0.91; 95% CI, 0.77–1.07), were associated with a small increase in pneumonia. A history of pneumonia was strongly associated with subsequent pneumonia (HR = 4.41; 95% CI, 3.70–5.27). Less than 15% of patients were vaccinated against pneumococcus, and this was not associated with a reduced risk of pneumonia (HR = 1.02; 95% CI, 0.80–1.30) in this cohort. Conclusion In a large US cohort, corticosteroids were confirmed to increase pneumonia risk. Tumor necrosis-alpha inhibitors were associated with a smaller increase in the risk of pneumonia. Surprisingly, pneumococcal vaccination did not reduce all-cause pneumonia in this population, though few patients were vaccinated.</description><subject>Bacterial pneumonia</subject><subject>Clinical Research</subject><subject>Comorbidity</subject><subject>Complications and side effects</subject><subject>Corticosteroids</subject><subject>Development and progression</subject><subject>Drug therapy</subject><subject>Gastrointestinal diseases</subject><subject>Pneumonia</subject><subject>Risk factors</subject><subject>Tumor necrosis factor</subject><subject>Vaccination</subject><issn>1078-0998</issn><issn>1536-4844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kV1rFTEQhhdRbK3e-AMkIIII2yabzSa5EY71q1BRpHobcpJJz-huctzsWtpfb45biwWRgcnHPPMyw1tVjxk9ZFTzI1z7I7y6YkrfqfaZ4F3dqra9W-5UqppqrfaqBzl_o7Qpoe9Xe5wJ2grO9it3tgGyyjk5tBOmSFIgH8Cj-_3KxEZPvlrnMC7lC5w25DPm7zvwU4R5SBEtwUhOYujtMNgpjZfkVbqAnrzGDDbDw-pesH2GR9fnQfXl7Zuz4_f16cd3J8er09q1Ukx1Gc5z0UDQ3DHdgWfKtrqVwXINrGQGqvEN7VoHKqy1tR0LjXdMgtPgPD-oXi6623k9gHcQp9H2ZjviYMdLkyya25WIG3OefhrJBRWCF4Hn1wJj-jFDnsyA2UHf2whpzqZplJJMCUoL-nRBz20PBmNIRdHtcLPqtKJMSqkLdfgPqoSHAV2KELD832p4sTS4MeU8QriZnlGzM9sUs81idoGf_L3vDfrH3QI8W4A0b_8n9AvLJrPP</recordid><startdate>20200512</startdate><enddate>20200512</enddate><creator>Gregory, Martin H</creator><creator>Ciorba, Matthew A</creator><creator>Wiitala, Wyndy L</creator><creator>Stidham, Ryan W</creator><creator>Higgins, Peter</creator><creator>Morley, S Celeste</creator><creator>Hou, Jason K</creator><creator>Feagins, Linda A</creator><creator>Govani, Shail M</creator><creator>Cohen-Mekelburg, Shirley A</creator><creator>Waljee, Akbar K</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200512</creationdate><title>The Association of Medications and Vaccination with Risk of Pneumonia in Inflammatory Bowel Disease</title><author>Gregory, Martin H ; Ciorba, Matthew A ; Wiitala, Wyndy L ; Stidham, Ryan W ; Higgins, Peter ; Morley, S Celeste ; Hou, Jason K ; Feagins, Linda A ; Govani, Shail M ; Cohen-Mekelburg, Shirley A ; Waljee, Akbar K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-202d352ef93c196ed18a4947fa39e1fa31e82d2064ce8fb9aa61f2dc17ec9ecd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Bacterial pneumonia</topic><topic>Clinical Research</topic><topic>Comorbidity</topic><topic>Complications and side effects</topic><topic>Corticosteroids</topic><topic>Development and progression</topic><topic>Drug therapy</topic><topic>Gastrointestinal diseases</topic><topic>Pneumonia</topic><topic>Risk factors</topic><topic>Tumor necrosis factor</topic><topic>Vaccination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gregory, Martin H</creatorcontrib><creatorcontrib>Ciorba, Matthew A</creatorcontrib><creatorcontrib>Wiitala, Wyndy L</creatorcontrib><creatorcontrib>Stidham, Ryan W</creatorcontrib><creatorcontrib>Higgins, Peter</creatorcontrib><creatorcontrib>Morley, S Celeste</creatorcontrib><creatorcontrib>Hou, Jason K</creatorcontrib><creatorcontrib>Feagins, Linda A</creatorcontrib><creatorcontrib>Govani, Shail M</creatorcontrib><creatorcontrib>Cohen-Mekelburg, Shirley A</creatorcontrib><creatorcontrib>Waljee, Akbar K</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Inflammatory bowel diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gregory, Martin H</au><au>Ciorba, Matthew A</au><au>Wiitala, Wyndy L</au><au>Stidham, Ryan W</au><au>Higgins, Peter</au><au>Morley, S Celeste</au><au>Hou, Jason K</au><au>Feagins, Linda A</au><au>Govani, Shail M</au><au>Cohen-Mekelburg, Shirley A</au><au>Waljee, Akbar K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Association of Medications and Vaccination with Risk of Pneumonia in Inflammatory Bowel Disease</atitle><jtitle>Inflammatory bowel diseases</jtitle><addtitle>Inflamm Bowel Dis</addtitle><date>2020-05-12</date><risdate>2020</risdate><volume>26</volume><issue>6</issue><spage>919</spage><epage>925</epage><pages>919-925</pages><issn>1078-0998</issn><eissn>1536-4844</eissn><abstract>Abstract Background Patients with inflammatory bowel disease (IBD) are at increased risk for pneumonia, and corticosteroids are reported to amplify this risk. Less is known about the impact of corticosteroid-sparing IBD therapies on pneumonia risk or the efficacy of pneumococcal vaccination in reducing all-cause pneumonia in real-world IBD cohorts. Methods We performed a population-based study using an established Veterans Health Administration cohort of 29,957 IBD patients. We identified all patients who developed bacterial pneumonia. Cox survival analysis was used to determine the association of corticosteroids at study entry and as a time-varying covariate, corticosteroid-sparing agents (immunomodulators and antitumor necrosis-alpha [TNF] inhibitors), and pneumococcal vaccination with the development of all-cause pneumonia. Results Patients with IBD who received corticosteroids had a greater risk of pneumonia when controlling for age, gender, and comorbidities (hazard ratio [HR] 2.21; 95% confidence interval [CI], 1.90–2.57 for prior use; HR = 3.42; 95% CI, 2.92–4.01 for use during follow-up). Anti-TNF inhibitors (HR 1.52; 95% CI, 1.02–2.26), but not immunomodulators (HR 0.91; 95% CI, 0.77–1.07), were associated with a small increase in pneumonia. A history of pneumonia was strongly associated with subsequent pneumonia (HR = 4.41; 95% CI, 3.70–5.27). Less than 15% of patients were vaccinated against pneumococcus, and this was not associated with a reduced risk of pneumonia (HR = 1.02; 95% CI, 0.80–1.30) in this cohort. Conclusion In a large US cohort, corticosteroids were confirmed to increase pneumonia risk. Tumor necrosis-alpha inhibitors were associated with a smaller increase in the risk of pneumonia. Surprisingly, pneumococcal vaccination did not reduce all-cause pneumonia in this population, though few patients were vaccinated.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>31504531</pmid><doi>10.1093/ibd/izz189</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source Oxford University Press Journals All Titles (1996-Current)
subjects Bacterial pneumonia
Clinical Research
Comorbidity
Complications and side effects
Corticosteroids
Development and progression
Drug therapy
Gastrointestinal diseases
Pneumonia
Risk factors
Tumor necrosis factor
Vaccination
title The Association of Medications and Vaccination with Risk of Pneumonia in Inflammatory Bowel Disease
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