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Risk of post‐operative surgical site infections after vedolizumab vs anti‐tumour necrosis factor therapy: a propensity score matching analysis in inflammatory bowel disease

Summary Background Perioperative vedolizumab (VDZ) and anti‐tumour necrosis factor (TNFi) therapies are implicated in causing post‐operative complications in inflammatory bowel disease (IBD). Aim To compare the risk of surgical site infections (SSIs) between VDZ‐ and TNFi‐treated IBD patients in pro...

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Published in:Alimentary pharmacology & therapeutics 2018-08, Vol.48 (3), p.340-346
Main Authors: Park, K. T., Sceats, L., Dehghan, M., Trickey, A. W., Wren, A., Wong, J. J., Bensen, R., Limketkai, B. N., Keyashian, K., Kin, C.
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container_title Alimentary pharmacology & therapeutics
container_volume 48
creator Park, K. T.
Sceats, L.
Dehghan, M.
Trickey, A. W.
Wren, A.
Wong, J. J.
Bensen, R.
Limketkai, B. N.
Keyashian, K.
Kin, C.
description Summary Background Perioperative vedolizumab (VDZ) and anti‐tumour necrosis factor (TNFi) therapies are implicated in causing post‐operative complications in inflammatory bowel disease (IBD). Aim To compare the risk of surgical site infections (SSIs) between VDZ‐ and TNFi‐treated IBD patients in propensity‐matched cohorts. Methods The Optum Research Database was used to identify IBD patients who received VDZ or TNFi within 30 days prior to abdominal surgery between January 2015 and December 2016. The date of IBD‐related abdominal surgery was defined as the index date. SSIs were determined by ICD‐9/10 and CPT codes related to superficial wound infections or deep organ space infections after surgery. Propensity score 1:1 matching established comparable cohorts based on VDZ or TNFi exposure before surgery based on evidence‐based risk modifiers. Results The propensity‐matched sample included 186 patients who received pre‐operative biologic therapy (VDZ, n = 94; TNFi, n = 92). VDZ and TNFi cohorts were similar based on age, gender, IBD type, concomitant immunomodulator exposure, chronic opioid or corticosteroid therapy, Charlson Comorbidity Index and malnutrition. VDZ patients were more likely to undergo an open bowel resection with ostomy. After propensity score matching, there was no significant difference in post‐operative SSIs (TNFi 12.0% vs VDZ 14.9%, P = 0.56). Multivariable analysis indicated that malnutrition was the sole risk factor for developing SSI (OR 3.1, 95% CI 1.11‐8.71) regardless of the type of biologic exposure. Conclusion In the largest, risk‐adjusted cohort analysis to date, perioperative exposure to VDZ therapy was not associated with a significantly higher risk of developing an SSI compared to TNFi therapy.
doi_str_mv 10.1111/apt.14842
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T. ; Sceats, L. ; Dehghan, M. ; Trickey, A. W. ; Wren, A. ; Wong, J. J. ; Bensen, R. ; Limketkai, B. N. ; Keyashian, K. ; Kin, C.</creator><creatorcontrib>Park, K. T. ; Sceats, L. ; Dehghan, M. ; Trickey, A. W. ; Wren, A. ; Wong, J. J. ; Bensen, R. ; Limketkai, B. N. ; Keyashian, K. ; Kin, C.</creatorcontrib><description>Summary Background Perioperative vedolizumab (VDZ) and anti‐tumour necrosis factor (TNFi) therapies are implicated in causing post‐operative complications in inflammatory bowel disease (IBD). Aim To compare the risk of surgical site infections (SSIs) between VDZ‐ and TNFi‐treated IBD patients in propensity‐matched cohorts. Methods The Optum Research Database was used to identify IBD patients who received VDZ or TNFi within 30 days prior to abdominal surgery between January 2015 and December 2016. The date of IBD‐related abdominal surgery was defined as the index date. SSIs were determined by ICD‐9/10 and CPT codes related to superficial wound infections or deep organ space infections after surgery. Propensity score 1:1 matching established comparable cohorts based on VDZ or TNFi exposure before surgery based on evidence‐based risk modifiers. Results The propensity‐matched sample included 186 patients who received pre‐operative biologic therapy (VDZ, n = 94; TNFi, n = 92). VDZ and TNFi cohorts were similar based on age, gender, IBD type, concomitant immunomodulator exposure, chronic opioid or corticosteroid therapy, Charlson Comorbidity Index and malnutrition. VDZ patients were more likely to undergo an open bowel resection with ostomy. After propensity score matching, there was no significant difference in post‐operative SSIs (TNFi 12.0% vs VDZ 14.9%, P = 0.56). Multivariable analysis indicated that malnutrition was the sole risk factor for developing SSI (OR 3.1, 95% CI 1.11‐8.71) regardless of the type of biologic exposure. Conclusion In the largest, risk‐adjusted cohort analysis to date, perioperative exposure to VDZ therapy was not associated with a significantly higher risk of developing an SSI compared to TNFi therapy.</description><identifier>ISSN: 0269-2813</identifier><identifier>ISSN: 1365-2036</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/apt.14842</identifier><identifier>PMID: 29876995</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Abdominal surgery ; Adult ; Anti-Inflammatory Agents - therapeutic use ; Antibodies, Monoclonal, Humanized - therapeutic use ; Combined Modality Therapy ; Complications ; Corticosteroids ; Digestive System Surgical Procedures - adverse effects ; Digestive System Surgical Procedures - methods ; Exposure ; Female ; Gangrene ; Health risks ; Humans ; Immunotherapy - adverse effects ; Immunotherapy - methods ; Infections ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Inflammatory Bowel Diseases - drug therapy ; Inflammatory Bowel Diseases - epidemiology ; Inflammatory Bowel Diseases - surgery ; Intestine ; Longitudinal Studies ; Male ; Malnutrition ; Opioids ; Postoperative Period ; Propensity Score ; Retrospective Studies ; Risk Factors ; Surgery ; Surgical site infections ; Surgical Wound Infection - epidemiology ; Surgical Wound Infection - etiology ; Tumor necrosis factor ; Tumor Necrosis Factor-alpha - antagonists &amp; inhibitors ; Tumor necrosis factor-TNF ; Tumors</subject><ispartof>Alimentary pharmacology &amp; therapeutics, 2018-08, Vol.48 (3), p.340-346</ispartof><rights>2018 John Wiley &amp; Sons Ltd</rights><rights>2018 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2018 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3882-11d78a310e91c1325a9f98846c0d98f7f48ee7b8397e493eb0ca07d4d633e6643</citedby><cites>FETCH-LOGICAL-c3882-11d78a310e91c1325a9f98846c0d98f7f48ee7b8397e493eb0ca07d4d633e6643</cites><orcidid>0000-0002-2133-3598</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29876995$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, K. T.</creatorcontrib><creatorcontrib>Sceats, L.</creatorcontrib><creatorcontrib>Dehghan, M.</creatorcontrib><creatorcontrib>Trickey, A. W.</creatorcontrib><creatorcontrib>Wren, A.</creatorcontrib><creatorcontrib>Wong, J. J.</creatorcontrib><creatorcontrib>Bensen, R.</creatorcontrib><creatorcontrib>Limketkai, B. N.</creatorcontrib><creatorcontrib>Keyashian, K.</creatorcontrib><creatorcontrib>Kin, C.</creatorcontrib><title>Risk of post‐operative surgical site infections after vedolizumab vs anti‐tumour necrosis factor therapy: a propensity score matching analysis in inflammatory bowel disease</title><title>Alimentary pharmacology &amp; therapeutics</title><addtitle>Aliment Pharmacol Ther</addtitle><description>Summary Background Perioperative vedolizumab (VDZ) and anti‐tumour necrosis factor (TNFi) therapies are implicated in causing post‐operative complications in inflammatory bowel disease (IBD). Aim To compare the risk of surgical site infections (SSIs) between VDZ‐ and TNFi‐treated IBD patients in propensity‐matched cohorts. Methods The Optum Research Database was used to identify IBD patients who received VDZ or TNFi within 30 days prior to abdominal surgery between January 2015 and December 2016. The date of IBD‐related abdominal surgery was defined as the index date. SSIs were determined by ICD‐9/10 and CPT codes related to superficial wound infections or deep organ space infections after surgery. Propensity score 1:1 matching established comparable cohorts based on VDZ or TNFi exposure before surgery based on evidence‐based risk modifiers. Results The propensity‐matched sample included 186 patients who received pre‐operative biologic therapy (VDZ, n = 94; TNFi, n = 92). VDZ and TNFi cohorts were similar based on age, gender, IBD type, concomitant immunomodulator exposure, chronic opioid or corticosteroid therapy, Charlson Comorbidity Index and malnutrition. VDZ patients were more likely to undergo an open bowel resection with ostomy. After propensity score matching, there was no significant difference in post‐operative SSIs (TNFi 12.0% vs VDZ 14.9%, P = 0.56). Multivariable analysis indicated that malnutrition was the sole risk factor for developing SSI (OR 3.1, 95% CI 1.11‐8.71) regardless of the type of biologic exposure. 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T.</creatorcontrib><creatorcontrib>Sceats, L.</creatorcontrib><creatorcontrib>Dehghan, M.</creatorcontrib><creatorcontrib>Trickey, A. W.</creatorcontrib><creatorcontrib>Wren, A.</creatorcontrib><creatorcontrib>Wong, J. J.</creatorcontrib><creatorcontrib>Bensen, R.</creatorcontrib><creatorcontrib>Limketkai, B. N.</creatorcontrib><creatorcontrib>Keyashian, K.</creatorcontrib><creatorcontrib>Kin, C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, K. T.</au><au>Sceats, L.</au><au>Dehghan, M.</au><au>Trickey, A. W.</au><au>Wren, A.</au><au>Wong, J. J.</au><au>Bensen, R.</au><au>Limketkai, B. N.</au><au>Keyashian, K.</au><au>Kin, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk of post‐operative surgical site infections after vedolizumab vs anti‐tumour necrosis factor therapy: a propensity score matching analysis in inflammatory bowel disease</atitle><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2018-08</date><risdate>2018</risdate><volume>48</volume><issue>3</issue><spage>340</spage><epage>346</epage><pages>340-346</pages><issn>0269-2813</issn><issn>1365-2036</issn><eissn>1365-2036</eissn><abstract>Summary Background Perioperative vedolizumab (VDZ) and anti‐tumour necrosis factor (TNFi) therapies are implicated in causing post‐operative complications in inflammatory bowel disease (IBD). Aim To compare the risk of surgical site infections (SSIs) between VDZ‐ and TNFi‐treated IBD patients in propensity‐matched cohorts. Methods The Optum Research Database was used to identify IBD patients who received VDZ or TNFi within 30 days prior to abdominal surgery between January 2015 and December 2016. The date of IBD‐related abdominal surgery was defined as the index date. SSIs were determined by ICD‐9/10 and CPT codes related to superficial wound infections or deep organ space infections after surgery. Propensity score 1:1 matching established comparable cohorts based on VDZ or TNFi exposure before surgery based on evidence‐based risk modifiers. Results The propensity‐matched sample included 186 patients who received pre‐operative biologic therapy (VDZ, n = 94; TNFi, n = 92). VDZ and TNFi cohorts were similar based on age, gender, IBD type, concomitant immunomodulator exposure, chronic opioid or corticosteroid therapy, Charlson Comorbidity Index and malnutrition. VDZ patients were more likely to undergo an open bowel resection with ostomy. After propensity score matching, there was no significant difference in post‐operative SSIs (TNFi 12.0% vs VDZ 14.9%, P = 0.56). Multivariable analysis indicated that malnutrition was the sole risk factor for developing SSI (OR 3.1, 95% CI 1.11‐8.71) regardless of the type of biologic exposure. Conclusion In the largest, risk‐adjusted cohort analysis to date, perioperative exposure to VDZ therapy was not associated with a significantly higher risk of developing an SSI compared to TNFi therapy.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29876995</pmid><doi>10.1111/apt.14842</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-2133-3598</orcidid><oa>free_for_read</oa></addata></record>
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1365-2036
1365-2036
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subjects Abdominal surgery
Adult
Anti-Inflammatory Agents - therapeutic use
Antibodies, Monoclonal, Humanized - therapeutic use
Combined Modality Therapy
Complications
Corticosteroids
Digestive System Surgical Procedures - adverse effects
Digestive System Surgical Procedures - methods
Exposure
Female
Gangrene
Health risks
Humans
Immunotherapy - adverse effects
Immunotherapy - methods
Infections
Inflammatory bowel disease
Inflammatory bowel diseases
Inflammatory Bowel Diseases - drug therapy
Inflammatory Bowel Diseases - epidemiology
Inflammatory Bowel Diseases - surgery
Intestine
Longitudinal Studies
Male
Malnutrition
Opioids
Postoperative Period
Propensity Score
Retrospective Studies
Risk Factors
Surgery
Surgical site infections
Surgical Wound Infection - epidemiology
Surgical Wound Infection - etiology
Tumor necrosis factor
Tumor Necrosis Factor-alpha - antagonists & inhibitors
Tumor necrosis factor-TNF
Tumors
title Risk of post‐operative surgical site infections after vedolizumab vs anti‐tumour necrosis factor therapy: a propensity score matching analysis in inflammatory bowel disease
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