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      Risk of Postoperative Surgical Site Infections after Vedolizumab versus Anti-Tumor Necrosis Factor Therapy: A Propensity-Score Matching Analysis in Inflammatory Bowel Disease

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          Abstract

          Background

          Perioperative vedolizumab (VDZ) and anti-tumor necrosis factor (TNFi) therapies are implicated in causing postoperative 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 preoperative 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 postoperative 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.

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          Author and article information

          Journal
          8707234
          1160
          Aliment Pharmacol Ther
          Aliment. Pharmacol. Ther.
          Alimentary pharmacology & therapeutics
          0269-2813
          1365-2036
          23 May 2018
          07 June 2018
          August 2018
          01 August 2019
          : 48
          : 3
          : 340-346
          Affiliations
          [1 ]Stanford Children’s Inflammatory Bowel Disease Center, Division of Gastroenterology, Department of Pediatrics, Stanford University School of Medicine
          [2 ]Division of Colorectal Surgery, Department of Surgery & Stanford-Surgery Policy Improvement Research and Education (S-SPIRE) Center, Stanford University School of Medicine
          [3 ]Health Services Research & Development, VA Palo Alto Health Care System, Palo Alto, CA
          [4 ]Division of Gastroenterology, Department of Medicine, Stanford University School of Medicine
          Author notes
          Correspondence: KT Park, MD, MS, 750 Welch Road, Ste 116, Palo Alto, CA 94304, Office: 650-723-5070, Fax: 650-498-5608, ktpark@ 123456stanford.edu

          DR KT PARK (Orcid ID : 0000-0002-2133-3598)

          Article
          PMC6043399 PMC6043399 6043399 nihpa970060
          10.1111/apt.14842
          6043399
          29876995
          24d7135a-ecee-4904-9379-02f10e74a13b
          History
          Categories
          Article

          biologic,vedolizumab,postoperative complications,Inflammatory bowel disease

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