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      Biologics and surgical outcomes in Crohn’s disease: is there a direct relationship?

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          Abstract

          Despite significant advances in medical therapy in the management of Crohn’s disease (CD), surgery is still required in a significant proportion of patients and constitutes an important tool in treatment algorithms. Recently, more options of biological agents have been made available, and most patients with CD undergoing surgical procedures have been previously exposed to this class of drugs. There is controversy in the literature as to whether anti-tumor necrosis factor (TNF) agents, anti-integrins, or anti-interleukins (ILs) have a direct relationship with increased postoperative complications.

          In this narrative review, the authors summarize the most important data regarding the effect of biologics on postoperative outcomes in CD.

          Most studies (with different designs) are based on the experience with anti-TNF agents, mostly with infliximab. Some studies outlined the relationship between vedolizumab and postoperative complications, and there is a lack of data with ustekinumab in this scenario. Most studies are retrospective, but few prospective data are available. A cause–effect (proof of concept) direct relationship between biologics and an increase in postoperative morbidity has not been demonstrated to date. Several confounding factors such as previous use of steroids, malnutrition, and unfavorable abdominal conditions have a definitely effect on postoperative complications in CD.

          Biologics seem safe to be used in the perioperative period, but available data are still controversial. Multidisciplinary individualized decisions should be made on a case-to-case basis, adapting the surgical strategy according to risk factors involved.

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          Most cited references51

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          Adalimumab for maintenance of clinical response and remission in patients with Crohn's disease: the CHARM trial.

          This study evaluated the efficacy and safety of adalimumab, a fully human, anti-tumor necrosis factor monoclonal antibody administered subcutaneously, in the maintenance of response and remission in patients with moderate to severe Crohn's disease (CD). Patients received open-label induction therapy with adalimumab 80 mg (week 0) followed by 40 mg (week 2). At week 4, patients were stratified by response (decrease in Crohn's Disease Activity Index > or =70 points from baseline) and randomized to double-blind treatment with placebo, adalimumab 40 mg every other week (eow), or adalimumab 40 mg weekly through week 56. Co-primary end points were the percentages of randomized responders who achieved clinical remission (Crohn's Disease Activity Index score <150) at weeks 26 and 56. The percentage of randomized responders in remission was significantly greater in the adalimumab 40-mg eow and 40-mg weekly groups versus placebo at week 26 (40%, 47%, and 17%, respectively; P < .001) and week 56 (36%, 41%, and 12%, respectively; P < .001). No significant differences in efficacy between adalimumab eow and weekly were observed. More patients receiving placebo discontinued treatment because of an adverse event (13.4%) than those receiving adalimumab (6.9% and 4.7% in the 40-mg eow and 40-mg weekly groups, respectively). Among patients who responded to adalimumab, both adalimumab eow and weekly were significantly more effective than placebo in maintaining remission in moderate to severe CD through 56 weeks. Adalimumab was well-tolerated, with a safety profile consistent with previous experience with the drug.
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            Ustekinumab as Induction and Maintenance Therapy for Ulcerative Colitis

            The efficacy of ustekinumab, an antagonist of the p40 subunit of interleukin-12 and interleukin-23, as induction and maintenance therapy in patients with ulcerative colitis is unknown.
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              ECCO-ESCP Consensus on Surgery for Crohn’s Disease

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                Author and article information

                Contributors
                Journal
                Therap Adv Gastroenterol
                Therap Adv Gastroenterol
                TAG
                sptag
                Therapeutic Advances in Gastroenterology
                SAGE Publications (Sage UK: London, England )
                1756-283X
                1756-2848
                16 July 2020
                2020
                : 13
                : 1756284820931738
                Affiliations
                [1-1756284820931738]Universidade do Oeste de Santa Catarina (UNOESC), Joaçaba, Brazil
                [2-1756284820931738]IBD Centre, Yokkaichi Hazu Medical Centre, Yokkaichi, Japan
                [3-1756284820931738]Outpatient clinics, Colorectal Surgery Unit, Catholic University of Paraná, Av Sao Jose 300, Curitiba, Parana 80050-350, Brazil
                Author notes
                Author information
                https://orcid.org/0000-0001-7551-5568
                https://orcid.org/0000-0002-9632-6691
                Article
                10.1177_1756284820931738
                10.1177/1756284820931738
                7366403
                c8bf926a-2d13-4133-9000-90910d4fc5ed
                © The Author(s), 2020

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                : 29 January 2020
                : 11 May 2020
                Categories
                Review
                Custom metadata
                January-December 2020
                ts1

                antibodies monoclonal,crohn’s disease,infections,integrins,postoperative complications,tumor necrosis factor-alpha,ustekinumab

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