Intra-abdominal septic complications after ileocolic resection increases risk for endoscopic and surgical postoperative Crohn's disease recurrence.


Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
23 Nov 2022
Historique:
pubmed: 16 6 2022
medline: 26 11 2022
entrez: 15 6 2022
Statut: ppublish

Résumé

Postoperative recurrence [POR] of Crohn's disease following ileocolonic resection is common. The impact of immediate postoperative intra-abdominal septic complications [IASC] on endoscopic and surgical recurrence has not been elucidated. To evaluate if IASC is associated with an increased risk for endoscopic and surgical POR. This was a retrospective study of adult Crohn's disease patients undergoing ileocolonic resection with primary anastomosis between 2009 and 2020. IASC was defined as anastomotic leak or intra-abdominal abscess within 90 days of the date of surgery. Multivariable logistic and Cox proportional hazard modelling were performed to assess the impact of IASC on endoscopic POR [modified Rutgeerts' score ≥ i2b] at index postoperative ileocolonoscopy and long-term surgical recurrence. In 535 Crohn's disease patients [median age 35 years, 22.1% active smokers, 35.7% one or more prior resection] had an ileocolonic resection with primary anastomosis. A minority of patients [N = 47; 8.8%] developed postoperative IASC. In total, 422 [78.9%] patients had one or more postoperative ileocolonoscopies, of whom 163 [38.6%] developed endoscopic POR. After adjusting for other risk factors for postoperative recurrence, postoperative IASC was associated with significantly greater odds (adjusted odds ratio [aOR]: 2.45 [1.23-4.97]; p = 0.01) and decreased time (adjusted hazards ratio [aHR]: 1.60 [1.04-2.45]; p = 0.03] to endoscopic POR. Furthermore, IASC was associated with increased risk (aOR: 2.3 [1.04-4.87] p = 0.03) and decreased survival-free time [aHR: 2.53 [1.31-4.87]; p = 0.006] for surgical recurrence. IASC is associated with an increased risk for endoscopic and surgical POR of Crohn's disease. Preoperative optimization to prevent IASC, in addition to postoperative biological prophylaxis, may help reduce the risk for endoscopic and surgical POR.

Sections du résumé

BACKGROUND BACKGROUND
Postoperative recurrence [POR] of Crohn's disease following ileocolonic resection is common. The impact of immediate postoperative intra-abdominal septic complications [IASC] on endoscopic and surgical recurrence has not been elucidated.
AIMS OBJECTIVE
To evaluate if IASC is associated with an increased risk for endoscopic and surgical POR.
METHODS METHODS
This was a retrospective study of adult Crohn's disease patients undergoing ileocolonic resection with primary anastomosis between 2009 and 2020. IASC was defined as anastomotic leak or intra-abdominal abscess within 90 days of the date of surgery. Multivariable logistic and Cox proportional hazard modelling were performed to assess the impact of IASC on endoscopic POR [modified Rutgeerts' score ≥ i2b] at index postoperative ileocolonoscopy and long-term surgical recurrence.
RESULTS RESULTS
In 535 Crohn's disease patients [median age 35 years, 22.1% active smokers, 35.7% one or more prior resection] had an ileocolonic resection with primary anastomosis. A minority of patients [N = 47; 8.8%] developed postoperative IASC. In total, 422 [78.9%] patients had one or more postoperative ileocolonoscopies, of whom 163 [38.6%] developed endoscopic POR. After adjusting for other risk factors for postoperative recurrence, postoperative IASC was associated with significantly greater odds (adjusted odds ratio [aOR]: 2.45 [1.23-4.97]; p = 0.01) and decreased time (adjusted hazards ratio [aHR]: 1.60 [1.04-2.45]; p = 0.03] to endoscopic POR. Furthermore, IASC was associated with increased risk (aOR: 2.3 [1.04-4.87] p = 0.03) and decreased survival-free time [aHR: 2.53 [1.31-4.87]; p = 0.006] for surgical recurrence.
CONCLUSION CONCLUSIONS
IASC is associated with an increased risk for endoscopic and surgical POR of Crohn's disease. Preoperative optimization to prevent IASC, in addition to postoperative biological prophylaxis, may help reduce the risk for endoscopic and surgical POR.

Identifiants

pubmed: 35705188
pii: 6608980
doi: 10.1093/ecco-jcc/jjac078
pmc: PMC9924045
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1696-1705

Subventions

Organisme : NIDDK NIH HHS
ID : K23 DK124570
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK123233
Pays : United States
Organisme : Cleveland Clinic Lerner Research Institute Research Program

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. All rights reserved. For permissions, please email: journals.permissions@oup.com.

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Auteurs

Salam P Bachour (SP)

Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH, USA.

Ravi S Shah (RS)

Cleveland Clinic Department of Gastroenterology, Hepatology, and Nutrition, Cleveland, OH, USA.

Florian Rieder (F)

Cleveland Clinic Department of Gastroenterology, Hepatology, and Nutrition, Cleveland, OH, USA.
Department of Inflammation and Immunity, Lerner Research Institute, Cleveland, OH, USA.

Taha Qazi (T)

Cleveland Clinic Department of Gastroenterology, Hepatology, and Nutrition, Cleveland, OH, USA.

Jean Paul Achkar (JP)

Cleveland Clinic Department of Gastroenterology, Hepatology, and Nutrition, Cleveland, OH, USA.

Jessica Philpott (J)

Cleveland Clinic Department of Gastroenterology, Hepatology, and Nutrition, Cleveland, OH, USA.

Bret Lashner (B)

Cleveland Clinic Department of Gastroenterology, Hepatology, and Nutrition, Cleveland, OH, USA.

Stefan D Holubar (SD)

Cleveland Clinic Department of Colorectal Surgery, Cleveland, OH, USA.

Amy L Lightner (AL)

Cleveland Clinic Department of Colorectal Surgery, Cleveland, OH, USA.

Edward L Barnes (EL)

University of North Carolina at Chapel Hill, Division of Gastroenterology and Hepatology, Chapel Hill, NC, USA.

Jordan Axelrad (J)

New York University Department of Gastroenterology and Hepatology, New York, NY, USA.

Miguel Regueiro (M)

Cleveland Clinic Department of Gastroenterology, Hepatology, and Nutrition, Cleveland, OH, USA.

Benjamin Click (B)

Cleveland Clinic Department of Gastroenterology, Hepatology, and Nutrition, Cleveland, OH, USA.

Benjamin L Cohen (BL)

Cleveland Clinic Department of Gastroenterology, Hepatology, and Nutrition, Cleveland, OH, USA.

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