Predictability of simple endoscopic score for Crohn's disease for postoperative outcomes in Crohn's disease.


Journal

Journal of gastroenterology and hepatology
ISSN: 1440-1746
Titre abrégé: J Gastroenterol Hepatol
Pays: Australia
ID NLM: 8607909

Informations de publication

Date de publication:
Oct 2021
Historique:
revised: 21 04 2021
received: 06 03 2021
accepted: 07 05 2021
pubmed: 12 5 2021
medline: 11 2 2022
entrez: 11 5 2021
Statut: ppublish

Résumé

Approximately half of patients with Crohn's disease (CD) who have surgery will experience clinical recurrence within 10 years of their surgery. This study aimed to assess the postoperative outcomes according to disease location and validated the simple endoscopic score for CD (SES-CD) to predict disease-related outcomes. We retrospectively assessed medical records of CD patients who underwent ileocolonoscopy within 12 months after surgery at the University of Chicago between 2005 and 2016. We defined patients with postoperative colonic inflammation at the first postoperative ileocolonoscopy or had Montreal classification L2 as colon-dominant disease and patients without colonic involvement or who had L1 as small intestine (SI)-dominant disease. The outcomes included clinical and surgical recurrence. Among 207 CD patients, 51 (24.6%) and 156 (75.4%) patients had colon-dominant and SI-dominant disease, respectively. Patients with colon-dominant disease had a greater risk of postoperative clinical recurrence compared with those with SI-dominant disease (P = 0.018). Colon-dominant disease was a risk of earlier surgical recurrence compared with SI-dominant disease, although there were no significant differences in the recurrence-free survivals. SES-CD > 2 at the first postoperative ileocolonoscopy was a significant risk of clinical recurrence on log-rank test (P < 0.001) and Cox proportional hazards model (hazard ratio = 2.25; 95% confidence interval = 1.14-4.47; P = 0.020). An SES-CD of 1 was an appropriate cut-off to predict the clinical recurrence of SI-dominant disease, but a higher SES-CD cut-off value of 5 was required for colon-dominant disease. We demonstrated that SES-CD predicts postoperative clinical recurrence of CD, regardless of disease location.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
Approximately half of patients with Crohn's disease (CD) who have surgery will experience clinical recurrence within 10 years of their surgery. This study aimed to assess the postoperative outcomes according to disease location and validated the simple endoscopic score for CD (SES-CD) to predict disease-related outcomes.
METHODS METHODS
We retrospectively assessed medical records of CD patients who underwent ileocolonoscopy within 12 months after surgery at the University of Chicago between 2005 and 2016. We defined patients with postoperative colonic inflammation at the first postoperative ileocolonoscopy or had Montreal classification L2 as colon-dominant disease and patients without colonic involvement or who had L1 as small intestine (SI)-dominant disease. The outcomes included clinical and surgical recurrence.
RESULTS RESULTS
Among 207 CD patients, 51 (24.6%) and 156 (75.4%) patients had colon-dominant and SI-dominant disease, respectively. Patients with colon-dominant disease had a greater risk of postoperative clinical recurrence compared with those with SI-dominant disease (P = 0.018). Colon-dominant disease was a risk of earlier surgical recurrence compared with SI-dominant disease, although there were no significant differences in the recurrence-free survivals. SES-CD > 2 at the first postoperative ileocolonoscopy was a significant risk of clinical recurrence on log-rank test (P < 0.001) and Cox proportional hazards model (hazard ratio = 2.25; 95% confidence interval = 1.14-4.47; P = 0.020). An SES-CD of 1 was an appropriate cut-off to predict the clinical recurrence of SI-dominant disease, but a higher SES-CD cut-off value of 5 was required for colon-dominant disease.
CONCLUSIONS CONCLUSIONS
We demonstrated that SES-CD predicts postoperative clinical recurrence of CD, regardless of disease location.

Identifiants

pubmed: 33973282
doi: 10.1111/jgh.15540
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2785-2793

Informations de copyright

© 2021 Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

Références

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Auteurs

Shintaro Akiyama (S)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.

Akihiro Yamada (A)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
Section of Gastroenterology, Department of Internal Medicine, Toho University Sakura Medical Center, Chiba, Japan.

Jacob E Ollech (JE)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
Inflammatory Bowel Disease Center, Rabin Medical Center, Petah Tikva, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Yuga Komaki (Y)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.

Fukiko Komaki (F)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.

Joel Pekow (J)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.

Sushila R Dalal (SR)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.

Russell D Cohen (RD)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.

David T Rubin (DT)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.

Atsushi Sakuraba (A)

Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.

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