Combined strategies following surgical drainage for perianal fistulizing Crohn's disease: failure rates and prognostic factors.


Journal

Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland
ISSN: 1463-1318
Titre abrégé: Colorectal Dis
Pays: England
ID NLM: 100883611

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 21 12 2019
accepted: 21 06 2020
pubmed: 9 7 2020
medline: 19 8 2021
entrez: 9 7 2020
Statut: ppublish

Résumé

The medico-surgical strategy for the treatment of perianal fistulizing Crohn's disease (CD) following surgical drainage remains challenging and debated. Our aims were to describe the failure rate of therapeutic interventions after drainage of the fistula tract and determine the factors associated with failure to optimize medico-surgical strategies. All consecutive patients with perianal fistulizing CD who underwent surgical drainage with at least a 12-week follow-up were included. Failure was defined as the occurrence of at least one of the following items: abscess recurrence, purulent discharge from the tract, visible external opening and further drainage procedure(s). One hundred and sixty-nine patients were included. The median follow-up was 4.0 years. The cumulative failure rates were 20%, 30% and 36% at 1, 3 and 5 years, respectively. The cumulative failure rates in patients who had sphincter-sparing surgeries or seton removal were significantly higher than in those who had a fistulotomy. Anterior fistula [hazard ratio (HR) = 2.52 (1.13-5.61), P = 0.024], supralevator extension [HR = 20.78 (3.38-127.80), P = 0.001] and the absence or discontinuation of immunosuppressants after anal drainage [HR = 3.74 (1.11-12.5), P = 0.032] were significantly associated with failure in the multivariate analysis model. Combined strategies for perianal fistulizing CD lead to a failure rate of 36% at 5 years. Where advisable, fistulotomy may be preferred because it has a lower rate of recurrence. The benefits of immunosuppressants require a dedicated prospective randomized trial.

Identifiants

pubmed: 32640112
doi: 10.1111/codi.15241
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

159-168

Subventions

Organisme : MSD Life Science Foundation, Public Interest Incorporated Foundation
Organisme : Takeda Pharmaceutical Company

Informations de copyright

© 2020 Association of Coloproctology of Great Britain and Ireland.

Références

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Auteurs

A Herissay (A)

CHU Rennes, Universitaire Rennes, Rennes, France.

L Siproudhis (L)

INSERM, CIC1414, Institut NUMECAN (Nutrition Metabolism and Cancer), CHU Rennes, Universitaire Rennes, Rennes, France.

E Le Balc'h (E)

CHU Rennes, Universitaire Rennes, Rennes, France.

M Dewitte (M)

CHU Rennes, Universitaire Rennes, Rennes, France.

T Wallenhorst (T)

CHU Rennes, Universitaire Rennes, Rennes, France.

G Bouguen (G)

INSERM, CIC1414, Institut NUMECAN (Nutrition Metabolism and Cancer), CHU Rennes, Universitaire Rennes, Rennes, France.

C Brochard (C)

INSERM, CIC1414, Institut NUMECAN (Nutrition Metabolism and Cancer), CHU Rennes, Universitaire Rennes, Rennes, France.

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