Anal ulcerations in Crohn's disease: Natural history in the era of biological therapy

Dig Liver Dis. 2017 Nov;49(11):1191-1195. doi: 10.1016/j.dld.2017.07.014. Epub 2017 Aug 4.

Abstract

Background: The natural history of anal ulcerations in Crohn's disease remains unknown.

Aims: To assess the long-term outcomes of anorectal ulcerations.

Methods: Data from consecutive patients with perineal Crohn's disease were prospectively recorded. The data of patients with anal ulceration were extracted.

Results: Anal ulcerations were observed in 154 of 282 patients (54.6%), and 77 cases involved cavitating ulcerations. The cumulative healing rates were 47%, 70% and 82% at 1, 2 and 3 years, respectively. Patients with a primary fistula phenotype had a shorter median time to healing of their anal ulceration (28 [13-83] weeks) than those with a stricture (81 [28-135] weeks) or those with isolated ulceration (74 [31-181] weeks) (p=0.004). Among patients with ulcerations but no fistula at referral (n=67), only 4 (6%) developed de novo abscesses and/or fistula during follow-up. There was no benefit associated with introducing or optimising biologics, nor with combining immunosuppressants and biologics.

Conclusion: Anal ulceration in Crohn's disease usually requires a long time to achieve sustained healing. Determining the impact of biologics on healing rates will require dedicated randomised trials although it does not show a significant healing benefit in the present study.

Keywords: Crohn’s disease; Fissure; Perianal Crohn’s disease; Ulceration.

MeSH terms

  • Adalimumab / therapeutic use
  • Adult
  • Constriction, Pathologic / etiology
  • Crohn Disease / complications*
  • Crohn Disease / drug therapy*
  • Crohn Disease / surgery
  • Female
  • Fissure in Ano / etiology*
  • Gastrointestinal Agents / therapeutic use
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Infliximab / therapeutic use
  • Male
  • Middle Aged
  • Phenotype
  • Rectal Fistula / etiology*
  • Rectal Fistula / surgery
  • Wound Healing

Substances

  • Gastrointestinal Agents
  • Immunosuppressive Agents
  • Infliximab
  • Adalimumab