Tight control using fecal calprotectin and early disease intervention increase the rates of transmural remission in Crohn's disease

Author:

Fernandes Samuel Raimundo123ORCID,Bernardo Sónia13,Saraiva Sofia13ORCID,Gonçalves Ana Rita13,Moura Santos Paula13,Valente Ana1,Correia Luís Araújo123,Cortez‐Pinto Helena12ORCID,Magro Fernando34ORCID

Affiliation:

1. Serviço de Gastrenterologia e Hepatologia Hospital Santa Maria Centro Hospitalar Universitário Lisboa Norte EPE Lisboa Portugal

2. Clínica Universitária de Gastrenterologia. Faculdade de Medicina, Universidade de Lisboa Lisboa Portugal

3. Portuguese Group of Studies in Inflammatory Bowel Disease Gedii Porto Portugal

4. CINTESIS@RISE Department of Biomedicine Faculty of Medicine of the University of Porto Porto Portugal

Abstract

AbstractBackgroundIncreasing evidence supports the use of transmural remission as a treatment target in Crohn's disease (CD), but it is seldom achieved in clinical practice. Tight monitoring of inflammation using fecal calprotectin with reactive treatment escalation may potentially improve these results.AimsTo evaluate if treatment escalation based on fecal calprotectin can improve the rates of transmural remission in CD. The influence of the timing of intervention on this strategy was also evaluated.MethodsRetrospective cohort study including 256 CD patients with 2 consecutive assessments by MRI‐enterography and colonoscopy and with regular monitoring using fecal calprotectin. For each occurrence of an elevated fecal calprotectin (≥250 μg/g), we evaluated whether a reactive adjustment of medical treatment was performed. The ratio of treatment escalation/elevated fecal calprotectin was correlated with the chances of reaching transmural remission. Early disease was defined as disease duration <18 months without previous exposure to immunomodulators and biologics.ResultsAfter a median follow‐up of 2 years (IQR 1–4), 61 patients (23.8%) reached transmural remission. Ratios of escalation ≥50% resulted in higher rates of transmural remission (34.2% vs. 15.1%, p < 0.001). The effect was more pronounced in patients with early disease (50.0% vs. 12.0%, p = 0.003). In multivariate analysis, a treatment escalation ratio ≥50% (OR 3.46, 95% CI 1.67–7.17, p = 0.001) and early disease intervention (OR 3.24, 95% CI 1.12–9.34, p = 0.030) were independent predictors of achieving transmural remission.ConclusionTight‐monitoring and reactive treatment escalation increase the rates of transmural remission in CD. Intervention in early disease further improves these results.

Publisher

Wiley

Subject

Gastroenterology,Oncology

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