Impact of faecal calprotectin measurement on clinical decision-making in patients with Crohn's disease and ulcerative colitis

PLoS One. 2019 Oct 24;14(10):e0223893. doi: 10.1371/journal.pone.0223893. eCollection 2019.

Abstract

Background: Faecal calprotectin (FC) seems to be the best available biomarker for the detection of intestinal inflammation in patients with inflammatory bowel disease (IBD). The aim of this study is to clarify whether the measurement of FC has changed the number of ultrasound and endoscopic procedures, drug modifications, as well as FC re-measurements in IBD patients.

Methods: This retrospective study included 242 IBD patients with available FC values (case cohort) and 46 patients without an available FC value (control cohort). Clinical consequences such as carrying out abdominal ultrasound, endoscopy, drug modification or FC re-measurement at the next ambulatory presentation or during in-patient stay were collected. Statistical analysis was performed to determine the association between clinical decision-making and patient's characteristics, especially FC value.

Results: Overall, 192 (67%) clinical consequences were noted in both cohorts. In the case cohort 174 (91%) implications were noted compared to 18 (9%) in the control cohort (P < 0.001). In the case cohort, significantly more clinical consequences were detected in patients with Crohn's disease (CD) as well as in ulcerative colitis (UC) patients with a FC value > 250 mg/Kg than in patients with a value of ≤ 250 mg/Kg. In CD patients with high FC values significantly increased numbers of abdominal ultrasounds, endoscopies and FC re-measurements were noted. In UC patients with high FC values significantly increased numbers of abdominal ultrasounds, drug modifications and FC re-measurements were noted.

Conclusion: Measurement of FC may alter physician's clinical decision-making in IBD patients beside other clinical and diagnostic parameters. Further prospective and survey studies are warranted to evaluate the influence of FC measurement in the daily clinical decision-making.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / metabolism*
  • Case-Control Studies
  • Clinical Decision-Making*
  • Colitis, Ulcerative / diagnosis*
  • Colitis, Ulcerative / metabolism
  • Crohn Disease / diagnosis*
  • Crohn Disease / metabolism
  • Diagnostic Tests, Routine / methods*
  • Feces / chemistry*
  • Female
  • Humans
  • Leukocyte L1 Antigen Complex / metabolism*
  • Male
  • Middle Aged
  • Prognosis
  • Retrospective Studies
  • Severity of Illness Index

Substances

  • Biomarkers
  • Leukocyte L1 Antigen Complex

Grants and funding

We acknowledge support by the Open Access Publication Funds of the Göttingen University and the German Council Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.