Standardisation of intestinal ultrasound scoring in clinical trials for luminal Crohn’s disease

Author:

Goodsall Thomas M.1,Jairath Vipul2ORCID,Feagan Brian G.2ORCID,Parker Claire E.2ORCID,Nguyen Tran M.2ORCID,Guizzetti Leonardo2,Asthana Anil K.3,Begun Jakob4,Christensen Britt3ORCID,Friedman Antony B.3ORCID,Kucharzik Torsten5,Lee Andrew4,Lewindon Peter J.4,Maaser Christian5,Novak Kerri L.6ORCID,Rimola Jordi7ORCID,Taylor Kirstin M.3,Taylor Stuart A.8,White Lauren S.4,Wilkens Rune9ORCID,Wilson Stephanie R.6,Wright Emily K.3,Bryant Robert V.1,Ma Christopher6ORCID

Affiliation:

1. Adelaide SA Australia

2. London ON Canada

3. Melbourne Vic. Australia

4. Brisbane Qld Australia

5. Lüneburg Germany

6. Calgary AB Canada

7. Barcelona Spain

8. London UK

9. Copenhagen Denmark

Abstract

SummaryBackgroundIntestinal ultrasound (IUS) is a valuable tool for assessment of Crohn’s disease (CD). However, there is no widely accepted luminal disease activity index.AimsTo identify appropriate IUS protocols, indices, items, and scoring methods for measurement of luminal CD activity and integration of IUS in CD clinical trials.MethodsAn expert international panel of adult and paediatric gastroenterologists (n = 15) and radiologists (n = 3) rated the appropriateness of 120 statements derived from literature review and expert opinion (scale of 1‐9) using modified RAND/UCLA methodology. Median panel scores of 1 to ≤3.5, >3.5 to <6.5 and ≥6.5 to 9 were considered inappropriate, uncertain and appropriate ratings respectively. The statement list and survey results were discussed prior to voting.ResultsA total of 91 statements were rated appropriate with agreement after two rounds of voting. Items considered appropriate measures of disease activity were bowel wall thickness (BWT), vascularity, stratification and mesenteric inflammatory fat. There was uncertainty if any of the existing IUS disease activity indices were appropriate for use in CD clinical trials. Appropriate trial applications for IUS included patient recruitment qualification when diseased segments cannot be adequately assessed by ileocolonoscopy and screening for exclusionary complications. At outcome assessment, remission endpoints including BWT and vascularity, with or without mesenteric inflammatory fat, were considered appropriate. Components of an ideal IUS disease activity index were identified based upon panel discussions.ConclusionsThe panel identified appropriate component items and applications of IUS for CD clinical trials. Empiric evidence, and development and validation of an IUS disease activity index are needed.

Publisher

Wiley

Subject

Pharmacology (medical),Gastroenterology,Hepatology

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