Intestinal ultrasound for monitoring therapeutic response in patients with ulcerative colitis: results from the TRUST&UC study.


Journal

Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R

Informations de publication

Date de publication:
09 2020
Historique:
received: 08 07 2019
revised: 05 12 2019
accepted: 10 12 2019
pubmed: 22 12 2019
medline: 7 4 2021
entrez: 22 12 2019
Statut: ppublish

Résumé

Prospective evaluation of intestinal ultrasound (IUS) for disease monitoring of patients with ulcerative colitis (UC) in routine medical practice. TRansabdominal Ultrasonography of the bowel in Subjects with IBD To monitor disease activity with UC (TRUST&UC) was a prospective, observational study at 42 German inflammatory bowel disease-specialised centres representing different care levels. Patients with a diagnosis of a proctosigmoiditis, left-sided colitis or pancolitis currently in clinical relapse (defined as Short Clinical Colitis Activity Index ≥5) were enrolled consecutively. Disease activity and vascularisation within the affected bowel wall areas were assessed by duplex/Colour Doppler ultrasonography. At baseline, 88.5% (n=224) of the patients had an increased bowel wall thickness (BWT) in the descending or sigmoid colon. Even within the first 2 weeks of the study, the percentage of patients with an increased BWT in the sigmoid or descending colon decreased significantly (sigmoid colon 89.3%-38.6%; descending colon 83.0%-42.9%; p<0.001 each) and remained low at week 6 and 12 (sigmoid colon 35.4% and 32.0%; descending colon 43.4% and 37.6%; p<0.001 each). Normalisation of BWT and clinical response after 12 weeks of treatment showed a high correlation (90.5% of patients with normalised BWT had symptomatic response vs 9.5% without symptomatic response; p<0.001). IUS may be preferred in general practice in a point-of-care setting for monitoring the disease course and for assessing short-term treatment response. Our findings give rise to the assumption that monitoring BWT alone has the potential to predict the therapeutic response, which has to be verified in future studies.

Identifiants

pubmed: 31862811
pii: gutjnl-2019-319451
doi: 10.1136/gutjnl-2019-319451
pmc: PMC7456734
doi:

Substances chimiques

Anti-Inflammatory Agents 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1629-1636

Investigateurs

Martin Faehndrich (M)
Martin Hoffstadt (M)
Stefan Schanz (S)
Klaus Fellermann (K)
Ulf Helwig (U)
Michael Karaus (M)
Henning Kempelmann (H)
Torsten Kucharzik (T)
Tanja Kuehbacher (T)
Diether Ludwig (D)
Andrea Pace (A)
Stefan Schreiber (S)
Carsten Buening (C)
Ulrich Graefe (U)
Harald Gruemmer (H)
Astrid Linde (A)
Stefan Schubert (S)
Martin Wetzel (M)
Ingrid Koenig (I)
Sven Pannach (S)
Ingolf Schiefke (I)
Jens Walldorf (J)
Olaf Engelke (O)
Susanne Erwig (S)
Barbara Lanyi (B)
Axel Naumann (A)
Ron Winograd (R)
Martin Dreier (M)
Theodor Kudlich (T)
Lars Langeloh (L)
Deike Strobel (D)
Dieter Witzemann (D)
Michael Boehmi (M)
Norbert Boerner (N)
Wolfgang Mohl (W)
Gero Moog (G)
Ursula Pohlmann (U)
Benjamin Simonis (B)
Hartmut Steinbrueck (H)
Gerd-Ruediger Franke (GR)
Johanna Vogelpohl (J)
Joachim Weber-Guskar (J)

Commentaires et corrections

Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: CM received honorary fees from AbbVie, Biogen, Celgene, Ferring, Falk Foundation, Janssen, MSD Sharp & Dome, Takeda Pharma and Vifor Pharma. UH received lecture and consulting fees from AbbVie, Celltrion, MSD, Ferring, Falk Foundation, Takeda, Mundipharma, Hospira, Pfizer, Amgen, Biogen, Shield, Janssen and Vifor Pharma. IF received consulting and honorary fees from AbbVie. AR, SR and DL are AbbVie employees, and may own AbbVie stock or options. TK received honorary fees from AbbVie, Biogen, Boehringer Ingelheim, Ferring, Hospira, Mundipharma, Falk Pharma GmbH, Janssen, MSD Sharp & Dome and Takeda Pharma.

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Auteurs

Christian Maaser (C)

Outpatients Department of Gastroenterology, IBD Center, Städtisches Klinikum Lüneburg gGmbH, Luneburg, Niedersachsen, Germany christian.maaser@klinikum-lueneburg.de.

Frauke Petersen (F)

Department of General Internal Medicine and Gastroenterology, University Teaching Hospital Lueneburg, Lueneburg, Germany.

Ulf Helwig (U)

Gastroenterology Practice, Oldenburg, Germany.

Imma Fischer (I)

Biostatistik - Tübingen, Tuebingen, Germany.

Alexander Roessler (A)

Medical Department, AbbVie Deutschland GmbH and Co KG, Wiesbaden, Hesse, Germany.

Stefan Rath (S)

Medical Department, AbbVie Deutschland GmbH and Co KG, Wiesbaden, Hesse, Germany.

Dorothee Lang (D)

Medical Department, AbbVie Deutschland GmbH and Co KG, Wiesbaden, Hesse, Germany.

Torsten Kucharzik (T)

Department of Gastroenterology, Stadtisches Klinikum Luneburg gGmbH, Luneburg, Germany.

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