Publication

Coeliac disease screening is suboptimal in a tertiary gastroenterology setting

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Last modified
  • 05/23/2025
Type of Material
Authors
    Heba N. Iskandar, Emory UniversityDarrell M. Gray, Washington UniversityHongha Vu, Washington UniversityFaiz Mirza, Washington UniversityMary Katherine Rude, Washington UniversityKara Regan, Washington UniversityAdil Abdalla, Washington UniversitySrinivas Gaddam, Washington UniversitySami Almaskeen, Washington UniversityMichael Mello, Washington UniversityEvelyn Marquez, Washington UniversityClaire Meyer, Washington UniversityAhmed Bolkhir, Washington UniversityNavya Kanuri, Washington UniversityGregory Sayuk, Washington UniversityC Prakash Gyawali, Washington University
Language
  • English
Date
  • 2017-08-01
Publisher
  • BMJ Publishing Group
Publication Version
Copyright Statement
  • © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0032-5473
Volume
  • 93
Issue
  • 1102
Start Page
  • 472
End Page
  • 475
Grant/Funding Information
  • Funding HI: 5T32DK007130-36, UL1TR000448; GS: K23 DK084113.
Abstract
  • Background and aims Coeliac disease (CD) is widely prevalent in North America, but case-finding techniques currently used may not be adequate for patient identification. We aimed to determine the adequacy of CD screening in an academic gastroenterology (GI) practice. Methods Consecutive initial visits to a tertiary academic GI practice were surveyed over a 3-month period as a fellow-initiated quality improvement project. All electronic records were reviewed to look for indications for CD screening according to published guidelines. The timing of screening was noted (before or after referral), as well as the screening method (serology or biopsy). Data were analysed to compare CD screening practices across subspecialty clinics. Results 616 consecutive patients (49±0.6 years, range 16-87 years, 58.5% females, 94% Caucasian) fulfilled inclusion criteria. CD testing was indicated in 336 (54.5%), but performed in only 145 (43.2%). The need for CD screening was highest in luminal GI and inflammatory bowel disease clinics, followed by biliary and hepatology clinics (p<0.0001); CD screening rate was highest in the luminal GI clinic (p=0.002). Of 145 patients screened, 4 patients (2.4%) had serology consistent with CD, of which 2 were proven by duodenal biopsy. Using this proportion, an additional 5 patients might have been diagnosed in 191 untested patients with indications for CD screening. Conclusions More than 50% of patients in a tertiary GI clinic have indications for CD screening, but <50% of indicated cases are screened. Case-finding techniques therefore are suboptimal, constituting a gap in patient care and an important target for future quality improvement initiatives.
Author Notes
  • Correspondence to: Dr Heba Iskandar, Digestive Diseases Division, Department of Medicine, Emory University, 1365 Clifton Rd NE Bldg B, Atlanta, GA 30322, USA; heba.iskandar@emory.edu
Keywords
Research Categories
  • Health Sciences, General
  • Health Sciences, Medicine and Surgery

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