Soonwook Hong1, Timothy A Zaki2, Michael Main3, Ashley M Hine4, Shannon Chang5, David Hudesman5, Jordan E Axelrad5. 1. Department of Medicine, NYU Langone Health, New York, New York, New York, USA. 2. Department of Medicine, UT Southwestern Medical Center, Dallas, Texas, USA. 3. Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA. 4. Department of Medicine, University of Connecticut School of Medicine, Farmington, Connecticut, USA. 5. Department of Gastroenterology, NYU Langone Health , New York, New York, USA.
Abstract
BACKGROUND: Differentiating between enteric infection and relapse of inflammatory bowel disease (IBD) is a common clinical challenge. Few studies have evaluated the impact of multiplex gastrointestinal polymerase chain reaction (GI PCR) pathogen panels on clinical practice compared to stool culture. Our aim was to compare the impact of PCR stool testing to conventional stool testing in outpatients presenting with relapse of IBD. METHODS: In a retrospective cohort study of outpatients with IBD presenting to NYU Langone Health with flare from September 2015 to April 2019, we compared patients who underwent stool testing with GI PCR to age-, sex-, and IBD-subtype-matched patients who underwent culture and ova and parasite exam (conventional testing). The primary outcome was IBD therapy escalation after testing. Secondary outcomes included rates of posttesting endoscopy, abdominal radiography, antibiotics, and IBD-related emergency department visits, hospitalizations, and abdominal surgeries. RESULTS: We identified 134 patients who underwent GI PCR matched to 134 patients who underwent conventional testing. Pathogens were more frequently identified on GI PCR (26 vs 5%; P < 0.01). We found that GI PCR was associated with less escalation in IBD therapy (16 vs 29%; P < 0.01) and fewer posttest endoscopies (10% vs 18%; P = 0.04), with no differences in IBD outcomes. On multivariate analysis, testing with GI PCR was associated with an odds ratio of 0.26 (95% confidence interval, 0.08-0.84; P = 0.02) for escalation of IBD therapies. CONCLUSIONS: Testing with GI PCR was associated with higher rates of pathogen detection and lower rates of IBD therapy escalation and endoscopy in the outpatient setting. These changes in management were not associated with a difference in IBD outcomes.
BACKGROUND: Differentiating between enteric infection and relapse of inflammatory bowel disease (IBD) is a common clinical challenge. Few studies have evaluated the impact of multiplex gastrointestinal polymerase chain reaction (GI PCR) pathogen panels on clinical practice compared to stool culture. Our aim was to compare the impact of PCR stool testing to conventional stool testing in outpatients presenting with relapse of IBD. METHODS: In a retrospective cohort study of outpatients with IBD presenting to NYU Langone Health with flare from September 2015 to April 2019, we compared patients who underwent stool testing with GI PCR to age-, sex-, and IBD-subtype-matched patients who underwent culture and ova and parasite exam (conventional testing). The primary outcome was IBD therapy escalation after testing. Secondary outcomes included rates of posttesting endoscopy, abdominal radiography, antibiotics, and IBD-related emergency department visits, hospitalizations, and abdominal surgeries. RESULTS: We identified 134 patients who underwent GI PCR matched to 134 patients who underwent conventional testing. Pathogens were more frequently identified on GI PCR (26 vs 5%; P < 0.01). We found that GI PCR was associated with less escalation in IBD therapy (16 vs 29%; P < 0.01) and fewer posttest endoscopies (10% vs 18%; P = 0.04), with no differences in IBD outcomes. On multivariate analysis, testing with GI PCR was associated with an odds ratio of 0.26 (95% confidence interval, 0.08-0.84; P = 0.02) for escalation of IBD therapies. CONCLUSIONS: Testing with GI PCR was associated with higher rates of pathogen detection and lower rates of IBD therapy escalation and endoscopy in the outpatient setting. These changes in management were not associated with a difference in IBD outcomes.
Authors: Joseph F Rodemann; Erik R Dubberke; Kimberly A Reske; Da Hea Seo; Christian D Stone Journal: Clin Gastroenterol Hepatol Date: 2007-03 Impact factor: 11.382
Authors: Jordan E Axelrad; Andrew Joelson; Peter H R Green; Garrett Lawlor; Simon Lichtiger; Ken Cadwell; Benjamin Lebwohl Journal: Am J Gastroenterol Date: 2018-08-03 Impact factor: 10.864
Authors: Waseem Ahmad; Nghia H Nguyen; Brigid S Boland; Parambir S Dulai; David T Pride; Daniel Bouland; William J Sandborn; Siddharth Singh Journal: Dig Dis Sci Date: 2018-10-25 Impact factor: 3.199
Authors: Julajak Limsrivilai; Zachary M Saleh; Laura A Johnson; Ryan W Stidham; Akbar K Waljee; Shail M Govani; Brian Gutermuth; Alexandra M Brown; Emily Briggs; Krishna Rao; Peter D R Higgins Journal: Dig Dis Sci Date: 2020-01-24 Impact factor: 3.199
Authors: Jordan E Axelrad; Andrew Joelson; Yael R Nobel; Garrett Lawlor; Peter H R Green; Simon Lichtiger; Benjamin Lebwohl Journal: Inflamm Bowel Dis Date: 2017-06 Impact factor: 7.290
Authors: Jordan E Axelrad; Ken H Cadwell; Jean-Frederic Colombel; Shailja C Shah Journal: Therap Adv Gastroenterol Date: 2021-03-31 Impact factor: 4.409