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.2023 Nov;11(9):894-903.
doi: 10.1002/ueg2.12473. Epub 2023 Oct 18.

The use of non-invasive stool tests for verification of Helicobacter pylori eradication and clarithromycin resistance

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The use of non-invasive stool tests for verification of Helicobacter pylori eradication and clarithromycin resistance

Michiel C Mommersteeg et al. United European Gastroenterol J.2023 Nov.

Abstract

Background: Clarithromycin resistance of Helicobacter pylori (H. pylori) represents a major challenge in eradication therapy. In this study, we assessed if non-invasive stool tests can be used to verify successful H. pylori eradication and determine clarithromycin resistance.

Materials and methods: In this prospective study, patients undergoing urea breath testing (UBT) for confirmation of H. pylori eradication were asked to collect the stool as both a dry fecal sample and fecal immunochemical test (FIT). Stool H. pylori antigen testing (SAT) was performed on these samples and assessed for its accuracy in eradication verification. Type and duration of antibiotic treatment were retrospectively collected from patient records and compared with clarithromycin resistance determined by PCR of stool samples.

Results: H. pylori eradication information was available for a total of 145 patients (42.7% male, median age: 51.2). Successful eradication was achieved in 68.1% of patients. SAT on FIT samples had similar accuracy for eradication assessment compared to dry fecal samples, 72.1% [95% CI 61.4-81.2] versus 72.2% [95% CI 60.9-81.7]. Clarithromycin resistance rate was 13.4%.

Conclusion: H. pylori antigen testing on FIT stool samples to verify H. pylori eradication is feasible and has similar accuracy as H. pylori antigen testing on dry stool samples. Dry stool, but not FIT, was suitable for non-invasive identification of H. pylori clarithromycin resistance by rt-PCR personalizing antibiotic treatment strategies without the need for invasive diagnostics is desirable, as the cure rate of first-line empirical H. pylori treatment remains low.

Keywords: Faecal Immunochemical Test (FIT); H. pylori eradication therapy; Helicobacter pylori; antibiotic resistance; clarithromycin; gastric cancer; stool antigen test; urea breath test.

© 2023 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology.

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Conflict of interest statement

MCM declares that he has no conflicts of interest. SAVN declares that she has no conflict of interest. LMMW declares that she has no conflict of interest. BHCMR declares that she has no conflict of interest. AJV declares that she has no conflicts of interest. APV declares that she has no conflict of interest. MPP declares that he has no conflicts of interest. GMF declares that she has no conflict of interest. MJB has received research grants from Boston Scientific, grants and personal fees from Cook Medical, grants from Pentax Medical, grants from 3M, grants from Mylan, and grants from InterScope, outside the submitted work. EJK declares that he has no conflict of interest. MCWS has received grants from sysmex, sentinel, Medtronic, Boston Scientific, Norgine, outside the submitted work. The authors have no potential conflicts of interest to disclose that are relevant to this manuscript. Full disclosures have been submitted to the journal.

Figures

FIGURE 1
FIGURE 1
Flowchart of patient inclusion in this study. The HELI cohort comprises 182 individuals invited for UBT for either a primary diagnosis ofHelicobacter pylori (H. pylori) or eradication thereof. We retrieved electronic patient records onH. pylori eradication for 145 of these patients, 88 of whom underwent UBT for verification of treatment efficacy and had stool and/or FIT samples available for stool antigen measurements of these patients. For the detection of antibiotic resistance using rt‐PCR, stool samples were obtained from 97 patients with and withoutH. pylori infection from the original HELI cohort (including those with primary infections and those tested for eradication ofH. pylori infection). UBT, urease breath test.
FIGURE 2
FIGURE 2
Visual representation ofHelicobacter pylori eradication treatments received by study cohort and success rates thereof. PAC, PPI + Amoxicillin + Clarithromycin; PAL, PPI + Amoxicillin + Levofloxacin; PCM, PPI + clarithromycin + Metronidazole; PAM, PPI + Amoxicillin + Metronidazole; PLM, PPI + Levofloxacin + Metronidazole; PTM, PPI + Tetracyclin + Metronidazole; PCL, PPI + Clarithromycin + Levofloxacin; PBTM, PPI + Bismuth + Tetracyclin + Metronidazole; PA, PPI + Amoxicillin; PAT, PPI + Amoxicillin + Tetracyclin; PDL, PPI + Doxycyclin + Levofoxacin; PCT, PPI + Clarithromycin + Tetracyclin; PLM, PPI + Levofloxacin + Metronidazole; ?, unknown therapy.
FIGURE 3
FIGURE 3
A diagnostic and treatment scheme incorporating a possible place for the fecal antibiotic susceptibility PCR. PCR, polymerase chain reaction; SAT, stool antigen test; UBT, urease breath test; standard triple therapy, PPI + clarithromycin + amoxicillin for 10–14 days; Bismuth containing quadruple therapy, PPI + bismuth + tetracyclin + metronidazole for 14 days.
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