ReviewJGH open : an open access journal of gastroenterology and hepatology2026
Current
Review in JGH open : an open access journal of gastroenterology and hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Aims: Accurate diagnosis of Methods and Results: A narrative review was conducted using PubMed/MEDLINE, Embase, Web of Science, the Cochrane Library, and Google Scholar, prioritizing clinical guidelines, systematic reviews, diagnostic accuracy studies, multicenter validation studies, and directly relevant method-development research. Histology, rapid urease testing, and culture remain established biopsy-based methods, whereas urea breath testing and validated monoclonal stool antigen testing are the leading non-invasive options for detecting active infection and confirming eradication. Serology is useful only in selected settings because it cannot reliably distinguish current from previous infection. Culture provides phenotypic susceptibility results but is technically demanding. qPCR and targeted PCR provide faster, target-specific genotypic information, while next-generation sequencing may broaden resistance-variant detection in specialist or surveillance settings. Genotypic findings require antibiotic-specific interpretation because genotype-phenotype concordance varies. AI-assisted endoscopic interpretation, biosensors, LAMP, CRISPR-based assays, and string test-based sampling may address specific workflow gaps, but most remain adjunctive, selectively implemented, early translational, or investigational. Conclusion: Diagnostic selection should begin with the clinical question and integrate patient risk, treatment history, medication exposure, local resistance patterns, specimen access, laboratory capacity, turnaround time, and available resources. Wider adoption of newer technologies requires external validation, standardization, quality assurance, regulatory readiness, economic assessment, and evidence that results improve clinical management.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.