Evidence map›Paper›PMID 42403498›Full record

ArticleJournal of the Association of Medical Microbiology and Infectious Disease Canada = Journal officiel de l'Association pour la microbiologie medicale et l'infectiologie Canada2026

Impact of direct from clinical sample sequencing assays for infectious diseases diagnostics: A single-centre retrospective cohort study.

Hugo Leprohon, Bouchra Tannir, Gisele Jolicoeur, Marc-Christian Domingo, Philippe J Dufresne, Philippe Morency-Potvin, Patrick Benoit, Simon Grandjean Lapierre

Abstract read
In one paragraph

Article in Journal of the Association of Medical Microbiology and Infectious Disease Canada = Journal officiel de l'Association pour la microbiologie medicale et l'infectiologie Canada, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Hugo LeprohonDepartment of Medicine, Université de Montréal, Montréal, Québec, Canada.
Bouchra TannirDepartment of Medicine, Université de Montréal, Montréal, Québec, Canada.
Gisele JolicoeurDepartment of Medicine, Université de Montréal, Montréal, Québec, Canada.
Marc-Christian DomingoInstitut National de Santé Publique du Québec, Laboratoire de Santé Publique du Québec (LSPQ), Montréal, Québec, Canada.
Philippe J DufresneInstitut National de Santé Publique du Québec, Laboratoire de Santé Publique du Québec (LSPQ), Montréal, Québec, Canada.
Philippe Morency-PotvinDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montréal, Québec, Canada.
Patrick BenoitDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montréal, Québec, Canada.
Simon Grandjean LapierreDepartment of Microbiology, Infectious Diseases and Immunology, Université de Montréal, Montréal, Québec, Canada.ORCID https://orcid.org/0000-0003-3646-1573

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The analytical performance of bacterial targeted sequencing (BTS), fungal targeted/panfungal sequencing (FTS), and metagenomic next-generation sequencing (mNGS) assays has been previously evaluated and their clinical use is increasing. Limited evidence is available on their true clinical impact on infectious disease diagnosis and treatment. Methods: We conducted a 3-year retrospective cohort study including all patients for whom broad-range sequencing assays were performed directly from clinical samples for the detection of bacterial and fungal pathogens. The operational characteristics, diagnostic and therapeutic impacts of the assays were assessed by reviewing patient clinical files and laboratory information system charts. Results: A total of 279 samples from 185 patients were included. The positivity rates for BTS, FTS, and mNGS were respectively 20.5% (47/229), 20% (9/45), and 20% (1/5). Of these 279 samples, 40 (14.3%) had an impact on patient management. The test results helped to establish a diagnosis in 26 (9.3%) cases and led to treatment modifications in 14 (5%). FTS achieved higher impact rates (26.7%) than both BTS (12.2%) and mNGS (0%). Short turnaround times increase impact rates, and the most impactful tests were those performed on bone and intervertebral disc samples, or in patients with negative culture results due to prior antibiotic administration. Conclusions: In this study, the overall diagnostic impact of BTS and FTS was high. Both the diagnostic and treatment impact of those assays can be increased if prescribed in well-selected clinical syndromes and performed on well-selected clinical samples.

Indexed as

direct sequencinginnovative diagnosticsmetagenomicsnext-generation sequencingrapid diagnostics

Identifiers

PMID42403498
PMCPMC13331621

What OpenQuestion holds

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Registered trials

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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.