Evidence map›Paper›PMID 40026774›Full record

ArticleAntimicrobial stewardship & healthcare epidemiology : ASHE2025

Jean Stanciu, Patrick Dolcé, Charles Frenette, Marie-Claude Roy, Lina Kouider, Yves Longtin

Abstract read
In one paragraph

Article in Antimicrobial stewardship & healthcare epidemiology : ASHE, 2025. 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

6 authors.

Jean StanciuMedical Microbiology and Infectious Diseases, Centre Intégré de Santé et de Services Sociaux du Bas-Saint-Laurent, Rimouski, QC, Canada.ORCID https://orcid.org/0009-0006-1595-8651
Patrick DolcéMedical Microbiology and Infectious Diseases, Centre Intégré de Santé et de Services Sociaux du Bas-Saint-Laurent, Rimouski, QC, Canada.
Charles FrenetteMedical Microbiology and Infectious Diseases, McGill University Health Centre, Montreal, QC, Canada.ORCID https://orcid.org/0000-0002-8996-0766
Marie-Claude RoyMedical Microbiology and Infectious Diseases, CHU de Québec-Université Laval, Quebec City, QC, Canada.ORCID https://orcid.org/0000-0002-5756-7193
Lina KouiderMedical Microbiology and Infectious Diseases, Centre Intégré de Santé et de Services Sociaux du Bas-Saint-Laurent, Rimouski, QC, Canada.
Yves LongtinMedical Microbiology and Infectious Diseases, Infection Prevention and Control Unit, Jewish General Hospital, Montreal, QC, Canada.ORCID https://orcid.org/0000-0002-4532-379X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To develop and validate an automated surveillance system for healthcare-associated Design: Multicenter cohort study. Setting: 16 acute care hospitals. Patients: Patients admitted to participating hospitals between 2013 and 2022. Methods: An automated surveillance system was developed with retrospective extraction from admission/discharge/transfer and laboratory databases and compared with conventional surveillance based on clinical definitions collected prospectively by infection control professionals. Comparison of HA-CDI incidence rates calculated by automated vs conventional surveillances were performed with χ Results: Overall, conventional surveillance reported 3,211 cases of HA-CDI for an incidence rate of 4.94 per 10,000 patient-days. Automated surveillance detected 4,708 cases, for an incidence rate of 7.24 per 10,000 patient-days (incidence rate ratio, 1.47; 95% CI, 1.40-1.53). Full concordance between both surveillance methods was observed in 62% of cases, while 34% of cases were detected only by automated surveillance, and 4% were detected by conventional surveillance only. Between 2013 and 2022, an identical declining trend in HA-CDI incidence rates of -0.54 cases per 10,000 patient-days was observed with both surveillance methods. A subset of 49 cases detected only by automated surveillance were reviewed; the main reasons for discrepancy were delayed testing (39%), colonization (24%), misclassifications (14%), and interinstitutional transfers (12%). Conclusions: HA-CDI incidence rates calculated by automated surveillance were higher than those of conventional surveillance, but the overestimation was consistent over time, suggesting that a correction factor could improve precision.

Identifiers

PMID40026774
PMCPMC11869069

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Registered trials

None linked

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.