Evidence map›Paper›PMID 42228012›Full record

ArticleIntensive care medicine2026

Impact of appropriate antimicrobial therapy on patient outcomes and antimicrobial use: a sub analysis of the DIANA Study Dataset.

José Pedro Cidade, Pedro Póvoa, Pieter Depuydt, Sofie Dhaese, Ken De Smet, Alexis Tabah, Murat Akova, Menino Osbert Cotta, Gennaro De Pascale, George Dimopoulos and 16 more

Abstract read
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In one paragraph

Article in Intensive care medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Hour-1 Sepsis Bundle: Updated Evidence.Journal of clinical medicine · 2026
    Review
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

26 authors.

José Pedro CidadeIntensive Care Unit 4, Department of Intensive Care, São Francisco Xavier Hospital, ULSLO, Lisbon, Portugal.ORCID http://orcid.org/0000-0002-8359-5171
Pedro PóvoaIntensive Care Unit 4, Department of Intensive Care, São Francisco Xavier Hospital, ULSLO, Lisbon, Portugal.
Pieter DepuydtDepartment of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.
Sofie DhaeseDivision of Nephrology and Infectious Diseases, AZ Sint-Jan Brugge, Bruges, Belgium.
Ken De SmetDepartment of Emergency Medicine, Leuven University Hospitals, Leuven, Belgium.
Alexis TabahIntensive Care Unit, Redcliffe Hospital, Redcliffe, QLD, Australia.
Murat AkovaDepartment of Infectious Diseases and Clinical Microbiology, Hacettepe University School of Medicine, Ankara, Turkey.
Menino Osbert CottaUniversity of Queensland Centre of Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.
Gennaro De PascaleDipartimento di Scienza dell'Emergenza, Anestesiologiche e della Rianimazione - UOC di Anestesia, Rianimazione, Terapia Intensiva e Tossicologia Clinica - Istituto di Anestesia e Rianimazione, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
George DimopoulosDepartment of Critical Care, EVGENIDIO Hospital, Athens, Greece.
Shigeki FujitaniEmergency Medicine and Critical Care Medicine, St. Marianna University Hospital, Kawasaki, Kanagawa, Japan.
Jose Garnacho-MonteroIntensive Care Clinical Unit, Hospital Universitario Virgen del Rocío, Seville, Spain.
Marc LeoneAix-Marseille Universite, Assistance Publique Hopitaux de Marseille, Hopital Nord, Service d'Anesthesie et de Reanimation, Marseille, France.
Jeffrey LipmanFaculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.
Marlies OstermannDepartment of Critical Care, King's College London, Guy's and St Thomas' Hospital, London, UK.
José-Artur PaivaIntensive Care Department, Unidade Local de Saude Sao Joao EPE, Porto, Portugal.
Jeroen SchoutenDepartment of Intensive Care Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Fredrik SjövallDepartment of Intensive and Perioperative Care, Skane University Hospital, Malmo, Sweden.
Jean-François TimsitUniversite de Paris, Sorbonne Paris Cite, UMR 1137, IAME, Medical and Infectious Diseases Intensive Care Unit, AP-HP, Bichat-Claude Bernard Hospital, 75018, Paris, France.
Jason A RobertsUR-UM 103, University of Montpellier, Division of Anesthesia, Critical Care, Emergency and Pain Medicine, Nîmes University Hospital, Nîmes, France.
Jean Ralph ZaharPrevention du Risque Infectieux et Maitrise de l'Antibiothérapie Unit, GH Paris Seine Saint Denis, APHP, Bobigny, France.
Farid ZandShiraz Anesthesiology and Critical Care Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Kapil ZirpeGrant Medical Foundation, Ruby Hall Clinic, Pune, Maharashtra, India.
Jan J De WaeleDepartment of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium.
Liesbet De BusDepartment of Intensive Care Medicine, Ghent University Hospital, Ghent, Belgium. liesbet.debus@ugent.be.
DIANA Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAlthough inappropriate therapy has been consistently associated with adverse outcomes, the magnitude and consistency of the benefit associated with appropriate empiric therapy in critically ill patients remain uncertain. We aimed to quantify the prevalence of appropriate empiric antimicrobial therapy and evaluate its association with outcomes and antimicrobial exposure in a large international ICU cohort.

methodsThis predefined sub-analysis of the DIANA study included adult ICU patients receiving empirical antimicrobials for suspected or confirmed bacterial infection. Only patients with microbiologically confirmed infections were analyzed, and therapy was classified as appropriate if at least one agent demonstrated in vitro activity against the identified pathogen. Associations with 28-day mortality and antimicrobial-free days were assessed using multivariable logistic and Cox regression models. Pre-specified interaction analyses explored effect modification by disease severity and diagnostic certainty.

resultsOf 845 patients with microbiologically confirmed infections, 87.7% received appropriate empirical antimicrobial therapy. Compared with inappropriate therapy, appropriate therapy was associated with significantly lower ICU mortality and longer 28-day antimicrobial-free days and mechanical ventilation-free days. After multivariable adjustment, appropriate therapy remained independently associated with reduced 28-day mortality [adjusted odds ratio (OR) 1.83, 95% confidence interval 1.11-3.06, p = 0.02; hazard ratio (HR) 1.51, 95% CI 1.03-2.21, p = 0.035]. Effect-modification analyses demonstrated that the survival benefit of appropriate therapy was consistent across levels of diagnostic certainty and was most pronounced in patients with moderate illness severity (SOFA 3-9).

conclusionIn critically ill ICU patients, appropriate empirical antimicrobial therapy is independently associated with reduced 28-day mortality rates.

Indexed as

Anti-Bacterial AgentsAnti-Infective AgentsBacterial InfectionsAgedCritical IllnessFemaleHospital MortalityHumansIntensive Care UnitsMaleMiddle AgedAnti-Bacterial AgentsAnti-Infective AgentsAntibiotic appropriatenessAntimicrobial StewardshipIntensive careMDR-causing infectionsSepsis and infectionSeptic shock

Identifiers

PMID42228012

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.