Evidence map›Paper›PMID 41494027›Full record

ArticlePloS one2026

Aetiology and impact of bacterial bloodstream infections in mechanically ventilated COVID-19 patients: A prospective Swedish multicenter cohort study.

Isak Olsson, Anna C Nilsson, Ingrid Didriksson, Attila Frigyesi, Hans Friberg, Anton Reepalu, Martin Spångfors

Abstract readMulticenter Study
In one paragraph

Article in PloS one, 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
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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

7 authors.

Isak OlssonDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.ORCID https://orcid.org/0009-0005-7955-4640
Anna C NilssonDepartment of Infectious Diseases, Skåne University Hospital, Malmö, Sweden.
Ingrid DidrikssonDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.
Attila FrigyesiDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.
Hans FribergDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.
Anton ReepaluDepartment of Infectious Diseases, Skåne University Hospital, Malmö, Sweden.ORCID https://orcid.org/0000-0003-1690-8921
Martin SpångforsDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, Lund, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCritically ill COVID-19 patients admitted to the intensive care unit (ICU) are at an increased risk of acquiring bacterial bloodstream infections (BSI). We aimed to describe patient characteristics, risk factors, and the microbiological spectrum in blood cultures and evaluate the impact of ICU-acquired BSI on outcomes in a Nordic setting.

methodsA prospective multicenter cohort study was conducted on adult invasively mechanically ventilated (IMV) COVID-19 patients. The primary aim was to identify the proportion of ICU-acquired BSI and its aetiology. Secondary outcomes were duration of IMV, length of stay (LOS), and mortality for individuals with and without BSI, respectively. Logistic regression was used to identify potential predictors of ICU-acquired BSI. Predictors were assessed by calculating an Area Under the Receiver Operating Characteristics (AUROC) curve.

resultsOf 354 included patients, 17% had an ICU-acquired BSI. Staphylococcus aureus was the most common pathogen. Patients with BSI had a longer duration of IMV (20 days versus 9 days, p < 0.001), longer ICU-LOS (24 days versus 11 days, p < 0.001), and hospital-LOS (38 days versus 24 days, p < 0.001). A BSI was associated with increased mortality; odds ratio (OR) 3.21, 95% CI: 1.61-6.38, p < 0.001. Adjusted analyses showed that higher BMI; OR 1.06, 95% CI: 1.01-1.11, p = 0.014, diabetes mellitus with organ complications; OR 2.66, 95% CI: 1.33-5.29, p = 0.005, and number of symptomatic days before ICU admission; OR 1.04, 95% CI: 1.01-1.07, p = 0.008, were associated with a BSI. The AUROC was 0.66 (95% CI: 0.58-0.74).

conclusionICU-acquired BSIs were found in 17% of critically ill COVID-19 patients and were associated with a longer duration of IMV and LOS as well as increased mortality. Staphylococcus aureus was the dominating pathogen. We found several factors associated with ICU-acquired BSIs at ICU admission. However, their ability to predict BSIs was poor.

Indexed as

BacteremiaCOVID-19Cross InfectionRespiration, ArtificialAgedCritical IllnessFemaleHumansIntensive Care UnitsLength of StayMaleMiddle AgedProspective StudiesRisk FactorsSARS-CoV-2Staphylococcus aureus

Identifiers

PMID41494027
PMCPMC12774336

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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.