Evidence map›Paper›PMID 37508292›Full record

ArticleAntibiotics (Basel, Switzerland)2023

Clinical and Microbiological Outcomes and Follow-Up of Secondary Bacterial and Fungal Infections among Critically Ill COVID-19 Adult Patients Treated with and without Immunomodulation: A Prospective Cohort Study.

Bálint Gergely Szabó, Eszter Czél, Imola Nagy, Dorina Korózs, Borisz Petrik, Bence Marosi, Zsófia Gáspár, Martin Rajmon, Márk Di Giovanni, István Vályi-Nagy and 3 more

Abstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2023. 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. Article
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

13 authors.

Bálint Gergely SzabóDivision of Infectology, Department of Haematology and Internal Medicine, Semmelweis University, Albert Florian ut 5-7, H-1097 Budapest, Hungary.
Eszter CzélSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Albert Florian ut 5-7, H-1097 Budapest, Hungary.
Imola NagyFaculty of Medicine, Semmelweis University, Ulloi ut 26, H-1085 Budapest, Hungary.ORCID 0000-0002-1616-0776
Dorina KorózsSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Albert Florian ut 5-7, H-1097 Budapest, Hungary.
Borisz PetrikSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Albert Florian ut 5-7, H-1097 Budapest, Hungary.
Bence MarosiSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Albert Florian ut 5-7, H-1097 Budapest, Hungary.
Zsófia GáspárDoctoral School of Clinical Medicine, Semmelweis University, Ulloi ut 26, H-1085 Budapest, Hungary.
Martin RajmonFaculty of Medicine, Semmelweis University, Ulloi ut 26, H-1085 Budapest, Hungary.
Márk Di GiovanniFaculty of Medicine, Semmelweis University, Ulloi ut 26, H-1085 Budapest, Hungary.
István Vályi-NagySouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Albert Florian ut 5-7, H-1097 Budapest, Hungary.
János SinkóDivision of Infectology, Department of Haematology and Internal Medicine, Semmelweis University, Albert Florian ut 5-7, H-1097 Budapest, Hungary.
Botond LakatosDivision of Infectology, Department of Haematology and Internal Medicine, Semmelweis University, Albert Florian ut 5-7, H-1097 Budapest, Hungary.
Ilona BobekSouth Pest Central Hospital, National Institute of Hematology and Infectious Diseases, Albert Florian ut 5-7, H-1097 Budapest, Hungary.

Funding

Excellence Program of the National Research, Development and Innovation Office Tématerületi Kiválósági Program TKP2021-EGA-08"Investment in the Future" Fund Befektetés a Jövőbe Alap 2020-1.1.6-JÖVŐ-2021-00011Ministry of Human Capacities, Human Resource Support Operator of Hungary NTP-NFTÖ-21-B-0338Ministry of Innovation and Technology of Hungary ÚNKP-19-3-I-SE-74Semmelweis University EFOP-3.6.3-VEKOP-16-2017-00009
6 · The paper itself

Abstract

backgroundNearly 10% of COVID-19 cases will require admission to the intensive care unit (ICU). Our aim was to assess the clinical and microbiological outcomes of secondary infections among critically ill COVID-19 adult patients treated with/without immunomodulation.

methodsA prospective observational cohort study was performed between 2020 and 2022 at a single ICU. The diagnosis and severity classification were established by the ECDC and WHO criteria, respectively. Eligible patients were included consecutively at admission, and followed for +30 days post-inclusion. Bloodstream-infections (BSIs), ventilator-associated bacterial pneumonia (VAP), and COVID-19-associated invasive pulmonary aspergillosis (CAPA) were defined according to international guidelines. Patient stratification was performed by immunomodulatory therapy administration (dexamethasone, tocilizumab, baricitinib/ruxolitinib). The primary outcome was any microbiologically confirmed major infectious complication, secondary outcomes were invasive mechanical ventilation (IMV) requirement and all-cause mortality.

resultsAltogether, 379 adults were included. At baseline, 249/379 (65.7%) required IMV and 196/379 (51.7%) had a cytokine storm. At +30 days post-inclusion, the rate of any microbiologically confirmed major infectious complication was 151/379 (39.8%), IMV requirement and all-cause mortality were 303/379 (79.9%) and 203/379 (53.6%), respectively. There were no statistically significant outcome differences after stratification. BSI, VAP, and CAPA episodes were mostly caused by

conclusionsSecondary infections among critically ill COVID-19 adult patients represent a relevant burden, probably irrespective of immunomodulatory treatment.

Indexed as

bloodstream infectionBSICAPAcoronavirus disease 2019COVID-19COVID-19-associated pulmonary aspergillosiscritically illimmunomodulationintensive care unitnosocomial infectionSARS-CoV-2severe acute respiratory syndrome coronavirus 2VAPventilatory-associated pneumonia

Identifiers

PMID37508292
PMCPMC10376198

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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.