Evidence map›Paper›PMID 37386603›Full record

ArticleJournal of anesthesia, analgesia and critical care2022

Epidemiology of ventilator-associated pneumonia in ICU COVID-19 patients: an alarming high rate of multidrug-resistant bacteria.

Nardi Tetaj, Alessandro Capone, Giulia Valeria Stazi, Maria Cristina Marini, Gabriele Garotto, Donatella Busso, Silvana Scarcia, Ilaria Caravella, Manuela Macchione, Giada De Angelis and 29 more

Abstract read
In one paragraph

Article in Journal of anesthesia, analgesia and critical care, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

39 authors.

Nardi TetajNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy. nardi.tetaj@inmi.it.ORCID http://orcid.org/0000-0002-2906-4855
Alessandro CaponeClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Giulia Valeria StaziNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Maria Cristina MariniNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Gabriele GarottoNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Donatella BussoNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Silvana ScarciaNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Ilaria CaravellaNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Manuela MacchioneNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Giada De AngelisNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Rachele Di LorenzoNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Alessandro CarucciNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Maria Vittoria AntonicaNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Ilaria GavianoNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Carlo InversiNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Elisabetta AgostiniNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Flaminia CanichellaNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Giorgia TaloniNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Francesca EvangelistaNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Ilaria OnnisNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Giulia MogaveroNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Maria Elena LamannaNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Dorotea RubinoNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Mattia Di FrischiaNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Candido PorcelliNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Elena CesiNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
Andrea AntinoriClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Fabrizio PalmieriClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Gianpiero D'OffiziClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Fabrizio TagliettiClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Carla NisiiClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Maria Adriana CataldoClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Stefania IannielloClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Paolo CampioniClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Francesco VaiaHealth Direction, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Emanuele NicastriClinical and Research Department of Infectious Diseases, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Enrico GirardiScientific Direction, National Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, 00149, Rome, Italy.
Luisa MarchioniNational Institute for Infectious Diseases IRCCS Lazzaro Spallanzani, Rome, Italy.
ICU COVID-19 Study Group

Funding

Ministero della Salute COVID-2020-12371675
6 · The paper itself

Abstract

backgroundCOVID‑19 is a novel cause of acute respiratory distress syndrome (ARDS) that leads patients to intensive care unit (ICU) admission requiring invasive ventilation, who consequently are at risk of developing of ventilator‑associated pneumonia (VAP). The aim of this study was to assess the incidence, antimicrobial resistance, risk factors, and outcome of VAP in ICU COVID-19 patients in invasive mechanical ventilation (MV).

methodsObservational prospective study including adult ICU admissions between January 1, 2021, and June 31, 2021, with confirmed COVID-19 diagnosis were recorded daily, including demographics, medical history, ICU clinical data, etiology of VAPs, and the outcome. The diagnosis of VAP was based on multi-criteria decision analysis which included a combination of radiological, clinical, and microbiological criteria in ICU patients in MV for at least 48 h.

resultsTwo hundred eighty-four COVID-19 patients in MV were admitted in ICU. Ninety-four patients (33%) had VAP during the ICU stay, of which 85 had a single episode of VAP and 9 multiple episodes. The median time of onset of VAP from intubation were 8 days (IQR, 5-13). The overall incidence of VAP was of 13.48 episodes per 1000 days in MV. The main etiological agent was Pseudomonas aeruginosa (39.8% of all VAPs) followed by Klebsiella spp. (16.5%); of them, 41.4% and 17.6% were carbapenem resistant, respectively. Patients during the mechanical ventilation in orotracheal intubation (OTI) had a higher incidence than those in tracheostomy, 16.46 and 9.8 episodes per 1000-MV day, respectively. An increased risk of VAP was reported in patients receiving blood transfusion (OR 2.13, 95% CI 1.26-3.59, p = 0.005) or therapy with Tocilizumab/Sarilumab (OR 2.08, 95% CI 1.12-3.84, p = 0.02). The pronation and PaO

conclusionsCOVID-19 patients have a higher incidence of VAP compared to the general ICU population, but it is similar to that of ICU ARDS patients in the pre-COVID-19 period. Interleukin-6 inhibitors and blood transfusions may increase the risk of VAP. The widespread use of empirical antibiotics in these patients should be avoided to reduce the selecting pressure on the growth of multidrug-resistant bacteria by implementing infection control measures and antimicrobial stewardship programs even before ICU admission.

Indexed as

Acute respiratory distress syndromeARDSCoronavirus disease 2019CorticosteroidCOVID-19Intensive care unitVentilator-associated pneumonia

Identifiers

PMID37386603
PMCPMC9389502

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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.