Evidence map›Paper›PMID 41144391›Full record

ArticlePloS one2025

Cytomegalovirus reactivation in mechanically ventilated patients with or without SARS-CoV-2 infection: A retrospective cohort study.

Octave Cannac, Vanessa Pauly, Christine Zandotti, Léa Luciani, Paul-Rémi Petit, Xavier de Lamballerie, Rémi Charrel, Laurent Papazian, Damien Barrau, Geoffray Agard and 1 more

Abstract read
In one paragraph

Article in PloS one, 2025. 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. 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

11 authors.

Octave CannacService de Médecine Intensive Réanimation, APHM, Hôpital Nord, Marseille, France.
Vanessa PaulyAix Marseille University, School of Medicine - La Timone Medical Campus, EA 3279, CEReSS - Health Services Research and Quality of life Center, Marseille, France.
Christine ZandottiUnité des Virus Émergents (UVE), Aix-Marseille Univ-IRD 190-Inserm 1207, Marseille, France.
Léa LucianiUnité des Virus Émergents (UVE), Aix-Marseille Univ-IRD 190-Inserm 1207, Marseille, France.
Paul-Rémi PetitUnité des Virus Émergents (UVE), Aix-Marseille Univ-IRD 190-Inserm 1207, Marseille, France.
Xavier de LamballerieUnité des Virus Émergents (UVE), Aix-Marseille Univ-IRD 190-Inserm 1207, Marseille, France.
Rémi CharrelUnité des Virus Émergents (UVE), Aix-Marseille Univ-IRD 190-Inserm 1207, Marseille, France.
Laurent PapazianAix-Marseille Université, Faculté de Médecine, Centre d'Études et de Recherches sur les Services de Santé et qualité de vie EA 3279, Marseille, France.
Damien BarrauService de Médecine Intensive Réanimation, APHM, Hôpital Nord, Marseille, France.ORCID https://orcid.org/0009-0007-8661-0094
Geoffray AgardService de Médecine Intensive Réanimation, APHM, Hôpital Nord, Marseille, France.ORCID https://orcid.org/0000-0002-5095-6268
Sami HraiechService de Médecine Intensive Réanimation, APHM, Hôpital Nord, Marseille, France.ORCID https://orcid.org/0000-0003-4652-1664

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundData comparing the incidence, risk factors and outcomes of cytomegalovirus (CMV) reactivation in SARS-CoV-2 positive and negative patients remain controversial.

designA retrospective cohort study in a tertiary center. PATIENTS: Patients admitted to the intensive care unit between December 2019 and May 2021, under invasive mechanical ventilation for 4 days or more and screened for CMV reactivation were included. MEASUREMENTS: The primary outcome was the incidence of CMV reactivation in SARS-CoV-2 negative and positive patients. Secondary outcomes included risk factors for CMV reactivation in both populations and survival analysis according to CMV reactivation in SARS-CoV-2 negative and positive patients.

resultsCMV reactivation occurred in 34.7% (n = 51/147) of SARS-CoV-2 negative patients and in 45.4% (83/183) of SARS-CoV-2 positive patients (p = 0.08). When considering competing factors, SARS-CoV-2 infection was not associated with CMV reactivation (sub-hazard ratio (SHR) = 1.01 [0.68-1.49], p = 0.98). Treatment with methylprednisolone was significantly associated with CMV reactivation in the unadjusted and adjusted analysis (SHR 2.81 [2.01-3.93] p < 0.001; SHR 2.84 [1.94-4.15] p < 0.001 respectively). Patients combining SARS-CoV-2 infection and CMV reactivation had a significantly higher all-cause mortality. Among patients presenting a CMV reactivation, the administration of ganciclovir was a protective factor for day-60 mortality (HR = 0.4; [0.22-0.74] p = 0.004).

conclusionIn this large retrospective cohort, CMV reactivation was not significantly associated with SARS-CoV-2 infection in patients undergoing invasive mechanical ventilation for at least 4 days. The major risk factor for CMV reactivation was treatment with methylprednisolone. The combination of CMV reactivation with SARS-CoV-2 infection was associated with a higher mortality whereas ganciclovir treatment reduced mortality.

Indexed as

COVID-19CytomegalovirusCytomegalovirus InfectionsRespiration, ArtificialVirus ActivationAgedFemaleHumansIntensive Care UnitsMaleMethylprednisoloneMiddle AgedRetrospective StudiesRisk FactorsSARS-CoV-2Methylprednisolone

Identifiers

PMID41144391
PMCPMC12558532

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.