Evidence map›Paper›PMID 40924239›Full record

ArticleInfection2026

Severe viral infections requiring intensive care unit admissions- aetiology, co-infections, respiratory interventions and outcomes.

M Brown, F Abeer, T Roe, R Beecham, O Arscott, B Eastwood, S Mahar, M Montague, D Neseam, P Patel and 9 more

Abstract read
In one paragraph

Article in Infection, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Challenges and opportunities in the management of severe pneumonia. Key concepts from the Seventh Annual Meeting of Spanish Experts 2025.Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia · 2026
    Review
  2. Review
  3. 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

19 authors.

M BrownGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
F AbeerGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
T RoeGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
R BeechamGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
O ArscottGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
B EastwoodGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
S MaharGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
M MontagueGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
D NeseamGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
P PatelGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
J SrinivasaGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
A GreenwellGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
K ThomasGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
D BrowningMicrobiology Department, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
E Wilson-DaviesSouthampton Specialist Virology Centre, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
A Conway MorrisDepartment of Medicine, Addenbrooke's Hospital, University Division of Anaesthesia, University of Cambridge, Hills Road, Cambridge, CB2 0QQ, UK.
Mpw GrocottGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
K SaeedGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK.
A DushianthanGeneral Intensive Care Unit, University Hospital Southampton NHS Foundation Trust, Tremona Road, Southampton, SO16 6YD, UK. a.dushianthan@soton.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSevere viral infections are common in patients requiring admission to intensive care units (ICU). Furthermore, these patients often have additional secondary or co-infections. Despite their prevalence, it remains uncertain to what extent those additional infections contribute to worse outcomes for patients with severe viral infections requiring ICU admission. This study aims to characterise severe viral infections requiring admission to intensive care, and describe their viral aetiology, the incidence of additional infections, and their clinical outcomes.

methodsThis retrospective single-centre cohort included consecutive adults admitted to the intensive care unit (ICU) with a positive polymerase chain reaction (PCR) test for viral infection from 2015 to 2024. Patients with SARS-CoV-2 were not included in this analysis. The data were retrieved from all available electronic databases. Patients were further stratified to compare severe viral infections alone to those with other microbiology confirmed co-infection (within 48 h of admission) and secondary infection (48 h after ICU admission).

resultsWe identified 222 with positive PCR for viral infection admitted to ICU. The majority were admitted with radiographic evidence of pneumonia (73.0%). Rhinovirus (28.4%), influenza A (18.5%), and RSV (16.2%) were the most common viral pathogens. Of the total, 149 patients had viral infection alone, 50 had co-infections, and 23 developed secondary infections. 30-day and ICU mortality were similar for viral alone, co-infection and secondary infection groups. Although those with secondary infection had a greater hospital and ICU length of stay, this was not reflected in the duration of mechanical ventilation or 30-day hospital mortality.

conclusionIn our large cohort of severe viral infections where Rhinovirus was the most common pathogen. This patient population constitute a high burden of respiratory support. The study also characterised 22.5% had co-infection, and 10% had subsequent secondary infection. While patients with secondary infections had prolonged ICU and hospital stay, the 30-day mortality was similar between all groups.

Indexed as

CoinfectionIntensive Care UnitsVirus DiseasesAdultAgedAged, 80 and overFemaleHospitalizationHumansLength of StayMaleMiddle AgedRetrospective StudiesTreatment OutcomeIntensive careMechanical ventilationPneumoniaViral infection

Identifiers

PMID40924239
PMCPMC12864227

What OpenQuestion holds

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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.