Evidence map›Paper›PMID 24428878›Full record

ArticleCritical care (London, England)2014

Pseudomonas aeruginosa serotypes in nosocomial pneumonia: prevalence and clinical outcomes.

Qin Lu, Philippe Eggimann, Charles-Edouard Luyt, Michel Wolff, Michael Tamm, Bruno François, Emmanuelle Mercier, Jorge Garbino, Pierre-François Laterre, Holger Koch and 7 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Critical care (London, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.7field-weighted citation impact, top 7% of its field
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

44 citing papers in PubMed, 86 citations in OpenAlex.

  1. Assessment of panobacumab as adjunctive immunotherapy for the treatment of nosocomial Pseudomonas aeruginosa pneumonia.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2014
    Trial
  2. Applicability of Nanopore-only whole-genome sequencing forJournal of clinical microbiology · 2026
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  11. Comprehensive Genomic Analysis ofAntibiotics (Basel, Switzerland) · 2025
    Article
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  20. Outbreak ofAntibiotics (Basel, Switzerland) · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 10 institutions in 3 countries.

Qin Lu
Philippe Eggimann
Charles-Edouard Luyt
Michel Wolff
Michael Tamm
Bruno François
Emmanuelle Mercier
Jorge Garbino
Pierre-François Laterre
Holger Koch
Verena Gafner
Michael P Rudolf
Erkan Mus
Antonio Perez
Hedvika Lazar
Jean Chastre
Jean-Jacques Rouby
Biognosys (Switzerland) · CHAssistance Publique – Hôpitaux de Paris · FRSorbonne Université · FRBretonneau Hospital · FRCliniques Universitaires Saint-Luc · BEHôpital Bichat-Claude-Bernard · FRHôpital Dupuytren · FRUniversity Hospital of Basel · CHUniversity Hospital of Geneva · CHUniversity Hospital of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPseudomonas aeruginosa frequently causes nosocomial pneumonia and is associated with poor outcome. The purpose of this study was to assess the prevalence and clinical outcome of nosocomial pneumonia caused by serotype-specific P. aeruginosa in critically ill patients under appropriate antimicrobial therapy management.

methodsA retrospective, non-interventional epidemiological multicenter cohort study involving 143 patients with confirmed nosocomial pneumonia caused by P. aeruginosa. Patients were analyzed for a period of 30 days from time of nosocomial pneumonia onset. Fourteen patients fulfilling the same criteria from a phase IIa studyconducted at the same time/centers were included in the prevalence calculations but not in the clinical outcome analysis.

resultsThe prevalence of serotypes was: O6 (29%), O11 (23%), O10 (10%), O2 (9%), and O1 (8%). Serotypes with a prevalence of less than 5% were found in 13% of patients, 8% were classified as not typeable. Across all serotypes, 19% mortality, 70% clinical resolution, 11% clinical continuation, and 5% clinical recurrence were recorded. Age and higher APACHE II (Acute Physiology and Chronic Health Evaluation II) were predictive risk factors associated with probability of death and lower clinical resolution for P. aeruginosa nosocomial pneumonia. Mortality tends to be higher with O1 (40%) and lower with O2 (0%); clinical resolution tends to be better with O2 (82%) compared to other serotypes. Persisting pneumonia with O6 and O11 was, respectively, 8% and 21%; clinical resolution with O6 and O11 was, respectively, 75% and 57%.

conclusionsIn P. aeruginosa nosocomial pneumonia, the most prevalent serotypes were O6 and O11. Further studies including larger group sizes are needed to correlate clinical outcome with virulence factors of P. aeruginosa in patients with nosocomial pneumonia caused by various serotypes; and to compare O6 and O11, the two serotypes most frequently encountered in critically ill patients.

Indexed as

AdultAgedCohort StudiesCross InfectionFemaleHumansMaleMiddle AgedPneumonia, BacterialPrevalencePseudomonas aeruginosaPseudomonas InfectionsRetrospective StudiesTreatment Outcome

Identifiers

PMID24428878
PMCPMC4057348
OpenAlexW2152250670

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.