Evidence map›Paper›PMID 22080633›Full record

ArticleCritical care medicine2012

Clinical outcomes of type III Pseudomonas aeruginosa bacteremia.

Ali A El-Solh, Angela Hattemer, Alan R Hauser, Ahmad Alhajhusain, Hardik Vora

Abstract read
In one paragraph

Article in Critical care medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

74 citing papers in PubMed, 118 citations in OpenAlex.

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  11. ThePathogens (Basel, Switzerland) · 2024
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  14. Review
  15. Age of Antibiotic Resistance in MDR/XDR Clinical Pathogen ofPharmaceuticals (Basel, Switzerland) · 2023
    Review
  16. Review
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  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Ali A El-SolhVeterans Affairs Western New York Healthcare System, Western New York Respiratory Research Center, Division of Pulmonary, Critical Care, and Sleep Medicine, Buffalo, NY, USA. solh@buffalo.edu
Angela Hattemer
Alan R Hauser
Ahmad Alhajhusain
Hardik Vora
Bipar · FRVA Western New York Healthcare System · US

Funding

Mechanistic Studies of Patatin-like ToxinsR01AI053674 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HAUSER, ALAN R · 2003 to 2017
$4.3M
Pseudomonas aeruginosa Genomic Islands and VirulenceR01AI075191 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HAUSER, ALAN R · 2009 to 2013
$1.7M
NIAID NIH HHS R01 AI053674NIAID NIH HHS R01AI053674NIAID NIH HHS R01 AI075191
6 · The paper itself

Abstract

backgroundPseudomonas aeruginosa bacteremia is a serious and life-threatening infection associated with high mortality. Among the multitude of virulence determinants possessed by P. aeruginosa, the type 3 secretion system has been implicated with more acute and invasive infection in respiratory diseases. However, the relationship between the type 3 secretion system and clinical outcomes in P. aeruginosa bacteremia has not been investigated.

objectivesTo determine the association between the type 3 secretion system virulence factor in P. aeruginosa bloodstream infection and 30-day mortality.

designRetrospective analysis of 85 cases of P. aeruginosa bacteremia.

settingTertiary care hospital.

interventionsBacterial isolates were assayed in vitro for secretion of type 3 exotoxins (ExoU, ExoT, and ExoS). Strain relatedness was analyzed using randomly amplified polymorphic DNA polymerase chain reaction genotyping. Antimicrobial susceptibilities were determined by means of the Kirby-Bauer disk-diffusion test. MEASUREMENTS AND MAIN

resultsAt least one of the type 3 secretion system proteins was detected in 37 out of the 85 isolates (44%). Septic shock was identified in 43% of bacteremic patients with type 3 secretion system+ isolates compared to 23% of patients with type 3 secretion system- isolates (p = .12). A high frequency of resistance in the type 3 secretion system+ isolates was observed to ciprofloxacin (59%), cefepime (35%), and gentamicin (38%). There was a significant difference in the 30-day cumulative probability of death after bacteremia between secretors and nonsecretors (p = .02). None of the type 3 secretion system+ patients who survived the first 30 days had a P. aeruginosa isolate which exhibited ExoU phenotype.

conclusionsThe expression of type 3 secretion system exotoxins in bacteremic isolates of P. aeruginosa confers poor clinical outcomes independent of antibiotic susceptibility profile.

Indexed as

ADP Ribose TransferasesAgedAnti-Bacterial AgentsBacteremiaBacterial ProteinsBacterial ToxinsExotoxinsFemaleGTPase-Activating ProteinsHumansMaleMicrobial Sensitivity TestsPseudomonas aeruginosaPseudomonas InfectionsRandom Amplified Polymorphic DNA TechniqueRetrospective StudiesADP Ribose TransferasesAnti-Bacterial AgentsBacterial ProteinsBacterial Toxinsexoenzyme SExotoxinsExoT protein, Pseudomonas aeruginosaGTPase-Activating Proteinspseudomonas exoprotein A protein, Pseudomonas aeruginosa

Identifiers

PMID22080633
PMCPMC3288436
OpenAlexW1978839325

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.