Evidence map›Paper›PMID 24863401›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2014

Pseudomonas aeruginosa phenotypes associated with eradication failure in children with cystic fibrosis.

Nicole Mayer-Hamblett, Bonnie W Ramsey, Hemantha D Kulasekara, Daniel J Wolter, Laura S Houston, Christopher E Pope, Bridget R Kulasekara, Catherine R Armbruster, Jane L Burns, George Retsch-Bogart and 5 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Article
  3. Changing profile of bacterial infection and microbiome in cystic fibrosis: when to use antibiotics in the era of CFTR-modulator therapy.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  4. Article
  5. Article
  6. Phage therapy to treat cystic fibrosisFrontiers in microbiology · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Increased sputum lactate during oral glucose tolerance test in cystic fibrosis.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2022
    Article
  11. Article
  12. Article
  13. The Effect of CFTR Modulators on Airway Infection in Cystic Fibrosis.International journal of molecular sciences · 2022
    Review
  14. Article
  15. Frontiers in cellular and infection microbiology · 2022
    Article
  16. Article
  17. Pathogens (Basel, Switzerland) · 2021
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Nicole Mayer-HamblettDepartment of Pediatrics Department of Biostatistics Department of Seattle Children's Hospital, Washington.
Bonnie W RamseyDepartment of Pediatrics Department of Seattle Children's Hospital, Washington.
Hemantha D KulasekaraDepartment of Microbiology.
Daniel J WolterDepartment of Pediatrics.
Laura S HoustonDepartment of Pediatrics.
Christopher E PopeDepartment of Pediatrics.
Bridget R KulasekaraDepartment of Microbiology.
Catherine R ArmbrusterDepartment of Microbiology.
Jane L BurnsDepartment of Pediatrics Department of Seattle Children's Hospital, Washington.
George Retsch-BogartDepartment of Pediatrics, University of North Carolina, Chapel Hill.
Margaret RosenfeldDepartment of Pediatrics Department of Seattle Children's Hospital, Washington.
Ronald L GibsonDepartment of Pediatrics Department of Seattle Children's Hospital, Washington.
Samuel I MillerDepartment of Microbiology Department of Genome Sciences Department of Medicine, University of Washington, Seattle.
Umer KhanDepartment of Seattle Children's Hospital, Washington.
Lucas R HoffmanDepartment of Pediatrics Department of Microbiology Department of Seattle Children's Hospital, Washington.
Seattle Children's Hospital · USUniversity of North Carolina at Chapel Hill · USUniversity of Washington · US

Funding

Translational Research Center to Expedite Novel Therapies in Cystic FibrosisP30DK089507 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Sonya Heltshe · 2010 to 2026
$21.4M
Pseudomonas aeruginosa Adaptation During Early CF Airway Infection and TreatmentR01HL098084 · NHLBI · UNIVERSITY OF WASHINGTON · PI HOFFMAN, LUCAS R · 2009 to 2012
$1.6M
Pseudomonas Aeruginosa Early CF Adaptive Changes: A Translational StudyK02HL105543 · NHLBI · UNIVERSITY OF WASHINGTON · PI HOFFMAN, LUCAS R · 2011 to 2014
$400k
NHLBI NIH HHS K02 HL105543NHLBI NIH HHS K02HL105543NHLBI NIH HHS R01 HL098084NHLBI NIH HHS R01HL098084NIDDK NIH HHS P30 DK089507
6 · The paper itself

Abstract

backgroundPseudomonas aeruginosa is a key respiratory pathogen in people with cystic fibrosis (CF). Due to its association with lung disease progression, initial detection of P. aeruginosa in CF respiratory cultures usually results in antibiotic treatment with the goal of eradication. Pseudomonas aeruginosa exhibits many different phenotypes in vitro that could serve as useful prognostic markers, but the relative relationships between these phenotypes and failure to eradicate P. aeruginosa have not been well characterized.

methodsWe measured 22 easily assayed in vitro phenotypes among the baseline P. aeruginosa isolates collected from 194 participants in the 18-month EPIC clinical trial, which assessed outcomes after antibiotic eradication therapy for newly identified P. aeruginosa. We then evaluated the associations between these baseline isolate phenotypes and subsequent outcomes during the trial, including failure to eradicate after antipseudomonal therapy, emergence of mucoidy, and occurrence of an exacerbation.

resultsBaseline P. aeruginosa isolates frequently exhibited phenotypes thought to represent chronic adaptation, including mucoidy. Wrinkly colony surface and irregular colony edges were both associated with increased risk of eradication failure (hazard ratios [95% confidence intervals], 1.99 [1.03-3.83] and 2.14 [1.32-3.47], respectively). Phenotypes reflecting defective quorum sensing were significantly associated with subsequent mucoidy, but no phenotype was significantly associated with subsequent exacerbations during the trial.

conclusionsPseudomonas aeruginosa phenotypes commonly considered to reflect chronic adaptation were observed frequently among isolates at early detection. We found that 2 easily assayed colony phenotypes were associated with failure to eradicate after antipseudomonal therapy, both of which have been previously associated with altered biofilm formation and defective quorum sensing.

Indexed as

BiofilmsChildChild, PreschoolCystic FibrosisFemaleGenotypeGlycosaminoglycansHumansInfantMalePhenotypePseudomonas aeruginosaPseudomonas InfectionsTreatment FailureGlycosaminoglycansmucoid exopolysaccharide (P aeruginosa)antibiotic treatmentcystic fibrosiseradicationphenotypic characterizationPseudomonas aeruginosa

Identifiers

PMID24863401
PMCPMC4148602
OpenAlexW2116228267

What OpenQuestion holds

Textmetadata
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.