Evidence map›Paper›PMID 20503282›Full record

ArticlePediatric pulmonology2010

Pulmonary exacerbations in cystic fibrosis with negative bacterial cultures.

Edith T Zemanick, Brandie D Wagner, J Kirk Harris, Jeffery S Wagener, Frank J Accurso, Scott D Sagel

Abstract read
In one paragraph

Article in Pediatric pulmonology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Vaping-Dependent Pulmonary Inflammation Is CaInternational journal of molecular sciences · 2024
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Nontuberculous Mycobacteria in Cystic Fibrosis.Current treatment options in infectious diseases · 2016
    Review
  16. The pediatric microbiome and the lung.Current opinion in pediatrics · 2015
    Review
  17. Review
  18. Treatment of pulmonary exacerbations in cystic fibrosis.European respiratory review : an official journal of the European Respiratory Society · 2013
    Review
  19. Molecular detection of CF lung pathogens: current status and future potential.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2013
    Review
  20. 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

6 authors.

Edith T ZemanickDepartment of Pediatrics, University of Colorado Denver, Aurora, Colorado 80045, USA. zemanick.edith@tchden.org
Brandie D Wagner
J Kirk Harris
Jeffery S Wagener
Frank J Accurso
Scott D Sagel

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR025780 · NCRR · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2008 to 2011
$61.3M
LABORATORY COREU01HL081335 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI ABMAN, STEVEN HERBERT · 2005 to 2008
$4.1M
NCRR NIH HHS 1UL1RR025780NCRR NIH HHS UL1 RR025780NHLBI NIH HHS 1U01HL081335-01NHLBI NIH HHS U01 HL081335
6 · The paper itself

Abstract

backgroundPulmonary exacerbations are a major cause of morbidity in cystic fibrosis (CF) and likely contribute to lung function decline. Exacerbations are often associated with characteristic airway bacteria [CF related bacteria (CFRB)]. However, some patients do not have CFRB detected by culture during exacerbations.

objectivesWe sought to determine the proportion of airway cultures negative for CFRB during pulmonary exacerbations, and to characterize patients who were CFRB-negative versus CFRB-positive.

methodsWe performed a retrospective study of patients with CF admitted for a pulmonary exacerbation. Patients were classified as CFRB-positive or CFRB-negative based on admission airway cultures. Demographics, clinical presentation, lung function, history of chronic Pseudomonas aeruginosa infection and improvement in lung function with treatment were compared between groups. MAIN

resultsThere were 672 admissions for exacerbation involving 211 patients over 5 years. Seventeen percent were classified as CFRB-negative. Forty-one percent of bronchoalveolar lavage (BAL), 32% of throat and 10% of sputum samples were CFRB-negative. Among patients capable of expectorating sputum, the CFRB-negative group was younger, less likely to have chronic P. aeruginosa, had higher lung function and body mass index (BMI), and had a lower systemic inflammatory response on admission compared to those with CFRB-positive cultures. The two groups had similar numbers of patients with three or more signs and symptoms of a pulmonary exacerbation (88% vs. 92%). Both groups returned to baseline lung function following treatment.

conclusionsA significant number of patients with CF and pulmonary exacerbation did not have typical CFRB detected by culture. Patients without CFRB still had characteristic signs and symptoms of pulmonary exacerbation and responded to treatment. Understanding the causes of illness in these patients may improve the diagnosis and treatment of pulmonary exacerbations in CF.

Indexed as

AdolescentAnti-Bacterial AgentsAzithromycinBronchoalveolar Lavage FluidChildCystic FibrosisDisease ProgressionFemaleHumansMalePseudomonas aeruginosaPseudomonas InfectionsRetrospective StudiesSputumTobramycinYoung AdultAnti-Bacterial AgentsAzithromycinTobramycin

Identifiers

PMID20503282
PMCPMC2937349

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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.