Evidence map›Paper›PMID 25690407›Full record

Trial reportJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2015

Factors associated with response to treatment of pulmonary exacerbations in cystic fibrosis patients.

Valerie J Waters, Sanja Stanojevic, Nicole Sonneveld, Michelle Klingel, Hartmut Grasemann, Yvonne C W Yau, Elizabeth Tullis, Pearce Wilcox, Andreas Freitag, Mark Chilvers and 1 more

Open access · bronzeAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 4 pooled it
7.2field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 4 syntheses or guidelines pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Article
  7. Review
  8. Article
  9. Article
  10. Re-examining baseline lung function recovery following IV-treated pulmonary exacerbations.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2023
    Article
  11. Diagnosis and Management of Cystic Fibrosis Exacerbations.Seminars in respiratory and critical care medicine · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Application of multiple event analysis as an alternative approach to studying pulmonary exacerbations as an outcome measure.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2020
    Observational
  19. Acute Pulmonary Exacerbations in Cystic Fibrosis.Seminars in respiratory and critical care medicine · 2019
    Review
  20. Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 1 country.

Valerie J WatersDivision of Infectious Diseases, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto. Electronic address: Valerie.Waters@sickkids.ca.
Sanja StanojevicDivision of Respiratory Medicine, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto. Electronic address: Sanja.Stanojevic@sickkids.ca.
Nicole SonneveldDivision of Respiratory Medicine, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto. Electronic address: n.sonneveld@erasmusmc.nl.
Michelle KlingelDivision of Respiratory Medicine, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto. Electronic address: michelle.klingel@sickkids.ca.
Hartmut GrasemannDivision of Respiratory Medicine, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto. Electronic address: Hartmut.Grasemann@sickkids.ca.
Yvonne C W YauDivision of Microbiology, Department of Pediatric Laboratory Medicine, Hospital for Sick Children, University of Toronto, Toronto. Electronic address: Yvonne.Yau@sickkids.ca.
Elizabeth TullisDivision of Respirology and Keenan Research Centre of Li Ka Shing Knowledge Institute, Department of Medicine, St. Michael's Hospital, University of Toronto, Toronto. Electronic address: Tullise@smh.ca.
Pearce WilcoxDivision of Respiratory Medicine, Department of Medicine, St Paul's Hospital, University of British Columbia, Vancouver. Electronic address: PWilcox@providencehealth.bc.ca.
Andreas FreitagDivision of Respiratory Medicine, Department of Medicine, Hamilton Health Sciences Center, McMaster University, Hamilton. Electronic address: freitaga@mcmaster.ca.
Mark ChilversDivision of Respiratory Medicine, Department of Pediatrics, British Columbia Children's Hospital, Vancouver. Electronic address: mchilvers@cw.bc.ca.
Felix A RatjenDivision of Respiratory Medicine, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto. Electronic address: Felix.Ratjen@sickkids.ca.
Hospital for Sick Children · CAUniversity of Toronto · CASickKids Foundation · CABC Children's Hospital · CAHamilton Health Sciences · CAUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPulmonary exacerbations are associated with significant lung function decline from baseline in cystic fibrosis (CF) and it is not well understood why some patients do not respond to antibiotic therapy. The objective of this study was to identify factors associated with lung function response to antibiotic treatment of pulmonary exacerbations.

methodsAs a secondary analysis of a randomized, controlled trial of intravenous antibiotic treatment for pulmonary exacerbations in CF patients, we investigated whether baseline factors and changes in sputum bacterial density, serum or sputum inflammatory markers were associated with recovery of lung function and risk of subsequent exacerbation.

resultsIn 36 of the 70 exacerbations (51%), patients' lung function returned to >100% of their baseline at day 14 of antibiotic treatment; 34 exacerbations were classified as non-responders. Baseline characteristics were not significantly different between responders and non-responders. Less of a drop in FEV1 from baseline to exacerbation (OR 1.09, 95% CI 1.0, 1.18, p=0.04) as well as a greater decrease in sputum neutrophil elastase (OR 2.94, 95% CI 1.07, 8.06, p=0.04) were associated with response to antibiotic treatment at day 14. In addition, higher CRP (HR 1.35 (95% CI: 1.01, 1.78), p=0.04) and sputum neutrophil elastase (HR 1.71 (95% CI: 1.02, 2.88), p=0.04) at day 14 of antibiotic therapy were associated with an increased risk of subsequent exacerbation.

conclusionsInadequate reduction of inflammation during an exacerbation is associated with failure to recover lung function and increased risk of subsequent re-exacerbation in CF patients.

Indexed as

AdolescentAdultChildCystic FibrosisDisease ProgressionDouble-Blind MethodFemaleHumansLung DiseasesMaleYoung Adultantibioticscystic fibrosisinflammationpulmonary exacerbations

Identifiers

PMID25690407
OpenAlexW2096694356

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.