Evidence map›Paper›PMID 22919584›Full record

ArticleFrontiers in cellular and infection microbiology2011

Can early Burkholderia cepacia complex infection in cystic fibrosis be eradicated with antibiotic therapy?

Alex Horsley, Kevin Webb, Rowland Bright-Thomas, John Govan, Andrew Jones

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 3 pooled it
1.7field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 3 syntheses or guidelines pooled it, 47 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Review
  5. Glycoproteomic and proteomic analysis ofMicrobiology spectrum · 2024
    Article
  6. Vaccines · 2024
    Review
  7. Phage therapy to treat cystic fibrosisFrontiers in microbiology · 2024
    Review
  8. Article
  9. Molecular Characterization of theAntibiotics (Basel, Switzerland) · 2020
    Article
  10. Article
  11. Loss ofmSphere · 2019
    Article
  12. Antimicrobial agents and chemotherapy · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Cystic Fibrosis: Microbiology and Host Response.Pediatric clinics of North America · 2016
    Review
  17. Burkholderia cepacia complex in Serbian patients with cystic fibrosis: prevalence and molecular epidemiology.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2016
    Article
  18. Article
  19. 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

5 authors at 2 institutions in 1 country.

Alex HorsleyManchester Adult Cystic Fibrosis Center, University Hospitals South Manchester Manchester, UK; Respiratory Research Group, School of Translational Medicine, University of Manchester, Manchester, UK. alexander.horsley@manchester.ac.uk
Kevin Webb
Rowland Bright-Thomas
John Govan
Andrew Jones
University of Manchester · GBUniversity of Edinburgh · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOrganisms of the Burkholderia cepacia complex (BCC) are important pathogens in cystic fibrosis (CF). The majority of those who acquire BCC develop chronic infection but it can also result in rapid decline in a significant minority. In addition, chronic infection with Burkholderia cenocepacia in particular is regarded as a contraindication to lung transplantation in many units. Whilst aggressive antibiotic therapy is employed in CF to eradicate Pseudomonas aeruginosa before infection becomes irreversibly established, no formal assessment of such strategies has been previously reported for BCC, despite the apparent widespread adoption of this practice.

methodsUK adult CF centers were surveyed about their current approach to new BCC infection. Outcomes of eradication therapy were assessed in patients attending the Manchester Adult CF Center with new BCC isolates between 1st January 2002 and 1st May 2011. Patients with previous infection with the same strain of BCC were excluded. BCC were identified at the national reference laboratories and confirmed by species-specific PCR and RecA sequencing.

resultsRoutine use of therapies to attempt eradication of new BCC is commonly used in the UK (12/17 centers who responded). This typically involves a combination of intravenous and nebulised antibiotics. Of 19 eligible cases of new BCC infection, the organism has been eradicated in 7 (37%). Three of these did not receive specific eradication therapy. Of 14 patients who have received eradication therapy and completed follow up, BCC were cleared in only 4 (29%).

conclusionsAttempted eradication of new BCC is a common practice in UK adult CF centers. A minority of patients clear the infection spontaneously and the effects of eradication therapies are at best modest. Early treatment may be associated with better outcomes, though there are insufficient data to support the use of any specific treatment regimen. A prospective, systematic evaluation of treatments and outcomes is required.

Indexed as

Burkholderia cepacia complexAdolescentAdultAnti-Bacterial AgentsBurkholderia InfectionsChronic DiseaseCystic FibrosisData CollectionHumansMiddle AgedRespiratory Tract InfectionsSecondary PreventionTreatment OutcomeUnited KingdomYoung AdultAnti-Bacterial AgentsBurkholderia cenocepaciaBurkholderia cepaciaBurkholderia multivoranscystic fibrosisEradication

Identifiers

PMID22919584
PMCPMC3417365
OpenAlexW1976917271

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.