Evidence map›Paper›PMID 24856776›Full record

ReviewJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2014

European Cystic Fibrosis Society Standards of Care: Framework for the Cystic Fibrosis Centre.

Steven Conway, Ian M Balfour-Lynn, Karleen De Rijcke, Pavel Drevinek, Juliet Foweraker, Trudy Havermans, Harry Heijerman, Louise Lannefors, Anders Lindblad, Milan Macek and 8 more

Abstract readReview
In one paragraph

Review in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 3 pooled it
–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

63 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. The globalization of cystic fibrosis care.Current opinion in pediatrics · 2025
    Review
  12. Article
  13. Collaboration between registered dietitians and gastroenterologists in cystic fibrosis care: Results of an international cross-sectional survey.Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition · 2025
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Cystic Fibrosis: From Tragedy to Triumph.American journal of respiratory and critical care medicine · 2023
    Article
  20. Clinical outcomes of adults and children with cystic fibrosis during the COVID-19 pandemic.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2023
    Article

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

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

18 authors.

Steven ConwayPaediatric and Adult CF Units, Leeds Teaching Hospitals Trust, UK. Electronic address: steven.conway@doctors.net.uk.
Ian M Balfour-LynnRoyal Brompton Hospital, Sydney Street, London, UK.
Karleen De RijckeCystic Fibrosis Europe, Belgium.
Pavel DrevinekDepartment of Medical Microbiology, 2nd Faculty of Medicine, Charles University, Prague, Czech Republic; Department of Paediatrics, 2nd Faculty of Medicine, Charles University, Prague, Czech Republic; University Hospital Motol, Prague, Czech Republic.
Juliet FowerakerDepartment of Microbiology, Papworth Hospital NHS Foundation Trust, Papworth Everard, Cambridge, UK.
Trudy HavermansCystic Fibrosis Centre, University Hospital Leuven, Belgium.
Harry HeijermanHagaZiekenhuis, Department of Pulmonology & Cystic Fibrosis, The Hague, The Netherlands.
Louise LanneforsCopenhagen CF Centre, Rigshospitalet, University Hospital, Copenhagen, Denmark.
Anders LindbladGothenburg CF Centre, Queen Silvia Children's Hospital, Göteborg, Sweden.
Milan MacekDepartment of Biology and Medical Genetics, University Hospital Motol, Prague, Czech Republic; Second School of Medicine, Charles University Prague, Prague, Czech Republic.
Sue MadgeDepartment of Respiratory Medicine, Royal Brompton Hospital, Sydney Street, London, UK.
Maeve MoranNational Referral Centre for Adult Cystic Fibrosis, Pharmacy Department, St. Vincent's University Hospital, Ireland.
Lisa MorrisonGartnavel General Hospital, West of Scotland Adult CF Unit, Glasgow, UK.
Alison MortonAdult Cystic Fibrosis Unit, St James's Hospital, Leeds, UK.
Jacquelien NoordhoekDutch Cystic Fibrosis Foundation, The Netherlands.
Dorota SandsDepartment of Pediatrics, Institute of Mother and Child, Warsaw, Poland.
Anneke VertommenCystic Fibrosis Centre, University Hospital Leuven, Belgium.
Daniel PeckhamAdult Cystic Fibrosis Unit, St James's Hospital, Leeds, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A significant increase in life expectancy in successive birth cohorts of people with cystic fibrosis (CF) is a result of more effective treatment for the disease. It is also now widely recognized that outcomes for patients cared for in specialist CF Centres are better than for those who are not. Key to the effectiveness of the specialist CF Centre is the multidisciplinary team (MDT), which should include consultants, clinical nurse specialist, microbiologist, physiotherapist, dietitian, pharmacist, clinical psychologist, social worker, clinical geneticist and allied healthcare professionals, all of whom should be experienced in CF care. Members of the MDT are also expected to keep up to date with developments in CF through continued professional development, attendance at conferences, auditing and involvement in research. Specialists CF Centres should also network with other Centres both nationally and internationally, and feed Centre data to registries in order to further the understanding of the disease. This paper provides a framework for the specialist CF Centre, including the organisation of the Centre and the individual roles of MDT members, as well as highlighting the value of CF organisations and disease registries.

Indexed as

Standard of CareAdolescentAdultChildChild, PreschoolCystic FibrosisEuropeHealth Services AccessibilityHospitals, SpecialHumansPatient Care TeamSocieties, MedicalYoung AdultCF CentreContinuing professional developmentMultidisciplinary team

Identifiers

PMID24856776
PMCPMC7105239

What Socratic 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 Socratic graph.