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ECFS best practice guidelines: the 2018 revision

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F18%3A10375277" target="_blank" >RIV/00216208:11130/18:10375277 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064203:_____/18:10375277

  • Result on the web

    <a href="https://doi.org/10.1016/j.jcf.2018.02.006" target="_blank" >https://doi.org/10.1016/j.jcf.2018.02.006</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jcf.2018.02.006" target="_blank" >10.1016/j.jcf.2018.02.006</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    ECFS best practice guidelines: the 2018 revision

  • Original language description

    Developments in managing CF continue to drive dramatic improvements in survival. As newborn screening rolls-out across Europe, CF centres are increasingly caring for cohorts of patients who have minimal lung disease on diagnosis. With the introduction of mutation-specific therapies and the prospect of truly personalised medicine, patients have the potential to enjoy good quality of life in adulthood with ever-increasing life expectancy. The landmark Standards of Care published in 2005 set out what high quality CF care is and how it can be delivered throughout Europe. This underwent a fundamental re-write in 2014, resulting in three documents; center framework, quality management and best practice guidelines. This document is a revision of the latter, updating standards for best practice in key aspects of CF care, in the context of a fast-moving and dynamic field. In continuing to give a broad overview of the standards expected for newborn screening, diagnosis, preventative treatment of lung disease, nutrition, complications, transplant/end of life care and psychological support, this consensus on best practice is expected to prove useful to clinical teams both in countries where CF care is developing and those with established CF centres. The document is an ECFS product and endorsed by the CF Network in ERN LUNG and CF Europe.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30203 - Respiratory systems

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Cystic Fibrosis

  • ISSN

    1569-1993

  • e-ISSN

  • Volume of the periodical

    17

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    26

  • Pages from-to

    153-178

  • UT code for WoS article

    000430763900005

  • EID of the result in the Scopus database

    2-s2.0-85042650897