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Insights into the cystic fibrosis care in Eastern Europe: Results of survey

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F18%3A10376346" target="_blank" >RIV/00216208:11130/18:10376346 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/18:10376346 RIV/00064203:_____/18:10376346

  • Result on the web

    <a href="https://doi.org/10.1016/j.jcf.2018.04.003" target="_blank" >https://doi.org/10.1016/j.jcf.2018.04.003</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jcf.2018.04.003" target="_blank" >10.1016/j.jcf.2018.04.003</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Insights into the cystic fibrosis care in Eastern Europe: Results of survey

  • Original language description

    Background: The European cystic fibrosis (CF) Society Standards of Care were set to facilitate the delivery of high-quality care throughout Europe. However, their implementation may be difficult for less economically advantaged countries. This survey was performed to explore the gap in the knowledge of the level of CF care in Eastern Europe. Methods: Questionnaires were sent online to one CF professional and one CF patient representative for every Eastern European country. Results: Although most respondents indicated the presence of CF centres, disparities in their framework among individual countries and between them and the European CF Standards of Care became apparent. A minority of countries achieved CF centre recognition by the government (6 of 16), provided CF care for adults (6 countries) and had a multidisciplinary team with all team members represented (2 countries). Patients were significantly more critical in the evaluation of various aspects of CF care than physicians, especially in the Balkan region. Conclusions: The survey results indicate that the organization and level of CF care across Eastern Europe is largely variable and lacks some of its fundamental attributes in several countries.

  • 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

    10606 - Microbiology

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

    4

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    3

  • Pages from-to

    475-477

  • UT code for WoS article

    000439672700010

  • EID of the result in the Scopus database

    2-s2.0-85045846427