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
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10606 - Microbiology
Result continuities
Project
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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
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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