Pregled bibliografske jedinice broj: 740708
Cystic fibrosis across Europe : EuroCareCF analysis of demographic data from 35 countries
Cystic fibrosis across Europe : EuroCareCF analysis of demographic data from 35 countries // Journal of cystic fibrosis, 9 (2010), S2; S5-S21 doi:.org/10.1016/j.jcf.2010.08.002 (međunarodna recenzija, članak, znanstveni)
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Naslov
Cystic fibrosis across Europe : EuroCareCF analysis of demographic data from 35 countries
Autori
Mehta, Gita ; Macek, Milan ; Mehta, Anil ; ... ; Tješić-Drinković, Dorian ; Tješić-Drinković, Duška ; ...
Kolaboracija
European Registry Working Group
Izvornik
Journal of cystic fibrosis (1569-1993) 9
(2010), S2;
S5-S21
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
registries/statistics & numerical data ; database ; rare disease ; Geography ; chronic disease ; genetics ; p.Phe508del ; CFTR
Sažetak
A 35 country European cystic fibrosis (CF) demographic registry was developed to compare outcomes (EuroCareCF EC-FP6). We applied methods that had successfully created country-specific registries inviting wide participation to obtain consent and collate demographic and CFTR genotype data. Among 29.095 patients, a widely different country-specific prevalence of childhood CF exists that cannot be explained by differential population frequency of mutant-CFTR or case under-ascertainment with a significant paucity of the homozygous p.Phe508del genotype that presents in childhood in >90% of cases. Excess premature childhood CF mortality may still occur. The better resourced Western Europe now has a ~5% mortality for childhood CF, which is not apparent in many of the European countries reported here. In addition, a female survival disadvantage exists. The reasons require further investigation. We showcase the value of simple data collection in one rare disease, which might interest those managing rare diseases across the globe.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti, Javno zdravstvo i zdravstvena zaštita, Demografija
Napomena
On behalf of the Eureopean Registry Working Group ; EuroCareCF: Report on the demographics of cystic fibrosis in 35 European countries (European Coordination Action for Research in Cystic Fibrosis ; EC FP6 project no. LSHM-CT-2005-018932) ; David N. Sheppard (ur.) ; str. S5-S21. kao autori na radu navedeni su: Mehta, Gita ; Macek, Milan ; Mehta, Anil on behalf of the European Registry Working Group
POVEZANOST RADA
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta,
Medicinski fakultet, Zagreb
Poveznice na cjeloviti tekst rada:
doi www.cysticfibrosisjournal.com www.sciencedirect.com dx.doi.orgCitiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE