The importance of data issues when comparing cystic fibrosis registry outcomes between countries: Are annual review FEV(1) in the UK only collected when subjects are well?

RATIONALE, AIMS AND OBJECTIVE: Cross‐country comparisons of cystic fibrosis (CF) outcomes can potentially identify variation in care but are dependent on data quality. An important assumption is that the UK annual review FEV(1) is only collected during periods of clinical stability. If this assumpti...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:J Eval Clin Pract
Päätekijät: Hoo, Zhe Hui, Curley, Rachael, Campbell, Michael J., Walters, Stephen J., Wildman, Martin J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: John Wiley and Sons Inc. 2018
Aiheet:
Original Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6099433/
https://ncbi.nlm.nih.gov/pubmed/29901239
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jep.12967
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia