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...

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Bibliografiska uppgifter
I publikationen:J Eval Clin Pract
Huvudupphovsmän: Hoo, Zhe Hui, Curley, Rachael, Campbell, Michael J., Walters, Stephen J., Wildman, Martin J.
Materialtyp: Artigo
Språk:Inglês
Publicerad: John Wiley and Sons Inc. 2018
Ämnen:
Original Articles
Länkar: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
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