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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...
שמור ב:
| הוצא לאור ב: | J Eval Clin Pract |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
John Wiley and Sons Inc.
2018
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| נושאים: | |
| גישה מקוונת: | 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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