The measurement properties of tests and tools used in cystic fibrosis studies: a systematic review-Reference-Cited by-同舟云学术

The measurement properties of tests and tools used in cystic fibrosis studies: a systematic review

Published:2021-05-11 Issue:160 Volume:30 Page:200354
ISSN:0905-9180
Container-title:European Respiratory Review
language:en
Short-container-title:Eur Respir Rev

Author:

McLeod Charlie^ORCID,Wood Jamie,Tong Allison,Schultz André,Norman Richard,Smith Sherie,Blyth Christopher C.,Webb Steve,Smyth Alan R.,Snelling Thomas L.

Abstract

There is no consensus on how best to measure responses to interventions among children and adults with cystic fibrosis (CF). We have systematically reviewed and summarised the characteristics and measurement properties of tests and tools that have been used to capture outcomes in studies among people with CF, including their reliability, validity and responsiveness. This review is intended to guide researchers when selecting tests or tools for measuring treatment effects in CF trials. A consensus set of these tests and tools could improve consistency in how outcomes are captured and thereby facilitate comparisons and synthesis of evidence across studies.

Publisher

European Respiratory Society (ERS)

Subject

Pulmonary and Respiratory Medicine

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