Comparison of Reporting Quality in National Cystic Fibrosis Patient Registries: Implications for Identifying Use of Novel CFTR Modulators

Both F508del prevalence and GDP are associated with variable CFTRm usage rates, although a predominant reason is unclear as a result of poor consistency in registry reporting. Urgent action is needed to create uniform reporting of registry data and increase availability of novel CFTRm therapies to the global CF population.

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Publication Details

Journal
Pulmonary Therapy
Published
2024-09-27
DOI
https://doi.org/10.1007/s41030-024-00274-y
Citations
1
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
0.42
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article

Comparison of Reporting Quality in National Cystic Fibrosis Patient Registries: Implications for Identifying Use of Novel CFTR Modulators

Owen W. Tomlinson, Craig Anthony Williams, Philip Mitchelmore
1 citations
Pulmonary Therapy
Cystic Fibrosis Research Advances
0.42
article

Comparison of Reporting Quality in National Cystic Fibrosis Patient Registries: Implications for Identifying Use of Novel CFTR Modulators

Owen W. Tomlinson, Craig Anthony Williams, Philip Mitchelmore
article en
1 citations

Abstract

Both F508del prevalence and GDP are associated with variable CFTRm usage rates, although a predominant reason is unclear as a result of poor consistency in registry reporting. Urgent action is needed to create uniform reporting of registry data and increase availability of novel CFTRm therapies to the global CF population.

Pulmonary TherapyVol. 10(4)
University of Exeter (GB), Royal Devon & Exeter NHS Foundation Trust (GB)
Openalex Percentile: Top 32%
Cystic Fibrosis Research Advances
0.42
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