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Pediatric Pulmonology
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Comparison of clinical features of cystic fibrosis patients eligible but not on CFTR modulators to ineligible for CFTR modulators

Authors: Halime Nayır Büyükşahin; Nagehan Emiralioğlu; Ebru Yalçın; Velat Şen; Hadice Selimoğlu Şen; Hüseyin Arslan; Azer Kılıç Başkan; +48 Authors

Comparison of clinical features of cystic fibrosis patients eligible but not on CFTR modulators to ineligible for CFTR modulators

Abstract

AbstractIntroductionCystic fibrosis transmembrane conductance regulator (CFTR) modulator drugs target the underlying defect and improve CFTR function. They are a part of standard care in many countries, but not all patients are eligible for these drugs due to age and genotype. Here, we aimed to determine the characteristics of non‐eligible patients for CFTR modulators in the CF registry of Turkey (CFRT) to highlight their clinical needs.MethodsThis retrospective cohort study included CF patient data from the CFRT in 2021. The decision of eligibility for the CFTR modulator was determined according to the ‘Vertex treatment‐Finder' on the Vertex® website. Demographic and clinical characteristics of patients were compared between eligible (group 1) and ineligible (group 2) groups for CFTR modulators.ResultsAmong the study population (N = 1527), 873 (57.2%) were in group 1 and 654 (42.8%) were in group 2. There was no statistical difference between groups regarding sex, meconium ileus history, diagnoses via newborn screening, FEV1 z‐score, CF‐associated complications, organ transplant history, and death. Patients in group 2 had a higher incidence of pancreatic insufficiency (87.7% vs. 83.2%, p = .010), lower median height z‐scores (−0.87 vs. −0.55, p < .001), lower median body mass index z‐scores (−0.65 vs. −0.50, p < .001), longer days receiving antibiotics due to pulmonary exacerbation (0 [interquartile range, IQR: 0–2] vs. 0 [IQR: 0–7], p = 0.001), and more non‐invasive ventilation support (2.6% vs. 0.9%, p = 0.008) than patients in group 1.ConclusionThe ineligible group had worse clinical outcomes than the eligible group. This highlights their need for life‐changing drugs to improve clinical outcomes.

Country
Turkey
Keywords

Male, Registry, clinical features, Cystic Fibrosis, Adolescent, Turkey, Cystic Fibrosis Transmembrane Conductance Regulator, registry, Cftr Modulators, Cystic fibrosis, cystic fibrosis, Young Adult, Humans, Registries, Child, eligibility, Fibrosiseligibility, Retrospective Studies, Eligibility, Clinical Features, Clinical Featurescystic, Patient Selection, Infant, Newborn, Infant, Clinical features, CFTR modulators, CFTR Modulators, Child, Preschool, Female, Exocrine Pancreatic Insufficiency

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    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
5
Top 10%
Average
Top 10%
Green