Relating Improvement in Gastrointestinal (CFAbd‐Score <sup>©</sup> ) and Sinonasal (SNOT) Symptoms During Therapy With Elexacaftor/Tezacaftor/Ivacaftor in CF Patients

The burden of symptoms captured with the CFAbd-Score and the SNOT-20-GAV significantly and markedly decreased after ETI initiation. The modest association between changes in both organ-specific symptom scores supports the previously reported individualized electrophysiological responses observed in nasal-potential and intestinal-current measurements.

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Publication Details

Journal
Pediatric Pulmonology
Published
2026-02-01
DOI
https://doi.org/10.1002/ppul.71507
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
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article

Relating Improvement in Gastrointestinal (CFAbd‐Score © ) and Sinonasal (SNOT) Symptoms During Therapy With Elexacaftor/Tezacaftor/Ivacaftor in CF Patients

Franziska Duckstein, Carlos Zagoya, Jochen G. Mainz, Olaf Eickmeier et al.
Pediatric Pulmonology
Cystic Fibrosis Research Advances
article

Relating Improvement in Gastrointestinal (CFAbd‐Score © ) and Sinonasal (SNOT) Symptoms During Therapy With Elexacaftor/Tezacaftor/Ivacaftor in CF Patients

Franziska Duckstein, Carlos Zagoya, Jochen G. Mainz, Olaf Eickmeier, Anton Barucha, Louise Polte, Ingo Philipp Fürchtegott Baumann, Pauline Sadrieh, Vivien Greiner, Suzanne van Dullemen
article en

Abstract

The burden of symptoms captured with the CFAbd-Score and the SNOT-20-GAV significantly and markedly decreased after ETI initiation. The modest association between changes in both organ-specific symptom scores supports the previously reported individualized electrophysiological responses observed in nasal-potential and intestinal-current measurements.

Pediatric PulmonologyVol. 61(2)
Goethe University Frankfurt (DE), Heidelberg University (DE), University Hospital Heidelberg (DE), Medizinische Hochschule Brandenburg Theodor Fontane (DE), Brandenburg University of Applied Sciences (DE), Universitätsklinikum Brandenburg an der Havel (DE)
Openalex Percentile: Top 58%
Cystic Fibrosis Research Advances
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