Clinical characteristics of patients requiring lung transplantation referral in national cystic fibrosis registry data

dc.contributor.authorOnay, Zeynep Reyhan
dc.contributor.authorEyuboglu, Tugba Sismanlar
dc.contributor.authorAslan, Ayse Tana
dc.contributor.authorGursoy, Tugba Ramasli
dc.contributor.authorYalcin, Ebru
dc.contributor.authorKiper, Nural
dc.contributor.authorDogru, Deniz
dc.date.accessioned2026-08-12T17:20:52Z
dc.date.issued2023
dc.departmentFırat Üniversitesi
dc.description.abstractBackground. We aimed to determine the number of cystic fibrosis (CF) patients recorded in the Cystic Fibrosis Registry of Turkiye (CFRT) who were in need of lung transplantation (LT) referral and examine clinical differences between patients who were LT candidates due to rapid forced expiratory volume in one second (FEV1) decline and LT candidates without rapid FEV1 decline in the last year to identify a preventable cause in patients with such rapid FEV1 decline. Methods. All CF patients recorded in the CFRT in 2018 were evaluated in terms of LT. Patients were divided into those with FEV1 below 50% and in need of LT due to a decrease of 20% or more in the previous year (Group 1) and those who did not have FEV1 decline of more than 20% in the previous year but had other indications for LT (Group 2). Demographic and clinical features were compared between the two groups. Results. Of 1488 patients registered in CFRT, 58 had a need for LT. Twenty patients were included in Group 1 and others in Group 2. Our findings did not reveal any significant variations in treatment, chronic infection status, or complications between the two groups. The average weight z-score was significantly higher in Group 1. Positive correlations were detected between weight z-score and FEV1 in 2017 in Group 1 and between FEV1 values in 2017 and 2018 in Group 2. Conclusions. There appears to be a relationship between the nutritional status and weight z-scores of CF patients and pulmonary function, which may indirectly affect the need for lung transplantation referral.
dc.identifier.doi10.24953/turkjped.2021.4930
dc.identifier.endpage268
dc.identifier.issn0041-4301
dc.identifier.issue2
dc.identifier.orcid0000-0002-2879-8910
dc.identifier.orcid0000-0002-7064-7585
dc.identifier.orcid0000-0002-1438-7854
dc.identifier.orcid0000-0002-0793-9710
dc.identifier.orcid0000-0002-9804-1200
dc.identifier.orcid0000-0003-4085-0256
dc.identifier.orcid0000-0001-7284-4999
dc.identifier.pmid37114691
dc.identifier.scopus2-s2.0-85159207631
dc.identifier.scopusqualityQ3
dc.identifier.startpage257
dc.identifier.trdizinid1177631
dc.identifier.urihttps://doi.org/10.24953/turkjped.2021.4930
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1177631
dc.identifier.urihttps://hdl.handle.net/11508/53728
dc.identifier.volume65
dc.identifier.wosWOS:000982312900009
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherTurkish J Pediatrics
dc.relation.ispartofTurkish Journal of Pediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectcystic fibrosis
dc.subjectlung transplantation
dc.subjectregistry
dc.titleClinical characteristics of patients requiring lung transplantation referral in national cystic fibrosis registry data
dc.typeArticle

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