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

dc.contributor.authorBingöl, Ayşen
dc.contributor.authorBaşaran, Erdem
dc.contributor.authorTuğcu, Gökçen Dilşa
dc.contributor.authorPolat, Sanem Eryılmaz
dc.contributor.authorÇollak, Abdulhamit
dc.contributor.authorUzuner, Selçuk
dc.contributor.authorCan, Demet
dc.date.accessioned2024-02-05T15:58:26Z
dc.date.available2024-02-05T15:58:26Z
dc.date.issued2023
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.description.abstractBackground. We aimed to determine the number of cystic fibrosis (CF) patients recorded in the Cystic Fibrosis Registry of Türkiye (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 (FEV?) decline and LT candidates without rapid FEV? decline in the last year to identify a preventable cause in patients with such rapid FEV? decline. Methods. All CF patients recorded in the CFRT in 2018 were evaluated in terms of LT. Patients were divided into those with FEV? 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 FEV? 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 FEV? in 2017 in Group 1 and between FEV? 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.en_US
dc.identifier.doi10.24953/turkjped.2021.4930
dc.identifier.endpage268en_US
dc.identifier.issn0041-4301
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-85159207631
dc.identifier.scopusqualityQ3
dc.identifier.startpage257en_US
dc.identifier.trdizinid1177631
dc.identifier.urihttps://doi.org/10.24953/turkjped.2021.4930
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/1177631
dc.identifier.urihttps://hdl.handle.net/20.500.12462/14065
dc.identifier.volume65en_US
dc.identifier.wosWOS:000982312900009
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.language.isoenen_US
dc.relation.ispartofTurkish Journal of Pediatricsen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.snmztrdizinidealen_US]
dc.subjectCystic Fibrosisen_US
dc.subjectLung Transplantationen_US
dc.subjectRegistryen_US
dc.titleClinical characteristics of patients requiring lung transplantation referral in national cystic fibrosis registry dataen_US
dc.typeArticleen_US

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