The success of the Cystic Fibrosis Registry of Turkey for improvement of patient care

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dc.authorid0000-0002-9232-5982en_US
dc.authorid0000-0002-2597-6646en_US
dc.contributor.authorAsfuroğlu, Pelin
dc.contributor.authorEyüboğlu, Tuğba Şişmanlar
dc.contributor.authorAslan, Ayşe Tana
dc.contributor.authorGürsoy, Tuğba Ramaslı
dc.contributor.authorEmiralioğlu, Nagehan
dc.contributor.authorYalçın, Ebru
dc.contributor.authorŞen, Velat
dc.contributor.authorŞen, Hadice Selimoğlu
dc.date.accessioned2023-03-16T11:18:18Z
dc.date.available2023-03-16T11:18:18Z
dc.date.issued2022en_US
dc.departmentDicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalıen_US
dc.description.abstractBackground Cystic fibrosis (CF) registries play an essential role in improving disease outcomes of people with CF. This study aimed to evaluate the association of newly established CF registry system in Turkey on follow-up, clinical, growth, treatment, and complications of people with this disease. Methods Age at diagnosis, current age, sex, z-scores of weight, height and body mass index (BMI), neonatal screening results, pulmonary function tests, history of meconium ileus, medications, presence of microorganisms, and follow-up were evaluated and compared to data of people with CF represented in both 2017 and 2019 registry data. Results There were 1170 people with CF in 2017 and 1637 in 2019 CF registry. Eight hundred and fourteen people were registered in both 2017 and 2019 of whom z-scores of heights and BMI were significantly higher in 2019 (p = 0.002, p =0.039, respectively). Inhaled hypertonic saline, bronchodilator, and azithromycin usages were significantly higher in 2019 (p =0.001, p = 0.001, p = 0.003, respectively). The percent predicted of forced expiratory volume in 1 sec and forced vital capacity were similar in 2017 and 2019 (88% and 89.5%, p = 0.248 and 84.5% and 87%, p =0.332, respectively). Liver diseases and osteoporosis were significantly higher, and pseudo-Bartter syndrome (PBS) was significantly lower in 2019 (p = 0.011, p = 0.001, p = 0.001, respectively). Conclusions The z-scores of height and BMI were higher, the use of medications that protect and improve lung functions was higher and incidence of PBS was lower in 2019. It was predicted that registry system increased the care of people with CF regarding their follow-up. The widespread use of national CF registry system across the country may be beneficial for the follow-up of people with CF.en_US
dc.identifier.citationAsfuroğlu, P., Eyüboğlu, T.Ş., Aslan, A.T., Gürsoy, T.R., Emiralioglu, N., Yalçın, E. ve diğerleri. (2022). The success of the Cystic Fibrosis Registry of Turkey for improvement of patient care. Pediatric Pulmonology, 57(5), 1245-1252.en_US
dc.identifier.doi10.1002/ppul.25852
dc.identifier.endpage1252en_US
dc.identifier.issn8755-6863
dc.identifier.issn1099-0496
dc.identifier.issue5en_US
dc.identifier.pmid35102722
dc.identifier.scopus2-s2.0-85124530692
dc.identifier.scopusqualityQ1
dc.identifier.startpage1245en_US
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/epdf/10.1002/ppul.25852
dc.identifier.urihttps://hdl.handle.net/11468/11428
dc.identifier.volume57en_US
dc.identifier.wosWOS:000753941000001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorŞen, Velat
dc.institutionauthorŞen, Hadice Selimoğlu
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofPediatric Pulmonology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChilden_US
dc.subjectCystic fibrosisen_US
dc.subjectRegistryen_US
dc.titleThe success of the Cystic Fibrosis Registry of Turkey for improvement of patient careen_US
dc.titleThe success of the Cystic Fibrosis Registry of Turkey for improvement of patient care
dc.typeArticleen_US

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