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dc.contributor.author김혜순*
dc.date.accessioned2025-03-24T16:30:02Z-
dc.date.available2025-03-24T16:30:02Z-
dc.date.issued2024*
dc.identifier.issn2287-1012*
dc.identifier.otherOAK-36893*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/271517-
dc.description.abstractRare endocrine diseases are complex conditions that require lifelong specialized care due to their chronic nature and associated long-term complications. In Korea, a lack of nationwide data on clinical practice and outcomes has limited progress in patient care. Therefore, the Multicenter Networks for Ideal Outcomes of Pediatric Rare Endocrine and Metabolic Disease (OUTSPREAD) study was initiated. This study involves 30 centers across Korea. The study aims to improve the long-term prognosis of Korean patients with rare endocrine diseases by collecting comprehensive clinical data, biospecimens, and patient-reported outcomes to identify complications and unmet needs in patient care. Patients with childhood-onset pituitary, adrenal, or gonadal disorders, such as craniopharyngioma, congenital adrenal hyperplasia (CAH), and Turner syndrome were prioritized. The planned enrollment is 1,300 patients during the first study phase (2022–2024). Clinical, biochemical, and imaging data from diagnosis, treatment, and follow-up during 1980–2023 were retrospectively reviewed. For patients who agreed to participate in the prospective cohort, clinical data and biospecimens will be prospectively collected to discover ideal biomarkers that predict the effectiveness of disease control measures and prognosis. Patient-reported outcomes, including quality of life and depression scales, will be evaluated to assess psychosocial outcomes. Additionally, a substudy on CAH patients will develop a steroid hormone profiling method using liquid chromatography-tandem mass spectrometry to improve diagnosis and monitoring of treatment outcomes. This study will address unmet clinical needs by discovering ideal biomarkers, introducing evidence-based treatment guidelines, and ultimately improving long-term outcomes in the areas of rare endocrine and metabolic diseases. © 2024 Annals of Pediatric Endocrinology & Metabolism.*
dc.languageEnglish*
dc.publisherKorean society of pediatric endocrinology*
dc.subjectChild*
dc.subjectCohort studies*
dc.subjectCongenital adrenal hyperplasia*
dc.subjectCraniopharyngioma*
dc.subjectEndocrine system diseases*
dc.subjectRare disease*
dc.subjectTreatment outcome*
dc.subjectTurner syndrome*
dc.titleCohort profile: Multicenter Networks for Ideal Outcomes of Rare Pediatric Endocrine and Metabolic Diseases in Korea (OUTSPREAD study)*
dc.typeArticle*
dc.relation.issue6*
dc.relation.volume29*
dc.relation.indexSCOPUS*
dc.relation.indexKCI*
dc.relation.startpage349*
dc.relation.lastpage355*
dc.relation.journaltitleAnnals of Pediatric Endocrinology and Metabolism*
dc.identifier.doi10.6065/apem.2448272.136*
dc.identifier.scopusid2-s2.0-85214379005*
dc.author.googleLee Y.J.*
dc.author.googleCheon C.K.*
dc.author.googleSuh J.*
dc.author.googleMoon J.-E.*
dc.author.googleAhn M.B.*
dc.author.googleChang S.H.*
dc.author.googleLee J.*
dc.author.googleChoi J.H.*
dc.author.googleKim M.*
dc.author.googleLim H.H.*
dc.author.googleKim J.*
dc.author.googleKim S.-H.*
dc.author.googleLee H.S.*
dc.author.googleLee Y.*
dc.author.googleKang E.*
dc.author.googleKim S.Y.*
dc.author.googleHong Y.H.*
dc.author.googleYang S.*
dc.author.googleHan H.-S.*
dc.author.googleChung S.*
dc.author.googleCho W.K.*
dc.author.googleKim E.Y.*
dc.author.googleKim J.K.*
dc.author.googleShim K.S.*
dc.author.googleYoo E.-G.*
dc.author.googleKim H.S.*
dc.author.googleYang A.*
dc.author.googleKim S.*
dc.author.googleNam H.-K.*
dc.author.googleCho S.Y.*
dc.author.googleLee Y.A.*
dc.contributor.scopusid김혜순(55663596500)*
dc.date.modifydate20250917123811*
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의과대학 > 의학과 > Journal papers
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