Searchable abstracts of presentations at key conferences in endocrinology

ea0090rc3.5 | Rapid Communications 3: Pituitary and Neuroendocrinology 1 | ECE2023

The Reassessment of Therapeutic Decisions by Clinicians According to the SAGIT® Instrument in Acromegaly: Results of a Multicenter Study

Turgut Seda , Ciftci Sema , Yilmaz Nusret , Uysal Serhat , Muradov İlkin , Kılıc Kan Elif , Cansu Guven Baris , Yenidunya Yalın Gulşah , Uc Ziynet ALphan , Sarıbeyliler Goktuğ , Pehlivan Esma , Bagir Gulay Simsek , Tanrikulu Seher , Yaylali Guzin , Mısıroğlu Fuat , Omma Tulay , Selcukbiricik Ozlem Soyluk , Cakir İlkay , Yurekli Banu Sarer , Ertorer Melek Eda , Kadioglu Pinar , Saygili Fusun , Yarman Sema

Objective: SAGIT, a new instrument designed for therapeutic decision, is not routinely used yet. While the medical treatment was mostly planned according to disease activity by hormonal evaluation, the therapeutic decision has tried to be standardized with the SAGIT instrument. The aim of this study is to reassess the therapeutic decisions by clinicians in the management of acromegaly according to the SAGIT instrument.Material and Method: This multicente...

ea0090ep19 | Adrenal and Cardiovascular Endocrinology | ECE2023

21-hydroxylase deficient congenital adrenal hyperplasia in adult endocrinology clinics of turkey: A nationwide multicenter study

Ertorer Melek Eda , Anaforoglu İnan , Yilmaz Nusret , Akkus Gamze , Turgut Seda , Unluhizarci Kursad , Selcukbiricik Ozlem Soyluk , Merdin Fatma Avcı , Karakilic Ersen , Pehlivan Esma , Yorulmaz Goknur , Gul Ozen Oz , Emral Rifat , Kebapci Medine Nur , Acubucu Fettah , Tuzun Dilek , Gorar Suheyla , Topuz Emek , Bagir Gulay Simsek , Genc Selin , Demir Kezban , Tamer Gonca , Yaylali Guzin , Omma Tulay , Firat Sevde Nur , Koc Gonul , Saygili Emre Sedar , Yurekli Banu Sarer

Introduction: Congenital adrenal hyperplasia (CAH) is a group of autosomal recessively inherited disorders that are characterised by inactivating mutations at various steps of adrenal steroidogenic pathways causing defective cortisol biosynthesis. 21-Hydroxylase enzyme deficiency (21-OHd) constitutes more than 95% of all CAH cases.Material & Methods: Medical records of patients with all forms of CAH from 19 adult endocrinology clinics located at six ...

ea0090rc7.5 | Rapid Communications 7: Pituitary and Neuroendocrinology 2 | ECE2023

Evaluation and follow-up data of patients diagnosed with hypophysitis: A multicentric nationwide study

Hacioglu Aysa , Karaca Zuleyha , Uysal Serhat , Ozkaya Hande Mefkure , Kadioglu Pinar , Selcukbiricik Ozlem Soyluk , Yarman Sema , Gul Nurdan , Koksalan Damla , Selek Alev , Cetinarslan Berrin , Canturk Zeynep , Tuğce Şah unal Fatma , Corapcıoğlu Demet , Sahin Mustafa , Babayeva Afruz , Akturk Mujde , Eraydin Ayten , Fenkci Semin , Piskinpasa Hamide , Ciftci Sema , Dokmetaş Meric , Şahin Onur , Sebile Dokmetas H. , Ozturk Sadettin , Akarsu Ersin , Kılıc Kan Elif , Atmaca Aysegul , Pehlivan Esma , Saygili Fusun , Erkan Buruc , Burhan Sebnem , Omma Tulay , Uc Ziynet Alphan , Elbuken Gulsah , Bayram Fahri , Yorulmaz Goknur , Cansu Guven Baris , Bostan Hayri , Turan Kubra , Sener Selcuk Yusuf , Gorar Suheyla , Pekkolay Zafer , Hekimsoy Zeliha , Dogruel Hakan , Ertorer Melek Eda , Topaloğlu Omercan , Celik Ozlem , Iyidir Ozlem , Kelestimur Fahrettin

Background: Hypophysitis is a rare group of disease characterized with infla mmation of the pituitary gland. Rarity of the disease obviates development of a treatment strategy. We aimed to present the nationwide data of the demographics, clinical and radiological characteristics, treatment modalities and responses of the patients diagnosed with hypophysitis in a retrospective manner.Methods: The endocrinology clinics all over the country were invited to ...