18 results match your criteria: "SBU Tepecik Training and Research Hospital[Affiliation]"
Saudi Med J
May 2024
From the Department of Anesthesiology and Reanimation Unit (Sen, Aydin), SBU Haseki Training and Research Hospital, Istanbul; and From the Department of Anesthesiology and Reanimation Unit (Uzun, Guldogan), SBU Tepecik Training and Research Hospital, İzmir, Turkey.
Objectives: To research the effects of blood cortisol and hemoglobinA1c (HBA1C) levels on mortality in patients admitted to the intensive care unit (ICU) and whether these factors could be used as reliable indicators for mortality risk assessment in these patients.
Methods: After receiving approval from the ethics committee, 79 patients admitted to ICU were included in the study. From patient files, we collected data on demographics (age, gender), presence of diabetes mellitus, and levels of cortisol, HbA1C, glucose, and lactate measured during hospitalization, along with acute physiology and chronic health evaluation (APACHE) II scores calculated within the first 24 hours.
Front Cardiovasc Med
November 2023
Department of Pediatric Cardiology Izmir, Katip Celebi University Faculty of Medicine, Izmir, Türkiye.
Introduction: Device closure of perimembranous ventricular septal defects (pmVSD) is a successful off-label treatment alternative. We aim to report and compare the outcomes of pmVSD closure in children weighing less than 10 kg using Amplatzer Duct Occluder II (ADOII) and Konar-MF VSD Occluder (MFO) devices.
Methods: Retrospective clinical data review of 52 children with hemodynamically significant pmVSD, and sent for transcatheter closure using ADOII and MFO, between January 2018 and January 2023.
Eur Rev Med Pharmacol Sci
September 2023
Department of Pediatrics, SBU Tepecik Training and Research Hospital, Izmir, Turkey.
Eur Rev Med Pharmacol Sci
May 2023
Department of Pediatric Cardiology, SBU Tepecik Training and Research Hospital, Izmir, Turkey.
Objective: Transcatheter closure of medium and large ventricular septal defects (VSDs) in young children is limited due to the use of over-sized devices that can cause hemodynamic instability and arrhythmia. In this study, we aimed to retrospectively evaluate the safety and efficacy of the device in the mid-term in children weighing less than 10 kg whose transcatheter VSD was closed only with the Konar-MFO device.
Patients And Methods: Among 70 children whose transcatheter VSD was closed between January 2018 and January 2023, 23 patients weighing less than 10 kg were included in the study.
Ther Apher Dial
October 2023
Department of İnternal Medicine, Afyonkarahisar Health Sciences University, Afyonkarahisar, Turkey.
Aim: To evaluate the inflammatory parameters and oxygenation in severe coronavirus disease-19 patients who underwent extracorporeal cytokine adsorption (CA).
Methods: Patients who underwent extracorporeal CA for cytokine storm were included in the study. The changes in oxygenation, laboratory parameters, and mortality rates were investigated.
Turk J Gastroenterol
June 2022
Department of Pediatric Infectious Diseases, Katip Celebi University - SBU Tepecik Training and Research Hospital, izmir, Turkey.
Background: Given that procedures involving gastrointestinal tract lumens are high-risk and aerosol forming, the functioning of endos- copy units has been reorganized during the coronavirus disease 2019 pandemic. Guidelines recommend that all personnel should carry out procedures in a negative-pressure room with personal protective equipment; in the absence of a negative-pressure room, an ade- quately ventilated room should be used. During the normalization of the coronavirus disease 2019 pandemic, this study aimed to evalu- ate children who were treated in our endoscopy unit without a negative-pressure chamber in terms of coronavirus disease 2019 after procedures.
View Article and Find Full Text PDFTurk Arch Pediatr
May 2022
İzmir Katip Çelebi University, Departments of Pediatric Gastroenterology, Hepatology, and Nutrition, İzmir, Turkey.
Objective: Gilbert syndrome (GS) is a disease characterized by mildly elevated indirect serum bilirubin levels due to mutation in the promoter of the UGT1A1 gene, which causes a decrease in uridine diphosphate glucuronyltransferase enzyme activity. Gilbert syndrome should be considered based on clinical and laboratory findings in differential diagnosis, which can be supported by genetic analysis. This study aimed to evaluate the clinical findings and UGT1A1 mutations of children with Gilbert syndrome.
View Article and Find Full Text PDFAm J Med
February 2022
Baskent University Adana Dr. Turgut Noyan Training and Research Hospital, General Surgery Department.
Turk J Med Sci
October 2021
Department of Anesthesiology and Reanimation, Intensive Care Unit, SBU Tepecik Training and Research Hospital, İzmir, Turkey.
Background: Biomarkers are useful for diagnosing infection and sepsis in adults, but data are limited in elderly patients. Furthermore, clinical symptoms of infection in elderly patients are usually atypical or unclear. We aimed to assess the usefulness of PCT, CRP, and WBC in distinguishing elderly patients infected with sepsis from infected without sepsis and those with no-infection.
View Article and Find Full Text PDFInt J Surg Case Rep
February 2021
Yeditepe University Faculty of Medicine, Department of Gastrointestinal Surgery, İstanbul, Turkey. Electronic address:
Introduction And Importance: In liver cyst hydatid surgery, presence of cysto-biliary communication (CBC) is important for the prevention of postoperative morbidity. If cysto-biliary connections are not obvious, diagnosis is not easy. Intraoperative bile leakage test has been shown to reduce postoperative biliary complications by revealing occult CBCs.
View Article and Find Full Text PDFTurk J Gastroenterol
September 2020
Department of Organ Transplantation and General Surgery, SBU Tepecik Training and Research Hospital, İzmir, Turkey.
Exp Clin Transplant
September 2020
From the Department of Pediatric Gastroenterology, Hepatology, and Nutrition, Izmir Katip Celebi University, SBU Tepecik Training and Research Hospital, Izmir, Turkey.
Waardenburg syndrome is a genetic disease characterized by hearing loss and pigmentation abnormalities. Waardenburg syndrome type 4 is very rare, and children with Waardenburg syndrome type 4 present with intestinal aganglionosis. The associated findings and severity of Waardenburg syndrome type 4 may also differ significantly between cases.
View Article and Find Full Text PDFEur J Gastroenterol Hepatol
January 2022
Department of Pediatric Gastroenterology, Hepatology and Nutrition, Cukurova University, Adana.
Introduction: Autoimmune hepatitis (AIH) is a common pediatric liver disease and long-term remission is usually maintained with low dose prednisolone and azathioprine (AZA). The aim of this study is to evaluate the efficiency of AZA monotherapy for maintenance treatment of children with AIH.
Materials And Methods: This study was a retrospective analysis of the 55 children with AIH.
Indian J Crit Care Med
May 2020
Department of Anesthesiology and Reanimation, Intensive Care Unit, SBU Tepecik Training and Research Hospital, Izmir, Turkey.
Objectives: Although high procalcitonin (PCT) levels are associated with poor neurological outcomes and increased mortality rates in patients treated with targeted temperature management (TTM) in the postcardiac arrest (CA) period, there are limited data about the correlation between PCT levels and infection. The aim of our study was to assess the relationship of PCT levels in the first 48 hours with early period infections, late period neurological prognosis, and mortality in patients treated with TTM after CA.
Materials And Methods: Serum PCT was measured on admission days 1 and 2.
J Pediatr Genet
June 2020
Department of Pediatric Nephrology, Izmir Katip Celebi University, SBU Tepecik Training and Research Hospital, Izmir, Turkey.
Renal-hepatic-pancreatic dysplasia-1 (RHPD1) is an ultra-rare genetic disorder with a high mortality. It is caused by biallelic pathogenic variants in , which encode nephrocytin, an important component of the ciliary protein complex. The -related disease phenotype is diverse with RHPD1, nephronophthisis-3, and Meckel syndrome-7.
View Article and Find Full Text PDFTurk J Gastroenterol
April 2019
Department of Pediatric Surgery, Izmir Katip Çelebi University - SBU Tepecik Training and Research Hospital, İzmir, Turkey.
Background/aims: Pediatric intestinal pseudo-obstruction (PIPO) is a severe disorder of gut motility. In this rare and difficult-to-manage disease, complex treatment method, such as intestinal transplantation, is sometimes needed. This study evaluated the management and follow-up results of patients with PIPO who received treatment at our center.
View Article and Find Full Text PDFIndian Pediatr
March 2018
Department of Pediatric Gastroenterology, Hepatology and Nutrition and Pediatric Surgery, Izmir Katip Celebi University, Izmir, Turkey.
Objective: The aim of this study was to examine the etiology of gallstones in children and responses to ursodeoxycholic acid (UDCA) treatment.
Methods: 74 children with cholelithiasis were recruited, and underwent ultrasonography to detect gallstones. All relevant clinical information was recorded in a structured proforma.
Gulf J Oncolog
May 2017
Dept of Radiation Oncology, Dokuz Eylül Univ Faculty of Medicine, Izmir, Turkey.
Aim Of The Study: To investigate the effects of dosevolume parameters of brain parenchyma, optic nerves (ONs) and cribriform plate (CP), which were determined on central nervous system (CNS) control in pediatric leukemia patients who have undergone prophylactic cranial irradiation (PCI) at our department.
Patients And Methods: In the current study, the records of 14 patients were examined retrospectively. Along with the minimum and maximum doses for brain and CP, D95% (minimal dose received by the 95% volume of a structure) and V95% (percent volume of target receiving 95% of prescribed dose) could be obtained from the dose-volume histogram.