İbrahim İlker Çetin
Başkent University
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Publication
Featured researches published by İbrahim İlker Çetin.
Echocardiography-a Journal of Cardiovascular Ultrasound and Allied Techniques | 2017
Mehmet Emre Ari; Filiz Ekici; İbrahim İlker Çetin; Emine Betül Tavil; Nese Yarali; Pamir Isik; Tuncay Hazirolan; Bahattin Tunç
The purpose of this study is to determine early myocardial dysfunction in β‐thalassemia major (BTM) patients. Where the myocardial dysfunction cannot be detected by conventional echocardiography, it could be detected by tissue Doppler imaging (TDI) or speckle tracking echocardiography (STE).
Echocardiography-a Journal of Cardiovascular Ultrasound and Allied Techniques | 2018
İbrahim İlker Çetin; Hazım A. Gursu; Ayşe Esin Kibar; Murat Sürücü; Ali Orgun; Utku Pamuk
To investigate myocardial deformation and function during treatment for Kawasaki disease (KD) in children.
Turkish Journal of Pediatrics | 2016
İbrahim İlker Çetin; Filiz Ekici; Abdullah Kocabaş; Berna Şaylan Çevik; Sancar Eminoğlu; Ayşe Esin Kibar; Mehmet Emre Ari; Murat Sürücü; Ali Orgun
This clinical study was designed to evaluate mortality rate and the factors that may affect survival in neonatal surgery unit. Randomly chosen 300 (ß: 0.20) patients among 1,439 patients treated in neonatal surgery unit during years 1983 to 2009, were evaluated retrospectively. The patients were separated into three groups according to date of treatment; Group A: 1983 - 1995, Group B: 1996 - 2005 and Group C: 2005 - 2009. M/F ratios did not differ between non-survived and survived patient populations. Mortality rates were 37%, 22% and 13% in Group A, B, and C respectively (p < 0.001). Parenteral nutrition, maternal age, time until admission and gestational age did not affect mortality rate, however median age of newborn was lower in non-survived cases (1 day vs. 3 days, p < 0.001). Associating abnormality, low birth weight ( < 1,500 g), associating sepsis, need of globulin and requirement of respiratory support were determinants of lower survival (p < 0.001). The mortality rate for patients that underwent thoracotomy (42%) and laparotomy (41%) were higher than patients that underwent other operations (8%) and observation (10%) (p < 0.001). Diaphragmatic hernia had higher mortality rates than the other pathologies (p < 0.001). Survival rate is increasing to date in newborn pediatric surgery unit; it is independent from parenteral nutrition, maternal age, time to admission and gestational age however it is affected adversely by the age of patient, associating abnormality, low birth weight, presence of sepsis and requirement of respiratory support. Increase in survival could be related to various additional factors such as development of delicate respiratory support machines, broad spectrum antibiotics, hospital infection control teams, central venous catheters, use of TPN by central route, volume adjustable infusion pumps, monitoring devices, neonatal surgical techniques, prenatal diagnosis of pediatric surgical conditions and developments of environmental control methods in neonatal surgical units.The objective was to compare the efficacy and safety of naproxen (NXN) to acetylsalicylic acid (ASA) in the treatment of acute rheumatic fever (ARF). The data of 338 children were retrospectively analyzed. The patients were grouped according to joint and valve involvement and also drug chosen [methyl prednisolone (mPSL), ASA or NXN]. The treatment results and adverse events in each group were compared. The mean age was 10.3 years and the median follow-up was 62 months. Median time for normalization of acute phase reactants was 1 week in patients given steroids and 2 weeks in patients given ASA or NXN. ASA was replaced with NXN in 18 patients (10.2%) due to hepatic toxicity. The rate of rebound, recurrence and the prevalence of rheumatic valve disease were not different in patients given NXN, ASA or mPSL. In conclusion, NXN is a safe and effective alternative to ASA in the treatment of ARF in children.
Pediatric Transplantation | 2015
Derya Özyörük; Ayşe Esin Kibar; Murat Sürücü; Suna Emir; İbrahim İlker Çetin; Bahattin Tunç; Namik Ozbek
PH is a rare condition with high mortality rate after pediatric HSCT. As clinical presentation is non‐specific and may mimic other conditions, a high degree of suspicion is required for diagnosis. Here, we present a patient with stage‐IV neuroblastoma who developed PAH after autologous HSCT. After exclusion of other causes of PH, we regarded that this condition was secondary to HSCT.
Cardiology in The Young | 2018
Hazım A. Gursu; İbrahim İlker Çetin
Paediatric cardiology is arguably the sub-specialty in which the greatest advances have been made in both disease diagnosis and treatment over the past half a century. Paediatric cardiology emerged as a discipline in the 1930s. Since then, advances in imaging techniques such as echocardiography, angiography, CT, or magnetic resonance and extracorporeal circulation have provided excellent diagnosis and treatment of CHD. The pioneers of paediatric cardiology are more than eponyms, for each used in new and original ways the tools and concepts available in his or her era. This brief overview of the history of paediatric cardiology on stamps begins from William Harvey up to our own time, and includes the milestones in paediatric cardiology.
Anatolian Journal of Cardiology | 2017
Sanliay Şahin; Mutlu Uysal Yazici; Ganime Ayar; Tülin Köksal; İbrahim İlker Çetin; Filiz Ekici; Abdullah Kocabaş
Objective: To determine the indication and necessity of echocardiographic assessment and therapeutic interventions in critically ill children. Methods: A total of 140 children, including 75 mechanically ventilated (MV) and 65 spontaneously breathing (SB) children, who were admitted consecutively from March to August 2013 were evaluated prospectively. Data regarding the indication for echocardiography and therapeutic approaches used were documented. For evaluating disease severity, the Pediatric Risk of Mortality Score III (PRISM) was ascertained. The correlation between PRISM score and the requirement of echocardiographic evaluations were analyzed. Results: Patients ages were between 45 days to 18 years. The male-to-female ratio was 1.33. In 35.4% patients who underwent echocardiographic evaluation, no definitive alteration occurred in treatment approach, whereas in the remaining 64.6% patients, decisive or supplemental information was gathered. Echocardiography was indicated in 88% MV children and 46.2% SB children. Echocardiographic evaluation was necessary in MV children and there was a positive correlation between the PRISM score and the requirement of echocardiographic assessment (p<0.001). Conclusion: Echocardiographic evaluation is an invaluable tool especially in MV children and the requirement of echocardiographic assessment increases according to clinical severity. Basic training for intensivists in this procedure is crucial and needs to be improved and supported in critically ill.
Archives of the Turkish Society of Cardiology | 2016
Hatice Tatar Aksoy; Handan Ünsal; İbrahim İlker Çetin
Atrioventricular (AV) block in the neonatal period is a rare disorder. It is frequently associated with underlying structural congenital heart disease and maternal lupus. Presently described is premature baby who developed 2:1 AV block and congestive heart failure due to hypocalcemia. Dramatic clinical improvement was observed following treatment of intravenous 10% calcium gluconate. Therefore, it is suggested that serum calcium level of newborns with AV block and congestive heart failure be measured.
Pediatrics International | 2005
İbrahim İlker Çetin; Arda Saygili; Beyhan Demirhan; Kürşad Tokel
Arrhythmogenic right ventricular dysplasia (ARVD) is a myocardial disease of unknown etiology and it is included among the cardiomyopathies in most of the classification systems. It is thought to be a consequence of myocyte loss either on a genetic or acquired basis causing transdifferentiation from myocytes to adipocytes. Familial occurance with an autosomal inheretence is also known. 1 Clinical manifestations include palpitations, syncopal episodes, findings of heart failure, stroke and sudden death. 2–4 Postmortem diagnosis of ARVD can be important in identification of possible affected family members in order to initiate early treatment modalities. The optimal treatment strategies are not clear but may include antiarrhythmic drugs, radiofrequency ablation, implantable defibrillators, and the treatment of heart failure if present. 5–7
CardioVascular and Interventional Radiology | 2005
İbrahim İlker Çetin; Utku Arman Örün; Birgül Varan; Mehmet Coskun; Kürşad Tokel
We have reported a patient with aortopulmonary window (APW) simulating truncus. In classically defined APW, aorta and main pulmonary artery separate again after a distance from the window and form the aortic arch and pulmonary arteries. However, in our case, there was no separation and they formed a very large pouch from which the great vessels originated. Thus, we believe that we have presented the first case of APW simulating truncus, but with two separate semilunar valves.
European Journal of Medical Genetics | 2005
İbrahim İlker Çetin; Dilek Aktas; Ergul Tuncbilek