Person: YAKUT, KAHRAMAN
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Publication Open Access Pulmonary Edema in the Acute Stage of Rheumatic Fever Treated with Double-Valve Replacement in a Pediatric Patient(2020-03-01T00:00:00Z) Yozgat, Yilmaz; Uzuner, Selcuk; YEŞİLBAŞ, OSMAN; Ogur, Mustafa; YAKUT, KAHRAMAN; Yozgat, Can Yilmaz; Temur, Hafize Otcu; AY, YASİN; YOZGAT, YILMAZ; UZUNER, SELÇUK; YAKUT, KAHRAMAN; AY, YASİNCardiogenic pulmonary edema (CPE) is a rare clinical condition of acute rheumatic fever (ARF) in the early stage. Generally, CPE can be convalesced by steroid and anticongestive treatment. Herein, we describe a case of a 14-year-old boy with ARF presenting with bilateral pulmonary edema secondary to acute mitral and aortic insufficiency. In this case, the pulmonary edema of ARF was successfully managed by combined surgical replacements of both valves.Publication Metadata only Management of pediatric cardiac transplantation candidates with pulmonary hypertension and high pulmonary vascular resistance(2020-06-01T00:00:00Z) Varan, Birgül; Gökdemir, Mahmut; Cındık, Nimet; Erdoğan, İlkay; Yakut, Kahraman; Sezgin, Atila; Tokel, N. Kürşad; Gümüş, Ayten; YAKUT, KAHRAMANPublication Metadata only Aortic balloon valvuloplasty and mid-term results in newborns: a single center experience.(2020-01-01T00:00:00Z) Varan, Birgül; Yakut, Kahraman; Erdoğan, İlkay; Özkan, Murat; Tokel, N. Kürşad; YAKUT, KAHRAMANPublication Metadata only Coronary artery fistulae and treatment in children(2020-08-01T00:00:00Z) Tokel, Niyazi Kürşad; Yakut, Kahraman; Varan, Birgül; Erdoğan, İlkay; Özkan, Murat; YAKUT, KAHRAMANPublication Open Access A Rare Cause of Pulmonary Hypertension in a 4-Year-Old Toddler: Association of Cor Triatriatum Sinister and Pulmonary Arteriovenous Malformation(2020-11-01T00:00:00Z) Yozgat, Can Yilmaz; ÇAKIR, Erkan; YAZAN, HAKAN; OTÇU TEMUR, Hafize; YAKUT, KAHRAMAN; YOZGAT, YILMAZ; ÇAKIR, ERKAN; YAZAN, HAKAN; OTÇU TEMUR, HAFİZE; YAKUT, KAHRAMAN; YOZGAT, YILMAZCor triatriatum sinister is a rare congenital cardiac anomaly. The anomaly is caused by a fibromuscular membrane that divides the left atrium into two cavities. This membrane can lead to the obstruction of left atrial flow and also create pulmonary venous hypertension. Pulmonary arteriovenous malformation (PAVM) is notorious for its aberrant blood flow between the pulmonary arteries and veins. Herein, we report a case of a 4-year-old toddler who had a unique form of pulmonary hypertension presenting with cor triatriatum sinister and diffuse PAVM. After the surgical treatment of cor triatriatum sinister, both pulmonary arteriovenous malformation and pulmonary hypertension disappeared.Publication Metadata only Acute Respiratory Distress Syndrome and MyocarditisCaused by Human Metapneumovirus in a Child(2020-04-01T00:00:00Z) Yakut, Kahraman; Varan, Birgül; Erdoğan, İlkay; Tokel, Niyazi Kürşad; YAKUT, KAHRAMANPublication Metadata only Evaluation of cardiac arrhythmias by electrocardiographic markers in pediatric patients who have tuberous sclerosis without cardiac rhabdomyoma(2021-04-01T00:00:00Z) Yozgat, Y.; Kus, H. D.; Kahraman, F. U.; Yuksel, M.; Firat, C. K.; Toprak, A.; Yozgat, C. Y.; Yakut, K.; Sahin, S. S.; Iscan, A.; Temur, H. O.; Ergor, S. N.; Erenberk, U.; Saritas, T.; USTABAŞ KAHRAMAN, FEYZA; TOPRAK, ALİ; YAKUT, KAHRAMANBackground: Tuberous sclerosis (TS) is an autosomal dominant and hereditary disorder. Cardiac rhabdomyoma and arrhythmias are the most deleterious risk factors linked to TS. Although arrhythmias in pediatric patients with TS who have cardiac rhabdomyoma have been frequently reported, arrhythmia in patients who have TS without rhabdomyoma is rarely reported in the literature. The study aimed to assess the susceptibility of pediatric patients who have TS without cardiac rhabdomyoma to cardiac arrhythmia using electrocardiographic (ECG) markers.Publication Open Access Management and Outcomes of Paediatric Patients with Palpitations Examined in Our Clinic(2020-07-01T00:00:00Z) YAKUT, KAHRAMANObjective: We retrospectively reviewed the data of patients who presented to the paediatric cardiology clinic with complaints of palpitations. We aimed to describe the characteristics of these patients, the rhythm disorders that were detected, and the treatment methods with a particular attention on rare and vital diseases. Methods: In total, 1,680 patients aged 5-18 years who presented with palpitations at the paediatric cardiology clinic between January 2016 and June 2019 were enrolled. Of these, 714 (42.5%) were male and 966 (57.5%) were female. All the hospital records including electrocardiography, echocardiography, cardiovascular stress test, 24-h Holter monitoring, event recorder and genetic analysis results were reviewed. Results: The mean age of the patients was 13.5 +/- 3.2 years (range: 5-17.8 years). Palpitation was accompanied with chest pain in 218 patients, shortness of breath in 152 patients and weakness in 67 patients. Also, 726 Holter monitoring, 165 event recorder and 104 cardiovascular stress test results were evaluated. Dysrhythmia was detected in 306 patients (18.2%). The most common dysrhythmias were supraventricular extrasystoles (n=171, 55.8%) and ventricular extrasystoles (n=82, 26.8%). Five patients were diagnosed with non-sustained ventricular tachycardia (VT) episodes, one with long QTc syndrome and one with catecholaminergic polymorphic VT. Two patients were followed-up for arrhythmogenic right ventricular dysplasia (ARVD), 12 patients had mitral valve prolapsed (MVP), 8 had valvular heart disease caused by acute rheumatic fever (ARF) and 7 had bicuspid aortic valve (BAV). Conclusion: Palpitation is one of the common causes of outpatient clinic visits in children and it may be the first symptom of serious arrhythmias, although it is frequently associated with benign pathologies. Most life-threatening dysrhythmias can be detected by a thorough analysis of the patient using basic cardiological examination methods.