Person:
YAKUT, KAHRAMAN

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Kurumdan Ayrılmıştır
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KAHRAMAN
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YAKUT
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Now showing 1 - 8 of 8
  • PublicationMetadata only
    A Report of Brugada Syndrome Presenting with Cardiac Arrest Triggered by Verapamil Intoxication
    (2017-11-01) Yakut, KAHRAMAN; Erdogan, Ilkay; Varan, Birgul; Atar, Ilyas; YAKUT, KAHRAMAN
    Background: Brugada syndrome is a disease characterized by a specific electrocardiographic pattern and an increased risk of sudden cardiac death. We present this case with the updated literature to emphasise the need to consider the diagnosis of Brugada syndrome in patients admitted to the emergency ward with sudden cardiac arrest.
  • PublicationMetadata only
    The results of interventional catheterization in infants weighing under 2,000 g
    (2019-07-01) Varan, Birgul; Tokel, N. Kursad; Yakut, KAHRAMAN; Erdogan, Ilkay; Ozkan, Murat; YAKUT, KAHRAMAN
    Background: The aim of this study was to evaluate the early and mid-term results of interventional cardiac catheterization and procedure-related complications in infants weighing <2,000 g.
  • PublicationMetadata only
    Asymptomatic giant congenital left atrial aneurysm
    (2019-01-01T00:00:00Z) Yakut, KAHRAMAN; Varan, Birgul; Erdogan, Ilkay; YAKUT, KAHRAMAN
    Congenital aneurysm of the left atrial appendage can be caused by congenital dysplasia of the pectinate muscles and may be accompanied by a congenital absence of the pericardium. Symptoms generally manifest after two decades and the most common symptom is atrial arrhythmia in the form of atrial fibrillation / flutter. A four year-old patient with no symptoms underwent an echocardiographic examination for the investigation of a heart murmur. Echocardiographic examination revealed a large cystic lesion occupying the left hemithorax and compressing the left ventricle. The patient was referred to our center. The lesion caused displacement of the heart rightward behind the sternum which made the examination difficult. We aimed to present this rare case of giant left atrial appendage aneurysm in the light of current literature.
  • PublicationMetadata only
    A rare cause of cyanosis in newborns: arteriovenous fistula between the right pulmonary artery and the left atrium and its treatment
    (2018-04-01T00:00:00Z) Yakut, KAHRAMAN; Varan, Birgul; Ozkan, Murat; YAKUT, KAHRAMAN
    The formation of a fistula between the right pulmonary artery and the left atrium via a sac is a very rare cyanotic congenital cardiopulmonary defect. A fistula between the pulmonary artery and left atrium may cause cardiac failure in utero. It can safely be treated surgically and in selected cases closure can be performed with transcatheter insertion of a device. In this article, we present a case with a fistula between the right pulmonary artery and the left atrium that was considered unsuitable for transcatheter closure and was safely treated surgically.
  • PublicationMetadata only
    A rare complication of balloon pulmonary angioplasty: Aortopulmonary window and its treatment
    (2019-01-01T00:00:00Z) Varan, Birgul; Yakut, KAHRAMAN; Tokel, Kursad; Ozkan, Suleyman; Aslamaci, Sait; YAKUT, KAHRAMAN
  • PublicationMetadata only
    Diagnosis and treatment of abnormal left coronary artery originating from the pulmonary artery: A single-center experience
    (2019-12-01T00:00:00Z) Yakut, KAHRAMAN; Tokel, Niyazi Kursad; Ozkan, Murat; Varan, Birgul; Erdogan, Ilkay; Aslamaci, Mehmet Sait; YAKUT, KAHRAMAN
    Objective: We aimed to review symptoms, findings, surgical treatment options, short- and mid-term outcomes, and reoperation rate of patients diagnosed with of left coronary artery from the pulmonary artery (ALCAPA) of an anomalous origin in our institution.
  • PublicationMetadata only
    Case report and the surgical treatment of two cases with pulmonary atresia in which pulmonary arteries is circulated by coronary arteries
    (2018-04-01) Yakut, KAHRAMAN; Tokel, Kursad; Varan, Birgul; Erdogan, Ilkay; Ozkan, Murat; YAKUT, KAHRAMAN
    Pulmonary atresia (PA) and ventricular septal defect (VSD) can occur in a variety of ways, from simple valve atresia to a condition in which circulation to the pulmonary bed occurs through collateral arteries separated from the aorta and there are no real pulmonary arteries, or they are present but hypoplastic. The size of the pulmonary arteries and concomitant complex cardiac lesions are important in making decisions about treatment and correctional alternatives. While complete correction surgeries in the style of a correction of tetralogy of Fallot are performed in simpler cases, many very invasive procedures are also performed and the resulting quality of life is very variable. The size of the pulmonary artery and its branches and the presence of accompanying collateral vessels are determining factors in the management of the disease. In this report, 2 cases of VSD and PA, in which the circulation of the pulmonary arteries was through the coronary arteries, diagnosed as a result of echocardiography performed following murmurs heard during examination, are described. The first patient was 40 days old and the second was 2 days old. In the second case, diagnosis was confirmed by catheter angiography, and in the first case, the final diagnosis was made during surgery. The aim of this report is to emphasize the importance of pulmonary artery size, the presence of pulmonary confluence, the origin of circulation, and concomitant collateral arteries when considering treatment methods.
  • PublicationMetadata only
    Diagnosis and surgical treatment of aortopulmonary window: Our single-center experience
    (2018-01-01) Yakut, KAHRAMAN; Ozkan, Murat; Varan, Birgul; Erdogan, Ilkay; Aslamact, Sait; YAKUT, KAHRAMAN
    Background: In this study, we aimed to report our single-center experience in aortopulmonary window and review clinical signs, symptoms, surgical correction techniques, and long-term outcomes.