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Dive into the research topics where Umut Kocabaş is active.

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Featured researches published by Umut Kocabaş.


Heart Rhythm | 2015

High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia

Can Hasdemir; Serdar Payzin; Umut Kocabaş; Hatice Sahin; Nihal Yildirim; Alpay Alp; Mehmet Aydin; Ryan Pfeiffer; Elena Burashnikov; Yuesheng Wu; Charles Antzelevitch

BACKGROUND Atrioventricular nodal reentrant tachycardia (AVNRT) may coexist with Brugada syndrome (BrS). OBJECTIVES The present study was designed to determine the prevalence of drug-induced type 1 Brugada ECG pattern (concealed BrS) in patients presenting with clinical spontaneous AVNRT and to investigate their electrocardiographic, electrophysiological, and genetic characteristics. METHODS Ninety-six consecutive patients without any sign of BrS on baseline electrocardiogram undergoing electrophysiological study and ablation for symptomatic, drug-resistant AVNRT and 66 control subjects underwent an ajmaline challenge to unmask BrS. Genetic screening was performed in 17 patients displaying both AVNRT and BrS. RESULTS A concealed BrS electrocardiogram was uncovered in 26 of 96 patients with AVNRT (27.1%) and in 3 of 66 control subjects (4.5%) (P ≤ .001). Patients with concealed BrS were predominantly female patients (n=23 [88.5%] vs n=44 [62.9%], P = .015), had higher prevalence of chest pain (n=10 [38.5%] vs n=13 [18.6%], p=0.042), migraine headaches (n=10 [38.5%] vs n=10 [14.2%], p=0.008), and drug-induced initiation and/or worsening of duration and/or frequency of AVNRT (n=4 [15.4%] vs n=1 [1.4%], p=0.006) as compared to patients with AVNRT without BrS. Genetic screening identified 19 mutations or rare variants in 13 genes in 13 of 17 patients with both AVNRT and BrS (yield = 76.5%). Ten of these 13 genotype-positive patients (76.9%) harbored genetic variants known or suspected to cause a loss of function of cardiac sodium channel current (SCN5A, SCN10A, SCN1B, GPD1L, PKP2, and HEY2). CONCLUSION Our results suggest that spontaneous AVNRT and concealed BrS co-occur, particularly in female patients, and that genetic variants that reduce sodium channel current may provide a mechanistic link between AVNRT and BrS and predispose to expression of both phenotypes.


Annals of Noninvasive Electrocardiology | 2017

Brugada syndrome, Brugada phenocopy or none?

Umut Kocabaş; Can Hasdemir; Esra Kaya; Cuneyt Turkoglu; Adrian Baranchuk

Brugada syndrome is a form of inherited arrhythmia syndrome characterized by a distinct ST‐segment elevation in the right precordial leads. Brugada phenocopies are clinical entities that present with an electrocardiographic pattern identical to Brugada syndrome and may obey to various clinical conditions. We present a case of a suicidal attempt using a high dose of propafenone causing a Brugada‐type electrocardiographic pattern. Is this a Brugada syndrome case, a Brugada phenocopy or something else?


Echo research and practice | 2016

A complicated trilogy: persistent left superior vena cava with hypertrophic cardiomyopathy and atrial septal defect

Umut Kocabaş; Esra Kaya; Cahide Soydas Cinar

Extract: A 28-year-old asymptomatic woman was referred to ourclinic for evaluation of a heart murmur. Transthoracic echocardiography (TTE) demonstrated ventricular hypertrophy with septal thickness of 26 mm., consistent with hypertrophic cardiomyopathy (HCM). The diagnosis of HCM was confirmed by contrast-enhanced magnetic resonance imaging, and late gadolinium enhancement was observed in the anterior wall ...


Pacing and Clinical Electrophysiology | 2018

Coexistence of atrioventricular accessory pathways and drug-induced type 1 Brugada pattern

Can Hasdemir; Jimmy Jyh-Ming Juang; Sedat Kose; Umut Kocabaş; Mehmet Orman; Serdar Payzin; Hatice Sahin; Candan Celen; Emin Evren Ozcan; Ching-Yu Julius Chen; Ramazan Gunduz; Oguzhan E. Turan; Oktay Senol; Elena Burashnikov; Charles Antzelevitch

Atrial arrhythmias, particularly atrioventricular nodal reentrant tachycardia, can coexist with drug‐induced type 1 Brugada electrocardiogram (ECG) pattern (DI‐Type1‐BrP). The present study was designed to determine the prevalence of DI‐Type1‐BrP in patients with atrioventricular accessory pathways (AV‐APs) and to investigate the clinical, electrocardiographic, electrophysiologic, and genetic characteristics of these patients.


Balkan Medical Journal | 2017

Not All Brugada Electrocardiogram Patterns are Brugada Syndrome or Brugada Phenocopy

Grace Xu; Byron H. Gottschalk; Umut Kocabaş; Adrian Baranchuk

Address for Correspondence: Dr. Grace Xu, Department of Medicine, Queen’s University School of Medicine, Kingston, Canada Phone: 647 234 6926 e-mail: [email protected] Received: 31 May 2017 Accepted: 15 September 2017 • DOI: 10.4274/balkanmedj.2017.0621 Available at www.balkanmedicaljournal.org Cite this article as: Xu G, Gottschalk BH, Kocabaş U, Baranchuk A. Not All Brugada Electrocardiogram Patterns are Brugada Syndrome or Brugada Phenocopy. Balkan Med J 2017;34:593 ©Copyright 2017 by Trakya University Faculty of Medicine / The Balkan Medical Journal published by Galenos Publishing House. Not All Brugada Electrocardiogram Patterns are Brugada Syndrome or Brugada Phenocopy


International Journal of the Cardiovascular Academy | 2016

Coronary injection ventriculography: Multiple coronary-cameral fistulas as a rare cause of stable angina pectoris

Umut Kocabaş; Esra Kaya; Mustafa Akin


International Journal of the Cardiovascular Academy | 2016

Novel oral anticoagulants in non-valvular atrial fibrillation: Pharmacological properties, clinical trials, guideline recommendations, new antidote drugs and real-world data☆

Umut Kocabaş; Esra Kaya; Gökhan Avcı


TÜRK KARDİYOLOJİ DERNEĞİ ARŞİVİ | 2018

Sinsi bir düşmanın histopatolojik tanısı ve çoklu model görüntülenmesi: Primeri bilinmeyen malign melanomun kardiyak metastazı

Umut Kocabaş; Esra Kaya; Cahide Soydas Cinar


International Journal of the Cardiovascular Academy | 2018

Congenital and acquired Lutembacher's syndrome presenting in two adults

Umut Kocabaş; UgurOnsel Turk


American Journal of Cardiology | 2018

Predictive Value of Cha2ds2-vasc and Cha2ds2-vasc-hs Scores for Failed Reperfusion after Thrombolytic Therapy in Patients with St-elevation Myocardial Infarction

Salih Kilic; Umut Kocabaş; Levent Can; Oguz Yavuzgil; Mustafa Cetin; Mehdi Zoghi

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