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15 results on '"Svjetlana Tisma-Dupanovic"'

1. Atrioventricular nodal reentrant tachycardia in patients with complex congenital heart disease and twin atrioventricular nodes

Author

John Papagiannis, MD, FHRS, Christopher Mathis, MD, Lindsey Malloy-Walton, DO, and Svjetlana Tisma-Dupanovic, MD, FHRS

Subjects
Ablation, Atrial isomerism, Atrioventricular nodal reentrant tachycardia, Congenital heart disease, Cryoablation, Twin atrioventricular nodes, Diseases of the circulatory (Cardiovascular) system, RC666-701
Published
2020
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3. PO-03-149 CURRENT STATE OF CARDIAC IMPLANTABLE ELECTRONIC DEVICE REMOTE MONITORING IN PEDIATRICS AND CONGENITAL HEART DISEASE: A PACES-SPONSORED QUALITY IMPROVEMENT INITIATIVE

Author

Bradley C. Clark, Douglas Y. Mah, Ronn E. Tanel, Caitlin Brateng, Patrick S. Connell, Brynn E. Dechert-Crooks, Svjetlana Tisma-Dupanovic, Arnold L. Fenrich, Allison C. Hill, Elizabeth E. Jarosz, Martin J. LaPage, Anthony C. McCanta, Lindsey E. Malloy-Walton, Melissa Olen, Andreas Pflaumer, Andrew E. Radbill, Karen A. Smoots, Robert D. Whitehill, and Aarti Dalal

Subjects
Physiology (medical), Cardiology and Cardiovascular Medicine
Published
2023
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6. B-PO05-194 UNEXPLAINED VENTRICULAR FIBRILLATION IN YOUNG

Author

Chandra Srinivasan, Sherrie Joy A. Baysa, Seshadri Balaji, Jennifer Nelson, John Papagiannis, Eric S. Silver, Patricia E. Thomas, Frank A. Fish, Mary C Niu, Sabrina Tsao, Harinder R. Singh, Susan P. Etheridge, Lindsey Malloy-Walton, Svjetlana Tisma-Dupanovic, Robert Whitehill, Ronald J. Kanter, and Reina Bianca Tan

Subjects
medicine.medical_specialty, business.industry, Physiology (medical), Internal medicine, Ventricular fibrillation, medicine, Cardiology, Cardiology and Cardiovascular Medicine, medicine.disease, business
Published
2021
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7. B-PO02-197 PATTERNS OF ELECTROCARDIOGRAPH ABNORMALITIES IN CHILDREN WITH HYPERTROPHIC CARDIOMYOPATHY

Author

Susan P. Etheridge, Andreas Pflaumer, Stephanie J. Nakano, Christopher M. Janson, Andrew D. Blaufox, Michaela Horndasch, Christopher C. Erickson, Shubhayan Sanatani, Margaret J. Strieper, Aneeq Malik, Maria Ilina, Richard T. Smith, Harinder R. Singh, Philip M. Chang, Peter F. Aziz, Walter Li, Peter Kubuš, Seshadri Balaji, Ilana Zeltser, Leonardo Liberman, Naomi J. Kertesz, Anjan S. Batra, Mayme Marshall, Michal J. Kantoch, Narayanswami Sreeram, Jason M. Garnreiter, Anne Fournier, George M. McDaniel, Frank A. Fish, Maully J. Shah, Frank Zimmermann, Robert M. Hamilton, Svjetlana Tisma-Dupanovic, Mitchell I. Cohen, Ian H. Law, Jeremy P. Moore, and Mark W. Russell

Subjects
medicine.medical_specialty, business.industry, Physiology (medical), Internal medicine, Cardiology, Hypertrophic cardiomyopathy, Medicine, Cardiology and Cardiovascular Medicine, business, medicine.disease
Published
2021
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8. B-PO05-167 ATRIAL TACHYARRHYTHMIAS IN CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA: A REPORT FROM THE INTERNATIONAL PEDIATRIC CPVT REGISTRY

Author

Anna N. Kamp, Dania Kallas, Santokh Dhillon, Sit-Yee Kwok, Thomas M. Roston, Susan P. Etheridge, Shubhayan Sanatani, Martin J. LaPage, Adam C. Kean, Rouzbeh Ghadiry-Tavi, Joseph Atallah, Prince J. Kannankeril, Georgia Sarquella Brugada, Linda M. Knight, James C. Perry, Andrew D. Krahn, Allison C. Hill, Peter Kubuš, Yung R. Lau, Christopher L. Johnsrude, Anne Fournier, Svjetlana Tisma-Dupanovic, Ian H. Law, Robert M. Hamilton, Sonia Franciosi, Jordana Kron, Joshua R. Kovach, Peter S. Fischbach, David Backhoff, and Seshadri Balaji

Subjects
medicine.medical_specialty, business.industry, Physiology (medical), Internal medicine, medicine, Cardiology, Cardiology and Cardiovascular Medicine, Catecholaminergic polymorphic ventricular tachycardia, medicine.disease, business
Published
2021
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9. B-AB20-04 PROSPECTIVE ASSESSMENT OF CHILDREN WITH WOLFF-PARKINSON-WHITE SYNDROME: HOW RARE ARE EVENTS, REALLY?

Author

Shubhayan Sanatani, Naomi J. Kertesz, David J. Bradley, Nicholas H. Von Bergen, Christopher M. Janson, Svjetlana Tisma-Dupanovic, Ian H. Law, Andrew E. Radbill, Mary C. Niu, Jennifer R. Maldonado, Jayaprakash Shenthar, Charles C. Anderson, Gregory Webster, Jinque Kuang, Brynn E. Dechert-Crooks, Gaurav Arora, Peter F. Aziz, David Gamboa, Cheyenne Beach, Ahmad Sami Chaouki, Ronn E. Tanel, Anna N. Kamp, Lindsey Malloy Walton, John Papagiannis, Sarah Yukiko Asaki, Prince J. Kannankeril, Susan P. Etheridge, Andrew D. Blaufox, Christopher C. Erickson, and Thomas A. Pilcher

Subjects
Pediatrics, medicine.medical_specialty, White (horse), business.industry, Physiology (medical), medicine, Cardiology and Cardiovascular Medicine, business
Published
2021
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10. B-PO03-182 PRIMARY PREVENTION IMPLANTABLE CARDIOVERTER-DEFIBRILLATORS IN CHILDREN WITH CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA: A PROSPECTIVE STUDY OF THE INTERNATIONAL PEDIATRIC CPVT REGISTRY

Author

Dania Kallas, Prince J. Kannankeril, David Backhoff, Susan P. Etheridge, Linda M. Knight, Andrew D. Krahn, Martin J. LaPage, Joseph Atallah, Seshadri Balaji, Joshua R. Kovach, Thomas M. Roston, Shubhayan Sanatani, Santokh S. Dhillon, Peter Kubuš, Anna N. Kamp, Sonia Franciosi, Christopher L. Johnsrude, Allison C. Hill, Peter S. Fischbach, Avani Lamba, Sit-Yee Kwok, Adam C. Kean, James C. Perry, Yung R. Lau, Anne Fournier, Svjetlana Tisma-Dupanovic, and Ian H. Law

Subjects
medicine.medical_specialty, business.industry, Physiology (medical), Internal medicine, Primary prevention, medicine, Cardiology, Cardiology and Cardiovascular Medicine, business, Prospective cohort study, Catecholaminergic polymorphic ventricular tachycardia, medicine.disease
Published
2021
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11. An Adolescent with Possible Arrhythmogenic Right Ventricular Dysplasia and Long QT Syndrome: Evaluation and Management

Author

Sanket Shah, Svjetlana Tisma-Dupanovic, Arthur J. Moss, B D O Jonathan Wagner, and David T. Huang

Subjects
congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, medicine.diagnostic_test, business.industry, medicine.medical_treatment, Long QT syndrome, Catheter ablation, General Medicine, medicine.disease, Arrhythmogenic right ventricular dysplasia, Physiology (medical), Internal medicine, medicine, Cardiology, cardiovascular diseases, Differential diagnosis, Cardiology and Cardiovascular Medicine, business, Electrocardiography, Genetic testing, Cardiac catheterization
Abstract

We describe a unique presentation of arrhythmogenic right ventricular dysplasia (ARVD) in a 14-year-old Caucasian male who was additionally diagnosed with long QT syndrome (LQTS). Genetic testing eventually confirmed the diagnosis of both ARVD and LQTS, which combined, to our knowledge, has not been reported in the literature.

Published
2013
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12. The Study of Antiarrhythmic Medications in Infancy (SAMIS)

Author

Harinder R. Singh, J. Philip Saul, Susan P. Etheridge, Kenny K. Wong, Yaniv Bar-Cohen, Pamela S. Ro, James E. Potts, Karen Gibbs, Anne Fournier, Svjetlana Tisma-Dupanovic, Shubhayan Sanatani, Charles C. Anderson, Elizabeth A. Stephenson, Ronald J. Kanter, Bertrand A. Ross, Anjan S. Batra, John H. Reed, Andrew D. Blaufox, Andrew S. Mackie, and Brian W. McCrindle

Subjects
Male, Tachycardia, Canada, Digoxin, Propranolol, law.invention, Double-Blind Method, Randomized controlled trial, Recurrence, law, Physiology (medical), Tachycardia, Supraventricular, Clinical endpoint, medicine, Humans, Adverse effect, Proportional Hazards Models, Chi-Square Distribution, business.industry, Infant, Newborn, Infant, medicine.disease, United States, Clinical trial, Treatment Outcome, Anesthesia, Female, Supraventricular tachycardia, medicine.symptom, Cardiology and Cardiovascular Medicine, business, Anti-Arrhythmia Agents, medicine.drug
Abstract

Background— Supraventricular tachycardia (SVT) is one of the most common conditions requiring emergent cardiac care in children, yet its management has never been subjected to a randomized controlled clinical trial. The purpose of this study was to compare the efficacy and safety of the 2 most commonly used medications for antiarrhythmic prophylaxis of SVT in infants: digoxin and propranolol. Methods and Results— This was a randomized, double-blind, multicenter study of infants P =0.25). No first recurrence occurred after 110 days of treatment. The 6-month recurrence-free status was 79% for patients on digoxin and 67% for patients on propranolol ( P =0.34), and there were no first recurrences in either group between 6 and 12 months. There were no deaths and no serious adverse events related to study medication. Conclusions— There was no difference in SVT recurrence in infants treated with digoxin versus propranolol. The current standard practice may be treating infants longer than required and indicates the need for a placebo-controlled trial. Clinical Trial Registration Information— http://clinicaltrials.gov ; NCT-00390546.

Published
2012
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13. Prolonged QT in a 13-Year-Old Patient with Down Syndrome and Complete Atrioventricular Canal Defect

Author

Ilan Goldenberg, David T. Huang, Svjetlana Tisma-Dupanovic, Rengasamy Gowdamarajan, Timothy Knilans, and Jeffrey A. Towbin

Subjects
Andersen Syndrome, Down syndrome, medicine.medical_specialty, medicine.diagnostic_test, business.industry, Prolonged QT, General Medicine, medicine.disease, Physiology (medical), Internal medicine, Cardiology, Medicine, Electrical conduction system of the heart, Atrioventricular canal defect, Cardiology and Cardiovascular Medicine, business, Atrioventricular cushions, Electrocardiography
Published
2011
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14. Impact of the permanent ventricular pacing site on left ventricular function in children: a retrospective multicentre survey

Author

Ward Y. Vanagt, Peter P. Karpawich, Petr Kubuš, Patrick Frias, Anita Hiippala, Andreas Blank, Kathryn K. Collins, Conceicao Trigo, Sabrina Tsao, John Papagiannis, Bert Nagel, Jan Marek, Jan Hendrik Nürnberg, Gisela Dann, Xavier Ganame, Irene E. van Geldorp, Fulvio Gabbarini, Svjetlana Tisma-Dupanovic, Jan Janoušek, Thierry Sluysmans, Roman Gebauer, Jan Elders, Maren Tomaske, Jean Benoit Thambo, Frits W. Prinzen, Mark K. Friedberg, Annette Rackowitz, Tammo Delhaas, Andreas Früh, Viera Illikova, S. A. Clur, ACS - Amsterdam Cardiovascular Sciences, AII - Amsterdam institute for Infection and Immunity, APH - Amsterdam Public Health, Paediatric Cardiology, Cardiologie, Biomedische Technologie, Kindergeneeskunde, Fysiologie, and RS: CARIM School for Cardiovascular Diseases

Subjects
Male, medicine.medical_specialty, Adolescent, Cardiomyopathy, 030204 cardiovascular system & hematology, Ventricular Function, Left, Electrocardiography, Ventricular Dysfunction, Left, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, medicine, Humans, 030212 general & internal medicine, cardiovascular diseases, Atrioventricular Block, Child, Retrospective Studies, Ventricular function, medicine.diagnostic_test, business.industry, Cardiac Pacing, Artificial, Stroke Volume, Atrial fibrillation, Retrospective cohort study, Stroke volume, Ventricular pacing, medicine.disease, Treatment Outcome, Echocardiography, Child, Preschool, Cardiology, cardiovascular system, Female, Cardiology and Cardiovascular Medicine, business, Atrioventricular block, Follow-Up Studies
Abstract

Chronic right ventricular (RV) pacing is associated with deleterious effects on cardiac function. In an observational multicentre study in children with isolated atrioventricular (AV) block receiving chronic ventricular pacing, the importance of the ventricular pacing site on left ventricular (LV) function was investigated. Demographics, maternal autoantibody status and echocardiographic measurements on LV end-diastolic and end-systolic dimensions and volumes at age 1 year) for isolated AV block. LV fractional shortening (LVFS) and, if possible LV ejection fraction (LVEF) were calculated. Linear regression analyses were adjusted for patient characteristics. From 27 centres, 297 children were included, in whom pacing was applied at the RV epicardium (RVepi, n = 147), RV endocardium (RVendo, n = 113) or LV epicardium (LVepi, n = 37). LVFS was significantly affected by pacing site (p = 0.001), and not by maternal autoantibody status (p = 0.266). LVFS in LVepi (39 ± 5%) was significantly higher than in RVendo (33 ± 7%, p < 0.001) and RVepi (35 ± 8%, p = 0.001; no significant difference between RV-paced groups, p = 0.275). Subnormal LVFS (LVFS < 28%) was seen in 16/113 (14%) RVendo-paced and 21/147 (14%) RVepi-paced children, while LVFS was normal (LVFS ≥ 28%) in all LVepi-paced children (p = 0.049). These results are supported by the findings for LVEF (n = 122): LVEF was

Published
2011
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15. Prolonged QT in a 13-year-old patient with Down syndrome and complete atrioventricular canal defect

Author

Svjetlana, Tisma-Dupanovic, Rengasamy, Gowdamarajan, Ilan, Goldenberg, David T, Huang, Timothy, Knilans, and Jeffrey A, Towbin

Subjects
Andersen Syndrome, Electrocardiography, Adolescent, Heart Conduction System, Humans, Female, Hereditary Arrhythmia Corner: Learning from Challenging Patients, Down Syndrome, Endocardial Cushion Defects
Abstract

Ann Noninvasive Electrocardiol 2011;16(4):403–406

Published
2011

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