Özel Hasta Gruplarında Aritmi Yönetimi
Özet
Referanslar
Wilde AA, Amin AS, Postema PG. Diagnosis, management and therapeutic strategies for congenital long QT syndrome. Heart. 2022; 108(5), 332-338. Doi: 10.1136/heartjnl-2020- 318259.
Sueblinvong V. Zhang S. Varga P. Atrial Arrhythmia and Bradycardia as a Presentation of Congenital Long QT Syndrome. Pediatric cardiology Published Jul 11, 2024
Tatlı E., Gül Ç. Brugada Syndrome: Clınıcal Evaluatıon, Dıagnosıs And Treatment Modalıtıes: Revıew Turkiye Klinikleri J Med Sci. 2005;25(4):560-4
Bergeman AT, Wilde AA, van der Werf, C. Catecholaminergic polymorphic ventricular tachycardia: a review of therapeutic strategies. Cardiac Electrophysiology Clinics. 2023;
Zeppenfeld K, Tfelt-Hansen J, De Riva M. et al. 2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: Developed by the task force for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death of the European Society of Cardiology (ESC) Endorsed by the Association for European Paediatric and Congenital Cardiology (AEPC). European heart journal. 2022; 43(40), 3997-4126
Wilde AA. Bhuiyan ZA, Crotti L. et al. Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia. N Engl J Med. 2008; 358, 2024- 2029.
Bjerregaard P. Diagnosis and management of short QT syndrome. Heart Rhythm. 2018; 15(8), 1261-1267. Doi: 10.1016/j.hrthm.2018.02.034
Chan CH, Lam YY, Wong N. et al. Abnormal developmental trajectory and vulnerability to cardiac arrhythmias in tetralogy of Fallot with DiGeorge syndrome. Communications Biology. 2023; 6(1), 969.Doi: 10.1038/s42003-023-05344-6
Alexandra Viktoria Busley , Óscar Gutiérrez-Gutiérrez , Elke Hammer. Mutation-induced LZTR1 polymerization provokes cardiac pathology in recessive Noonan syndrome.2 3 July 2024, DOI: 10.1016/j.celrep.2024.114448
Algaze C, Chubb H, Deitch AM. et al. Electrocardiograms do not detect myocardial ıschemia in patients with williams syndrome and nonsyndromic elastin arteriopathy with coronary artery stenosis. The American Journal of Cardiology. 2024; 215, 50-55. Doi: 10.1016/j.amjcard.2023.11.020
Akbulut A. Aşkıntaş K. Duchenne musküler distrofi taşıyıcı kadınlarda görülen semptomlar: geleneksel derleme Yıl 2023, Cilt: 8 Sayı: 2, 39- 46, 25.08.2023 https://doi.org/10.52881/gsbdergi.1255489
Güler GB, Gürsoy MO, Kürklü TST, et al. Multimodality ımaging in cardiomyopathies. Ars. 2024; 52(1), S1-S206. Doi:10.5543/tkda.2024.13636
Teekakirikul P. Kelly M. Rehm H. Inherited Cardiomyopathies: Molecular Genetics and Clinical Genetic Testing in the Postgenomic Era The Journal of Molecular Diagnostics Volume 15, Issue 2, March 2013, Pages 158-170
Marian A. Braunwald E. Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy 2017 Sep 15;121(7):749–770 doi: 10.1161/CIRCRESAHA.117.311059
Basit H, Wallen TJ, Sergent BN. Eisenmenger syndrome. 2018. Erişim adresi:https://europepmc.org/article/nbk/nbk507800?utmmedium=email&utm_source=transaction&clie nt=bot&client=bot#free-full-text
Çuvadar A. Taylan G. Pregnancy-Related Arrhythmias, Management and Nursing/Midwifery Approach Unika Sag. Bil. Derg. 2022; 2(1): 241-247
Kamala P. Tamirisa, Uri Elkayam Gebelikte Aritmiler Klinik Elektrofizyoloji cilt 8 sayı 1 2022 Ocak;8(1):120-135.
Haïssaguerre, M., Derval, N., Sacher, F., Jesel, L., Deisenhofer, I., de Roy, L., ... & Hocini, M. (2008). Sudden cardiac arrest associated with early repolarization. New England Journal of Medicine, 358(19), 2016–2023. https://doi.org/10.1056/NEJMoa071968
Patel, R. B., & Deo, R. (2020). Early repolarization syndrome: Electrocardiographic features, pathophysiology, and clinical outcomes. Circulation: Arrhythmia and Electrophysiology, 13(2), e007759. https://doi.org/10.1161/CIRCEP.119.007759
Nademanee, K., Haïssaguerre, M., Hocini, M., & Nogami, A. (2019). J-wave syndromes: Brugada and early repolarization syndromes—recent advances and controversies. Circulation: Arrhythmia and Electrophysiology, 12(10), e007206. https://doi.org/10.1161/CIRCEP.119.007206