РОЛЬ ХОЛТЕРОВСКОГО МОНИТОРИРОВАНИЯ ЭКГ В ДИАГНОСТИКЕ ГЕНЕТИЧЕСКИХ СИНДРОМОВ (КАНАЛОПАТИИ) С РИСКОМ ЖИЗНЕУГРОЖАЮЩИХ АРИТМИЙ

Данная лекция посвящена группе наследственных заболеваний - «первичные электрические болезни сердца» или «каналопатии». Представлены диагностические критерии и показания для проведения Холтеровского мониторирования ЭКГ.

Л.К. Каражанова, А.А. Чиныбаева, М.А. Капакова

 

Государственный медицинский университет города Семей

1. Резник А.В., Федоров В.В., Розенштраух Л.В. Ион-ные каналы и токи в кардиомиоцитах. Кардиология 2006; 2:4-18. 2. Jewell A.; Lange-Nielsen, F. Congenital deaf-mutism, functional heart disease with prolongation of Q-T interval and sudden death. Am. Heart J. 54: 59-68, 1957. 3. Romano, С; Gemme, G.; Pongiglione, R. Aritmie cardiache rare dell eta pediatrica. II. Accessi sincopali per fibrillazione ventricolare parossistica. (Presentazione del primo caso della letteraturapediatrica Italiana.) Clin. Pediat. 45: 656-683, 1963. 4. Ward О. С A new familial cardiac syndrome in children. J. Irish Med. Assoc. 54: 103-106, 1964. 5. London B. Overview of inherited diseases that pre-dispose to the development of cardiac arrhythmias (LQTS, ARVD. AF. Brugada). North America Society of Pacing and Electrophysiology (NASPE) 21st Annual Scientific Sessions. 6. Schwartz P. Idiopathic long QT syndrome: progress and guestions. Am Heart.1985:109:399-411. 7. Crotti L, Celano G, Federica Dagradi F and J Schwartz P. Congenital long QT syndrome. Orphanet Journal of Rare Diseases 2008, 3:18 8. Moss A, Goldenberg 1. Importance of Knowing the Genotype and the Specific Mutation When Mmciging Patients With Long-QT Syndrome. Circ Arrhythmia Electrophysiol 2008; 1 ;219-226. 9. Makarov L.M., Belokon N.A., Laan M.I., Belozerov Y.M., Shkolnicova M.A.. Kruglikov I.V., Holter monitoring in the long QT syndrome of children and adolescents// COR VASA. - 32(6). - 414-483/ - 1990. 10. Gertie СМ., Beaufort-Krol, Maarten P et a/. Devel-opmental aspects of Long QT syndrome eype 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhood J Am Coll Cardiol 2005:46:331-7 11. Etheridge SP, Compton SJ. Tristani-Firouzi M, Mason JW. A new oral therapy for long QT syndrome: long-term oral potassium improves repolarization in patients with HERG mutations. J Am Coll Cardiol 2003 Nov 19;42(10): 1777-82. 12. Tristani-Firouzi, M, Jensen JL, Donaldson MR. ct ai. Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome). J Clin invest 2002; 110:381-388. 13. Andersen ED, Krasilnikoff PA, Overvad H. Intermit-tent muscular weakness, extrasystoles, and multiple devel-opmental abnormalities: a new syndrome Acta Pediatr Scand 1971;60:559 -564. 14. Макаров Л.М., Комолятова В.Н., Колосов В.О. и соавт. Синдром Андерсена-Тавила. Эффективность препаратов IС класса. Описание случая. Кардиология 2012 (в печати). 15. Neyrod N.. Maison-Blanche, I.Denjoi, Chevret S., Danger C, Dausse E., Fayn J., Badilini F., Menhabi N., Scwartz K., Guicheney P., Coumel P. Diagnostic perfomance of QT variables from 24-hour electrocardiography in the long QT syndrome. European Heart J 1998; 19:158-165. 16. Lande G, Kyndt F, Baro I, Chabannes D Boisseau P, Pony JC, Escande D, Lе Маrес Н. Dynamic analysis of the QT interval in long QTI syndrome patients with a normal phenotype. 17. Merri M, Moss A., Benhorin J, Locati K, Aalberti M, Badilini F. et al. Relation between ventricular repolarisation duration and cardiac cycle length during 24-hour Halter recordings: findings in normal patients and patients with long QT syndrome. Circulation 1992;85:1816-1821. 18. Makarov L. The QT interval and "QT dynamicity" during Halter monitoring in children and adolescents. Turk Aritmi, Pacemaker ve Elektrofizyoloji Dergisi. 2010; 8(1): 7-14. 19. Locati E. QT interval duration and adaptation to heart rate. In: Zareba W., Maison-Blanche P., Locati E. (eds). Noninvasive Electrocardiology in Clinical Practice. Futura Puhl. Co., Armonk, NY, 2001, 71- 96 p. 20.G Lande, F.Kyndt, I. Baro et al. Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype Eur Heart J.2001 Mar;22(5):410-22. 21. Gussak I, Brugada P, Brugada J, Wright RS, Ko-pecky SL, Chaitman BR, Bjerregaard P. Idiopathic short QT interval: a new clinical syndrome? Cardiology 2000; 94(2):99-102. 22. Gussak I, Brugada P., Brugada J, Antzelevitch C, Osbakken M. Bjerregard P. ECG phenomen of idiopathic and paradoxical short QT intervals. Cardiac Electrophysiology Review 2002; 6: 49-53. 23. Rasmussen V, Jensen .J, Hansen .J. QT interval in 24-hour ambulatory ECG recordings from 60 healthy adult subjects. J Electrocardiol 1991;24:91-95. 24. Brugada P, Brugada J. Right bundle branche black, persistent ST segment elevation and sudden cardiac death: A distict clinical and electrocariographic syndrome. J Am Coll Cardiol 1992:20:1391-1396. 25. Silvia G. Priori, Maurizio Gasparini, Carlo Napolitano et al Risk Stratification in Brugada Syndrome Results of the PRELUDE (Programmed ELectrical stimulation preDictive valuE) Registry. J Am Coll Cardiol2012:59:37-45. 26. Larsson E., Wesslen L., Lindquist O. et al. Sudden unexpected cardiac death among young Swedish orienteers-morphological changes in heart and other organs. APMIS, 1999, 107 (3): 325-336. 27. Leenhardt A, Lucet V, Denjoy I, et al. Catechola-minergic Polymorphic Ventricular Tachycardia in Children A 7-Year Follow-up of 21 Patients. Circulation. 1995:91:1512-1519. 28. Sumitomo N, Harada K, Nagashima M, et al. Cate-cholaminergic polymorphic ventricular tachycardia: electro-cardiographs ch aracteristics and optimal therapeutic strat-egies to prevent sudden death // Heart. 2003 Jan;89(l):66-70. 29. Veerakul G, Nademanee К What is the sudden death syndrome in Southeast Asian males? Cardiol Rev 2000 Mar-Apr;8(2):90-5.
Количество просмотров: 363

Ключевые слова:

Библиографическая ссылка

Л.К. Каражанова, А.А. Чиныбаева, М.А. Капакова

РОЛЬ ХОЛТЕРОВСКОГО МОНИТОРИРОВАНИЯ ЭКГ В ДИАГНОСТИКЕ ГЕНЕТИЧЕСКИХ СИНДРОМОВ (КАНАЛОПАТИИ) С РИСКОМ ЖИЗНЕУГРОЖАЮЩИХ АРИТМИЙ. //НАУКА И ЗДРАВООХРАНЕНИЕ 2012.№ 5. С. 18-21

 

L.K. Karazhanova, A.A. Chinybaeva, M.A. Kapakova

ROLE OF CHOLTER ECG MONITORING IN THE DIAGNOSIS OF GENETIC SYNDROMES

(CHANNELOPATHIES) WITH THE RISK OF LIFE-THREATENING ARRHYTHMIAS. // NAUKA I ZDRAVOOKHRANENIE 2012.№ 5. С. 18-21

 

Л.К. Каражанова, А.А. Чиныбаева, М.А. Капакова

ӨМІРГЕ ҚАТЕРЛІ АРИТМИЯЛАР ҚАУПІ БАР ГЕНЕТИКАЛЫҚ СИНДРОМДАР (КАНАЛОПАТИЯЛАР) ДИАГНОСТИКАСЫНДА ЭКГ-НІҢ ХОЛТЕРЛІК МОНИТОРЛАУ. // ҒЫЛЫМ ЖӘНЕ ДЕНСАУЛЫҚ САҚТАУ. 2012.№ 5. С. 18-21


Авторизируйтесь для отправки комментариев