GL検索 v0.1.0
画像は 93 ページを描画したものです
page 93

p.93 抽出テキスト

dysfunction is a risk factor for sudden cardiac death in adults late after repair of tetralogy of Fallot. J Am Coll Cardiol 2002; 40: 1675-1680. PMID: 12427422 525. Harrison DA, Harris L, Siu SC, et al. Sustained ventricular tachycardia in adult patients late after repair of tetralogy of Fallot. J Am Coll Cardiol 19 9 7; 3 0 : 13 6 8 - 137 3. PMID: 9350941 526. Knauth AL, Gauvreau K, Powell AJ, et al. Ventricular size and function assessed by cardiac MRI predict major adverse clinical outcomes late after tetralogy of Fallot repair. Heart 2008; 94: 211-216. PMID: 17135219 527. Khairy P, Landzberg MJ, Gatzoulis MA, et al. Value of programmed ventricular stimulation after tetralogy of fallot repair: A multicenter study. Circulation 20 0 4; 10 9: 1994 - 2000. PMID: 15051640 528. Xiao L, Koopmann TT, Ördög B, et al. Unique cardiac Purkinje fiber transient outward current β-subunit composition: A potential molecular link to idiopathic ventricular fibrillation. Circ Res 2013; 112: 1310 -1322. PMID: 23532596 529. Leenhardt A, Glaser E, Burguera M, et al. Short-coupled variant of torsade de pointes: A new electrocardiographic entity in the spectrum of idiopathic ventricular tachyarrhythmias. Circulation 1994; 89: 206-215. PMID: 8281648 530. Alders M, Koopmann TT, Christiaans I, et al. Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation. Am J Hum Genet 2009; 84: 468-476. PMID: 19285295 531. Koizumi A, Sasano T, Kimura W, et al. Genetic defects in a His-Purkinje system transcription factor, IRX 3, cause lethal cardiac arrhythmias. Eur Heart J 2016; 37: 1469-1475. PMID: 26429810 532. Fujii Y, Itoh H, Ohno S, et al. A type 2 ryanodine receptor variant associated with reduced Ca

2+ release and short-coupled torsades de pointes ventricular arrhythmia. Heart Rhythm 2017; 14: 98- 107. PMID: 27756708 533. Kajiyama T, Miyazawa K, Kondo Y, et al. SCN5A mutation and a short coupled variant of Torsades de Pointes originating from the right ventricle: A case report. J Cardiol Cases 2020; 21: 104- 105. PMID: 32153684 534. Herman AR, Cheung C, Gerull B, et al. Outcome of apparently unexplained cardiac arrest: Results from investigation and follow-up of the Prospective Cardiac Arrest Survivors With Preserved Ejection Fraction Registry. Circ Arrhythm Electrophysiol 2016; 9: e003619. PMID: 26783233 535. Visser M, van der Heijden JF, Doevendans PA, et al. Idiopathic ventricular fibrillation: The struggle for definition, diagnosis, and follow-up. Circ Arrhythm Electrophysiol 2016; 9: e003817. PMID: 27103090 536. Krahn AD, Healey JS, Chauhan V, et al. Systematic assessment of patients with unexplained cardiac arrest: Cardiac Arrest Survivors With Preserved Ejection Fraction Registry (CASPER). Circulation 2009; 120: 278-285. PMID: 19597050 537. Jiménez-Jáimez J, Peinado R, Grima EZ, et al. Diagnostic approach to unexplained cardiac arrest (from the FIVI-Gen Study). Am J Cardiol 2015; 116: 894-899. PMID: 26189708 538. Deif B, Roberts JD. Diagnostic evaluation and arrhythmia mechanisms in survivors of unexplained cardiac arrest. Pacing Clin Electrophysiol 2019; 42: 1320-1330. PMID: 31411341 539. Conte G, Caputo ML, Regoli F, et al. True idiopathic ventricular fibrillation in out-of-hospital cardiac arrest survivors in the Swiss Canton Ticino: prevalence, clinical features, and longterm follow-up. Europace 2017; 19: 259-266. PMID: 28175278 540. Waldmann V, Bougouin W, Karam N, et al. Paris-SDEC investigators. Characteristics and clinical assessment of unexplained sudden cardiac arrest in the real-world setting: focus on idiopathic ventricular fibrillation. Eur Heart J 2018; 39: 1981- 1987. PMID: 29566157 541. Vittoria Matassini M, Krahn AD, Gardner M, et al. Evolution of clinical diagnosis in patients presenting with unexplained cardiac arrest or syncope due to polymorphic ventricular tachycardia. Heart Rhythm 2014; 11: 274-281. PMID: 24239842 542. Wilde AA, Moss AJ, Kaufman ES, et al. Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study. Circulation 2016; 134: 872-882. PMID: 27566755 543. Villain E, Denjoy I, Lupoglazoff JM, et al. Low incidence of cardiac events with beta-blocking therapy in children with long QT syndrome. Eur Heart J 2004; 25: 1405-1411. PMID: 15321698 544. Shimizu W, Moss AJ, Wilde AA, et al. Genotype-phenotype aspects of type 2 long QT syndrome. J Am Coll Cardiol 2009; 54: 2052-2062. PMID: 19926013 545. Moss AJ, Zareba W, Hall WJ, et al. Effectiveness and limitations of β-blocker therapy in congenital long-QT syndrome. Circulation 2000; 101: 616-623. PMID: 10673253 546. Moss AJ, Shimizu W, Wilde AA, et al. Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ 1 gene. Circulation 2007; 115: 2481-2489. PMID: 17470695 547. Dorostkar PC, Eldar M, Belhassen B, et al. Long-term follow-up of patients with long-QT syndrome treated with β-blockers and continuous pacing. Circulation 1999; 100: 2431-2436. PMID: 10595956 548. Abu-Zeitone A, Peterson DR, Polonsky B, et al. Efficacy of different beta-blockers in the treatment of long QT syndrome. J Am Coll Cardiol 2014; 64: 1352-1358. PMID: 25257637 549. Schwartz PJ. Idiopathic long QT syndrome: Progress and questions. Am Heart J 1985; 109: 399-411. PMID: 3966369 550. Schwartz PJ, Moss AJ, Vincent GM, et al. Diagnostic criteria for the long QT syndrome: An update. Circulation 1993; 88: 782- 784. PMID: 8339437 551. Schwartz PJ. The congenital long QT syndromes from genotype to phenotype: clinical implications. J Intern Med 2006; 259: 39- 47. PMID: 16336512 552. Schwartz PJ, Crotti L. QTc behavior during exercise and genetic testing for the long-QT syndrome. Circulation 2011; 124: 2181- 2184. PMID: 22083145 553. 日本循環器学会 / 日本小児循環器学会.学校心臓検診のガイドライン(2016 年版).https://www.j-circ.or.jp/cms/wp-content/uploads/

2020/02/JCS2016_sumitomo_h.pdf 554. Shimizu W, Kamakura S, Arakaki Y, et al. T wave alternans in idiopathic long-QT syndrome: Insight from body surface mapping. Pacing Clin Electrophysiol 1996; 19: 1130-1133. PMID: 8823845 555. Jervell A, Lange-Nielsen F. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death. Am Heart J 1957; 54: 59-68. PMID: 13435203 556. Vincent GM, Jaiswal D, Timothy KW. Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome. Am J Cardiol 1991; 68: 498- 503. PMID: 1872278 557. Swan H, Toivonen L, Viitasalo M. Rate adaptation of QT intervals during and after exercise in children with congenital long QT syndrome. Eur Heart J 1998; 19: 508-513. PMID: 9568456 558. Chattha IS, Sy RW, Yee R, et al. Utility of the recovery electrocardiogram after exercise: a novel indicator for the diagnosis and genotyping of long QT syndrome? Heart Rhythm 2010; 7: 906- 911. PMID: 20226272 559. Sy RW, van der Werf C, Chattha IS, et al. Derivation and validation of a simple exercise-based algorithm for prediction of genetic testing in relatives of LQTS probands. Circulation 2011; 124: 2187-2194. PMID: 22042885 560. Laksman ZW, Hamilton RM, Chockalingam P, et al. Mutation location effect on severity of phenotype during exercise testing in type 1 long-QT syndrome: Impact of transmembrane and C-loop location. J Cardiovasc Electrophysiol 2013; 24: 1015- 1020. PMID: 23691991 561. Takenaka K, Ai T, Shimizu W, et al. Exercise stress test amplifies genotype-phenotype correlation in the LQT 1 and LQT 2 forms of the long-QT syndrome. Circulation 2003; 107: 838- 844. PMID: 12591753 562. Horner JM, Horner MM, Ackerman MJ. The diagnostic utility of recovery phase QTc during treadmill exercise stress testing in the evaluation of long QT syndrome. Heart Rhythm 2011; 8: 1698-1704. PMID: 21699858 563. Krahn AD, Klein GJ, Yee R. Hysteresis of the RT interval with exercise: A new marker for the long-QT syndrome? Circulation 1997; 96: 1551-1556. PMID: 9315546 564. Andrsova I, Novotny T, Kadlecova J, et al. Clinical characteristics of 30 Czech families with long QT syndrome and KCNQ 1 and KCNH 2 gene mutations: importance of exercise testing. J Electrocardiol 2012; 45: 746-751. PMID: 22727609 565. Shimizu W, Noda T, Takaki H, et al. Diagnostic value of epinephrine test for genotyping LQT 1, LQT 2, and LQT 3 forms of congenital long QT syndrome. Heart Rhythm 2004; 1: 276-283. PMID: 15851169 566. Shimizu W. Update of diagnosis and management of inherited cardiac arrhythmias. Circ J 2013; 77: 2867- 2872. PMID: 24200848 567. Schwartz PJ, Priori SG, Spazzolini C, et al. Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias. Circulation 2001; 103: 89- 95.