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State-of–the-Art Management of Hypertrophic Cardiomyopathy in Children

Published online by Cambridge University Press:  01 November 2009

Stuart Berger ,
Anwer Dhala  and
Joseph A. Dearani
Stuart Berger*
Affiliation:
Professor of Pediatrics, The Medical College of Wisconsin, Milwaukee, Wisconsin
Anwer Dhala
Affiliation:
Professor of Pediatrics, The Medical College of Wisconsin, Milwaukee, Wisconsin
Joseph A. Dearani
Affiliation:
Professor of Surgery, Mayo Clinic School of Medicine
*
Correspondence to: Stuart Berger, MD, Professor of Pediatrics, Children’s Hospital of Wisconsin-Herma Heart Center, 9000 W. Wisconsin Avenue, Milwaukee, Wisconsin 53226. 414-266-2434 (office); 414-266-2294 (fax); E-mail: sberger@mcw.edu
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Abstract

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Keywords

Cardiomyopathyleft ventricular hypertrophymyomectomy
Type
Original Article
Information
Cardiology in the Young , Volume 19 , Issue S2: Innovation associated with the treatment of patients with congenital and pediatric cardiac disease , November 2009 , pp. 66 - 73
Copyright
Copyright © Cambridge University Press 2009

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References

1.Maron, BJ. Hypertrophic cardiomyopathy in childhood. In Pediatric Clinics of North America 51 (2004): 1305–1346.CrossRefGoogle Scholar
2.Ganame, J, Pignatelli, RH, Eidem, BW, et al. Myocardial deformation abnormalities in pediatric hypertrophic cardiomyopathy: are all etiologies identical? Eur J Echocardiogr 2008; 9 (6): 784–790; Epub 2008 Apr 27.CrossRefGoogle ScholarPubMed
3.Morita, H, Rehm, HL, Mennices, A. Shared genetic causes of cardiac hypertrophy in children and adults. NEJM 2008; 358 (18): 1899–1908; Epub 2008 Apr 9.CrossRefGoogle ScholarPubMed
4.Bos, JM, Ommen, SR, Ackerman, MJ. Genetics of hypertrophic cardiomyopathy: one, two, or more diseases? Curr Opinion Cardiol 2007; 22 (3): 193–199.CrossRefGoogle ScholarPubMed
5.Maron, BJ, Casey, SA, Poliac, LC, et al. Clinical course of hypertrophic cardiomyopathy in a regional United States cohort. JAMA 1999: 281–650–655.Google Scholar
6.Maron, BJ. Echocardiographic assessment of left ventricular hypertrophy in patients with obstructive or nonobstructive hypertrophic cardiomyopathy. Eur Heart J 1983; 4 Suppl F: 73–91.CrossRefGoogle ScholarPubMed
7.Rawlins, J, Bahn, A, Sharma, S. Left ventricular hypertrophy in athletes. Eur J Echocardiograph 2009; 10 (3): 350–356; Epub 2009 Feb 26.CrossRefGoogle ScholarPubMed
8.Maron, BJ, Spirito, P, Wesley, , et al. Development and progression of left ventricular hypertrophy in children with hypertrophic cardiomyopathy. NEJM 1986; 315: 610–614.CrossRefGoogle ScholarPubMed
9.Maron, BJ, Seidman, JG, Seidman, CE. Proposal for contemporary screening strategies in families with hypertrophic cardiomyopathy. J Am Coll Cardiol 2004; 44 (11): 2125–2132.CrossRefGoogle ScholarPubMed
10.Maron, MS, Olivotto, I, Betochhi, S, et al. Effect of left ventricular outflow tract obstruction on clinical outcome in hypertrophic cardiomyopathy. NEJM 2003; 348: 295–303.CrossRefGoogle ScholarPubMed
11.Poutanen, T, Tikanoja, T, Jaaskelainen, P. Diastolic dysfunction without left ventricular hypertrophy is an early finding in children with hypertrophic cardiomyopathy-causing mutations in the beta-myosin heavy chain, alpha-tropomyosin, and myosin-binding protein C genes. Am Heart J 2006; 151 (3): 725.e1–725.e9.CrossRefGoogle ScholarPubMed
12.Sotgia, B, Sciagra, R, Olivotto, I, et al. Spatial relationship between coronary microvascular dysfunction and delayed contrast enhancement in patients with hypertrophic cardiomyopathy. J Nucl Med 2008; 49 (7): 1090–1096.CrossRefGoogle ScholarPubMed
13.Sherrid, MV, Barac, I, McKenna, WJ, et al. Multicenter study of the efficacy and safety of disopyramide in obstructive hypertrophic cardiomyopathy. J Am Coll Cardiol 2005; 45 (8): 1252–1258.CrossRefGoogle ScholarPubMed
14.Koffland, MJ, Waldstein, DJ, Vos, J, ten Cate, FJ. Prognosis in hypertrophic cardiomyopathy observed in a large clinic population. Am J Cardiol 1993; 72: 939–943.CrossRefGoogle Scholar
15.Maron, BJ, Olovetto, I, Spirito, P, et al. Epidemiology of hypertrophic cardiomyopathy-related death: revisited in a large non-referral-based patient population. Circulation 2000; 102: 858–864.CrossRefGoogle Scholar
16.Maron, BJ, Shen, WK, Link, MS, et al. Efficiacy of implantable cardioverter-defibrillators for the prevention of sudden death in patients with hypertrophic cardiomyopathy. NEJM 2000; 342: 363–373.CrossRefGoogle Scholar
17.Elliott, PM, Poloniecki, J, Dickie, S, et al. Sudden death in hypertrophic cardiomyopathy: identification of high risk patients. J Am Coll Cardiol 2000; 36: 2212–2218.CrossRefGoogle ScholarPubMed
18.Spirito, P, Seidman, CE, McKenna, WJ, Maron, BJ. Management of hypertrophic cardiomyopathy. NEJM 1997; 336: 775–785.CrossRefGoogle ScholarPubMed
19.Ostman-Smith, I, Wettrell, G, Riesenfeld, T. A cohort study of childhood hypertrophic cardiomyopathy: improved survival following high-dose beta adrenoceptor antagonisy treatment. J Am Coll Cardiol 1999; 34: 1813–1822.CrossRefGoogle ScholarPubMed
20.Cairns, JA, Connolly, SJ, Roberts, R, et al. Randomized trial of outcome after myocardial infarction I patients with frequent or repetitive ventricular premature depolarizations: CAMIAT. Lancet 1997; 349: 675–682.CrossRefGoogle ScholarPubMed
21.Julian, DJ, Camm, AJ, Frangin, GA, et al. Randomized trial of effect of amiodarone on mortalityt in patients with left ventricular dysfunction after recent myocardial infarction: AMIAT. Lancet 1997; 349: 667–674.CrossRefGoogle Scholar
22.Moss, AJ, Hall, WJ, Cannom, DS, et al. Improved survival with an implanted defibrillator in patients with coronary disease at high risk for arrhythmia. NEJM 1996; 335: 1933–1940.CrossRefGoogle ScholarPubMed
23.Silka, MJ, Kron, J, Dunnigan, A, Dick, M. Sudden cardiac death and the use of implantable cardioverter-defibrillators in pediatric patients. Circulation 1993; 87: 800–807.CrossRefGoogle ScholarPubMed
24.Elliott, PM, Sharma, S, Varnava, A, et al. Survival after cardiac arrest in patients with hypertrophic cardiomyopathy. J Am Coll Cardiol 1999; 33: 1596–1601.CrossRefGoogle ScholarPubMed
25.Berul, CI, Van Hare, GF, Kertesz, NJ, et al. Results of a multicenter retrospective implantable cardioverter-defibrillator registry of pediatric and congenital heart disease patients. J Am Coll Cardiol 2008; 51: 1685–1691.CrossRefGoogle ScholarPubMed
26.Nishimura, RA, Giuliani, ER, Brandenburg, RO, et al. Hypertrophic cardiomyopathy. Mayo Clinic Practice of Cardiology, 3rd Edition Chapter 20. In: Giuliani ER, Gersh BJ, McGoon MD, Hayes DL, Schaff HV (eds). Mosby-Year Book Inc., St. Louis, MO, 1996, pp 689–711.Google Scholar
27.Theodoro, DA, Danielson, GK, Feldt, RH, Anderson, BJ. Hypertrophic obstructive cardiomyopathy in pediatric patients: Results of surgical treatment. J Thorac Cardiovasc Surg 1996; 112: 1589–1599.CrossRefGoogle ScholarPubMed
28.Maron, BJ, McKenna, WJ, Danielson, GK, et al. American College of Cardiology/European Society of Cardiology Clinical Expert Consensus Document on Hypertrophic Cardiomyopathy. A report of the ACC Task Force on Clinical Expert Consensus Documents and the Committee to Develop an Expert Consensus Document on Hypertrohic Cardiomyopathy. J Am Coll Cardiol 2003; 42: 1687–1713.CrossRefGoogle Scholar
29.Maron, BJ. Hypertrophic cardiomyopathy: a systematic review. JAMA 2002; 287: 1308–1320.CrossRefGoogle ScholarPubMed
30.Dearani, JA, Danielson, GK. Septal myectomy for hypertrophic cardiomyopathy. Operative Techniques in Thoracic and Cardiovascular Surgery 2004; 9: 278–292.CrossRefGoogle Scholar
31.McKenna, WJ, Deanfield, J, Faruqui, A, et al. Prognosis in hypertrophic cardiomyopathy: Role of age and clinical, electrocardiographic and hemodynamic features. Am J Cardiol 1981; 47: 532–538.CrossRefGoogle ScholarPubMed
32.Minakata, K, Dearani, JA, O’Leary, PW, et al. Septal myectomy for obstructive hypertrophic cardiomyopathy in pediatric patients: early and late results. Ann Thorac Surg 2005; 80: 1424–1430.CrossRefGoogle ScholarPubMed
33.McCully, RB, Nishimura, RA, Tajik, AJ, et al. Extent of clinical improvement after surgical treatment of hypertrophic cardiomyopathy. Circulation 1996; 94: 467–471.CrossRefGoogle Scholar
34.Seiler, C, Hess, OM, Schoenbeck, M, et al. Long-term follow-up of medical versus surgical therapy for hypertrophic cardiomyopathy: a retrospective study. J Am Coll Cardiol 1991; 17: 634–645.CrossRefGoogle ScholarPubMed
35.Ommen, SR, Maron, BJ, Olivotto, I, et al. Long-term effects of surgical septal myectomy on survival in patients with obstructive hypertrophic cardiomyopathy. J Am Coll Cardiol 2005; 46 (3): 470–476.CrossRefGoogle ScholarPubMed
36.Minaka, K, Dearani, JA, Nishimura, RA, et al. Extended septal myectomy for hypertrophic obstructive cardiomyopathy with anomalous papillary muscles or chordae. J Thorac Cardiovasc Surg 2004; 127: 481.CrossRefGoogle Scholar