Current management of hypertrophic cardiomyopathy

Current Treatment Options in Cardiovascular Medicine

Volumn 10, Issue 6, 2008, Pages 496-504

  Coats, Caroline J ^a   Elliott, Perry M ^a  

^a UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL; ALDOSTERONE; AMIODARONE; ANGIOTENSIN; ANGIOTENSIN RECEPTOR ANTAGONIST; ANTIBIOTIC AGENT; ATENOLOL; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; BISOPROLOL; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; DISOPYRAMIDE; DIURETIC AGENT; LOSARTAN; METOPROLOL; PERHEXILINE; PRACTOLOL; PROPRANOLOL; RENIN; SARCOMERE PROTEIN; SPIRONOLACTONE; STRUCTURAL PROTEIN; UNCLASSIFIED DRUG; VERAPAMIL; WARFARIN;

ANTICHOLINERGIC EFFECT; ARTIFICIAL HEART PACEMAKER; ATRIOVENTRICULAR BLOCK; BACTERIAL ENDOCARDITIS; BRADYCARDIA; CARDIAC RESYNCHRONIZATION THERAPY; CLINICAL TRIAL; DEFIBRILLATION; DISEASE COURSE; DRUG MEGADOSE; DRUG POTENTIATION; DRUG SAFETY; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; ELECTROLYTE BLOOD LEVEL; EXERCISE TEST; FAMILY STUDY; FATIGUE; GENE MUTATION; GENERAL ANESTHESIA; GENETIC ANALYSIS; GENETIC COUNSELING; GENETIC SCREENING; GENOMICS; GENOTYPE PHENOTYPE CORRELATION; HEART ATRIUM FIBRILLATION; HEART FAILURE; HEART MUSCLE CONTRACTILITY; HEART OUTFLOW TRACT OBSTRUCTION; HEART SURGERY; HEART TRANSPLANTATION; HEREDITY; HETEROZYGOSITY; HOLTER MONITORING; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; HYPOTENSION; IMPOTENCE; LIVER FUNCTION; MEDICAL DECISION MAKING; MEDICAL RESEARCH; METABOLOMICS; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; PATIENT MONITORING; PHYSICAL ACTIVITY; PREGNANCY; PROTEOMICS; QT PROLONGATION; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; REVIEW; RISK ASSESSMENT; SIDE EFFECT; SLEEP DISORDER; SPORT; SUDDEN DEATH; SURVIVAL RATE; THYROID FUNCTION;

EID: 58849115974     PISSN: 10928464     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11936-008-0042-9     Document Type: Review

References (54)

1. Elliott P, McKenna WJ: Hypertrophic cardiomyopathy. Lancet 2004, 363:1881-1891.
2. Maron BJ: Hypertrophic Aardiomyopathy: a systematic review. JAMA 2002, 287:1308-1320.
3. Arad M, Seidman JG, Seidman CE: Phenotypic diversity in hypertrophic cardiomyopathy. Hum Mol Genet 2002, 11:2499-2506.
4. Hilfiker-Kleiner D, Knoll R: Disease-modifying mutations in familial hypertrophic cardiomyopathy: Complexity from simplicity. Circulation 2008, 117:1775-1777.
5. Keren A, Syrris P, McKeTna WJ: Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression. Nat Clin Pract Cardiovasc Med 2008, 5:158-168.
6. Elliott P, Andersson B, Arbustini E, et al.: Classification of the cardiomyopathies: A position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases. Eur Heart J 2008, 29:270-276.
7. Maron BJ, Towbin JA, Thiene G, et al.: Contemporary definitions and classification of the cardiomyopathies: An American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention. Circulation 2006, 113:1807-1816.
8. 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 American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines. J Am Coll Cardiol 2003, 42:1687-1713.
9. Maron MS, Olivotto I, Zenovich AG, et al.: Hypertrophic cardiomyopathy is predominantly a disease of left ventricular outflow tract obstruction. Circulation 2006, 114:2232-2239.
10. Maron MS, Olivotto I, Betocchi S, et al.: Effect of left ventricular outflow tract obstruction on clinical outcome in hypertrophic cardiomyopathy. N Engl J Med 2003, 348:295-303.
11. Sherrid MV, Pearle G, Gunsburg DZ: Mechanism of benefit of negative inotropes in obstructive hypertrophic cardiomyopathy. Circulation 1998, 97:41-47.
12. Harrison DC, Braunwald E, Glick G, et al.: Effects of beta adrenergic blockade on the circulation with particular reference to observations in patients with hypertrophic subaortic stenosis. Circulation 1964, 29:84-98.
13. Hubner PJ, Ziady GM, Lane GK, et al.: Double-blind trial of propranolol and practolol in hypertrophic cardiomyopathy. Br Heart J 1973, 35:1116-1123.
14. Ostman-Smith I, Wettrell G, Riesenfeld T: A cohort study of childhood hypertrophic cardiomyopathy: Improved survival following high-dose beta-adrenoceptor antagonist treatment. J Am Coll Cardiol 1999, 34:1813-1822.
15. EpsteIn SE, Rosing DR: Verapamil: its potential for causing serious complications in patients with hypertrophic cardiomyopathy. Circulation 1981, 64:437-441.
16. Rosing DR, KeAt KM, Maron BJ, Epstein SE: Verapamil therapy: a new approach to the pharmacologic treatment of hypertrophic cardiomyopathy. II. Effects on exercise capacity and symptomatic status. Circulation 1979, 60:1208-1213.
17. Pollick C, Kimball B, Henderson M, Wigle ED: Disopyramide in hypertrophic cardiomyopathy. I. Hemodynamic assessment after intravenous administration. Am J Cardiol 1988, 62:1248-1251.
18. 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, 45:1251-1258.
19. McKenna WJ, Oakley CM, Krikler DM, Goodwin JF: Improved survival with amiodarone in patients with hypertrophic cardiomyopathy and ventricular tachycardia. Br Heart J 1985, 53:412-416.
20. Maron BJ, Olivotto I, Bellone P, et al.: Clinical profile of stroke in 900 patients with hypertrophic cardiomyopathy. J Am Coll Cardiol 2002, 39:301-307.
21. Biagini E, Coccolo F, Ferlito M, et al.: Dilated-hypokinetic evolution of hypertrophic cardiomyopathy: Prevalence, incidence, risk factors, and prognostic implications in pediatric and adult patients. J Am Coll Cardiol 2005, 46:1543-1550.
22. Tsybouleva N, Zhang L, Chen S, et al.: Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy. Circulation 2004, 109:1284-1291.
23. Lim DS, Lutucuta S, Bachireddy P, et al.: Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy. Circulation 2001, 103:789-791.
24. Araujo AQ, Arteaga E, Ianni BM, et al.: Effect of Losartan on left ventricular diastolic function in patients with nonobstructive hypertrophic cardiomyopathy. Am J Cardiol 2005, 96:1563-1567.
25. Spirito P, Rapezzi C, Bellone P, et al.: Infective endocarditis in hypertrophic cardiomyopathy: Prevalence, incidence, and indications for antibiotic prophylaxis. Circulation 1999, 99:2132-2137.
26. Wilson W, Taubert KA, Gewitz M, et al.: Prevention of infective endocarditis: Guidelines from the AmericanAHeart Association: a guideline from the American Heart Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee, Council on Cardiovascular Disease in the Young, and the Council on Clinical Cardiology, Council on Cardiovascular Surgery and Anesthesia, and the Quality of Care and Outcomes Research Interdisciplinary Working Group. Circulation 2007, 116:1736-1754.
27. Team NSCGT: Prophylaxis Against Infective Endocarditis in Adults and Children Undergoing Interventional Procedures. London: National Institute for Health and Clinical Excellence; 2008.
28. Olivotto I, Ommen SR, Maron MS, et al.: Surgical myectomy versus alcohol septal ablation for obstructive hypertrophic cardiomyopathy. Will there ever be a randomized trial? J Am Coll Cardiol 2007, 50:831-834.
29. Woo A, Williams WG, Choi R, et al.: Clinical and echocardiographic determinants of long-term survival after surgical myectomy in obstructive hypertrophic cardiomyopathy. Circulation 2005, 111:2033-2041.
30. 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, 46:470-476.
31. Seggewiss H, Rigopoulos A, Welge D, et al.: Long-term follow-up after percutaneous septal ablation in hypertrophic obstructive cardiomyopathy. Clin Res Cardiol 2007, 96:856-863.
32. Maron BJ, Nishimura RA, McKenna WJ, et al.: Assessment of permanent dual-chamber pacing as a treatment for drug-refractory symptomatic patients with obstructive hypertrophic cardiomyopathy. A randomized, double-blind, crossover study (M-PATHY). Circulation 1999, 99:2927-2933.
33. Kappenberger L, Linde C, Daubert C, et al.: Pacing in hypertrophic obstructive cardiomyopathy. A randomized crossover study PIC. Study Group. Eur Heart J 1997, 18:1249-1256.
34. Kilicaslan F, Verma A, Saad E, et al.: Efficacy of catheter ablation of atrial fibrillation in patients with hypertrophic obstructive cardiomyopathy. Heart Rhythm 2006, 3:275-280.
35. Gaita F, Di Donna P, Olivotto I, et al.: Usefulness and safety of transcatheter ablation of atrial fibrillation in patients with hypertrophic cardiomyopathy. Am J Cardiol 2007, 99:1575-1581.
36. Jeanrenaud X, Schlapfer J, Fromer M, et al.: Dual chamber pacing in hypertrophic obstructive cardiomyopathy: Beneficial effect of atrioventricular junction ablation for optimal left ventricular capture and filling. Pacing Clin Electrophysiol 1997, 20:293-300.
37. Ashrafian H, Mason MJ, Mitchell AG: Regression of dilated-hypokinetic hypertrophic cardiomyopathy by biventricular cardiac pacing. Europace 2007, 9:50-54.
38. Rogers DP, Marazia S, Chow AW, et al.: Effect of biventricular pacing on symptoms and cardiac remodelling in patients with end-stage hypertrophic cardiomyopathy. Eur J Heart Fail 2008, 10:507-513.
39. Lenarczyk R, Kowalski O, Kukulski T, et al.: Resynchronization or dyssynchronization-successful treatment with biventricular stimulation of a child with obstructive hypertrophic cardiomyopathy without dyssynchrony. J Cardiovasc Electrophysiol 2007, 18:542-544.
40. Biagini E, Spirito P, Leone O, et al.: Heart transplantation in hypertrophic cardiomyopathy. Am J Cardiol 2008, 101:387-392.
41. Elliott PM, Gimeno JR, Thaman R, et al.: Historical trends in reported survival rates in patients with hypertrophic cardiomyopathy. Heart 2006, 92:785-791.
42. 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.
43. Zipes DP, Camm AJ, Borggrefe M, et al.: ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death-executive summary: A report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Develop Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death): developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society. Eur Heart J 2006, 27:2099-2140.
44. Watkins H: Sudden death in hypertrophic cardiomyopathy. N Engl J Med 2000, 342:422-424.
45. Maron BJ, Maron MS, Lesser JR, et al.: Sudden cardiac arrest in hypertrophic cardiomyopathy in the absence of conventional criteria for high risk status. Am J Cardiol 2008, 101:544-547.
46. Moon JC, McKenna WJ, McCrohon JA, et al.: Toward clinical risk assessment in hypertrophic cardiomyopathy with gadolinium cardiovascular magnetic resonance. J Am Coll Cardiol 2003, 41:1561-1567.
47. Maron BJ, Spirito P: Implications of left ventricular remodeling in hypertrophic cardiomyopathy. Am J Cardiol 1998, 81:1339-1344.
48. Maron BJ, Seidman JG, Seidman CE: Proposal for contemporary screening strategies in families with hypertrophic cardiomyopathy. J Am Coll Cardiol 2004, 44:2125-2132.
49. Autore C, Conte MR, Piccininno M, et al.: Risk associated with pregnancy in hypertrophic cardiomyopathy. J Am Coll Cardiol 2002, 40:1864-1869.
50. Thompson RC, Liberthson RR, Lowenstein E: Perioperative anesthetic risk of noncardiac surgery in hypertrophic obstructive cardiomyopathy. JAMA 1985, 254:2419-2421.
51. Pelliccia A, Fagard R, Bjornstad HH, et al.: Recommendations for competitive sports participation in athletes with cardiovascular disease: A consensus document from the Study Group of Sports Cardiology of the Working Group of Cardiac Rehabilitation and Exercise Physiology and the Working Group of Myocardial and Pericardial Diseases of the European Society of Cardiology. Eur Heart J 2005, 26:1422-1445.
52. Maron BJ, Chaitman BR, Ackerman MJ, et al.: Recommendations for physical activity and recreational sports participation for young patients with genetic cardiovascular diseases. Circulation 2004, 109:2807-2816.
53. Maron BJ, Moller JH, Seidman CE, et al.: Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases: Hypertrophic cardiomyopathy, long-QT syndrome, and Marfan syndrome. A statement for healthcare professionals from the Councils on Clinical Cardiology, Cardiovascular Disease in the Young, and Basic Science, American Heart Association. Circulation 1998, 98:1460-1471.
54. Corrado D, Pelliccia A, Bjornstad HH, et al.: Cardiovascular pre-participation screening of young competitive athletes for prevention of sudden death: Proposal for a common European protocol. Consensus Statement of the Study Group of Sport Cardiology of the Working Group of Cardiac Rehabilitation and Exercise Physiology and the Working Group of Myocardial and Pericardial Diseases of the European Society of Cardiology. Eur Heart J 2005, 26:516-524.