Literature DB >> 4039188

Improved survival with amiodarone in patients with hypertrophic cardiomyopathy and ventricular tachycardia.

W J McKenna, C M Oakley, D M Krikler, J F Goodwin.   

Abstract

The effect of amiodarone on survival was assessed in patients with hypertrophic cardiomyopathy and ventricular tachycardia in a drug trial with historical controls. During 1976 and 1977, 24 hour (seven) or 48 hour (79) electrocardiographic monitoring was performed in 86 consecutive patients; 24 had ventricular tachycardia and received conventional antiarrhythmic agents. Nineteen clinical, echocardiographic, and haemodynamic features were assessed. Seven patients died suddenly during follow up of three years; of these, five had continued to have ventricular tachycardia and two had no documented ventricular tachycardia. During 1978 and 1979, ventricular tachycardia was detected during 48 hour electrocardiographic monitoring in 21 of the next 82 consecutive patients with hypertrophic cardiomyopathy. They received amiodarone (150-400 mg/day, median 300); ventricular tachycardia was suppressed in all during repeat 48 hour electrocardiographic examination. Two patients died suddenly during a three year follow up, but neither belonged to the amiodarone treated group with ventricular tachycardia. The clinical and haemodynamic variables were similar in patients taking amiodarone and conventional agents. The fact that control of ventricular arrhythmia with amiodarone is significantly associated with improved survival suggests that amiodarone may prevent sudden death in patients with hypertrophic cardiomyopathy and ventricular tachycardia.

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Year:  1985        PMID: 4039188      PMCID: PMC481782          DOI: 10.1136/hrt.53.4.412

Source DB:  PubMed          Journal:  Br Heart J        ISSN: 0007-0769


  14 in total

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Authors:  D TEARE
Journal:  Br Heart J       Date:  1958-01

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Authors:  S Frank; E Braunwald
Journal:  Circulation       Date:  1968-05       Impact factor: 29.690

3.  Arrhythmia in hypertrophic cardiomyopathy. II: Comparison of amiodarone and verapamil in treatment.

Authors:  W J McKenna; L Harris; G Perez; D M Krikler; C Oakley; J F Goodwin
Journal:  Br Heart J       Date:  1981-08

Review 4.  The natural history of hypertrophic cardiomyopathy.

Authors:  W J McKenna; J F Goodwin
Journal:  Curr Probl Cardiol       Date:  1981-07       Impact factor: 5.200

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Authors:  R E Ingham; R M Rossen; D J Goodman; D C Harrison
Journal:  Chest       Date:  1975-12       Impact factor: 9.410

6.  Arrhythmia in hypertrophic cardiomyopathy. I: Influence on prognosis.

Authors:  W J McKenna; D England; Y L Doi; J E Deanfield; C Oakley; J F Goodwin
Journal:  Br Heart J       Date:  1981-08

7.  Prevalence of arrhythmias during 24-hour electrocardiographic monitoring and exercise testing in patients with obstructive and nonobstructive hypertrophic cardiomyopathy.

Authors:  D D Savage; S F Seides; B J Maron; D J Myers; S E Epstein
Journal:  Circulation       Date:  1979-05       Impact factor: 29.690

8.  Amiodarone for long-term management of patients with hypertrophic cardiomyopathy.

Authors:  W J McKenna; L Harris; E Rowland; A Kleinebenne; D M Krikler; C M Oakley; J F Goodwin
Journal:  Am J Cardiol       Date:  1984-10-01       Impact factor: 2.778

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Authors:  L M Shapiro; W J McKenna
Journal:  J Am Coll Cardiol       Date:  1983-09       Impact factor: 24.094

10.  Sudden death in patients with hypertrophic cardiomyopathy: characterization of 26 patients with functional limitation.

Authors:  B J Maron; W C Roberts; J E Edwards; H A McAllister; D D Foley; S E Epstein
Journal:  Am J Cardiol       Date:  1978-05-01       Impact factor: 2.778

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  46 in total

Review 1.  Hypertrophic cardiomyopathy: management, risk stratification, and prevention of sudden death.

Authors:  William J McKenna; Elijah R Behr
Journal:  Heart       Date:  2002-02       Impact factor: 5.994

2.  Contemporary considerations for risk stratification, sudden death and prevention in hypertrophic cardiomyopathy.

Authors:  B J Maron
Journal:  Heart       Date:  2003-09       Impact factor: 5.994

3.  Hypertrophic cardiomyopathy in the elderly.

Authors:  L M Shapiro
Journal:  Br Heart J       Date:  1990-05

Review 4.  Implications of arrhythmias and prevention of sudden death in hypertrophic cardiomyopathy.

Authors:  A Selcuk Adabag; Barry J Maron
Journal:  Ann Noninvasive Electrocardiol       Date:  2007-04       Impact factor: 1.468

Review 5.  Problems in diagnosis and management of hypertrophic cardiomyopathy.

Authors:  O Odemuyiwa; W J McKenna
Journal:  Postgrad Med J       Date:  1991-08       Impact factor: 2.401

Review 6.  The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.

Authors:  J Burn; J Camm; M J Davies; L Peltonen; P J Schwartz; H Watkins
Journal:  Heart       Date:  1997-08       Impact factor: 5.994

7.  Sudden death in young people due to hypertrophic cardiomyopathy.

Authors:  A L Gourdie; C E Robertson; A Busuttil
Journal:  Arch Emerg Med       Date:  1989-09

8.  Genetic testing for familial hypertrophic cardiomyopathy in newborn infants. Hypertrophic cardiomyopathy can be treated but not cured.

Authors:  J F Goodwin
Journal:  BMJ       Date:  1995-07-01

9.  Therapeutic options in hypertrophic cardiomyopathy: a pediatric perspective.

Authors:  Edward K Rhee; John J Nigro; Stephen G Pophal
Journal:  Curr Treat Options Cardiovasc Med       Date:  2008-09

10.  Haemodynamic effects of short term intravenous amiodarone for hypertrophic cardiomyopathy.

Authors:  A Branzi; C Rapezzi; P M Benenati; G Binetti; G Piovaccari; M Bacchi; R Roncuzzi; R Zannoli; B Magnani
Journal:  Br Heart J       Date:  1988-04
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