Literature DB >> 28944179

Hypertrophic cardiomyopathy in children.

Arman Arghami1, Joseph A Dearani1, Sameh M Said1, Patrick W O'Leary2, Hartzell V Schaff1.   

Abstract

Hypertrophic cardiomyopathy (HCM) occurs in 1 of 500 adults and is considered to be one of the most common causes of death in young people under 35 years of age. Children with HCM are usually asymptomatic and the overall annual mortality beyond the first year of life is 1%. Septal myectomy is safe and effective in children with obstructive HCM and published data shows improved late survival compared to untreated HCM. Patient selection and surgical expertise remain critical components to ensuring successful outcomes of septal myectomy, particularly when considering prophylactic myectomy in a seemingly asymptomatic patient.

Entities:  

Keywords:  Hypertrophic cardiomyopathy (HCM); septal myectomy

Year:  2017        PMID: 28944179      PMCID: PMC5602192          DOI: 10.21037/acs.2017.07.04

Source DB:  PubMed          Journal:  Ann Cardiothorac Surg        ISSN: 2225-319X


  33 in total

1.  Surgical relief of diffuse subvalvular aortic stenosis.

Authors:  J W KIRKLIN; F H ELLIS
Journal:  Circulation       Date:  1961-10       Impact factor: 29.690

2.  2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.

Authors:  Bernard J Gersh; Barry J Maron; Robert O Bonow; Joseph A Dearani; Michael A Fifer; Mark S Link; Srihari S Naidu; Rick A Nishimura; Steve R Ommen; Harry Rakowski; Christine E Seidman; Jeffrey A Towbin; James E Udelson; Clyde W Yancy
Journal:  J Thorac Cardiovasc Surg       Date:  2011-12       Impact factor: 5.209

3.  Apical myectomy: a new surgical technique for management of severely symptomatic patients with apical hypertrophic cardiomyopathy.

Authors:  Hartzell V Schaff; Morgan L Brown; Joseph A Dearani; Martin D Abel; Steve R Ommen; Paul Sorajja; A Jamil Tajik; Rick A Nishimura
Journal:  J Thorac Cardiovasc Surg       Date:  2010-03       Impact factor: 5.209

Review 4.  Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

Authors:  A J Marian; L Salek; S Lutucuta
Journal:  Minerva Med       Date:  2001-12       Impact factor: 4.806

5.  Epidemiology of hypertrophic cardiomyopathy-related death: revisited in a large non-referral-based patient population.

Authors:  B J Maron; I Olivotto; P Spirito; S A Casey; P Bellone; T E Gohman; K J Graham; D A Burton; F Cecchi
Journal:  Circulation       Date:  2000-08-22       Impact factor: 29.690

6.  Hypertrophic obstructive cardiomyopathy in pediatric patients: results of surgical treatment.

Authors:  D A Theodoro; G K Danielson; R H Feldt; B J Anderson
Journal:  J Thorac Cardiovasc Surg       Date:  1996-12       Impact factor: 5.209

7.  Prognosis in hypertrophic cardiomyopathy: role of age and clinical, electrocardiographic and hemodynamic features.

Authors:  W McKenna; J Deanfield; A Faruqui; D England; C Oakley; J Goodwin
Journal:  Am J Cardiol       Date:  1981-03       Impact factor: 2.778

8.  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

9.  Hypertrophic cardiomyopathy in infants: clinical features and natural history.

Authors:  B J Maron; A J Tajik; H D Ruttenberg; T P Graham; G F Atwood; B E Victorica; J T Lie; W C Roberts
Journal:  Circulation       Date:  1982-01       Impact factor: 29.690

10.  A contemporary European experience with surgical septal myectomy in hypertrophic cardiomyopathy.

Authors:  Attilio Iacovoni; Paolo Spirito; Caterina Simon; Maria Iascone; Giovanni Di Dedda; Paolo De Filippo; Samuele Pentiricci; Luca Boni; Michele Senni; Antonello Gavazzi; Paolo Ferrazzi
Journal:  Eur Heart J       Date:  2012-04-20       Impact factor: 29.983

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