Literature DB >> 24464640

Long-term prognostic impact of therapeutic strategies in patients with idiopathic dilated cardiomyopathy: changing mortality over the last 30 years.

Marco Merlo1, Alberto Pivetta, Bruno Pinamonti, Davide Stolfo, Massimo Zecchin, Giulia Barbati, Andrea Di Lenarda, Gianfranco Sinagra.   

Abstract

AIMS: ACE-inhibitors, β-blockers, implantable cardioverter-defibrillator (ICD) and cardiac resynchronization therapy (CRT) improved prognosis of heart failure. We sought to analyse the long-term prognostic impact of evidence-based integrated therapeutic strategies in patients with idiopathic dilated cardiomyopathy (IDCM). METHODS AND
RESULTS: From 1978 to 2007, 853 IDCM patients (45 ± 15 years, 72% males) were enrolled and classified as follows: Group 1, 110 patients (12.8%) enrolled during 1978-1987; Group 2, 376 patients (44.1%) enrolled during 1988-1997; Group 3, 367 patients (43.1%) enrolled during 1998-2007. ACE-inhibitors/angiotensin receptor blockers were administered in 34%, 93%, and 93% (P <0.001), and β-blockers in 11%, 82%, and 86% (P <0.001) in Groups 1, 2, and 3, respectively; ICDs were implanted in 2%, 14%, and 13% (P = 0.005); mean time to device implantation was lower in Group 3. At 8 years, heart transplant (HTx)-free survival rates were 55%, 71%, and 87% in Groups 1, 2, and 3, respectively (P <0.001). Similar progressive improvement was found for pump-failure death (DHF)/HTx, while survival free from sudden death (SD) was significantly improved only in Group 3. Multivariable models considering competing risk indicated early diagnosis (i.e. a baseline less advanced disease stage) and tailored medical therapy (HR 0.44, CI 95% 0.19-0.98) as independent protectors against DHF/HTx. Concerning SD, lower left ventricular ejection fraction emerged as a predictor, while ICD was the only therapy with a protective role (HR 0.08, CI 95% 0.01-0.61). Treatment with digitalis emerged as a predictor of both DHF/HTx and SD.
CONCLUSIONS: An effective management and evidence-based integrated therapeutic approach progressively and significantly improved the long-term prognosis of IDCM during the last three decades.
© 2013 The Authors. European Journal of Heart Failure © 2013 European Society of Cardiology.

Entities:  

Keywords:  Dilated cardiomyopathy; Follow-up study; Heart failure; Prognosis; Sudden death

Mesh:

Substances:

Year:  2013        PMID: 24464640     DOI: 10.1002/ejhf.16

Source DB:  PubMed          Journal:  Eur J Heart Fail        ISSN: 1388-9842            Impact factor:   15.534


  47 in total

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Review 7.  Genetics of Dilated Cardiomyopathy: Clinical Implications.

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8.  Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy.

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Review 9.  Emerging concepts in arrhythmogenic dilated cardiomyopathy.

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Journal:  Heart Fail Rev       Date:  2021-09       Impact factor: 4.214

10.  Next-Generation Sequencing Reveals Novel Genetic Variants for Dilated Cardiomyopathy in Pediatric Chinese Patients.

Authors:  Yan Wang; Bo Han; Youfei Fan; Yingchun Yi; Jianli Lv; Jing Wang; Xiaofei Yang; Diandong Jiang; Lijian Zhao; Jianjun Zhang; Hui Yuan
Journal:  Pediatr Cardiol       Date:  2021-08-04       Impact factor: 1.655

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