Efficacy and Safety of PARACHUTE® Device: systematic review

SUMMARY INTRODUCTION Heart failure due to an acute myocardial infarction is a very frequent event, with a tendency to increase according to improvements in the treatment of acute conditions which have led to larger numbers of infarction survivors. OBJECTIVE The aim of this study is to synthesize...

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Main Authors: Roberta da Silva Teixeira, Bruna Medeiros Gonçalves de Veras, Kátia Marie Simões e Senna, Rosângela Caetano
Format: Article
Language:English
Published: Associação Médica Brasileira
Series:Revista da Associação Médica Brasileira
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302018000900853&lng=en&tlng=en
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spelling doaj-1976aa8c59844f789d5f4f9f870d55642020-11-25T00:48:55ZengAssociação Médica BrasileiraRevista da Associação Médica Brasileira1806-928264985386010.1590/1806-9282.64.09.853S0104-42302018000900853Efficacy and Safety of PARACHUTE® Device: systematic reviewRoberta da Silva TeixeiraBruna Medeiros Gonçalves de VerasKátia Marie Simões e SennaRosângela CaetanoSUMMARY INTRODUCTION Heart failure due to an acute myocardial infarction is a very frequent event, with a tendency to increase according to improvements in the treatment of acute conditions which have led to larger numbers of infarction survivors. OBJECTIVE The aim of this study is to synthesize the evidence, through a systematic review, on efficacy and safety of the device in patients with this basic condition. METHODS Studies published between January 2002 and October 2016 were analysed, having as reference databases Embase, Medline, Cochrane Library, Lilacs, Web of Science and Scopus. The selection of studies, data extraction and methodological quality assessment of studies were examined by two independent reviewers, with disagreements resolved by consensus. RESULTS Only prospective studies without control group were identified. Six studies were included, with averages of 34 participants and follow-up of 13 months. Clinical, functional, hemodynamic and quality of life outcomes were evaluated. The highest mortality rate was 8.4% with 12-month follow-up for unspecified cardiovascular reasons, and heart failure rehospitalization was 29.4% with 36-month follow-up. Statistically significant improvements were found only in some of the studies which evaluating changes in left ventricular volume indices, the distance measured by the six-minute walk test, New York Heart Association functional classification, and quality of life, in pre and post-procedure analysis. CONCLUSIONS The present review indicates that no available quality evidence can assert efficacy and safety of PARACHUTE® in the treatment of heart failure after apical or anterior wall myocardial infarction.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302018000900853&lng=en&tlng=enInsuficiência cardíacaInfarto do miocárdioEquipamentos e provisõesAvaliação da tecnologia biomédicaLiteratura de revisão como assunto
collection DOAJ
language English
format Article
sources DOAJ
author Roberta da Silva Teixeira
Bruna Medeiros Gonçalves de Veras
Kátia Marie Simões e Senna
Rosângela Caetano
spellingShingle Roberta da Silva Teixeira
Bruna Medeiros Gonçalves de Veras
Kátia Marie Simões e Senna
Rosângela Caetano
Efficacy and Safety of PARACHUTE® Device: systematic review
Revista da Associação Médica Brasileira
Insuficiência cardíaca
Infarto do miocárdio
Equipamentos e provisões
Avaliação da tecnologia biomédica
Literatura de revisão como assunto
author_facet Roberta da Silva Teixeira
Bruna Medeiros Gonçalves de Veras
Kátia Marie Simões e Senna
Rosângela Caetano
author_sort Roberta da Silva Teixeira
title Efficacy and Safety of PARACHUTE® Device: systematic review
title_short Efficacy and Safety of PARACHUTE® Device: systematic review
title_full Efficacy and Safety of PARACHUTE® Device: systematic review
title_fullStr Efficacy and Safety of PARACHUTE® Device: systematic review
title_full_unstemmed Efficacy and Safety of PARACHUTE® Device: systematic review
title_sort efficacy and safety of parachute® device: systematic review
publisher Associação Médica Brasileira
series Revista da Associação Médica Brasileira
issn 1806-9282
description SUMMARY INTRODUCTION Heart failure due to an acute myocardial infarction is a very frequent event, with a tendency to increase according to improvements in the treatment of acute conditions which have led to larger numbers of infarction survivors. OBJECTIVE The aim of this study is to synthesize the evidence, through a systematic review, on efficacy and safety of the device in patients with this basic condition. METHODS Studies published between January 2002 and October 2016 were analysed, having as reference databases Embase, Medline, Cochrane Library, Lilacs, Web of Science and Scopus. The selection of studies, data extraction and methodological quality assessment of studies were examined by two independent reviewers, with disagreements resolved by consensus. RESULTS Only prospective studies without control group were identified. Six studies were included, with averages of 34 participants and follow-up of 13 months. Clinical, functional, hemodynamic and quality of life outcomes were evaluated. The highest mortality rate was 8.4% with 12-month follow-up for unspecified cardiovascular reasons, and heart failure rehospitalization was 29.4% with 36-month follow-up. Statistically significant improvements were found only in some of the studies which evaluating changes in left ventricular volume indices, the distance measured by the six-minute walk test, New York Heart Association functional classification, and quality of life, in pre and post-procedure analysis. CONCLUSIONS The present review indicates that no available quality evidence can assert efficacy and safety of PARACHUTE® in the treatment of heart failure after apical or anterior wall myocardial infarction.
topic Insuficiência cardíaca
Infarto do miocárdio
Equipamentos e provisões
Avaliação da tecnologia biomédica
Literatura de revisão como assunto
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302018000900853&lng=en&tlng=en
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