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Using left ventricular assist devices in advanced heart failure patients

Advanced Heart Failure (AHF) is a complex syndrome that affects the physiology of the heart to maintain efficient blood circulation resulting in multiorgan failure and, eventually, death. Left Ventricular Assist Devices (LVADs) have become the cornerstone therapy for AHF patients, both as a bridge t...

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Autores principales: Shah, Syed Raza, Issa Najim, Najla, Shah, Syed Arbab, Shahnawaz, Waqas, Ahmed Jangda, Muhammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292364/
https://www.ncbi.nlm.nih.gov/pubmed/30559944
http://dx.doi.org/10.1080/20009666.2018.1536240
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author Shah, Syed Raza
Issa Najim, Najla
Shah, Syed Arbab
Shahnawaz, Waqas
Ahmed Jangda, Muhammad
author_facet Shah, Syed Raza
Issa Najim, Najla
Shah, Syed Arbab
Shahnawaz, Waqas
Ahmed Jangda, Muhammad
author_sort Shah, Syed Raza
collection PubMed
description Advanced Heart Failure (AHF) is a complex syndrome that affects the physiology of the heart to maintain efficient blood circulation resulting in multiorgan failure and, eventually, death. Left Ventricular Assist Devices (LVADs) have become the cornerstone therapy for AHF patients, both as a bridge to transplantation and as a decisive therapy. Recently the results of the MOMENTUM 3 Trial were published. The trial compared HeartMate 3 LVAD with HeartMate II LVAD in a randomized trial in The Multicenter Study of MagLev Technology in Patients Undergoing Mechanical Circulatory Support Therapy with HeartMate 3 (MOMENTUM 3). Of 366 patients, 190 were assigned to the centrifugal-flow pump group (HeartMate 3) and 176 to the axial-flow (HeartMate II) pump group. In the intention-to-treat population, the primary end point occurred in 151 patients (79.5%) in the centrifugal-flow pump group, as compared with 106 (60.2%) in the axial-flow pump group (P < 0.001 for noninferiority). Reoperation for pump malfunction was less frequent in the centrifugal-flow pump group than in the axial-flow pump group (P < 0.001).The results of the MOMENTUM 3 Trial are a big achievement in the cardiovascular world. Any improvement in LVADs that reduces the risk of stroke, perhaps the most feared complication of these devices, would be meaningful. Besides, given the observed lower rate of pump thrombosis and reoperation for pump malfunction, it already seems likely that the HeartMate 3 will supplant the HeartMate II in clinical practice. In addition, the risks that are associated with reoperation undoubtedly counterbalanced any unintentional bias in performing that intervention.
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spelling pubmed-62923642018-12-17 Using left ventricular assist devices in advanced heart failure patients Shah, Syed Raza Issa Najim, Najla Shah, Syed Arbab Shahnawaz, Waqas Ahmed Jangda, Muhammad J Community Hosp Intern Med Perspect Perspective Advanced Heart Failure (AHF) is a complex syndrome that affects the physiology of the heart to maintain efficient blood circulation resulting in multiorgan failure and, eventually, death. Left Ventricular Assist Devices (LVADs) have become the cornerstone therapy for AHF patients, both as a bridge to transplantation and as a decisive therapy. Recently the results of the MOMENTUM 3 Trial were published. The trial compared HeartMate 3 LVAD with HeartMate II LVAD in a randomized trial in The Multicenter Study of MagLev Technology in Patients Undergoing Mechanical Circulatory Support Therapy with HeartMate 3 (MOMENTUM 3). Of 366 patients, 190 were assigned to the centrifugal-flow pump group (HeartMate 3) and 176 to the axial-flow (HeartMate II) pump group. In the intention-to-treat population, the primary end point occurred in 151 patients (79.5%) in the centrifugal-flow pump group, as compared with 106 (60.2%) in the axial-flow pump group (P < 0.001 for noninferiority). Reoperation for pump malfunction was less frequent in the centrifugal-flow pump group than in the axial-flow pump group (P < 0.001).The results of the MOMENTUM 3 Trial are a big achievement in the cardiovascular world. Any improvement in LVADs that reduces the risk of stroke, perhaps the most feared complication of these devices, would be meaningful. Besides, given the observed lower rate of pump thrombosis and reoperation for pump malfunction, it already seems likely that the HeartMate 3 will supplant the HeartMate II in clinical practice. In addition, the risks that are associated with reoperation undoubtedly counterbalanced any unintentional bias in performing that intervention. Taylor & Francis 2018-12-11 /pmc/articles/PMC6292364/ /pubmed/30559944 http://dx.doi.org/10.1080/20009666.2018.1536240 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of Greater Baltimore Medical Center. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Perspective
Shah, Syed Raza
Issa Najim, Najla
Shah, Syed Arbab
Shahnawaz, Waqas
Ahmed Jangda, Muhammad
Using left ventricular assist devices in advanced heart failure patients
title Using left ventricular assist devices in advanced heart failure patients
title_full Using left ventricular assist devices in advanced heart failure patients
title_fullStr Using left ventricular assist devices in advanced heart failure patients
title_full_unstemmed Using left ventricular assist devices in advanced heart failure patients
title_short Using left ventricular assist devices in advanced heart failure patients
title_sort using left ventricular assist devices in advanced heart failure patients
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292364/
https://www.ncbi.nlm.nih.gov/pubmed/30559944
http://dx.doi.org/10.1080/20009666.2018.1536240
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