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Temporary Right-Ventricular Assist Devices: A Systematic Review
Acute right-sided heart failure (RHF) is a complex clinical syndrome, with a wide range of clinical presentations, associated with increased mortality and morbidity, but about which there is a scarcity of evidence-based literature. A temporary right-ventricular assist device (t-RVAD) is a potential...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837135/ https://www.ncbi.nlm.nih.gov/pubmed/35160064 http://dx.doi.org/10.3390/jcm11030613 |
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author | Abdelshafy, Mahmoud Caliskan, Kadir Guven, Goksel Elkoumy, Ahmed Elsherbini, Hagar Elzomor, Hesham Tenekecioglu, Erhan Akin, Sakir Soliman, Osama |
author_facet | Abdelshafy, Mahmoud Caliskan, Kadir Guven, Goksel Elkoumy, Ahmed Elsherbini, Hagar Elzomor, Hesham Tenekecioglu, Erhan Akin, Sakir Soliman, Osama |
author_sort | Abdelshafy, Mahmoud |
collection | PubMed |
description | Acute right-sided heart failure (RHF) is a complex clinical syndrome, with a wide range of clinical presentations, associated with increased mortality and morbidity, but about which there is a scarcity of evidence-based literature. A temporary right-ventricular assist device (t-RVAD) is a potential treatment option for selected patients with severe right-ventricular dysfunction as a bridge-to-recovery or as a permanent solution. We sought to conduct a systematic review to determine the safety and efficacy of t-RVAD implantation. Thirty-one studies met the inclusion criteria, from which data were extracted. Successful t-RVAD weaning ranged between 23% and 100%. Moreover, 30-day survival post-temporary RAVD implantation ranged from 46% to 100%. Bleeding, acute kidney injury, stroke, and device malfunction were the most commonly reported complications. Notwithstanding this, t-RVAD is a lifesaving option for patients with severe RHF, but the evidence stems from small non-randomized heterogeneous studies utilizing a variety of devices. Both the etiology of RHF and time of intervention might play a major role in determining the t-RVAD outcome. Standardized endpoints definitions, design and methodology for t-RVAD trials is needed. Furthermore, efforts should continue in improving the technology as well as improving the timely provision of a t-RVAD. |
format | Online Article Text |
id | pubmed-8837135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88371352022-02-12 Temporary Right-Ventricular Assist Devices: A Systematic Review Abdelshafy, Mahmoud Caliskan, Kadir Guven, Goksel Elkoumy, Ahmed Elsherbini, Hagar Elzomor, Hesham Tenekecioglu, Erhan Akin, Sakir Soliman, Osama J Clin Med Review Acute right-sided heart failure (RHF) is a complex clinical syndrome, with a wide range of clinical presentations, associated with increased mortality and morbidity, but about which there is a scarcity of evidence-based literature. A temporary right-ventricular assist device (t-RVAD) is a potential treatment option for selected patients with severe right-ventricular dysfunction as a bridge-to-recovery or as a permanent solution. We sought to conduct a systematic review to determine the safety and efficacy of t-RVAD implantation. Thirty-one studies met the inclusion criteria, from which data were extracted. Successful t-RVAD weaning ranged between 23% and 100%. Moreover, 30-day survival post-temporary RAVD implantation ranged from 46% to 100%. Bleeding, acute kidney injury, stroke, and device malfunction were the most commonly reported complications. Notwithstanding this, t-RVAD is a lifesaving option for patients with severe RHF, but the evidence stems from small non-randomized heterogeneous studies utilizing a variety of devices. Both the etiology of RHF and time of intervention might play a major role in determining the t-RVAD outcome. Standardized endpoints definitions, design and methodology for t-RVAD trials is needed. Furthermore, efforts should continue in improving the technology as well as improving the timely provision of a t-RVAD. MDPI 2022-01-26 /pmc/articles/PMC8837135/ /pubmed/35160064 http://dx.doi.org/10.3390/jcm11030613 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Abdelshafy, Mahmoud Caliskan, Kadir Guven, Goksel Elkoumy, Ahmed Elsherbini, Hagar Elzomor, Hesham Tenekecioglu, Erhan Akin, Sakir Soliman, Osama Temporary Right-Ventricular Assist Devices: A Systematic Review |
title | Temporary Right-Ventricular Assist Devices: A Systematic Review |
title_full | Temporary Right-Ventricular Assist Devices: A Systematic Review |
title_fullStr | Temporary Right-Ventricular Assist Devices: A Systematic Review |
title_full_unstemmed | Temporary Right-Ventricular Assist Devices: A Systematic Review |
title_short | Temporary Right-Ventricular Assist Devices: A Systematic Review |
title_sort | temporary right-ventricular assist devices: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837135/ https://www.ncbi.nlm.nih.gov/pubmed/35160064 http://dx.doi.org/10.3390/jcm11030613 |
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