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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.
Afiliação
  • Abdelshafy M; Discipline of Cardiology, Saolta Group, Galway University Hospital, Health Service Executive and CORRIB Core Lab, National University of Ireland Galway (NUIG), H91 V4AY Galway, Ireland.
  • Caliskan K; Department of Cardiology, Al-Azhar University, Al-Hussein University Hospital, Cairo 11311, Egypt.
  • Guven G; Department of Cardiology, Erasmus MC University Medical Center, 3015 GD Rotterdam, The Netherlands.
  • Elkoumy A; Department of Intensive Care Medicine, Erasmus MC University Medical Center, 3015 GD Rotterdam, The Netherlands.
  • Elsherbini H; Division of Internal Medicine Intensive Care, Hacettepe University Faculty of Medicine, 06230 Ankara, Turkey.
  • Elzomor H; Discipline of Cardiology, Saolta Group, Galway University Hospital, Health Service Executive and CORRIB Core Lab, National University of Ireland Galway (NUIG), H91 V4AY Galway, Ireland.
  • Tenekecioglu E; Islamic Center of Cardiology and Cardiac Surgery, Al-Azhar University, Nasr City, Cairo 11651, Egypt.
  • Akin S; Department of Cardiology, Erasmus MC University Medical Center, 3015 GD Rotterdam, The Netherlands.
  • Soliman O; Discipline of Cardiology, Saolta Group, Galway University Hospital, Health Service Executive and CORRIB Core Lab, National University of Ireland Galway (NUIG), H91 V4AY Galway, Ireland.
J Clin Med ; 11(3)2022 Jan 26.
Article em En | MEDLINE | ID: mdl-35160064
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article