The Biocompatibility Challenges in the Total Artificial Heart Evolution.


Journal

Annual review of biomedical engineering
ISSN: 1545-4274
Titre abrégé: Annu Rev Biomed Eng
Pays: United States
ID NLM: 100883581

Informations de publication

Date de publication:
04 06 2019
Historique:
pubmed: 24 2 2019
medline: 3 7 2020
entrez: 24 2 2019
Statut: ppublish

Résumé

There are limited therapeutic options for final treatment of end-stage heart failure. Among them, implantation of a total artificial heart (TAH) is an acceptable strategy when suitable donors are not available. TAH development began in the 1930s, followed by a dramatic evolution of the actuation mechanisms operating the mechanical pumps. Nevertheless, the performance of TAHs has not yet been optimized, mainly because of the low biocompatibility of the blood-contacting surfaces. Low hemocompatibility, calcification, and sensitivity to infections seriously affect the success of TAHs. These unsolved issues have led to the withdrawal of many prototypes during preclinical phases of testing. This review offers a comprehensive analysis of the pathophysiological events that may occur in the materials that compose TAHs developed to date. In addition, this review illustrates bioengineering strategies to prevent these events and describes the most significant steps toward the achievement of a fully biocompatible TAH.

Identifiants

pubmed: 30795701
doi: 10.1146/annurev-bioeng-060418-052432
doi:

Substances chimiques

Biocompatible Materials 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

85-110

Auteurs

Eleonora Dal Sasso (E)

Cardiovascular Regenerative Medicine Group, Department of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua and Veneto Institute of Molecular Medicine, 35128 Padua, Italy; email: eleonora.dalsasso@studenti.unipd.it , gino.gerosa@unipd.it , laura.iop@unipd.it.
Padua Heart Project, Division of Cardiac Surgery, University Hospital of Padua, 35128 Padua, Italy; email: silvia.scuri@yahoo.it.

Andrea Bagno (A)

Department of Industrial Engineering, University of Padua, 35128 Padua, Italy; email: andrea.bagno@unipd.it.

Silvia T G Scuri (STG)

Padua Heart Project, Division of Cardiac Surgery, University Hospital of Padua, 35128 Padua, Italy; email: silvia.scuri@yahoo.it.

Gino Gerosa (G)

Cardiovascular Regenerative Medicine Group, Department of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua and Veneto Institute of Molecular Medicine, 35128 Padua, Italy; email: eleonora.dalsasso@studenti.unipd.it , gino.gerosa@unipd.it , laura.iop@unipd.it.
Padua Heart Project, Division of Cardiac Surgery, University Hospital of Padua, 35128 Padua, Italy; email: silvia.scuri@yahoo.it.

Laura Iop (L)

Cardiovascular Regenerative Medicine Group, Department of Cardiac, Thoracic and Vascular Sciences and Public Health, University of Padua and Veneto Institute of Molecular Medicine, 35128 Padua, Italy; email: eleonora.dalsasso@studenti.unipd.it , gino.gerosa@unipd.it , laura.iop@unipd.it.
Padua Heart Project, Division of Cardiac Surgery, University Hospital of Padua, 35128 Padua, Italy; email: silvia.scuri@yahoo.it.

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