Cavopulmonary assist: Long-term reversal of the Fontan paradox.


Journal

The Journal of thoracic and cardiovascular surgery
ISSN: 1097-685X
Titre abrégé: J Thorac Cardiovasc Surg
Pays: United States
ID NLM: 0376343

Informations de publication

Date de publication:
12 2019
Historique:
received: 02 05 2019
revised: 13 06 2019
accepted: 14 06 2019
pubmed: 1 10 2019
medline: 3 3 2020
entrez: 1 10 2019
Statut: ppublish

Résumé

Fontan circulatory inefficiency can be addressed by replacing the missing subpulmonary power source to reverse the Fontan paradox. An implantable cavopulmonary assist device is described that will simultaneously reduce systemic venous pressure and increase pulmonary arterial pressure, improving preload and cardiac output, in a univentricular Fontan circulation on a long-term basis. A rotary blood pump that was based on the von Karman viscous pump was designed for implantation into the total cavopulmonary connection (TCPC). It will impart modest pressure energy to augment Fontan flow without risk of obstruction. In the event of rotational failure, it is designed to default to a passive flow diverter. Pressure-flow performance was characterized in vitro in a Fontan mock circulatory loop with blood analog. The pump performed through the fully specified operating range, augmenting flow in all 4 directions of the TCPC. Pressure rise of 6 to 8 mm Hg was readily achieved, ranging to 14 mm Hg at highest speed (5600 rpm). Performance was consistent across a wide range of cardiac outputs. In stalled condition (0 rpm), there was no discernible pressure loss across the TCPC. A blood pump technology is described that can reverse the Fontan paradox and may permit a surgical strategy of long-term biventricular maintenance of a univentricular Fontan circulation. The technology is intended for Fontan failure in which right-sided circulatory inefficiencies predominate and ventricular systolic function is preserved. It may also apply before clinical Fontan failure as health maintenance to preempt the progression of Fontan disease.

Identifiants

pubmed: 31564543
pii: S0022-5223(19)31676-9
doi: 10.1016/j.jtcvs.2019.06.112
pii:
doi:

Types de publication

Journal Article Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

1627-1636

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 The American Association for Thoracic Surgery. Published by Elsevier Inc. All rights reserved.

Auteurs

Mark D Rodefeld (MD)

Section of Cardiothoracic Surgery, Department of Surgery, Indiana University School of Medicine and James Whitcomb Riley Hospital for Children, Indianapolis, Ind. Electronic address: rodefeld@iupui.edu.

Alison Marsden (A)

Department of Bioengineering and Pediatrics, Stanford University, Stanford, Calif.

Richard Figliola (R)

Department of Mechanical Engineering, Clemson University, Clemson, SC.

Travis Jonas (T)

Mechanical Solutions Inc, Whippany, NJ.

Michael Neary (M)

Rotor Bearing Technology and Software Inc, Phoenixville, Pa.

Guruprasad A Giridharan (GA)

Department of Bioengineering, University of Louisville, Louisville, Ky.

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