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A High-Fidelity Porcine Model of Orthotopic Heart Transplantation Following Donation after Circulatory Death.

Publication ,  Journal Article
Dewan, KC; Benkert, AR; Lobo, AA; Chen, J; Gross, RT; Salinas, M; Evans, A; Achanta, S; Mehta, S; Cutrone, M; Johnston, V; Rivera, K ...
Published in: J Vis Exp
June 6, 2025

The number of advanced heart failure patients who can receive a heart transplant is limited by a shortage of suitable organ donors. In efforts to expand the donor pool, alternative donation and procurement methods have been developed, including heart transplantation following donation after circulatory death (DCD HT). While short-term survival following DCD HT is non-inferior to heart transplantation with brain-dead donors, there may be an increased rate of primary graft dysfunction (PGD) associated with DCD HT allografts. The underlying etiology of PGD is multifactorial and incompletely understood. For DCD HT allografts, the period of warm ischemic injury during DCD procurement is a potential risk factor for PGD to which brain death allografts are not exposed. The functional warm ischemic time thus may be an important driver of PGD in DCD HT. However, the mechanisms underlying PGD in this clinical scenario are poorly understood at the molecular level. The work presented herein aims to describe the development and validation of a high-fidelity non-survival porcine model of DCD orthotopic heart transplantation. We hypothesize that the use of this translational large animal model is critical to elucidate molecular mechanisms contributing to PGD, as well as to investigate interventions designed to optimize allograft preservation and early performance. This model replicates the perioperative and surgical approach used in DCD HT clinically, with modifications to account for porcine anatomy and physiology. The development of this large animal surgical model will not only provide mechanistic insights into the development of PGD but also can be modified to enhance translational research efforts aimed at improving organ recovery following DCD HT.

Duke Scholars

Published In

J Vis Exp

DOI

EISSN

1940-087X

Publication Date

June 6, 2025

Issue

220

Location

United States

Related Subject Headings

  • Tissue Donors
  • Swine
  • Primary Graft Dysfunction
  • Models, Animal
  • Heart Transplantation
  • Animals
  • 3101 Biochemistry and cell biology
  • 1702 Cognitive Sciences
  • 1701 Psychology
  • 0601 Biochemistry and Cell Biology
 

Citation

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MLA
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Dewan, K. C., Benkert, A. R., Lobo, A. A., Chen, J., Gross, R. T., Salinas, M., … Keenan, J. E. (2025). A High-Fidelity Porcine Model of Orthotopic Heart Transplantation Following Donation after Circulatory Death. J Vis Exp, (220). https://doi.org/10.3791/68090
Dewan, Krish C., Abigail R. Benkert, Alejandro A. Lobo, Jengwei Chen, Ryan T. Gross, Martha Salinas, Amy Evans, et al. “A High-Fidelity Porcine Model of Orthotopic Heart Transplantation Following Donation after Circulatory Death.J Vis Exp, no. 220 (June 6, 2025). https://doi.org/10.3791/68090.
Dewan KC, Benkert AR, Lobo AA, Chen J, Gross RT, Salinas M, et al. A High-Fidelity Porcine Model of Orthotopic Heart Transplantation Following Donation after Circulatory Death. J Vis Exp. 2025 Jun 6;(220).
Dewan, Krish C., et al. “A High-Fidelity Porcine Model of Orthotopic Heart Transplantation Following Donation after Circulatory Death.J Vis Exp, no. 220, June 2025. Pubmed, doi:10.3791/68090.
Dewan KC, Benkert AR, Lobo AA, Chen J, Gross RT, Salinas M, Evans A, Achanta S, Mehta S, Cutrone M, Johnston V, Rivera K, Tran KD, Ngeve S, McCartney S, Milano C, Bowles DE, Keenan JE. A High-Fidelity Porcine Model of Orthotopic Heart Transplantation Following Donation after Circulatory Death. J Vis Exp. 2025 Jun 6;(220).

Published In

J Vis Exp

DOI

EISSN

1940-087X

Publication Date

June 6, 2025

Issue

220

Location

United States

Related Subject Headings

  • Tissue Donors
  • Swine
  • Primary Graft Dysfunction
  • Models, Animal
  • Heart Transplantation
  • Animals
  • 3101 Biochemistry and cell biology
  • 1702 Cognitive Sciences
  • 1701 Psychology
  • 0601 Biochemistry and Cell Biology