Development of a Simple and Active Shunt System in the Anhepatic Stage for Surgical Training of Orthotopic Liver Transplantation.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
Historique:
received: 27 01 2020
accepted: 12 03 2020
pubmed: 30 5 2020
medline: 20 4 2021
entrez: 30 5 2020
Statut: ppublish

Résumé

A pig model has been commonly used for technical training for clinical liver transplantation (LT). However, as the healthy pigs have no shunt bypassing the portal vein (PV), it is necessary to complete LT within 30 minutes after shutting off the PV flow. While a model that uses an ex vivo shunt system has been used to alleviate the constraints of the anhepatic phase, it has been often difficult to keep sufficient blood flow rate and prevent the intestinal congestion because the blood vessels were occluded easily with the suction pressure by using the conventional shunt system. We designed a portable shunt system and a novel connector that can prevent the blood vessel from occluding. The system can separately control the flow rate of PV and inferior vena cava (IVC) and detect whether the blood vessels were occluded. By reducing the solution volume in the circuit, the effected blood loss ex vivo could be minimized. The stability of this system was verified with 15 medical doctors in an advanced medical professional education course. The system enabled the blood flow to maintain ≥ 20 mL/minute and prevented the intestinal congestion. The perioperative hemodynamics of the recipient were stable without a blood transfusion using 25 to 40 kg pigs. We confirmed that all LT training were completed, even 60 minutes after shutting off the PV flow. Our system greatly contributed to training on LT for conducting the survival experiments.

Sections du résumé

BACKGROUND BACKGROUND
A pig model has been commonly used for technical training for clinical liver transplantation (LT). However, as the healthy pigs have no shunt bypassing the portal vein (PV), it is necessary to complete LT within 30 minutes after shutting off the PV flow. While a model that uses an ex vivo shunt system has been used to alleviate the constraints of the anhepatic phase, it has been often difficult to keep sufficient blood flow rate and prevent the intestinal congestion because the blood vessels were occluded easily with the suction pressure by using the conventional shunt system.
METHODS METHODS
We designed a portable shunt system and a novel connector that can prevent the blood vessel from occluding. The system can separately control the flow rate of PV and inferior vena cava (IVC) and detect whether the blood vessels were occluded. By reducing the solution volume in the circuit, the effected blood loss ex vivo could be minimized. The stability of this system was verified with 15 medical doctors in an advanced medical professional education course.
RESULTS RESULTS
The system enabled the blood flow to maintain ≥ 20 mL/minute and prevented the intestinal congestion. The perioperative hemodynamics of the recipient were stable without a blood transfusion using 25 to 40 kg pigs. We confirmed that all LT training were completed, even 60 minutes after shutting off the PV flow.
CONCLUSIONS CONCLUSIONS
Our system greatly contributed to training on LT for conducting the survival experiments.

Identifiants

pubmed: 32466955
pii: S0041-1345(20)30245-1
doi: 10.1016/j.transproceed.2020.03.028
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

42-48

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Hiroo Kasamatsu (H)

SCREEN Holdings Co, Ltd, Kyoto, Japan.

Syuhei Yoshimoto (S)

SCREEN Holdings Co, Ltd, Kyoto, Japan.

Shinji Torai (S)

SCREEN Holdings Co, Ltd, Kyoto, Japan.

Takahiro Kimura (T)

SCREEN Holdings Co, Ltd, Kyoto, Japan.

Masaki Yoshioka (M)

SCREEN Holdings Co, Ltd, Kyoto, Japan.

Soichi Nadahara (S)

SCREEN Holdings Co, Ltd, Kyoto, Japan.

Hidekazu Yamamoto (H)

Department of Transplantation and Pediatric Surgery, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.

Yukihiro Inomata (Y)

Department of Transplantation and Pediatric Surgery, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.

Eiji Kobayashi (E)

SCREEN Holdings Co, Ltd, Kyoto, Japan; Department of Organ Fabrication, Keio University School of Medicine, Tokyo, Japan. Electronic address: organfabri@keio.jp.

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