Abigail Meyers, Varun Lingaiah Kopparthy, Jacob Lammers, Mazen Al-Malak, Brian Figueroa, Ying Ku, Lianne Mulvihill, Ryan Khalaf, Jose Reyes, Diane Jo, R'ay Fodor, Payam Sadeghi, Antonio Rampazzo, Bahar Bassiri Gharb
{"title":"Ex Vivo Preservation of Porcine Vascularized Composite Soft Tissue Allografts.","authors":"Abigail Meyers, Varun Lingaiah Kopparthy, Jacob Lammers, Mazen Al-Malak, Brian Figueroa, Ying Ku, Lianne Mulvihill, Ryan Khalaf, Jose Reyes, Diane Jo, R'ay Fodor, Payam Sadeghi, Antonio Rampazzo, Bahar Bassiri Gharb","doi":"10.1111/aor.14969","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The aim of this study was to evaluate ex vivo perfusion (EVP) for vascularized composite tissue preservation. We hypothesized that EVP could maintain allografts in near-physiologic conditions for ≥ 24 h.</p><p><strong>Methods: </strong>Twenty superior epigastric artery perforator-based abdominal flaps were procured from 10 Yorkshire pigs. Flaps were preserved for 12 h (n = 5) or 24 h (n = 5) using EVP with an oxygenated colloid solution containing HBOC-201 oxygen carrier (HbO<sub>2</sub> Therapeutics, Souderton, PA). Contralateral flaps were cold storage controls (4°C) (n = 10). Hemodynamics, temperature, gases, metabolites, electrolytes, indocyanine green (ICG) angiography, and weight were analyzed. Biopsies were taken every 6 h for histology.</p><p><strong>Results: </strong>Ischemia time was 16 ± 6 min. There were no significant differences between the 12 h EVP and 24 h EVP groups at perfusion end for the following parameters: MAP (p = 0.63), pH (p = 0.77), pO2 (p = 0.20), venous pCO<sub>2</sub> (p = 0.22), lactate (p = 0.28), creatine kinase (p = 0.89), or myoglobin (p = 0.95). Electrolytes were also comparable at perfusion termination: sodium (p = 0.31), potassium (p = 0.61), and calcium (p = 0.29). After 12 h, flaps in the 24 h EVP group demonstrated a significant weight decrease (-4.5% [-4.6%, -4.1%] weight change), compared to the 12 h EVP group (1.2% [-1.1%, 1.6%] weight change) (p = 0.03). At perfusion end, weight did not differ from baseline between the 24 h EVP (2.3% [0%, 3%]) and 12 h EVP groups (p = 0.37). SCS flap weight was unchanged from baseline at 12 h (p = 0.954) and 24 h (p = 0.616). ICG revealed well-perfused flaps. H&E staining revealed preserved skin architecture without histopathological changes.</p><p><strong>Conclusion: </strong>EVP preserved flaps for 24 h within physiologic parameters and without development of edema. EVP may extend preservation time for VCAs.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Artificial organs","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1111/aor.14969","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: The aim of this study was to evaluate ex vivo perfusion (EVP) for vascularized composite tissue preservation. We hypothesized that EVP could maintain allografts in near-physiologic conditions for ≥ 24 h.
Methods: Twenty superior epigastric artery perforator-based abdominal flaps were procured from 10 Yorkshire pigs. Flaps were preserved for 12 h (n = 5) or 24 h (n = 5) using EVP with an oxygenated colloid solution containing HBOC-201 oxygen carrier (HbO2 Therapeutics, Souderton, PA). Contralateral flaps were cold storage controls (4°C) (n = 10). Hemodynamics, temperature, gases, metabolites, electrolytes, indocyanine green (ICG) angiography, and weight were analyzed. Biopsies were taken every 6 h for histology.
Results: Ischemia time was 16 ± 6 min. There were no significant differences between the 12 h EVP and 24 h EVP groups at perfusion end for the following parameters: MAP (p = 0.63), pH (p = 0.77), pO2 (p = 0.20), venous pCO2 (p = 0.22), lactate (p = 0.28), creatine kinase (p = 0.89), or myoglobin (p = 0.95). Electrolytes were also comparable at perfusion termination: sodium (p = 0.31), potassium (p = 0.61), and calcium (p = 0.29). After 12 h, flaps in the 24 h EVP group demonstrated a significant weight decrease (-4.5% [-4.6%, -4.1%] weight change), compared to the 12 h EVP group (1.2% [-1.1%, 1.6%] weight change) (p = 0.03). At perfusion end, weight did not differ from baseline between the 24 h EVP (2.3% [0%, 3%]) and 12 h EVP groups (p = 0.37). SCS flap weight was unchanged from baseline at 12 h (p = 0.954) and 24 h (p = 0.616). ICG revealed well-perfused flaps. H&E staining revealed preserved skin architecture without histopathological changes.
Conclusion: EVP preserved flaps for 24 h within physiologic parameters and without development of edema. EVP may extend preservation time for VCAs.
期刊介绍:
Artificial Organs is the official peer reviewed journal of The International Federation for Artificial Organs (Members of the Federation are: The American Society for Artificial Internal Organs, The European Society for Artificial Organs, and The Japanese Society for Artificial Organs), The International Faculty for Artificial Organs, the International Society for Rotary Blood Pumps, The International Society for Pediatric Mechanical Cardiopulmonary Support, and the Vienna International Workshop on Functional Electrical Stimulation. Artificial Organs publishes original research articles dealing with developments in artificial organs applications and treatment modalities and their clinical applications worldwide. Membership in the Societies listed above is not a prerequisite for publication. Articles are published without charge to the author except for color figures and excess page charges as noted.