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Partial Replacement of Left Hemidiaphragm in Dogs by Either Cryopreserved or Decellularized Heterograft Patch Publisher Pubmed



Davari HR1 ; Rahim MB2 ; Tanideh N3 ; Sani M4 ; Tavakoli HR2 ; Rasekhi AR5 ; Monabati A6 ; Koohihosseinabadi O7 ; Gholami S8
Authors
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Authors Affiliations
  1. 1. General Thoracic Surgery Ward, Thorax Advanced Research Center, Tehran University of Medical Sciences and Health Services, Valiasr Hospital, Imam Khomeini Hospital Complex, Kheshavarz Boulevard, Tehran, 1419733141, Iran
  2. 2. General Thoracic Surgery Ward, Tehran University of Medical Sciences and Health Services, Tehran, Iran
  3. 3. Transgenic Technology Research Center, Shiraz University of Medical Sciences and Health Services, Shiraz, Iran
  4. 4. Department of Anatomy, Shiraz University of Medical Sciences and Health Services, Shiraz, Iran
  5. 5. Department of Radiology, Shiraz University of Medical Sciences and Health Services, Shiraz, Iran
  6. 6. Department of Pathology, Shiraz University of Medical Sciences and Health Services, Shiraz, Iran
  7. 7. Animal Laboratory, Shiraz University of Medical Sciences and Health Services, Shiraz, Iran
  8. 8. Transplant Coordinator, Shiraz University of Medical Sciences and Health Services, Shiraz, Iran

Source: Interactive Cardiovascular and Thoracic Surgery Published:2016


Abstract

OBJECTIVES Large diaphragmatic defects are still a challenging issue for reconstruction using either synthetic prosthesis or bioprosthesis. To evaluate the possibility of using diaphragm allograft as a natural bioprosthesis in humans, we conducted a two-group study and compared cryopreserved and decellularized diaphragmatic heterograft patched in a canine model. METHODS At the end of organ harvesting from a human donor, the left hemidiaphragm was taken to the laboratory in phosphate-buffered saline solution. The next step was freezing the grafts at -80°C, and preserving them for up to 2 months in Group 1. It was subjected to a detergent-enzymatic method (containing sodium deoxycholate/DNase lavations) of decellularization for 25 cycles in Group 2. Through left thoracotomy in the eighth intercostal space, cryopreserved patches in six dogs and decellularized patches in five dogs replaced the diaphragm. During the follow-up, sonography was done in all animals, but three and two dogs in Group 1 and 2 underwent computed tomography (CT) scan, respectively. The animals were euthanized after 6 months. RESULTS There was no mortality. Sonography showed only motion impairment of the patches in all cases. In Group 1, CT scan showed mild atelectasis and scattered infiltration in the left lower lobe, fibrotic bands and minimal fluid collection under the diaphragm. In Group 2, CT scan showed scattered fibrotic bands and mild to moderate elevation of the left hemidiaphragm. There was no evidence of gross disruption and complete healing of the suture line. Necropsy in both groups showed patches were completely replaced with a dense fibrous tissue. In Group 1, focal calcification was noticeable in every case and foreign body-type granulomas were clearly seen all over the grafted tissue. Histology in Group 2 animals showed less inflammatory cell infiltration and scattered foreign body granulomas in comparison with the cryopreserved patch graft. CONCLUSIONS The gross healing process in the decellularized heterograft is similar to the cryopreserved diaphragm but with fewer inflammatory cells and foreign body granulomas on histology. Both of them can be used instead of bioprostheses with regard to the fact that the decellularized patch technique is more complex and expensive. It is recommended to compare them with commercial bioprostheses. © 2016 The Author 2016. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.