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First Experience in Living Liver Donation From Donors With Sickle Cell Trait

Living donor liver transplantation is the main source of organs in the Middle East. Therefore, well balanced criteria are needed to avoid unnecessary exclusion of potential donors, while prioritizing donor safety. We face a high incidence of sickle cell trait (SCT; and disease). Therefore, there is...

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Autores principales: Schulze, Maren, Zidan, Ahmed, Sturdevant, Mark, Aljudaibi, Sultan, Shagrani, Mohammad, Bzeizi, Khalid, Alqahtani, Saleh, Broering, Dieter C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088231/
https://www.ncbi.nlm.nih.gov/pubmed/35557991
http://dx.doi.org/10.1097/TXD.0000000000001332
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author Schulze, Maren
Zidan, Ahmed
Sturdevant, Mark
Aljudaibi, Sultan
Shagrani, Mohammad
Bzeizi, Khalid
Alqahtani, Saleh
Broering, Dieter C.
author_facet Schulze, Maren
Zidan, Ahmed
Sturdevant, Mark
Aljudaibi, Sultan
Shagrani, Mohammad
Bzeizi, Khalid
Alqahtani, Saleh
Broering, Dieter C.
author_sort Schulze, Maren
collection PubMed
description Living donor liver transplantation is the main source of organs in the Middle East. Therefore, well balanced criteria are needed to avoid unnecessary exclusion of potential donors, while prioritizing donor safety. We face a high incidence of sickle cell trait (SCT; and disease). Therefore, there is vast experience in general and cardiac surgeries in SCT carriers at our center. After studying their management in detail, we considered accepting SCT carriers as living liver donors, on an exceptional basis. This the first single-center case series of living donor liver transplantation with SCT. METHODS. Between January 2012 and September 2021, 20 donors with SCT were reviewed for age, gender, relation to the recipient, hemoglobin, hemoglobin S (HbS), surgical approach, intensive care unit stay, donor and recipients’ complications, and graft and recipient survival. RESULTS. Average age of donors was 28.4 y. Sixteen donated the left lateral segment, 4 the left lobe. Recipients were related children or adults. HbS ranged from 21.2% to 39.9%, being ≥30% in 14 donors. HbS was reduced by phlebotomy or exchange transfusion. We performed 7 open, one laparoscopic, and 12 robotic donor surgeries. Operating room time, blood loss, and intensive care unit stay were comparable to non-SCT donors. There was no SCT-related complication. All donors are alive and free of thromboembolic events. Graft and recipient survival is 100% until follow-up. CONCLUSION. Our experience should encourage other countries with high incidence of SCT to report their experience with this donor population.
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spelling pubmed-90882312022-05-11 First Experience in Living Liver Donation From Donors With Sickle Cell Trait Schulze, Maren Zidan, Ahmed Sturdevant, Mark Aljudaibi, Sultan Shagrani, Mohammad Bzeizi, Khalid Alqahtani, Saleh Broering, Dieter C. Transplant Direct Liver Transplantation Living donor liver transplantation is the main source of organs in the Middle East. Therefore, well balanced criteria are needed to avoid unnecessary exclusion of potential donors, while prioritizing donor safety. We face a high incidence of sickle cell trait (SCT; and disease). Therefore, there is vast experience in general and cardiac surgeries in SCT carriers at our center. After studying their management in detail, we considered accepting SCT carriers as living liver donors, on an exceptional basis. This the first single-center case series of living donor liver transplantation with SCT. METHODS. Between January 2012 and September 2021, 20 donors with SCT were reviewed for age, gender, relation to the recipient, hemoglobin, hemoglobin S (HbS), surgical approach, intensive care unit stay, donor and recipients’ complications, and graft and recipient survival. RESULTS. Average age of donors was 28.4 y. Sixteen donated the left lateral segment, 4 the left lobe. Recipients were related children or adults. HbS ranged from 21.2% to 39.9%, being ≥30% in 14 donors. HbS was reduced by phlebotomy or exchange transfusion. We performed 7 open, one laparoscopic, and 12 robotic donor surgeries. Operating room time, blood loss, and intensive care unit stay were comparable to non-SCT donors. There was no SCT-related complication. All donors are alive and free of thromboembolic events. Graft and recipient survival is 100% until follow-up. CONCLUSION. Our experience should encourage other countries with high incidence of SCT to report their experience with this donor population. Lippincott Williams & Wilkins 2022-05-09 /pmc/articles/PMC9088231/ /pubmed/35557991 http://dx.doi.org/10.1097/TXD.0000000000001332 Text en Copyright © 2022 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Liver Transplantation
Schulze, Maren
Zidan, Ahmed
Sturdevant, Mark
Aljudaibi, Sultan
Shagrani, Mohammad
Bzeizi, Khalid
Alqahtani, Saleh
Broering, Dieter C.
First Experience in Living Liver Donation From Donors With Sickle Cell Trait
title First Experience in Living Liver Donation From Donors With Sickle Cell Trait
title_full First Experience in Living Liver Donation From Donors With Sickle Cell Trait
title_fullStr First Experience in Living Liver Donation From Donors With Sickle Cell Trait
title_full_unstemmed First Experience in Living Liver Donation From Donors With Sickle Cell Trait
title_short First Experience in Living Liver Donation From Donors With Sickle Cell Trait
title_sort first experience in living liver donation from donors with sickle cell trait
topic Liver Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088231/
https://www.ncbi.nlm.nih.gov/pubmed/35557991
http://dx.doi.org/10.1097/TXD.0000000000001332
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