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Published on: May 7, 2015
First Experience in Living Liver Donation From Donors With Sickle Cell Trait
Maren Schulze1, Ahmed Zidan1, Mark Sturdevant2
1Department of Abdominal Transplant and Hepatobiliary Surgery, Organ Transplant Centre of Excellence, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Insights
Living donor liver transplantation in sickle cell trait (SCT) carriers is safe and effective. This study shows no SCT-related complications in donors, with excellent graft and recipient survival rates.
Area of Science:
- Transplantation Surgery
- Hematology
- Organ Donation
Background:
- Living donor liver transplantation (LDLT) is crucial in the Middle East, necessitating donor safety protocols.
- High incidence of sickle cell trait (SCT) in the region requires careful donor selection criteria.
- Prior surgical experience with SCT patients informed the decision to evaluate SCT carriers as potential living liver donors.
Purpose of the Study:
- To assess the safety and outcomes of accepting living donors with sickle cell trait (SCT) for liver transplantation.
- To evaluate donor and recipient complications and survival rates in LDLT involving SCT donors.
- To establish a precedent for considering SCT carriers as living liver donors on an exceptional basis.
Main Methods:
- A retrospective review of 20 living donors with SCT undergoing liver donation between January 2012 and September 2021.
- Analysis included donor demographics, hemoglobin S (HbS) levels, surgical approach, and perioperative outcomes.
- Management of HbS levels (phlebotomy or exchange transfusion) and follow-up for donor/recipient complications and survival were recorded.
Main Results:
- Twenty SCT donors (average age 28.4 years) donated liver segments (left lateral or left lobe) to related recipients.
- HbS levels ranged from 21.2% to 39.9%, with 14 donors having ≥30% HbS, managed effectively.
- Surgical outcomes, including OR time, blood loss, and ICU stay, were comparable to non-SCT donors, with no SCT-related complications and 100% graft/recipient survival.
Conclusions:
- Living donor liver transplantation with sickle cell trait carriers is feasible and safe.
- This single-center experience demonstrates excellent outcomes, supporting the acceptance of SCT donors under specific criteria.
- Encourages other high-SCT prevalence countries to report similar experiences to expand donor pools.
Abstract:
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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