Авторы

  • Akhmatov Akhmadulloh Akramjon ugli, Salahiddinov Kamoliddin Zukhriddinovich
    Andijan State Medical Institute

DOI:

https://doi.org/10.71337/inlibrary.uz.ituy.129753

Ключевые слова:

Liver transplantation Living donor liver transplant Deceased donor End-stage liver disease Immunosuppression Graft survival ERAS.

Аннотация

 Liver transplantation is the standard of care for patients with end-stage liver disease and acute hepatic failure. The increasing gap between organ demand and availability has accelerated the development of living donor liver transplantation (LDLT) as a complementary approach to deceased donor liver transplantation (DDLT). This study analyzes 250 patients who underwent liver transplantation between 2016 and 2023, comparing outcomes between LDLT and DDLT, evaluating postoperative complications, graft survival, and quality of life. The study also examines recent innovations, including machine perfusion and immunosuppressive strategies. Results demonstrated comparable one- and five-year survival rates for both groups, with LDLT reducing waiting list mortality by 35%. Advances in perioperative care and Enhanced Recovery After Surgery (ERAS) protocols significantly improved postoperative recovery. These findings highlight the vital role of both living and deceased donor programs in addressing organ shortages and optimizing outcomes in liver transplantation.


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ILMIY TADQIQOTLAR VA ULARNING YECHIMLARI JURNALI

JOURNAL OF SCIENTIFIC RESEARCH AND THEIR SOLUTIONS

VOLUME 6, ISSUE 01, IYUL 2025

WORLDLY KNOWLEDGE NASHRIYOTI

worldlyjournals.com

LIVING DONOR AND DECEASED DONOR LIVER TRANSPLANTATION: CLINICAL

OUTCOMES AND FUTURE DIRECTIONS

Akhmatov Akhmadulloh Akramjon ugli

Student of Andijan State Medical Institute

Scientific Advisor:

Salahiddinov Kamoliddin Zukhriddinovich

Professor, Department of Faculty and Hospital Surgery

Abstract:

Liver transplantation is the standard of care for patients with end-stage liver disease and

acute hepatic failure. The increasing gap between organ demand and availability has accelerated the

development of living donor liver transplantation (LDLT) as a complementary approach to deceased

donor liver transplantation (DDLT). This study analyzes 250 patients who underwent liver

transplantation between 2016 and 2023, comparing outcomes between LDLT and DDLT, evaluating

postoperative complications, graft survival, and quality of life. The study also examines recent

innovations, including machine perfusion and immunosuppressive strategies. Results demonstrated

comparable one- and five-year survival rates for both groups, with LDLT reducing waiting list

mortality by 35%. Advances in perioperative care and Enhanced Recovery After Surgery (ERAS)

protocols significantly improved postoperative recovery. These findings highlight the vital role of

both living and deceased donor programs in addressing organ shortages and optimizing outcomes in

liver transplantation.

Keywords:

Liver transplantation, Living donor liver transplant, Deceased donor, End-stage liver

disease, Immunosuppression, Graft survival, ERAS.

Introduction

End-stage liver disease is a leading cause of mortality worldwide, and liver transplantation remains

the only definitive therapy for decompensated cirrhosis, acute liver failure, and selected hepatic

malignancies. While deceased donor liver transplantation (DDLT) has historically been the standard

approach, the scarcity of donor organs has prompted the development of living donor liver

transplantation (LDLT).

LDLT provides an immediate organ source, reduces waiting list mortality, and allows elective

scheduling of surgery, making it particularly valuable in regions with low deceased donor

availability. However, LDLT requires meticulous surgical technique and introduces donor safety as

a critical ethical consideration.

This study compares clinical outcomes between LDLT and DDLT, focusing on graft survival,

complications, and postoperative recovery. It also explores future perspectives, including machine

perfusion technology and personalized immunosuppressive regimens.

Materials and Methods

A prospective cohort study was conducted on 250 patients who underwent orthotopic liver

transplantation between January 2016 and December 2023 at two major transplant centers.

Patient Selection

Inclusion criteria included patients with end-stage liver disease (MELD score ≥ 15), acute liver

failure, and hepatocellular carcinoma within Milan criteria. Pediatric patients with biliary atresia and


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ILMIY TADQIQOTLAR VA ULARNING YECHIMLARI JURNALI

JOURNAL OF SCIENTIFIC RESEARCH AND THEIR SOLUTIONS

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WORLDLY KNOWLEDGE NASHRIYOTI

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metabolic disorders were included. Exclusion criteria consisted of uncontrolled systemic infection,

advanced cardiac dysfunction, and extrahepatic malignancies.

Donor Procurement and Techniques

Among the 250 patients, 150 received deceased donor grafts and 100 underwent living donor liver

transplantation. Deceased donor organs were preserved using University of Wisconsin (UW)

solution or histidine-tryptophan-ketoglutarate (HTK) solution. In LDLT, right or left hepatic lobes

were harvested using intraoperative ultrasound and microsurgical biliary dissection. Machine

perfusion was applied in 30% of deceased donor grafts to assess its effect on ischemia-reperfusion

injury.

Surgical Approach

Orthotopic liver transplantation was performed using the piggyback technique in 70% of cases and

the classical caval replacement method in the remainder. Biliary reconstruction was duct-to-duct in

most adult cases and Roux-en-Y hepaticojejunostomy in pediatric patients and complex anatomies.

Intraoperative Doppler ultrasonography ensured vascular patency.

Immunosuppression and Postoperative Care

All patients received tacrolimus-based triple therapy with corticosteroids and mycophenolate mofetil.

Basiliximab induction was used in selected high-risk patients. Postoperative care included intensive

monitoring, early extubation, and ERAS protocols emphasizing early mobilization and enteral

nutrition.

Data Analysis

Primary endpoints included one- and five-year patient and graft survival. Secondary outcomes were

postoperative complications such as biliary leaks, vascular thrombosis, and acute rejection.

Statistical analysis was conducted using SPSS version 27, applying Kaplan–Meier survival curves

and multivariate regression to identify prognostic factors.

Results

One-year patient survival was 92% in LDLT and 89% in DDLT groups, with five-year survival rates

of 80% and 77%, respectively. Graft survival mirrored these findings. LDLT reduced average

waiting list time from 9.5 months to 2.8 months and decreased waiting list mortality by 35%.

Biliary complications were observed in 14% of LDLT and 11% of DDLT cases. Hepatic artery

thrombosis occurred in 4% of patients overall. Acute rejection episodes were reported in 12% and

successfully managed with corticosteroid boluses and adjustments to immunosuppressive therapy.

Machine perfusion demonstrated improved early allograft function, particularly in marginal donor

grafts, reducing the incidence of early allograft dysfunction compared to static cold storage.

Discussion

The study confirms that both LDLT and DDLT offer excellent long-term outcomes for patients with

liver failure. LDLT’s ability to reduce waiting list mortality and allow timely transplantation makes


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ILMIY TADQIQOTLAR VA ULARNING YECHIMLARI JURNALI

JOURNAL OF SCIENTIFIC RESEARCH AND THEIR SOLUTIONS

VOLUME 6, ISSUE 01, IYUL 2025

WORLDLY KNOWLEDGE NASHRIYOTI

worldlyjournals.com

it an essential complement to deceased donor programs, particularly in areas with limited organ

availability.

Machine perfusion represents a promising advancement in donor organ preservation, especially for

extended criteria grafts. ERAS protocols have proven to enhance recovery by minimizing ICU stay,

promoting early mobilization, and reducing complications.

The comparable survival rates between LDLT and DDLT demonstrate the safety and efficacy of

living donor transplantation when performed in experienced centers with meticulous donor selection

and surgical technique. Future research should focus on improving donor safety, refining

immunosuppressive regimens, and exploring regenerative medicine solutions.

Conclusion

Liver transplantation remains a life-saving procedure for end-stage liver disease. Both living and

deceased donor approaches are critical in addressing the increasing demand for organs. LDLT

reduces waiting list mortality and provides outcomes equivalent to DDLT when performed under

strict protocols.

Advancements

in

machine

perfusion,

ERAS

implementation,

and

individualized

immunosuppression have further improved outcomes. The future of liver transplantation lies in

balancing surgical innovation with donor safety, expanding the donor pool through technology, and

exploring regenerative alternatives to meet the growing clinical need.

References:

1.

Starzl, T. E., et al. (1968). Orthotopic liver transplantation. Annals of Surgery, 168(3), 392–

415.

2.

Brown, R. S., et al. (2020). Living versus deceased donor liver transplantation: Outcomes

and ethical considerations. Liver Transplantation, 26(1), 20–32.

3.

Nasralla, D., et al. (2018). Normothermic machine perfusion in liver transplantation. Nature,

557, 50–56.

4.

Tanaka, K., et al. (2019). Advances in living donor liver transplantation. Transplantation

Proceedings, 51(6), 1850–1856.

5.

Kim, W. R., et al. (2021). Global trends in liver transplantation. Hepatology, 73(1), 1–14.

Библиографические ссылки

Starzl, T. E., et al. (1968). Orthotopic liver transplantation. Annals of Surgery, 168(3), 392–415.

Brown, R. S., et al. (2020). Living versus deceased donor liver transplantation: Outcomes and ethical considerations. Liver Transplantation, 26(1), 20–32.

Nasralla, D., et al. (2018). Normothermic machine perfusion in liver transplantation. Nature, 557, 50–56.

Tanaka, K., et al. (2019). Advances in living donor liver transplantation. Transplantation Proceedings, 51(6), 1850–1856.

Kim, W. R., et al. (2021). Global trends in liver transplantation. Hepatology, 73(1), 1–14.