Hepatobiliary & Liver Transplant SurgeryDr. Sandeep JhaLiving Donor Liver Transplant

Sr. Consultant, Liver Transplant, HPB & GI Surgery, Metro Heart Institute with Multispeciality, Faridabad

Part 4 of 9 in Basics of Living Donor Liver Transplant

Evaluating a Living Liver Donor: Criteria and Safety Protocol

July 20, 2025

Donor evaluation is treated as the single most important step in living donor liver transplant, because donor safety failures in the past, including a cluster of donor deaths in the United States in 1984, once shut down an entire country's living donor programme. A potential donor must be 18-55, free of known medical disorders, of a lean build, able to give fully informed consent, and, under Indian law, related to the recipient.

A multidisciplinary team, with authority to reject at any stage

Every donor is evaluated by a team including a liver transplant surgeon, hepatologist, gastroenterologist, anaesthesiologist, cardiologist, pulmonologist, and, for female donors, a gynaecologist. At any point in this process, if there is even a suspicion a donor might have future problems, the donor is rejected outright; the surgical team proceeds only after a government-appointed authorisation committee formally clears the case.

The imaging and lab workup that actually clears a donor

A triple-phase contrast-enhanced CT scan, arterial, portal and delayed venous phases, maps the portal vein, hepatic veins and arterial anatomy to confirm the donor's liver can be safely divided; an MRCP maps the biliary anatomy, which has significant natural variation. A non-contrast CT-derived liver attenuation index screens for fatty liver, a donor with an index below zero is declared unfit; MRI or, in doubtful cases, a liver biopsy can confirm graft quality further. Blood group compatibility follows standard rules: an A recipient can receive from an A or O donor, a B recipient from B or O, an O recipient only from an O donor, and an AB recipient from any blood group; Rh status does not matter.

This article is based on a Jivo Masterclass session conducted by Dr. Sandeep Jha, Consultant, Liver Transplantation, Shalby Sanar International Hospital, Gurugram. The article has been summarised with the assistance of an AI tool from the original masterclass recording. Watch the full Masterclass recording

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This guide is based on a live Jivo Masterclass — Dr. Sandeep Jha taught doctors across Africa on July 20, 2025.

FROM THE LIVE Q&A

DR

Dr. Nasuro

In cases I've seen, liver transplant patients often survive only three to five years and have poor mobility afterward. How effective would a second transplant be if the first graft fails, and what dietary or other measures can help a patient's recovery and prognosis?

SJ

Dr. Sandeep Jha

There's no diet that prevents cirrhosis itself, prevention means treating the underlying cause: stopping alcohol, treating hepatitis B or C, and controlling diabetes and obesity. Once cirrhosis has developed, a high-protein, low-salt diet with frequent small protein-containing meals is recommended. On outcomes: large international studies show one-year survival of 85-90% and five-year survival over 70%, with emerging twenty-year data also showing around 70% survival, this is achievable when there is continuity of care. The shorter survival seen in some international patients usually reflects a lack of follow-up after they return home, working directly through local doctors and structured referral, not going straight through informal medical tourism, is what closes this gap.

See all 5 questions from this masterclass →

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Frequently Asked Questions

Why is metabolic liver disease becoming the leading cause of liver transplant, and is there any outcome difference between receiving a right lobe versus a left lobe graft?

Metabolic-associated fatty liver disease is rising because of uncontrolled diabetes, obesity and sedentary lifestyle, a pattern first seen in the US, where it became the leading transplant indication in 2024, and now increasingly in India too, even as hepatitis B and C become easier to control through treatment and vaccination. On lobe choice: there is no outcome difference between right and left lobe transplantation when the technique is sound, the choice simply reflects that adults need more liver mass (right lobe) while children need less (left lateral segment or left lobe). The only practical difference is for the donor, recovery from a left lobe donation is somewhat faster with slightly fewer complications, since less liver volume is removed.

A patient from Ethiopia underwent a successful liver transplant in India a couple of years ago but later developed a serious infection that couldn't be controlled and the patient died. Why are post-transplant infections so difficult to control, and how can this be addressed?

Transplant recipients are on immunosuppression to protect the new liver, so even minor infections can escalate very quickly. The approach has to be to hit them early and hit them hard: get full blood work and cultures done immediately, look for a source of infection as fast as possible, and start empirical high-grade antibiotics well ahead of what a normal patient would need, often one or two steps more aggressive. Better collaboration between the treating team in India and the doctor in the patient's home country would meaningfully improve outcomes in these situations.

What is the cost-effectiveness of this surgery, and what are the side effects and post-operative complications?

It is extremely cost-effective: a modest cost can buy 40-50 years of additional life for a patient dying of cirrhosis. Most complications and side effects happen in the first month after transplant; by one year, 80-85% of patients are doing well, patients who would not have survived at all without the transplant. Compared to a 57% one-year mortality without transplant in patients with bleeding and ascites, this represents a dramatic survival benefit, and outcomes are even more stark for patients with cancer, encephalopathy or severe sarcopenia, who have even poorer survival without it.

What is the fate of the donor after donating their liver, and what are the possible complications?

Donors are absolutely fine after a complete evaluation; the risk to life is now around 0.5%, and even that figure is based on older data, current donor safety protocols are stricter still. Donors are walking around and eating within two to three days, discharged by day six or seven, and most can travel home within about ten days to two to three weeks. They can resume office work and light household activity almost immediately; the only restriction is avoiding heavy weightlifting for three months, after which there are no restrictions at all.

In cases I've seen, liver transplant patients often survive only three to five years and have poor mobility afterward. How effective would a second transplant be if the first graft fails, and what dietary or other measures can help a patient's recovery and prognosis?

There's no diet that prevents cirrhosis itself, prevention means treating the underlying cause: stopping alcohol, treating hepatitis B or C, and controlling diabetes and obesity. Once cirrhosis has developed, a high-protein, low-salt diet with frequent small protein-containing meals is recommended. On outcomes: large international studies show one-year survival of 85-90% and five-year survival over 70%, with emerging twenty-year data also showing around 70% survival, this is achievable when there is continuity of care. The shorter survival seen in some international patients usually reflects a lack of follow-up after they return home, working directly through local doctors and structured referral, not going straight through informal medical tourism, is what closes this gap.

What are the basic criteria for a living liver donor?

Age 18-55, no known medical disorders, a lean build, the capacity to give fully informed consent, and, under Indian law, a blood relationship to the recipient.

What imaging is required before a living liver donation?

A triple-phase contrast-enhanced CT scan to map the portal vein, hepatic veins and arterial anatomy, an MRCP to map biliary anatomy, and a liver attenuation index (or MRI/biopsy in doubtful cases) to screen for fatty liver.

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