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Journal of Medicine Vol 2 - Amrita Institute of Medical Sciences and ...

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<strong>Amrita</strong> <strong>Journal</strong> <strong>of</strong> <strong>Medicine</strong><br />

Living Donor Liver Transplantation in Acute Hepatic Failure – viable option in Indian context<br />

King’s College criteria for transplantation in acute liver failure:<br />

Non – acetaminophen cause<br />

INR >6.7<br />

Or any three <strong>of</strong><br />

Unfavorable cause (eg. Drug induced, non A<br />

non B hepatitis, Halothane hepatitis)<br />

Age 40 years<br />

Acute/Subacute presentation<br />

Bilirubin level >300mmol/L<br />

Acetaminophen<br />

Arterial pH 300mmol/L<br />

INR > 6.5<br />

INR > 3.5<br />

cipient received 8 units <strong>of</strong> packed cells <strong>and</strong> 9 units <strong>of</strong><br />

plasma. The donor hepatectomy was accomplished without<br />

the need for red cell transfusion. The donor was<br />

extubated immediately postoperatively while the recipient<br />

was extubated the next day.<br />

Initial immunosuppression was with injectable methyl<br />

prednisolone alone. Oral steroids, Tacrolimus <strong>and</strong><br />

Mycophenolate M<strong>of</strong>etil were started on the third postoperative<br />

day. Tacrolimus dose was adjusted to maintain<br />

serum trough levels between 5 <strong>and</strong> 15ng/ml. The convalescence<br />

was rather smooth <strong>and</strong> she was discharged on<br />

24 th postoperative day. At follow up in 3 rd month, she is<br />

back to near normal life. The donor is back to his routine<br />

activities <strong>of</strong> daily living.<br />

DISCUSSION<br />

AHF is a clinical syndrome that results from sudden<br />

loss <strong>of</strong> hepatic parenchymal <strong>and</strong> metabolic functions <strong>and</strong><br />

manifests as coagulopathy <strong>and</strong> encephalopathy. The<br />

causes differ in various parts <strong>of</strong> the world. In U.K <strong>and</strong><br />

USA 5 acetaminophen <strong>and</strong> idiosyncratic drug reactions are<br />

the most commonly identified etiologic agents while in<br />

Japan <strong>and</strong> India acute hepatitis B is the leading cause <strong>of</strong><br />

AHF 6 . It is known that spontaneous survival rates from<br />

AHF due to acetaminophen toxicity <strong>and</strong> Hepatitis A are<br />

high 4 , while the rates for other viral hepatitis <strong>and</strong> idiosyncratic<br />

drug reactions are low.<br />

AHF constitutes a medical emergency associated with<br />

a high mortality due to the development <strong>of</strong> cerebral<br />

edema, coagulopathy <strong>and</strong> bleeding complications. The<br />

role <strong>of</strong> LT in AHF has been established beyond doubt.<br />

The essential challenge is identifying the crucial timing<br />

for transplantation. This involves maintaining the fine<br />

balance between possible reversibility <strong>of</strong> the condition<br />

through hepatic regeneration versus development <strong>of</strong> complications,<br />

which may either contraindicate transplant or<br />

render the condition irretrievable despite a transplant! A<br />

useful tool to assess whether a patient is likely to become<br />

irreversible is the Kings college criteria 7 , for early<br />

identification <strong>of</strong> indices with a poor prognosis.<br />

Traditional cadaveric graft if available <strong>and</strong> in a good<br />

condition, is considered ideal because patients with AHF<br />

have a huge metabolic dem<strong>and</strong>. However, even in countries<br />

with an established cadaveric organ-sharing program,<br />

a suitable donor may not be easily available in the emergency<br />

setting <strong>of</strong> AHF. Over the last few years, the use <strong>of</strong><br />

living donor liver transplantation (LDLT) has been evaluated<br />

<strong>and</strong> the benefits in the setting <strong>of</strong> AHF are<br />

well-established 8 . The advantages are that graft function<br />

is usually excellent as cold ischaemia time can be kept<br />

to a minimum <strong>and</strong> the procedure can be completed on<br />

an emergency basis before the patient’s condition deteriorates<br />

irreversibly. The potential disadvantage is possible<br />

inadequacy <strong>of</strong> available liver volume; hence the safer left<br />

liver grafts (Fig.1) have given way to the functionally larger<br />

right liver, albeit at the cost <strong>of</strong> significantly higher donor<br />

morbidity <strong>and</strong> mortality 9 .<br />

Donor related complications can be kept to a minimum<br />

by careful preoperative estimation <strong>of</strong> the donor liver<br />

volume <strong>and</strong> a careful delineation <strong>of</strong> the vascular <strong>and</strong> biliary<br />

anatomy <strong>of</strong> the two lobes <strong>of</strong> the liver. The size <strong>of</strong> the<br />

graft required by the recipient is estimated by the graft to<br />

recipient weight ratio (GRWR), which is the weight <strong>of</strong><br />

the graft divided by the weight <strong>of</strong> the recipient multiplied<br />

by 100 (ideal GRWR = 1), <strong>and</strong> balanced against<br />

the 40% <strong>of</strong> the original liver volume that has to be retained<br />

in the donor. CT volumetry is invaluable in this<br />

regard 10 . It is imperative while planning the parenchymal<br />

transection to ensure adequate vascular inflow <strong>and</strong> outflow<br />

<strong>and</strong> biliary drainage <strong>of</strong> all the segments in both the<br />

lobes <strong>of</strong> the liver to avoid functional parenchymal loss in<br />

either the donor or recipient. The information obtained<br />

34

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