Liver transplantation in the UK

Abstract

INTRODUCTION: This paper provides a review of the practice of liver transplantation with the main emphasis on UK practice and indications for transplantation. Referral and Assessment: This section reviews the process of referral and assessment of patients with liver disease with reference to UK practice.

Donor Organs: The practice of brainstem death and cadaveric organ donation is peculiar to individual countries and rates of donation and potential areas of improvement are addressed.

Operative Technique: The technical innovations that have led to liver transplantation becoming a semi-elective procedure are reviewed. Specific emphasis is made to the role of liver reduction and splitting and living related liver transplantation and how this impacts on UK practice are reviewed. The complications of liver transplantation are also reviewed with reference to our own unit.

Immunosuppression: The evolution of immunosuppression and its impact on liver transplantation are reviewed with some reference to future protocols. Retransplantation: The role of retransplantation is reviewed.

Outcome and Survival: The results of liver transplantation are reviewed with specific emphasis on our own experience. Future: The future of liver transplantation is addressed.

INTRODUCTION

Recent years have seen dramatic changes in the practice of liver transplantation. In 1980 in Europe fewer than 30 liver grafts were performed compared to over 3000 in 1995 (Figure 1). During this period liver transplantation has evolved from a rare procedure in patients with end-stage liver disease, to a semi-elective operation with current predictable success rates of approximately 90% in patients with chronic disease. In the early period of liver transplantation it was reserved for patients with end stage chronic liver disease or unresectable primary liver malignancy, but in recent years there has been a considerable broadening of the accepted indications. Improving results have led to liver transplantation becoming a semi-elective procedure with both quantity and quality of life being of major concern. Patients who may not be in immediate risk of death from liver decompensation but have significantly impaired quality of life are now considered as candidates.

Figure 1.

Evolution of european liver transplantation.

The current indications can be classified into four broad groups; chronic liver failure, acute liver failure, primary hepatic malignancy not treatable by conventional resection and inborn errors of metabolism due to a liver based enzyme defect but without parenchymal liver disease (Table 1).

Table 1.

Common indications for liver transplantation

		Birmingham series
		n	%
Chronic liver failure	Primary biliary cirrhosis	434	24.7
	Primary sclerosing cholangitis	158	9
	Autoimmune chronic active hepatitis	96	5.5
	Alcoholic cirrhosis	122	6.9
	Cryptogenic cirrhosis	92	5.2
	HBV or HBC cirrhosis	165	9.4
	Biliary atresia	142	8
	Alpha-1 anti-trypsin deficiency	65	3.7
	Budd-Chiari syndrome	8	0.1
Acute liver failure	Viral hepatitis (non-A, non B, HBV, HAV)	10	8
	Drugs (Paracetamol, anti-tuberculosis therapy, halothane)	66	3.8
	Toxins and solvents	0
Primary hepatic malignancy	Unresectable HCC	20	0.4
	Small HCC in cirrhotic liver	78	10.2
Inborn errors of metabolism	Crigler-Najjar type 1	1	0.05
	Proprionic acidaemia	6	0.08
	Primary oxalosis	8	0.1
	Urea cycle defects	0

Chronic liver failure is the most common indication for liver replacement and can be caused by a wide variety of diseases including autoimmune, viral, congenital and alcohol induced liver disease. Primary biliary cirrhosis (PBC) is the commonest indication for liver transplantation in the UK. Several studies on survival in PBC have led to the development of a prognostic index that is helpful in planning the timing of liver replacement[1]. Primary sclerosing cholangitis (PSC) is a condition that is usually found in patients with inflammatory bowel disease. Progression of PSC is less predictable than PBC but approximately 30% of patients with PSC will develop cholangiocarcinoma that is usually incurable at diagnosis. Autoimmune hepatitis (AIH) is less common than PBC and PSC but immunosuppressive therapy can delay progression. Excess immunosuppression prior to transplantation however, may increase the morbidity and mortality associated with liver replacement and the optimal timing of liver replacement is a finely balanced decision.

An estimated 300 million people worldwide carry the hepatitis B virus (HBV). In Western Europe and North America the carrier rate is low (0.5%) and is mainly confined to high-risk groups including intravenous drug users, homosexuals and immigrants from high prevalence areas. HBV is a significant problem however, because of the risks of early recurrence after liver replacement. Patients who are HBV-DNA positive at time of transplant develop rapid recurrence with early death. The results of trials of antiviral therapy using agents such as lamivudine and HBV specific immunoglobulins prior to transplantation suggest that viral replication can be suppressed prior to and post liver replacement with encouraging early results[2-5]. Hepatitis C virus (HCV) is an increasing public health problem. Most patients seen in the UK have become infected following transfusion of blood products or from intravenous drug abuse. The development of cirrhosis following HCV infection is slow but with a significant risk of subsequent hepatocellular carcinoma development[6]. Recurrence of HCV after transplantation is common but not usually problematic in the early years[7,8]. The evolving strategies for anti-viral therapy in this group of patients are likely to have a significant impact on survival in this group of patients[9-11].

Alcoholic liver disease (ALD) is the commonest cause of cirrhosis in many parts of the western world although during the evolution of liver transplantation very few cases were accepted. Many transplant physicians were initially reluctant to consider liver replacement in these patients because of the risks of returning to alcohol and public attitudes[12]. The alcoholic who can prove abstinence prior to grafting has an equivalent survival to those transplanted for other chronic liver disease and recidivism is surprisingly uncommon[13]. There has therefore been an increasing pressure to accept reformed alcoholics and an increasing proportion are now being grafted[14].

The commonest cause of chronic liver failure in children is biliary atresia. If diagnosed early and treated surgically with a portoenterostomy (Kasai operation), the progression of liver disease is delayed and up to 40% of children will survive long term[15]. Many children however, will develop end stage liver disease and die within the first few years of life if not transplanted. Failure to thrive is a common sequelae of chronic liver disease in children and should be considered an indication for grafting.

The development of hepatic encephalopathy within eight weeks of onset of symptoms in a patient without previous liver disease is defined as acute fulminant hepatic failure (AFHF)[16]. Sub-acute or late onset hepatic failure has al so been recognised with encephalopathy developing between eight weeks and six months of onset of symptoms. The commonest causes of AFHF in the UK include drugs and toxins[17-20], viral hepatitis (Hepatitis A, B, and non-A non-B) [21,22] and miscellaneous causes including Wilson's disease, fatty liver of pregnancy and Budd-Chiari syndrome[23-26]. Specific prognostic factors for spontaneous recovery from AFHF have been published and are helpful in decision making about transplantation[27].

An increasing number of inborn errors of metabolism with a deficiency of a single hepatic enzyme are being treated by liver transplantation, even though the liver is otherwise structurally and functionally normal (Table 1). Timing is important and transplantation should be performed before irretrievable damage is done to other organs e.g. renal failure in primary oxalosis or cerebral damage in Crigler-Najjar syndrome[28,29].

Hepatocellular carcinoma (HCC) is the commonest primary liver malignancy and although it is rare in the UK it is one of the commonest cancers worldwide[30]. The majority of cases occur in the background of liver cirrhosis with the presence of HCV and HBV being additional risk factors (Figure 2). It has been recommended that transplantation be restricted to patients with HCC who have lesions up to 3 cm and up to three in number[31-33]. There are other rare unresectable hepatic tumours that are occasionally conside red for transplantation. These include epithelioid haemangioendothelioma, sarcomata, cholangiocarcinoma and secondary neuroendocrine tumours[34-36]. Hilar cholangiocarcinomas almost invariably recur early after grafting and are no longer considered appropriate candidates[37].

Figure 2.

CT Scan showing HCC in cirrhotic liver with ascites and splenomegaly.

REFERRAL AND ASSESSMENT

In patients with acute or chronic liver failure timely referral is necessary if a successful outcome is to be achieved[38-40]. Many patients with chronic liver disease can remain stable for long periods and decompensation may occur secondary to a complication such as variceal bleeding, portal vein thrombosis, development of hepatic malignancy or spontaneous bacterial peritonitis. The ability to intervene before any major deterioration is dependent on the recognition of early indicators of disease progression; in cholestatic conditions (PBC and PSC) the level of bilirubin is an obvious indicator of the underlying disease severity and is likely to lead to an early referral for specialist opinion but for many liver conditions the appearance of jaundice is a late feature and other signs of a deterioration in liver synthetic function, such as a falling albumin or rising prothrombin time are a better indicator of the need for referral.

A multi-disciplinary team including hepatologists and transplant surgeons usually assess patients in the UK. A careful review is required to determine the diagnosis of the liver disease and this will include a specialist pathologist at the transplant centre reporting on the liver histology. Often patients who drink moderate amounts of alcohol are labelled as having alcoholic liver disease but an open mind for these cases is encouraged because modest alcohol intake may unmask an underlying liver condition such as alpha-1 anti-trypsin deficiency or haemochromatosis[41,42].

Assessment for transplantation includes both physical fitness for major surgery as well as psychological evaluation and counselling. A detailed evaluation of the cardio-respiratory system is often indicated and this may require ECG, echocardiogram, exercise ECG, coronary angiography and pulmonary artery catheter isation in those with evidence of ischaemic heart disease, pulmonary hypertension or suspected major pulmonary shunts as seen in the hepatopulmonary syndrome[43].

Technical considerations such as patency of the portal vein are also required and this can be determined by Doppler ultrasound, angiography, spiral computerised tomography (CT) or magnetic resonance imaging (MRI). An absent portal vein is not a contraindication to transplantation if a patent superior mesenteric vein or large coronary vein can be identified which would be suitable for anastomosis to the donor portal vein[44]. Patients with primary HCC require detailed investigation for evidence of disease outside the liver and this should include laparoscopy to detect peritoneal disease or transcapsular spread[45], isotope bone scanning and computerised tomographic studies of the abdomen and chest. Difficulty may occur in patients with PSC in trying to differentiate between malignant and benign hilar strictures (Figure 3). In our series malignancy was present in 25% of the patients with significant biliary dilatation but that pre-transplant diagnosis was difficult (unpublished data).

Figure 3.

Cholangiogram showing dominant hilar stricture in a patient with PSC.

DONOR ORGANS

The number of liver transplants performed annually in the UK has remained largely stable over the last five years and this has been despite a slight fall in the number of cadaveric organ donors. The total number of liver transplants has been maintained in the UK by an increase in the number of split liver grafts performed and a wider use of more marginal liver donors. Over the last ten years the introduction of seatbelt laws and stricter drink driving legislation has reduced the number of cadaveric donors being derived from road traffic accident victims. Donor numbers have been largely maintained by utilising older donors who have usually died from cerebro-vascular disease and have concomitant co-morbidity. The use of such marginal donors does not seem to have been at the expense of worse outcomes. Successful outcome from liver transplantation is possible even in haemodynamically unstable donors and in those with abnormal liver function tests[46].

Assessment of the liver by an experienced transplant surgeon at time of retrieval is a useful guide to subsequent function but if there is evidence of fatty change, a frozen section histological assessment prior to implantation can be helpful[47-49]. A fit recipient can often cope with a marginal graft but a poor recipient will need a graft which functions well immediately for the best chance for survival.

Size matching of donor and recipient is attempted when selecting a patient for a particular liver. Attempting to place a large graft in a small recipient can cause major technical problems. Patients with cholestatic diseases such as PSC and particularly PBC often have large livers and will accept grafts from significantly larger donors, as can patients with marked ascites.

Approximately 60% of potentially suitable organ donors (approximately 1000 per year) are missed each year in the UK[50]. UK organ donation rates remain some of the lowest in Europe but a more aggressive approach to the identification and confirmation of brainstem death and improved family requesting could achieve significant improvements in organ donation in the UK[51]. A number of initiatives such as presumed donor consent and elective ventilation are currently being considered[50].

OPERATIVE TECHNIQUE

Many factors can be identified which have contributed to the improved early outcome after liver replacement. Semi-elective daytime operating ensures that the surgical and anaesthetic team produce the best technical results. The ability to store livers long enough to allow this came from the development of University of Wisconsin preservation fluid which allows satisfactory immediate graft function for storage periods of eighteen hours or more[52].

Meticulous attention to haemostasis has been aided by developments in surgical techniques and instruments (conventional diathermy, argon beam coagulator, fibrin glue, etc.). The monitoring of coagulation parameters in the operating room with the help of the thromboelastogram (TEG) means that blood coagulation is optimised and that predictable deteriorations in clotting which often occur on reperfusion can be anticipated and minimised[53]. The role of anti-fibrinolytic agents such as aprotinin (Trasyslol) and human recombinant factors (Novoseven) remains unclear but are the subject of clinical study[54,55].

Technical innovations

The INTRODUCTION of venovenous bypass for the anhepatic phase produced a significant stabilisation of haemodynamic parameters during portal vein and caval clamping with a clear reduction in transfusion requirements and an improvement in renal function[56]. The alternative to venovenous bypass is to preserve the vena cava at the time of hepatectomy and anastomose the back of the donor vena cava to the front of the recipient cava (piggyback technique)[57]. Several techniques have been described but the piggyback technique is not without its complications[58-62]. Most units currently utilise a combination of techniques and a minority of units still perform liver replacement without either bypass or the piggyback technique.

Early techniques of biliary reconstruction involved utilising the donor gall bladder as a conduit between the donor and recipient duct. This technique has been abandoned because of the almost universal development of stones in the conduit. An end-to-end duct anastomosis is now the routine but this has been followed by stricture formation in up to 13% of cases[63-65] and techniques of anastomosing the ducts obliquely with the ends spatulated or by utilising a side- to-side anastomosis are gaining wider acceptance [66,67]. The use of a T-tube has been abandoned by most units[63-65,68].

Liver reduction and splitting

The shortfall in size matched grafts for small children led to the development of reduced grafts in the mid 1980′s[69-71]. The most commonly used technique is to transplant the left lateral lobe segments II and III with venous outflow based on the left hepatic vein which is anastomosed to the retained recipient vena cava[72]. Weight ratios as high as ten-to-one between donor and recipient have been reported[73] the ideal weight ratio however, is four, five or six to one. Reduced liver grafts are not without their comp lications[74] but there appears to be a low incidence of hepatic artery thrombosis[75,76]. The INTRODUCTION of this technique has led to a significant reduction in mortality from liver disease in children[77]. The techniques of graft reduction have led to the development of splitting livers where the left lobe (or left lateral segments) is transplanted into a paediatric recipient and the right lobe is grafted usually into an adult recipient (split-liver)[78-80]. This technique was de veloped on the backbench following removal of the cadaveric donor organ. The pro cedure can take approximately two hours and during this time the donor organ is subject to some re -warming that might be detrimental to its initial function. Recently the technique of in situ splitting of cadaveric donor organs has been developed as an extension of the development of living related liver transplantation. The advantage of this technique is that the splitting of the liver is performed during the warm phase dissection prior to organ perfusion and cooling and the organ is the n not subject to re-warming during a subsequent splitting procedure. The results of this technique appear to result in better initial graft function[81-83].

Living related liver transplantation

In countries that do not have legal recognition of brainstem death and therefore have no access to cadaveric organs, solid organ transplantation has been limited to living related organ donation and this has led to the development of living related liver transplantation[84]. The increasing donor organ shortfall with the increasing number of potential recipients; despite the option of organ splitting, has meant that even in countries that do recognise brainstem death living related liver transplantation has had to be undertaken[85-88]. The organ shortfall in the UK for patients with liver disease is less than in other countries and the number of units performing this procedure is small with only 12 being performed in 1999[89,90]. The greatest experience with this technique has been with adult-to-child left lateral lobe because of the obvious size discrepancy and donor to recipient weight ratios[91] but increasing experience of the technique has led to the expansion of the technique to include adult-to-adult donation[92-96]. The increasing demand for liver transplantation in the UK and the reduction in cadaveric donor organs [90] suggest that this technique is likely to become established practice but careful preoperative evaluation of the donor is needed[97-100].

Complications

The one-year survival following liver transplantation has improved from approximately 30% in the 1960s and 1970s to more than 80% in the 1990s[14,101,102]. The immediate complications following liver transplantation include primary non-function, haemorrhage and acute renal failure. The incidence of these is significantly influenced by the quality of the donor liver and technical aspects of the transplant operation itself. Over the last 10 years in the UK there has been an increase in the use of marginal organs[46] but this has been offset by improvements in technical aspects of the surgical procedure, per-operative anaesthetic management and post-operative intensive care management. In our own unit the incidence of these complications between 1985 to 1989 and 1995 to 1999 was; primary non-function 1.9% and 1.7%, return to theatre for pack removal or haemorrhage 8.4% and 2.4% and post-operative renal failure 18.6% and 16.4% respectively (unpublished data). Despite the use of an increasingly marginal donor pool the incidence of these complications hastherefore reduced.

Primary non-function may be due to pre-existing but occult problems in the donor, poor retrieval or preservation, or injury caused by reperfusion (post-reperfusion syndrome). The clinical picture mimics acute fulminant hepatic failure and death rapidly follow unless urgent regrafting can be undertaken. Fortunately primary non-function is rare although primary dysfunction occurs in 5% to 10% of cases and is associated with a worse long-term outcome[103,104].

The majority of routine liver transplants require minimal or no transfused blood. In our own series 47% of liver transplants required four units or less of blood per-operatively (unpublished data). Patients with severe portal hypertension and previous major upper abdominal operations can pose a major surgical challenge, meticulous haemostasis, venovenous bypass, warming of blood and blood products and strict control of coagulation parameters will usually be effective.

A significant number of transplant candidates already have impaired renal function and a combination of factors lead to a rise in the serum creatinine after surgery[105-107]. This will usually respond to optimisation of hydration and pharmacological manipulation but a proportion of patients will develop anuria and require renal replacement therapy at least in the short term[108].

Histological evidence of acute rejection can be documented in approximately 80% of liver grafts at the end of the first week but many of these do not require additional immunosuppression if other parameters of graft function are improving[109]. Histological evidence of severe cellular rejection and less severe histological forms associated with significant biochemical abnormalities (approximately 30% of liver grafts) are usually treated with high dose steroids[110,111]. Steroid resistant rejection may respond to other agents including monoclonal (OKT3) and polyclonal antibodies (ATG) or by switching immunosuppression regimes[112,113]. Chronic or irreversible rejection in the liver is a biliary rather than a vascular phenomenon in which the small bile radicals are destroyed[114,115]. This can occur very early on after grafting and if progressive leads to loss of the graft although predicting which patients might require regrafting can be difficult[116,117]. Chronic rejection accounts for approximately 5% of graft loss within the first three to five years following transplantation [118]. Lower rates of chronic rejection and graft salvage in early chronic rejection may occur with newer immunosuppressive regimes[119-121]. Histological examination of the transplanted liver in stable long-term patients often shows evidence of chronic post-transplant hepatitis[122]. The causes of the histological changes are unknown although unrecognised viral infections may be responsible for some cases and the steroid sparing immunosuppression regimes may also be partly responsible.

Serious cytomegalovirus (CMV) infections tend to be primary (transmitted by the donor liver) rather than reactivation infections and should be avoidable if CMV -matched donors are used. Clinical infection usually presents between four and eight weeks with fever and leucopenia but asymptomatic sero-conversion does not require treatment. This will respond well to a combination of reduction in base line immunosuppression and ganciclovir therapy[123]. The traditional serological tests vary between centres, take time and are less sensitive than PCR tests[124]. In patients with symptoms specific to an organ histological analysis should be used in conjunction with PCR tests[125,126]. Significant CMV infection is associated with acute rejection and may result in a worse long-term outcome[127]. The routine use of prophylactic ganciclovir reduces the incidence of clinical CMV infection although a high index of suspicion and prompt treatment will also result in negligible mortality[128-132].

Biliary complications are a significant problem in most units undertaking liver transplantation and these include bile leaks, anastomotic strictures, non-anastomotic strictures of the donor bile duct and sludge formation. The overall incidence in adults is approximately 10% but is higher in children[74,133]. In our own series the overall incidence of biliary complications requiring intervention is 12%, this rises to 27% in those patients undergoing re-transplantation (unpublished data). The ability to image the biliary tree effectively using ultrasound, MRI cholangiography, endoscopic retrograde cholangiography (ERCP) or percutaneous transhepatic cholangiography (PTC) has led to most biliary complications being managed without reoperation[134]. The presence of a major biliary disruption or an associated biliary obstruction is an indication for urgent biliary reconstruction[135]. Biliary obstruction without leakage will usually be evident from simple ultrasound, can be confirmed by ERCP or PTC and can usually be managed without recourse to open surgery[136-138]. Non-anastomotic biliary strictures involving the confluence or intra -hepatic bile ducts are a rare but serious complication that were once attributed to prolonged preservation times[139]. These strictures are complicated but a proportion can be resolved using a PTC approach by a skilled radiologist although a number of cases will require regrafting. In any patient with a biliary complication patency of the hepatic artery should be confirmed, as hepatic artery thrombosis will cause ischaemia and necrosis of the biliary tree[140]. The late biliary complications seen after transplantation are usually obstruction with possible secondary sepsis and cholangitis. The commonest cause is an anastomotic stricture, with or without stone or sludge formation in the proximal dilated biliary tree. An ERCP may enable duct clearance, dilatation of any stricture and stent insertion. Most strictures will recur and therefore formal biliary reconstruction is usually required.

Hepatic arterial thrombosis (HAT) after liver transplantation occurs most frequently in the first postoperative month and leads to graft necrosis, intra-hepatic abscess or biliary necrosis and bile leakage. In all suspected cases patency of the artery should be checked with Doppler ultrasound and confirmed with spiral CT or angiography[141-143]. Per-cutaneous attempts at revascularizati on of stenosed or thrombosed hepatic arteries can be attempted and urgent thrombectomy has been successful in some cases but the majority of cases of early HAT will need regrafting[144-148]. Late arterial thrombosis may be occult and if asymptomatic can probably be ignored. In our own series HAT has occurred in 4.6% of adult grafts and 9.1% of paediatric grafts (unpublished data). Technical problems account for the majority of cases but over transfusion at the time of surgery, producing a high a haematocrit, has been reported as a risk factor[149,150].

Malignancy is well recognised as a potential complication of long term immunosup pression. Longer survival is seen with the liver compared to other solid organ transplants and therefore the time exposed to the risk of malignancy is greater. The most common malignancies seen secondary to prolonged immunosuppression are the lymphoproliferative diseases and lymphoma and skin malignancy[151,152]. Reduction in the level of immunosuppression is often enough to treat lymphoproliferative disease[153]. A proportion of liver transplants are performed for primary hepatic malignancy and paradoxically the donor liver (free from malignancy at the time of transplant) is the commonest site of recurrence. The predilection for circulating malignant cells to return and then grow in the liver is well recognised.

IMMUNOSUPPRESSION

The widespread INTRODUCTION of cylosporine A in the early 1980s was responsible for the improvement in liver graft survival from 35% to 70% survival at one-year[154]. Immunosuppression with cylosporine, azathioprine and steroids remained the main immunosuppressive regimen until the development of tacrolimus in 1989[155]. Tacrolimus was initially used to salvage grafts failing from rejection on cylosporine based regimens[156] but has subsequently been increasingly used as first line immunosuppression by many units. Although structurally different to cylosporine, it also acts by inhibiting calcineurin and subsequent interleukin (IL) 2 production and therefore prevents T cell proli feration[157]. Three prospective randomised trials have compared the efficacy of tacrolimus and cylosporine in liver transplant recipients[158-160]. The incidence of rejection was significantly lower with tacrolimus in all studies but there was no difference in one-year patient and graft survival. Long-term follow up has shown a trend towards en hanced survival in patients treated with tacrolimus[161]. The toxicity profile of tacrolimus is similar to that of cylosporine (nephrotoxicity, neurotoxicity, hypertension and diabetogenic potential) but without the gingival hyperplasia and hirsutism commonly seen with cylosporine[162].

Mycophenolate mofetil (MMF) is another new agent that blocks purine metabolism by inhibiting inosine monophosphate dehydrogenase in T and B lymphocytes[163]. The role of MMF in liver transplant recipients remains to be fully defined but initial reports suggest that when combined with tacrolimus the incidence of acute rejection is reduced[164,165]. MMF has haematological and gastrointestinal side effects but is not nephrotoxic and may be useful in patients with compromised renal function so that the dose of tacrolimus can be reduced[166]. New immunosuppressants continue to be developed and some are currently under evaluation including sirolimus (inhibits action of IL2), basiliximab (chimeric IL2 receptor monoclonal antibody) and daclizumab (humanised IL2 receptor monclonal antibody)[167,168]. Polyclonal antibody therapy that has previously been used to treat steroid resistant rejection has however, been rendered almost obsolete by current immunosuppressant protocols. In our own centre the current immunosuppression regimen is tacrolimus combined with azathioprine and prednisolone, with steroid taper and withdrawal over three months. MMF is used in place of azathioprine to allow low dose tacrolimus regime ns in those patients with renal impairment prior to transplantation and is also used in place of azathioprine in those patients undergoing retransplantation for chronic rejection.

The available immunosuppressive options will continue to increase and with it the permutations of immunosuppressive regimens. This may make it difficult to effectively evaluate individual regimens. Immunosuppression will however, continue to be a balancing act, with over immunosuppression culminating in toxicity, life threatening infections and malignancy and under immunosuppression leading to rejection and graft loss.

RETRANSPLANTATION

In our own series 10% of nearly 2000 liver transplants were regrafts, although the proportion of patients requiring a regraft is decreasing[169]. HAT accounts for 30% of regrafts, primary non-function for 16%, chronic rejection for 31% and recurrent disease for 6%, although the incidence of HAT and primary non-function is decreasing and the incidence of recurrent disease (PSC and HCV) is increasing[169]. Early re-transplantation is technically straight forward and usually performed for HAT or primary non-function. In an era of donor shortage and donor/recipient number mismatch the role of re-transplantation has been questioned but the outcome of re- transplantation is good with survival rates only slightly worse than those achieved for the first graft[170].

SURVIVAL

One-year survival rates for elective liver transplant in patients with benign disease now exceed 90% in many centres, with predicted 10 year survival rates expected to exceed 70%[102,171]. Patients transplanted for AFHF have a worse one-year survival with higher post-operative death rates usually related to cerebral complications and multi-organ failure. Experienced centres have however, obtained one-year survival rates of approximately 70%[172-174]. The long-term outcome for patients undergoing liver transplant for AFHF is as good as those transplanted for chronic disease. The increasing interest in living related transplantation offers a new opportunity for those patients with AFHF who cannot wait for a cadaveric organ[175]. The outcome in children undergoing liver transplantation is equally good, even in high-risk groups such as children age under 1 year in whom donor organ shortage might prevent grafting at the optimal time[75].

Survival rates for patients grafted for primary liver cancer (HCC) are less good however, patients transplanted for asymptomatic lesions up to 3 cm in diameter have survival rates close to those seen in patients grafted for benign disease[32]. In our own unit overall survival (including fulminant hepatic failure) at one-year is 81% for adults and 86% for children with different long -term survival depending on disease type (Figure 4).

Figure 4.

Survival following liver transplantation by disease type: birmingham series 1988-2000.

THE FUTURE

The most serious issue currently facing liver transplant physicians is the short fall in donor organs needed to meet demand. This deficit is greater in the US than in the UK. If the UK could increase its rates of organ donation to levels seen in other European centres and split all livers that meet appropriate criteri a (approximately 25% of UK cadaveric organs) then current organ demand could be met. Patient demand will however, mean that increasingly transplant physicians will be asked to justify why certain categories of patient are not considered suitable for transplantation. The limited supply of cadaveric organs allows these physicians to justify transplantation criteria on the basis of the scarcity of this resource. The continued success of living related liver transplant programmes around the world is likely to lead to increasing pressure to relax the criteria for liver transplantation for those patients able to provide their ‘own’ source of suitable transplant organs. This will require strict control and the application of new National guidelines if the UK is to avoid an expensive and potentially dangerous situation in the application of universal standards of care. A successful UK living related programme would certainly help to ease the deficit in urgent organs for those with AFHF and could address the deficit that currently exists for liver transplantation in chronic liver disease but we believe that this should only occur after the UK has exhausted the potential that is currently untapped in potential cadaveric organs.

The use of genetically modified xenografts could be potential major breakthrough for organ recipients but is not easily applicable to liver failure patients and there remain many biological and ethical obstacles before these organs become a sustainable source[176].