Liver transplantation for acute-on-chronic liver failure

From November 1991 to December 2007, 517 adult patients (≥17 years old) underwent liver transplantation at Queen Mary Hospital, The University of Hong Kong. All of the liver explants were examined histologically. On the basis of the explant pathology reports, the patients, other than those with polycystic liver (n = 5), metabolic disease (n = 7), or retransplantation for liver graft non-function (n = 18), were categorized into four groups according to their conditions: group 1, patients with fulminant hepatic failure (n = 37); group 2, patients with acute exacerbation of chronic hepatitis B (n = 50); group 3, cirrhotic patients with acute deterioration (n = 99); and group 4, patients with cirrhosis only (n = 301). Massive or submassive hepatocyte necrosis was a prominent feature in the first two conditions. Differentiating fulminant hepatic failure from acute exacerbation of chronic hepatitis B was based on findings of fibrous bands and ductular proliferation in the latter condition. Cirrhosis was diagnosed on the basis of typical findings of nodules enveloped by fibrous septae. Differentiation between cirrhosis with acute deterioration and cirrhosis only was based on the presence of hepatocyte necrosis and features of acute hepatitis in the former condition. Patients in groups 2 and 3 were those with acute-on-chronic liver failure and the focus of this study.

Clinical records of these four groups of patients were reviewed with the aim to ascertain that their clinical presentations did fulfill the definition of acute-on-chronic liver failure as described in the Asian Pacific Association for the Study of the Liver Consensus Meeting. Presence of hyperbilirubinemia and coagulopathy was confirmed by laboratory tests. Presence of ascites was documented by imaging studies and/or laparotomy. Hepatic encephalopathy was documented when there was disturbance in central nervous system function and the severity was graded from 1 to 4 according to the system devised by Conn and Bircha [2].

Patients in groups 1, 2, and 3 all presented clinical features of acute liver failure. Once their clinical status fulfilled the King’s College Hospital criteria [3] and contraindications to liver transplantation were ruled out, the family was informed of the need for liver transplantation and the options of deceased donor liver transplantation (DDLT) and living donor liver transplantation (LDLT). While waiting for a liver graft, supportive treatment was continued. Lamivudine was given to patients with hepatitis B immediately if they had not been on nucleoside analogue. Patients with suspected infection were prescribed with broad-spectrum antibiotics after appropriate cultures had been performed. Only patients with positive bacterial or fungal culture in blood, urine, sputum, bronchoalveolar lavage fluid, or ascites were considered to have infection before transplantation. Presence of infection was not considered a contraindication to liver transplantation. If the condition of the patient was not critical, infection was treated with potent antibiotic before transplantation. Otherwise, heavy doses of broad-spectrum antibiotic were administered perioperatively. Patients with oliguria or rapidly deteriorating renal function received hemodialysis or continuous venovenous hemofiltration. Thirteen patients received molecular adsorbents recirculating system treatment as well [4]. Endotracheal intubation and mechanical ventilation were not routinely performed unless the patient was comatose and control of airway was considered necessary. Intracranial pressure was monitored in the first few patients, but the monitoring was not done in the subsequent patients because serious complications related to insertion of intracranial pressure monitoring device were encountered. Instead, these patients were monitored by their neurological signs, and workup for the recipients and living donors (if available) was proceeded quickly to allow the patients to receive transplantation in time [5]. Computed tomography of the brain was routinely performed in all patients with impaired conscious state to rule out severe brain edema and intracranial bleeding, which were contraindications to liver transplantation.

Liver transplantation was performed with deceased donor or living donor livers by the technique previously described [6]. All deceased donor grafts were whole grafts except 6, which were right trisegment grafts derived from splitting of livers. All, except 2, living donor grafts contained the middle hepatic vein. The living donor grafts were from right livers (n = 284), left livers (n = 17), or domino livers (n = 3). Venovenous bypass was used intraoperatively in the first 115 patients, but it was not used thereafter because the procedure was found not beneficial [7]. Intraoperative hemodialysis was performed in seven patients because of fluid overload, anuria, or difficulty maintaining a stable hemodynamic state and acid–base balance.

After operation, the patients were routinely maintained on mechanical ventilation until spontaneous breathing effort was evident and hemodynamic stability had been achieved. Renal support therapy was rendered when the patients had oliguria, fluid overload, or increasing serum levels of urea and creatinine.

The immunosuppressive protocol included steroid and FK506 in the initial period of the study for up to patient no. 216 in our series, and thereafter a combination of FK506, steroid, mycophenolate mofetil, and IL-2 receptor antagonist was used [8]. In the immediate postoperative period, FK506 was prescribed only when renal function had improved and adequate urine output was shown. After about 3 months, monotherapy with FK506 was maintained. Patients with hepatitis B continued to receive lifelong lamivudine. Adefovir was added when YMDD mutant was detected. Hepatitis B immunoglobulin was not given. Patients with hepatitis C were not given any antiviral treatment unless their liver graft showed evidence of recurrent infection.

In this study, possible causes of acute deterioration of liver function and types of hepatic insults were documented prospectively. Variceal bleeding was considered a manifestation of elevated portal pressure but not a hepatic insult leading to the onset of acute-on-chronic liver failure. Hepatorenal syndrome (type 1) was diagnosed by urine sodium concentration of less than 10 mmol/l in the absence of ultrasonographic evidence of obstructive uropathy or parenchymal disease and lack of improvement in renal function after plasma volume expansion [9]. The severity of illness before liver transplantation was reflected by the model for end-stage liver disease (MELD) score [10]. Hospital mortality was defined as death within the same hospital admission for liver transplantation. All patients were followed up regularly in the outpatient clinic by the same team of surgeons. There was no default of follow-up. The last census date for this study was August 31, 2008. The overall patient and graft survival rates (all-cause mortalities as an end point) were estimated by the life-table method and compared between groups by the log-rank test. Discrete variables were compared by the χ ² test, and continuous variables were compared by the Mann–Whitney U test. Stepwise logistic regression analysis was used to define factors related to hospital mortality. Multivariate analysis of factors of patient survival was performed with the Cox proportional hazards model. All statistical analyses were performed by SPSS, Version 12.0, for Windows (SPSS Inc., Chicago, IL). A value P < 0.05 was considered statistically significant.

The study demonstrated that patients with acute-on-chronic liver failure were at high risk of dying because of a high incidence of concomitant infection (including septicemia) and renal and respiratory failure. The severity of pretransplant illness of the patients with acute-on-chronic liver failure was reflected by their high MELD scores. Such patients probably belonged to status IIA in the United Network for Organ Sharing classification of waiting list for liver transplantation. However, with timely liver transplantation, particularly with the availability of LDLT, most of them were salvaged with rapid normalization of hepatic and renal functions. Their long-term survival rates are also satisfactory. Comparing them with the patients with fulminant hepatic failure and those with cirrhosis only, all treated in the same center and period, the outcome is equally satisfactory. Compared with the scanty data from the literature, the outcome of the patients reported in this study is probably superior [11‐14].

The patients with acute-on-chronic liver failure had two hepatic insults: acute liver injury on top of chronic liver damage. Those with chronic hepatitis B had various degrees of liver fibrosis but preserved liver function. Their pretransplant conditions were similar to those of the patients with fulminant hepatic failure. However, because their clinical deterioration was less fulminant, the incidence of intensive care unit admission in this group was lower. Patients having established cirrhosis with superimposed acute liver injury represented the highest risk group. They might be nutritionally depleted or might have suffered ill effects of portal hypertension. In previous studies, the outcome of liver transplantation for these patients was unfavorable [11‐14]. The unfavorable outcome was probably related to the timing of liver transplantation and graft quality. If liver transplantation could be carried out before irreversible multiorgan failure, and if the liver grafts were optimal in function, as shown in this series, even patients with preoperative infection and renal and respiratory failure could be salvaged. The results of our patients who underwent LDLT are favorable because nearly all our living grafts contained the middle hepatic vein, which allows uniform and complete venous drainage of the graft [15].

In our center, we offer options of both LDLT and DDLT. Supply of deceased donor liver grafts in our locality is scarce. The donor rate is about three per million population per year. Patients on the waiting list for DDLT are prioritized by MELD score. Thus, patients with acute-on-chronic liver failure are always on the top of the list and receive deceased donor grafts once they are available. Nevertheless, only a fortunate few can be supported in the intensive care unit and undergo DDLT in time. The molecular adsorbents recirculation system has been especially useful in bridging some of our patients to DDLT [16].

In this study, the 5-year overall survival rate of patients with acute-on-chronic liver failure exceeded 90%. Patients with cirrhosis only had less favorable long-term survival because many of them developed HCC and died of tumor recurrence. HCC was also present in 11% of the cirrhotic patients with acute deterioration, but their long-term survival was not affected, probably because the tumors were in early stage. However, even with exclusion of HCC patients, the cirrhotic patients with acute deterioration still had significantly better survival rates than the patients with cirrhosis only. The exact reason is not known.

In conclusion, the short-term and long-term survival rates after liver transplantation for acute-on-chronic liver failure are similar to those after transplantation for other liver conditions. Timely transplantation, especially by LDLT in regions with scarcity of deceased donor livers, is the only modality that can salvage patients of acute-on-chronic liver failure. However, the timing and indication for transplantation for this illness are not yet well defined. In the present study, the timing was determined according to the King’s College Hospital criteria. Patients with acute exacerbation of chronic hepatitis B demonstrate many clinical features similar to those demonstrated by patients with fulminant hepatic failure, so the King’s College Hospital criteria may be applicable to them. For cirrhotic patients with acute deterioration, their underlying cirrhosis status may prevent them from recovering spontaneously. For such patients, the King’s College Hospital criteria may not be applicable. In fact, there exists a set of criteria established previously for acute-on-chronic liver failure [17], but it carries the deficiency that the criteria were established on a relatively small patient database. At present, a large-scale study based on data of all patients with acute-on-chronic liver failure admitted to our center is on the way. Identification of factors predicting mortality and the need for liver transplantation will allow earlier transplantation and a higher salvage rate.