To analyze the impact of model for end-stage liver disease (MELD) allocation policy on survival outcomes after liver transplantation (LT).
INTRODUCTION:Considering that an ideal system of grafts allocation should also ensure improved survival after transplantation, changes in allocation policies need to be evaluated in different contexts as an evolutionary process.
METHODS:A retrospective cohort study was carried out among patients who underwent LT at the University of Pernambuco. Two groups of patients transplanted before and after the MELD allocation policy implementation were identified and compared using early postoperative mortality and post-LT survival as end-points.
RESULTS:Overall, early postoperative mortality did not significantly differ between cohorts (16.43% vs. 8.14%; p = 0.112). Although at 6 and 36-months the difference between pre- vs. post-MELD survival was only marginally significant (p = 0.066 and p = 0.063; respectively), better short, medium and long-term post-LT survival were observed in the post-MELD period. Subgroups analysis showed special benefits to patients categorized as non-hepatocellular carcinoma (non-HCC) and moderate risk, as determined by MELD score (15-20).
DISCUSSION:This study ensured a more robust estimate of how the MELD policy affected post-LT survival outcomes in Brazil and was the first to show significantly better survival after this new policy was implemented. Additionally, we explored some potential reasons for our divergent survival outcomes.
CONCLUSION:Better survival outcomes were observed in this study after implementation of the MELD criterion, particularly amongst patients categorized as non-HCC and moderate risk by MELD scoring. Governmental involvement in organ transplantation was possibly the main reason for improved survival.
Initially described by Malinchoc et al.1 as a mathematical model for predicting survival in the first three months postoperatively for patients who underwent percutaneous placement of transjugular intrahepatic porto-systemic shunt (TIPS), the model for end-stage liver disease (MELD) score was quickly validated as a predictor of mortality for a wide variety of liver diseases,2-4 including cirrhotic patients awaiting liver transplantation (LT).5-8
Afterwards, to reduce mortality amongst patients on the waiting list9,10 and to eliminate possible confounding factors, the MELD criterion was incorporated as a more transparent and objective system, based on easily measurable laboratory tests.11-13 The implementation of this model was based on the recognition that time on the list was an inadequate criterion for prioritizing candidates for LT, since it had little relationship to mortality in these patients.12,13
Therefore, considering that an ideal system of graft allocation should ensure the best use of available livers for mortality reduction amongst patients on waiting lists and improvement of survival after transplantation,5 changes in allocation policies need to be evaluated in different contexts over time. In addition, as the MELD criterion has only recently been implemented in Brazil (2006), only medium-term post-transplant survivals could be compared with those observed in the period before its introduction.14
This current study describes a Brazilian single-center experience and provides a comparison between pre- vs. post-MELD cohorts to analyze the impact of MELD allocation policy on survival outcomes after LT at the Department of Surgery and Liver Transplantation of the Oswaldo Cruz University Hospital (HUOC), University of Pernambuco.
MATERIALS AND METHODSStudy Population and Data CollectionA retrospective cohort study was carried out on patients transplanted by the Department of General Surgery and Liver Transplantation of the Oswaldo Cruz University Hospital, University of Pernambuco, from July 15, 2003 to July 14, 2009. Using our own database, two groups of patients transplanted before and after MELD allocation policy implementation were identified: pre-MELD group—those undergoing LT from July 15, 2003 to July 14, 2006 (n = 113); and Post-MELD group—those undergoing LT between July 15, 2006 and July 14, 2009 (n = 185).
The same surgical team performed all procedures using standard technique without veno-venous bypass and with conventional or piggyback hepato-venous reconstruction. After LT, tacrolimus, mycophenolate (sodium or mofetil) and prednisone were used as immunosuppressive treatment, with no changes in the protocols applied from 2003 to 2009. All patients were followed for at least one year in order to determine the primary endpoint (death).
We limited our study to adults and adolescent patients (>16 years) who received deceased donor orthotopic LT. For patients who had undergone re-transplantations, data were collected from the first procedure only and recipients of split-liver or sequential (domino) transplants were not eligible for this study. We also excluded patients transplanted as a result of fulminant hepatic failure, as well as patients with incomplete data in their medical records.
Variables and OutcomesDescriptive statistics include donor and recipient ages, cold (CIT) and warm ischemia times (WIT), amounts of red blood cells (RBC) and platelets transfused at the surgery, MELD score and monthly transplant rates as continuous variables. As categorical variables, Child-Pugh classing, ABO blood grouping, pre-transplant diagnosis, recipient gender and hepato-venous reconstruction type were studied.
Two different survival outcomes were compared between pre- vs. post-MELD groups: early postoperative mortality and patient post-LT survival. Early postoperative mortality rates were defined as the proportion of deaths in the first 30 days after LT. Patient survival, as a function of time after transplantation until the date of death or end of the study, was explored as short- (3 and 6 months), medium- (1 year) and long-term (3 years) outcomes. Data on deaths not related to liver disease or transplant procedure, and data on those patients alive at the end of the study, were “censored” for cumulative survival estimation.
MELD score was calculated using laboratory results collected immediately prior to the LT15 with no adjustments for malignancy or other “special” conditions used to prioritize these patients on the waiting list.16 Serum markers were used to confirm viral hepatitis diagnosis. The pre-operative diagnosis of hepatocellular carcinoma (HCC) was based on the Barcelona-2000 conference diagnostic criteria17 and confirmed by explant pathology. The Milan criteria were applied as a basis for selecting patients with HCC for LT.
Sample CharacteristicsOur group performed 298 LTs in 288 patients during the period described earlier. Eighty patients were not eligible or excluded from this study, and 208 patients were included in the analysis (pre-MELD = 73 vs. post-MELD = 135). Patient characteristics, as well as transplant Center and donor variables, are summarized in Table 1. Seventy-seven percent of HCC patients had other associated diagnoses, among which viral C hepatitis was the most common disease (52.45%).
Descriptive statistics of measured variables.
| Study Cohorts Median (interquartile range) or n (%) | ||||
|---|---|---|---|---|
| Variables | Overall Median (interquartile range) or n (%) | Pre-MELD | Post-MELD | p-value1 |
| Recipient variables | ||||
| Recipient age (years) | 54 (44.5-60.5) | 52 (45-59) | 55 (44-61) | 0.207 |
| MELD Score | 15 (12-19) | 15 (12-17) | 15 (12-20) | 0.073 |
| HCC | 13 (10-15) | 13 (12-16) | 13 (10-15) | 0.501 |
| Non-HCC | 17 (13-20) | 15 (11-17) | 18.5 (14-21.5) | <0.001 |
| Gender | 0.858 | |||
| Male | 137 (65.86) | 47 (64.38) | 90 (66.66) | |
| Female | 71 (34.13) | 26 (35.61) | 45 (33.33) | |
| ABO blood group | 0.953 | |||
| A | 84 (40.38) | 32 (43.83) | 52 (38.51) | |
| B | 24 (11.53) | 7 (9.58) | 17 (12.59) | |
| AB | 11 (5.28) | 2 (2.73) | 9 (6.66) | |
| O | 89 (42.78) | 32 (43.83) | 57 (42.22) | |
| Child-Pugh class | 0.926 | |||
| A | 53 (25.48) | 17 (23.28) | 36 (26.66) | |
| B | 94 (45.19) | 37 (50.68) | 57 (42.22) | |
| C | 61 (29.32) | 19 (26.02) | 42 (31.11) | |
| Diagnosis2 | ||||
| Chronic viral hepatitis | 86 (41.34) | 32 (43.83) | 54 (40) | 0.697 |
| HCC | 61 (29.32) | 10 (13.69) | 51 (37.77) | <0.001 |
| Alcoholic cirrhosis | 53 (25.48) | 21 (28.76) | 32 (23.70) | 0.526 |
| Cryptogenic cirrhosis | 25 (12.01) | 10 (1.36) | 15 (11.11) | 0.745 |
| Autoimmune chronic Hepatitis | 13 (6.25) | 6 (2.88) | 7 (5.18) | 0.385 |
| Cholestatic liver Disease3 | 11 (5.28) | 3 (1.44) | 8 (5.92) | 0.750 |
| Miscellaneous | 51 (24.51) | 16 (21.91) | 35 (25.92) | 0.636 |
| Donor and center variables | ||||
| Monthly transplant rate | 6 (4-8) | 4 (3-6) | 6 (5-8) | <0.001 |
| Donor age (years) | 40.5 (25.5-51) | 42 (26-51) | 39 (25-51) | 0.974 |
| Cold ischemia time (hours) | 6.8 (5.4-8.7) | 7 (5.6-8.6) | 6.6 (5.4-8.7) | 0.533 |
| Warm ischemia time (minutes) | 47.5 (40-55) | 55 (45-60) | 45 (37-51) | <0.001 |
| Red blood cells Transfusion (units) | 3 (1-5) | 3 (2-5) | 3 (1-5) | 0.626 |
| Platelets transfusion (units) | 0 (0-9) | 0 (0-7) | 0 (0-10) | 0.666 |
| Hepato-venous reconstruction | 0.039 | |||
| Conventional | 127 (61.06) | 52 (71.23) | 75 (55.56) | |
| Piggyback | 81 (38.94) | 21 (28.77) | 60 (44.44) | |
Follow-up data were available for the entire study group (n = 208). Over the 82.6 month follow-up period, 68 liver allograft recipients died (36.7%) and 7 (3.4%) underwent re-transplantations. The main causes of death were infection, malignancy recurrence and liver failure/transplant rejection.
Analytic ApproachThe statistical analyses were performed using the STATISTICA Data Analysis Software System, Version 8.0 (Statsoft, Inc., Tulsa, OK, USA), and all analyses considered a two-tailed p-value of 0.05 as statistically significant. Normal distribution was not proven for the clinical variables available (Kolmogorov–Smirnov test, p<0.05); then, nonparametric tests were applied to all data analysis. For descriptive analyses, we summarized the continuous variables using medians (interquartile range) and categorical variables as proportions.
Comparisons between pre- vs. post-MELD groups were conducted using the Mann-Whitney U-test for continuous variables and chi-square tests for categorical variables, including Yates's correction or Fischer's exact test as appropriate. Rates of postoperative early mortality were compared using chi-square tests and survival probabilities were constructed using Kaplan–Meier survival estimates and compared using the log-rank test.
Furthermore, as a result of the introduction of the MELD allocation policy to prioritize the sickest patients and the well-known increase in the rates of LT for HCC in the post-MELD era,10–12,14,18-24 we also stratified the patients according to MELD score and diagnosis, in order to control for these variables. Patients were stratified according to MELD score to low-risk (<15), medium-risk (15–20) or high-risk (>20) categories.9 According to diagnosis, these patients were stratified as HCC or non-HCC.
Additionally, we explored some potential reasons for divergent survival outcomes after implementation of the MELD-based policy, using a cross-sectional strategy. For this analysis, we applied c-statistic, univariate and multivariate analyses to check our hypothesis, as described below.
The prognostic value of MELD score in predicting post-LT survival was assessed using receiver operating characteristic (ROC) curve analysis. The c-statistic, equivalent to the area under the ROC curve (AUC), was adopted to establish the overall diagnostic accuracy of the MELD score. Usually, AUC between 0.8 and 0.9 indicates excellent diagnostic accuracy; a score with an AUC>0.7 should be considered clinically useful and AUC ≤ 0.5 is considered to be indicative of a lack of discriminating power.9,25,26
The association of each demographic variable with long-term post-LT survival was also tested using the log-rank test in a univariate analysis. For this approach, we categorized the continuous variables using current cut-off points.9,21,27–31 Then, factors whose association with survival showed a p-value <0.20 were used in a multivariate Cox's proportional-hazards model to identify the independent predictors. We also adjusted this multivariate analysis for transplantation era (first vs. second transplantation era) and allocation criterion (pre- vs. post-MELD).
Finally, we explored survival in consecutive transplantations eras using the Kaplan-Meier method and the log-rank test. As follow-up of patients who have recently undergone transplantation is often small, we limited this study to a one-year analysis of four successive transplantation periods (quartiles) and to a two-year analysis of two successive transplantation eras. The significant variables highlighted in the previous multivariate analysis were also compared among the transplantation quartiles using the Kruskal-Wallis test.
Ethical CommentsThis study was registered in the Brazilian National System of Human Research – SISNEP (CAAE - 0003.0.106.000/10) and approved by the HUOC Ethics Research Committee (protocol number 12/2010). All procedures complied with the standards of the Declaration of Helsinki and current ethical guidelines.
RESULTSAs summarized in Table 1, a statistically significant increase in monthly transplant rates (p<0.001), proportion of HCC patients (p<0.001) and use of the piggyback hepato-venous technique (p = 0.039) were found in the post-MELD cohort. A significant reduction of WIT was also observed after implementation of the MELD criterion (p<0.001) and the overall median MELD score remained unchanged after its introduction (p<0.073). In the HCC sub-group, this score was lower than among non-HCC patients (p<0.001) and displayed no change during the post-MELD era (p = 0.501). On the other hand, the median MELD score rose 3.5 points in this period in the non-HCC sub-group (p<0.001).
The overall early postoperative mortality was 11.05% and showed no statistical difference between the cohorts (16.43% vs. 8.14%; p = 0.112). Similarly, the inter-group study showed no statistical difference between patients categorized according to diagnosis (p = 0.545) or MELD score (p = 0.994). However, the subgroups analysis showed a statistically significant reduction in mortality rate after introduction of the MELD criterion in the patients categorized as moderate-risk by MELD score (p = 0.039). We also found a borderline statistical significance in the non-HCC subgroup (p = 0.054) (Table 2).
Early postoperative mortality rates.
| Study Cohorts n (%) | ||||
|---|---|---|---|---|
| Mortality Rates | n (%) | Pre-MELD | Post-MELD | p-value1 |
| Overall | 23 (11.05) | 12 (16.43) | 11 (8.14) | 0.112 |
| Diagnostic Categories | ||||
| HCC | 5 (8.19) | 0 (0) | 5 (9.80) | 0.579 |
| Non-HCC | 18 (12.24) | 12 (19.04) | 6 (7.14) | 0.054 |
| p-value2 | 0.545 | |||
| MELD Score Risk Categories | ||||
| MELD <15 | 9 (9.67) | 5 (14.28) | 4 (6.89) | 0.289 |
| MELD 15-20 | 10 (12.82) | 7 (23.33) | 3 (6.25) | 0.039 |
| MELD >20 | 4 (10.81) | 0 (0) | 4 (13.79) | 0.557 |
| p-value2 | 0.994 | |||
Patients 3, 6, 12 and 36-months overall cumulative survivals were 85.1, 79.3, 74.5 and 67.5%, respectively. Although the difference between pre- vs. post-MELD survival rates was sometimes only marginally significant, better rates of post-LT survival were observed in the post-MELD era (Figure 1). The inter-group analysis showed no statistical difference in survival amongst patients stratified according to diagnosis or MELD score (Figure 2), but statistically higher cumulative survivals were found in the sub-group analysis of non-HCC and moderate-risk MELD score categories in the post-MELD period (Table 3).
Overall patient survival (Kaplan-Meier) before and after the model for end-stage liver disease (MELD) criterion implementation. There was improved patient survival at three years (with a borderline statistical significance) among the post-MELD cohort as compared to the pre-MELD cohort (60.27% vs. 72.62%, p = 0.063, by the log-rank test).
Kaplan-Meier analysis of patients stratified according to diagnosis (A) and model for end-stage liver disease (MELD) score risk category (B). Inter-group analysis showed no difference in patient survival at three years (p = 0.350 and p = 0.887, respectively, by the log-rank test).
Stratified cumulative proportion surviving after liver transplantation.
| Cumulative Proportion Surviving (%) 1 | |||||
|---|---|---|---|---|---|
| Groups and Categories | n (%) | 3 months | 6 months | 12 months | 36 months |
| Overall | |||||
| Pre-MELD | 73 (35.10) | 77.62 | 72.57 | 65.75 | 60.27 |
| Post-MELD | 135 (64.90) | 88.76 | 82.96 | 79.25 | 72.62 |
| p-value2 | 0.036 | 0.066 | 0.028 | 0.063 | |
| HCC | |||||
| Pre-MELD | 10 (16.39) | 100.00 | 100.00 | 90.00 | 80.00 |
| Post-MELD | 51 (83.60) | 86.00 | 76.47 | 70.58 | 57.27 |
| p-value2 | 0.217 | 0.090 | 0.174 | 0.141 | |
| Non-HCC | |||||
| Pre-MELD | 63 (42.85) | 73.98 | 68.21 | 61.90 | 57.14 |
| Post-MELD | 84 (57.14) | 90.41 | 86.90 | 84.52 | 83.28 |
| p-value2 | 0.009 | 0.005 | 0.001 | 0.001 | |
| MELD <15 | |||||
| Pre-MELD | 35 (37.63) | 79.41 | 74.28 | 68.57 | 62.85 |
| Post-MELD | 58 (62.36) | 87.71 | 82.75 | 79.31 | 70.35 |
| p-value2 | 0.292 | 0.313 | 0.241 | 0.402 | |
| MELD 15-20 | |||||
| Pre-MELD | 30 (38.46) | 72.41 | 66.66 | 63.33 | 60.00 |
| Post-MELD | 48 (61.53) | 91.66 | 85.41 | 85.41 | 78.32 |
| p-value2 | 0.029 | 0.042 | 0.021 | 0.056 | |
| MELD >20 | |||||
| Pre-MELD | 8 (21.62) | 87.50 | 87.50 | 62.50 | 50.00 |
| Post-MELD | 29 (78.38) | 85.96 | 79.31 | 68.96 | 68.96 |
| p-value2 | 0.874 | 0.588 | 0.785 | 0.604 | |
According to c-statistic, the accuracy of preoperative MELD score in predicting post-LT survival was 0.526, 0.524, 0.5 and 0.519, at 3, 6, 12 and 36-months, respectively. After univariate and multivariate analyses, only transfusion of RBC (≥5 units) was an independent predictor of poorer 3-year post-LT survival, although differences in CIT (≥12 hours) were also of borderline statistical significance. These findings remained unchanged after adjustment for transplantation era and allocation criterion (Table 4).
Predictors of 3-year post-liver transplantation survival.
| Multivariate3 | ||||
|---|---|---|---|---|
| Variables1 | Univariate 2 | Unadjusted | Allocation Criterion | Transplantation Era4 |
| Diagnostic categories5 | 0.350 | – | – | – |
| ABO blood group | 0.120 | 0.279 | 0.361 | 0.320 |
| Receptor gender | 0.635 | – | – | – |
| Recipient age (<55 vs. ≥55) | 0.973 | – | – | – |
| MELD (<15 vs.15-20 vs. >20) | 0.887 | – | – | – |
| Child-Pugh class | 0.400 | – | – | – |
| Donor age (<50 vs. ≥50) | 0.660 | – | – | – |
| Cold ischemia (<12 vs. ≥12) | 0.018 | 0.062 | 0.050 | 0.060 |
| Warm ischemia (<45 vs. ≥45) | 0.048 | 0.419 | 0.694 | 0.825 |
| Red blood cells (<5 vs. ≥5) | <0.001 | 0.002 | 0.002 | 0.003 |
| Platelets (yes vs. no) | 0.027 | 0.547 | 0.573 | 0.666 |
| Transplant rate (<5 vs. ≥5) | 0.424 | – | – | – |
| Hepato-venous Reconstruction6 | 0.006 | 0.119 | 0.135 | 0.128 |
The patients transplanted with piggyback hepato-venous anastomosis presented significantly better post-LT survival in the univariate analysis (60.44% vs. 79.15%. p = 0.006); however, this statistical significance was lost in the multivariate analysis. This technique was also associated with lower RBC transfusion and WIT (p = 0.032 and p<0.001, respectively).
We found increased survival from first to fourth transplantation quartiles in a one-year survival analysis (61.5% vs. 73.1% vs. 75% vs. 88.5%, respectively. p = 0.027), as well as in the first vs. second transplantation era, as determined using two-year survival as an end-point (62.5% vs. 80.4%, respectively, p = 0.005). There were no significant differences in RBC transfusion or CIT into the transplantation quartiles (p = 0.177 and p = 0.608, respectively).
DISCUSSIONSince July 2006, the MELD criterion has been adopted to guide organ allocation at the national level for LT in Brazil.16 The implementation of this new allocation policy was followed by significant increases in the monthly rates of LT and, therefore, the total number of procedures performed by our department. This also occurred at other Centers,10,11,21,32 likely reflecting recent increase in Public Health System involvement in the transplantation of organs and tissues.10,33
As a result of the prioritization of patients in “special situations” dictated by the new liver grafts allocation policy,16 there was a significant increase in the number of patients transplanted as a result of HCC in our department, as well as around the world.11,12,14,18-24,32,34
Contrary to the findings of other authors, we did not find an overall increased severity of liver disease in the patients transplanted after the introduction of the MELD-based policy.11,21,35 However, this may be as a result of the higher proportion of HCC patients transplanted in the post-MELD period. Such patients typically have better hepatic functional reserves10,21,36 and exhibit no change in the severity of their liver disease after adoption of the MELD criterion. Moreover, “dilution” of the MELD scores by the increase in monthly transplant rates21 and the shorter time spent awaiting LT in our State during the post-MELD period10 may have reduced MELD scores.
Although the difference between pre- vs. post-MELD survival has sometimes been only marginally significant, analysis of our liver transplant database reveals that the most important post-transplantation outcome—namely patient survival—has improved since the implementation of the MELD-based liver allocation system. In order to explore these divergent outcomes,11,14,21,37 we conducted some additional exploratory analyses to elucidate our findings further.
First, as factors related to cancer alone are not enough to predict the prognosis of patients with HCC4 and because such patients exhibit better liver function at the time of LT,5,10,21,36 we expected better survival for these patients and supposed it as the main reason for our improved post-LT survival during the post-MELD period.36 However, our data have shown that HCC patient survival did not improve after introduction of the MELD criterion. Furthermore, there was no significant difference in early postoperative mortality or post-LT survival between HCC vs. non-HCC patients. Therefore, the best results observed during the post-MELD period did not result from the greater proportion of HCC patients transplanted in this period. We also noticed a trend of worsening survival after one year of LT in this patient subgroup, which probably resulted from the influence of tumor-related factors.38
A second possible explanation is that transplant recipients are simply not sicker in the post- vs. pre-MELD periods. Nonetheless, our data failed to confirm this hypothesis. Despite the lack of any change in liver disease severity in the HCC subgroup, the non-HCC patients exhibited a 3.5-point increase in median MELD score during the post-MELD era. This approach also demonstrated an apparent disconnect between liver disease severity and survival outcomes in the non-HCC subgroup, which presented significantly higher cumulative survival after adoption of the MELD criterion. Similarly, a lower early postoperative mortality rate, with borderline statistical significance, could also be observed amongst these patients in the post-MELD era.
Although it is plausible to hypothesize that patients transplanted with higher MELD scores had worse survival,10,21,22 our data show there was no significant difference among patient groups with different MELD scores. This finding suggests MELD score is not a good predictor of post-LT survival. We also used the c-statistic to confirm that preoperative MELD score had poor discriminatory power in predicting post-LT survival among patients treated in our department.
Similarly, in a systematic review about the performance of MELD in the setting of LT, Colongita et al. concluded that MELD score is not a good predictor for short-term mortality after LT and that further studies were needed to assess long-term performance.5 In addition, it has been demonstrated that this score does not have the same prognostic accuracy among patients with milder degrees of hepatic cirrhosis and that the effect of hepatic dysfunction may not be evident at MELD score values lower than 30.5,39 This suggests only high MELD values affect post-LT survival.21 Therefore, although statistically significant, the 3.5-point increases that represent shifts to milder degrees of hepatic dysfunction (i.e. MELD 15-20), may not translate into a clinically relevant difference in survival.
On the other hand, worse survival in recipients with higher MELD scores has been cited by some authors9,14,35 and higher MELD scores have also been linked to greater postoperative morbidity.40,41 However, even in patients with more severe disease, there is a clear survival benefit from LT, because of their corresponding lower survival rates on the waiting list without LT42-44 As demonstrated by Merion et al.,42 the benefit of LT would become evident only in patients with MELD scores higher than 18 and the magnitude of this benefit increased with increasing MELD score. Similar results were also described by Gleisner et al., who suggested a MELD score of 15 as a transition point in terms of overall survival benefit.44
Although the MELD criterion was established to prioritize the sickest patients, a large proportion of transplanted recipients do not have severe liver disease, as evaluated by MELD score.5 Accordingly, in our department the median MELD score did not change with the introduction of the MELD criterion and remained low (15 points) after implementation (HCC = 13 and non-HCC = 18.5). Similarly, only 3.4% of patients had MELD scores greater than 30 (data not shown). These low proportions of patients with high MELD scores have also been found in other studies5,22,35,42 and probably contributed to reducing the accuracy of this score in predicting post-LT survival in our department.
Other potential explanations were that better survival outcomes in the post-MELD period may have resulted from our increased case volume and/or from a higher proportion of patients transplanted with the piggyback technique. In order to explore this hypothesis, we additionally performed a secondary statistical approach to explore long-term predictors of survival using univariate and multivariate analysis. According to this approach, transfusion of RBC alone (≥5 units) was an independent predictor of poorer three-year post-LT survival; however, CIT ≥12 hours also exhibited borderline statistical significance as an independent predictor.
In a previous study at our department, the piggyback technique was associated with reduced length of hospital stay, surgical time and WIT, as well as a better 30-day post-LT survival.45 Accordingly, in our long-term univariate analysis, we found better post-LT survival amongst patients transplanted with the piggyback hepato-venous anastomosis. However, our multivariate analysis revealed this outcome probably resulted from the reduced RBC transfusion that accompanies this technique. The higher proportion of patients transplanted with this technique in the post-MELD era also served to explain our lower WIT observed during this last period.
As our department changed from a medium case volume center (20-50 LT /year) in the pre-MELD period of the study to a high case volume center (>50LT/year) in the post-MELD era,21 as well as the better outcomes observed at LT Centers performing more than 20 procedures per year,46 we hypothesized that increased LT volume was a plausible reason for better survival after implementation of the MELD allocation plan. Nevertheless, our monthly transplantation rates did not correlate with patient survival in this study. Furthermore, because our study started after more than 40 LTs had been performed by our department, center- and team-related factors (i.e. case volume and transplantation experience) appear to not have significantly influenced patient survival at our department. Similarly, Northup et al. explored the impact of transplant center case volume on survival of 9909 adult liver transplants performed in the USA since the beginning of the MELD allocation system.47 After adjusting for disease severity and multiple donor and recipient factors, transplant center volume was no longer a significant predictor of post-LT survival, according to these authors.
As alternative reasons for our better survival outcomes in the post-MELD period, we finally hypothesized that involvement of the Public Health System in the transplantation of organs and tissues played a role.10,33 To support this hypothesis, we explored our analysis of patient survival to include successive transplantation periods. Using this approach, we found increased survival from first to fourth transplantation quartiles in a one-year survival analysis as well as in the first vs. second transplantation era, using two-year survival as the end-point. Moreover, we also confirmed there were no differences in RBC transfusion or CIT among successive transplantation quartiles.
Notably, in the post-MELD period, governmental efforts to encourage organ transplantation improved the logistics of the donation-transplant process, allowing for an increase in the number of potential donors in brain-death notifications and in the amount of donations and transplants in the State of Pernambuco.10,33 Furthermore, governmental involvement also included some educational, structural and financial improvements that gradually impacted on regional medical assistance33 and may have contributed to better survival during the most recent periods of our LT activity.
Our analysis has three main strengths: firstly, whereas a previous report14 with similar methods measured medium-term post-LT survival (1-year), we provided a 3-year survival analysis. This approach ensured a more robust estimate of how the MELD policy affected post-LT survival outcomes in Brazil; secondly, we were the first center to show significantly better survival after the implementation of a MELD-based policy.11,14,21,37 Similarly, although MELD-based policy has not significantly reduced waiting list mortality throughout the country,48,49 our State presented lower waiting list mortality after adoption of this new system;10 and lastly, we explored potential reasons for our divergent survival outcomes after LT.
However, there were also limitations with our study. Firstly, few patients in the HCC and MELD >20 subgroups underwent transplantation during the pre-MELD era at our department, which limited their subgroup analyses to comparisons between the pre- vs. post-MELD periods. Secondly, a small proportion of our patients had high “calculated” MELD scores [i.e. only 3.4% had MELD scores >30 and just 8.2% had MELD scores ≥25 (data not shown)]. Notably, a low proportion of patients with high MELD scores probably minimized the accuracy of this score in predicting post-LT survival, as well as the impact of MELD-based policy on our post-LT survival outcomes. Lastly, analysis of additional donor-related variables could provide additional information, because a large proportion of extended-criteria donors were used at our department.28,50
CONCLUSIONIn conclusion, better survival outcomes were observed in our department after implementation of the MELD allocation policy, particularly amongst patients categorized as non-HCC and moderate-risk, as determined by MELD score (15-20 points). Gradual involvement of the Public Health System in organ transplantation was possibly the main reason for the improvement in survival outcomes.
CONFLICTS OF INTERESTAll the authors declare that there are no conflicts of interest, financial support or disclaimers related to this study.
The authors would like to thank Ms. Tânia M. Xavier, Ms. Juliana S. Gomes and Dr. Isaac Esmeraldino for their help with data collection. We also thank Dr. Gedson A. Maia and Dr. José A. Morais for English review and Dr. José N. Figueiroa and Dr. Ulisses Montarroyos for their excellent technical assistance.