<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJEpi</journal-id><journal-title-group><journal-title>Open Journal of Epidemiology</journal-title></journal-title-group><issn pub-type="epub">2165-7459</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojepi.2023.134019</article-id><article-id pub-id-type="publisher-id">OJEpi-128869</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Temporal Variations in Mortality after Liver Transplantation: Retrospective Investigation of Potential Risk Factors Using Propensity Score
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rana</surname><given-names>A. Almousa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mohamed</surname><given-names>M. Shoukri</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Internal Medicine, King Saud Medical City, Riyadh, Saudi Arabia</addr-line></aff><aff id="aff2"><addr-line>Department of Epidemiology and Biostatistics, Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario Canada</addr-line></aff><pub-date pub-type="epub"><day>18</day><month>09</month><year>2023</year></pub-date><volume>13</volume><issue>04</issue><fpage>250</fpage><lpage>259</lpage><history><date date-type="received"><day>13,</day>	<month>August</month>	<year>2023</year></date><date date-type="rev-recd"><day>3,</day>	<month>November</month>	<year>2023</year>	</date><date date-type="accepted"><day>6,</day>	<month>November</month>	<year>2023</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Objective: We aim to detect over-time variations in mortality of liver transplant recipients stratified by the period of transplant. Since this is a retrospective investigation, bias reduction caused by possible confounding effects can be achieved by using propensity score weighting in a multivariate logistic regression model. 
  Methods: Medical charts of all adult liver transplant recipients (
  <em>n</em> = 250) who were transplanted in three periods 2005-2009, 2010-2014 and 2015-2019 were retrospectively reviewed. The following recipient factors were analyzed: recipients and donors’ ages, sex, renal impairment, body mass index (BMI), presence of bacterial or viral infections, MELD (Model for end-stage diseases). Multivariate logistic model adjusted by Propensity Scores (PS) was used to identify the effect of the risk factors on mortality, and death within five years, in the targeted time frame. Patient outcomes are recorded as; (patient status = 1 if dead, or patient status = 0 if alive). 
  Results: Meld score, recipient age, and renal impairments were shown to be predictors of mortality in transplanted patients. Multivariate regression model was used to identify the significance of the specified risk factors, followed by pairwise comparisons between periods. Pairwise comparisons between periods using logistic regression weighted by the inverse propensity score, correcting for the possible confounding effect of measured covariates showed that the death rate is significantly reduced in subsequent periods as compared to the initial period. 
  Conclusions: The clinical implications of these findings are the ability to stratify patients at high risk of posttransplant death by planning more intensive and accurate management for them.
 
</p></abstract><kwd-group><kwd>Liver Transplantation</kwd><kwd> Age</kwd><kwd> Body Mass Index</kwd><kwd> Renal Impairment</kwd><kwd> Inverse Propensity Score Weighting</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Data on liver transplantation are globally available and to name but a few in [<xref ref-type="bibr" rid="scirp.128869-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref3">3</xref>] . Liver transplantation is still a complex and cost-intensive procedure [<xref ref-type="bibr" rid="scirp.128869-ref4">4</xref>] and the results are influenced by many interrelated factors. As liver transplantation has become a universally accepted treatment for end-stage liver disease, the number of patients accumulating on the waiting list has gradually outweighed the scarce resources of available organs. Fair allocation of donor livers to patients with end-stage liver disease remains a difficult task. In this study we addressed several questions, the first being whether there is a change in the rate of death among transplant recipients. Furthermore, we investigated the effect of several risk factors on patients’ survival.</p><sec id="s1_1"><title>1.1. MELD Score</title><p>The first risk factor being investigated is model for end-stage liver disease (MELD) score [<xref ref-type="bibr" rid="scirp.128869-ref5">5</xref>] . The usually adopted policy stratifies the patients based on their risk of death while on the waiting list [<xref ref-type="bibr" rid="scirp.128869-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref7">7</xref>] . The impact of the MELD score on postoperative mortality remains unclear. There are reports of reduced survival in groups with high MELD scores [<xref ref-type="bibr" rid="scirp.128869-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref9">9</xref>] but also reports of no influence of MELD score on survival [<xref ref-type="bibr" rid="scirp.128869-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref11">11</xref>] .</p><p>The MELD score incorporates three simple laboratory parameters (serum creatinine and bilirubin, and INR for prothrombin time) and stratiﬁes patients according to their disease severity in an objective and continuous ranking scale. Concordance statistics have demonstrated its high accuracy in stratifying patients according to their risk of dying in the short term (three months) [<xref ref-type="bibr" rid="scirp.128869-ref12">12</xref>] .</p></sec><sec id="s1_2"><title>1.2. Age</title><p>The second risk factor for mortality after liver transplant that we study in this paper is age.</p><p>Our second aim is to establish whether there is a relationship between the donor’s age and patient and survival among liver transplant recipients and to determine the age at which this relationship emerges. A donor’s age is one factor that determines the choice of a graft for transplant. However, the shortage of organs for a large number of waiting patients limits this decision. Thus, donors show a tendency toward older age, particularly in Europe compared with the United States [<xref ref-type="bibr" rid="scirp.128869-ref13">13</xref>] . Several factors may reduce the quality of grafts from older donors, including an increased degree of hepatic steatosis, a higher incidence of primary dysfunction or failure, a reduced functional capacity, and a greater extent of parenchymatous necrosis and fibrosis. [<xref ref-type="bibr" rid="scirp.128869-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref8">8</xref>] As a result, during the last decade several studies reported a decline in the survival rates of patients who receive organs from donors older than 45, 50, or 60 years [<xref ref-type="bibr" rid="scirp.128869-ref13">13</xref>] . The aim of this study was to determine whether there is a relationship between donor age and recipient survival, and to establish a cut-off age.</p></sec><sec id="s1_3"><title>1.3. Renal Impairment</title><p>The third risk factor is chronic renal dysfunction which has also been shown to have a significant association with cardiovascular events in retrospective analyses [<xref ref-type="bibr" rid="scirp.128869-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref17">17</xref>] . One study of data from the Organ Procurement and Transplant Network (OPTN) assessed risk factors for cardiovascular mortality in 5057 patients undergoing liver transplant for nonalcoholic steatohepatitis and found moderate or severe kidney disease (estimated GFR [eGFR] &lt; 60 mL/min/1.73 m<sup>2</sup>) to incur a 1.8-fold increase in risk (p &lt; 0.001) [<xref ref-type="bibr" rid="scirp.128869-ref14">14</xref>] . A single-center retrospective analysis of 202 primary liver transplants has reported a doubling of the risk for both cardiovascular events and cardiovascular mortality in patients with eGFR &lt; 60 mL/min/1.73 m<sup>2</sup> [<xref ref-type="bibr" rid="scirp.128869-ref18">18</xref>] .</p></sec><sec id="s1_4"><title>1.4. Infections (Bacterial, Viral, and Fungal)</title><p>Virtually any bacteria can cause disease after liver transplantation [<xref ref-type="bibr" rid="scirp.128869-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref20">20</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref22">22</xref>] . Risk factors for resistant bacterial pathogens are prior antibiotic One of the most common bacterial infections found to manifest itself early after liver transplantation, is surgical site infection, which has been estimated to occur in about 10% of patients. Intra-abdominal infections account for 27% - 47% of early bacterial infections after liver transplantation [<xref ref-type="bibr" rid="scirp.128869-ref23">23</xref>] . Intraabdominal abscesses, peritonitis, and cholangitis commonly present during the first few weeks after liver transplant as fever, leukocytosis, and abdominal pain, although clinically asymptomatic cases which are mainly manifested with elevated liver enzymes are not uncommon.</p><p>Liver recipients are somewhat unique among transplant recipients because they are commonly chronically infected with hepatitis B or C viruses, often with an accelerated clinical course [<xref ref-type="bibr" rid="scirp.128869-ref24">24</xref>] . Respiratory and gastrointestinal viruses may occur throughout the post-liver transplant period, with seasonal variations for some viruses such as influenza and parainfluenza [<xref ref-type="bibr" rid="scirp.128869-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref27">27</xref>] .</p><p>Although various fungal species infect liver transplant recipients, by far the most common are the Candida species followed by the Aspergillus species. Cryptococcus neoformans occurs much less commonly in the form of meningitis, lung disease and cellulitis [<xref ref-type="bibr" rid="scirp.128869-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref30">30</xref>] .</p></sec><sec id="s1_5"><title>1.5. Patient BMI</title><p>The fifth risk factor we studied is patients’ body mass index (BMI). In the general population, a high BMI is associated with the development of cardiovascular diseases, diabetes, musculoskeletal disorders and cancer, resulting in increased morbidity and mortality [<xref ref-type="bibr" rid="scirp.128869-ref31">31</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref32">32</xref>] .</p></sec></sec><sec id="s2"><title>2. Methods of Analysis</title><p>Data analyses are done using the SAS software version 9.4. Among the 250 transplant recipients, 17/55 died within the first five years, 16/75 died in the subsequent five years, 16/120 died in the third five years. We used the Cochran-Armitage chi-square test for trend and found that the rate of death varied significantly among the three periods with p-value = 0.010. Descriptive statistics of variables measured on the continuous scale are summarized in <xref ref-type="table" rid="table1">Table 1</xref>. MELD score was significantly higher among the dead recipients (p-value = 0.0001). Donor’s BMI was not significantly different (p-value = 0.253). Dead donors had mean age (30.64 years) which was significantly larger than the mean age of the survivors (32.5 years) with a p-value = 0.0001. Donors BMI was slightly higher among the survivors (mean = 23.84) as compared to the dead recipients (mean = 22.8), but the difference was marginally significant (p-value = 0.044).</p><p>We used the chi-square test to compare categorical variables in the two groups of transplant recipients. There was no significant difference in the death rate in males (30/154) when compared to females (20/96), the p-value = 0.795. The death rate in the infected recipients (whether viral or bacterial infection) was higher (24/66) as compared to the infection-free recipients (26/184) with p-value = 0.0001. Similarly, we found that the death rate of patients with renal impairment (14/19) was significantly higher than the rate of death in patients with no renal impairment (36/231) with p-value = 0.0001.</p><p>Several studies [<xref ref-type="bibr" rid="scirp.128869-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.128869-ref9">9</xref>] attempted to find a cut-off for MELD that will dis</p><p>The ROC area = 0.716 with 95% confidence interval (0.63 - 0.802) p-value = 0.0001.</p><p>Optimal cut-offs point for MELD is (24.5) giving sensitivity = 0.44 and specificity = 0.833.</p><p>The ROC area = 0.727 with 95% confidence interval (0.646 - 0.807) p-value = 0.0001.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Summary statistics of the transplanted patients stratified by patient status</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="2"  >Patient Status</th><th align="center" valign="middle" >MELD</th><th align="center" valign="middle" >BMI</th><th align="center" valign="middle" >Donor age</th><th align="center" valign="middle" >Donor BMI</th></tr></thead><tr><td align="center" valign="middle"  rowspan="3"  >0</td><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >19.02</td><td align="center" valign="middle" >26.68</td><td align="center" valign="middle" >25.93</td><td align="center" valign="middle" >23.84</td></tr><tr><td align="center" valign="middle" >N</td><td align="center" valign="middle" >200</td><td align="center" valign="middle" >200</td><td align="center" valign="middle" >200</td><td align="center" valign="middle" >200</td></tr><tr><td align="center" valign="middle" >Std. Deviation</td><td align="center" valign="middle" >5.567</td><td align="center" valign="middle" >4.808</td><td align="center" valign="middle" >5.491</td><td align="center" valign="middle" >3.246</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >1</td><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >24.82</td><td align="center" valign="middle" >27.68</td><td align="center" valign="middle" >30.64</td><td align="center" valign="middle" >22.80</td></tr><tr><td align="center" valign="middle" >N</td><td align="center" valign="middle" >50</td><td align="center" valign="middle" >50</td><td align="center" valign="middle" >50</td><td align="center" valign="middle" >50</td></tr><tr><td align="center" valign="middle" >Std. Deviation</td><td align="center" valign="middle" >7.951</td><td align="center" valign="middle" >7.875</td><td align="center" valign="middle" >5.934</td><td align="center" valign="middle" >3.295</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >Total</td><td align="center" valign="middle" >Mean</td><td align="center" valign="middle" >20.18</td><td align="center" valign="middle" >26.88</td><td align="center" valign="middle" >26.87</td><td align="center" valign="middle" >23.63</td></tr><tr><td align="center" valign="middle" >N</td><td align="center" valign="middle" >250</td><td align="center" valign="middle" >250</td><td align="center" valign="middle" >250</td><td align="center" valign="middle" >250</td></tr><tr><td align="center" valign="middle" >Std. Deviation</td><td align="center" valign="middle" >6.527</td><td align="center" valign="middle" >5.553</td><td align="center" valign="middle" >5.882</td><td align="center" valign="middle" >3.276</td></tr></tbody></table></table-wrap><p>The optimal cut-off point for donor’s age at donation was 32.5 years giving sensitivity = 0.45 and specificity = 0.834.</p><p>Our second objective is to model the joint effect of the selected risk factors on patients’ survival using a multivariate logistic regression model.</p></sec><sec id="s3"><title>3. Multivariate Analysis</title><p><xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref> show the ROC curves for MELD and donor’s age, respectively and the related information on such areas under the curves and the significance of the departure of each area from the 50% null point. We shall utilize the Propensity Score (PS) method to build a multivariate regression model that links the outcome of interest (mortality) to all the measured risk factors. The PS method involves calculating the conditional probability (propensity) of being in a specific period given a set of covariates, weighting the data based on these propensity scores, and then analyzing the outcome (mortality) using the weighted data. The fundamental objective of using the PS is to bring an observational or a retrospective investigation closer to the randomized prospective study design. The method of weighting we used in this paper is “weighting by the inverse PS”. It was proposed by Imbens [<xref ref-type="bibr" rid="scirp.128869-ref33">33</xref>] and further discussed by Hirano and Imbens [<xref ref-type="bibr" rid="scirp.128869-ref34">34</xref>] . It was shown that weighing based on the inverse of the PS produces unbiased estimates of the group effect. This method has nice mathematical properties as was demonstrated in [<xref ref-type="bibr" rid="scirp.128869-ref35">35</xref>] .</p><p>In <xref ref-type="table" rid="table2">Table 2</xref> we present the results of the maximum likelihood estimation of the</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> The maximum likelihood analysis of logistic regression</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="7"  >Analysis of Maximum Likelihood Estimates</th></tr></thead><tr><td align="center" valign="middle" >Parameter</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >DF</td><td align="center" valign="middle" >Estimate</td><td align="center" valign="middle" >Standard Error</td><td align="center" valign="middle" >Wald Chi-Square</td><td align="center" valign="middle" >Pr &gt; ChiSq</td></tr><tr><td align="center" valign="middle" >Intercept</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >9.3468</td><td align="center" valign="middle" >2.7973</td><td align="center" valign="middle" >11.1651</td><td align="center" valign="middle" >0.0008</td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.00871</td><td align="center" valign="middle" >0.0176</td><td align="center" valign="middle" >0.2436</td><td align="center" valign="middle" >0.6216</td></tr><tr><td align="center" valign="middle" >Sex</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.1582</td><td align="center" valign="middle" >0.2272</td><td align="center" valign="middle" >0.4845</td><td align="center" valign="middle" >0.4864</td></tr><tr><td align="center" valign="middle" >MELD</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >−0.1528</td><td align="center" valign="middle" >0.0385</td><td align="center" valign="middle" >15.7735</td><td align="center" valign="middle" >&lt;0.0001</td></tr><tr><td align="center" valign="middle" >BMI</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >−0.0946</td><td align="center" valign="middle" >0.0423</td><td align="center" valign="middle" >4.9973</td><td align="center" valign="middle" >0.0254</td></tr><tr><td align="center" valign="middle" >period</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >−0.2306</td><td align="center" valign="middle" >0.2590</td><td align="center" valign="middle" >0.7932</td><td align="center" valign="middle" >0.3731</td></tr><tr><td align="center" valign="middle" >Donors Age</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >−0.2052</td><td align="center" valign="middle" >0.0399</td><td align="center" valign="middle" >26.4858</td><td align="center" valign="middle" >&lt;0.0001</td></tr><tr><td align="center" valign="middle" >Donor BMI</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.1154</td><td align="center" valign="middle" >0.0686</td><td align="center" valign="middle" >2.8294</td><td align="center" valign="middle" >0.0926</td></tr><tr><td align="center" valign="middle" >infection</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >0.4200</td><td align="center" valign="middle" >0.2307</td><td align="center" valign="middle" >3.3138</td><td align="center" valign="middle" >0.0687</td></tr><tr><td align="center" valign="middle" >Renal impairment</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.0220</td><td align="center" valign="middle" >0.3513</td><td align="center" valign="middle" >8.4617</td><td align="center" valign="middle" >0.0036</td></tr></tbody></table></table-wrap><p>logistic regression model. As can be seen, MELD, patient’s BMI, donor’s age, and renal impairment have joint significant effects and are considered potential risk factors for death within five years from liver transplantation.</p><p>From <xref ref-type="table" rid="table3">Table 3</xref>, we conclude that when period 1 is the reference period the odds of death during that period are significantly higher than the odds of death in the subsequent two periods. One can then conclude that the quality of patients’ care has improved in the second and third periods relative to the first period.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Pairwise comparison of odds of death between periods</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  colspan="4"  >Odds Ratio Estimates: Pairwise comparison</th></tr></thead><tr><td align="center" valign="middle" >Effect</td><td align="center" valign="middle" >Point Estimate</td><td align="center" valign="middle"  colspan="2"  >95% Wald Confidence Limits</td></tr><tr><td align="center" valign="middle" >period 2 vs 1</td><td align="center" valign="middle" >1.954</td><td align="center" valign="middle" >1.562</td><td align="center" valign="middle" >2.445</td></tr><tr><td align="center" valign="middle" >period 3 vs 1</td><td align="center" valign="middle" >3.293</td><td align="center" valign="middle" >2.612</td><td align="center" valign="middle" >4.153</td></tr></tbody></table></table-wrap></sec><sec id="s4"><title>4. Discussion</title><p>It is well known that there is a global shortage of organs that can be used for transplant in patients with liver diseases. It is therefore very important to identify patients who benefit most from a liver transplantation and to detect risk factors associated with poor outcomes (mortality). The main findings of this study were that donor’s age, patient’s BMI, MELD, renal impairment are relevant for prediction of long-term patient survival. The association between infection and donor’s BMI was not significant in the multivariate logistic regression model. This finding contrasts with numerous previous studies that demonstrated a significantly decreased survival in recipients of older donations. Based on our work, strict recommendations for the acceptance or refusal of potential liver donors cannot be made. Moreover, we conclude that careful donor organ and recipient selection can lead to excellent results. One of the major strengths of this paper is the multivariate modeling and the use of propensity score weights which leads to bias reduction in the estimations of covariate effects.</p></sec><sec id="s5"><title>5. Conclusions</title><p>The main limitation of this study is the retrospective data collection. More studies involving larger samples are necessary to confirm the results obtained. In conclusion, knowing the factors that can determine a specific cause of early death in the post-transplant liver transplantation will allow us to stratify more accurately those patients at high risk of death.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Almousa, R.A. and Shoukri, M.M. (2023) Temporal Variations in Mortality after Liver Transplantation: Retrospective Investigation of Potential Risk Factors Using Propensity Score. 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