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. 2021 Nov 25;21:444. doi: 10.1186/s12876-021-02026-7

Prognosis of liver transplantation: Does postoperative ileus matter?

Ruiping Bai 1, Rui An 1, Kunyu Han 1, Mengwen Xue 1, Simei Zhang 2, Xin Shen 1, Shaohua Zheng 1,
PMCID: PMC8620943  PMID: 34823485

Abstract

Background

Nowadays, liver transplantation has become a main therapy for end-stage liver disease. However, studies show that there are high mortality and severe complications after liver transplantation. Although gastrointestinal dysfunction is a common and major complication after liver transplantation, there was rarely relative research. This study aims to elucidate the factors about ileus after liver transplantation and patients’ survival.

Methods

We collected and analyzed the data (n = 318, 2016–2019) from the First Affiliated Hospital of Xi’an Jiaotong University. After excluding cases, a total of 293 patients were included for this study. The subjects were divided into a non-ileus group and an ileus group. We reviewed 38 variables (including preoperative, operative and postoperative relative factors). Additionally, other complications after liver transplantation and survival data were compared between two groups.

Results

Of the 293 patients, 23.2% (n = 68) experienced postoperative ileus. Ileus patients were not different with non-ileus patients in preoperative, operative and postoperative factors. HBV-positive patients with ileus had a lower MELD score (P = 0.025), and lower postoperative total bilirubin was correlated with ileus (P = 0.049). Besides, Child–Pugh score of HCC patients with ileus was low (P = 0.029). The complications after liver transplantation were not different between two groups. Compared with the patients without ileus, the patients with ileus had a higher mortality rate.

Conclusion

According to our research, ileus-patients had a lower 1-year survival rates. The preoperative MELD score and postoperative total bilirubin of HBV-positive patients with ileus were lower, and Child–Pugh score of HCC patients with ileus was also lower.

Keywords: Liver transplantation, Postoperative ileus, MELD score, Child–Pugh score

Background

Liver disease accounts for approximately 2 million deaths every year worldwide [1]. Apart from cirrhosis and hepatocellular carcinoma due to viral hepatitis as well as alchohol, non-alchoholic fatty liver disease and drug induced hepatitis continue to increase as a main cause of acute liver injury. Liver diseases were estimated to become the 12th leading cause of mortality by 2020 [2]. Liver transplantation (LT) becomes a major therapy for liver diseases, especially the end-stage liver disease [1, 3, 4]. However, the needs of liver transplantation far exceed the supply. Current liver transplantation rates were less than 10% needs of organ transplantation [1]. Although the survival rate of liver transplantation has improved greatly in recent years, there are still many complications that affect prognosis and life span [5].

The clinical researches about cardiovascular disease, acute kidney injury and thrombosis after LT are most common, and gastrointestinal dysfunction is an ordinary complication after surgery, but postoperative ileus (POI) after LT is rare [68]. Postoperative ileus is a common complication following especially open abdominal surgery. Preoperative malnutrition, operative procedure, anesthesia and postoperative managements may increase the risk of gastrointestinal dysfunction [9]. According to clinical experience, once the gastrointestinal function is abnormal, the recovery of LT patients is delayed, even may affect survival rate of patients. Our study is designed to identify risk factors, obtain possible predictive factors and the effects of ileus to survival rate after LT patients.

Methods

Data collection

We collected the data from the First Affiliated Hospital of Xi’an Jiaotong University from January 2016 to March 2019 all recipients that underwent orthotopic liver transplantation (OLT). All of the liver grafts were from cardiac-dead donors. We excluded the candidates who were in gastrointestinal dysfunction before surgery, needed enteral feeding or nasogastric tube after surgery, homeostasis disturbance, secondary liver transplantation, multiple organ dysfunction syndrome (MODS) before surgery, critically ill after surgery (included extended immobility or narcotic use) and incomplete data. The duct-to-duct biliary reconstruction was performed for every patient, and there were no any cases of biliodigestive anastomosis. Data elements included preoperative, operative and postoperative factors. Additionally, patients were classified as postoperative ileus when the time of the first passage of flatus and the first defecation was over 72 h, or normal. In our study, all ileus-patients were paralytic ileus without requiring reoperation for adhesiolysis, and there were no patients with mechanical ileus.

Follow up

In view of regular check-up of post-LT patients, we used the inhospital or outhospital numbers, which are unique to each patient, to obtain patients’ outcome in this study. The single endpoint of the study was all-cause mortality. Observations were stopped at the date of one year after surgery. Finally, 293 patients finished follow up.

Statistic analysis

The patients were categorized into 2 groups according to postoperative ileus. Continuous variables were summarized as means ± standard deviation or median and interquartile ranges, whereas frequencies and percentages were used for categorical variables. Student’s t-test or Mann–Whitney U-test for continuous independent variables, the Pearson chi2 test or Fisher’s exact test was used to compare qualitative variables. The log-rank test (Mantel-Cox) was used to compare group survival curves. Statistical significance for all analyses was determined at P < 0.05. All analyses were undertaken by using Statistical Package for Social Sciences (SPSS) software, version 25.0 (IBM SPSS, Armonk, NY, USA).

Results

Patient’s characteristics of eligible transplanted cohort

There were 293 patients who were eligible and finished the follow up. The mean age of the transplanted population was 48 (40.00–55.00) and 76.5% were males. The most common atiology of liver diseases were chronic hepatitis B (46.4%), primary hepatic carcinoma (31.4%), and chronic hepatitis C (4.1%). Less common atiology included alcohol liver disease (7 patients), autoimmune hepatitis (7 patients), cholestatic hepatitis (7 patient), and NASH (31 patients) (Table 1).

Table 1.

Preoperative and operative relative factors

Over all (n = 293) Ileus (n = 68) Non-ileus (n = 225) P value
Preoperative characteristics
 Age (years) 48.0 (40.00–55.00) 48.0 (37.00–54.75) 47.9 ± 10.08 0.676
 Male 224.0 (76.50%) 53.0 (77.90%) 171.0 (76.00%) 0.741
 BMI (kg/m2) 22.5 (20.76–24.47) 22.6 ± 3.19 22.3 (20.76–24.39) 0.952
 History of abdominal surgery 75.0 (25.60%) 20.0 (29.40%) 55.0 (24.40%) 0.411
 Hepatic encephalopathy 33.0 (11.30%) 7.0 (10.30%) 26.0 (11.60%) 0.773
 Portal hypertension 197.0 (67.20%) 47.0 (69.10%) 150.0 (66.70%) 0.706
 Pleural fluid or ascites 143.0 (48.80%) 31.0 (45.60%) 112.0 (49.80%) 0.545
 Child–Pugh 10.0 (9.00–11.00) 10.0 (8.00–11.00) 10.0 (9.00–11.00) 0.289
 MELD score 15.0 (11.00–23.00) 14.5 (10.00–19.75) 16.0 (11.50–23.00) 0.058
 Albumin (g/L) 36.8 (32.90–42.20) 36.7 ± 6.57 37.0 (32.95–42.25) 0.432
 Total bilirubin (umol/L) 44.8 (25.05–135.40) 44.8 (22.30–98.40) 44.8 (26.10–168.35) 0.363
 Serum creatinine (umol/L) 56.0 (46.00–67.00) 57.0 (45.50–75.00) 55.0 (46.00–66.00) 0.370
 Preoperative lactic acid 1.5 (1.10–1.90) 1.5 (1.00–2.00) 1.4 (1.10–1.90) 0.725
 Atiology of liver disease
  Chronic hepatitis B 136.0 (46.40%) 34.0 (50.00%) 102.0 (45.30%) 0.499
  Primary hepatic carcinoma 92.0 (31.40%) 18.0 (26.50%) 74.0 (32.90%) 0.318
  Chronic hepatitis C 12.0 (4.10%) 1.0 (1.50%) 11.0 (4.90%) 0.370
  Alcoholic hepatitis 7.0 (2.40%) 1.0 (1.50%) 6.0 (2.70%) 0.910
  Autoimmune hepatitis 7.0 (2.40%) 4.0 (5.90%) 3.0 (1.30%) 0.089
  Cholestatic Cirrhosis 7.0 (2.40%) 1.0 (1.50%) 6.0 (2.70%) 0.910
  Other 31.0 (10.60%) 9.0 (13.20%) 22.0 (9.80%) 0.417
Intraoperative factors
 Operation time (min) 365.0 (330.00–420.00) 377.0 ± 81.52 367.0 (330.00–420.00) 0.668
 Anhepatic phase (min) 50.0 (45.00–57.00) 51.4 ± 11.59 51.0 (45.00–57.00) 0.578
 Portal vein clamping time (min) 58.0 (52.50–65.00) 57.0 (52.00–65.50) 58.0 (53.00–65.00) 0.546
 Blood loss during operation (ml) 1000.0 (650–2000) 1000.0 (625–1600) 1000.0 (650–2000) 0.661
 Total infusion fluid (ml) 5660.0 (4735–6690) 5750.7 ± 1653.65 5700.0 (4780–6710) 0.385
 Intraoperative RBC transfusion (units) 8.0 (4.00–12.00) 8.0 (4.00–11.75) 8.0 (6.00–12.00) 0.167
 Intraoperative cryoprecipitate transfusion(units) 1200.0 (800–1600) 1000.0 (800.00–1550.00) 1200.0 (800.00–1600.00) 0.177
 Retention time of tracheal tube (hours) 7.2 (5.25–9.63) 7.3 (5.50–9.44) 7.2 (5.00–9.88) 0.917
 Length of SICU (days) 6.0 (5.00–10.00) 6.0 (5.00–9.50) 7.0 (5.00–10.00) 0.394
 Length of hospital stay (days) 19.0 (15.00–24.50) 19.5 (15.00–23.75) 19.0 (15.00–26.00) 0.947
 Anesthesia factors
  Propofol (mg) 1500.0 (1300.00–1820.00) 1500.0 (1200.00–1930.00) 1500.0 (1300.00–1800.00) 0.826
  Sufentanil (ug) 30.0 (30.00–40.00) 30.0 (30.00–40.00) 30.0 (30.00–40.00) 0.101
  Renifentanil (ug) 3000.0 (2517–3800) 3000.0 (2400–3956) 3000.0 (2600–3600) 0.773
  Sevoflurane (ml) 60.0 (50.00–80.00) 60.0 (50.00–70.00) 60.0 (50.00–80.00) 0.796
  Dexmedetomidine (ug) 120.0 (100.00–180.00) 111.0 (100.00–150.00) 120.0 (85.00–180.00) 0.881
  Etomidate (mg) 14.0 (10.00–16.00) 14.0 (11.25–16.00) 14.00 (10.00–16.00) 0.572

Preoperative risk factors of postoperative ileus

The study demonstrated that age, male, BMI (body mass index), history of abdominal surgery, hepatic encephalopathy, portal hypertension, Model for End-Stage Liver Disease (MELD score), platelet counts, albumin, total bilirubin, serum creatinine, lactic acid and atiology of liver disease were not significantly different between groups (Table 1).

Table 2 shows the results of risk factors for HBV-positive patients with and without ileus. Except for MELD score (P = 0.025), no significant differences were observed between patients with and without ileus for other factors analyzed.

Table 2.

Preoperative and operative relative factors of patients with HBV

Over all (n = 192) Ileus (n = 47) Non-ileus (n = 145) P value
Preoperative characteristics
 Age (years) 45.4 ± 9.17 45.7 ± 9.25 46.5 ± 9.41 0.633
 Male 158.0 (82.30%) 40.0 (85.10%) 118.0 (81.40%) 0.561
 BMI (kg/m2) 22.2 (20.76–24.22) 22.8 ± 2.94 22.328 (20.76–24.39) 0.772
 History of abdominal surgery 49.0 (25.50%) 14.0 (29.80%) 35.0 (24.10%) 0.440
 Hepatic encephalopathy 21.0 (10.90%) 4.0 (8.50%) 17.0 (11.70%) 0.540
 Portal hypertension 135.0 (70.30%) 34.0 (72.30%) 101.0 (69.70%) 0.726
 Pleural fluid or ascites 89.0 (46.40%) 20.0 (42.60%) 69.0 (47.60%) 0.548
 Child–Pugh 10.0 (9.00–12.00) 9.4 ± 2.06 10.0 (9.00–11.50) 0.055
 MELD score 16.0 (12.00–24.00) 13.0 (9.00–19.00) 16.0 (11.00–23.00) 0.025
 Albumin (g/L) 35.7 (31.80–41.48) 37.0 ± 6.90 37.1 (32.90–43.30) 0.536
 Total bilirubin (umol/L) 45.9 (25.93–127.05) 32.7 (21.30–98.50) 46.8 (26.05–126.70) 0.140
 Serum creatinine (umol/L) 57.0 (46.00–71.75) 57.0 (44.00–76.00) 55.0 (46.00–66.00) 0.499
 Preoperative lactic acid 1.5 (1.10–1.88) 1.5 (1.00–1.80) 1.4 (1.10–1.80) 0.722
Intraoperative factors
 Operation time (min) 390.0 (330.00–420.00) 371.4 ± 93.24 365.0 (330.00–420.00) 0.401
 Anhepatic phase (min) 50.0 (45.00–57.00) 50.0 (45.00–59.00) 51.0 (45.00–57.50) 0.862
 Portal vein clamping time (min) 58.50 (53.00–65.75) 58.0 (53.00–67.00) 59.0 (52.50–65.50) 0.930
 Blood loss during operation (ml) 1200.0 (800–2000) 1000.0 (600–1600) 1200.0 (800–2000) 0.446
 Total infusion fluid (ml) 5830.0 (5032–6820) 5410.0 (4490–6524) 5710.0 (4690–6725) 0.210
 Intraoperative RBC transfusion (units) 8.0 (6.00–12.00) 6.0 (4.00–12.00) 8.0 (4.50–12.00) 0.167
 Intraoperative cryoprecipitate transfusion (units) 1400.0 (1000–1600) 1000.0 (800.00–1600.00) 1200.0 (1000–1600) 0.245
 Retention time of tracheal tube (hours) 7.0 (5.00–9.50) 6.3 (5.25–11.00) 7.3 (5.00–9.63) 0.328
 Length of SICU (days) 6.0 (4.00–10.00) 6.0 (4.00–8.00) 7.0 (5.00–10.00) 0.213
 Length of hospital stay (days) 18.0 (14.00–23.00) 18.0 (14.00–23.00) 18.0 (15.00–26.00) 0.721
 Anesthesia factors
  Propofol (mg) 1500.0 (1400–1885) 1609.6 ± 452.87 1500.0 (1300–1990) 0.985
  Sufentanil (ug) 30.0 (30.00–40.00) 30.0 (25.00–40.00) 30.0 (30.00–40.00) 0.209
  Renifentanil (ug) 3000.0 (2725–4000) 3219.6 ± 996.15 3000.0 (2600–4000) 0.868
  Sevoflurane (ml) 60.0 (50.00–80.00) 60.0 (50.00–80.00) 60.0 (50.00–70.00) 0.355
  Dexmedetomidine (ug) 116.0 (80.25–186.75) 100.0 (100.00–150.00) 120.0 (80.00–189.50) 0.627
  Etomidate (mg) 14.0 (10.00–16.00) 14.0 (12.00–16.00) 14.0 (10.00–16.00) 0.288

Bold italics means P < 0.05

There were not different between with and without ileus of HCC (hepatocellular carcinoma) patients for intraoperative risk factors, except for Child–Pugh score (P = 0.029; Table 3).

Table 3.

Preoperative and operative relative factors of patients with HCC

Over all (n = 92) Ileus (n = 18) Non-ileus (n = 74) P value
Preoperative characteristics
 Age (years) 50.1 ± 9.33 50.2 ± 8.83 50.0 ± 9.51 0.959
 Male 77.0 (83.70%) 18.0 (100.00%) 59.0 (79.70%) 0.083
 BMI (kg/m2) 23.3 ± 3.33 23.4 ± 2.75 23.2 ± 3.47 0.832
 History of abdominal surgery 17.0 (18.50%) 4.0 (22.20%) 13.0 (17.60%) 0.906
 Hepatic encephalopathy 3.0 (3.30%) 0 (0.0%) 3.0 (4.10%) 1.000
 Portal hypertension 47.0 (51.10%) 10.0 (55.60%) 37.0 (50.00%) 0.672
 Pleural fluid or ascites 30.0 (32.60%) 6.0 (33.30%) 24.0 (32.40%) 0.942
 Child–Pugh 9.0 (8.00–11.00) 8.0 (6.00–10.25) 9.0 (8.00–11.00) 0.029
 MELD score 12.0 (9.00–18.00) 11.6 ± 4.46 12.0 (10.00–19.25) 0.081
 Albumin (g/L) 39.7 ± 5.97 36.0 ± 7.06 39.9 ± 6.12 0.488
 Total bilirubin (umol/L) 34.9 (19.47–77.48) 30.9 (15.48–68.48) 35.5 (19.63–87.63) 0.425
 Serum creatinine (umol/L) 55.0 (46.00–64.75) 63.1 ± 26.72 54.5 (46.00–63.25) 0.394
 Preoperative lactic acid 1.3 (1.03–1.70) 1.4 (1.00–1.80) 1.3 (1.08–1.70) 0.657
Intraoperative factors
 Operation time (min) 360.0 (300.00–420.00) 369.2 ± 71.71 360.0 (300.00–412.50) 0.726
 Anhepatic phase (min) 50.0 (45.00–57.75) 52.4 ± 12.67 50.0 (45.00–57.25) 0.976
 Portal vein clamping time (min) 58.5 (52.75–65.25) 58.0 (51.00–67.00) 59.0 (53.00–65.00) 0.774
 Blood loss during operation (ml) 800.0 (500.00–1200.00) 800.0 (575.00–1050.00) 800.0 (500.00–1225.00) 0.832
 Total infusion fluid (ml) 4915.0 (4285–5960) 4656.2 ± 1190.72 5070.0 (4308–6145) 0.080
 Intraoperative RBC transfusion (units) 5.0 (2.00–9.50) 4.0 (1.50–6.50) 6.0 (2.00–10.00) 0.181
 Intraoperative cryoprecipitate transfusion (units) 800.0 (600.00–1200.00) 800.0 (750.00–1000.00) 800.0 (600.00–1200.00) 0.420
 Retention time of tracheal tube (hours) 7.0 (5.00–9.88) 9.2 ± 4.63 6.8 (5.00–9.31) 0.162
 Length of SICU (days) 6.0 (5.00–9.00) 6.0 (5.00–8.00) 6.0 (5.00–9.00) 0.714
 Length of hospital stay (days) 18.0 (15.00–25.75) 17.5 (14.00–22.50) 19.0 (15.00–26.00) 0.427
 Anesthesia factors
  Propofol (mg) 1500.0 (1200–1970) 1522.2 ± 542.93 1500.0 (1300–1909) 0.432
  Sufentanil (ug) 30.0 (30.00–40.00) 30.0 (30.00–40.00) 30.0 (30.00–40.00) 0.791
  Renifentanil (ug) 3000.0 (2500–3750) 3116.7 ± 1169.84 3000.0 (2500–3650) 0.596
  Sevoflurane (ml) 50.0 (50.00–80.00) 50.0 (50.00–62.50) 55.0 (47.50–80.00) 0.920
  Dexmedetomidine (ug) 100.0 (100.00–160.00) 100.0 (100.00–162.50) 100.0 (89.25–160.00) 0.783
  Etomidate (mg) 14.0 (12.00–16.00) 14.0 (12.00–16.00) 14.0 (11.50–16.00) 0.284

Bold italics means P < 0.05

Intraoperative and postoperative risk factors of postoperative ileus

Intraoperative factors included duration of surgery, anhepatic phase, blood loss, total infusion fluid, red cell transfusion, cryoprecipitate transfusion and anesthesia (drug doses of propofol, sufentanil, renifentanil, sevoflurane, dexmedetomidine and etomidate) were not different among groups (Table 1). Retention time of tracheal tube, length of Intensive Care Unit of Surgery (SICU), length of hospital-stay, total bilirubin, lactic acid, platelet counts were postoperative possible risk factors. All were not different (Table 4).

Table 4.

Postoperative characteristics and complications

Over all (n = 293) Ileus (n = 68) Non-ileus (n = 225) P value
Postoperative characteristics
 Total bilirubin (umol/L) 62.1 (40.53–106.05) 58.0 (40.30–94.28) 65.0 (41.13–112.90) 0.315
 Lactic acid 2.1 (1.40–3.53) 2.3 (1.40–4.58) 2.0 (1.40–3.23) 0.123
 Platelet (× 10^9/L) 48.5 (35.00–73.00) 50.5 (39.00–82.75) 48.0 (32.75–70.25) 0.217
Complications
 Pulmonary infection 6 (2.04%) 3 (4.41%) 3 (1.33%) 0.140
 Kidney injury 3 (1.02%) 1 (1.47%) 2 (0.89%) 0.549
 Biliary infection 12 (4.10%) 5 (7.35%) 7 (3.11%) 0.158
 Vascular complication 5 (1.71%) 2 (2.94%) 3 (1.33%) 0.329
 Others 16 (5.46%) 4 (5.88%) 12 (5.33%) 0.770

There were not different between with and without ileus of HBV-positive patients for intraoperative risk factors (Table 2), but postoperative total bilirubin was significantly different between groups (P = 0.049; Table 5).

Table 5.

Postoperative characteristics and complications of patients with HBV

Over all (n = 192) Ileus (n = 47) Non-ileus (n = 145) P value
Postoperative characteristics
 Total bilirubin (umol/L) 62.7 (43.00–106.73) 61.1 ± 30.44 66.4 (44.65–116.58) 0.049
 Lactic acid 2.2 (1.30–3.53) 2.3 (1.55–4.05) 2.1 (1.30–3.18) 0.186
 Platelet (× 10^9/L) 49.5 (35.00–70.75) 47.0 (38.75–75.50) 50.0 (35.00–69.75) 0.820
Complications
 Pulmonary infection 4 (2.08%) 2 (4.26%) 2 (1.38%) 0.252
 Kidney injury 3 (1.56%) 1 (2.13%) 2 (1.38%) 0.571
 Biliary infection 6 (3.13%) 2 (4.26%) 4 (2.76%) 0.636
 Vascular complication 2 (1.04%) 1 (2.13%) 1 (0.69%) 0.431
 Others 8 (4.17%) 2 (4.26%) 6 (4.14%) 1.000

Bold italics means P < 0.05

Tables 3 and 6 showed that no significant differences were observed in HCC patients with and without ileus for intraoperative and postoperative risk factors.

Table 6.

Postoperative characteristics and complications of patients with HCC

Over all (n = 92) Ileus (n = 18) Non-ileus (n = 74) P value
Postoperative characteristics
 Total bilirubin (umol/L) 61.8 (35.15–115.60) 60.3 (36.93–115.13) 62.9 (34.85–115.60) 0.686
 Lactic acid 2.0 (1.40–3.40) 2.8 ± 1.62 1.9 (1.40–3.40) 0.401
 Platelet (× 10^9/L) 50.5 (35.25–69.50) 57.8 ± 28.36 50.0 (35.00–64.75) 0.638
Complications
 Pulmonary infection 3 (3.26%) 1 (5.56%) 2 (2.70%) 0.484
 Kidney injury 2 (2.17%) 1 (5.56%) 1 (1.35%) 0.355
 Biliary infection 3 (3.26%) 1 (5.56%) 2 (2.70%) 0.484
 Vascular complication 2 (11.80%) 1 (5.56%) 1 (1.35%) 0.355
 Others 4 (11.80%) 1 (5.56%) 3 (4.05%) 1.000

Complications of transplanted cohort

Within the 30 days after surgery, the most common complications were biliary infection or stricture (4.1%), pulmonary infection (2.04%), vascular complication (1.71%), and kidney injury (1.02%). Other complications included acute injection (3 patients), abdominal infection (2 patients), recurrence of hepatocellular carcinoma (5 patients), sepsis (1 patients), coagulation disorders (4 patients), and acute pancreas (1 patient). Between ileus group and non-ileus group were not different (all P > 0.05; Table 4). There were no differences in complications between patients with and without ileus of HBV-positive patients (Table 5). Furthermore, no significant differences were observed in HCC (hepatocellular carcinoma) patients with and without ileus (Table 6).

Overall survival rates of ileus and normal patients

Univariate analysis of 52 patients showed that 1-, 2- and 3-year overall survival rates post-LT were 89%, 89% and 89% in ileus patients, respectively, and 91%, 88% and 88% in non-ileus patients, respectively. The mean survival time was 11.24 months in patients with ileus and 11.76 months in patients without ileus in 1-year overall survival analysis. Kaplan–Meier survival curves showed that the overall survival rate was significantly different (P = 0.008) between groups (Fig. 1A).

Fig. 1.

Fig. 1

Overall (A), HBV-positive (B) and HCC (C) survival rates of ileus and non-ileus patients

1-, 2- and 3-year overall survival rates post-LT of HBV-positive patients were 87%, 87% and 87% in ileus patients, respectively, and 91%, 91% and 91% in normal patients, respectively. 1-year overall survival rates post-LT were not different among groups (P = 0.174; Fig. 1B).

1-, 2- and 3-year overall survival rates post-LT of HCC patients were 88%, 88% and 88% in ileus patients, respectively, and 93%, 88% and 88% in normal patients, respectively. 1-year overall survival rates post-LT were not different among groups (P = 0.580; Fig. 1C).

Donor's characteristics of ileus and normal patients

Table 7 shows the results of donor's characteristics for patients with and without ileus. There were no significant differences between patients with and without ileus for the factors analyzed.

Table 7.

The donor's characteristics

Over all (n = 293) Ileus (n = 68) Non-ileus (n = 225) P value
Age (years) 50.0 (39.00–58.00) 52.0 (39.25–59.00) 50.0 (39.00–58.00) 0.439
Male 257.0 (87.70%) 60.0 (88.20%) 197.0 (87.60%) 0.881
BMI (kg/m2) 22.5 (20.52–24.31) 22.5 (20.76–24.35) 22.2 ± 3.13 0.502
Warm ischemia time (min) 14.0 (11.00–15.00) 12.5 (10.25–15.00) 14.0 (11.00–15.50) 0.180
Cold ischemia time (hours) 6.0 (5.00–6.00) 6.0 (5.00–6.00) 6.0 (5.00–6.00) 0.527

Discussion

Liver transplantation is not only a definitive treatment for liver diseases, but also is the second most common solid organ transplantation. Although doctors and researchers take complications of liver transplantation seriously and carry out treatments, POI is ignored by researchers. Postoperative ileus is a common complication after most abdominal surgeries, which is associated with longer hospitalization and increased medical costs [10]. Fluid overload, exogenous opioids, surgical procedure are key mechanisms of POI [11, 12]. Among the 293 patients enrolled in this study with liver diseases who underwent LT, univariate analysis indicated that there was no significant difference in preoperative, intraoperative and postoperative factors between patients with and without POI, apart from the lower MELD score and postoperative total bilirubin in HBV-patients with ileus, and Child-pugh score of HCC patients with ileus was low. Study has reported that goal-directed fluid therapy does not reduce postoperative ileus in gastrointestinal surgery. It is possible that fluid overload is not necessary risk factor [13], which also been proved in our results. Besides, patients with POI had worse overall survival rates than patients without POI.

Model of end-stage liver disease (MELD) and Child–Pugh scores have been widely used to assess the prognosis and predict the outcomes of cirrhotic patients [14]. MELD score is incorporated only 3 objective variables, including total bilirubin, creatinine and INR. Studies has proved that the MELD score system could reduce the mortality in patients waiting for a liver transplantation, and downgrading MELD score can improve the outcomes after liver transplantation in patients with acute-on-chronic hepatitis B liver failure [15, 16]. The Child–Pugh score, based on clinical symptoms of insufficient liver function (ascites/encephalopathy), and laboratory analysis of parameters of liver function (albumin, bilirubin, and PT) can be used to identify low or high-risk patients [17]. And the Child–Pugh score has been proved that it is not only as a predictor of postoperative mortality after portocaval shunt surgery but also predicts mortality risk associated with other major operations [18].The preoperative MELD score and postoperative total bilirubin of HBV-positive patients with ileus were lower than without ileus. And Child–Pugh score of HCC patients with ileus was lower than without ileus. There were no differences in other observed factors and overall survival rates among groups. MELD and Child–Pugh scores are lower, the liver function is better. According to the results, we can get that POI after liver transplantation may predict the recovery of normal liver function. Then, complications after liver transplantation including biliary infection, vascular complication, pulmonary infection, kidney injury were not different in LT patients with ileus and without ileus according to our study. We demonstrated that compared with the patients without ileus, the patients with ileus had a higher mortality rate within one year after surgery, which is consistent with the clinical observation.

Several limitations of this study must be considered. First, this study was retrospective. Second, postoperative ileus was determined based on medical history, and the diagnosis of postoperative ileus lacks objective standards, which needs further research and discussion of professionals, especially ileus after liver transplantation. However, this study indicate that ileus of liver transplantation is a worthy research direction and demands sufficient clinical attention.

Conclusion

In conclusion, compared with non-ileus patients, we didn’t obtain the risk factors of patients with ileus. Ileus-patients didn’t increase complications after liver transplantation, but decrease post-LT one-year survival rates. But the preoperative MELD score and postoperative total bilirubin of HBV-positive patients with ileus were lower, and Child–Pugh score of HCC patients with ileus was also lower. A future prospective cohort study with larger a sample size should be conducted to confirm these observations, or POI may not be vital in the liver transplantation patients.

Acknowledgements

Not applicable.

Abbreviations

LT

Liver transplantation

POI

Postoperative ileus

OLT

Orthotopic liver transplantation

MODS

Multiple organ dysfunction syndrome

BMI

Body mass index

MELD score

Model for End-Stage Liver Disease

HCC

Hepatocellular carcinoma

SICU

Intensive Care Unit of Surgery

Authors' contributions

RpB contributed to the methodology, data collection, data analysis and writing-original draft; RA and KyH contributed to the data collection, software, data analysis; MwX and SmZ contributed to the writing-review; XScontributed to the research design, writing-review & editing; ShZ contributed to the research design, project administration, writing-review & editing. All authors have read and approved the manuscript.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for profit sectors.

Availability of data and materials

The data that support the findings of this study are available from the corresponding authors.

Declarations

Ethics approval and consent to participate

The institutional review board of the First Affiliated Hospital of Xi’an Jiaotong University approved this retrospective study.

Consent for publication

Not applicable.

Competing interest

The authors declare that they have no conflict of interest.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data that support the findings of this study are available from the corresponding authors.


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