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Int J Med Sci 2017; 14(2):173-180. doi:10.7150/ijms.17502 This issue Cite

Research Paper

Risk factors for intraoperative massive transfusion in pediatric liver transplantation: a multivariate analysis

Seok-Joon Jin¹, Sun-Key Kim¹, Seong-Soo Choi¹, Keum Nae Kang², Chang Joon Rhyu², Shin Hwang³, Sung-Gyu Lee³, Jung-Man Namgoong³ , Young-Kug Kim¹

1. Department of Anesthesiology and Pain Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea;
2. Department of Anesthesiology and Pain Medicine, National Police Hospital, Seoul, Republic of Korea;
3. Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.

✉ Corresponding authors: Young-Kug Kim, MD, PhD, Professor, Department of Anesthesiology and Pain Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Republic of Korea. Tel: +82-2-3010-5976; Fax: +82-2-3010-6790; Email: kykseoul.kr; Jung-Man Namgoong, MD, PhD, Assistant Professor, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea. Tel: +82-2-3010-1512; Fax: +82-2-3010-6701; Email: namgoong2940com. More

Abstract

Background: Pediatric liver transplantation (LT) is strongly associated with increased intraoperative blood transfusion requirement and postoperative morbidity and mortality. In the present study, we aimed to assess the risk factors associated with massive transfusion in pediatric LT, and examined the effect of massive transfusion on the postoperative outcomes.

Methods: We enrolled pediatric patients who underwent LT between December 1994 and June 2015. Massive transfusion was defined as the administration of red blood cells ≥100% of the total blood volume during LT. The cases of pediatric LT were assigned to the massive transfusion or no-massive transfusion (administration of red blood cells <100% of the total blood volume during LT) group. Univariate and multivariate logistic regression analyses were performed to evaluate the risk factors associated with massive transfusion in pediatric LT. Kaplan-Meier survival analysis, with the log rank test, was used to compare graft and patient survival within 6 months after pediatric LT between the 2 groups.

Results: The total number of LT was 112 (45.0%) and 137 (55.0%) in the no-massive transfusion and massive transfusion groups, respectively. Multivariate logistic regression analysis indicated that high white blood cell (WBC) count, low platelet count, and cadaveric donors were significant predictive factors of massive transfusion during pediatric LT. The graft failure rate within 6 months in the massive transfusion group tended to be higher than that in the no-massive transfusion group (6.6% vs. 1.8%, P = 0.068). However, the patient mortality rate within 6 months did not differ significantly between the massive transfusion and no-massive transfusion groups (7.3% vs. 7.1%, P = 0.964).

Conclusion: Massive transfusion during pediatric LT is significantly associated with a high WBC count, low platelet count, and cadaveric donor. This finding can provide a better understanding of perioperative blood transfusion management in pediatric LT recipients.

Keywords: pediatric liver transplantation, massive transfusion, risk factors.

Introduction

Liver transplantation (LT) has been introduced as a curative treatment for children with end stage liver disease. Since Starzl performed the first successful pediatric LT in 1967 [1], the advances in the surgical techniques, anesthetic management, and immunosuppressant therapy have led to improvements in the long-term survival rate to >80% [2]. Nevertheless, hepatic graft failure may still develop, and often affects patient survival after LT. Death in most cases of pediatric LT occurs within 6 months of the LT [3]. In addition, massive blood loss and subsequent blood transfusion, which are associated with higher morbidity and mortality, are frequently noted during pediatric LT [4-8]. Liver cirrhosis, associated with a bleeding tendency during LT as a result of a complex hemostatic disorder, is not commonly observed in children. In contrast, biliary atresia, a very common disease requiring pediatric LT, is associated with peritoneal adhesion and recurrent inflammation of the bile tree, as most of these patients have previously undergone hepatoportoenterostomy and experience recurrent cholangitis [9]. Thus, peritoneal adhesion in these patients requires a greater amount of blood products and a longer operation time during intraabdominal surgery [10].

The total blood volume of neonates and children is usually small, and hence, there is a greater possibility of massive transfusion during major operations in pediatric patients. Although major advances have been made in surgical and anesthetic management to reduce the use of blood products during LT, the incidence of large blood loss during LT remains high. As the intraoperative blood transfusion requirement is directly related to poor outcomes [11-13], minimizing and predicting the need for massive transfusion during pediatric LT are important. However, only limited information is available regarding the risk factors for intraoperative massive transfusion in pediatric LT recipients.

In the present study, we aimed to evaluate the risk factors associated with massive transfusion during pediatric LT. Moreover, we examined the effect of massive transfusion on postoperative outcomes, such as graft failure and patient mortality, after pediatric LT.

Materials and Methods

Patient characteristics

The institutional review board of Asan Medical Center, Seoul, Republic of Korea approved this study. The medical records from the general ward and intensive care units, as well as data on the operation and anesthesia used, were retrospectively reviewed. We enrolled pediatric patients who underwent LT between December 1994 and June 2015. The exclusion criteria were as follows: incomplete data from medical records, preoperative anticoagulant use, and simultaneous transplantation of another organ. The demographic data, primary diagnosis, donor type, surgical technique for the donor, preoperative laboratory values, and intraoperative variables, as well as the presence of elective/emergent surgery, re-LT, ascites, chronic kidney disease, esophageal varix, fulminant hepatic failure, hepatic encephalopathy, peritonitis, previous abdominal surgery, and portal vein thrombosis were recorded to evaluate the risk factors for intraoperative massive transfusion.

General anesthesia

After routine monitoring (pulse oximetry, electrocardiography, and non-invasive blood pressure recording), general anesthesia was induced by using an intravenous bolus injection of thiopental sodium (5 mg/kg), fentanyl (0.5-1 μg/kg), and rocuronium (0.6 mg/kg) or vecuronium (0.15 mg/kg). After tracheal intubation, anesthesia was maintained using 1-2 vol% sevoflurane, 50% oxygen in medical air, a continuous infusion of fentanyl (3-5 μg/kg/h), and rocuronium (0.2 mg/kg/h) or vecuronium (0.05 mg/kg/h). Patients were mechanically ventilated at a constant tidal volume of 8-10 ml/kg, and the respiratory rate was adjusted to maintain the end-tidal carbon dioxide partial pressure between 35 and 40 mmHg during the operation. Arterial and central venous catheters were placed for hemodynamic monitoring and blood sampling. Crystalloid (plasma solution A, CJ Pharmaceutical, Seoul, Korea) and colloid (albumin) were administered during LT.

Surgical procedure

The surgical technique comprised a bilateral subcostal incision, with extension to the xiphoid, or an inverted T-shaped incision. Total hepatectomy was performed in the recipients after clamping the inferior vena cava, portal vein, and hepatic artery; a venous-venous bypass was not adopted. Prior to engraftment, the donor liver was flushed with 1000 ml of Histidine-Tryptophan-Ketoglutarate solution via the portal vein. Venoplasty of the hepatic vein and/or portal vein in the recipient was preceded by the an-hepatic phase, and engraftment was performed with the anastomosis of the hepatic vein, portal vein, and hepatic artery. We routinely checked the vascular perfusion of the liver graft using Doppler sonography after engraftment. Hemostasis was achieved by direct suture ligation or electrocoagulation. A Roux-en-Y hepaticojejunostomy was performed using interrupted sutures.

Definition of massive transfusion

Since the total blood volume in children varies according to age, the definition of massive transfusion in children should be relative to the total body volume of specific age groups [8]. The total blood volume in children aged >3 months was considered to be 70 ml/kg [14]. Massive transfusion was defined as the administration of red blood cells ≥100% of the total blood volume. The cases of pediatric LT were assigned to the massive transfusion group (administration of red blood cells ≥100% of the total blood volume during LT) or no-massive transfusion group (administration of red blood cells <100% of the total blood volume during LT). Intraoperative red blood cell transfusion was performed in cases where the hemoglobin level was <8.0 mg/dl.

Postoperative outcomes

The postoperative outcome measures included graft failure and patient mortality. We used the definition of early graft failure reported in previous studies [15-17]. We limited the survival analysis of grafts to 6 months in order to evaluate the influence of massive transfusion on early graft dysfunction and to minimize other factors that may contribute to late graft dysfunction, such as newly developed liver disease. We also defined early patient mortality as death that occurred within 6 months of the surgery.

Statistical analysis

Data were expressed as means ± standard deviation or number (%), as appropriate. Continuous variables were compared using Student's t-test or Mann-Whitney U test, whereas categorical variables were compared using the χ² test or Fisher's exact test, as appropriate. The most relevant risk factors associated with intraoperative massive transfusion were selected in the univariate logistic regression analysis. Variables with a P value <0.2 in the univariate logistic regression analysis were included in the final multivariate logistic regression analysis. In all other analyses, except for univariate logistic regression analysis, a P value <0.05 was considered statistically significant. Kaplan-Meier survival analysis, with a log rank test, was used to compare graft and patient survival within 6 months of pediatric LT, between the massive transfusion and no-massive transfusion groups. Statistical analyses were conducted using R (version 3.1.2; R Foundation for Statistical Computing, Vienna, Austria), SigmaStat for Windows (version 3.5; Systat Software, Inc., Chicago, IL), and SPSS for Windows (version 23.0.0; IBM Corporation, Chicago, IL).

Results

Of the 257 pediatric LT procedures conducted during the study period, 249 were included in the analysis (Figure 1). The recipient age ranged from 3 months to 17 years. The total volume of red blood cell transfusion for all patients was 126.7 ± 175.4 ml/kg. The distribution of the red blood cell transfusion amount is illustrated in Figure 2. Intraoperative massive transfusion was observed in 137 (55.0%) of 249 LT procedures, whereas 14 (5.6%) LT procedures did not require blood transfusion (Figure 2).

 Figure 1 

Study flow chart.

 Figure 2 

Histogram representing the distribution of the ratio of transfused red blood cell volume to total blood volume. No-massive transfusion (blue bars) indicates the administration of red blood cell <100% of the total blood volume during liver transplantation. Massive transfusion (red bars) indicates the administration of red blood cell ≥100% of the total blood volume during liver transplantation. LT, liver transplantation.

Preoperative characteristics were compared between the massive transfusion group and no-massive transfusion group (Table 1). The sex, donor type, and surgical technique for the donor excluding the left lateral segment, as well as the presence of ascites and chronic kidney disease significantly differed between the massive transfusion and no-massive transfusion groups (Table 1). The WBC, hemoglobin, platelet, protein, and C-reactive protein values were also significantly different between the 2 groups (Table 2). A greater amount of cryoprecipitate, fresh frozen plasma, platelet concentrate, crystalloid, and colloid was administered in the massive transfusion group than in the no-massive transfusion group (Table 2).

The results of univariate analysis are summarized in Table 3. Sex, cadaveric donor, and surgical technique for the donor; WBC, hemoglobin, platelet, albumin, and creatinine values; presence of emergent LT, re-LT, ascites, and chronic kidney disease; and operation time were selected for inclusion in the multivariate logistic regression analysis (P <0.2). Multivariate logistic regression analysis indicated that high WBC count, low platelet count, and cadaveric donor were significant predictive risk factors of massive transfusion during pediatric LT (Table 4).

The graft failure rate within 6 months of LT in the massive transfusion group tended to be higher than that in the no-massive transfusion group, although the values did not significantly differ (6.6% vs. 1.8%, P = 0.068) (Figure 3). However, the mortality rate within 6 months of LT did not differ significantly between the massive transfusion and no-massive transfusion groups (7.3% vs. 7.1%, P = 0.964) (Figure 3).

Discussion

In the present study, we found that the risk factors for intraoperative massive transfusion in pediatric LT were high WBC count, low platelet count, and cadaveric donor. We also found that early graft failure tended to be higher in the massive transfusion group than in the no-massive transfusion group.

Massive transfusion may be associated with serious complications such as hypothermia, electrolyte abnormalities, immunologic complications, coagulopathy, transfusion reactions, and postoperative mortality [14, 18, 19]. Although the factors predicting blood loss and transfusion during LT have been previously evaluated, those studies primarily included adult patients [13, 20-24]. Moreover, the factors influencing blood transfusion in pediatric LT were evaluated under preoperative conditions, with varying anatomical and surgical factors [4, 5]. However, the results have not been consistent, due to the differences in the preoperative status, surgical techniques [22], massive transfusion definitions [5], and transfusion triggers between studies. In our present study, we followed a commonly used definition of massive transfusion in children [14] and divided the cases into the massive blood transfusion and no-massive blood transfusion groups. Furthermore, we believe that our current results are reliable because the data were collected from a single institution that had highly experienced surgical and anesthetic teams [25-27].

 Figure 3 

Kaplan-Meier curves of graft survival (A) and patient survival (B) within 6 months of the pediatric liver transplantation. The blue solid line indicates patient or graft survival in the no-massive transfusion group. The red solid line indicates patient or graft survival in the massive transfusion group.

In our present series, a high WBC count was a unique factor that predicted intraoperative massive transfusion during pediatric LT. Previous studies have indicated that bacterial infections are common in patients with upper gastrointestinal hemorrhage [28-30], possibly because of preoperative invasive procedures, bacterial translocation in the intestine, and defects in the scavenging system [29, 31]. Bernard et al. showed that bacterial infection is not only an independent factor of bleeding in liver dysfunction patients, but is also an important prognostic factor for mortality [30]. The relationship between bleeding and bacterial infection in these studies supports our finding that leukocytosis can produce massive bleeding in patients with liver dysfunction. Moreover, peritoneal adhesion is inevitable after trans-peritoneal surgery. Children with biliary atresia, recurrent peritonitis, or cholangitis, which cause inevitable peritoneal adhesion, are commonly encountered, particularly among those with hepatoportoenterostomy. Adhesiolysis during LT can lead to increased blood loss [10], which may then contribute to massive transfusion in patients with coagulopathy or hemodynamic instability. Moreover, bacterial infection can lead to failure of bleeding control in the esophageal varix [32]. Our study suggests that massive transfusion during LT occurs more easily in children who are susceptible to bacterial infection and recurrent inflammation of the abdominal cavity.

Our finding of the association between low platelet count and massive transfusion is consistent with that observed in previous studies [22, 33]. Deakin et al. demonstrated that low platelet count was the best predictor of massive transfusion. Similarly, the intraoperative transfusion requirement during LT was strongly associated with lower platelet count [33]. Marino et al. showed that patients who could not maintain normal platelet levels, despite the preoperative correction of platelet counts, were likely to have a high level of blood usage [34]. Importantly, a lower platelet count is associated with impaired coagulation function, which can lead to bleeding and blood transfusion during pediatric LT.

We found that the incidence of massive transfusion was higher in patients who underwent cadaveric donor LT than in those who underwent living-donor LT [35]. Fasco et al. reported that patients who underwent living-donor LT required 66% fewer total blood products, as compared to those who underwent cadaveric donor LT, and that patients in the living-donor LT group had milder disease and more preserved coagulation function than those in the cadaveric donor LT group. In our present study, cadaveric donor LT was selected if the patient was undergoing an emergent operation or had fulminant hepatic failure, and if the patient did not have a living donor. However, some other studies have indicated conflicting results [7, 36, 37]. Pirate et al. did not observe a significant difference in blood transfusion between cadaveric donor LT and living-donor LT. The reasons for such discrepancies may be due to the differences in the preoperative conditions of patients, blood transfusion triggers, and inclusion criteria for LT recipients.

In our present analysis, the incidence of early graft failure tended to be higher in the massive transfusion group than in the no-massive transfusion group (6.6% vs. 1.8%, P = 0.068). Previous studies showed that massive transfusion was commonly associated with a wide range of complications, such as transfusion reactions to liver graft, systemic immunological deteriorations, metabolic deteriorations, and coagulopathy [14], and indicated the need for careful monitoring and strategy to reduce large blood loss and subsequent massive transfusion. Moreover, studies have reported a wide variation in graft survival [38, 39]. Hence, further study is needed to clarify the association between massive transfusion and graft failure in pediatric LT.

There is a possibility of selection bias due to the retrospective nature of the present study. As patients were not enrolled according to predefined criteria, the wide range of age, weight, height, or disease entity may affect our results. However, we assessed almost all the possible variables associated with massive transfusion. Hence, there is minimal possibility of bias in the selection of study patients.

In conclusion, we have found that high WBC count, low platelet count, and cadaveric donor are significant factors for predicting massive transfusion during pediatric LT. This result may offer valuable information on perioperative transfusion management in pediatric recipients who have a high risk of massive bleeding during LT.

Abbreviations

LT, liver transplantation; WBC, white blood cell.

Conflict of interests

The authors have no funding or other conflicts of interest to disclose.

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Author contact

Corresponding authors: Young-Kug Kim, MD, PhD, Professor, Department of Anesthesiology and Pain Medicine, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 05505, Republic of Korea. Tel: +82-2-3010-5976; Fax: +82-2-3010-6790; Email: kykseoul.kr; Jung-Man Namgoong, MD, PhD, Assistant Professor, Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul, 05505, Republic of Korea. Tel: +82-2-3010-1512; Fax: +82-2-3010-6701; Email: namgoong2940com.

Received 2016-9-7
Accepted 2016-12-21
Published 2017-2-8

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