Abstracts
INTRODUCTION:
Liver transplantation is the best therapeutic option for end-stage liver disease. Non-selective beta-blocker medications such as propranolol act directly on the cardiovascular system and are often used in the prevention of gastrointestinal bleeding resulting from HP. The effects of propranolol on cardiovascular system of cirrhotic patients during liver transplantation are not known.
OBJECTIVE:
Evaluate the influence of propranolol used preoperatively on cardiac index during the anhepatic phase of liver transplantation.
METHOD:
101 adult patients (73 male [72.2%]) who underwent cadaveric donor orthotopic liver transplantation by piggyback technique with preservation of the retrohepatic inferior vena cava performed at Hospital das Clinicas, Federal University of Minas Gerais were evaluated. There was no difference in severity between groups by the MELD system, p = 0.70. The preoperative use of propranolol and the cardiac index outcome were compared during the anhepatic phase of liver transplantation in 5 groups (I: increased cardiac index, II: cardiac index reduction lower than 16%, III: cardiac index reduction equal to or greater than 16% and less than 31%, IV: cardiac index reduction equal to or greater than 31% and less than 46%, V: cardiac index reduction equal to or greater than 46%).
RESULTS:
Patients in group I (46.4%) who received propranolol preoperatively were statistically similar to groups II (60%), III (72.7%), IV (50%) and V (30.8%), p = 0.57.
CONCLUSION:
The use of propranolol before transplantation as prophylaxis for gastrointestinal bleeding may be considered safe, as it was not associated with worsening of cardiac index in anhepatic phase of liver transplantation.
Liver transplant; Cardiac output; Beta-adrenergic antagonist; Propranolol
INTRODUÇÃO:
O transplante hepático (TH) é a melhor opção terapêutica para doença hepática em estágio terminal (DHET). As medicações betabloqueadoras não seletivas, como o propranolol, atuam diretamente no sistema cardiovascular (SCV) e são frequentemente usadas na prevenção de hemorragia digestiva decorrente da HP. Os efeitos do propranolol no SCV de cirróticos durante o TH não são conhecidos.
OBJETIVO:
Avaliar a influência do uso pré-operatório do propranolol no índice cardíaco (IC) durante a fase anepática do TH.
MÉTODO:
Avaliaram-se 101 pacientes adultos (73 homens, 72,2%) submetidos a transplante ortotópico de fígado doador cadáver, pela técnica de piggyback com preservação da veia cava inferior retro-hepática, feito no Hospital das Clínicas da Universidade Federal de Minas Gerais. Não houve diferença de gravidade pelo sistema MELD entre os grupos, p = 0,70. Foram comparados o uso pré-operatório de propranolol com o desfecho do IC durante a fase anepática do TH em cinco grupos (I: aumento do IC; II: redução do IC inferior a 16%; III: redução do IC igual a ou maior do que 16% e menor do que 31%; IV: redução do IC igual a ou maior do que 31% e menor do que 46%;V: redução do IC igual a ou maior do que 46%).
RESULTADOS:
Pacientes que fizeram uso pré-operatório de propranolol no grupo I (46,4%) foram estatisticamente semelhantes aos dos grupos II (60%), III (72,7%), IV (50%) e V (30,8%), p = 0,57.
CONCLUSÃO:
O propranolol no pré-transplante, como profilaxia para hemorragia digestiva, pode ser considerado seguro, pois não se associou à pioria do IC na fase anepática do TH.
Transplante de fígado; Débito cardíaco; Antagonista adrenérgico beta; Propranolol
INTRODUCCIÓN:
El trasplante hepático (TH) es la mejor opción terapéutica para la enfermedad hepática en estado terminal. Los betabloqueantes no selectivos, como el propranolol, actúan directamente en el sistema cardiovascular y a menudo son usadas en la prevención de la hemorragia digestiva proveniente de la hipertensión portal. Los efectos del propranolol en el sistema cardiovascular de cirróticos durante el TH no se conocen.
OBJETIVO:
Evaluar la influencia del uso preoperatorio del propranolol en el índice cardíaco (IC) durante la fase anhepática del TH.
MÉTODO:
Se estudiaron 101 pacientes adultos (73 hombres [72,2%]) sometidos a trasplante ortotópico de hígado de donante cadáver, por la técnica de piggyback con preservación de la vena cava inferior retrohepática, en el Hospital das Clínicas de la Universidad Federal de Minas Gerais. No hubo diferencia respecto a la gravedad por el sistema Meld entre los grupos (p = 0,70). Se comparó el uso preoperatorio del propranolol con el resultado del IC durante la fase anhepática del TH en 5 grupos (i: aumento del IC; ii: reducción del IC < 16%; iii: reducción del IC ≥ 16% y < 31%; iv: reducción del IC ≥ 31% y < 46%;v: reducción del IC ≥ 46%).
RESULTADOS:
El número de pacientes que usaron el propranolol en el preoperatorio en el grupo i (46,4%) fue estadísticamente similar a los grupos ii (60%), iii (72,7%), iv (50%) y v (30,8%), p = 0,57.
CONCLUSIÓN:
El propranolol en el pretrasplante, como profilaxis para la hemorragia digestiva, puede ser considerado seguro porque no se asoció con el empeoramiento del IC en la fase anhepática del TH.
Trasplante de hígado; Gasto cardíaco; Antagonista betaadrenérgico; Propranolol
Introduction
Since the first liver transplantation (LT) performed in humans by Starzl in Denver, USA, in 1963, major advances such as better preservation of organs, improvement of surgical techniques, better knowledge of anesthesiology, and immunosuppressive therapy evolution have made liver transplantation the best treatment option for end-stage liver disease (ESLD).11 Starzl TE, Marchioro TL, Vonkaulla KN, et al. Homotrans- plantation of the liver in humans. Surg Gynecol Obstet. 1963;117:659-76. Currently, post-LT survival is approximately 90%, 85% and 80% at 1, 3 and 5 years, respectively.22 Menon KV, Hakeem AR, Heaton ND. Meta-analysis: recurrence and survival following the use of sirolimus in liver transplan- tation for hepatocellular carcinoma. Aliment Pharmacol Ther. 2013;37:411-9.
Cirrhosis is the most common cause of portal hypertension (PH) and causes increase in both intrahepatic vascular resistance and portal flow. PH is associated with serious complications, such as ascites, hepatic encephalopathy, and bleeding from esophagogastric varices.33 Garcia-Tsao G, Sanyal AJ, Grace NDC, et al. Preven- tion and management of gastroesophageal varices and variceal hemorrhage in cirrhosis. Hepatology. 2007;46: 922-38. The hepatic venous pressure gradient (HVPG) reduction below 12 mmHg is essential to minimize the risk of upper gastrointestinal bleeding in patients with PH. Non-selective beta-blockers drugs, such as propranolol and pindolol, reduce PH by decreasing the cardiac output (CO) and splanchnic vasoconstriction and, thus, the portal blood flow.33 Garcia-Tsao G, Sanyal AJ, Grace NDC, et al. Preven- tion and management of gastroesophageal varices and variceal hemorrhage in cirrhosis. Hepatology. 2007;46: 922-38. , 44 De Franchis R, Faculty BV. Revising consensus in portal hyper- tension: report of the Baveno V consensus workshop on methodology of diagnosis and therapy in portal hypertension. J Hepatol. 2010;53:762-8. and 55 La Mura V, Abraldes JG, Raffa S, et al. Prognostic value of acute hemodynamic response to i.v. propranolol in patients with cirrhosis and portal hypertension. J Hepatol. 2009;51: 279-87. The pharmacological effects of beta-blockers interfere with the cardiovascular system (CVS) during the perioperative period of LT and affect the transplanted liver functionality.66 Schepis F, Vukotic R, Berzigotti A, et al. Hemodynamic response to propranolol in patients with recurrent HCV-related cirrhosis after liver transplantation: a case-control study. Liver Transpl. 2013;19:450-6.
LT intraoperative period is classically divided into three phases: pre-anhepatic, anhepatic, and neohepatic. During the anhepatic phase, severe hemodynamic changes may occur and it is important that the anesthesiologist be prepared to optimize this patient during graft reperfusion, a critical time with a high incidence of CVS instability.77 Ozier Y, Klinck JR. Anesthetic management of hepatic transplantation. Curr Opin Anaesthesiol. 2008;21: 391-400.
Thus, it is important to know the effects of preoperative propranolol during LT.
Objectives
Evaluate the effect of preoperative use of propranolol and CI clinical and surgical variables during the anhepatic phase of orthotopic transplantation of cadaver donor orthotopic liver transplantation.
Method
Prospective study was performed at the Gastroenterology Alfa Institute of the Hospital das Clinicas, Federal University of Minas Gerais (HC-UFMG). This research was approved by the Research Ethics Committee of UFMG, CAAE 0244.0.203.000-08 and CAAE 0406.0.203.000-11 projects.
During the study period, from August 29, 2008 to January 5, 2012, 218 liver transplants were performed, wherein 13 of them are of retransplantation. A total of 114 patients, who agreed with and signed the informed consent after the invitation to participate, met the inclusion criteria. Thirteen patients were excluded because of hemodynamic data collection failure.
Inclusion criteria were age ≥18 years, transplantation with cadaver donor by piggyback technique, and signing the informed consent. Exclusion criteria were previous LT and hepatectomy, preoperative hemodynamic instability characterized by the need for vasopressor agents, acute liver failure, and autoimmune hepatitis.
One hundred and one patients participated in the study, 73 male (72.2%). LT indications were: post-viral C cirrhosis (33.7%), ethanol cirrhosis (28.7%), cryptogenic cirrhosis (20.8%), post-viral B cirrhosis (6.9%), primary biliary cirrhosis (3.9%), and others (5.9%). Fifty-four patients were receiving beta-blockers in the pretransplant period (53.5%), and propranolol was the drug used for prophylaxis of gastroesophageal varices bleeding.33 Garcia-Tsao G, Sanyal AJ, Grace NDC, et al. Preven- tion and management of gastroesophageal varices and variceal hemorrhage in cirrhosis. Hepatology. 2007;46: 922-38.
The study patients underwent balanced general anesthesia. Anesthesia was induced with etomidate (0.3 mg kg-1), fentanyl (5 µg kg-1), and rocuronium (1.2 mg kg-1), maintained with isoflurane (1 MAC), and monitored by the anesthetic gas analyzer. Additional doses of rocuronium and fentanyl were used as needed.
Before surgical incision, all patients underwent the following monitoring: intra-arterial pressure by radial artery catheterization, pulmonary artery pressures, pulmonary artery occlusion pressure, and continuous cardiac output using the Swan-Ganz DDC-Edwards(r) catheter and Vigilance-Edwards(r) monitor. Data included intra-arterial mean pressure (IAP), central venous pressure (CVP), mean pulmonary artery pressure (PAP), pulmonary capillary pressure (PCP), heart rate (HR), and cardiac output (CO). In addition to the hemodynamic data the dosage of vasopressor drugs used in intraoperative was recorded.
Measurements were performed at the following times: induction of anesthesia (T1); beginning of anhepatic phase characterized as the portal vein clamping (T2); 5 min before graft reperfusion, characterized as the end of anhepatic phase (T3). In this study the time between T2 and T3 was considered the anhepatic phase duration.
From collected data, the body surface area (BSA), peripheral vascular resistance index (PVRI), and CI were calculated using the Vigilance-Edwards(r) monitor. Body mass index (BMI) was calculated using the following formula: BMI = weight (kg) × height (m)- 22 Menon KV, Hakeem AR, Heaton ND. Meta-analysis: recurrence and survival following the use of sirolimus in liver transplan- tation for hepatocellular carcinoma. Aliment Pharmacol Ther. 2013;37:411-9.. The Meld (model for end-stage liver disease) used in this study was the calculated and not the corrected Meld.
According to the percentage change in CI, occurring between the beginning (T2) and the end (T3) of the anhepatic phase, and the severity of myocardial impairment function, the patients' results were divided into five groups: Group I: increased CI; Group II: CI reduction lower than 16%; Group III: CI reduction equal to or greater than 16% and less than 31%; Group IV: CI reduction equal to or greater than 31% and less than 46%; and Group V: CI reduction equal to or greater than 46%). Groups II, III, IV, and V had an unfavorable outcome of cardiac index.
Statistical analysis
SPSS version 18 was the software used in the analysis. The reference level of significance in univariate analysis was 0.20. In the multivariate analysis, a 0.05 significance level was considered.
Shapiro-Wilk normality test was used for continuous variables in order to decide for parametric or non-parametric tests in data analysis.
In the descriptive analysis, continuous variables were expressed as mean values and standard deviations and categorical variables as frequency and percentage.
For comparison of continuous variables in the five independent groups (I, II, III, IV, and V), the mean comparison test ANOVA was used when the variables had normal Gaussian distribution and the Kruskal-Wallis test for median comparison when the variables did not reach Gaussian distribution.
To evaluate the association of categorical variables in the five groups, the linear trend chi-square test was used because in this case the groups have an importance of ordering.
Results
Descriptive analysis of the patients' clinical characteristics is shown in Table 1.
Table 2 shows the frequency and percentage of some categorical variables.
Table 3 shows the association between categorical variables and CI variation in the different groups.
Table 4 shows the association between continuous variables with CI variation in different groups.
Discussion
Since the development of propranolol by James Black88 Black JW, Crowther AF, Shanks RG, et al. A new adrenergic betarecptor antagonist. Lancet. 1964;1:1080-1. for more than four decades, the adrenergic beta-blockers have been used for treatment of hypertension, coronary artery disease, myocardial infarction, and heart failure, standing out mainly by the action on beta-adrenergic receptors in the CVS. In the heart, beta-1 receptors are present in the sinoatrial node (speeding depolarization), cardiac muscle (increasing contractility), and transmission tissue (increasing conduction velocity) and determine increase in cardiac output. Beta-2 receptors act on the peripheral vascular muscle (causing vasodilation).99 Chrysant SG, Chrysant GS. Current status of β-blockers for the treatment of hypertension: an update. Drugs Today (Barc). 2012;48:353-66. In drug prevention of upper gastrointestinal bleeding by esophagogastric varices in patients with PH, the beta-blocker is indicated at low initial doses (propranolol 20 mg day-1) with a progressive increase according to patient tolerance and HR reduction.1010 Chen Yl, Ghali P. Prevention and management of gastro- esophageal varices in cirrhosis. lnt J Hepatol. 2012;2012: 150-750.
Systolic ventricular function is determined by preload, afterload, and myocardial contractility - factors that affect the CI. During preoperative evaluation of ESLD patients CVS should be considered because terminal liver disease may be associated with cirrhotic cardiomyopathy. In these patients, CO might be increased due to reduced afterload even in the presence of contractile dysfunction. However, when the CVS is highly demanded as during LT the myocardial dysfunction may manifest and cardiac response may be unsatisfactory and determine an unfavorable outcome.1111 Lee RF, Glenn TK, Lee SS. Cardiac dysfunction in cirrhosis. Best Pract Res Clin Gastroenterol. 2007;21:125-40. Wong et al., evaluating myocardial function of asymptomatic cirrhotic patients for cardiovascular disease during exercise found a smaller increase in CO compared with control. The decrease in cardiac performance has as factors left ventricular hypertrophy, diastolic dysfunction, and reduced chronotropic response.1212 Wong F, Girgrah N, Graba J, et al. The cardiac response to exercise in cirrhosis. Gut. 2001;49:268-75. In this study, we evaluated the CI variation during LT anhepatic phase which is a very demanding period for the CVS, in order to find preoperative factors that may be associated with an unfavorable outcome, which is the worsening of myocardial performance.
The classical technique of LT involves the donor hepatectomy with retrohepatic vena cava resection associated with temporary occlusion of the portal and cava veins during the anhepatic phase, which causes decreased venous return to the heart, decreased renal perfusion, and congestion of the splanchnic venous system in this phase.1313 Figueras J, Llado L, Ramos E, et al. Temporary portocaval shunt during liver transplantation with vena cava preserva- tion. Results of a prospective randomized study. Liver Transpl. 2001;7:904-11. During the surgical procedure, to avoid interference of the technique used on the analyzed data, we included only the LT performed with the piggyback technique, in which there is preservation of the inferior vena cava. Even with the piggyback technique, the portal vein needs to be occluded causing increased portal pressure with splanchnic bed congestion and intestinal edema. In 1993, Tzakis et al. described the use of piggyback technique with the placement of temporary portocaval shunt (TPCS) for portal vein communication with the infrahepatic inferior vena cava during the anhepatic phase.1414 Tzakis AG, Reyes J, Nour B, et al. Temporary end to side por- tacaval shunt in orthotopic hepatic transplantation in humans. Surg Gynecol Obstet. 1993;176:180-2. Figueras et al., in order to assess whether TPCS would improve the hemodynamic and metabolic evolution during LT with piggyback technique, found an improved hemodynamic profile with less need for blood products in TPCS group, but this benefit was more evident in a subgroup of patients with portal flow exceeding 1000 mL min-1 or portocaval gradient greater than or equal to 16 mmHg.1313 Figueras J, Llado L, Ramos E, et al. Temporary portocaval shunt during liver transplantation with vena cava preserva- tion. Results of a prospective randomized study. Liver Transpl. 2001;7:904-11. Margarit et al.1515 Margarit C, de Cenarruzabeitia lL, Lázaro JL, et al. Portacaval shunt and inferior vena cava preservation in orthotopic liver transplantation. Transplant Proc. 2005;37: 3896-8. evaluated the advantages of TPCS during LT and concluded that TPCS during the anhepatic phase reduces the need for packed red blood cell transfusion and improves postoperative renal function, only in patients with portal vein flow exceeding 800 mL min-1. Muscari et al.,1616 Muscari F, Suc B, Aguirre J, et al. Orthotopic liver transplan- tation with vena cava preservation in cirrhotic patients: is systematic temporary portacaval anastomosis a justified pro- cedure? Transplant Proc. 2005;37:2159-62. evaluating 84 patients undergoing LT with the piggyback technique, concluded that the routine use of TPCS is not justified. In the present study, TPCS was performed during the anhepatic phase in only 15.8% of patients (Table 2), and there was no association between TPCS and percentage change in CI during anhepatic phase (Table 3).
Table 4 shows that some moderating variables that could influence the outcome were controlled. Important factors in this evaluation were the duration of anhepatic phase (T2/T3), which could be increased by surgical difficulty. The CVPm, which could be influenced by partial clamping of vena cava with the piggyback surgical technique and influence CI, was statistically similar in all groups evaluated. Raval et al., in a review article, reported that ESLD patients with compromised systolic and diastolic function not observed at rest, but during periods of high demand, which reduces the CI by compromising the contractile function, diastolic relaxation, and myocardial electrophysiological conduction. These changes in cirrhotic patients are known as cirrhotic cardiomyopathy and are directly related to the ESLD severity.1717 Raval Z, Harinstein ME, Skaro Al, et al. Cardiovascular risk assessment of the liver transplant candidate. J Am Coll Cardiol. 2011;58:223-31. In our study, based on Meld system, all groups were statistically similar and showed that there was no interference of the liver disease severity on CI.
In a review article of the pathophysiology and clinical implications of cirrhotic cardiomyopathy, Yang and Lin reported the importance of beta-adrenergic receptors for heart contractile function and the involvement of these receptors in ESLD patients.1818 Yang YY, Lin HC. The heart: pathophysiology and clinical implications of cirrhotic cardiomyopathy. J Chin Med Assoc. 2012;75:619-23. Zenghua et al., in an experimental study, concluded that myocardial contractility in response to beta-adrenergic receptor stimulation was attenuated in cirrhotic rats due to decreased density associated with the signaling pathway involvement of these receptors.1919 Ma Z, Miyamoto A, Lee SS. Role of altered beta-adrenoceptor signal transduction in the pathogenesis of cirrhotic cardiomyopathy in rats. Gastroenterology. 1996;110: 1191-8. Villas-Boas et al., studying the effects of propranolol on renin-angiotensin system in cirrhotic patients, reported changes in hemodynamic parameters with reduced CI in LT pre-anhepatic phase in patients treated with propranolol preoperatively.2020 Vilas-Boas WW, Ribeiro-Oliveira A, Ribeiro Rda C, et al. Effect of propranolol on the splanchnic and peripheral renin angiotensin system in cirrhotic patients. World J Gastroenterol. 2008;14:6824-30. Aiming at evaluating the effect of propranolol on myocardial function during the anhepatic phase, we correlated the patients receiving propranolol with CI change during the anhepatic phase and found no statistically significant association (Table 3). The propranolol dose of our patients ranged from 20 mg to 120 mg day. The clinical condition of ESLD patients rarely allows improved administration of the adrenergic beta-blocker medication.1010 Chen Yl, Ghali P. Prevention and management of gastro- esophageal varices in cirrhosis. lnt J Hepatol. 2012;2012: 150-750. Non-interference of propranolol on CI variation may be due to the preoperative dose be considered low, so there is significant beta-adrenergic receptor blockade in the heart and myocardial contractile function impairment in this moment of myocardial stress, which is the anhepatic phase.
We believe that myocardial depression during the anhepatic phase may occur due to pro-inflammatory cytokine accumulation,2121 Arranz J, Soriano A, Garcia l, et al. Effect of proinflammatory cytokines (lL-6, TNF-alpha, lL-1beta) on hemodynamic perfor- mance during orthotopic liver transplantation. Transplant Proc. 2003;35:1884-7. occurred during the LT and intensified at the end of this phase, associated with latent cirrhotic cardiomyopathy. This association between inflammatory cytokine and worsening of myocardial performance has been studied in septic shock,2222 Hartemink KJ, Groeneveld AB. Vasopressors and inotropes in the treatment of human septic shock: effect on innate immunity? lnflammation. 2012;35:206-13. and 2323 Zanotti-Cavazzoni SL, Hollenberg SM. Cardiac dysfunction in severe sepsis and septic shock. Curr Opin Crit Care. 2009;15:392-7. which can bring substrate for a future understanding of this event in LT.
Conclusion
The use of propranolol in cirrhotic liver pre-transplantation for prophylaxis of bleeding by esophagogastric varices is safe for CVS during the anhepatic phase of liver transplantation.
References
-
1Starzl TE, Marchioro TL, Vonkaulla KN, et al. Homotrans- plantation of the liver in humans. Surg Gynecol Obstet. 1963;117:659-76.
-
2Menon KV, Hakeem AR, Heaton ND. Meta-analysis: recurrence and survival following the use of sirolimus in liver transplan- tation for hepatocellular carcinoma. Aliment Pharmacol Ther. 2013;37:411-9.
-
3Garcia-Tsao G, Sanyal AJ, Grace NDC, et al. Preven- tion and management of gastroesophageal varices and variceal hemorrhage in cirrhosis. Hepatology. 2007;46: 922-38.
-
4De Franchis R, Faculty BV. Revising consensus in portal hyper- tension: report of the Baveno V consensus workshop on methodology of diagnosis and therapy in portal hypertension. J Hepatol. 2010;53:762-8.
-
5La Mura V, Abraldes JG, Raffa S, et al. Prognostic value of acute hemodynamic response to i.v. propranolol in patients with cirrhosis and portal hypertension. J Hepatol. 2009;51: 279-87.
-
6Schepis F, Vukotic R, Berzigotti A, et al. Hemodynamic response to propranolol in patients with recurrent HCV-related cirrhosis after liver transplantation: a case-control study. Liver Transpl. 2013;19:450-6.
-
7Ozier Y, Klinck JR. Anesthetic management of hepatic transplantation. Curr Opin Anaesthesiol. 2008;21: 391-400.
-
8Black JW, Crowther AF, Shanks RG, et al. A new adrenergic betarecptor antagonist. Lancet. 1964;1:1080-1.
-
9Chrysant SG, Chrysant GS. Current status of β-blockers for the treatment of hypertension: an update. Drugs Today (Barc). 2012;48:353-66.
-
10Chen Yl, Ghali P. Prevention and management of gastro- esophageal varices in cirrhosis. lnt J Hepatol. 2012;2012: 150-750.
-
11Lee RF, Glenn TK, Lee SS. Cardiac dysfunction in cirrhosis. Best Pract Res Clin Gastroenterol. 2007;21:125-40.
-
12Wong F, Girgrah N, Graba J, et al. The cardiac response to exercise in cirrhosis. Gut. 2001;49:268-75.
-
13Figueras J, Llado L, Ramos E, et al. Temporary portocaval shunt during liver transplantation with vena cava preserva- tion. Results of a prospective randomized study. Liver Transpl. 2001;7:904-11.
-
14Tzakis AG, Reyes J, Nour B, et al. Temporary end to side por- tacaval shunt in orthotopic hepatic transplantation in humans. Surg Gynecol Obstet. 1993;176:180-2.
-
15Margarit C, de Cenarruzabeitia lL, Lázaro JL, et al. Portacaval shunt and inferior vena cava preservation in orthotopic liver transplantation. Transplant Proc. 2005;37: 3896-8.
-
16Muscari F, Suc B, Aguirre J, et al. Orthotopic liver transplan- tation with vena cava preservation in cirrhotic patients: is systematic temporary portacaval anastomosis a justified pro- cedure? Transplant Proc. 2005;37:2159-62.
-
17Raval Z, Harinstein ME, Skaro Al, et al. Cardiovascular risk assessment of the liver transplant candidate. J Am Coll Cardiol. 2011;58:223-31.
-
18Yang YY, Lin HC. The heart: pathophysiology and clinical implications of cirrhotic cardiomyopathy. J Chin Med Assoc. 2012;75:619-23.
-
19Ma Z, Miyamoto A, Lee SS. Role of altered beta-adrenoceptor signal transduction in the pathogenesis of cirrhotic cardiomyopathy in rats. Gastroenterology. 1996;110: 1191-8.
-
20Vilas-Boas WW, Ribeiro-Oliveira A, Ribeiro Rda C, et al. Effect of propranolol on the splanchnic and peripheral renin angiotensin system in cirrhotic patients. World J Gastroenterol. 2008;14:6824-30.
-
21Arranz J, Soriano A, Garcia l, et al. Effect of proinflammatory cytokines (lL-6, TNF-alpha, lL-1beta) on hemodynamic perfor- mance during orthotopic liver transplantation. Transplant Proc. 2003;35:1884-7.
-
22Hartemink KJ, Groeneveld AB. Vasopressors and inotropes in the treatment of human septic shock: effect on innate immunity? lnflammation. 2012;35:206-13.
-
23Zanotti-Cavazzoni SL, Hollenberg SM. Cardiac dysfunction in severe sepsis and septic shock. Curr Opin Crit Care. 2009;15:392-7.
Publication Dates
-
Publication in this collection
May-Jun 2015
History
-
Received
03 Nov 2013 -
Accepted
05 Feb 2014