Pharmacological prophylaxis of hepatic encephalopathy after transjugular intrahepatic portosystemic shunt: a randomized controlled study

Hepatic encephalopathy is a frequent event after transjugular-intrahepatic-portosystemic-shunt (TIPS), especially during the first months. Aim of this study was to compare two different treatments (lactitol 60 g/day, rifaximin 1200 mg/day) with no-treatment in the prevention of post-TIPS hepatic enc...

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Veröffentlicht in:Journal of hepatology 2005-05, Vol.42 (5), p.674-679
Hauptverfasser: Riggio, O., Masini, A., Efrati, C., Nicolao, F., Angeloni, S., Salvatori, Filippo M., Bezzi, M., Attili, Adolfo F., Merli, M.
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container_end_page 679
container_issue 5
container_start_page 674
container_title Journal of hepatology
container_volume 42
creator Riggio, O.
Masini, A.
Efrati, C.
Nicolao, F.
Angeloni, S.
Salvatori, Filippo M.
Bezzi, M.
Attili, Adolfo F.
Merli, M.
description Hepatic encephalopathy is a frequent event after transjugular-intrahepatic-portosystemic-shunt (TIPS), especially during the first months. Aim of this study was to compare two different treatments (lactitol 60 g/day, rifaximin 1200 mg/day) with no-treatment in the prevention of post-TIPS hepatic encephalopathy. Seventy-five consecutive cirrhotics submitted to TIPS were randomized to receive either one of the above treatments or no-treatment. The main end-point was the occurrence of an episode of overt hepatic encephalopathy during the first month post-TIPS. Before the procedure and weekly thereafter the patients were evaluated by examining their mental status, asterixis, ammonia and trail-making-test Part-A (TMT-A). The three groups were comparable for age, sex, etiology, Child-Pugh-score, post-TIPS porto-systemic gradient, previous hepatic encephalopathy, basal values of ammonia and psychometric performance. Twenty-five patients developed hepatic encephalopathy (33%, CI 95%=22–45%). One-month incidence was similar in the three groups ( P=0.97). Previous hepatic encephalopathy (Relative Hazard=3.79;1.27–11.31) and basal-TMT-A Z-score>1.5 (RH=3.55;1.24–10.2) were predictors of post-TIPS encephalopathy at multivariate analysis. A
doi_str_mv 10.1016/j.jhep.2004.12.028
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Previous hepatic encephalopathy (Relative Hazard=3.79;1.27–11.31) and basal-TMT-A Z-score&gt;1.5 (RH=3.55;1.24–10.2) were predictors of post-TIPS encephalopathy at multivariate analysis. A &lt;5 mmHg porto-systemic gradient was also significantly related to the occurrence of encephalopathy. Our data show that treatment with lactitol or rifaximin is not effective in the prophylaxis of hepatic encephalopathy during the first month after a TIPS.</description><subject>Adult</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Cathartics - administration &amp; dosage</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. 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Aim of this study was to compare two different treatments (lactitol 60 g/day, rifaximin 1200 mg/day) with no-treatment in the prevention of post-TIPS hepatic encephalopathy. Seventy-five consecutive cirrhotics submitted to TIPS were randomized to receive either one of the above treatments or no-treatment. The main end-point was the occurrence of an episode of overt hepatic encephalopathy during the first month post-TIPS. Before the procedure and weekly thereafter the patients were evaluated by examining their mental status, asterixis, ammonia and trail-making-test Part-A (TMT-A). The three groups were comparable for age, sex, etiology, Child-Pugh-score, post-TIPS porto-systemic gradient, previous hepatic encephalopathy, basal values of ammonia and psychometric performance. Twenty-five patients developed hepatic encephalopathy (33%, CI 95%=22–45%). One-month incidence was similar in the three groups ( P=0.97). Previous hepatic encephalopathy (Relative Hazard=3.79;1.27–11.31) and basal-TMT-A Z-score&gt;1.5 (RH=3.55;1.24–10.2) were predictors of post-TIPS encephalopathy at multivariate analysis. A &lt;5 mmHg porto-systemic gradient was also significantly related to the occurrence of encephalopathy. Our data show that treatment with lactitol or rifaximin is not effective in the prophylaxis of hepatic encephalopathy during the first month after a TIPS.</abstract><cop>Oxford</cop><pub>Elsevier B.V</pub><pmid>15826716</pmid><doi>10.1016/j.jhep.2004.12.028</doi><tpages>6</tpages></addata></record>
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subjects Adult
Aged
Biological and medical sciences
Cathartics - administration & dosage
Female
Gastroenterology. Liver. Pancreas. Abdomen
Gastrointestinal Agents - administration & dosage
Hepatic encephalopathy
Hepatic Encephalopathy - epidemiology
Hepatic Encephalopathy - prevention & control
Humans
Incidence
Liver cirrhosis
Liver Cirrhosis - drug therapy
Liver Cirrhosis - epidemiology
Liver Cirrhosis - surgery
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical sciences
Middle Aged
Other diseases. Semiology
Portal hypertension
Portasystemic Shunt, Transjugular Intrahepatic
Postoperative Complications - epidemiology
Postoperative Complications - prevention & control
Rifamycins - administration & dosage
Sugar Alcohols - administration & dosage
TIPS
Treatment Failure
title Pharmacological prophylaxis of hepatic encephalopathy after transjugular intrahepatic portosystemic shunt: a randomized controlled study
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