Hepatic encephalopathy in liver cirrhosis - Pathogenesis, diagnosis and management

被引:68
作者
Gerber, T [1 ]
Schomerus, H [1 ]
机构
[1] Diakoniekrankenhaus Rotenburg, Med Clin 2, D-27342 Rotenburg, Germany
关键词
D O I
10.2165/00003495-200060060-00008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pathogenesis of hepatic encephalopathy (HE) is unknown. Many theories have been proposed. Most established therapies are based on such theories but since no theory has have ever been proved, therapies have to he considered empiric. The spectrum of HE ranges from minimal cerebral functional deficits, which can only be found by sensitive psychometric tests, to coma with signs of decerebration. HE has arbitrarily been divided into stages. A number of precipitating factors are known and the first line of therapy should always be the elimination of these factors. The differential diagnosis includes all states of impaired consciousness and deficits in cerebral function in patients with chronic liver disease, and clinical and biochemical tests to differentiate are indicated. The therapeutic options for HE include: protein restriction only for a limited time in comatous patients; nonabsorbable antibiotics (aminoglycosides), which because of adverse effects are also limited to higher grades of HE; intestinal cleansing which is applicable in all degrees of HE; lactulose, branched chain aminoacids and ornithin aspartate which have been proven to he effective and can be applied long term in patients with lower grades of HE.
引用
收藏
页码:1353 / 1370
页数:18
相关论文
共 134 条
[1]  
ADAMS RD, 1953, ELECTROEN CLIN NEURO, V3, P51
[2]  
AGGARWAL A, 1999, TURK J GASTROENTEROL, V10, P18
[3]  
[Anonymous], 1979, The Hepatic Coma Syndromes and Lactulose
[4]   NEOMYCIN-SORBITOL AND LACTULOSE IN TREATMENT OF ACUTE PORTAL-SYSTEMIC ENCEPHALOPATHY - CONTROLLED, DOUBLE-BLIND CLINICAL-TRIAL [J].
ATTERBURY, CE ;
MADDREY, WC ;
CONN, HO .
AMERICAN JOURNAL OF DIGESTIVE DISEASES, 1978, 23 (05) :398-405
[5]   MECHANISM OF THE EXCESSIVE SEDATIVE RESPONSE OF CIRRHOTICS TO BENZODIAZEPINES - MODEL EXPERIMENTS WITH TRIAZOLAM [J].
BAKTI, G ;
FISCH, HU ;
KARLAGANIS, G ;
MINDER, C ;
BIRCHER, J .
HEPATOLOGY, 1987, 7 (04) :629-638
[6]   EXPERIMENTAL HEPATIC-ENCEPHALOPATHY - CHANGES IN THE BINDING OF GAMMA-AMINOBUTYRIC ACID [J].
BARALDI, M ;
ZENEROLI, ML .
SCIENCE, 1982, 216 (4544) :427-429
[7]   Flumazenil for hepatic encephalopathy grade III and IVa in patients with cirrhosis: An Italian multicenter double-blind, placebo-controlled, cross-over study [J].
Barbaro, G ;
Di Lorenzo, G ;
Soldini, M ;
Giancaspro, G ;
Bellomo, G ;
Belloni, G ;
Grisorio, B ;
Annese, M ;
Bacca, D ;
Francavilla, R ;
Barbarini, G .
HEPATOLOGY, 1998, 28 (02) :374-378
[8]   ELEVATED BRAIN CONCENTRATIONS OF 1,4-BENZODIAZEPINES IN FULMINANT HEPATIC-FAILURE [J].
BASILE, AS ;
HUGHES, RD ;
HARRISON, PM ;
MURATA, Y ;
PANNELL, L ;
JONES, EA ;
WILLIAMS, R ;
SKOLNICK, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (07) :473-478
[9]   BRAIN CONCENTRATIONS OF BENZODIAZEPINES ARE ELEVATED IN AN ANIMAL-MODEL OF HEPATIC-ENCEPHALOPATHY [J].
BASILE, AS ;
PANNELL, L ;
JAOUNI, T ;
GAMMAL, SH ;
FALES, HM ;
JONES, EA ;
SKOLNICK, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (14) :5263-5267
[10]   DEAFNESS COMPLICATING ANTIBIOTIC THERAPY OF HEPATIC ENCEPHALOPATHY [J].
BERK, DP ;
CHALMERS, T .
ANNALS OF INTERNAL MEDICINE, 1970, 73 (03) :393-+