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1.
Transplant Proc ; 40(9): 3253-5, 2008 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19010246

RESUMO

UNLABELLED: Living donor liver transplantation (LDLT) for patients with acute liver failure (ALF) is still controversial. To be considered a feasible alternative, this therapeutic option should offer similar results to transplants performed with cadaveric grafts, without significant risks for donors. The aim of this study was to compare the outcomes of pediatric patients with ALF who were transplanted with either cadaveric or living donor grafts. PATIENTS AND METHODS: Between March 1994 and February 2007, 149 patients under 18 years were transplanted, including 43 (28.8%) with ALF. We reviewed the demography, etiology, surgical technique, complications, and long-term results in this group. Patient actuarial survival was determined by Kaplan-Meier analysis. RESULTS: The median age of the recipients was 4.8 years (range 1.2 to 18) including 26 boys and 17 girls. Sixteen (37.2%) underwent LDLT. Three patients in the living donor group needed a second graft (18.7%) versus 7 (26%) among the cadaveric group. No mortality or serious morbidity was observed in living donors. Fifteen patients died. Septic and neurologic complications, and primary graft non-function were the most frequent causes of death. All patients died during the first year after liver transplant. Actuarial 1- and 5-year survivals were 65% without a significant difference between the groups. CONCLUSION: Considering that patients with ALF have no chance of survival without transplantation and that cadaveric grafts remain a limited resource, especially in our country, these results showed that LDLT was a valid option for these patients, as well as a secure procedure for the donors.


Assuntos
Falência Hepática Aguda/cirurgia , Transplante de Fígado/métodos , Doadores Vivos , Adolescente , Causas de Morte , Criança , Feminino , Humanos , Transplante de Fígado/efeitos adversos , Transplante de Fígado/mortalidade , Doadores Vivos/estatística & dados numéricos , Masculino , Pais , Estudos Retrospectivos , Segurança , Análise de Sobrevida , Sobreviventes , Resultado do Tratamento
2.
J Nutr ; 131(9): 2300-3, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11533270

RESUMO

It has been reported that intake of (n-3) polyunsaturated fatty acids (PUFA) reduces the risk of coronary heart disease and decreases biliary cholesterol saturation in the bile of gallstone patients. We investigated the effect of n-3 PUFA on cholesterol saturation index (CSI) and nucleation time (NT) in obese subjects who were losing weight. This was a double-blind, placebo-controlled clinical trial. Obese women (n = 35) with a body mass index (BMI) > or = 30 kg/m(2), with no prior history of gallstones or cholecystectomy by ultrasound were first studied to ensure absence of stones or biliary sludge. The women were then assigned to a hypocaloric regimen [5.02 MJ (1200 kcal)/d] and to receive 1200 mg/d of ursodeoxycholic acid (UDCA), 11.3 g/d of (n-3) PUFA or a placebo for 6 wk. BMI, CSI and NT were recorded at baseline and at the end of the experimental period. BMI decreased 5.75 +/- 2.7%/mo (range, 1.5-12.42%/mo) during the experiment. The CSI did not change in any of the groups. Cholesterol NT decreased significantly in the UDCA and placebo groups, but not in the (n-3) PUFA group. None of the women had developed gallstones at 6 wk. These results suggest that (n-3) PUFA maintain the CSI and NT in obese women during rapid weight loss, which probably results in the prevention of cholesterol gallstone formation.


Assuntos
Bile/metabolismo , Colelitíase/prevenção & controle , Colesterol/fisiologia , Ácidos Graxos Ômega-3/farmacologia , Óleos de Peixe/farmacologia , Obesidade/metabolismo , Redução de Peso , Adulto , Dieta Redutora , Método Duplo-Cego , Feminino , Humanos , Pessoa de Meia-Idade , Obesidade/dietoterapia , Obesidade/patologia , Fatores de Tempo
3.
Br J Haematol ; 103(2): 568-81, 1998 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-9827938

RESUMO

In order to better define which cell subset contained in graft products might be the most predictive of haemopoietic recovery following autologous blood cell transplantation (ABCT), the relationships between the amounts of reinfused mononuclear cells (MNC), CFU-GM, total CD34+ cells and their CD33 and CD38 subsets. and the successive stages of trilineage engraftment kinetics, were studied in 45 cancer patients, using the Spearman correlation test, a linear regression model and a log-inverse model. No relationship was found between the infused numbers of MNC, CD33+ and CD33- subsets observed and the numbers of days to reach predetermined absolute neutrophil (ANC), platelet and reticulocyte counts. The infused numbers of CFU-GM, CD34+ and CD34+ 38+ cells correlated inconstantly with haemopoietic recovery parameters. The strongest and the most constant correlations were significantly observed between the infused numbers of CD34+ 38- cells and each trilineage engraftment parameter. The log-inverse model determined a threshold dose of 0.05 x 10(6) (= 5 x 10(4)) CD34+ 38- cells/kg, below which the trilineage engraftment kinetics were significantly slower and unpredictable. Post-transplant TBI-conditioning regimens increased the low cell dose-related delay of engraftment kinetics whereas post-transplant administration of haemopoietic growth factors (HGF) seemed to abrogate this delay. This would justify clinical use of HGF only in patients transplanted with CD34+ 38- cell amounts lower than the proposed threshold value. This study suggests that the CD34+ 38- subpopulation, although essentially participating in late complete haemopoietic recovery, is also composed of committed progenitor cells involved in early trilineage engraftment.


Assuntos
Antígenos CD34/sangue , Antígenos CD , Transfusão de Sangue Autóloga , Neoplasias Hematológicas/terapia , ADP-Ribosil Ciclase , ADP-Ribosil Ciclase 1 , Adolescente , Adulto , Idoso , Antígenos de Diferenciação/sangue , Antígenos de Neoplasias/sangue , Contagem de Células Sanguíneas , Ensaio de Unidades Formadoras de Colônias , Feminino , Sobrevivência de Enxerto/imunologia , Fatores de Crescimento de Células Hematopoéticas/uso terapêutico , Humanos , Masculino , Glicoproteínas de Membrana , Pessoa de Meia-Idade , NAD+ Nucleosidase/sangue , Estudos Prospectivos , Irradiação Corporal Total
5.
Rev Gastroenterol Mex ; 62(4): 266-72, 1997.
Artigo em Espanhol | MEDLINE | ID: mdl-9580234

RESUMO

Nearly 30% of the obese patients treated with hypoenergetic diets for weight reduction develop gallstone disease (GD). Until the present time, the use of ursodeoxycholic acid (UDA) is the only available therapeutic measure to avoid the development of GD. Dietary fiber induce a bile acid synthesis. A double-blind clinical trial was conducted to compare the effect of rational diet plus UDA vs a rational diet supplemented with Psyllium plantago (Pp) for the prevention of GD in obese subjects undergoing a weight-reduction diet. Patients with a body mass index (BMI = weight in Kg/square height in m) of 30 Kg/m2 or more and with normal gallbladder and biliary tree ultrasound (GBUS) were included. Weight-reduction diets were individually calculated for each patient according to their energy expenditure (EE). Patients were randomly and blindly assigned either to group I (diet + 750 mg UDA + fiber placebo) or group II (diet + 15 g Pp+ UDA placebo). An anthropometric evaluation was performed to each patient before and after the two-month treatment, as well as resting EE by indirect calorimetry, GBUS and endoscopy for the determination of cholesterol crystals in duodenal bile. Weight reduction was similar in both groups (group I = 6 +/- 2 Kg vs group II = 6 +/- 3 Kg). GD development was observed in one patient of group I (5.5%) and two patients of group II (p > 0.05). All patients with GD lost a minimum of 4 Kg during the study period. GD development did not correlate with the presence of crystals in the duodenal bile at the beginning of the study. Our results suggest a beneficial effect of a rational diet with fiber supplementation to prevent GD development in obese patients included in a weight reduction program.


Assuntos
Colelitíase/prevenção & controle , Dieta Redutora , Fibras na Dieta , Obesidade/terapia , Adulto , Colagogos e Coleréticos/administração & dosagem , Colelitíase/etiologia , Interpretação Estatística de Dados , Fibras na Dieta/administração & dosagem , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Obesidade/complicações , Psyllium/administração & dosagem , Ácido Ursodesoxicólico/administração & dosagem
6.
Ren Fail ; 17(1): 13-20, 1995 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-7770639

RESUMO

UNLABELLED: The mechanism of renal function abnormalities in experimental biliary cirrhosis can be partially explained by the absence of gastrointestinal bile flow, which predisposes to translocation of intestinal endotoxin, a potent renal vasoconstrictor. Since bile acids prevent the absorption of intestinal endotoxins, we aimed to evaluate the effects of ursodeoxycholic acid (UDCA) administration on renal function and hemodynamic abnormalities induced by 1 week of obstructive jaundice in rats. METHODS: Fifty-two rats were used; 30 had ligation of the common bile duct, 22 were sham operated. Bile duct ligated rats were randomly and blindly assigned to receive UDCA (25 mg/kg/day, n = 14) or placebo (n = 16) during 1 week. Sham rats received no treatment. Portal pressure (PP) as well as creatinine clearance (CrCl), urinary sodium (US), and plasma renin activity (PRA) were evaluated. Results are mean +/- SEM, with a significant value of p < 0.05. RESULTS: Portal pressure (10.4 +/- 1.1 vs. 12.1 +/- 0.8 mm Hg) was significantly lower in UDCA than in placebo-treated rats. ALT serum levels were also significantly lower in bile duct ligated rats receiving UDCA (77.3 +/- 28 IU/L) than in placebo-treated rats (162 +/- 65 IU/L). US (1.1 +/- 0.5 vs. 2.1 +/- 0.3 mEq/24 h) was significantly lower and PRA (6.0 +/- 2.6 vs. 1.9 +/- 1.0 ng Ang 1/mL/h) higher in bile duct ligated than in sham-operated rats. No differences were found between UDCA or placebo-treated bile duct ligated rats. CrCl was similar between sham (0.39 +/- 0.12 mL/min/100 g BW) and UDCA (0.32 +/- 0.16) but significantly lower in placebo-treated (0.28 +/- 0.07) than sham-operated rats (p < 0.05). CONCLUSION: UDCA administration had very mild effects on renal function abnormalities induced by experimental obstructive jaundice in rats. However, portal hypertension and biochemical abnormalities were partially improved.


Assuntos
Colestase/tratamento farmacológico , Rim/efeitos dos fármacos , Ácido Ursodesoxicólico/uso terapêutico , Análise de Variância , Animais , Colestase/fisiopatologia , Avaliação Pré-Clínica de Medicamentos , Hemodinâmica/efeitos dos fármacos , Hipertensão Portal/tratamento farmacológico , Hipertensão Portal/fisiopatologia , Rim/fisiopatologia , Masculino , Distribuição Aleatória , Ratos , Ratos Wistar , Ácido Ursodesoxicólico/farmacologia
7.
CES med ; 6(1): 61-65, ene.-jun. 1992. tab
Artigo em Espanhol | LILACS | ID: lil-515458

RESUMO

Se revisan 125 casos de cierre de ostomía, 119 colostomías y 6 ileostomías en la Unidad Intermedia Manuel Uribe Angel de Envigado (SSSA) durante un período de tres afios (1987-1990). Todos los pacientes fueron preparados por el mismo sistema (preparación oral) manejados con una misma técnica quirúrgica estandarizada. La mayor parte de los pacientes fueron de sexo masculino (92 por ciento), con un promedio de edad de 30 afios, siendo el principal agente causal el trauma por arma de fuego (75). Se observó que el colon por enema fue normal en un 99 por ciento de los pacientes; hubo 33 complicaciones en 25 pacientes (26.4 por ciento) de los cuales 8 por ciento requirieron corrección quirúrgica y 18 por ciento se manejaron médicamente. Se observó una tendencia a disminuir las complicaciones cuando el Intervalo de tiempo al cierre era mayor. La técnica extra peritoneal y cierre primario mostró ser la de menor morbilidad. Se observó que el cierre de la piel no aumentó esta morbilidad. Se hacen recomendaciones derivadas de los resultados...


Assuntos
Colostomia , Ileostomia , Estomia
8.
J Cardiothorac Anesth ; 4(6): 711-4, 1990 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-2131900

RESUMO

Large doses of heparin given as a bolus may produce hypotension; however, conflicting reports exist about the mechanisms involved. This study was undertaken to determine the role of histamine in beef lung heparin-induced hypotension and the efficacy of histamine-receptor blockade in attenuating this undesirable side effect in patients undergoing cardiac surgery. Two hundred patients with good ventricular function were studied after they were randomized into four equal groups. Group I (control) received no histamine-receptor blockade, group II received 1 mg/kg of diphenhydramine 30 minutes prior to heparin administration, group III received 5 mg/kg of cimetidine 4 hours and again 30 minutes before heparin administration, and group IV received 1 mg/kg of diphenhydramine 30 minutes prior to heparin administration and 5 mg/kg of cimetidine 4 hours and 30 minutes before heparin administration. Hemodynamic variables, plasma histamine, and ionized calcium levels were measured before and after heparin administration. Significant hypotension occurred in group I patients after heparin administration. Mean arterial pressure decreased from 95 +/- 5 to 67 +/- 1.5 mm Hg (P less than 0.005) after 1 minute and to 85 +/- 2 mm Hg (P less than 0.05) at 4 minutes. Those changes were significantly greater than in group II (P less than 0.025) and Group IV (P less than 0.005) patients, in whom no significant hypotension was found. In group III, mean arterial pressure decreased from 92 +/- 3 to 75 +/- 1 mm Hg (P less than 0.05) after 1 minute and returned toward baseline values after 4 minutes. Histamine levels increased significantly in all groups of patients.(ABSTRACT TRUNCATED AT 250 WORDS)


Assuntos
Cimetidina/uso terapêutico , Difenidramina/uso terapêutico , Heparina/efeitos adversos , Histamina/fisiologia , Hipotensão/induzido quimicamente , Pressão Sanguínea/efeitos dos fármacos , Cálcio/sangue , Débito Cardíaco/efeitos dos fármacos , Ponte de Artéria Coronária , Histamina/sangue , Humanos , Hipotensão/fisiopatologia , Hipotensão/prevenção & controle , Fatores de Tempo
9.
Rev Invest Clin ; 42 Suppl: 101-5, 1990 Jul.
Artigo em Espanhol | MEDLINE | ID: mdl-19256146

RESUMO

Sodium benzoate is widely used in the Alimentary Industry at low doses for its antimicrobial action. It has also been used as a liver function test. The principle is to evaluate the liver capacity for conjugation of glycine to benzoic acid and to form hippuric acid which is excreted in the urine. In hyperammonemic syndromes, secondary to enzymatic deficiency of the urea cicle, sodium benzoate has the property to act as an alternative way of nitrogen excretion to urinary hippurate instead of urea. Recently, it has been proposed as a therapeutic alternative in cirrhotic patients with portal systemic encephalopathy. Historical, biochemical and clinical data which constitute the principles to validate its clinical application in Hepatology are reviewed in this manuscript.


Assuntos
Hiperamonemia/tratamento farmacológico , Cirrose Hepática/tratamento farmacológico , Benzoato de Sódio/uso terapêutico , Acetatos/toxicidade , Adulto , Animais , Criança , Ensaios Clínicos como Assunto , Avaliação Pré-Clínica de Medicamentos , Glicina/metabolismo , Encefalopatia Hepática/tratamento farmacológico , Encefalopatia Hepática/metabolismo , Hipuratos/metabolismo , Humanos , Hiperamonemia/metabolismo , Cirrose Hepática/metabolismo , Testes de Função Hepática , Masculino , Erros Inatos do Metabolismo/tratamento farmacológico , Erros Inatos do Metabolismo/enzimologia , Erros Inatos do Metabolismo/urina , Camundongos , Estrutura Molecular , Ratos , Benzoato de Sódio/química , Benzoato de Sódio/farmacocinética , Ureia/metabolismo
10.
Rev Invest Clin ; 42 Suppl: 120-6, 1990 Jul.
Artigo em Espanhol | MEDLINE | ID: mdl-19256150

RESUMO

Five patients with mild chronic portal systemic encephalopathy (PSE) were studied. The study was designed in a double cross over fashion in which each patient received during period I a 40 g vegetable protein diet as single treatment. During period II three g/day of oral kanamycin were added and then new periods of single vegetable protein diet (period III) and vegetable protein diet plus kanamycin (period IV) were introduced (identical to periods I and II respectively). Each period lasted two weeks. Several biweekly assessements-tests were determined including: mental state, asterixis grade, electroencephalograms, number connection tests, figure connection tests, blood ammonia levels and stool counts of total aerobes/anaerobes per g/feces were done. During the study none of the patients developed acute encephalopathy. In any case it was detected a significant improvement of the PSE parameters assessed with the addition of oral kanamycin. Fecal counts were very similar during the various periods of the study. We conclude that in mild portal systemic encephalopathy controlled with vegetable protein diet, the addition of non absorbable antibiotics is not mandatory for the management of these patients and may represent a potential risk of serious side effects. At the beginning of treatment vegetable protein diet should be administered and only in case of failure, antibiotics are to be indicated.


Assuntos
Antibacterianos/uso terapêutico , Encefalopatia Hepática/dietoterapia , Canamicina/uso terapêutico , Proteínas de Vegetais Comestíveis/uso terapêutico , Idoso , Antibacterianos/farmacocinética , Terapia Combinada , Estudos Cross-Over , Discinesias/dietoterapia , Discinesias/tratamento farmacológico , Discinesias/etiologia , Fezes/microbiologia , Feminino , Frutas , Encefalopatia Hepática/sangue , Encefalopatia Hepática/tratamento farmacológico , Encefalopatia Hepática/microbiologia , Humanos , Hiperamonemia/dietoterapia , Hiperamonemia/tratamento farmacológico , Hiperamonemia/etiologia , Absorção Intestinal , Canamicina/farmacocinética , Masculino , Pessoa de Meia-Idade , Testes Neuropsicológicos , Proteínas de Plantas/uso terapêutico
11.
Rev Invest Clin ; 42 Suppl: 141-8, 1990 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19256154

RESUMO

The management of hepatic encephalopathy should be considered accordingly with the precipitating factor and the type of encephalopathy. Ideally the therapeutic approach must be useful for both acute and chronic forms of encephalopathy. Current treatment of hepatic encephalopathy consists of certain well-established measures attempting to identify and treat the precipitating factors, and to reduce the intestinal nitrogenous compounds formation and absorption by dietary restriction or bowel-cleansing with catartics or antibiotics such as neomycin, metronidazol, etc. This review describes briefly several therapeutic modalities.


Assuntos
Encefalopatia Hepática/terapia , Bromocriptina/uso terapêutico , Ensaios Clínicos como Assunto , Colo/microbiologia , Proteínas Alimentares/efeitos adversos , Dissacarídeos/uso terapêutico , Método Duplo-Cego , Enema , Antagonistas GABAérgicos/uso terapêutico , Hemorragia Gastrointestinal/complicações , Encefalopatia Hepática/dietoterapia , Encefalopatia Hepática/tratamento farmacológico , Encefalopatia Hepática/etiologia , Humanos , Hiperamonemia/complicações , Laxantes/uso terapêutico , Levodopa/uso terapêutico , Cirrose Hepática/complicações , Cirrose Hepática/dietoterapia , Desnutrição/complicações , Redes e Vias Metabólicas , Proteínas de Vegetais Comestíveis/uso terapêutico , Benzoato de Sódio/uso terapêutico , Zinco/uso terapêutico
12.
Hepatology ; 7(4): 639-43, 1987.
Artigo em Inglês | MEDLINE | ID: mdl-3301614

RESUMO

A double-blind, controlled trial to study the efficacy of acidifying enemas of lactitol, a new galactoside-sorbitol disaccharide, and lactose vs. nonacidifying tap-water enemas was performed in 45 episodes of acute portal-systemic encephalopathy. At the time of randomization, all patients had encephalopathy of at least Grade 2+ severity, delay in the performance of number connection tests and hyperammonemia. A sequential analysis was performed which revealed after the inclusion of the first 20 patients, a significant failure of the nonacidifying enemas as compared to the lactitol enemas (p less than 0.004). The tap-water enema group was, therefore, suspended but the rest of the study continued after rerandomization for lactose and lactitol groups. A favorable response to treatment was obtained in 19 (86%) of the patients receiving lactitol enemas and in 14 (78%) of those receiving lactose enemas. A similar significant improvement in portal-systemic encephalopathy parameters and index was observed after both treatments. Both types of acidifying enemas induced a significant pH decrease in stool (p less than 0.05). These data suggest that acidifying agents like lactose and lactitol are effective and superior to tap-water enemas for the treatment of acute nitrogenous portal-systemic encephalopathy.


Assuntos
Enema/métodos , Encefalopatia Hepática/terapia , Lactose/uso terapêutico , Álcoois Açúcares/uso terapêutico , Água/uso terapêutico , Amônia/sangue , Conscientização , Ensaios Clínicos como Assunto , Método Duplo-Cego , Fezes/análise , Encefalopatia Hepática/psicologia , Humanos , Concentração de Íons de Hidrogênio , Testes de Inteligência , Distribuição Aleatória
16.
Gastroenterology ; 88(4): 901-7, 1985 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-2982694

RESUMO

A controlled crossover study was performed in 8 diabetic patients with chronic portal-systemic encephalopathy. After a basal period the patients were treated during periods A and B. During period A, a meat protein diet (0.8 g/kg body wt, approximately 1800 kcal/day) was consumed and neomycin plus laxatives were given. During period B patients received vegetable protein (0.8 g/kg body wt, 1800 kcal/day). This diet was supplemented with psyllium fiber to reach 35 g of fiber per day. Four patients were randomly assigned to receive the treatments in the order A-B and the other 4 patients in the order B-A. At the end of the first experimental period, fasting glucose levels were 204 +/- 86 mg% in the meat protein diet group and 127 +/- 8 mg% in the vegetable protein diet group (p less than 0.014). The patients were receiving 2.5 +/- 0.2 g/day and 2.1 +/- 0.5 g/day of tolbutamide at the end of the meat protein diet and vegetable protein diet, respectively. In all cases, fasting glucose levels decreased at the end of the vegetable diet period regardless of the previous treatment. An improvement of greater than or equal to 25 mg% of fasting glucose levels was observed in 7 of the 8 patients after the vegetable protein diet and in no case after the meat protein diet (p less than 0.0078). The parameters of encephalopathy were comparable at the end of both the meat protein diet and the vegetable protein diet. A significant increase in the number of bowel movements was noticed after the vegetable diet plus fiber (p less than 0.01). We propose the use of vegetable diet plus fiber to facilitate the treatment of patients with both diabetes and hepatic encephalopathy.


Assuntos
Diabetes Mellitus/dietoterapia , Proteínas Alimentares/administração & dosagem , Encefalopatia Hepática/dietoterapia , Proteínas de Plantas/administração & dosagem , Psyllium/administração & dosagem , Adulto , Aminoácidos/análise , Bilirrubina/sangue , Diabetes Mellitus/sangue , Fibras na Dieta/administração & dosagem , Ingestão de Energia , Feminino , Alimentos Fortificados , Glucagon/sangue , Encefalopatia Hepática/sangue , Humanos , Insulina/sangue , Cirrose Hepática/dietoterapia , Masculino , Pessoa de Meia-Idade , Neomicina/administração & dosagem , Tolbutamida/administração & dosagem
17.
Am J Gastroenterol ; 78(8): 517-22, 1983 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-6881119

RESUMO

In a single-blind, cross-over fashion we assessed the therapeutic value of the dopamine agonist bromocriptine at doses of 15 and 20 mg/day plus cleansing enemas, versus the vigorous standard treatment of neomycin 6 g/day plus cleansing enemas. We studied four patients with severe chronic portal systemic encephalopathy. All the patients presented elevated prolactin levels. During the study the following parameters were assessed: mental state, number connection test times, frequency of asterixis, EEG, blood ammonia, and serum prolactin levels. In all but one patient, portal systemic encephalopathy parameters improved during the standard therapy, as opposed to both bromocriptine periods. During the period with 30 mg/day of bromocriptine all four patients developed precoma, although later one patient improved. Serum prolactin levels were rapidly suppressed during both bromocriptine periods. Prolactin levels did not correlate with changes in mental state. In patients with severe portal systemic encephalopathy, treatments with 15 and 30 mg of bromocriptine plus cleansing enemas were no better than the standard therapy.


Assuntos
Bromocriptina/administração & dosagem , Encefalopatia Hepática/tratamento farmacológico , Bromocriptina/efeitos adversos , Bromocriptina/uso terapêutico , Enema , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Neomicina/uso terapêutico , Prolactina/sangue , Inconsciência/tratamento farmacológico
19.
Gastroenterology ; 81(1): 101-6, 1981 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-7239110

RESUMO

A randomized, double-blind comparison of lactose enemas plus placebo tablets vs. starch enemas plus neomycin tablets was performed on 18 patients with acute portal systemic encephalopathy. Ten patients received starch enemas (10%; 1000 ml t.i.d.) plus neomycin tablets and 8 patients received lactose enemas (20%; 1000 ml t.i.d.) plus placebo tablets. A significant mental state improvement was demonstrated in the group of patients treated with starch enemas-neomycin tablets (p less than 0.05) and in the group of patients treated with lactose enemas-placebo tablets (p less than 0.025). Both treatments significantly improved the frequency of asterixis, ammonia blood levels, and electroencephalograms. In addition, patients treated with lactose enemas showed significant improvement in number-connection test times (p less than 0.02), and their stools showed a more acid pH (p less than 0.05). No side effects were evident with either treatment. Lactose enemas are a safe and effective treatment for acute portal systemic encephalopathy.


Assuntos
Encefalopatia Hepática/terapia , Lactose/uso terapêutico , Neomicina/uso terapêutico , Amido/uso terapêutico , Doença Aguda , Adulto , Método Duplo-Cego , Enema , Fezes/análise , Feminino , Humanos , Concentração de Íons de Hidrogênio , Lactose/efeitos adversos , Masculino , Pessoa de Meia-Idade , Placebos , Distribuição Aleatória , Amido/efeitos adversos
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