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1.
Frontline Gastroenterol ; 14(4): 282-286, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37409332

RESUMO

The European Association for the Study of the Liver has recently updated guidance on haemochromatosis with a more extensive discussion on investigation and management.[ The new guidance focuses on non-invasive methods for fibrosis assessment and early diagnosis to include more extensive genetic testing if needed. Early diagnosis and treatment is vital as it reduces morbidity and mortality. We review this guideline and offer key updated messages with a focus on new developments since the last guidance and key aspects of current practice.

3.
Lancet Gastroenterol Hepatol ; 7(8): 755-769, 2022 08.
Artigo em Inglês | MEDLINE | ID: mdl-35490698

RESUMO

Non-alcoholic fatty liver disease (NAFLD) is common, affecting approximately 25% of the general population. The evidence base for the investigation and management of NAFLD is large and growing, but there is currently little practical guidance to support development of services and delivery of care. To address this, we produced a series of evidence-based quality standard recommendations for the management of NAFLD, with the aim of improving patient care. A multidisciplinary group of experts from the British Association for the Study of the Liver and British Society of Gastroenterology NAFLD Special Interest Group produced the recommendations, which cover: management of people with, or at risk of, NAFLD before the gastroenterology or liver clinic; assessment and investigations in secondary care; and management in secondary care. The quality of evidence for each recommendation was evaluated by the Grading of Recommendation Assessment, Development and Evaluation tool. An anonymous modified Delphi voting process was conducted individually by each member of the group to assess the level of agreement with each statement. Statements were included when agreement was 80% or greater. From the final list of statements, a smaller number of auditable key performance indicators were selected to allow services to benchmark their practice. It is hoped that services will review their practice against our recommendations and key performance indicators and institute service development where needed to improve the care of patients with NAFLD.


Assuntos
Gerenciamento Clínico , Hepatopatia Gordurosa não Alcoólica , Indicadores de Qualidade em Assistência à Saúde , Consenso , Técnica Delphi , Humanos , Hepatopatia Gordurosa não Alcoólica/diagnóstico , Hepatopatia Gordurosa não Alcoólica/terapia , Indicadores de Qualidade em Assistência à Saúde/normas , Sociedades Médicas , Reino Unido
4.
Frontline Gastroenterol ; 13(1): 32-38, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-34966531

RESUMO

OBJECTIVE: Primary biliary cholangitis (PBC) is a progressive, autoimmune, cholestatic liver disease affecting approximately 15 000 individuals in the UK. Updated guidelines for the management of PBC were published by The European Association for the Study of the Liver (EASL) in 2017. We report on the first national, pilot audit that assesses the quality of care and adherence to guidelines. DESIGN: Data were collected from 11 National Health Service hospitals in England, Wales and Scotland between 2017 and 2020. Data on patient demographics, ursodeoxycholic acid (UDCA) dosing and key guideline recommendations were captured from medical records. Results from each hospital were evaluated for target achievement and underwent χ2 analysis for variation in performance between trusts. RESULTS: 790 patients' medical records were reviewed. The data demonstrated that the majority of hospitals did not meet all of the recommended EASL standards. Standards with the lowest likelihood of being met were identified as optimal UDCA dosing, assessment of bone density and assessment of clinical symptoms (pruritus and fatigue). Significant variations in meeting these three standards were observed across UK, in addition to assessment of biochemical response to UDCA (all p<0.0001) and assessment of transplant eligibility in high-risk patients (p=0.0297). CONCLUSION: Our findings identify a broad-based deficiency in 'real-world' PBC care, suggesting the need for an intervention to improve guideline adherence, ultimately improving patient outcomes. We developed the PBC Review tool and recommend its incorporation into clinical practice. As the first audit of its kind, it will be used to inform a future wide-scale reaudit.

5.
Eur J Gastroenterol Hepatol ; 28(7): 757-61, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27254536

RESUMO

OBJECTIVES: Liver cirrhosis is associated with osteoporosis leading to an increased risk of fractures. We aimed to establish whether a risk stratification strategy using a fracture risk calculation tool (FRAX) to determine which patients should receive a dual-energy X-ray absorptiometry (DXA) scan is effective in reducing scan rates without compromising sensitivity for detecting osteoporosis. METHODS: A retrospective analysis of 252 patients with liver cirrhosis attending hepatoma surveillance clinics. Receiver operating characteristic analysis was performed to assess sensitivity and specificity at 10-year fracture risk thresholds of 5, 10 and 15%. RESULTS: DXA scans were performed among 252 patients. Mean age was 61.6±10.2 years, of which 53.2% were male. Cirrhosis aetiology was largely a result of alcohol excess (n=33.3%), chronic hepatitis C virus infection (n=20.2%) and nonalcoholic fatty liver disease (n=15.9%). The majority of patients were in good prognostic groups (87.4% Child-Pugh A, 11.3% Child-Pugh B, 1.3% Child-Pugh C). Osteoporosis was present in 19.0% of those who underwent DXA scanning. The optimum 10-year fracture risk threshold was found to be 10% using the FRAX tool. This retained a high sensitivity of 95.8%, specificity 64.7%, and negative predictive value 98.5%. Introduction of a 10% FRAX threshold would result in a reduction of the DXA scanning rate to 46.8% of the current rate. CONCLUSION: A risk stratification strategy for DXA scanning using a fracture risk assessment tool (FRAX) and a 10-year fracture risk threshold of 10% leads to a significant reduction in scan rates without compromising osteoporosis detection rates.


Assuntos
Cirrose Hepática/complicações , Osteoporose/diagnóstico por imagem , Osteoporose/etiologia , Fraturas por Osteoporose/etiologia , Absorciometria de Fóton/métodos , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Seleção de Pacientes , Curva ROC , Encaminhamento e Consulta/organização & administração , Estudos Retrospectivos , Medição de Risco/métodos , Fatores de Risco , Sensibilidade e Especificidade
6.
Hepatology ; 51(1): 191-200, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-20034024

RESUMO

UNLABELLED: Acute fatty liver of pregnancy (AFLP) is a rare disorder which is fatal if not recognized and treated early. Delivery of the feto-placental unit results in dramatic improvement in maternal liver function, suggesting a role for the placenta. However, the mechanisms by which defects in the fetus or placenta lead to maternal liver damage are not well understood and form the focus of this study. Placenta and serum were obtained at delivery from patients with AFLP, and placental mitochondria and peroxisomes were isolated. Placental mitochondrial function, oxidative stress, and fatty acid composition as well as serum antioxidants, oxidative and nitrosative stress markers, and fatty acid analysis were carried out. Hepatocytes in culture were used to evaluate cell death, mitochondrial function, and lipid accumulation on exposure to fatty acids. Oxidative stress was evident in placental mitochondria and peroxisomes of patients with AFLP, accompanied by compromised mitochondrial function. Increased levels of arachidonic acid were also seen in AFLP placenta when compared to control. Patients with AFLP also had a significant increase in oxidative and nitrosative stress markers in serum, along with decreased antioxidant levels and elevated levels of arachidonic acid. These levels of arachidonic acid were capable of inducing oxidative stress in hepatocyte mitochondria accompanied by induction of apoptosis. Exposure to arachidonic acid also resulted in increased lipid deposition in hepatocytes. CONCLUSION: Oxidative stress in placental mitochondria and peroxisomes is accompanied by accumulation of toxic mediators such as arachidonic acid, which may play a causative role in maternal liver damage seen in AFLP.


Assuntos
Fígado Gorduroso/metabolismo , Mitocôndrias/metabolismo , Placenta/metabolismo , Complicações na Gravidez/metabolismo , Antioxidantes/metabolismo , Feminino , Humanos , Estresse Oxidativo/efeitos dos fármacos , Gravidez , Espécies Reativas de Oxigênio/metabolismo
7.
Indian J Med Res ; 128(1): 32-7, 2008 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-18820356

RESUMO

BACKGROUND & OBJECTIVE: An outbreak of symptomatic viral hepatitis in children less than 10 yr of age in Vellore, south India, was investigated and the disease pattern studied using serological and epidemiological methods, supplemented by geographic information systems (GIS) mapping. METHODS: Three cases of hepatitis A were identified during routine surveillance in a birth cohort House-to-house visits were undertaken to identify other symptomatic cases and samples collected for anti- HAV IgM, ELISA testing. All cases and controls were mapped and geo-referenced using Arc View GIS 3.3. Spatial clustering was investigated using SaTScan 7.0.1 software. Drinking water sources were tested for coliform counts with the most probable number technique. RESULTS: Of the 965 children surveyed, 26 (2.78%) had jaundice between February to July 2006. From the 26 patients, 11 (42.3%) blood samples were obtained and tested for anti-HAV IgM; 10 (90.9%) were found to be positive. Water analysis showed high coliform counts in all samples. No spatial clustering of cases could be detected. INTERPRETATION & CONCLUSION: The outbreak was identified because of the symptomatic presentation of the cases. Our study highlighted the increasing detection of symptomatic children with hepatitis A virus infection. Water sources in the area were contaminated and may have served as the source of infection. The lack of clustering in GIS analysis could be due to the common water source.


Assuntos
Surtos de Doenças/estatística & dados numéricos , Hepatite A/epidemiologia , Áreas de Pobreza , População Urbana/estatística & dados numéricos , Criança , Pré-Escolar , Feminino , Humanos , Índia/epidemiologia , Masculino , Abastecimento de Água
8.
J Gastroenterol Hepatol ; 23(11): 1734-8, 2008 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18713304

RESUMO

BACKGROUND AND AIM: The localization of hepatitis B virus (HBV) core antigen to the nucleus or cytoplasm of hepatocytes has biological implications for viral packaging and persistence. This study examined the relationship between the localization of hepatitis B virus antigens, histological activity, and viral titer in patients with chronic HBV infection. METHODS: Liver biopsies from 110 patients with chronic HBV infection were studied. Ishak's scoring system was used for the histological analysis. The localization of hepatitis B surface antigen (HBsAg) and hepatitis B core antigen (HBcAg) and the percentage of hepatocytes stained positive by immunohistochemistry were correlated with viral titer, histological activity, and fibrosis indices using Spearman rank correlation. RESULTS: In 88 hepatitis B e-antigen (HBeAg)-positive individuals, the nuclear localization of HBcAg correlated significantly with DNA titer (r = 0.435, P = 0.001) and negatively with fibrosis (r = -0.297, P = 0.005). The cytoplasmic localization correlated significantly with histological activity (r = 0.211, P = 0.049). In 22 HBeAg-negative individuals, the nuclear localization of HBcAg correlated significantly with histological activity (r = 0.625, P = 0.002), DNA titer (r = 0.651, P = 0.009), and fibrosis (r = 0.447, P = 0.042). The cytoplasmic localization correlated significantly with DNA titer (r = 0.524, P = 0.045) and fibrosis (r = 0.528, P = 0.012). There was no correlation of HBsAg expression with DNA titer, histological activity index, or fibrosis in both groups. HBeAg-positive patients presented at a younger age. CONCLUSION: In HBeAg-positive individuals, nuclear core antigen correlated with DNA titer, and cytoplasmic localization with histological activity, whereas in HBeAg-negative individuals, nuclear localization correlated with DNA titer, histological activity, and fibrosis, and cytoplasmic localization correlated with DNA titer and fibrosis, but not with histological activity. These observations suggest biological differences between HBeAg-positive and -negative disease.


Assuntos
Antígenos da Hepatite B/análise , Vírus da Hepatite B/imunologia , Hepatite B Crônica/diagnóstico , Hepatócitos/virologia , Imuno-Histoquímica , Cirrose Hepática/virologia , Adolescente , Adulto , Biópsia , Núcleo Celular/virologia , Criança , Pré-Escolar , Citoplasma/virologia , DNA Viral/sangue , Feminino , Antígenos do Núcleo do Vírus da Hepatite B/análise , Antígenos de Superfície da Hepatite B/análise , Antígenos E da Hepatite B/análise , Vírus da Hepatite B/genética , Hepatite B Crônica/complicações , Hepatite B Crônica/imunologia , Hepatócitos/patologia , Humanos , Cirrose Hepática/patologia , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Adulto Jovem
9.
Eur J Gastroenterol Hepatol ; 20(8): 810-2, 2008 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-18617789

RESUMO

We report an unusual case of pravastatin-induced colitis in an 80-year old lady. Onset of symptoms was noted within 48 h of starting the medication. Colonoscopy revealed diffuse ulceration throughout the colon with relative sparing of the rectum, with the biopsies showing ulceration and inflammation. The patient received a short course of steroid therapy and 5 months after stopping pravastatin, there was complete macroscopic and microscopic resolution of the colonic lesions. Drug interaction of pravastatin with amitryptiline could have resulted in this uncommon complication.


Assuntos
Colite/induzido quimicamente , Inibidores de Hidroximetilglutaril-CoA Redutases/efeitos adversos , Pravastatina/efeitos adversos , Idoso de 80 Anos ou mais , Colite/diagnóstico , Colite/patologia , Colonoscopia , Feminino , Humanos
10.
Biochim Biophys Acta ; 1782(5): 349-54, 2008 May.
Artigo em Inglês | MEDLINE | ID: mdl-18346470

RESUMO

Human serum albumin binds ligands such as fatty acids and metals in circulation. Oxidative stress can modify albumin and affect ligand binding. This study examines the role of oxidative stress and fatty acids in modulating cobalt binding to albumin in patients with fatty liver. Elevated levels of malondialdehyde and protein carbonyls, indicative of oxidative stress were evident in serum of patients with fatty liver. A significant decrease in albumin-cobalt binding was also observed. Albumin isolated from patient serum also showed an increase in bound fatty acids. In vitro experiments indicated that while oxidant exposure or removal of fatty acids independently decreased cobalt binding to albumin, removal of fatty acids from the protein prior to oxidant exposure did not influence the oxidant effect on albumin-cobalt binding. These results suggest that oxidative stress and fatty acids on albumin can influence albumin-cobalt binding in patients with fatty liver by independent mechanisms.


Assuntos
Cobalto/metabolismo , Ácidos Graxos/metabolismo , Fígado Gorduroso/metabolismo , Albumina Sérica/metabolismo , Adulto , Estudos de Casos e Controles , Sulfato de Cobre/farmacologia , Fígado Gorduroso/enzimologia , Feminino , Humanos , Peróxido de Hidrogênio/farmacologia , Masculino , Malondialdeído/metabolismo , Ligação Proteica/efeitos dos fármacos , Carbonilação Proteica/efeitos dos fármacos , Albumina Sérica/isolamento & purificação , Xantina/metabolismo , Xantina Oxidase/metabolismo
11.
Gastroenterology ; 134(1): 111-9, 2008 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-18166350

RESUMO

BACKGROUND & AIMS: It has been proposed that activation of the sympathetic nervous system causes a rightward shift in the renal autoregulatory curve such that renal blood flow is critically dependent on renal perfusion pressure and that this contributes to the development of the hepatorenal syndrome. The aims of the study were to determine the relationship of renal blood flow and renal perfusion pressure in patients with liver cirrhosis and the effect on renal hemodynamics following insertion of a transjugular intrahepatic portosystemic shunt (TIPS). METHODS: Fifty-six patients were recruited into groups (1) with no ascites, (2) with diuretic-responsive ascites, (3) with intractable ascites, (4) with type II hepatorenal syndrome, and (5) requiring a TIPSs for refractory ascites. We measured cardiac hemodynamics, renal blood flow, renal perfusion pressure, and portal pressure and norepinephrine levels and mathematically modeled the renal autoregulatory curve. RESULTS: Renal blood flow correlated with renal perfusion pressure (r(2) = 0.78; P < .001) and inversely with the hepatic venous pressure gradient (r(2) = 0.61; P < .0001) and plasma norepinephrine levels (r(2) = 0.78; P < .0001). Norepinephrine levels increased with increasing disease severity, and this was associated with a rightward and downward shift of the renal blood flow/renal perfusion pressure autoregulatory curve. TIPS insertion reduced portal pressure and plasma norepinephrine levels (P < .001), and the renal blood flow/renal perfusion pressure curve was shifted upward. CONCLUSIONS: The relationship between renal blood flow and renal perfusion pressure involves a critical interplay between the sympathetic nervous system and the kidney. TIPS insertion decreases sympathetic activation and improves renal function through positive effects on renal blood flow autoregulation.


Assuntos
Síndrome Hepatorrenal/fisiopatologia , Homeostase/fisiologia , Cirrose Hepática/fisiopatologia , Pressão na Veia Porta/fisiologia , Circulação Renal/fisiologia , Sistema Nervoso Simpático/fisiopatologia , Estudos de Coortes , Feminino , Síndrome Hepatorrenal/sangue , Humanos , Cirrose Hepática/sangue , Cirrose Hepática/terapia , Masculino , Pessoa de Meia-Idade , Norepinefrina/sangue , Derivação Portossistêmica Transjugular Intra-Hepática
12.
J Gastroenterol Hepatol ; 22(2): 177-81, 2007 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17295868

RESUMO

BACKGROUND AND AIM: Spontaneous bacterial peritonitis (SBP) is a major complication of liver cirrhosis and accounts for significant mortality. Although oxygen free radicals and nitric oxide been implicated in the pathophysiology of liver cirrhosis, information on their role during the development of SBP is scarce. This study examined these active species in ascitic fluid from patients with SBP, and in response to treatment. METHODS: Forty-nine consecutive patients with cirrhosis and ascitic fluid neutrophil counts less than 250/cumm were studied as controls. Another 21 patients whose ascitic neutrophil count exceeded 250/cumm were treated as cases. Ascitic fluid was collected from these patients at entry and 48 h after treatment with antibiotics. Nitrate and markers of oxidative stress such as malondialdehyde, protein carbonyl content and total and protein thiols were measured. RESULTS: A significant increase in malondialdehyde and protein carbonyl levels was seen in ascites from patients with SBP when compared to controls. This was accompanied by a decrease in total thiols and protein thiols. In addition, there was a significant increase in ascitic fluid nitrate in patients with SBP when compared to control patients. After antibiotic treatment, malondialdehyde, protein carbonyl and nitrate levels dropped back towards control values, and total thiols also recovered. CONCLUSIONS: This study demonstrated the presence of oxidative stress in ascitic fluid from patients with SBP, and showed that ascitic fluid nitrate may be a marker for diagnosing SBP and a useful index in determining therapeutic response to antibiotic treatment.


Assuntos
Líquido Ascítico/metabolismo , Infecções Bacterianas/metabolismo , Óxido Nítrico/metabolismo , Estresse Oxidativo , Peritonite/metabolismo , Feminino , Humanos , Peroxidação de Lipídeos , Cirrose Hepática/metabolismo , Masculino , Pessoa de Meia-Idade , Oxirredução , Proteínas/metabolismo
13.
Indian J Gastroenterol ; 25(3): 128-31, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16877824

RESUMO

BACKGROUND AND OBJECTIVES: The relationship between hepatocyte expression of hepatitis B virus (HBV) antigens, liver histology and viral replication in asymptomatic subjects with incidental detection of hepatitis B surface antigen (HBsAg) remains unclear. We evaluated the histological activity index (HAI) and hepatocyte expression of viral antigens with replicative status in asymptomatic chronic HBV infection. METHODS: Asymptomatic subjects with incidental detection of HBsAg and ALT levels less than twice the upper limit of normal were grouped as follows: Group A - negative for HBeAg and HBV DNA (no HBV replication); B - HBeAg negative, HBV DNA positive (low HBV replication or pre-core mutant); C - positive HBeAg and HBV DNA (high viral replication). Liver biopsies were assessed for HAI (Ishak's scoring system). These were also subjected to immunohistochemistry for expression of HBsAg and hepatitis B core antigen (HBcAg); distribution, staining pattern and quantitative measurement of antigen expression were assessed. RESULTS: Median HAI was similar in the three groups (1.0, 2.0 and 2.0 in groups A, B and C, respectively). All subjects in Group C showed discrete cytoplasmic expression of HBsAg, whereas the other two groups showed heterogeneity in distribution and pattern of HBsAg staining. Quantitative measurement of cytoplasmic HBsAg revealed similar results in the three groups. Core antigen (nuclear) was detected in 4 of 5 subjects in Group C and none of those in Groups A and B. Ground-glass hepatocytes were seen in 20 and orcein-positive cells in 26 cases. HBsAg was detected by immunohistochemistry in 37 biopsies. CONCLUSIONS: Among asymptomatic subjects with chronic HBV infection, those with high rate of viral replication had discrete cytoplasmic HBsAg expression and nuclear expression of core antigen; these findings were uncommon in subjects with low or no viral replication.


Assuntos
Vírus da Hepatite B/isolamento & purificação , Hepatite B Crônica/diagnóstico , Achados Incidentais , Fígado/patologia , Adulto , Alanina Transaminase/metabolismo , Biomarcadores/sangue , DNA Viral/metabolismo , Feminino , Antígenos do Núcleo do Vírus da Hepatite B/metabolismo , Antígenos de Superfície da Hepatite B/metabolismo , Vírus da Hepatite B/imunologia , Hepatite B Crônica/patologia , Hepatócitos/metabolismo , Humanos , Imuno-Histoquímica , Fígado/virologia , Masculino , Sensibilidade e Especificidade , Replicação Viral
14.
World J Gastroenterol ; 12(29): 4764-6, 2006 Aug 07.
Artigo em Inglês | MEDLINE | ID: mdl-16937455

RESUMO

The triple A or Allgrove's syndrome is an autosomal recessive disorder characterized by the triad of achalasia cardia, alacrima and ACTH resistant adrenocortical insufficiency. Mutations of the Achalasia-Addisonianism-Alacrima-Syndrome (AAAS) gene on chromosome 12q13 are associated with this syndrome. We report an Indian family where two siblings were homozygous for a known mutation of the AAAS gene and presented with the classical triad of symptoms. The mother and the brother were heterozygous and asymptomatic. The affected siblings had iron deficiency anemia and the younger sister had pes cavus and palmoplantar keratosis. Neurological symptoms were absent in both affected children. Recognition of this syndrome can lead to early treatment of adrenal insufficency and genetic counselling.


Assuntos
Anormalidades Múltiplas/genética , Doença de Addison/genética , Acalasia Esofágica/diagnóstico , Doenças do Aparelho Lacrimal/genética , Mutação , Complexo de Proteínas Formadoras de Poros Nucleares/genética , Anormalidades Múltiplas/diagnóstico , Doença de Addison/complicações , Doença de Addison/diagnóstico , Adolescente , Acalasia Esofágica/genética , Feminino , Humanos , Índia , Doenças do Aparelho Lacrimal/complicações , Doenças do Aparelho Lacrimal/diagnóstico , Proteínas do Tecido Nervoso , Síndrome , População Branca/genética
15.
Trop Gastroenterol ; 27(3): 105-10, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17310552

RESUMO

Hepatitis C is a global health problem with an estimated 170 million people infected with this virus worldwide. It is an emerging infection in India and is a major public health concern. The exact magnitude of this infection in India has not been defined and the relative contribution of various risk factors has not been clearly elucidated. This review outlines the prevalence of hepatitis C in various population subsets in India, the association of hepatitis C and liver disease in India and the existing genotypes in India.


Assuntos
Hepacivirus/patogenicidade , Hepatite C/epidemiologia , Genótipo , Hepacivirus/genética , Hepatite C/genética , Humanos , Índia/epidemiologia , Prevalência , Fatores de Risco
16.
Indian J Gastroenterol ; 23(1): 26-7, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-15106714

RESUMO

Spontaneous rupture of amyloid liver is a fatal complication. A 48-year-old man with systemic amyloidosis secondary to multiple myeloma presented with acute hemoperitoneum. Emergency angiogram showed extravasation of contrast from the liver into the sub-hepatic space, which was successfully stopped by embolization of the right hepatic artery.


Assuntos
Amiloidose/complicações , Embolização Terapêutica , Hemoperitônio/terapia , Hepatopatias/complicações , Hemoperitônio/etiologia , Artéria Hepática , Humanos , Masculino , Pessoa de Meia-Idade , Ruptura Espontânea
17.
J Gastroenterol Hepatol ; 19(2): 134-8, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-14731121

RESUMO

BACKGROUND AND AIMS: The adverse effect of acute hepatitis A in chronic liver disease is well known. The outcome of acute hepatitis E in chronic liver disease has not been extensively studied. The present study aimed to examine the clinical profile and outcome of patients with chronic liver disease and hepatitis E virus (HEV) superinfection, and the seroprevalence of hepatitis A and E infections in patients with chronic liver disease and controls in India. METHODS: A retrospective study of patients with chronic liver disease and acute icteric hepatitis E was performed. Acute hepatitis E was diagnosed by immunoglobulin (Ig)M ELISA. Seroprevalence studies were carried out using IgG ELISA in 100 patients with chronic liver disease and 79 age- and sex-matched controls. RESULTS: From June 2001 to December 2002, nine patients with chronic liver disease were found to have superinfection with HEV. Out of these, six patients died of advanced liver failure. The etiology of liver disease was Wilson's disease in six, hepatitis B virus in one, autoimmune in one and cryptogenic in one case. The seroprevalence of hepatitis A was 99 and 100% and 56 and 21% for HEV in cases and controls, respectively. CONCLUSIONS: Acute HEV in patients with chronic liver disease has a grave prognosis. Wilson's disease was the most common cause of chronic liver disease complicated by acute HEV. Seroprevalence studies showed that 44% of patients with chronic liver disease were at risk of developing hepatitis E. Hepatitis E vaccine, when available, is indicated for use in this group.


Assuntos
Hepatite E/complicações , Hepatopatias/virologia , Superinfecção/complicações , Doença Aguda , Adolescente , Adulto , Idoso , Anticorpos Antivirais/sangue , Criança , Doença Crônica , Feminino , Hepatite A/complicações , Hepatite E/diagnóstico , Vírus da Hepatite E/isolamento & purificação , Humanos , Imunoglobulina G/sangue , Hepatopatias/fisiopatologia , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Superinfecção/fisiopatologia
18.
J Clin Gastroenterol ; 36(2): 147-8, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12544199

RESUMO

Mycobacterium fortuitum is a rapidly growing Mycobacterium , which usually colonizes the soil, dust and water. It commonly causes skin and soft tissue infections especially in patients who have preceding trauma. We report a case of perianal fistulae caused by M. fortuitum.


Assuntos
Mycobacterium fortuitum , Fístula Retal/microbiologia , Adulto , Diagnóstico Diferencial , Humanos , Masculino , Infecções por Mycobacterium não Tuberculosas/diagnóstico , Infecções por Mycobacterium não Tuberculosas/microbiologia , Fístula Retal/diagnóstico
19.
Eur J Gastroenterol Hepatol ; 14(8): 877-8, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12172409

RESUMO

Extrahepatic manifestations of hepatitis A are very unusual. We describe a case of prolonged cholestatic hepatitis A in a patient with generalized lymphadenopathy. With normalization of transaminases, there was an accompanying reduction in size of these lymph nodes. Lymphadenopathy reflects ongoing hepatic inflammation in prolonged cholestatic hepatitis A.


Assuntos
Colestase/patologia , Hepatite A/patologia , Doenças Linfáticas/patologia , Adulto , Biomarcadores , Biópsia por Agulha , Colestase/diagnóstico , Doença Crônica , Diagnóstico Diferencial , Seguimentos , Hepatite A/diagnóstico , Humanos , Testes de Função Hepática , Doenças Linfáticas/diagnóstico , Masculino , Índice de Gravidade de Doença
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