11 results on '"Edison R. Parise"'
Search Results
2. Utility and limitations of APRI and FIB4 to predict staging in a cohort of nonselected outpatients with hepatitis C
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Ana Cláudia de Oliveira, Ibrahin El-Bacha, Mônica V. Vianna, and Edison R. Parise
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Chronic hepatitis C ,Noninvasive serum markers ,Hepatic fibrosis ,Low-middle income country ,Accuracy ,Specialties of internal medicine ,RC581-951 - Abstract
Background. Chronic hepatitis C(CHC) staging is important for therapeutic decision-making. Identification of noninvasive markers can provide alternatives to liver biopsy.Aim. To assess the value of APRI and FIB4 for CHC fibrosis staging in a cohort of nonselected outpatients from a referral center in Sao Paulo, Brazil.Material and methods. Medical records of 798 adult outpatients were analyzed retrospectively. For calculations of APRI and FIB4, the original descriptions were considered, and markers were compared with degree of liver injury.Results. Overall, 49.3% of participants were female, and mean age was 56.9 ± 12.5 years. Genotype 1 was predominant (71.7vs. 23.7% genotype 3); 64% had significant fibrosis, 44% had advanced fibrosis, and 28% had cirrhosis. The areas under the receiver operating curve for significant fibrosis, advanced fibrosis, and cirrhosis, respectively, were 0.809, 0.819, and 0.815 for the APRI marker and 0.803, 0.836 and 0.852 for FIB4. Using the recommended cut off values, approximately 30-40% of the patients could not be classified. In the remainder, either APRI or FIB4 alone correctly diagnosed 80-85% of cases. Concomitant or consecutive use of both APRI and FIB4 increased the number of the cases correctly diagnosed only slightly, but also increased the number of patients not classified within the cutoff values.Conclusions. In conclusion, use of the APRI or FIB4 markers for detection of hepatic fibrosis may be a viable alternative at referral centers for treatment of CHC in low- and middleincome countries. Despite relatively good accuracy, a significant number of patients could not be assessed by these methods.
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- 2016
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3. Re-treatment of previous non-responders and relapsers to interferon plus ribavirin with peginterferon alfa-2a (40KD), ribavirin ± amantadine in patients with chronic hepatitis C: randomized multicentre clinical trial
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Mario G. Pessôa, Hugo Cheinquer, Paulo R.L. Almeida, Giovanni F. Silva, Maria Patelli J.S. Lima, Raymundo Paraná, Marco A. Lacerda, Edison R. Parise, José R.B. Pernambuco, Suelene S. Pedrosa, Rosângela Teixeira, Hoel Sette, Jr, and Fernando Tatsch
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Hepatitis C ,Re-treatment ,Peginterferon alfa-2a (40KD) ,Amantadine ,Specialties of internal medicine ,RC581-951 - Abstract
Introduction. A large number of patients with chronic hepatitis C have not been cured with interferon-based therapy. Therefore, we evaluated the efficacy of amantadine combined with the standard of care (pegylated interferon plus ribavirin) in patients who had not responded to or had relapsed after ≥ 24 weeks of treatment with conventional interferon plus ribavirin.Material and methods. Patients stratified by previous response (i.e., non-response or relapse) were randomized to 48 weeks of open-label treatment with peginterferon alfa-2a (40KD) 180 μg/week plus ribavirin 1,000/1,200 mg/day plus amantadine 200 mg/ day (triple therapy), or the standard of care (peginterferon alfa-2a [40KD] plus ribavirin).Results. The primary outcome was sustained virological response (SVR), defined as undetectable hepatitis C virus RNA in serum (< 50 lU/mL) at end of follow-up (week 72). Among patients with a previous non-response, 12/53 (22.6%; 95% confidence interval [CI] 12.3-36.2%) randomized to triple therapy achieved an SVR compared with 16/52 (30.8%; 95% CI 18.7-45.1%) randomized to the standard of care. Among patients with a previous relapse 22/39 (56.4%; 95% CI 39.6-72.2%) randomized to triple therapy achieved an SVR compared with 23/38 (60.5%; 95% CI 43.4-76.0%) randomized to the standard of care. Undetectable HCV RNA (< 50 IU/mL) at week 12 had a high positive predictive value for SVR. A substantial proportion of non-responders and relapsers to conventional interferon plus ribavirin achieve an SVR when re-treated with peginterferon alfa-2a (40KD) plus ribavirin.Conclusion. Amantadine does not enhance SVR rates in previously treated patients with chronic hepatitis C and cannot be recommended in this setting.
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- 2012
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4. Nonalcoholic fatty liver disease in Brazil. Clinical and histological profile
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Helma P. Cotrim, Edison R. Parise, Claudia P.M.S. Oliveira, Natalhie Leite, Ana Martinelli, Joào Galizzi, Rita de Càssia Silva, Ângelo Mattos, Leila Pereira, Waldir Amorim, Claúdia Ivantes, Francisco Souza, Marcelo Costa, Lizomar Maia, Màrio Pessoa, and Frederico Oliveira
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Nonalcoholic steatohepatitis ,Metabolic Syndrome ,Insulin resistance ,NAFLD in South America ,NASH ,MeSH ,Specialties of internal medicine ,RC581-951 - Abstract
Background. The epidemiology and clinical characteristics of nonalcoholic fatty liver disease (NAFLD) in South America are not well known. Brazil is a largest country in this part of the world and the present study aimed to contribute with this information.Methods. This descriptive study included patients from medical centers around Brazil, who had diagnosis of NAFLD. They were selected from chart review and also prospectively in Hepatology out-clinics. Patients with history of alcohol intake and others liver diseases were excluded. Histological diagnosis included: steatosis or steatohepatitis (steatosis, ballooning of hepatocytes or fibrosis). The criteria to perform a liver biopsy was ALT or AST > 1.5 × normal levels.Results. A total of 1280 patients from 16 Brazilian centers and all five regions were included. The mean age was 49.68 ± 13.59 years; 53.3% were males and 85% were asymptomatic. Hyperlipidemia was observed in 66.8% cases, obesity in 44.7%, overweight in 44.4%, diabetes in 22.7%, and toxins exposure in 10%. Metabolic syndrome was observed in 41.3% cases. Elevated levels of ALT, AST and GGT were observed in 55.8%, 42.2% and 63.1% cases, respectively. Liver biopsy performed in 437 cases showed: isolate steatosis in 42% cases, steatohepatitis in 58% and 27% of them also presented fibrosis. Cirrhosis was observed in 15.4% and hepatocellular carcinoma in 0.7%.Conclusions. NAFLD in Brazil is more frequent in asymptomatic males; steatohepatitis with fibrosis and cirrhosis were a significant diagnosis. The genetic predisposition and lifestyle should be influenced in the spectrum; however these findings deserve a future investigation.
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- 2011
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5. Latin American Association for the Study of the Liver Recommendations on Treatment of Hepatitis C
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Nahum Méndez-Sánchez, Raymundo Paraná, Hugo Cheinquer, Angelo Alves de Mattos, Adrian Gadano, Marcelo Silva, Mario G. Pessôa, Maria L. Gomes-Ferraz, Alejandro Soza, M. Cassia Mendes-Correa, Norberto C. Chávez-Tapia, Lucy Dagher, Martín Padilla, Nelia Hernandez, Juan F. Sánchez-Avila, Fernando Contreras, Henrique S. Moraes-Coelho, Edison R. Parise, Fernando Bessone, and Misael Uribe
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Hepatitis C ,Pegylated interferon ,Ribavarin ,Direct-acting antiviral ,Specialties of internal medicine ,RC581-951 - Published
- 2014
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6. Serum bile acids in schistosomotic hepatic fibrosis
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Edison R. Parise
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Arctic medicine. Tropical medicine ,RC955-962 - Published
- 1992
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7. Laminina e hipertensão portal Laminin and portal hypertension
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Edison R. Parise
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Microbiology ,QR1-502 ,Infectious and parasitic diseases ,RC109-216 - Published
- 1991
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8. Cardiometabolic disorders, inflammation and the incidence of non-alcoholic fatty liver disease: A longitudinal study comparing lean and non-lean individuals
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Ehimen C. Aneni, Gul Jana Saeed, Marcio Sommer Bittencourt, Miguel Cainzos-Achirica, Chukwuemeka U. Osondu, Matthew Budoff, Edison R. Parise, Raul D. Santos, Khurram Nasir, and Senechal, Martin
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Inflammation ,Blood Glucose ,Multidisciplinary ,General Science & Technology ,Incidence ,Prevention ,Liver Disease ,Chronic Liver Disease and Cirrhosis ,nutritional and metabolic diseases ,Cardiovascular ,Body Mass Index ,Alcoholism ,C-Reactive Protein ,Risk Factors ,Non-alcoholic Fatty Liver Disease ,Clinical Research ,Hypertension ,Humans ,2.1 Biological and endogenous factors ,Longitudinal Studies ,Aetiology ,Digestive Diseases - Abstract
Background There is limited knowledge about the risk of non-alcoholic fatty liver disease (NAFLD) associated with cardiometabolic disorders in lean persons. This study examines the contribution of cardiometabolic disorders to NAFLD risk among lean individuals and compares to non-lean individuals. Methods We analyzed longitudinal data from 6,513 participants of a yearly voluntary routine health testing conducted at the Hospital Israelita Albert Einstein, Brazil. NAFLD was defined as hepatic ultrasound diagnosed fatty liver in individuals scoring below 8 on the alcohol use disorders identification test. Our main exposure variables were elevated blood glucose, elevated blood pressure (BP), presence of atherogenic dyslipidemia (AD, defined as the combination of elevated triglycerides and low HDL cholesterol) and physical inactivity ( Results Over 15,580 person-years (PY) of follow-up, the incidence rate of NAFLD was 7.7 per 100 PY. In multivariate analysis adjusting for likely confounders, AD was associated with a 72% greater risk of NAFLD (IRR: 1.72 [95% CI:1.32–2.23]). Elevated blood glucose (IRR: 1.71 [95%CI: 1.29–2.28]) and physical inactivity (IRR: 1.46 [95%CI: 1.28–1.66]) were also independently associated with increased risk of NAFLD. In lean individuals, AD, elevated blood glucose and elevated BP were significantly associated with NAFLD although for elevated blood glucose, statistical significance was lost after adjusting for possible confounders. Physical inactivity and elevations in HsCRP were not associated with the risk of NAFLD in lean individuals only. Among lean (and non-lean) individuals, there was an independent association between progressively increasing waist circumference and NAFLD. Conclusion Cardiometabolic risk factors are independently associated with NAFLD. However, there are significant differences in the metabolic risk predictors of NAFLD between lean and non-lean individuals. Personalized cardiovascular disease risk stratification and appropriate preventive measures should be considered in both lean and non-lean individuals to prevent the development of NAFLD.
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- 2022
9. Re-treatment of previous non-responders and relapsers to interferon plus ribavirin with peginterferon alfa-2a (40KD), ribavirin ± amantadine in patients with chronic hepatitis C: randomized multicentre clinical trial
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Mario G, Pessôa, Hugo, Cheinquer, Paulo R L, Almeida, Giovanni F, Silva, Maria Patelli J S, Lima, Raymundo, Paraná, Marco A, Lacerda, Edison R, Parise, José R B, Pernambuco, Suelene S, Pedrosa, Rosângela, Teixeira, Hoel, Sette, and Fernando, Tatsch
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Adult ,Male ,Dose-Response Relationship, Drug ,Interferon-alpha ,Hepacivirus ,Hepatitis C, Chronic ,Middle Aged ,Antiviral Agents ,Recombinant Proteins ,Polyethylene Glycols ,Treatment Outcome ,Drug Resistance, Viral ,Ribavirin ,Amantadine ,Secondary Prevention ,Humans ,RNA, Viral ,Drug Therapy, Combination ,Female ,Follow-Up Studies - Abstract
A large number of patients with chronic hepatitis C have not been cured with interferon-based therapy. Therefore, we evaluated the efficacy of amantadine combined with the standard of care(pegylated interferon plus ribavirin) in patients who had not responded to or had relapsed after ≥ 24 weeks of treatment with conventional interferon plus ribavirin.Patients stratified by previous response (i.e., non-response or relapse) were randomized to 48 weeks of open-label treatment with peginterferon alfa-2a (40KD) 180 µg/week plus ribavirin 1,000/1,200 mg/day plus amantadine 200 mg/day (triple therapy), or the standard of care (peginterferon alfa-2a [40KD] plus ribavirin).The primary outcome was sustained virological response (SVR), defined as undetectable hepatitis C virus RNA in serum (50 IU/mL) at end of follow-up (week 72). Among patients with a previous non-response, 12/53 (22.6%; 95% confidence interval [CI] 12.3-36.2%) randomized to triple therapy achieved an SVR compared with 16/52 (30.8%; 95% CI 18.7-45.1%) randomized to the standard of care. Among patients with a previous relapse 22/39 (56.4%; 95% CI 39.6-72.2%) randomized to triple therapy achieved an SVR compared with 23/38 (60.5%; 95% CI 43.4-76.0%) randomized to the standard of care. Undetectable HCV RNA (50 IU/mL) at week 12 had a high positive predictive value for SVR. A substantial proportion of non-responders and relapsers to conventional interferon plus ribavirin achieve an SVR when re-treated with peginterferon alfa-2a (40KD) plus ribavirin.Amantadine does not enhance SVR rates in previously treated patients with chronic hepatitis C and cannot be recommended in this setting.
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- 2011
10. NONALCOHOLIC FATTY LIVER DISEASE BRAZILIAN SOCIETY OF HEPATOLOGY CONSENSUS
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Helma P COTRIM, Edison R PARISE, Cláudio FIGUEIREDO-MENDES, João GALIZZI-FILHO, Gilda PORTA, and Claudia P OLIVEIRA
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Fígado gorduroso ,terapia. Hepatopatia gordurosa não alcoólica ,diagnóstico. Consenso. ,Diseases of the digestive system. Gastroenterology ,RC799-869 - Abstract
ABSTRACT The prevalence of obesity-related metabolic syndrome has rapidly increased in Brazil, resulting in a high frequency of nonalcoholic fatty liver disease, that didn't receive much attention in the past. However, it has received increased attention since this disease was identified to progress to end-stage liver diseases, such as cirrhosis and hepatocellular carcinoma. Clinical practice guidelines for the diagnosis and treatment of nonalcoholic fatty liver disease have not been established in Brazil. The Brazilian Society of Hepatology held an event with specialists' members from all over Brazil with the purpose of producing guideline for Nonalcoholic Fatty Liver Disease based on a systematic approach that reflects evidence-based medicine and expert opinions. The guideline discussed the following subjects: 1-Concepts and recommendations; 2-Diagnosis; 3-Non-medical treatment; 4-Medical treatment; 5-Pediatrics - Diagnosis; 6-Pediatrics - Non-medical treatment; 7-Pediatrics - Medical treatment; 8-Surgical treatment.
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11. Brazilian society of hepatology recommendations for the diagnosis and treatment of hepatocellular carcinoma
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Flair J Carrilho, Angelo Alves de Mattos, Alex F Vianey, Denise Cerqueira P Vezozzo, Fábio Marinho, Francisco J Souto, Helma P Cotrim, Henrique Sergio M Coelho, Ivonete Silva, José Huygens P Garcia, Luciana Kikuchi, Patricia Lofego, Wellington Andraus, Edna Strauss, Giovanni Silva, Isaac Altikes, Jose Eymard Medeiros, Paulo L Bittencourt, and Edison R Parise
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Carcinome hepatocelular ,Tumores malignos do fígado ,Rastreamento de tumores hepáticos ,Diagnósticos e tratamento do carcinoma hepatocelular ,Carcinoma hepatocelular em fígado não cirrótico ,Diseases of the digestive system. Gastroenterology ,RC799-869 - Abstract
ABSTRACT Hepatocellular carcinoma is a malignancy of global importance and is associated with a high rate of mortality. Recent advances in the diagnosis and treatment of this disease make it imperative to update the recommendations on the management of the disease. In order to draw evidence-based recommendations concering the diagnosis and management of hepatocellular carcinoma, the Brazilian Society of Hepatology has sponsored a single-topic meeting in João Pessoa (PB). All the invited pannelists were asked to make a systematic review of the literature and to present topics related to the risk factors for its development, methods of screening, radiological diagnosis, staging systems, curative and palliative treatments and hepatocellular carcinoma in noncirrhotic liver. After the meeting, all panelists gathered together for the discussion of the topics and the elaboration of those recommendations. The text was subsequently submitted for suggestions and approval of all members of the Brazilian Society of Hepatology through its homepage. The present paper is the final version of the reviewed manuscript containing the recommendations of the Brazilian Society of Hepatology.
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