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1.
Ann Hepatol ; 18(6): 849-854, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-31537509

RESUMO

INTRODUCTION AND OBJECTIVES: Direct antiviral agents (DAAs) including sofosbuvir (SOF), daclatasvir (DCV), simeprevir (SIM) and ombitasvir, paritaprevir and dasabuvir were introduced 2015 in Brazil for treatment of hepatitis C virus (HCV) infection. The aims of this study were to assess effectiveness and safety of HCV treatment with DAA in real-life world in a highly admixed population from Brazil. MATERIALS AND METHODS: All Brazilian reference centers for HCV treatment were invited to take part in a web-based registry, prospectively conducted by the Brazilian Society of Hepatology, to assess outcomes of HCV treatment in Brazil with DAAs. Data to be collected included demographics, disease severity and comorbidities, genotype (GT), viral load, DAA regimens, treatment side effects and sustained virological response (SVR). RESULTS: 3939 patients (60% males, mean age 58±10 years) throughout the country were evaluated. Most had advanced fibrosis or cirrhosis, GT1 and were treated with SOF/DCV or SOF/SIM. Overall SVR rates were higher than 95%. Subjects with decompensated cirrhosis, GT2 and GT3 have lower SVR rates of 85%, 90% and 91%, respectively. Cirrhosis and decompensated cirrhosis in GT1 and male sex and decompensated cirrhosis in GT3 were significantly associated with no SVR. Adverse events (AD) and serious AD occurred in 18% and 5% of those subjects, respectively, but less than 1% of patients required treatment discontinuation. CONCLUSION: SOF-based DAA regimens are effective and safe in the heterogeneous highly admixed Brazilian population and could remain an option for HCV treatment at least in low-income countries.


Assuntos
Antivirais/uso terapêutico , Hepatite C Crônica/tratamento farmacológico , Imidazóis/uso terapêutico , Cirrose Hepática/patologia , Ribavirina/uso terapêutico , Simeprevir/uso terapêutico , Sofosbuvir/uso terapêutico , Idoso , Brasil , Carbamatos , Quimioterapia Combinada , Feminino , Genótipo , Hepacivirus/genética , Hepatite C Crônica/complicações , Humanos , Cirrose Hepática/diagnóstico por imagem , Cirrose Hepática/etiologia , Masculino , Pessoa de Meia-Idade , Prognóstico , Estudos Prospectivos , Pirrolidinas , Fatores Sexuais , Resposta Viral Sustentada , Valina/análogos & derivados
2.
Rev Soc Bras Med Trop ; 51(1): 14-20, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29513836

RESUMO

INTRODUCTION: In 2013, combination therapy using peginterferon, ribavirin, and boceprevir or telaprevir was introduced to treat hepatitis C virus genotype 1 infection in Brazil. The effectiveness of this therapy in four Brazilian regions was evaluated. METHODS: Clinical and virological data were obtained from patients of public health institutions in five cities, including sustained virological response (SVR) and side effects. Patients with advanced fibrosis (F3/4), moderate fibrosis (F2) for > 3 years, or extra-hepatic manifestations were treated according to Ministry of Health protocol. Treatment effectiveness was verified by using bivariate and multivariate analysis; p-values of < 0.05 were considered significant. RESULTS: Of 275 patients (64.7% men; average age, 57 years old), most (61.8%) were treatment-experienced; 53.9% had subgenotype 1a infection, 85.1% had advanced fibrosis, and 85.5% were treated with telaprevir. SVR was observed in 54.2%. Rapid virological response (RVR) was observed in 54.6% of patients (data available for 251 patients). Overall, 87.5% reported side effects and 42.5% did not complete treatment. Skin rash, severe infection, and death occurred in 17.8%, 2.5%, and death in 1.4% of cases, respectively. SVR was associated with treatment completion, RVR, and anemia. CONCLUSIONS: The effectiveness of hepatitis C virus triple therapy was lower than that reported in phase III clinical trials, possibly owing to the prioritized treatment of patients with advanced liver fibrosis. The high frequency of side effects and treatment interruptions observed supported the decision of the Brazilian authorities to suspend its use when safer and more effective drugs became available in 2015.


Assuntos
Hepacivirus/genética , Hepatite C Crônica/tratamento farmacológico , Inibidores de Proteases/administração & dosagem , Adulto , Idoso , Protocolos Clínicos , Quimioterapia Combinada , Feminino , Genótipo , Hepatite C Crônica/virologia , Humanos , Interferons/administração & dosagem , Masculino , Pessoa de Meia-Idade , Oligopeptídeos/administração & dosagem , Prolina/administração & dosagem , Prolina/análogos & derivados , Ribavirina/administração & dosagem , Resposta Viral Sustentada , Resultado do Tratamento
3.
Rev. Soc. Bras. Med. Trop ; 51(1): 14-20, Jan.-Feb. 2018. tab
Artigo em Inglês | LILACS | ID: biblio-897052

RESUMO

Abstract INTRODUCTION: In 2013, combination therapy using peginterferon, ribavirin, and boceprevir or telaprevir was introduced to treat hepatitis C virus genotype 1 infection in Brazil. The effectiveness of this therapy in four Brazilian regions was evaluated. METHODS: Clinical and virological data were obtained from patients of public health institutions in five cities, including sustained virological response (SVR) and side effects. Patients with advanced fibrosis (F3/4), moderate fibrosis (F2) for > 3 years, or extra-hepatic manifestations were treated according to Ministry of Health protocol. Treatment effectiveness was verified by using bivariate and multivariate analysis; p-values of < 0.05 were considered significant. RESULTS: Of 275 patients (64.7% men; average age, 57 years old), most (61.8%) were treatment-experienced; 53.9% had subgenotype 1a infection, 85.1% had advanced fibrosis, and 85.5% were treated with telaprevir. SVR was observed in 54.2%. Rapid virological response (RVR) was observed in 54.6% of patients (data available for 251 patients). Overall, 87.5% reported side effects and 42.5% did not complete treatment. Skin rash, severe infection, and death occurred in 17.8%, 2.5%, and death in 1.4% of cases, respectively. SVR was associated with treatment completion, RVR, and anemia. CONCLUSIONS: The effectiveness of hepatitis C virus triple therapy was lower than that reported in phase III clinical trials, possibly owing to the prioritized treatment of patients with advanced liver fibrosis. The high frequency of side effects and treatment interruptions observed supported the decision of the Brazilian authorities to suspend its use when safer and more effective drugs became available in 2015.


Assuntos
Humanos , Masculino , Feminino , Adulto , Idoso , Inibidores de Proteases/administração & dosagem , Hepacivirus/genética , Hepatite C Crônica/tratamento farmacológico , Oligopeptídeos/administração & dosagem , Ribavirina/administração & dosagem , Prolina/administração & dosagem , Prolina/análogos & derivados , Protocolos Clínicos , Interferons/administração & dosagem , Resultado do Tratamento , Hepatite C Crônica/virologia , Quimioterapia Combinada , Resposta Viral Sustentada , Genótipo , Pessoa de Meia-Idade
4.
São Paulo med. j ; 133(6): 525-530, Nov.-Dec. 2015. tab, graf
Artigo em Inglês | LILACS | ID: lil-770149

RESUMO

CONTEXT: Orthotopic liver transplantation (OLT) is the treatment of choice for end-stage liver disease. Cirrhosis due to hepatitis C infection is the leading indication for liver transplantation worldwide. However, patients who are given transplants because of viral liver diseases often present clinical coinfections, including hepatitis B together with hepatitis D. Currently, different strategies exist for patient management before and after liver transplantation, and these are based on different protocols developed by the specialized transplantation centers. CASE REPORT: We present a rare case of a 58-year-old man with chronic hepatitis B, C and D coinfection. The patient developed cirrhosis and hepatocellular carcinoma. His treatment comprised antiviral therapy for the three viruses and OLT. The patient's outcome was satisfactory. CONCLUSION: OLT, in association with antiviral therapy using entecavir, which was administered before and after transplantation, was effective for sustained clearance of the hepatitis B and D viruses. A recurrence of hepatitis C infection after transplantation responded successfully to standard treatment comprising peginterferon alfa-2A and ribavirin.


CONTEXTO: O transplante ortotópico de fígado (TOF) é o tratamento de escolha em pacientes com doença hepática terminal. A cirrose por hepatite C é a principal indicação de transplante hepático no mundo. No entanto, pacientes transplantados por hepatopatias virais frequentemente apresentam coinfecções, como hepatite B associada a hepatite D. Atualmente, existem diferentes estratégias de manejo em pacientes pré e pós-transplantados conforme diferentes protocolos de conduta de serviços especializados em transplante. RELATO DE CASO: Apresentamos o raro caso de um homem de 58 anos diagnosticado com as hepatites crônicas B, C e D. O paciente evoluiu com cirrose e carcinoma hepatocelular. O tratamento consistiu de terapia antiviral para os três vírus e de transplante ortotópico de fígado. O desfecho do paciente foi satisfatório. CONCLUSÃO: O transplante ortotópico de fígado, associado à terapia antiviral com entecavir antes e após o procedimento, foi eficaz na depuração sustentada dos vírus B e D. A recidiva do vírus C após o transplante respondeu com sucesso ao tratamento padrão com alfapeginterferon 2A e ribavirina.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Carcinoma Hepatocelular/cirurgia , Hepatite Viral Humana/tratamento farmacológico , Hepatite Viral Humana/cirurgia , Cirrose Hepática/cirurgia , Neoplasias Hepáticas/cirurgia , Transplante de Fígado/métodos , Antivirais/uso terapêutico , Coinfecção/tratamento farmacológico , Coinfecção/cirurgia , Hepatite B/tratamento farmacológico , Hepatite B/cirurgia , Hepatite C/tratamento farmacológico , Hepatite C/cirurgia , Hepatite D/tratamento farmacológico , Hepatite D/cirurgia , Interferon-alfa/uso terapêutico , Cirrose Hepática/virologia , Polietilenoglicóis/uso terapêutico , Proteínas Recombinantes/uso terapêutico , Recidiva , Ribavirina/uso terapêutico , Resultado do Tratamento
5.
Sao Paulo Med J ; 133(6): 525-30, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26176835

RESUMO

CONTEXT: Orthotopic liver transplantation (OLT) is the treatment of choice for end-stage liver disease. Cirrhosis due to hepatitis C infection is the leading indication for liver transplantation worldwide. However, patients who are given transplants because of viral liver diseases often present clinical coinfections, including hepatitis B together with hepatitis D. Currently, different strategies exist for patient management before and after liver transplantation, and these are based on different protocols developed by the specialized transplantation centers. CASE REPORT: We present a rare case of a 58-year-old man with chronic hepatitis B, C and D coinfection. The patient developed cirrhosis and hepatocellular carcinoma. His treatment comprised antiviral therapy for the three viruses and OLT. The patient's outcome was satisfactory. CONCLUSION: OLT, in association with antiviral therapy using entecavir, which was administered before and after transplantation, was effective for sustained clearance of the hepatitis B and D viruses. A recurrence of hepatitis C infection after transplantation responded successfully to standard treatment comprising peginterferon alfa-2A and ribavirin.


Assuntos
Carcinoma Hepatocelular/cirurgia , Hepatite Viral Humana/tratamento farmacológico , Hepatite Viral Humana/cirurgia , Cirrose Hepática/cirurgia , Neoplasias Hepáticas/cirurgia , Transplante de Fígado/métodos , Antivirais/uso terapêutico , Coinfecção/tratamento farmacológico , Coinfecção/cirurgia , Hepatite B/tratamento farmacológico , Hepatite B/cirurgia , Hepatite C/tratamento farmacológico , Hepatite C/cirurgia , Hepatite D/tratamento farmacológico , Hepatite D/cirurgia , Humanos , Interferon-alfa/uso terapêutico , Cirrose Hepática/virologia , Masculino , Pessoa de Meia-Idade , Polietilenoglicóis/uso terapêutico , Proteínas Recombinantes/uso terapêutico , Recidiva , Ribavirina/uso terapêutico , Resultado do Tratamento
6.
São Paulo; s.n; 2011. 166 p.
Tese em Português | LILACS | ID: lil-643279

RESUMO

Introdução: Vários fatores têm sido apontados como associados à progressão da hepatite B crônica para cirrose, entre eles o genótipo, mutações do VHB, status do HBeAg, infecção concorrentes com o VHD, HIV, VHC, assim como o uso de álcool, alterações metabólicas e idade em que ocorreu a infecção. No entanto, essa questão ainda não foi estudada na Amazônia Ocidental brasileira, área hiperendêmica de hebatite B. Objetivo: descrever os aspectos clínico-epidemiológicos e investigar fatores associados à progressão da cirrose numa coorte de pacientes com hepatite crônica pelo vírus B residente no estado do Acre, atendidos em serviço especializado entre 2000 e 2009. Métodos: estudo de coorte retrospectiva, abrangendo 672 pacientes com hepatite crônica pelo vírus B matriculados no Serviço de Assistência Especializada, Rio Branco, Acre, na Amazônia Ocidental, selecionados no período de 2000 a 2009 e acompanhados até 2010. Os dados foram obtidos mediante consulta a prontuários, complementados por entrevista, exames físicos e laboratoriais. Os casos de cirrose hepática foram confirmados pela presença de fibrose, formação de nódulos parenquimatosos regenerados ou em regeneração ao exame anatomopatológico (F3 e F4) e/ou pela presença de sinais de descompensação hepática ou de hipertensão portal demonstrada através da ultrasonografia abdominal e endoscopia. Foram excluídos do estudo os pacientes que apresentaram hepatocarcinoma, coinfecção com o HIV no momento da primeira avaliação. As variáveis de interesse foram: sócio-demográficas; características relativas à transmissão, aspectos clínicos e laboratoriais. Inicialmente, descreveram-se as características dos pacientes mediante comparações de proporções e médias aplicando-se para variáveis categóricas o teste do qui quadrado e exato de Fisher; e para as variáveis contínuas o teste de Kruskall-Walis.


Assuntos
Humanos , Cirrose Hepática/diagnóstico , Cirrose Hepática/etiologia , Hepatite B Crônica/complicações , Hepatite B Crônica/epidemiologia , Ambulatório Hospitalar , Brasil , Estudos de Coortes , Prognóstico , Estudos Retrospectivos
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