Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomes

Detalhes bibliográficos
Autor(a) principal: Porta,Gilda
Data de Publicação: 2019
Outros Autores: Carvalho,Elisa de, Santos,Jorge L., Gama,Jorge, Borges,Cristian V., Seixas,Renata B.P.M., Ferreira,Alexandre R., Miura,Irene K., Silveira,Themis R., Silva,Luciana R., Fagundes,Eleonora D.T., Bellomo-Brandao,Maria A., Sawamura,Regina, Vieira,Sandra M., Melere,Melina U., Marques,Cibele D.F., Pugliese,Renata P., Danesi,Vera L., Porta,Adriana, Marsillac,Marise E., Valladares,Marcia A., Menezes,Daniela G., Kieling,Carlos, Paula,Mariana N. de, Vasconcelos,Juliana R., Ferreira,Cristina T., Perin,Nilza, Resende,Leonardo R., Maia,Jussara, Tommaso,Adriana M.A. De, Hessel,Gabriel
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Jornal de Pediatria (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572019000500419
Resumo: Abstract Objective: This large study with a long-term follow-up aimed to evaluate the clinical presentation, laboratory findings, histological profile, treatments, and outcomes of children and adolescents with autoimmune hepatitis. Methods: The medical records of 828 children and adolescents with autoimmune hepatitis were reviewed. A questionnaire was used to collect anonymous data on clinical presentation, biochemical and histological findings, and treatments. Results: Of all patients, 89.6% had autoimmune hepatitis-1 and 10.4% had autoimmune hepatitis-2. The female sex was predominant in both groups. The median age at symptom onset was 111.5 (6; 210) and 53.5 (8; 165) months in the patients with autoimmune hepatitis 1 and autoimmune hepatitis-2, respectively. Acute clinical onset was observed in 56.1% and 58.8% and insidious symptoms in 43.9% and 41.2% of the patients with autoimmune hepatitis-1 and autoimmune hepatitis-2, respectively. The risk of hepatic failure was 1.6-fold higher for autoimmune hepatitis-2. Fulminant hepatic failure occurred in 3.6% and 10.6% of the patients with autoimmune hepatitis-1 and autoimmune hepatitis-2, respectively; the risk was 3.1-fold higher for autoimmune hepatitis-2. The gamma globulin and immunoglobulin G levels were significantly higher in autoimmune hepatitis-1, while the immunoglobulin A and C3 levels were lower in autoimmune hepatitis-2. Cirrhosis was observed in 22.4% of the patients; biochemical remission was achieved in 76.2%. The actuarial survival rate was 93.0%. A total of 4.6% underwent liver transplantation, and 6.9% died (autoimmune hepatitis-1: 7.5%; autoimmune hepatitis-2: 2.4%). Conclusions: In this large clinical series of Brazilian children and adolescents, autoimmune hepatitis-1 was more frequent, and patients with autoimmune hepatitis-2 exhibited higher disease remission rates with earlier response to treatment. Patients with autoimmune hepatitis-1 had a higher risk of death.
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spelling Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomesAutoimmune hepatitisClinicalLaboratoryTreatmentsOutcomesBrazilAbstract Objective: This large study with a long-term follow-up aimed to evaluate the clinical presentation, laboratory findings, histological profile, treatments, and outcomes of children and adolescents with autoimmune hepatitis. Methods: The medical records of 828 children and adolescents with autoimmune hepatitis were reviewed. A questionnaire was used to collect anonymous data on clinical presentation, biochemical and histological findings, and treatments. Results: Of all patients, 89.6% had autoimmune hepatitis-1 and 10.4% had autoimmune hepatitis-2. The female sex was predominant in both groups. The median age at symptom onset was 111.5 (6; 210) and 53.5 (8; 165) months in the patients with autoimmune hepatitis 1 and autoimmune hepatitis-2, respectively. Acute clinical onset was observed in 56.1% and 58.8% and insidious symptoms in 43.9% and 41.2% of the patients with autoimmune hepatitis-1 and autoimmune hepatitis-2, respectively. The risk of hepatic failure was 1.6-fold higher for autoimmune hepatitis-2. Fulminant hepatic failure occurred in 3.6% and 10.6% of the patients with autoimmune hepatitis-1 and autoimmune hepatitis-2, respectively; the risk was 3.1-fold higher for autoimmune hepatitis-2. The gamma globulin and immunoglobulin G levels were significantly higher in autoimmune hepatitis-1, while the immunoglobulin A and C3 levels were lower in autoimmune hepatitis-2. Cirrhosis was observed in 22.4% of the patients; biochemical remission was achieved in 76.2%. The actuarial survival rate was 93.0%. A total of 4.6% underwent liver transplantation, and 6.9% died (autoimmune hepatitis-1: 7.5%; autoimmune hepatitis-2: 2.4%). Conclusions: In this large clinical series of Brazilian children and adolescents, autoimmune hepatitis-1 was more frequent, and patients with autoimmune hepatitis-2 exhibited higher disease remission rates with earlier response to treatment. Patients with autoimmune hepatitis-1 had a higher risk of death.Sociedade Brasileira de Pediatria2019-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572019000500419Jornal de Pediatria v.95 n.4 2019reponame:Jornal de Pediatria (Online)instname:Sociedade Brasileira de Pediatria (SBP)instacron:SBPE10.1016/j.jped.2018.04.007info:eu-repo/semantics/openAccessPorta,GildaCarvalho,Elisa deSantos,Jorge L.Gama,JorgeBorges,Cristian V.Seixas,Renata B.P.M.Ferreira,Alexandre R.Miura,Irene K.Silveira,Themis R.Silva,Luciana R.Fagundes,Eleonora D.T.Bellomo-Brandao,Maria A.Sawamura,ReginaVieira,Sandra M.Melere,Melina U.Marques,Cibele D.F.Pugliese,Renata P.Danesi,Vera L.Porta,AdrianaMarsillac,Marise E.Valladares,Marcia A.Menezes,Daniela G.Kieling,CarlosPaula,Mariana N. deVasconcelos,Juliana R.Ferreira,Cristina T.Perin,NilzaResende,Leonardo R.Maia,JussaraTommaso,Adriana M.A. DeHessel,Gabrieleng2019-09-09T00:00:00Zoai:scielo:S0021-75572019000500419Revistahttp://www.jped.com.br/https://old.scielo.br/oai/scielo-oai.php||jped@jped.com.br1678-47820021-7557opendoar:2019-09-09T00:00Jornal de Pediatria (Online) - Sociedade Brasileira de Pediatria (SBP)false
dc.title.none.fl_str_mv Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomes
title Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomes
spellingShingle Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomes
Porta,Gilda
Autoimmune hepatitis
Clinical
Laboratory
Treatments
Outcomes
Brazil
title_short Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomes
title_full Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomes
title_fullStr Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomes
title_full_unstemmed Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomes
title_sort Autoimmune hepatitis in 828 Brazilian children and adolescents: clinical and laboratory findings, histological profile, treatments, and outcomes
author Porta,Gilda
author_facet Porta,Gilda
Carvalho,Elisa de
Santos,Jorge L.
Gama,Jorge
Borges,Cristian V.
Seixas,Renata B.P.M.
Ferreira,Alexandre R.
Miura,Irene K.
Silveira,Themis R.
Silva,Luciana R.
Fagundes,Eleonora D.T.
Bellomo-Brandao,Maria A.
Sawamura,Regina
Vieira,Sandra M.
Melere,Melina U.
Marques,Cibele D.F.
Pugliese,Renata P.
Danesi,Vera L.
Porta,Adriana
Marsillac,Marise E.
Valladares,Marcia A.
Menezes,Daniela G.
Kieling,Carlos
Paula,Mariana N. de
Vasconcelos,Juliana R.
Ferreira,Cristina T.
Perin,Nilza
Resende,Leonardo R.
Maia,Jussara
Tommaso,Adriana M.A. De
Hessel,Gabriel
author_role author
author2 Carvalho,Elisa de
Santos,Jorge L.
Gama,Jorge
Borges,Cristian V.
Seixas,Renata B.P.M.
Ferreira,Alexandre R.
Miura,Irene K.
Silveira,Themis R.
Silva,Luciana R.
Fagundes,Eleonora D.T.
Bellomo-Brandao,Maria A.
Sawamura,Regina
Vieira,Sandra M.
Melere,Melina U.
Marques,Cibele D.F.
Pugliese,Renata P.
Danesi,Vera L.
Porta,Adriana
Marsillac,Marise E.
Valladares,Marcia A.
Menezes,Daniela G.
Kieling,Carlos
Paula,Mariana N. de
Vasconcelos,Juliana R.
Ferreira,Cristina T.
Perin,Nilza
Resende,Leonardo R.
Maia,Jussara
Tommaso,Adriana M.A. De
Hessel,Gabriel
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Porta,Gilda
Carvalho,Elisa de
Santos,Jorge L.
Gama,Jorge
Borges,Cristian V.
Seixas,Renata B.P.M.
Ferreira,Alexandre R.
Miura,Irene K.
Silveira,Themis R.
Silva,Luciana R.
Fagundes,Eleonora D.T.
Bellomo-Brandao,Maria A.
Sawamura,Regina
Vieira,Sandra M.
Melere,Melina U.
Marques,Cibele D.F.
Pugliese,Renata P.
Danesi,Vera L.
Porta,Adriana
Marsillac,Marise E.
Valladares,Marcia A.
Menezes,Daniela G.
Kieling,Carlos
Paula,Mariana N. de
Vasconcelos,Juliana R.
Ferreira,Cristina T.
Perin,Nilza
Resende,Leonardo R.
Maia,Jussara
Tommaso,Adriana M.A. De
Hessel,Gabriel
dc.subject.por.fl_str_mv Autoimmune hepatitis
Clinical
Laboratory
Treatments
Outcomes
Brazil
topic Autoimmune hepatitis
Clinical
Laboratory
Treatments
Outcomes
Brazil
description Abstract Objective: This large study with a long-term follow-up aimed to evaluate the clinical presentation, laboratory findings, histological profile, treatments, and outcomes of children and adolescents with autoimmune hepatitis. Methods: The medical records of 828 children and adolescents with autoimmune hepatitis were reviewed. A questionnaire was used to collect anonymous data on clinical presentation, biochemical and histological findings, and treatments. Results: Of all patients, 89.6% had autoimmune hepatitis-1 and 10.4% had autoimmune hepatitis-2. The female sex was predominant in both groups. The median age at symptom onset was 111.5 (6; 210) and 53.5 (8; 165) months in the patients with autoimmune hepatitis 1 and autoimmune hepatitis-2, respectively. Acute clinical onset was observed in 56.1% and 58.8% and insidious symptoms in 43.9% and 41.2% of the patients with autoimmune hepatitis-1 and autoimmune hepatitis-2, respectively. The risk of hepatic failure was 1.6-fold higher for autoimmune hepatitis-2. Fulminant hepatic failure occurred in 3.6% and 10.6% of the patients with autoimmune hepatitis-1 and autoimmune hepatitis-2, respectively; the risk was 3.1-fold higher for autoimmune hepatitis-2. The gamma globulin and immunoglobulin G levels were significantly higher in autoimmune hepatitis-1, while the immunoglobulin A and C3 levels were lower in autoimmune hepatitis-2. Cirrhosis was observed in 22.4% of the patients; biochemical remission was achieved in 76.2%. The actuarial survival rate was 93.0%. A total of 4.6% underwent liver transplantation, and 6.9% died (autoimmune hepatitis-1: 7.5%; autoimmune hepatitis-2: 2.4%). Conclusions: In this large clinical series of Brazilian children and adolescents, autoimmune hepatitis-1 was more frequent, and patients with autoimmune hepatitis-2 exhibited higher disease remission rates with earlier response to treatment. Patients with autoimmune hepatitis-1 had a higher risk of death.
publishDate 2019
dc.date.none.fl_str_mv 2019-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572019000500419
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.jped.2018.04.007
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Pediatria
publisher.none.fl_str_mv Sociedade Brasileira de Pediatria
dc.source.none.fl_str_mv Jornal de Pediatria v.95 n.4 2019
reponame:Jornal de Pediatria (Online)
instname:Sociedade Brasileira de Pediatria (SBP)
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instname_str Sociedade Brasileira de Pediatria (SBP)
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reponame_str Jornal de Pediatria (Online)
collection Jornal de Pediatria (Online)
repository.name.fl_str_mv Jornal de Pediatria (Online) - Sociedade Brasileira de Pediatria (SBP)
repository.mail.fl_str_mv ||jped@jped.com.br
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