Gastroenterologia e hepatologia em pediatria: diagnóstico e tratamento

Silva, Giselia Alves Pontes da

doi:10.1590/s1519-38292004000100010

Cited by 3 publications

(3 citation statements)

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“…In the present study, it was concluded that individuals with CHF and PVT had a higher chance of developing EV (odds ratio [OR] 6.15) than cirrhotic patients. This result ratifies what was only suggested based on experience of the service and on isolated case reports (8,9). Such results corroborate the importance of detecting EV and grading their size in these patients, who could be enrolled in a research protocol for primary prophylaxis.…”

Section: Discussionsupporting

confidence: 87%

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Clinical and Laboratory Predictors of Esophageal Varices in Children and Adolescents With Portal Hypertension Syndrome

Fagundes

Ferreira

Roquete

et al. 2008

J. pediatr. gastroenterol. nutr.

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In reference services and research protocols, endoscopic screening should be performed in all patients with portal vein thrombosis and congenital hepatic fibrosis. Among cirrhotic patients, the indication should be conditioned to clinical evidence of splenomegaly or hypoalbuminemia. For clinicians, the recommendation is to emphasize the orientations given to guardians of patients with portal vein thrombosis and congenital hepatic fibrosis as to the risk of digestive bleeding. Cirrhotic patients with hypoalbuminemia and splenomegaly should receive the same orientations.

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Section: Discussionsupporting

confidence: 87%

“…Although a consensus has been reached for adults, in spite of some controversy, there is no formal recommendation for endoscopic screening in children (8,9). In practice, data and recommendations related to adults have been used in the management of pediatric cases, and may not be adequate because of differences inherent to age.…”

mentioning

confidence: 99%

Clinical and Laboratory Predictors of Esophageal Varices in Children and Adolescents With Portal Hypertension Syndrome

Fagundes

Ferreira

Roquete

et al. 2008

J. pediatr. gastroenterol. nutr.

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“…Consiste em um estudo epidemiológico descritivo, com dados obtidos por meio de consulta de dados secundários de um banco de domínio público, sendo assim não foi necessário submeter a pesquisa ao Comitê de Ética em Pesquisa. (GONCALVES, 2002;SILVA, 2003).…”

Section: Aspectos éTicosunclassified

Patologia das doenças

Salgado¹

2018

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Alpha1 antitrypsin deficiency: case report

Vasconcelos¹,

Coelho²,

Schmidt³

2015

Revista Médica De Minas Gerais

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Este relato alerta para a deficiência de alfa1antitripsina em neonato, que se apresentou como síndrome colestática. Seu subdiagnóstico constitui-se em importante limitação para o seu reconhecimento e tratamento adequado. A boa evolução ocorre em cerca de 50% dos pacientes. Associa-se, na maioria das vezes, a acometimento extra e intra-hepático e ausência de manifestações clínicas que indiquem o seu diagnóstico. A deficiência de alfa1antitripsina está entre as doenças que precisam ser excluídas frente à colestase neonatal.

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Gastroenterologia e hepatologia em pediatria: diagnóstico e tratamento

Cited by 3 publications

References 0 publications

Clinical and Laboratory Predictors of Esophageal Varices in Children and Adolescents With Portal Hypertension Syndrome

Clinical and Laboratory Predictors of Esophageal Varices in Children and Adolescents With Portal Hypertension Syndrome

Patologia das doenças

Alpha1 antitrypsin deficiency: case report

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