2001
DOI: 10.1046/j.1365-2036.2001.00915.x
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Usefulness of Helicobacter pylori stool antigen test to monitor response to eradication treatment in children

Abstract: Background: The monitoring of the results of eradication treatment is a crucial step for patients with Helicobacter pylori gastritis. A non‐invasive test for H. pylori antigens in stools (HpSA) was recently validated for children. Aim: To evaluate the accuracy of HpSA in monitoring eradication treatment in children. Methods: In 60 children, H. pylori gastritis was diagnosed by endoscopy and the 13C‐urea breath test. The children were treated and returned for a follow‐up 13C‐urea breath test 6 weeks after the e… Show more

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Cited by 41 publications
(32 citation statements)
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“…Monoclonal antibodybased tests are widely accepted for clinical practice with humans since they are sensitive, specific, noninvasive, and easy to perform (1,7,8). Our results show a high sensitivity and specificity of the test for stool samples from mice, which is in agreement with the values given for humans by the manufacturer.…”
supporting
confidence: 78%
“…Monoclonal antibodybased tests are widely accepted for clinical practice with humans since they are sensitive, specific, noninvasive, and easy to perform (1,7,8). Our results show a high sensitivity and specificity of the test for stool samples from mice, which is in agreement with the values given for humans by the manufacturer.…”
supporting
confidence: 78%
“…(7,26). The lack of IgG seroconversion or IgM seropositivity in a small subsample supports the transient nature of these infections, although the validity of serology in young children is not well established (8,15,25).…”
Section: Discussionmentioning
confidence: 95%
“…A presença de anticorpos no soro, sem antígenos nas fezes, pode representar o desaparecimento da infecção, uma vez que o teste sorológico empregado nesta pesquisa indica unicamente uma exposição prévia ao microrganismo, mas não discrimina indivíduos sadios ou com infecção ativa 24 34 . Já o teste nas fezes pode ser usado para o diagnóstico inicial da infecção, quando o indivíduo ainda não apresenta níveis de anticorpos detectáveis, bem como para confirmar a erradicação da Helicobacter pylori após quatro semanas do término do tratamento, quando ainda são verificados anticorpos no soro 24 . O imunoensaio nas fezes foi aprovado pela Food and Drug Administration desde 1998, tanto para o diagnóstico como para o controle da terapia, inclusive em crianças 24 34 .…”
Section: Tabelaunclassified