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Functional dyspesia

Dyspepsia is a functional GI disorder consisting in a wide range of symptoms. The main diagnostic challenge has been whether to perform an EGD or an abdominal US in order not to miss organic lesions, but to avoid unnecessary and sometimes invasive tests. Pepsinogen serology has been proposed as an u...

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Autores principales: Crafa, Pellegrino, Franceschi, Marilisa, Rodriguez Castro, Kryssia Isabel, Barchi, Alberto, Russo, Michele, Franzoni, Lorella, Antico, Antonio, Baldassarre, Gianluca, Panozzo, Maria Piera, Di Mario, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716988/
https://www.ncbi.nlm.nih.gov/pubmed/32921764
http://dx.doi.org/10.23750/abm.v91i3.10150
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author Crafa, Pellegrino
Franceschi, Marilisa
Rodriguez Castro, Kryssia Isabel
Barchi, Alberto
Russo, Michele
Franzoni, Lorella
Antico, Antonio
Baldassarre, Gianluca
Panozzo, Maria Piera
Di Mario, Francesco
author_facet Crafa, Pellegrino
Franceschi, Marilisa
Rodriguez Castro, Kryssia Isabel
Barchi, Alberto
Russo, Michele
Franzoni, Lorella
Antico, Antonio
Baldassarre, Gianluca
Panozzo, Maria Piera
Di Mario, Francesco
author_sort Crafa, Pellegrino
collection PubMed
description Dyspepsia is a functional GI disorder consisting in a wide range of symptoms. The main diagnostic challenge has been whether to perform an EGD or an abdominal US in order not to miss organic lesions, but to avoid unnecessary and sometimes invasive tests. Pepsinogen serology has been proposed as an useful non-invasive test to explore the status of the gastric mucosa, suggesting this strategy as an adequate approach in management of dyspepsia. In a primary care setting, 266 dyspeptic patients were investigated to establish the proper diagnosis. The workup included upper GI endoscopy with biopsies, a structured questionnaire including type and severity of symptoms, serological determination of serum pepsinogens, gastrin 17 and IgG against Hp. Inclusion criteria were dyspeptic symptoms (epigastric pain, nausea and/or vomiting, post prandial fullness, early satiation) lasting more than 1 year and the association between symptoms and food ingestion. Helicobacter pylori infection was present in 114 subjects, characterized by high levels of pepsinogen II and IgG against Hp. Twenty subjects were classified according with the diagnosis of chronic body atrophic gastritis. Nausea and post prandial fullness were the most frequent symptoms (48% and 41%, respectively) in the studied population, followed by epigastric pain and early satiation (37% and 26% respectively). A diagnosis of normality by serological diagnosis was found in half of patients experiencing epigastric pain and in about 60% of subjects with the three other symptoms (nausea, post prandial fullness, and early satiation). In conclusion, this experience confirms the clinical usefulness of serology in dyspepsia, contributing to correctly diagnosing CAG and H.p. infection in such patients and providing a good correlation with the clinical picture. (www.actabiomedica.it)
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spelling pubmed-77169882020-12-07 Functional dyspesia Crafa, Pellegrino Franceschi, Marilisa Rodriguez Castro, Kryssia Isabel Barchi, Alberto Russo, Michele Franzoni, Lorella Antico, Antonio Baldassarre, Gianluca Panozzo, Maria Piera Di Mario, Francesco Acta Biomed Original Article Dyspepsia is a functional GI disorder consisting in a wide range of symptoms. The main diagnostic challenge has been whether to perform an EGD or an abdominal US in order not to miss organic lesions, but to avoid unnecessary and sometimes invasive tests. Pepsinogen serology has been proposed as an useful non-invasive test to explore the status of the gastric mucosa, suggesting this strategy as an adequate approach in management of dyspepsia. In a primary care setting, 266 dyspeptic patients were investigated to establish the proper diagnosis. The workup included upper GI endoscopy with biopsies, a structured questionnaire including type and severity of symptoms, serological determination of serum pepsinogens, gastrin 17 and IgG against Hp. Inclusion criteria were dyspeptic symptoms (epigastric pain, nausea and/or vomiting, post prandial fullness, early satiation) lasting more than 1 year and the association between symptoms and food ingestion. Helicobacter pylori infection was present in 114 subjects, characterized by high levels of pepsinogen II and IgG against Hp. Twenty subjects were classified according with the diagnosis of chronic body atrophic gastritis. Nausea and post prandial fullness were the most frequent symptoms (48% and 41%, respectively) in the studied population, followed by epigastric pain and early satiation (37% and 26% respectively). A diagnosis of normality by serological diagnosis was found in half of patients experiencing epigastric pain and in about 60% of subjects with the three other symptoms (nausea, post prandial fullness, and early satiation). In conclusion, this experience confirms the clinical usefulness of serology in dyspepsia, contributing to correctly diagnosing CAG and H.p. infection in such patients and providing a good correlation with the clinical picture. (www.actabiomedica.it) Mattioli 1885 2020 2020-06-25 /pmc/articles/PMC7716988/ /pubmed/32921764 http://dx.doi.org/10.23750/abm.v91i3.10150 Text en Copyright: © 2020 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Original Article
Crafa, Pellegrino
Franceschi, Marilisa
Rodriguez Castro, Kryssia Isabel
Barchi, Alberto
Russo, Michele
Franzoni, Lorella
Antico, Antonio
Baldassarre, Gianluca
Panozzo, Maria Piera
Di Mario, Francesco
Functional dyspesia
title Functional dyspesia
title_full Functional dyspesia
title_fullStr Functional dyspesia
title_full_unstemmed Functional dyspesia
title_short Functional dyspesia
title_sort functional dyspesia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716988/
https://www.ncbi.nlm.nih.gov/pubmed/32921764
http://dx.doi.org/10.23750/abm.v91i3.10150
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