Cargando…
Case-management protocol for bloody diarrhea as a model to reduce the clinical impact of Shiga toxin-producing Escherichia coli infections. Experience from Southern Italy
To describe an operating protocol for bloody diarrhea (BD) in a pediatric population as a rapid response to a public health threat represented by an excess of pediatric HUS cases in the Apulia region (Southern Italy) starting from 2013. The protocol was set up with the goal of correct clinical manag...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7040055/ https://www.ncbi.nlm.nih.gov/pubmed/31776873 http://dx.doi.org/10.1007/s10096-019-03755-0 |
_version_ | 1783500911998402560 |
---|---|
author | Loconsole, Daniela Giordano, Mario Laforgia, Nicola Torres, Diletta Santangelo, Luisa Carbone, Vincenza Parisi, Antonio Quarto, Michele Scavia, Gaia Chironna, Maria |
author_facet | Loconsole, Daniela Giordano, Mario Laforgia, Nicola Torres, Diletta Santangelo, Luisa Carbone, Vincenza Parisi, Antonio Quarto, Michele Scavia, Gaia Chironna, Maria |
author_sort | Loconsole, Daniela |
collection | PubMed |
description | To describe an operating protocol for bloody diarrhea (BD) in a pediatric population as a rapid response to a public health threat represented by an excess of pediatric HUS cases in the Apulia region (Southern Italy) starting from 2013. The protocol was set up with the goal of correct clinical management of Shiga toxin-producing Escherichia coli (STEC) infections, reductions in subsequent cases of hemolytic uremic syndrome (HUS), and improved short- and long-term disease outcomes. The protocol consisted of rapid hospitalization of children with bloody diarrhea (BD), hematochemical laboratory tests every 12–24 hours, and prompt laboratory diagnosis of STEC. No antibiotics were recommended until diagnosis. Children positive for STEC infections underwent early vigorous volume expansion. In June–December 2018, 438 children with BD were hospitalized, of which 53 (12.1%) had a STEC infection. The most common serogroups were O26 (36.1%), O111 (23.0%), and O157 (14.8%). Thirty-one samples carried the stx2 gene. Four cases evolved into HUS (7.5%), all with favorable outcome despite neurological involvement in two cases. Prompt and accurate laboratory diagnosis of STEC infections is of the utmost importance in patients with BD for correct clinical management. The strict adherence to the protocol could reduce the progression rate of STEC infections to HUS and prevents complications. Enhanced BD surveillance may help reduce cases of pediatric HUS in Southern Italy. |
format | Online Article Text |
id | pubmed-7040055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70400552020-03-10 Case-management protocol for bloody diarrhea as a model to reduce the clinical impact of Shiga toxin-producing Escherichia coli infections. Experience from Southern Italy Loconsole, Daniela Giordano, Mario Laforgia, Nicola Torres, Diletta Santangelo, Luisa Carbone, Vincenza Parisi, Antonio Quarto, Michele Scavia, Gaia Chironna, Maria Eur J Clin Microbiol Infect Dis Original Article To describe an operating protocol for bloody diarrhea (BD) in a pediatric population as a rapid response to a public health threat represented by an excess of pediatric HUS cases in the Apulia region (Southern Italy) starting from 2013. The protocol was set up with the goal of correct clinical management of Shiga toxin-producing Escherichia coli (STEC) infections, reductions in subsequent cases of hemolytic uremic syndrome (HUS), and improved short- and long-term disease outcomes. The protocol consisted of rapid hospitalization of children with bloody diarrhea (BD), hematochemical laboratory tests every 12–24 hours, and prompt laboratory diagnosis of STEC. No antibiotics were recommended until diagnosis. Children positive for STEC infections underwent early vigorous volume expansion. In June–December 2018, 438 children with BD were hospitalized, of which 53 (12.1%) had a STEC infection. The most common serogroups were O26 (36.1%), O111 (23.0%), and O157 (14.8%). Thirty-one samples carried the stx2 gene. Four cases evolved into HUS (7.5%), all with favorable outcome despite neurological involvement in two cases. Prompt and accurate laboratory diagnosis of STEC infections is of the utmost importance in patients with BD for correct clinical management. The strict adherence to the protocol could reduce the progression rate of STEC infections to HUS and prevents complications. Enhanced BD surveillance may help reduce cases of pediatric HUS in Southern Italy. Springer Berlin Heidelberg 2019-11-27 2020 /pmc/articles/PMC7040055/ /pubmed/31776873 http://dx.doi.org/10.1007/s10096-019-03755-0 Text en © The Author(s) 2019, corrected publication December 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Loconsole, Daniela Giordano, Mario Laforgia, Nicola Torres, Diletta Santangelo, Luisa Carbone, Vincenza Parisi, Antonio Quarto, Michele Scavia, Gaia Chironna, Maria Case-management protocol for bloody diarrhea as a model to reduce the clinical impact of Shiga toxin-producing Escherichia coli infections. Experience from Southern Italy |
title | Case-management protocol for bloody diarrhea as a model to reduce the clinical impact of Shiga toxin-producing Escherichia coli infections. Experience from Southern Italy |
title_full | Case-management protocol for bloody diarrhea as a model to reduce the clinical impact of Shiga toxin-producing Escherichia coli infections. Experience from Southern Italy |
title_fullStr | Case-management protocol for bloody diarrhea as a model to reduce the clinical impact of Shiga toxin-producing Escherichia coli infections. Experience from Southern Italy |
title_full_unstemmed | Case-management protocol for bloody diarrhea as a model to reduce the clinical impact of Shiga toxin-producing Escherichia coli infections. Experience from Southern Italy |
title_short | Case-management protocol for bloody diarrhea as a model to reduce the clinical impact of Shiga toxin-producing Escherichia coli infections. Experience from Southern Italy |
title_sort | case-management protocol for bloody diarrhea as a model to reduce the clinical impact of shiga toxin-producing escherichia coli infections. experience from southern italy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7040055/ https://www.ncbi.nlm.nih.gov/pubmed/31776873 http://dx.doi.org/10.1007/s10096-019-03755-0 |
work_keys_str_mv | AT loconsoledaniela casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT giordanomario casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT laforgianicola casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT torresdiletta casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT santangeloluisa casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT carbonevincenza casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT parisiantonio casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT quartomichele casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT scaviagaia casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT chironnamaria casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly AT casemanagementprotocolforbloodydiarrheaasamodeltoreducetheclinicalimpactofshigatoxinproducingescherichiacoliinfectionsexperiencefromsouthernitaly |