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Oral administration of tannins and flavonoids in children with acute diarrhea: a pilot, randomized, control-case study
BACKGROUND: AG is the most common cause of pediatric consultations among children between 2 and 5 years of age and it still leads to high mortality and morbidity. Its management is based on rehydration therapy, but this treatment is not effective in reducing duration of diarrhea. For this reason, ot...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987560/ https://www.ncbi.nlm.nih.gov/pubmed/29866147 http://dx.doi.org/10.1186/s13052-018-0497-6 |
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author | Russo, Marina Coppola, Vincenzo Giannetti, Eleonora Buonavolontà, Roberta Piscitelli, Antonio Staiano, Annamaria |
author_facet | Russo, Marina Coppola, Vincenzo Giannetti, Eleonora Buonavolontà, Roberta Piscitelli, Antonio Staiano, Annamaria |
author_sort | Russo, Marina |
collection | PubMed |
description | BACKGROUND: AG is the most common cause of pediatric consultations among children between 2 and 5 years of age and it still leads to high mortality and morbidity. Its management is based on rehydration therapy, but this treatment is not effective in reducing duration of diarrhea. For this reason, other safer and less expensive interventions, which could be added to oral rehydration therapy, are of great interest. METHODS: A pilot, randomized, case-controlled trial was conducted in 60 children affected by AG (< 7 days) with mild-moderate dehydration, according to WHO recommendations, from1 year to 17 years old. Patients were divided into 2 Groups: Group 1 consisting of 30 children treated with Actitan F and standard oral rehydration (SOR); Group 2 consisting of 30 children who received only SOR. Both groups received treatment for seven days, respectively. Patients of Group 1 stopped for their own choice, SOR after the first 24 h and continued only with Actitan F. RESULTS: After 24 h of treatment, the median number of stools was 3.5 for Group 1, and 4 for Group 2. In Group 1 the difference between the number of stools at baseline (n = 5) and after 24 h of treatment (n = 3.5) was significant (p < 0.0001). At the end of treatment, the median duration of diarrhea in Group 1 was 5 days, compared with 4 days in the Group 2, this difference was not statically significant (p 0.48). CONCLUSIONS: Oral administration of Actitan F associated with SOR seems safe and effective treatment in shortening the duration of AG in children. Further studies confirming these data are needed. TRIAL REGISTRATION: NCT03356327 (retrospectively registered). |
format | Online Article Text |
id | pubmed-5987560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59875602018-07-10 Oral administration of tannins and flavonoids in children with acute diarrhea: a pilot, randomized, control-case study Russo, Marina Coppola, Vincenzo Giannetti, Eleonora Buonavolontà, Roberta Piscitelli, Antonio Staiano, Annamaria Ital J Pediatr Research BACKGROUND: AG is the most common cause of pediatric consultations among children between 2 and 5 years of age and it still leads to high mortality and morbidity. Its management is based on rehydration therapy, but this treatment is not effective in reducing duration of diarrhea. For this reason, other safer and less expensive interventions, which could be added to oral rehydration therapy, are of great interest. METHODS: A pilot, randomized, case-controlled trial was conducted in 60 children affected by AG (< 7 days) with mild-moderate dehydration, according to WHO recommendations, from1 year to 17 years old. Patients were divided into 2 Groups: Group 1 consisting of 30 children treated with Actitan F and standard oral rehydration (SOR); Group 2 consisting of 30 children who received only SOR. Both groups received treatment for seven days, respectively. Patients of Group 1 stopped for their own choice, SOR after the first 24 h and continued only with Actitan F. RESULTS: After 24 h of treatment, the median number of stools was 3.5 for Group 1, and 4 for Group 2. In Group 1 the difference between the number of stools at baseline (n = 5) and after 24 h of treatment (n = 3.5) was significant (p < 0.0001). At the end of treatment, the median duration of diarrhea in Group 1 was 5 days, compared with 4 days in the Group 2, this difference was not statically significant (p 0.48). CONCLUSIONS: Oral administration of Actitan F associated with SOR seems safe and effective treatment in shortening the duration of AG in children. Further studies confirming these data are needed. TRIAL REGISTRATION: NCT03356327 (retrospectively registered). BioMed Central 2018-06-04 /pmc/articles/PMC5987560/ /pubmed/29866147 http://dx.doi.org/10.1186/s13052-018-0497-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Russo, Marina Coppola, Vincenzo Giannetti, Eleonora Buonavolontà, Roberta Piscitelli, Antonio Staiano, Annamaria Oral administration of tannins and flavonoids in children with acute diarrhea: a pilot, randomized, control-case study |
title | Oral administration of tannins and flavonoids in children with acute diarrhea: a pilot, randomized, control-case study |
title_full | Oral administration of tannins and flavonoids in children with acute diarrhea: a pilot, randomized, control-case study |
title_fullStr | Oral administration of tannins and flavonoids in children with acute diarrhea: a pilot, randomized, control-case study |
title_full_unstemmed | Oral administration of tannins and flavonoids in children with acute diarrhea: a pilot, randomized, control-case study |
title_short | Oral administration of tannins and flavonoids in children with acute diarrhea: a pilot, randomized, control-case study |
title_sort | oral administration of tannins and flavonoids in children with acute diarrhea: a pilot, randomized, control-case study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987560/ https://www.ncbi.nlm.nih.gov/pubmed/29866147 http://dx.doi.org/10.1186/s13052-018-0497-6 |
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