OM-85BV na prevenção de infecções recorrentes de vias aéreas: um estudo randomizado, duplo cego, placebo controlado
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Tipo de documento: | Tese |
Idioma: | por |
Título da fonte: | Repositório Institucional PUCRS |
Texto Completo: | http://hdl.handle.net/10923/10800 |
Resumo: | Introduction: Acute respiratory tract infections (ARTI) are one of the most important causes of mortality in children under 5 years old. In developed countries ARTI account for 20% of emergency consultations and 75% of antibiotic prescriptions. Children in attending day care are more prone to recurrence of respiratory infections. Bacterial immunostimulants, resulting from the chemical lysis of microorganisms associated with most respiratory tract infections, have been propagated as possibly useful intervention for prevention of recurrent respiratory infections. Objective: To analyze the effectiveness of OM-85 Broncho-vaxom (OM-85 BV) on the prevention of upper respiratory tract infections in healthy children attending preschool during the 6-month period. Methods: A randomized, double-blind, placebo controlled study was conducted in 54 healthy children aged between 6 months to 5 years attending in the School for Early Childhood Education between the months of April and September. Use of OM-85 BV for 3 months and observed for a further 3 months the following outcomes: upper respiratory tract infection, bronchopneumonia, other infections, use of antibiotics, emergency consultations, need for hospital stay, side effects of the medication. Results: Of the 54 children included, 57% were male. All completed the study and there were no significant differences between the groups. Of the 27 patients in group OM-85 BV, 19 (70,4%), attending daycare full-time and 16 (64,85%) half period, morning or evening. Breastfeeding was exclusive until 6 months in 6 patients (22,2%) on the OM-85 BV group and in 7 (25,9%) patients in the control group. Family history of smoking was positive in 11 (40,7%) patients in the OM-85 BV group and in 13 (48,1%) patients in the control group. Regarding the number of respiratory infections, the mean in the OM-85 BV group in the first 3 months was 0,92± 0,87 and in the placebo group was 0,74± 1,02 and in the 6 months was 1,62± 1,47 and 1,03±1,34, respectively. Antibiotic was used in 10 (37%) children of the OM-85BV group in the 3 months of treatment and in 13 (48,1%) of the placebo group, and in the 6 months of follow-up the use was 48,1% in both groups. The mean number of hospitalizations was very low in the period of the study. The mean number of emergency visits during the first 3 months was 0,81±1,21 in the OM-85 BV group and 1,29±1,48 in the placebo group and at 6 months was 1,77±1,80 in the OM-85 BV group and 2,03±1,76 in the placebo group. Conclusions: OM-85 BV was not effective as an intervention in daycare children with no history of IRR. No statistically significant difference was observed between the groups in the use of antibiotics, emergency consultations and hospitalizations. |
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Souza, Fátima Cleonice dePinto, Leonardo Araújo2017-10-14T12:01:24Z2017-10-14T12:01:24Z2017http://hdl.handle.net/10923/10800Introduction: Acute respiratory tract infections (ARTI) are one of the most important causes of mortality in children under 5 years old. In developed countries ARTI account for 20% of emergency consultations and 75% of antibiotic prescriptions. Children in attending day care are more prone to recurrence of respiratory infections. Bacterial immunostimulants, resulting from the chemical lysis of microorganisms associated with most respiratory tract infections, have been propagated as possibly useful intervention for prevention of recurrent respiratory infections. Objective: To analyze the effectiveness of OM-85 Broncho-vaxom (OM-85 BV) on the prevention of upper respiratory tract infections in healthy children attending preschool during the 6-month period. Methods: A randomized, double-blind, placebo controlled study was conducted in 54 healthy children aged between 6 months to 5 years attending in the School for Early Childhood Education between the months of April and September. Use of OM-85 BV for 3 months and observed for a further 3 months the following outcomes: upper respiratory tract infection, bronchopneumonia, other infections, use of antibiotics, emergency consultations, need for hospital stay, side effects of the medication. Results: Of the 54 children included, 57% were male. All completed the study and there were no significant differences between the groups. Of the 27 patients in group OM-85 BV, 19 (70,4%), attending daycare full-time and 16 (64,85%) half period, morning or evening. Breastfeeding was exclusive until 6 months in 6 patients (22,2%) on the OM-85 BV group and in 7 (25,9%) patients in the control group. Family history of smoking was positive in 11 (40,7%) patients in the OM-85 BV group and in 13 (48,1%) patients in the control group. Regarding the number of respiratory infections, the mean in the OM-85 BV group in the first 3 months was 0,92± 0,87 and in the placebo group was 0,74± 1,02 and in the 6 months was 1,62± 1,47 and 1,03±1,34, respectively. Antibiotic was used in 10 (37%) children of the OM-85BV group in the 3 months of treatment and in 13 (48,1%) of the placebo group, and in the 6 months of follow-up the use was 48,1% in both groups. The mean number of hospitalizations was very low in the period of the study. The mean number of emergency visits during the first 3 months was 0,81±1,21 in the OM-85 BV group and 1,29±1,48 in the placebo group and at 6 months was 1,77±1,80 in the OM-85 BV group and 2,03±1,76 in the placebo group. Conclusions: OM-85 BV was not effective as an intervention in daycare children with no history of IRR. No statistically significant difference was observed between the groups in the use of antibiotics, emergency consultations and hospitalizations.Introdução: As infecções agudas do trato respiratório estão entre as causas mais importantes de mortalidade na faixa etária abaixo dos 5 anos, sendo, em países desenvolvidos, responsáveis por 20% das consultas nas emergências e 75% das prescrições de antibióticos. Crianças que frequentam creche são mais propensas à recorrência das infecções respiratórias. Os imunoestimulantes bacterianos, resultantes da lise química de microrganismos associados com a maioria das infecções respiratórias, têm sido propagados como intervenção possivelmente útil para a prevenção das infecções respiratórias recorrentes (IRR). Objetivo: Analisar a eficácia do OM-85 Broncho Vaxom (OM-85 BV) na prevenção de infecções respiratórias do trato respiratório superior em crianças hígidas que frequentam pré-escola, durante o período de 6 meses. Métodos: Desenvolveu-se um estudo randomizado duplo cego placebo controlado em 54 crianças previamente hígidas, com idade entre 6 meses e 5 anos, que frequentavam a Escola de Educação Infantil entre os meses de abril e setembro. Usado OM-85 BV por 3 meses e observado por mais 3 meses os seguintes desfechos: presença de infecção do trato respiratório superior, broncopneumonia, outras infecções, uso de antibióticos, consultas na emergência, necessidade de internação hospitalar, dias de ausência à creche e efeitos colaterais da medicação. Resultados: Das 54 crianças incluídas, 57% eram do sexo masculino. Todos completaram o estudo e não houve diferenças significativas entre os grupos. Dos 27 pacientes do grupo OM-85 BV, 19 (70,4%), frequentavam a creche em turno integral e dos 27 pacientes do grupo controle, 16 (64,8%). O aleitamento materno, foi exclusivo até o 6º mês em 6 (22,2%) pacientes do grupo OM-85 BV em 7 (25,9%) pacientes do grupo controle. Quanto à história familiar de fumo, foi positiva em 11 (40,7%) pacientes do grupo OM-85 BV e em 13 (48,1%) pacientes do grupo controle. Em relação ao número de infecções respiratórias, a média no grupo OM-85 BV nos primeiros 3 meses foi 0,92±0,87 e no grupo placebo foi 0,74±1,02 e nos 6 meses foi 1,62±1,47 e 1,03±1,34, respectivamente. Antibiótico foi usado em 10 (37%) crianças do grupo OM-85BV nos 3 meses de tratamento e em 13 (48,1%) do grupo placebo, já nos 6 meses de acompanhamento o uso foi de 48,1% nos dois grupos. A média de internações foi muito baixa no período estudado. A média de consultas na emergência nos primeiros 3 meses foi de 0,81±1,21 no grupo OM-85 BV e 1,29±1,48 no grupo placebo e nos 6 meses foi de 1,77±1,80 no grupo OM-85 BV e 2,03±1,76 no grupo placebo. Conclusões: OM-85 BV não foi eficaz como intervenção em crianças que frequentam creche, sem história de IRR. Não houve diferença estatisticamente significativa no uso de antibióticos, consultas na emergência e internações hospitalaresMade available in DSpace on 2017-10-14T12:01:24Z (GMT). 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dc.title.pt_BR.fl_str_mv |
OM-85BV na prevenção de infecções recorrentes de vias aéreas: um estudo randomizado, duplo cego, placebo controlado |
title |
OM-85BV na prevenção de infecções recorrentes de vias aéreas: um estudo randomizado, duplo cego, placebo controlado |
spellingShingle |
OM-85BV na prevenção de infecções recorrentes de vias aéreas: um estudo randomizado, duplo cego, placebo controlado Souza, Fátima Cleonice de INFECÇÕES RESPIRATÓRIAS DOENÇAS RESPIRATÓRIAS PEDIATRIA MEDICINA |
title_short |
OM-85BV na prevenção de infecções recorrentes de vias aéreas: um estudo randomizado, duplo cego, placebo controlado |
title_full |
OM-85BV na prevenção de infecções recorrentes de vias aéreas: um estudo randomizado, duplo cego, placebo controlado |
title_fullStr |
OM-85BV na prevenção de infecções recorrentes de vias aéreas: um estudo randomizado, duplo cego, placebo controlado |
title_full_unstemmed |
OM-85BV na prevenção de infecções recorrentes de vias aéreas: um estudo randomizado, duplo cego, placebo controlado |
title_sort |
OM-85BV na prevenção de infecções recorrentes de vias aéreas: um estudo randomizado, duplo cego, placebo controlado |
author |
Souza, Fátima Cleonice de |
author_facet |
Souza, Fátima Cleonice de |
author_role |
author |
dc.contributor.author.fl_str_mv |
Souza, Fátima Cleonice de |
dc.contributor.advisor1.fl_str_mv |
Pinto, Leonardo Araújo |
contributor_str_mv |
Pinto, Leonardo Araújo |
dc.subject.por.fl_str_mv |
INFECÇÕES RESPIRATÓRIAS DOENÇAS RESPIRATÓRIAS PEDIATRIA MEDICINA |
topic |
INFECÇÕES RESPIRATÓRIAS DOENÇAS RESPIRATÓRIAS PEDIATRIA MEDICINA |
description |
Introduction: Acute respiratory tract infections (ARTI) are one of the most important causes of mortality in children under 5 years old. In developed countries ARTI account for 20% of emergency consultations and 75% of antibiotic prescriptions. Children in attending day care are more prone to recurrence of respiratory infections. Bacterial immunostimulants, resulting from the chemical lysis of microorganisms associated with most respiratory tract infections, have been propagated as possibly useful intervention for prevention of recurrent respiratory infections. Objective: To analyze the effectiveness of OM-85 Broncho-vaxom (OM-85 BV) on the prevention of upper respiratory tract infections in healthy children attending preschool during the 6-month period. Methods: A randomized, double-blind, placebo controlled study was conducted in 54 healthy children aged between 6 months to 5 years attending in the School for Early Childhood Education between the months of April and September. Use of OM-85 BV for 3 months and observed for a further 3 months the following outcomes: upper respiratory tract infection, bronchopneumonia, other infections, use of antibiotics, emergency consultations, need for hospital stay, side effects of the medication. Results: Of the 54 children included, 57% were male. All completed the study and there were no significant differences between the groups. Of the 27 patients in group OM-85 BV, 19 (70,4%), attending daycare full-time and 16 (64,85%) half period, morning or evening. Breastfeeding was exclusive until 6 months in 6 patients (22,2%) on the OM-85 BV group and in 7 (25,9%) patients in the control group. Family history of smoking was positive in 11 (40,7%) patients in the OM-85 BV group and in 13 (48,1%) patients in the control group. Regarding the number of respiratory infections, the mean in the OM-85 BV group in the first 3 months was 0,92± 0,87 and in the placebo group was 0,74± 1,02 and in the 6 months was 1,62± 1,47 and 1,03±1,34, respectively. Antibiotic was used in 10 (37%) children of the OM-85BV group in the 3 months of treatment and in 13 (48,1%) of the placebo group, and in the 6 months of follow-up the use was 48,1% in both groups. The mean number of hospitalizations was very low in the period of the study. The mean number of emergency visits during the first 3 months was 0,81±1,21 in the OM-85 BV group and 1,29±1,48 in the placebo group and at 6 months was 1,77±1,80 in the OM-85 BV group and 2,03±1,76 in the placebo group. Conclusions: OM-85 BV was not effective as an intervention in daycare children with no history of IRR. No statistically significant difference was observed between the groups in the use of antibiotics, emergency consultations and hospitalizations. |
publishDate |
2017 |
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2017-10-14T12:01:24Z |
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2017-10-14T12:01:24Z |
dc.date.issued.fl_str_mv |
2017 |
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info:eu-repo/semantics/doctoralThesis |
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doctoralThesis |
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http://hdl.handle.net/10923/10800 |
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Pontifícia Universidade Católica do Rio Grande do Sul Porto Alegre |
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Pontifícia Universidade Católica do Rio Grande do Sul Porto Alegre |
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