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1.
Clinics (Sao Paulo) ; 79: 100384, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38754226

RESUMO

OBJECTIVE: This article focused on the correlation between the changes of serum total Immunoglobulin E (IgE) and Fractional exhaled Nitric Oxide (FeNO) and idiosyncratic reactions in children with bronchiolitis. METHODS: One hundred children with bronchiolitis and fifty healthy children were enrolled. Serum total IgE and FeNO were assessed, and the diagnostic value for bronchiolitis and the correlation with the severity of bronchiolitis were analyzed. Bronchiolitis children were divided into idiosyncratic + bronchiolitis and non-idiosyncratic + bronchiolitis groups, the relationship between serum total IgE and FeNO and idiosyncratic reaction was determined, and the diagnostic value of serum total IgE and FeNO for idiosyncratic bronchiolitis was examined. RESULTS: FeNO in bronchiolitis children was lower than that in healthy children but there was no significant difference in serum total IgE levels between the two populations. Serum total IgE increased while FeNO decreased with the aggravation of bronchiolitis in bronchiolitis children. The serum total IgE was positively correlated while FeNO was negatively correlated with the severity of bronchiolitis. Serum total IgE was higher in children with idiosyncratic bronchiolitis, but serum total IgE and FeNO were not the risk factors for idiosyncratic bronchiolitis; Area Under the Curve (AUC) of serum total IgE and FeNO for the diagnosis of idiosyncratic bronchiolitis was less than 0.7. CONCLUSION: Serum total IgE and FeNO in children with bronchiolitis are related to disease severity and idiosyncratic reaction. FeNO has a diagnostic value for bronchiolitis, but not for idiosyncratic bronchiolitis.


Assuntos
Bronquiolite , Imunoglobulina E , Óxido Nítrico , Índice de Gravidade de Doença , Humanos , Imunoglobulina E/sangue , Bronquiolite/sangue , Bronquiolite/imunologia , Feminino , Masculino , Lactente , Óxido Nítrico/análise , Óxido Nítrico/sangue , Estudos de Casos e Controles , Pré-Escolar , Teste da Fração de Óxido Nítrico Exalado , Biomarcadores/sangue , Biomarcadores/análise , Valores de Referência , Estatísticas não Paramétricas
2.
J Pediatr ; 203: 416-422.e1, 2018 12.
Artigo em Inglês | MEDLINE | ID: mdl-30243543

RESUMO

OBJECTIVE: To investigate the association between circulating 25-hydroxyvitamin D [25(OH)D] status at admission and disease severity among infants hospitalized for bronchiolitis and to determine whether the association differs by the form of 25(OH)D-total, bioavailable or free 25(OH)D. STUDY DESIGN: We conducted a 17-center prospective cohort study of 1016 US infants <12 months old hospitalized with bronchiolitis. Vitamin D status was defined by total 25(OH)D levels, and by calculated levels of bioavailable and free 25(OH)D. Bronchiolitis severity was defined by requirement for intensive care and hospital length-of-stay (LOS). Logistic and Poisson regression were used for unadjusted and multivariable analyses. RESULTS: The median age of hospitalized infants was 3.2 months (IQR 1.6-6.0). The median total 25(OH)D was 26.5 ng/mL (IQR 18.0-33.1); 298 (29%) infants had total 25(OH)D <20 ng/mL. In multivariable models, infants with total 25(OH)D <20 ng/mL had higher risk of requiring intensive care (aOR 1.72, 95% CI 1.12-2.64) and longer LOS (adjusted rate ratio 1.39, 95% CI 1.17-1.65) compared with infants with total 25(OH)D ≥30 ng/mL. Infants with the lowest tertile of bioavailable 25(OH)D, compared with those with the highest tertile, had longer LOS (adjusted rate ratio 1.32, 95% CI 1.07-1.62); admission to the intensive care unit was not statistically significant in the adjusted model (aOR 1.39, 95% CI 0.96-2.64). Free 25(OH)D level was not associated with severity of bronchiolitis in either unadjusted or adjusted models. CONCLUSION: In a large, multicenter cohort of US infants hospitalized for bronchiolitis, infants with total 25(OH)D <20 ng/mL had increased risk of intensive care and longer hospital LOS.


Assuntos
Bronquiolite/sangue , Hospitalização , Deficiência de Vitamina D/sangue , Bronquiolite/complicações , Pré-Escolar , Cuidados Críticos , Feminino , Humanos , Lactente , Unidades de Terapia Intensiva , Tempo de Internação , Masculino , Modelos Estatísticos , Análise Multivariada , Distribuição de Poisson , Estudos Prospectivos , Índice de Gravidade de Doença , Estados Unidos , Vitamina D/análogos & derivados , Vitamina D/sangue , Deficiência de Vitamina D/complicações
3.
Acta Paediatr ; 103(3): e111-5, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24188330

RESUMO

AIM: To investigate the influence of hypotonic parenteral hydration on serum and urinary sodium and osmolality in infants with moderate bronchiolitis. METHODS: We studied 36 infants (mean age 3.7 ± 2.3 months), with a diagnosis of moderate bronchiolitis admitted to a paediatric emergency unit in São Paulo, Brazil. Patients received a standard parenteral hypotonic solution, according to Holliday and Segar, during the first 24 h, due to respiratory distress. The disease was monitored by a respiratory severity score (RDAI-Respiratory Distress Assessment Instrument), respiratory rate and oxygen saturation. Serum and urinary sodium and osmolality were monitored at admission, 24 and 48 h after admission. RESULTS: All respiratory parameters improved during hospitalisation. Serum sodium and osmolality dropped after 24 h (136.8 ± 2.8 and 135.8 ± 2.6 mEq/L, p = 0.031; 283.4 ± 4.1 and 281.6 ± 3.9 mOsm/kg, p = 0.004 respectively) as well as urinary osmolality (486.8 ± 243.4 mOsm/kg and 355.7 ± 205.0 mOsm/kg, p < 0.001) when compared to admission. CONCLUSION: This study reinforces the occurrence of hyponatraemia in bronchiolitis even in patients with moderate disease and highlights the risk of serum sodium drop caused by hypotonic parenteral hydration.


Assuntos
Bronquiolite/complicações , Hiponatremia/prevenção & controle , Soluções Hipotônicas/uso terapêutico , Brasil/epidemiologia , Bronquiolite/sangue , Bronquiolite/urina , Estudos de Coortes , Progressão da Doença , Serviços Médicos de Emergência , Feminino , Humanos , Hiponatremia/epidemiologia , Hiponatremia/etiologia , Incidência , Recém-Nascido , Infusões Intravenosas , Masculino , Estudos Prospectivos
4.
Rev Med Chil ; 141(5): 574-81, 2013 May.
Artigo em Espanhol | MEDLINE | ID: mdl-24089271

RESUMO

BACKGROUND: An increased inflammatory innate response may play a role in pathogenesis of respiratory syncytial virus (RSV) infection. AIM: To quantify pro-inflammatory cytokines (IL-6-IL-8, ÍL-2-P and TNF-a) in nasopharyngeal aspirate (NPA) and plasma, and plasma cortisol in previously healthy infants with RSV bronchiolitis. PATIENTS AND METHODS: We studied 49 infants aged less than one year of age with RSV bronchiolitis and 25 healthy controls. Severity was defined using a previously described modified score. We quantified interleukins in NPA and plasma by flow cytometry and plasma cortisol by radioimmunoanalysis. RESULTS: Among patients with RSV bronchiolitis, 25 were classified as severe and 24 as moderate or mild. Significantly higher levels of IL-6 and IL-8 in NPA and plasma and IL-lfi in NPA were found in children classified as severe, when compared to those with moderate or mild disease and controls. There was a positive correlation between IL-6 and cortisol in plasma (r = 0,55; p < 0,0001) and both were correlated with the severity of the disease. CONCLUSIONS: RSV bronchiolitis severity was associated with higher levéis of inflammatory interleukins and plasma cortisol.


Assuntos
Bronquiolite/sangue , Hidrocortisona/sangue , Interleucinas/sangue , Infecções por Vírus Respiratório Sincicial/sangue , Fator de Necrose Tumoral alfa/sangue , Bronquiolite/imunologia , Bronquiolite/virologia , Estudos de Casos e Controles , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Lactente , Masculino , Nasofaringe/virologia , Infecções por Vírus Respiratório Sincicial/imunologia , Infecções por Vírus Respiratório Sincicial/virologia , Índice de Gravidade de Doença
5.
Rev. méd. Chile ; 141(5): 574-581, mayo 2013. graf, tab
Artigo em Espanhol | LILACS | ID: lil-684364

RESUMO

Background: An increased inflammatory innate response may play a role in pathogenesis of respiratory syncytial virus (RSV) infection. Aim: To quantify pro-inflammatory cytokines (IL-6-IL-8, ÍL-2-P and TNF-a) in nasopharyngeal aspirate (NPA) and plasma, and plasma cortisol in previously healthy infants with RSV bronchiolitis. Patients and Methods: We studied 49 infants aged less than one year of age with RSV bronchiolitis and 25 healthy controls. Severity was defined using a previously described modified score. We quantified interleukins in NPA and plasma by flow cytometry and plasma cortisol by radioimmunoanalysis. Results: Among patients with RSV bronchiolitis, 25 were classified as severe and 24 as moderate or mild. Significantly higher levels ofIL-6 and IL-8 in NPA and plasma and IL-lfi in NPA were found in children classified as severe, when compared to those with moderate or mild disease and controls. There was a positive correlation between IL-6 and cortisol in plasma (r = 0,55; p < 0,0001) and both were correlated with the severity of the disease. Conclusions: RSV bronchiolitis severity was associated with higher levéis of inflammatory interleukins and plasma cortisol.


Assuntos
Feminino , Humanos , Lactente , Masculino , Bronquiolite/sangue , Hidrocortisona/sangue , Interleucinas/sangue , Infecções por Vírus Respiratório Sincicial/sangue , Fator de Necrose Tumoral alfa/sangue , Bronquiolite/imunologia , Bronquiolite/virologia , Estudos de Casos e Controles , Ensaio de Imunoadsorção Enzimática , Nasofaringe/virologia , Infecções por Vírus Respiratório Sincicial/imunologia , Infecções por Vírus Respiratório Sincicial/virologia , Índice de Gravidade de Doença
7.
J Pediatr ; 120(1): 28-32, 1992 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-1731020

RESUMO

Eosinophil cationic protein (ECP), a cytotoxic protein contained in the granules of eosinophils, has been suggested as having an important role in the pathogenesis of asthma. To determine whether ECP plays a similar role in bronchiolitis, we tested samples of nasopharyngeal secretions, obtained from a group of 47 children with various forms of illness related to respiratory syncytial virus (RSV) and from 26 children with non-RSV upper respiratory tract illness or bacterial pneumonia, for the presence of ECP by means of a double-antibody radioimmunoassay. Concentrations of ECP in children with RSV bronchiolitis were significantly higher (166.8 ng/ml) than the mean concentration of ECP in both groups of children with RSV upper respiratory tract illness (43.5 ng/ml, p less than 0.002) and RSV lower respiratory tract disease without wheezing (29.1 ng/ml; p less than 0.0002). Children with non-RSV upper respiratory tract illness or bacterial pneumonia had levels of ECP in nasopharyngeal secretions similar to those of children with RSV upper respiratory tract illness or RSV pneumonia. High ECP levels in nasopharyngeal secretions (greater than 50 ng/ml) were predictive of the development of bronchiolitis at the time of RSV infection (p less than 0.001), and the individual ECP levels correlated with severity of the disease as determined by the initial PaO2 concentrations (p less than 0.05). These data suggest that eosinophil degranulation in the respiratory tract occurs during RSV bronchiolitis and may play a significant role in the development of virus-induced airway obstruction.


Assuntos
Proteínas Sanguíneas/farmacocinética , Degranulação Celular , Eosinófilos/fisiologia , Vírus Sinciciais Respiratórios , Infecções Respiratórias/metabolismo , Infecções por Respirovirus/metabolismo , Ribonucleases , Infecções Bacterianas/metabolismo , Infecções Bacterianas/fisiopatologia , Proteínas Sanguíneas/análise , Bronquiolite/sangue , Bronquiolite/metabolismo , Bronquiolite/fisiopatologia , Degranulação Celular/fisiologia , Criança , Pré-Escolar , Proteínas Granulares de Eosinófilos , Eosinófilos/metabolismo , Humanos , Hipóxia/sangue , Lactente , Nasofaringe/metabolismo , Oxigênio/sangue , Pressão Parcial , Pneumonia/metabolismo , Pneumonia/fisiopatologia , Pneumonia Viral/sangue , Pneumonia Viral/metabolismo , Pneumonia Viral/fisiopatologia , Probabilidade , Infecções Respiratórias/sangue , Infecções Respiratórias/fisiopatologia , Infecções por Respirovirus/sangue , Infecções por Respirovirus/fisiopatologia
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