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OBJECTIVE: Characterization of partial remission using the insulin dose-adjusted HbA1c (IDAA1c) ≤ 9 definition in a multiethnic Brazilian population of children and adolescents with type 1 diabetes (T1D), in addition with the determination of both Class II HLA genotype and autoantibodies. METHODS: We analyzed the prevalence of partial remission in 51 new-onset T1D patients with a median time follow-up of 13 months from diagnosis. For this study, anti-GAD65, anti-IA2 and HLA class II genotyping were considered. RESULTS: Partial remission occurred in 41.2% of T1D patients until 3 months after diagnosis, mainly in those aged 5-15 years. We have demonstrated a significant increase in the haplotypes of class II HLA DRB1*0301-DQB1*0201 in children and adolescents with a partial remission phase of the disease (42.9% vs 21.7% in non-remitters, P = .0291). This haplotype was also associated with the reduction of anti-IA2 antibodies production. Homozygote DRB1*03-DQB1*0201/DRB1*03-DQB1*0201 children had the lowest prevalence of IA-2A antibodies (P = .0402). However, this association does not correlate with the time of the remission phase. CONCLUSION: Although the number of patients studied was reduced, our data suggested that the association between genetics and decrease in antibody production to certain islet auto-antigen may contribute, at least in part, to the remission phase of T1D.

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OBJECTIVE: To determine whether the presence of opacification in the paranasal sinuses of children and adolescents without rhinosinusitis implies an increased risk of later development of upper respiratory tract symptoms. METHODS: This was a prospective study of a cohort of patients aged 0 to 18 years who underwent computerized tomography (CT) scans for indications unrelated to rhinosinusitis. Sinus opacification was evaluated using an opacification/development ratio score. The patients' clinical progression was followed up using a questionnaire for 1 month after the scans. RESULTS: Fifty-six percent (56%) of the 106 patients enrolled in the study had opacity, the majority due to mucosal thickening. Intense opacification was defined as "suspected" (score ≥ 15) and patients in this subset had a greater risk of developing symptoms during follow-up (odds ratio = 2.74; 95%CI 1.10-6.83) compared to those with no findings or discrete findings. CONCLUSIONS: Intense incidental sinus opacity on CT indicates a risk of future development of a clinical respiratory condition.

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OBJETIVO: Verificar se, em crianças e adolescentes sem rinossinusite, a presença de opacificações dos seios paranasais implica em maior risco de desenvolvimento posterior de sintomas do trato respiratório superior. MÉTODOS: Estudo prospectivo de coorte, com pacientes entre 0 e 18 anos, submetidos à tomografia computadorizada do crânio por indicações não relacionadas à rinossinusite. As opacificações sinusais foram aferidas pelo escore razão opacificação/desenvolvimento. A evolução clínica dos pacientes foi então avaliada por questionários durante o mês que se seguia ao exame. RESULTADOS: Dos 106 pacientes incluídos, as opacidades acometeram 56 por cento, a maioria de espessamento mucoso. Opacidades intensas, ditas suspeitas (escore > 15), impuseram maior risco de desenvolvimento de sintomas no seguimento (odds ratio = 2,74; IC95 por cento:1,10-6,83), em comparação aos exames normais ou às opacidades discretas. CONCLUSÃO: Opacidades tomográficas sinusais incidentais em crianças e adolescentes oferecem risco de desenvolvimento futuro de quadro clínico respiratório quando intensas.

OBJECTIVE: To determine whether the presence of opacification in the paranasal sinuses of children and adolescents without rhinosinusitis implies an increased risk of later development of upper respiratory tract symptoms. METHODS: This was a prospective study of a cohort of patients aged 0 to 18 years who underwent computerized tomography (CT) scans for indications unrelated to rhinosinusitis. Sinus opacification was evaluated using an opacification/development ratio score. The patients’ clinical progression was followed up using a questionnaire for 1 month after the scans. RESULTS: Fifty-six percent (56 percent) of the 106 patients enrolled in the study had opacity, the majority due to mucosal thickening. Intense opacification was defined as "suspected" (score > 15) and patients in this subset had a greater risk of developing symptoms during follow-up (odds ratio = 2.74; 95 percentCI 1.10-6.83) compared to those with no findings or discrete findings. CONCLUSION: Intense incidental sinus opacity on CT indicates a risk of future development of a clinical respiratory condition.

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This report describes the clinical features and outcome of 61 pediatric hospitalized patients with influenza-like infection. Fever, cough and respiratory distress were the most common symptoms of the infection. Fifteen patients presented positive RT-PCR results for influenza A (H1N1). The group with positive results was compared with the negative one. The main significant difference was antibiotic usage and the need of mechanical ventilation in the patients with H1N1-virus infection. Among the 11 patients who required intensive care due to respiratory failure, 3 from the positive group died and none from the negative group.

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OBJECTIVE: To detect factors associated with greater risk of death in infants after an apparent life-threatening event (ALTE). METHODS: This cross-sectional, retrospective, descriptive and analytic study evaluated infants younger than 12 months who had a sudden event of cyanosis, pallor, hypotonia or apnea and were seen in the emergency department of a tertiary university hospital. Forward stepwise logistic regression (Wald) was used to calculate and adjust odds ratios to evaluate associations. RESULTS: Mean age of the 145 patients included in the study was 105 days (median = 65 days). Eleven (7.6%) died, and their mean age was 189 days (median = 218 days). Mean age of survivors was 98 days (median = 62 days) (p = 0.003). Activity before the event, prematurity and number of events were not associated with death. A significant association was found with pallor. Of the 11 infants, 3 had spontaneous resolution of ALTE, whereas 8 patients [27.6%; p < 0.001; OR = 14.3 (95%CI 3.51-58.3)] did not. The associations with respiratory or cardiovascular disease were also significant. In multivariate analysis, immediate spontaneous resolution [p = 0.015; OR = 6.06 (95%CI 1.02-35.94)] and diagnosis of cardiovascular disease [p = 0.047; OR = 164.27 (95%CI 7.34-3.673.78)] remained statistically significant. CONCLUSION: Infants who experienced an ALTE had a higher risk of subsequent death when their age was greater than 6 months and the event had a long duration, particularly when ALTE was associated with cardiovascular disease.

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OBJETIVO: Identificar, na admissão dos lactentes com após eventos com aparente risco de morte (apparent life-threatening event, ALTE), fatores que possam indicar maior risco de evolução para o óbito. MÉTODOS: Estudo transversal retrospectivo, descritivo e analítico com lactentes menores de 12 meses, com evento súbito de cianose, palidez, hipotonia e/ou apneia, atendidos na unidade de emergência de hospital universitário de nível terciário. Para avaliação da associação, determinaram-se os valores de odds ratio bruto e ajustado por regressão logística (método stepwise forward Wald). RESULTADOS: Foram avaliados 145 pacientes com idade média de 105 dias (mediana = 65 dias). Onze (7,6 por cento) evoluíram para óbito, com idade média de 189 dias (mediana = 218 dias), enquanto que a idade média dos sobreviventes foi de 98 dias (mediana = 62 dias) (p = 0,003). Atividades que precederam o evento, antecedente de prematuridade e número de episódios não apresentaram associação com o óbito. Apresentou relação significativa o relato de palidez pelos observadores. Entre os 11 lactentes, 3 apresentaram melhora imediata e espontânea; já 8 pacientes [27,6 por cento; p < 0,001; OR = 14,3 (IC95 por cento 3,51-58,3)] não tiveram melhora espontânea. Os diagnósticos de doença do trato respiratório e do sistema cardiocirculatório também foram significantes. Na análise multivariada, mostraram significância estatística: não melhora imediata e espontânea [p = 0,015; OR = 6,06 (IC95 por cento 1,02-35,94)] e diagnóstico de doença do sistema cardiocirculatório [p = 0,047; OR = 164,27 (IC95 por cento 7,34-3.673,78)]. CONCLUSÃO: Os lactentes que apresentaram ALTE tiveram maior risco de óbito quando presentes na faixa etária acima dos 6 meses e quando os eventos tiveram duração prolongada, principalmente quando ocorreram como manifestação de doenças do sistema cardiocirculatório.

OBJECTIVE: To detect factors associated with greater risk of death in infants after an apparent life-threatening event (ALTE). METHODS: This cross-sectional, retrospective, descriptive and analytic study evaluated infants younger than 12 months who had a sudden event of cyanosis, pallor, hypotonia or apnea and were seen in the emergency department of a tertiary university hospital. Forward stepwise logistic regression (Wald) was used to calculate and adjust odds ratios to evaluate associations. RESULTS: Mean age of the 145 patients included in the study was 105 days (median = 65 days). Eleven (7.6 percent) died, and their mean age was 189 days (median = 218 days). Mean age of survivors was 98 days (median = 62 days) (p = 0.003). Activity before the event, prematurity and number of events were not associated with death. A significant association was found with pallor. Of the 11 infants, 3 had spontaneous resolution of ALTE, whereas 8 patients [27.6 percent; p < 0.001; OR = 14.3 (95 percentCI 3.51-58.3)] did not. The associations with respiratory or cardiovascular disease were also significant. In multivariate analysis, immediate spontaneous resolution [p = 0.015; OR = 6.06 (95 percentCI 1.02-35.94)] and diagnosis of cardiovascular disease [p = 0.047; OR = 164.27 (95 percentCI 7.34-3.673.78)] remained statistically significant. CONCLUSION: Infants who experienced an ALTE had a higher risk of subsequent death when their age was greater than 6 months and the event had a long duration, particularly when ALTE was associated with cardiovascular disease.

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OBJECTIVES: To compare leukotriene antagonists (LTA) to other groups of drugs used in asthma and allergic rhinitis treatment. SOURCES: MEDLINE, LILACS and Cochrane Library. KEYWORDS: leukotrienes, antileukotrienes, asthma treatment, allergic rhinitis treatment, asthma and allergic rhinitis. An attempt was made to group the main studies and reviews about this topic. SUMMARY OF THE FINDINGS: LTA are more efficient than placebo and enhance the effects of inhaled corticosteroids. The association of inhaled corticosteroids with long-acting Beta2 agonists is more efficient than the association of inhaled corticosteroids + LTA. Although use of LTA in acute asthma attacks and allergic rhinitis seems reasonable, more studies are needed to confirm this benefit. LTA reduce hospitalization time and the number of wheezing attacks in infants with acute viral bronchiolitis caused by respiratory syncytial virus, as well as recurrent wheezing after acute viral bronchiolitis. LTA are less efficient than intranasal corticosteroids for allergic rhinitis management. LTA are efficient in exercise-induced asthma, although they are not the first-line treatment. CONCLUSION: Controlled and randomized studies show that inhaled corticosteroids are the drugs of choice to treat persistent asthma and allergic rhinitis. There is not enough evidence to recommend the use of LTA as first-line drug (monotherapy) in children with asthma (level I). For children who cannot use inhaled corticosteroids, LTA may be a good alternative (level II).

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OBJETIVO: Comparar os antagonistas de leucotrienos (ARLT) aos outros grupos de medicamentos utilizados para tratar a asma e a rinite alérgica. FONTES DOS DADOS: MEDLINE, LILACS e Biblioteca Cochrane. Palavras chaves: leucotrienos, antileucotrienos, tratamento da asma, tratamento da rinite alérgica, asma e rinite alérgica. Procurou-se agrupar os principais trabalhos e revisões sobre o assunto. SíNTESE DOS DADOS: Os ARLT são mais eficazes do que placebo e potencializam os efeitos dos corticosteróides inalados. A associação de corticosteróides inalados com agentes beta2 agonistas de longa duração (LABA) é mais eficaz do que a associação de cortiscoteróides inalados + ARLT. Embora pareça racional o uso de ARLT na crise aguda de asma e rinite alérgica, mais estudos são necessários para comprovar esse benefício. Os ARLT promovem redução no tempo de hospitalização e no número de crises de sibilância em lactentes com bronquiolite viral aguda pelo vírus respiratório sincicial e na sibilância recorrente após bronquiolite viral aguda. Os ARLT são menos eficazes que os corticosteróides intranasais no manejo da rinite alérgica. Os ARLT são eficazes na asma induzida por exercício (AIE), embora não constituam a primeira linha de tratamento. CONCLUSÃO: Estudos controlados e randomizados mostram que os corticosteróides inalados são as drogas de escolha para o tratamento da asma persistente e rinite alérgica. :Não existem evidências suficientes para recomendar o uso de ARLT como medicamento de primeira linha (monoterapia) em crianças com asma (nível I). Nas crianças que não podem usar corticosteróides inalados, os ARLT podem ser uma alternativa (nível II).

OBJECTIVE: To compare leukotriene antagonists (LTA) to other groups of drugs used in asthma and allergic rhinitis treatment. SOURCES: MEDLINE, LILACS and Cochrane Library. Keywords: leukotrienes, antileukotrienes, asthma treatment, allergic rhinitis treatment, asthma and allergic rhinitis. An attempt was made to group the main studies and reviews about this topic. SUMMARY OF THE FINDINGS: LTA are more efficient than placebo and enhance the effects of inhaled corticosteroids. The association of inhaled corticosteroids with long-acting beta2-agonists is more efficient than the association of inhaled corticosteroids + LTA. Although use of LTA in acute asthma attacks and allergic rhinitis seems reasonable, more studies are needed to confirm this benefit. LTA reduce hospitalization time and the number of wheezing attacks in infants with acute viral bronchiolitis caused by respiratory syncytial virus, as well as recurrent wheezing after acute viral bronchiolitis. LTA are less efficient than intranasal corticosteroids for allergic rhinitis management. LTA are efficient in exercise-induced asthma, although they are not the first-line treatment. CONCLUSIONS: Controlled and randomized studies show that inhaled corticosteroids are the drugs of choice to treat persistent asthma and allergic rhinitis. There is not enough evidence to recommend the use of LTA as first-line drug (monotherapy) in children with asthma (level I). For children who cannot use inhaled corticosteroids, LTA may be a good alternative (level II).

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OBJECTIVE: To review the literature on acute toxic exposure in children, excluding envenomations. SOURCES OF DATA: MEDLINE review (emphasis on the past decade), including the American Academy of Clinical Toxicology and the European Association of Poison Centres and Clinical Toxicologists position statements and position papers (peer-reviewed information based on scientific evidence and broad consensus) on gastrointestinal decontamination, multiple-dose activated charcoal and urine alkalinization. SUMMARY OF THE FINDINGS: Acute toxic exposure in children is a common event, mainly in children under six years of age. Death is rare. Although widely employed, there is no evidence that gastrointestinal decontamination and multiple-dose activated charcoal improve the outcome of poisoned patients. Very few efficient antidotes are used on a consistent basis, and some of them are very expensive and not available in Brazil. CONCLUSIONS: Ipecac syrup and cathartics should not be administered on a routine basis in acute toxic exposures in outpatient treatment. Excluding the contraindications, single-dose activated charcoal and gastric lavage may be considered within one hour of ingestion if a patient ingested a potentially toxic amount or a potentially lethal amount, respectively. Whole bowel irrigation, multiple-dose activated charcoal and urine alkalinization may be considered in a few situations. Fomepizole and octreotide are safe and efficient antidotes, which can be used in the treatment of alcohol (methanol and ethylene glycol) and sulfonylureas poisoning, respectively.

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OBJETIVO: Revisar a literatura das exposições tóxicas em pediatria, excluindo os acidentes por animais peçonhentos. FONTES DE DADOS: Revisão narrativa dos principais trabalhos indexados no MEDLINE, especialmente da última década, incluindo as revisões de consenso baseadas em evidências sobre as medidas de descontaminação gastrintestinal e de aumento da eliminação de agentes tóxicos, estabelecidas em conjunto pela Academia Americana de Toxicologia Clínica e Associação Européia dos Centros de Intoxicação e dos Toxicologistas Clínicos. SíNTESE DOS DADOS: A exposição tóxica em pediatria é um evento comum, principalmente em crianças abaixo de 6 anos. A letalidade é baixa. Embora amplamente empregadas, não há evidências de que as medidas de descontaminação gastrintestinal e de aumento de eliminação de agentes tóxicos melhore o prognóstico dos pacientes intoxicados. São poucos os antídotos disponíveis e eficazes, sendo alguns de alto custo, e vários não disponíveis no Brasil; seu uso é limitado para indicações precisas. CONCLUSÕES: Não há evidências que apóiem a recomendação do uso do xarope de ipeca e de catárticos, seja no atendimento pré-hospitalar ou nas salas de emergência. O uso de carvão ativado em dose única e da lavagem gástrica, afastadas as contra-indicações, somente deve ser considerado se o procedimento puder ser realizado até 60 minutos da ingestão de doses potencialmente tóxicas ou potencialmente letais. A irrigação intestinal, a administração de carvão ativado em doses múltiplas e a alcalinização urinária podem ser consideradas em situações isoladas. Fomepizol e octreotida são antídotos seguros e eficazes no tratamento das intoxicações graves por álcoois (metanol e etilenoglicol) e sulfoniluréias, respectivamente.

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BACKGROUND: Describe clinical and epidemiological characteristics of pediatric patients diagnosed with acute diarrhea and shock, admitted to the pediatric intensive care unit, in order to compare the evolution of clinical data between the survival and non-survival groups, thereby identifying the risk factors of death. METHODS: In the Pediatric Intensive Care Unit of the Clinical Hospital at the State University of Campinas (UNICAMP), a non-controlled, descriptive and retrospective study was carried out from February 1994 to January 1998 The epidemiological and clinical/evolution data were analyzed and the groups of those who survived (56) and did not survive (15) were compared. For continuous variables, the Chi-Square test was used and for categorical variables, the Fisher's Exact test, for values lower than five. RESULTS: Seventy one children aged from 0.4 to 13.9 months were admitted, 15 of them died (21.2%). Low birth weight was found in 18.1% and the mean breast-feeding time was 1.1 months. The average length of stay was 5.6 days. 52/71 children needed mechanical ventilation, use of vasoactive drugs and sodium bicarbonate was necessary in 23/71 and 15/71, respectively. 93% of children were given antibiotics. The use of sodium bicarbonate, vasoactive drugs and mechanical ventilation showed an association with risk of death, but only vasoactive drugs (OR=18.56) and an age less than 3 months (OR=0.10) showed a statistically significant difference in multivariate analysis. CONCLUSIONS: Acute diarrhea and shock occurred mainly in children under 3 months of age with a severe clinical/laboratorial condition. During clinical evolution, the high risk of death was related to the use of vasoactive drugs, a support therapy used in critical patients.

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OBJETIVOS: Descrever características clínicas e epidemiológicas de criancas com diarréia aguda e choque, admitidas em unidade de terapia intensiva pediátrica, e comparar a evolucão clínica entre os grupos óbito e sobrevida, identificando fatores associados ao óbito. MÉTODOS: Estudo descritivo, retrospectivo, não controlado, no período de fevereiro de 1994 a janeiro de 1998. Os dados epidemiológicos e clínico-evolutivos dos pacientes foram analisados e os grupos de pacientes com sobrevida e com óbito foram comparados. O teste Qui-quadrado foi utilizado para variáveis contínuas, e o teste exato de Fisher para as variáveis categóricas (valores menores que cinco). RESULTADOS: Foram admitidas 71 criancas, com idade entre 0,4 e 13,9 meses. Evoluíram para óbito 15. Baixo peso de nascimento foi encontrado em 18,1 por cento dos pacientes, tempo médio de aleitamento materno de 1,1 mês e de internacão de 5,6 dias. Receberam antibióticos 93 por cento das criancas. Necessitaram de ventilacão pulmonar mecânica 52/71 criancas, uso de drogas vasoativas 23/70 e uso de bicarbonato de sódio 15/71; estas variáveis estiveram associadas com maior risco de óbito, na análise univariada. No modelo multivariado, permaneceram como significantes o parâmetro droga vasoativa (OR=18,56) e idade menor que três meses (OR=0,10). CONCLUSÕES: A diarréia aguda e choque ocorreram principalmente em criancas com menos de três meses de idade, com apresentacão clínica e laboratorial de gravidade. Na evolucão clínica, a utilizacão de terapia de suporte em paciente crítico esteve associada ao óbito, com destaque para o uso de droga vasoativa.

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Objetivos: Avaliar prospectivamente acidentes em unidades hospitalar, deterninando as causas mais freqüentes, com a finalidade de estabelecer bases para programas de prevenção. Métodos: O estudo abrangeu de março de 1997 a fevereiro de 1998. Todas as crianças até 14 anos vítimas de acidente tiveram seus dados de entrada anotados em ficha padronizada. Resultados: Foram atendidas 3.214 crianças vítimas de acidentes, representando 11,4 por cento do total. Predominou o sexo masculino (62,1 por cento). Os acidentes foram mais freqüêntes entre 9 e 13 anos (33,4 por cento), 2 e 5 anos (27,2 por cento) e 5 a 9 anos (25,5 por cento). Em 74 por cento houve traumatismo, devido principalmente quedas. O TCE foi importante nos menores de 1 ano, e o de membros entre 9 e 13 anos. Picadas e mordeduras ocorreram predominantemente entre os 5 e 13 anos e as intoxicações exógenas e acidentes com corpo estranho 2 e 5 anos. As queimaduras, entre os menores de 5 anos. 89,7 por cento dos atendimentos foram de baixa complexidade, mas 20 pacientes foram encaminhados para a UTI e ocorreram 4 óbitos em sala de emergência. Conclusões: A criança acima de 9 anos, menino, com traumatismo de membros por queda foi o caso de acidente mais freqüente. Programas de prevenção devem ter como alvo faixas etárias específicas. Os acidentes sobrecarregam serviços terciários com atendimentos de baixa complexidade. É necessário habilitar os centros de atenção primária para os casos de baixa complexidade

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No periodo de janeiro de 1984 a maio de 1994, de 239 criancas com ate 15 anos de idade, picadas por escorpioes pertencentes as especies T. bahiensis (84,9 por cento) e T. serrulatus (15,1 por cento), 17 apresentaram envenenamento grave...

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