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1.
J Infect Dis ; 212(1): 57-66, 2014.
Artigo em Inglês | LILACS, SES-SP, SESSP-IALPROD, SES-SP, SESSP-IALACERVO | ID: biblio-1022226

RESUMO

BACKGROUND: Congenital rubella syndrome (CRS) case identification is challenging in older children since laboratory markers of congenital rubella virus (RUBV) infection do not persist beyond age 12 months. METHODS: We enrolled children with CRS born between 1998 and 2003 and compared their immune responses to RUBV with those of their mothers and a group of similarly aged children without CRS. Demographic data and sera were collected. Sera were tested for anti-RUBV immunoglobulin G (IgG), IgG avidity, and IgG response to the 3 viral structural proteins (E1, E2, and C), reflected by immunoblot fluorescent signals. RESULTS: We enrolled 32 children with CRS, 31 mothers, and 62 children without CRS. The immunoblot signal strength to C and the ratio of the C signal to the RUBV-specific IgG concentration were higher (P < .029 for both) and the ratio of the E1 signal to the RUBV-specific IgG concentration lower (P = .001) in children with CRS, compared with their mothers. Compared with children without CRS, children with CRS had more RUBV-specific IgG (P < .001), a stronger C signal (P < .001), and a stronger E2 signal (P ≤ .001). Two classification rules for children with versus children without CRS gave 100% specificity with >65% sensitivity. CONCLUSIONS: This study was the first to establish classification rules for identifying CRS in school-aged children, using laboratory biomarkers. These biomarkers should allow improved burden of disease estimates and monitoring of CRS control programs. Published by Oxford University Press on behalf of the Infectious Diseases Society of America 2014. This work is written by (a) US Government employee(s) and is in the public domain in the US.


Assuntos
Instituições Acadêmicas , Estudantes , Síndrome da Rubéola Congênita/diagnóstico , Biomarcadores/sangue , Adolescente , Anticorpos Antivirais , Afinidade de Anticorpos
2.
Braz. j. med. biol. res ; 40(12): 1681-1687, Dec. 2007. graf, tab
Artigo em Inglês | LILACS | ID: lil-466743

RESUMO

The introduction of routine vaccination against tetanus and diphtheria in Brazil has decreased the incidence and changed the epidemiology of both diseases. We then investigated the prevalence of Corynebacterium diphtheriae carrier status and diphtheria and tetanus immunity in São Paulo, Brazil. From November 2001 to March 2003, 374 individuals were tested for the presence of C. diphtheriae in the naso-oropharynx and of serum diphtheria and tetanus antibodies. Participants were all healthy individuals without acute or chronic pathologies and they were stratified by age as follows: 0-12 months and 1-4, 5-9, 10-14, 15-24, 25-39, 40-59, and ³60 years. Antibodies were assessed using a double-antigen ELISA. C. diphtheriae species were identified by biochemical analysis and toxigenicity was assessed by the Elek test. For diphtheria, full protection (antibodies ³0.1 IU/mL) was present in 84 percent of the individuals, 15 percent had basic protection (antibodies ³0.01 and <0.1 IU/mL) and 1 percent were susceptible (antibodies <0.01 IU/mL). Full tetanus protection (antibodies ³0.1 IU/mL) was present in 79 percent of the participants, 18 percent had basic protection (antibodies ³0.01 and <0.1 IU/mL) and 3 percent were susceptible (antibodies <0.01 IU/mL). The geometric mean of diphtheria and tetanus antibodies reached the highest values at 5-9 years and decreased until the 40-59-year age range, increasing again in individuals over 60 years. Three participants (0.8 percent) were carriers of C. diphtheriae, all non-toxigenic strains. The present results demonstrate the clear need of periodic booster for tetanus and diphtheria vaccine in adolescents and adults after primary immunization in childhood.


Assuntos
Adolescente , Adulto , Criança , Pré-Escolar , Humanos , Lactente , Recém-Nascido , Pessoa de Meia-Idade , Anticorpos Antibacterianos/sangue , Clostridium tetani/imunologia , Corynebacterium diphtheriae/imunologia , Difteria/imunologia , Tétano/imunologia , Distribuição por Idade , Anticorpos Antibacterianos/imunologia , Brasil , Vacina contra Difteria, Tétano e Coqueluche/imunologia , Difteria/prevenção & controle , Ensaio de Imunoadsorção Enzimática , Tétano/prevenção & controle
3.
Braz. j. med. biol. res ; 39(4): 519-523, Apr. 2006. ilus, tab
Artigo em Inglês | LILACS | ID: lil-425090

RESUMO

Epidemiological data regarding tetanus and diphtheria immunity in elderly people in Brazil are scarce. During the First National Immunization Campaign for the Elderly in Brazil in April 1999, 98 individuals (median age: 84 years) received one tetanus-dyphtheria (Td) vaccine dose (Butantan Institute, lot number 9808079/G). Inclusion criteria were elderly individuals without a history of severe immunosuppressive disease, acute infectious disease or use of immunomodulators. Blood samples were collected immediately before the vaccine and 30 days later. Serum was separated and stored at -20°C until analysis. Tetanus and diphtheria antibodies were measured by the double-antigen ELISA test. Tetanus and diphtheria antibody concentrations lower than 0.01 IU/mL were considered to indicate the absence of protection, between 0.01 and 0.09 IU/mL were considered to indicate basic immunity, and values of 0.1 IU/mL or higher were considered to indicate full protection. Before vaccination, 18 percent of the individuals were susceptible to diphtheria and 94 percent were susceptible to tetanus. After one Td dose, 78 percent became fully immune to diphtheria, 13 percent attained basic immunity, and 9 percent were still susceptible to the disease. In contrast, 79 percent remained susceptible to tetanus, 4 percent had basic immunity and 17 percent were fully immune. Although one Td dose increases immunity to diphtheria in many elderly people who live in Brazil, a complete vaccination series appears to be necessary for the prevention of tetanus.


Assuntos
Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Anticorpos Antibacterianos/sangue , Vacina contra Difteria e Tétano/imunologia , Difteria/prevenção & controle , Tétano/prevenção & controle , Anticorpos Antibacterianos/imunologia , Brasil , Difteria/imunologia , Ensaio de Imunoadsorção Enzimática , Tétano/imunologia
4.
Braz. j. infect. dis ; 9(2): 162-168, Apr. 2005. tab
Artigo em Inglês | LILACS | ID: lil-408459

RESUMO

The bacteriological and clinical efficacy and the safety of gatifloxacin for the treatment of non-complicated acute rhinosinusitis was evaluated in 49 adult patients in an open-label multicenter study in Brazil. Patients under age 18, or with associated systemic diseases, were excluded. Diagnosis was based on symptoms, otorhinolaryngological examination, and X-rays of the sinus. At the first visit, all patients were treated with a single daily dose of 400 mg gatifloxacin for 10 days. Middle nasal meatus secretion was collected and sent for culture before and after treatment. Patients were all reevaluated at days 3 to 5; days + 1 to + 5 and 18 to 25 days + 7 to + 14 . Ninety three percent of the patients were considered clinically cured at the end of the treatment. The most frequent bacteria isolated were Haemophilus influenzae, Streptococcus pneumoniae and Moraxella catarrhalis, and at the end of the treatment, presumed bacteriological eradication was observed in almost all patients. Adverse effects were observed in 19 of the cases, mostly mild and self limiting, including diarrhea, abdominal pain, nausea and vomiting. Treatment had to be interrupted in two cases. Gatifloxacin was found to be efficacious and safe for the treatment of acute rhinosinusitis in adults.


Assuntos
Adolescente , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Antibacterianos/uso terapêutico , Fluoroquinolonas/uso terapêutico , Rinite/tratamento farmacológico , Sinusite/tratamento farmacológico , Doença Aguda , Fluoroquinolonas/efeitos adversos , Resultado do Tratamento
5.
Braz. j. med. biol. res ; 38(2): 215-220, fev. 2005. tab
Artigo em Inglês | LILACS | ID: lil-393658

RESUMO

Gastroesophageal reflux (GER) disorder was studied in children and adolescents with chronic and/or recurrent rhinosinusitis not associated with bronchial asthma. Ten children with a clinical and radiological diagnosis of chronic and/or recurrent rhinosinusitis, consecutively attended at the Pediatric Otolaryngology Outpatient Clinic, Federal University of São Paulo, were evaluated. Prolonged esophageal pH monitoring was used to investigate GER disorder. The mean age of the ten patients evaluated (eight males) was 7.4 ± 2.4 years. Two patients presented vomiting as a clinical manifestation and one patient presented retrosternal pain with a burning sensation. Twenty-four-hour esophageal pH monitoring was performed using the Sandhill apparatus. An antimony probe electrode was placed in the lower third of the esophagus, confirmed by fluoroscopy and later by a chest X-ray. The parameters analyzed by esophageal pH monitoring included: total percent time of the presence of acid esophageal pH, i.e., pH below 4 (<4.2 percent); total number of acid episodes (<50 episodes); number of reflux episodes longer than 5 min (3 or less), and duration of the longest reflux episode (<9.2 min). One patient (1/10, 10 percent) presented a 24-h esophageal pH profile compatible with GER disorder. This data suggest that an association between chronic rhinosinusitis not associated with bronchial asthma and GER disorder may exist in children and adolescents, especially in those with compatible GER disorder symptoms. In these cases, 24-h esophageal pH monitoring should be performed before indicating surgery, since the present data suggest that 10 percent of chronic rhinosinusitis surgeries can be eliminated.


Assuntos
Humanos , Masculino , Feminino , Pré-Escolar , Criança , Asma/complicações , Refluxo Gastroesofágico/etiologia , Rinite/complicações , Sinusite/complicações , Doença Crônica , Refluxo Gastroesofágico/diagnóstico , Concentração de Íons de Hidrogênio , Recidiva
6.
Rev. Hosp. Säo Paulo Esc. Paul. Med ; 1(2): 69-73, Jun. 1989. ilus, tab
Artigo em Inglês | LILACS | ID: lil-188364

RESUMO

The histochemical study of 25 pregnant rats liver submitted to nasal drop instillation of saline and naphazoline at increasing concentrations, at the 19th day pregnancy, showed glycogen decrease and total lipid increase, only at a concentration of 1:1,000 of naphazoline. In this group occured also an increase of fetal liver lipids.


Assuntos
Animais , Feminino , Gravidez , Ratos , Feto/efeitos dos fármacos , Fígado , Nafazolina/farmacologia , Fígado/patologia , Glicogênio/análise , Lipídeos/análise , Fotomicrografia , Ratos Wistar
7.
RBM rev. bras. med ; 41(3): 89-97, passim, 1984.
Artigo em Português | LILACS | ID: lil-20830

Assuntos
Humanos , Sinusite
11.
AMB rev. Assoc. Med. Bras ; 29(11/12): 218-9, 1983.
Artigo em Português | LILACS | ID: lil-17398

RESUMO

Os autores apresentam um estudo bacteriologico em infeccoes sinusais, atraves de material colhido por puncao transmeatica inferior do seio maxiliar. Em 26 pacientes estudados, 27% das culturas foram negativas; 61,5% revelaram a presenca de 1 ou mais germes anaerobios, de forma isolada ou associada com germes anaerobios; e apenas 11,5% apresentaram somente germes anaerobios, unicos ou multiplos


Assuntos
Adolescente , Adulto , Pessoa de Meia-Idade , Humanos , Masculino , Feminino , Infecções Bacterianas , Sinusite
13.
Acta AWHO ; 2(1): 12-8, 1983.
Artigo em Português | LILACS | ID: lil-15164

RESUMO

Vinte e cinco ratas prenhes, divididas em cinco grupos, foram tratadas durante todo o 19o. dia de gestacao, com instilacao de gotas nasais de 4 em 4 horas; o primeiro grupo considerado controle recebeu soro fisiologico e os restantes concentracoes crescentes de adrenalina. Apos 24 horas de tratamento, observou-se alteracao dos niveis de lipemia e de fosfatase acida no plasma, apenas quando foi empregado adrenalina em super dosagens, enquanto os niveis de glicemia mantiveram-se inalterados em todos os grupos


Assuntos
Feminino , Animais , Ratos , Epinefrina , Glucose , Lipídeos , Monoéster Fosfórico Hidrolases , Solução Salina Hipertônica
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