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1.
J. pediatr. (Rio J.) ; 99(supl.1): S1-S3, Mar.-Apr. 2023.
Article in English | LILACS-Express | LILACS | ID: biblio-1430722
2.
Braz. j. infect. dis ; 27(2): 102746, 2023. tab
Article in English | LILACS-Express | LILACS | ID: biblio-1439688

ABSTRACT

ABSTRACT Background: Chronic conditions increase the risk of invasive pneumococcal diseases (IPD). Pneumococcal vaccination remarkably reduced IPD morbimortality in vulnerable populations. In Brazil, pneumococcal vaccines are included in the National Immunization Program (PNI): PCV10 for < 2 years-old, and PPV23 for high risk-patients aged ≥ 2 years and institutionalized ≥ 60 years. PCV13 is available in private clinics and recommended in the PNI for individuals with certain underlying conditions. Methods: A retrospective study was performed using clinical data from all inpatients from five hospitals with IPD from 2016 to 2018 and the corresponding data on serotype and antimicrobial-non-susceptibility of pneumococcus. Vaccine-serotype-coverage was estimated. Patients were classified according to presence of comorbidities: healthy, without comorbidities; at-risk, included immunocompetent persons with specific medical conditions; high-risk, with immunocompromising conditions and others Results: 406 IPD cases were evaluated. Among 324 cases with information on medical conditions, children < 5 years were mostly healthy (55.9%), while presence of comorbidity prevailed in adults ≥ 18 years old (> 82.0%). Presence of ≥1 risk condition was reported in ≥ 34.8% of adults. High-risk conditions were more frequent than at-risk in all age groups. Among high-risk comorbidity (n = 211), cancer (28%), HIV/AIDS (25.7%) and hematological diseases (24.5%) were the most frequent. Among at-risk conditions (n = 89), asthma (16.5%) and diabetes (8.1%) were the most frequent. Among 404 isolates, 42.9% belonged to five serotypes: 19A (14.1%), 3 (8.7%), 6C (7.7%), 4 and 8 (6.2% each); 19A and 6C expressed antimicrobial-non-susceptibility. The vaccine-serotype-coverage was: PCV10, 19.1%, PCV13, 43.8%; PCV15, 47.8%; PCV20, 62.9%; PCV21, 65.8%, and PPV23, 67.3%. Information on hospital outcome was available for 283 patients, of which 28.6% died. Mortality was 54.2% for those with meningitis. Conclusion: Vaccine with expanded valence of serotypes is necessary to offer broad prevention to IPD. The present data contribute to pneumococcal vaccination public health policies for vulnerable patients, mainly those with comorbidity and the elderly.

3.
Braz J Infect Dis ; 27(6)2023.
Article in English | LILACS, CONASS, ColecionaSUS, SES-SP, SESSP-IALPROD, SES-SP | ID: biblio-1417653

ABSTRACT

Background: Chronic conditions increase the risk of invasive pneumococcal diseases (IPD). Pneumococcal vaccination remarkably reduced IPD morbimortality in vulnerable populations. In Brazil, pneumococcal vaccines are included in the National Immunization Program (PNI): PCV10 for < 2 years-old, and PPV23 for high risk-patients aged ≥ 2 years and institutionalized ≥ 60 years. PCV13 is available in private clinics and recommended in the PNI for individuals with certain underlying conditions. Methods: A retrospective study was performed using clinical data from all inpatients from five hospitals with IPD from 2016 to 2018 and the corresponding data on serotype and antimicrobial-non-susceptibility of pneumococcus. Vaccine-serotype-coverage was estimated. Patients were classified according to presence of comorbidities: healthy, without comorbidities; at-risk, included immunocompetent persons with specific medical conditions; high-risk, with immunocompromising conditions and others RESULTS: 406 IPD cases were evaluated. Among 324 cases with information on medical conditions, children < 5 years were mostly healthy (55.9%), while presence of comorbidity prevailed in adults ≥ 18 years old (> 82.0%). Presence of ≥1 risk condition was reported in ≥ 34.8% of adults. High-risk conditions were more frequent than at-risk in all age groups. Among high-risk comorbidity (n = 211), cancer (28%), HIV/AIDS (25.7%) and hematological diseases (24.5%) were the most frequent. Among at-risk conditions (n = 89), asthma (16.5%) and diabetes (8.1%) were the most frequent. Among 404 isolates, 42.9% belonged to five serotypes: 19A (14.1%), 3 (8.7%), 6C (7.7%), 4 and 8 (6.2% each); 19A and 6C expressed antimicrobial-non-susceptibility. The vaccine-serotype-coverage was: PCV10, 19.1%, PCV13, 43.8%; PCV15, 47.8%; PCV20, 62.9%; PCV21, 65.8%, and PPV23, 67.3%. Information on hospital outcome was available for 283 patients, of which 28.6% died. Mortality was 54.2% for those with meningitis. Conclusion: Vaccine with expanded valence of serotypes is necessary to offer broad prevention to IPD. The present data contribute to pneumococcal vaccination public health policies for vulnerable patients, mainly those with comorbidity and the elderly. Keywords: Antimicrobial resistance; Chronic diseases; Comorbidity; Invasive pneumococcal diseases; Pneumococcal conjugate vaccine; Pneumococcal serotypes; Pneumococcal vaccine.


Subject(s)
Asthma , Streptococcus pneumoniae , HIV , Vaccines, Conjugate , Meningitis
4.
Epidemiol. serv. saúde ; 30(4): e2021267, 2021. tab, graf
Article in English, Portuguese | LILACS | ID: biblio-1346032

ABSTRACT

Objetivo: Caracterizar o perfil clínico-epidemiológico da síndrome inflamatória multissistêmica pediátrica temporalmente associada à COVID-19 (SIM-P) e identificar fatores associados aos óbitos de SIM-P no Brasil, 2020. Métodos: Estudo seccional, utilizando dados do monitoramento nacional da SIM-P. Empregou-se regressão logística para estimar razões de chances (OR, odds ratios ) brutas e ajustadas. Resultados: Os casos (n=652) apresentaram mediana de idade de 5 anos; 57,1% eram do sexo masculino e 52,0% de raça/cor da pele parda; 6,4% evoluíram a óbito. A chance de óbito foi significativamente maior nos que apresentaram saturação de O2<95% (ORa=4,35 - IC95% 1,69;11,20) e resultado alterado de ureia (ORa=5,18 - IC95% 1,91;14,04); e menor na ausência de manchas vermelhas pelo corpo (ORa=0,23 - IC95% 0,09;0,62), com uso de anticoagulantes (ORa=0,32 - IC95% 0,12;0,89) e imunoglobulinas (ORa=0,38 - IC95% 0,15;1,01). Conclusão: A letalidade foi maior entre casos que apresentaram saturação de O2<95% e ureia alterada; e menor nos que apresentaram manchas vermelhas, usaram imunoglobulinas e anticoagulantes.


Objetivo: Caracterizar el perfil clínico-epidemiológico de los casos por síndrome inflamatorio multisistémico pediátrico asociado temporalmente a la COVID-19 (SIM-PedS) e identificar factores asociados a los óbitos por SIM-PedS en Brasil, 2020. Métodos: Estudio transversal basado en datos del monitoreo nacional de la SIM-PedS, Brasil, 2020. Se utilizó regresión logística para estimar razones de probabilidades brutas y ajustadas (OR, odds ratio). Resultados: Los casos (n=652) presentaron edad mediana de 5 años, 57,1% eran hombres, 52,0% de raza/color pardo y 6,4% falleció. La probabilidad de muerte fue significativamente mayor entre aquellos con saturación de O2<95% (ORa=4,35 - IC95%1,69;11,20) y resultado alterado de urea (ORa=5,18 - IC95% 1,91;14,04); menor en ausencia de manchas rojas como erupción (ORa=0,23 - IC95% 0,09;0,62), con uso de anticoagulantes (ORa=0,32 - IC95% 0,12;0,89) e inmunoglobulinas (ORa=0,38 - IC95%0,15;1,01). Conclusión: La letalidad fue mayor entre casos que presentaron saturación de O2<95% y urea alterada, y menor entre aquellos con manchas rojas, que usaron inmunoglobulinas y anticoagulantes.


Objective: To characterize the clinical-epidemiological profile of multisystem inflammatory syndrome in children temporally associated with COVID-19 (MIS-C), and to identify factors associated with MIS-C deaths in Brazil, 2020. Methods: This was a cross-sectional study, using national MIS-C monitoring data. Logistical regression was performed to estimate crude and adjusted odds ratios (OR). Results: Median case (n=652) age was 5 years, 57.1% were male, 52.0% were of brown race/skin color and 6.4% died. Likelihood of death was greater among those who presented O2 saturation <95% (ORa=4.35 - 95%CI 1.69;11.20) and altered urea results (ORa=5.18 - 95%CI 1.91;14.04); likelihood of death was lower when red skin blotches were not present (ORa=0.23 - 95%CI 0.09;0.62), when anticoagulants were used (ORa=0.32 - 95%CI 0.12;0.89) and when immunoglobulins were used (ORa=0.38 - 95%CI 0.15;1.01). Conclusion: Fatality ratios were higher among cases that presented O2 saturation <95% and altered urea results. Fatality ratios were lower among those with red skin blotches, and those who used immunoglobulins and anticoagulants.


Subject(s)
Humans , Male , Female , Child, Preschool , Child , Cross-Sectional Studies , Systemic Inflammatory Response Syndrome/epidemiology , COVID-19/epidemiology , Brazil/epidemiology , Pandemics , Epidemiological Monitoring
5.
REME rev. min. enferm ; 25: e1381, 2021. graf
Article in English, Portuguese | LILACS, BDENF | ID: biblio-1340539

ABSTRACT

RESUMO Objetivo: analisar e descrever as fake news e a infodemia divulgadas no Brasil em tempos de pandemia por COVID-19. Materiais e métodos: estudo exploratório descritivo com abordagem quantitativa, realizado a partir do levantamento de dados e de informações relacionadas à pandemia da COVID-19 na plataforma "Saúde sem Fake News". O acesso à plataforma foi realizado por meio dos canais oficiais do Ministério da Saúde e a busca totalizou 85 registros que foram encaminhados, analisados e divulgados, visando à comprovação ou não da veracidade dos dados. A análise e síntese dos resultados foram realizadas de forma descritiva. Resultados: verificou-se a difusão e veiculação de informações em redes e mídias sociais. Dentre os registros identificados, 94,1% foram classificados como fake news, envolvendo diferentes categorias, como medidas de prevenção, métodos terapêuticos e cura, que se destacaram por predominar nesta investigação. Apesar da maior concentração de informações no mês de fevereiro, a redução do número de publicações foi verificada diante do progresso da doença no país. Outros desfechos avaliados envolveram a origem, os mecanismos de transmissão e a relação com outras condições clínicas. Conclusão: diante do cenário incerto, as fake news e a infodemia constituem uma segunda pandemia vivenciada no cenário brasileiro, capaz de impactar negativamente nas medidas de prevenção e controle da COVID-19. Diante disso, destaca-se a necessidade de investimentos em recursos tecnológicos para proteger a sociedade da disseminação de informações falsas, assim como para a conscientização popular em buscar esclarecimentos oficiais, antes de compartilhar notícias sem verificar a veracidade das notícias.


RESUMEN Objetivo: analizar y describir noticias falsas e infodemias difundidas en Brasil en tiempos de pandemia por Covid-19. Materiales y métodos: estudio exploratorio descriptivo con enfoque cuantitativo, realizado a partir de la recolección de datos e información relacionada con la pandemia Covid-19 en la plataforma "Saúde sem Fake News". El acceso a la plataforma se realizó a través de los canales oficiales del Ministerio de Salud y la búsqueda totalizó 85 registros que fueron remitidos, analizados y difundidos, con el objetivo de acreditar o no la veracidad de los datos. El análisis y síntesis de los resultados se realizó de forma descriptiva. Resultados: se verificaron difusión y transmisión de información en medios de comunicación sociales. Entre los registros identificados, el 94,1% fueron clasificados como noticias falsas, involucrando diferentes categorías como medidas de prevención, métodos terapéuticos y curación, que se destacaron por predominar en esta investigación. A pesar de la mayor concentración de información en febrero, la reducción en el número de publicaciones se verificó a la luz del avance de la enfermedad en el país. Otros resultados evaluados involucraron origen, mecanismos de transmisión y relación con otras condiciones clínicas. Conclusión: ante el escenario incierto, las noticias falsas y la infodemia constituyen una segunda pandemia vivida en el escenario brasileño, capaz de impactar negativamente las medidas de prevención y control de Covid-19. Por tanto, es necesaria la inversión en recursos tecnológicos para proteger a la sociedad de la difusión de información falsa, así como la concienciación popular en la búsqueda de aclaraciones oficiales, antes de compartir una noticia sin verificar la veracidad de la noticia.


ABSTRACT Objective: to analyze and describe fake news and infodemic disseminated in Brazil in times of pandemic caused by COVID-19. Materials and methods: descriptive exploratory study with a quantitative approach, based on the collection of data and information related to the COVID-19 pandemic on the "Saúde sem Fake News" platform. Access to the platform was carried out through the official channels of the Ministry of Health and the search totaled 85 records that were forwarded, analyzed, and disseminated, with a view to proving or not the veracity of the data. The analysis and synthesis of the results were carried out in a descriptive way. Results: there was the dissemination and dissemination of information on social networks and media. Among the identified records, 94.1% were classified as fake news, involving different categories, such as prevention measures, therapeutic methods, and cure, which stood out for predominating in this investigation. Despite the greater concentration of information in February, the reduction in the number of publications was verified due to the progress of the disease in the country. Other evaluated outcomes involved the origin, transmission mechanisms and relationship with other clinical conditions. Conclusion: in view of the uncertain scenario, fake news and infodemia constitute a second pandemic experienced in the Brazilian scenario, capable of negatively impacting COVID-19 prevention and control measures. Therefore, there is a need for investments in technological resources to protect society from the dissemination of false information, as well as for popular awareness in seeking official clarification, before sharing news without verifying the veracity of the news.


Subject(s)
Humans , Information Dissemination , Social Networking , Social Media , COVID-19 , Persuasive Communication , Pandemics , Internet Use/ethics
6.
Rev. Soc. Bras. Med. Trop ; 54: e03832021, 2021. tab, graf
Article in English | LILACS | ID: biblio-1347098

ABSTRACT

Abstract In this study, we report the occurrence of multisystemic inflammatory syndrome among 64 children (2 deaths) with recent severe acute respiratory syndrome-related coronavirus 2 (SARS-COV-2) infections in the northeast region of Brazil. The major clinical symptoms and signs reported were exanthema (60.9%), abdominal pain (56.3%), nausea and vomiting (46.9%), diarrhea (37.5%), and dyspnea (37.5%). Laboratory findings revealed that the levels of C-reactive protein (75.0%), hemoglobin (51.6%), D-dimer (48.4%), lymphocytes (43.8%), LDH (45.3%), AST (42.2%), ALT (51.6%), and ferritin (48.4%) were above the reference values for a given age and gender. The clinical findings were similar to those observed in Kawasaki disease, although it represents a separate entity, emphasizing the need for proactive surveillance and early treatment.


Subject(s)
Humans , Child , COVID-19 , Mucocutaneous Lymph Node Syndrome/epidemiology , Brazil/epidemiology , Pandemics , SARS-CoV-2
8.
J. pediatr. (Rio J.) ; 96(2): 233-239, Mar.-Apr. 2020. tab, graf
Article in English | LILACS, ColecionaSUS, SES-SP | ID: biblio-1135018

ABSTRACT

Abstract Objective: Respiratory syncytial virus is a pathogen frequently involved in nosocomial outbreaks. Although several studies have reported nosocomial outbreaks in neonatal intensive care units, molecular epidemiology data are scarce. Here, the authors describe two consecutive respiratory syncytial virus outbreaks caused by genotypes ON-1 and NA-2 in a neonatal intensive care unit in São Paulo, Brazil. Methods: A prospective search for respiratory syncytial virus was performed after diagnosing the index case and four other symptomatic newborns in the neonatal intensive care unit. Nasopharyngeal aspirate samples of all patients in the neonatal intensive care unit were tested for 17 respiratory viruses using real-time reverse transcriptase polymerase chain reaction. Genotyping was performed using nucleotide sequencing. Results: From May to August 2013, two different outbreaks were detected in the neonatal intensive care unit. A total of 20 infants were infected with respiratory syncytial virus-A (ten and 14 with ON-1 and NA-2 genotypes, respectively). The mean age of the infants was 10 days, mean birth weight was 1,961 g, and the mean gestational age was 33 weeks. Risk factors (heart disease, lung disease, and prematurity) were present in 80% and 85.7% of infants in the ON-1 and NA-2 groups, respectively. In total, 45.8% of infants were asymptomatic and 20.8% required mechanical ventilation. Coinfections were not detected during the outbreaks. Conclusions: Infants in a neonatal intensive care unit who develop abrupt respiratory symptoms should be tested for respiratory viruses, especially respiratory syncytial virus. Even in the absence of severe symptoms, respiratory syncytial virus detection can prevent nosocomial transmission through infection control measures. A better understanding of respiratory syncytial virus molecular epidemiology is essential for developing new vaccines and antiviral drugs against respiratory syncytial virus.


Resumo Objetivo O vírus sincicial respiratório é um patógeno frequentemente envolvido em surtos nosocomiais. Embora vários estudos tenham relatado tais surtos em unidades de terapia intensiva neonatal, os dados epidemiológicos moleculares são escassos. Neste artigo, descrevemos dois surtos consecutivos de vírus sincicial respiratório causados pelos genótipos ON-1 e NA-2 em uma unidade de terapia intensiva neonatal em São Paulo, Brasil. Métodos Uma busca prospectiva por vírus sincicial respiratório foi realizada após o diagnóstico do caso índice e outros quatro recém-nascidos sintomáticos na unidade de terapia intensiva neonatal. Amostras de aspirado nasofaríngeo de todos os pacientes da unidade de terapia intensiva neonatal foram testadas para 17 vírus respiratórios com reação em cadeia da polimerase via transcriptase reversa em tempo real. A genotipagem realizada utilizando sequenciamento de nucleotídeos. Resultados De maio a agosto de 2013, foram detectados dois surtos diferentes na unidade de terapia intensiva neonatal. Vinte e quatro crianças foram infectadas com vírus sincicial respiratório-A (10 e 14 com os genótipos ON-1 e NA-2, respectivamente). A média da idade dos lactentes era de 10 dias, o peso médio ao nascer foi de 1961 g e a idade gestacional média de 33 semanas. Fatores de risco (doença cardíaca, doença pulmonar e prematuridade) estavam presentes em 80% e 85,7% dos bebês nos grupos ON-1 e NA-2, respectivamente. No total, 45,8% dos lactentes eram assintomáticos e 20,8% necessitaram de ventilação mecânica. Não foram detectadas coinfecções durante os surtos. Conclusões Bebês em unidade de terapia intensiva neonatal que desenvolvem sintomas respiratórios abruptos devem ser testados para vírus respiratórios, especialmente o vírus sincicial respiratório. Mesmo na ausência de sintomas graves, a detecção de vírus sincicial respiratório pode prevenir a transmissão nosocomial através de medidas de controle de infecção. Um melhor entendimento da epidemiologia molecular do vírus sincicial respiratório é essencial para o desenvolvimento de novas vacinas e drogas antivirais contra o vírus sincicial respiratório.


Subject(s)
Humans , Infant, Newborn , Intensive Care Units, Neonatal , Cross Infection , Brazil , Disease Outbreaks , Prospective Studies , Respiratory Syncytial Virus Infections , Genotype
9.
Rev. Soc. Bras. Med. Trop ; 53: e20180046, 2020. graf
Article in English | LILACS | ID: biblio-1057293

ABSTRACT

Abstract Hepatopulmonary hydatidosis in young children is a rare and atypical presentation of Echinococcus granulosus infection. We report the first case of cystic echinococcosis caused by a microvariant of E. granulosus sensu stricto. Chemotherapy and systemic corticoids were administered before curative surgery was performed. Recurrence was not observed for more than 24 months of follow-up.


Subject(s)
Humans , Animals , Female , Albendazole/administration & dosage , Echinococcus granulosus/isolation & purification , Echinococcosis, Hepatic/drug therapy , Echinococcosis, Pulmonary/diagnostic imaging , Thoracoscopy , Tomography, X-Ray Computed , Follow-Up Studies , Treatment Outcome , Echinococcosis, Hepatic/therapy , Echinococcosis, Pulmonary/therapy
10.
J. pediatr. (Rio J.) ; 95(supl.1): S95-S101, 2019.
Article in English | LILACS | ID: biblio-1002484

ABSTRACT

Abstract Objective: Weight and height growth impairment is one of the most frequent manifestations in HIV-infected children and may be the first sign of disease, being considered a marker of disease progression and an independent risk factor for death. The aim of this review is to evaluate the influence of antiretroviral therapy on the growth pattern of children and adolescents living with HIV/AIDS. Source of data: A non-systematic review was carried out in the PubMed database, with the terms "HIV", "Weight and height growth", "ART" and "children". The most relevant publications were selected. Data Synthesis: Antiretroviral therapy has significantly reduced morbidity and mortality in HIV-infected children and is clearly associated with recovery of weight and height-for-age Z-scores, especially when started early, in the asymptomatic child still without weight-height impairment. Therapeutic strategies involving the GH/IGF-1 axis, especially for children with growth impairment, are still being studied. Conclusions: HIV-infected children show early weight-height impairment; antiretroviral therapy improves the anthropometric profile of these children.


Resumo Objetivo: O acometimento do desenvolvimento pondero-estatural é uma das manifestações mais frequentes nas crianças infectadas pelo HIV e pode ser o primeiro sinal de doença, é considerado um marcador de progressão para doença e um fator de risco independente para morte. O objetivo desta revisão é avaliar a influência da terapia antirretroviral no padrão de crescimento em crianças e adolescentes vivendo com HIV/Aids. Fonte dos dados: Foi feita uma revisão não sistemática na base de dados PubMed, com os termos "HIV", "desenvolvimento pondero estatural", "TARV" e "crianças". Foram selecionadas as publicações mais relevantes. Síntese dos dados: A terapia antirretroviral reduziu substancialmente a morbimortalidade em crianças infectadas pelo HIV e está claramente associada à recuperação do escore-z de peso e de estatura para idade, principalmente quando iniciada precocemente, na criança assintomática e ainda sem comprometimento pondero-estatural. Estratégias terapêuticas que envolvem o eixo GH/IGF-1, principalmente para crianças com comprometimento do crescimento, ainda estão em estudo. Conclusões: As crianças infectadas pelo HIV apresentam comprometimento pondero-estatural precoce e a terapia antirretroviral melhora o perfil antropométrico dessas crianças.


Subject(s)
Humans , Male , Female , Infant, Newborn , Infant , Child, Preschool , Child , Adolescent , Body Height/drug effects , HIV Infections/drug therapy , Child Development/physiology , Anti-HIV Agents/therapeutic use , Growth and Development/drug effects , Growth Disorders/physiopathology , HIV Infections/physiopathology , Child Development/drug effects , Disease Progression , Anti-HIV Agents/adverse effects , Antiretroviral Therapy, Highly Active , Growth and Development/physiology , Growth Disorders/chemically induced
12.
Mem. Inst. Oswaldo Cruz ; 110(6): 786-792, Sept. 2015. tab, graf
Article in English | LILACS | ID: lil-763094

ABSTRACT

Group A human rotaviruses (HuRVA) are causative agents of acute gastroenteritis. Six viral structural proteins (VPs) and six nonstructural proteins (NSPs) are produced in RV-infected cells. NSP4 is a diarrhoea-inducing viral enterotoxin and NSP4 gene analysis revealed at least 15 (E1-E15) genotypes. This study analysed the NSP4 genetic diversity of HuRVA G2P[4] strains collected in the state of São Paulo (SP) from 1994 and 2006-2010 using reverse transcription-polymerase chain reaction, sequencing and phylogenetic analysis. Forty (97.6%) G2P[4] strains displayed genotype E2; one strain (2.4%) displayed genotype E1. These results are consistent with the proposed linkage between VP4/VP7 (G2P[4]) and the NSP4 (E2) genotype of HuRVA. NSP4 phylogenetic analysis showed distinct clusters, with grouping of most strains by their genotype and collection year, and most strains from SP were clustered together with strains from other Brazilian states. A deduced amino acid sequence alignment for E2 showed many variations in the C-terminal region, including the VP4-binding domain. Considering the ability of NSP4 to generate host immunity, monitoring NSP4 variations, along with those in the VP4 or VP7 protein, is important for evaluating the circulation and pathogenesis of RV. Finally, the presence of one G2P[4]E1 strain reinforces the idea that new genotype combinations emerge through reassortment and independent segregation.


Subject(s)
Adult , Child , Humans , Antigens, Viral/isolation & purification , Glycoproteins/genetics , RNA, Viral/genetics , Rotavirus/genetics , Toxins, Biological/genetics , Viral Nonstructural Proteins/genetics , Amino Acid Sequence , Base Sequence , Brazil , Feces/virology , Genetic Variation , Genotype , Genetic Linkage/genetics , Immunoenzyme Techniques , Molecular Sequence Data , Phylogeny , Reverse Transcriptase Polymerase Chain Reaction , RNA, Viral/isolation & purification , Rotavirus/classification , Rotavirus/immunology , Sequence Alignment
13.
Braz. j. infect. dis ; 18(3): 300-307, May-June/2014. tab, graf
Article in English | LILACS, SES-SP | ID: lil-712953

ABSTRACT

Management of children with HIV/AIDS is specially challenging. Age-related issues do not allow for direct transposition of adult observations to this population. CXCR4 tropism has been associated with disease progression in adults. The geno2pheno web-base is a friendly tool to predict viral tropism on envelope V3 sequences, generating a false positive rate for a CXCR4 prediction. We evaluated the association of HIV-1 tropism prediction with clinical and laboratory outcome of 73 children with HIV/AIDS in São Paulo, Brazil. The CXCR4 tropism was strongly associated with a lower (nadir) CD4 documented during follow-up (p < 0.0001) and with disease severity (clinical event and/or CD4 below 200 cells/mm3) at the last observation, using commonly applied clinical cutoffs, such as10%FPRclonal (p = 0.001). When variables obtained during follow-up are included, both treatment adherence and viral tropism show a significant association with disease severity. As for viremia suppression, 30% (22/73) were undetectable at the last observation, with only adherence strongly associated with suppression after adjustment. The study brings further support to the notion that antiretroviral treatment adherence is pivotal to management of HIV disease, but suggests that tropism prediction may provide an additional prognostic marker to monitor HIV disease in children.


Subject(s)
Adolescent , Child , Child, Preschool , Female , Humans , Infant , Male , HIV-1 , Disease Progression , HIV Infections/virology , /physiology , Viral Tropism/physiology , Anti-Retroviral Agents/therapeutic use , Genotype , HIV Infections/drug therapy , HIV Infections/physiopathology , RNA, Viral/blood , Viral Load
15.
J. pediatr. (Rio J.) ; 88(3): 195-202, maio-jun. 2012. ilus, tab
Article in Portuguese | LILACS | ID: lil-640772

ABSTRACT

OBJETIVOS: Analisar a epidemiologia da doença meningocócica no Brasil e o impacto que as recentes evidências acumuladas com a incorporação das vacinas meningocócicas C conjugadas nos programas de imunização podem ter nas diferentes estratégias de uso dessas vacinas. FONTES DOS DADOS: Revisão nas bases de dados MEDLINE, SciELO e LILACS no período de 2000 a 2011. SÍNTESE DOS DADOS: No Brasil, a doença meningocócica é endêmica, com ocorrência periódica de surtos. Os maiores coeficientes de incidência ocorrem em lactentes, sendo o sorogrupo C responsável pela maioria dos casos, motivando a introdução da vacina meningocócica C conjugada no Programa Nacional de Imunizações, em 2010, para crianças menores de 2 anos. A introdução das vacinas meningocócicas C conjugadas nos programas de imunização na Europa, Canadá e Austrália mostrou-se efetiva, com dramática redução na incidência de doença causada pelo sorogrupo C, não apenas nos vacinados, mas também em não vacinados. A efetividade em longo prazo dessas vacinas mostrou-se dependente de uma combinação de persistência de anticorpos, memória imunológica e proteção indireta. Recentes evidências indicando que a persistência de anticorpos não é duradoura em crianças pequenas imunizadas e que a memória imunológica não é rápida o suficiente para protegê-las contra a doença enfatizam a importância da proteção indireta para manutenção da população protegida. CONCLUSÕES: A rápida queda de títulos de anticorpos em crianças vacinadas nos primeiros anos de vida sugere a necessidade de incorporarmos doses de reforço antes da adolescência, especialmente em locais como o Brasil, onde ainda não contamos com o efeito da proteção indireta da população.


OBJECTIVES: To assess the epidemiology of meningococcal disease (MD) in Brazil and the impact that recent evidence and lessons learned from the introduction of meningococcal C conjugate (MCC) vaccines into immunization programs may have on different strategies of vaccine use. SOURCES: Non-systematic review of the MEDLINE, SciELO and LILACS databases covering the period from 2000 to 2011. SUMMARY OF THE FINDINGS: Meningococcal disease is endemic in Brazil, with periodic occurrence of outbreaks. Most cases are associated with serogroup C and the highest incidence rates are observed in infants, encouraging the introduction of MCC vaccine in the National Immunization Program in 2010 for children under 2 years old. The introduction of MCC vaccines into immunization programs in Europe, Canada and Australia proved to be effective, with dramatic reduction in the incidence of serogroup C meningococcal disease, not only in the vaccinated, but also in the unvaccinated individuals. Long-term effectiveness of MCC vaccines was dependent on a combination of antibody persistence, immunologic memory and herd protection. Recent evidence indicating that antibody persistence is not long-lasting in young immunized children, and that immunologic memory is not fast enough to protect them against the disease, emphasize the importance of herd protection to maintain the population protected. CONCLUSIONS: The rapid decline of antibody titers in children vaccinated in the first years of life suggests the need to incorporate booster doses before adolescence, especially in locations like Brazil, where the immunization program did not incorporate catch-up campaigns including adolescents, lacking the herd immunity effect.


Subject(s)
Humans , Immunization Programs/statistics & numerical data , Meningitis, Meningococcal/epidemiology , Meningitis, Meningococcal/prevention & control , Meningococcal Vaccines/therapeutic use , Neisseria meningitidis, Serogroup C/immunology , Australia , Brazil/epidemiology , Europe , Immunity, Herd , Incidence , North America , Vaccines, Conjugate/therapeutic use
16.
Rev. panam. salud pública ; 26(6): 518-528, dic. 2009. ilus, tab, graf
Article in English | LILACS | ID: lil-536492

ABSTRACT

OBJECTIVE: To compare the costs and benefits of pneumococcal conjugate vaccination compared with no vaccination from the perspectives of the health care system and society. METHODS: Using data from established sources, we estimated the incidence and mortality due to invasive pneumococcal disease, pneumonia, and acute otitis media (AOM) for a hypothetical birth cohort of children from birth to 5 years. RESULTS: A universal pneumococcal conjugate vaccination program was estimated capable of annually avoiding 1 047 cases of invasive disease, 58 226 cases of pneumonia, and 209 862 cases of AOM. When herd immunity effects were considered, the program prevented 1.3 million cases of pneumococcal disease and over 7 000 pneumococcal deaths. At a vaccination cost of R$ 51.12 (US$ 26.35) per dose, vaccination would cost annually R$ 4 289 (US$ 2,211) per disability-adjusted life years averted. This does not take into account herd immunity effects. CONCLUSIONS: At the current vaccine price, conjugate vaccination could be a cost-effective investment compared to other options to control childhood diseases. Further analysis is required to determine whether vaccination at the current price is affordable to Brazil.


OBJETIVO: Comparar los costos y los beneficios de la aplicación de la vacuna conjugada antineumocócica en comparación con la no vacunación, desde las perspectivas del sistema de salud y la sociedad. MÉTODOS: A partir de fuentes reconocidas, se estimaron la incidencia y la mortalidad por enfermedad neumocócica invasora, neumonía y otitis media aguda (OMA) para una cohorte hipotética de niños desde su nacimiento hasta los 5 años. RESULTADOS: Se estimó que un programa de vacunación universal con una vacuna conjugada antineumocócica sería capaz de evitar anualmente 1 047 casos de la enfermedad invasora, 58 226 casos de neumonía y 209 862 casos de OMA. Si se considera el efecto de la inmunidad de grupo, el programa evitaría 1,3 millones de casos de enfermedad y más de 7 000 muertes por infección neumocócica. A R$ 51,12 (US$ 26,35) por dosis, la vacunación costaría anualmente R$ 4 286 (US$ 2,211) por cada año de vida ajustado por discapacidad evitado, sin tomar en cuenta el efecto de la inmunidad de grupo. CONCLUSIONES: En comparación con otras opciones de control de estas enfermedades infantiles y con los precios actuales de la vacuna conjugada, la vacunación antineumocócica podría ser una inversión efectiva en función del costo. Se requieren más estudios para determinar si la vacunación es costeable para Brasil a los precios actuales.


Subject(s)
Humans , Pneumococcal Infections/epidemiology , Pneumococcal Infections/prevention & control , Pneumococcal Vaccines/economics , Brazil , Cost-Benefit Analysis , Incidence , Spouse Abuse , Vaccines, Conjugate
19.
Pediatr. mod ; 43(5): 251-255, set-out. 2007.
Article in Portuguese | LILACS | ID: lil-469184

ABSTRACT

Infecções causadas pelo S. pneumoniae são associadas à elevada morbidade e mortalidade, particularmente em lactentes e crianças pequenas. As vacinas polissacarídicas conjugadas a um complexo protéico demonstraram ser extremamente imunogênicas em lactentes, induzindo imunidade dependente de células T. Uma vacina pneumocócica conjugada heptavalente, usando como carreador protéico para os sete sorotipos o mutante diftérico CRM197, foi licenciada nos Estados Unidos no ano 2000, demonstrando ser segura, induzindo elevados títulos de anticorpos séricos, memória imunológica e ainda reduzindo, entre os vacinados, o estado de portador em nasofaringe dos sorotipos incluídos em sua composição. Neste momento, encontra-se em estágio avançado de desenvolvimento várias vacinas pneumocócicas conjugadas. Com o objetivo precípuo de estabelecer um parâmetro para ser utilizado no licenciamento de novas vacinas pneumocócicas conjugadas candidatas, em função de limitações de ordem ética e prática para realização de estudos de eficácia clínica, e baseando-se nos dados de três grandes estudos controlados, duplo-cegos, de eficácia clínica (dois nos EUA e um na África do Sul) a OMS recomendou, recentemente, a adoção de títulos de anticorpos anticapsulares polissacarídicos da classe IgG, medidos pelo método de ELISA, ³ 0,35 µg/mL, avaliados um mês após o término da imunização primária como sendo a concentração mínima de anticorpos associados à eficácia clínica protetora contra doença pneumocócica invasiva.


Subject(s)
Humans , Child , Pneumococcal Vaccines , Otitis/therapy , Pneumonia/immunology , Pneumonia/therapy , Streptococcus , Vaccines/adverse effects
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