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1.
J Genet Couns ; 32(4): 916-925, 2023 08.
Artigo em Inglês | MEDLINE | ID: mdl-36994658

RESUMO

Disease-specific knowledge allows individuals with sickle cell disease, sickle cell trait, and unaffected family members alike to make informed decisions and support those affected by the condition. The current study assesses how sickle cell knowledge varies by disease status within families affected by sickle cell disease. One hundred seventy-nine participants from 84 families completed an online survey and telephone interview. Generalized linear models, with generalized estimating equations, were fitted to evaluate differences in both item-level responses and total scores on the Sickle Cell Knowledge Scale by sickle cell status. Those with negative or unknown sickle cell status scored significantly lower than those with sickle cell disease or trait, despite being related to someone with sickle cell disease (χ2 (2) = 9.72, p = 0.008). Overall, participants performed poorly on items related to sickle cell trait, with limited understanding of autosomal recessive inheritance patterns. The study's findings suggest a need to move beyond patient-centered approaches to family-centered education efforts that reach those with sickle cell traits and negative or unknown status. Findings point to knowledge gaps related to sickle cell trait and patterns of inheritance, representing key enhancement areas for future sickle cell education efforts.


Assuntos
Anemia Falciforme , Traço Falciforme , Humanos , Traço Falciforme/genética , Conhecimentos, Atitudes e Prática em Saúde , Anemia Falciforme/genética , Inquéritos e Questionários , Escolaridade
2.
J Infect Dis ; 205(2): 280-8, 2012 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-22128315

RESUMO

BACKGROUND: We assessed the impact of 12 years of pneumococcal conjugate vaccine (PCV7) use on pneumococcal nasopharyngeal carriage and serotype-specific invasive disease potential among Native Americans. METHODS: Families were enrolled in a carriage study from 2006 to 2008; nasopharyngeal specimens and risk factor information were collected monthly for 7 visits. Pneumococcal carriage prevalence was compared with that before (1998-2000) and during (2001-2002) PCV7 introduction. We compared invasive disease incidence and carriage prevalence before and after PCV7 introduction to estimate changes in serotype-specific invasive potential. RESULTS: We enrolled 1077 subjects from 302 households. There was an absolute reduction in carriage prevalence of 8.0% (95% confidence interval [CI], 4.5%-11.4%) in children aged <5 years and 3.1% (95% CI, 1.1%-5.1%) in adults. In children aged <5 years, vaccine-serotype carriage prevalence decreased by 22.8% (95% CI, 20.1%-25.3%), and nonvaccine serotype (NVT) increased by 15.9% (95% CI, 12.4%-19.3%). No significant change was detected in serotype-specific invasive potential after PCV7 introduction. CONCLUSIONS: Pneumococcal carriage prevalence decreased in all ages since PCV7 introduction; vaccine-serotype carriage has been nearly eliminated, whereas the prevalence of NVT carriage has increased. The increase in the NVT invasive disease rate seems to be proportional to the increase in colonization prevalence.


Assuntos
Portador Sadio/epidemiologia , Indígenas Norte-Americanos , Vacinas Pneumocócicas , Pneumonia Pneumocócica/epidemiologia , Streptococcus pneumoniae , Vacinação , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Distribuição de Qui-Quadrado , Criança , Pré-Escolar , Intervalos de Confiança , Feminino , Humanos , Incidência , Masculino , Pessoa de Meia-Idade , Nasofaringe/microbiologia , Pneumonia Pneumocócica/patologia , Pneumonia Pneumocócica/prevenção & controle , Prevalência , Fatores de Risco , Sorotipagem , Adulto Jovem
3.
Clin Infect Dis ; 51(11): 1258-65, 2010 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-21034194

RESUMO

BACKGROUND: A second-generation 13-valent pneumococcal conjugate vaccine, PCV13, was recently licensed. Although PCV13 includes serotype 6A, the usefulness of that antigen may be limited by the emergence of a new serotype, 6C, which was identified among isolates initially characterized (Quellung reaction) as serotype 6A. The epidemiology of serotype 6C prior to and after 7-valent PCV (PCV7) introduction is incompletely understood. METHODS: We analyzed conventionally serotyped 6A (CS6A) pneumococci from invasive disease case patients of all ages and carriage isolates from children and adults obtained in population-based studies among Navajo and White Mountain Apache communities during 1994-2009. Samples were tested by triplex polymerase chain reaction to resolve serotypes 6C and 6A. RESULTS: A total of 74 invasive CS6A episodes occurred. All were retyped by polymerase chain reaction; 40 (54.1%) were serotype 6C. The mean annual incidence of serotype 6C invasive disease was 0.3 (95% confidence interval, 0.03-0.9), 0.7 (95% confidence interval, 0.2-1.3), and 1.5 (95% confidence interval, 1.0-2.1) cases per 100,000 population in the years prior to the PCV7 efficacy trial, during the time the PCV7 trial was conducted, and following PCV7 introduction and routine use, respectively (P = .01). In the routine vaccination era, 76% of invasive CS6As were serotype 6C; nearly all cases occurred in adults. The proportion of serotype 6C among CS6A carriage isolates increased from 42% to 61% to 94% in the prevaccine, early vaccine, and routine vaccination eras, respectively. CONCLUSION: In the PCV7 routine use era, virtually all serogroup 6 invasive pneumococcal disease and carriage strains among Navajo and White Mountain Apache communities are 6C. Monitoring and evaluation of this and other emerging serotypes among invasive disease and carriage isolates is warranted.


Assuntos
Portador Sadio/epidemiologia , Portador Sadio/prevenção & controle , Infecções Pneumocócicas/epidemiologia , Infecções Pneumocócicas/prevenção & controle , Vacinas Pneumocócicas/imunologia , Streptococcus pneumoniae/classificação , Streptococcus pneumoniae/isolamento & purificação , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Técnicas de Tipagem Bacteriana , Portador Sadio/microbiologia , Criança , Pré-Escolar , DNA Bacteriano/genética , Etnicidade , Feminino , Humanos , Incidência , Lactente , Recém-Nascido , Masculino , Pessoa de Meia-Idade , Infecções Pneumocócicas/microbiologia , Reação em Cadeia da Polimerase/métodos , Sorotipagem , Streptococcus pneumoniae/genética , Streptococcus pneumoniae/imunologia , Adulto Jovem
4.
J Public Health Manag Pract ; 14(1): 56-61, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18091041

RESUMO

OBJECTIVES: Disease surveillance by clinicians is critical to public health activities, yet studies have demonstrated significant underreporting of reportable diseases by clinicians. We sought to determine whether an intervention utilizing electronic media increases public health reporting by clinicians. METHODS: A nonrandomized, controlled design with 24-week baseline and intervention outcome periods was used. Five intervention hospitals in the county of Philadelphia received a three-component intervention that included e-mail memoranda, a Web site, and a handheld computer program. Intervention components provided education and information to assist with reporting. Control hospitals comprised all remaining hospitals in the county. RESULTS: E-mails were sent to more than 16500 clinicians and administrative personnel at five hospitals on each of three occasions. The Web site received 866 visits, and the handheld computer program was downloaded 130 times. Intervention hospitals had a mean increase of 5.6 reports, whereas control hospitals had a mean decrease of 3.0 reports (P = .02). CONCLUSIONS: The electronic information-based intervention led to a significant increase in clinician reporting of reportable diseases. Considering the ease and low cost of implementing such programs, they are an attractive method for increasing clinician reporting of public health conditions.


Assuntos
Notificação de Doenças/normas , Administradores Hospitalares/educação , Internet/estatística & dados numéricos , Corpo Clínico Hospitalar/educação , Vigilância da População/métodos , Informática em Saúde Pública , Computadores de Mão/estatística & dados numéricos , Notificação de Doenças/estatística & dados numéricos , Correio Eletrônico/estatística & dados numéricos , Fidelidade a Diretrizes , Humanos , Governo Local , Philadelphia , Avaliação de Programas e Projetos de Saúde , Software
5.
Pediatr Neurol ; 31(5): 345-8, 2004 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-15519116

RESUMO

Attention deficit hyperactivity disorder is a prevalent disorder characterized by hyperactivity, impulsivity, and attentional dysfunction. It is familial and heritable. Its pathophysiology is thought to involve an abnormality of the brain's dopaminergic neurotransmitter system. Recent work has identified a distinct polymorphism of the dopamine D4 receptor gene in normal people with a behavioral temperament profile characterized by features of "novelty seeking" which include impulsive and exploratory behaviors. These personality traits are also characteristic of children with attention deficit hyperactivity disorder, especially the hyperactive-impulsive type. This study investigated the relationship between dopamine D4 receptor gene polymorphism, temperament categories, and attention deficit hyperactivity disorder in 81 children with the disorder and 24 control subjects. There was no significant association between dopamine D4 receptor gene alleles, Novelty Seeking traits, and the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition diagnosis of attention deficit hyperactivity disorder--Hyperactive impulsive type or Inattentive type.


Assuntos
Transtorno do Deficit de Atenção com Hiperatividade/genética , Comportamento Exploratório , Polimorfismo Genético , Receptores de Dopamina D2/genética , Adolescente , Comportamento do Adolescente , Alelos , Transtorno do Deficit de Atenção com Hiperatividade/psicologia , Criança , Comportamento Infantil , Feminino , Humanos , Masculino , Receptores de Dopamina D4 , Sequências Repetitivas de Ácido Nucleico
6.
J Clin Microbiol ; 42(11): 4974-6, 2004 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-15528682

RESUMO

Several studies have shown that nasopharyngeal sampling is more sensitive than oropharyngeal sampling for the detection of pneumococcal carriage in children. The data for adults are limited and conflicting. This study was part of a larger study of pneumococcal carriage on the Navajo and White Mountain Apache Reservation following a clinical trial of a seven-valent pneumococcal conjugate vaccine. Persons aged 18 years and older living in households with children enrolled in the vaccine trial were eligible. We collected both nasopharyngeal and oropharyngeal specimens by passing a flexible calcium alginate wire swab either nasally to the posterior nasopharynx or orally to the posterior oropharynx. Swabs were placed in skim milk-tryptone-glucose-glycerin medium and frozen at -70 degrees C. Pneumococcal isolation was performed by standard techniques. Analyses were based on specimens collected from 1,994 adults living in 1,054 households. Nasopharyngeal specimens (11.1%; 95% confidence interval [CI], 9.8 and 12.6%) were significantly more likely to grow pneumococci than were oropharyngeal specimens (5.8%; 95% CI, 4.8 to 6.9%) (P < 0.0001). Few persons had pneumococcal growth from both specimens (1.7%). Therefore, both tests together were more likely to identify pneumococcal carriage (15.2%; 95% CI, 13.7 to 16.9%) than either test alone. Although we found that nasopharyngeal sampling was more sensitive than oropharyngeal sampling, nasopharyngeal sampling alone would have underestimated the prevalence of pneumococcal carriage in this adult population. Sampling both sites may give more accurate results than sampling either site alone in studies of pneumococcal carriage in adults.


Assuntos
Portador Sadio/microbiologia , Nasofaringe/microbiologia , Orofaringe/microbiologia , Infecções Pneumocócicas/microbiologia , Manejo de Espécimes/métodos , Streptococcus pneumoniae/isolamento & purificação , Adulto , Feminino , Humanos , Masculino
7.
J Clin Microbiol ; 41(11): 5288-90, 2003 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-14605186

RESUMO

We evaluated the Strep B optical immunoassay (OIA; ThermoBiostar, Inc.) for detecting light and heavy group B streptococcus colonization in 1,306 pregnant women. The women were examined at 20 to 32 weeks gestation and were from six countries. Compared to culture, the sensitivity and specificity of OIA were 13.3 and 98.4%, respectively, for light colonization and 41.5 and 97.7%, respectively, for heavy colonization.


Assuntos
Complicações Infecciosas na Gravidez/diagnóstico , Infecções Estreptocócicas/epidemiologia , Streptococcus agalactiae/isolamento & purificação , Feminino , Humanos , Imunoensaio/métodos , Irlanda/epidemiologia , Mianmar/epidemiologia , Philadelphia/epidemiologia , Filipinas/epidemiologia , Gravidez , Complicações Infecciosas na Gravidez/epidemiologia , Prevalência , Infecções Estreptocócicas/diagnóstico , Zimbábue/epidemiologia
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