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2.
Emerg Infect Dis ; 23(13)2017 12.
Artigo em Inglês | MEDLINE | ID: mdl-29154748

RESUMO

Response to sudden epidemic infectious disease emergencies can demand intensive and specialized training, as demonstrated in 2014 when Ebola virus disease (EVD) rapidly spread throughout West Africa. The medical community quickly became overwhelmed because of limited staff, supplies, and Ebola treatment units (ETUs). Because a mechanism to rapidly increase trained healthcare workers was needed, the US Centers for Disease Control and Prevention developed and implemented an introductory EVD safety training course to prepare US healthcare workers to work in West Africa ETUs. The goal was to teach principles and practices of safely providing patient care and was delivered through lectures, small-group breakout sessions, and practical exercises. During September 2014-March 2015, a total of 570 participants were trained during 16 course sessions. This course quickly increased the number of clinicians who could provide care in West Africa ETUs, showing the feasibility of rapidly developing and implementing training in response to a public health emergency.


Assuntos
Educação , Pessoal de Saúde , Doença pelo Vírus Ebola/epidemiologia , Doença pelo Vírus Ebola/prevenção & controle , Vigilância em Saúde Pública , Saúde Pública/educação , Alabama/epidemiologia , Humanos , Vigilância em Saúde Pública/métodos
3.
Health Secur ; 15(3): 261-267, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28636446

RESUMO

The International Health Regulations (IHR), an international law under the auspices of the World Health Organization (WHO), mandates that countries notify other countries of "travelers under public health observation." Between November 10, 2014, and July 12, 2015, the US Centers for Disease Control and Prevention (CDC) made 2,374 notifications to the National IHR Focal Points in 114 foreign countries of travelers who were monitored by US health departments because they had been to an Ebola-affected country in West Africa. Given that countries have preidentified focal points as points of contacts for sharing of public health information, notifications could be made by CDC to a trusted public health recipient in another country within 24 hours of receipt of the traveler's information from a US health department. The majority of US health departments used this process, offered by CDC, to notify other countries of travelers intending to leave the United States while being monitored in their jurisdiction.


Assuntos
Centers for Disease Control and Prevention, U.S. , Doença pelo Vírus Ebola/prevenção & controle , Vigilância em Saúde Pública , Viagem , África Ocidental , Monitoramento Epidemiológico , Doença pelo Vírus Ebola/epidemiologia , Humanos , Cooperação Internacional , Internacionalidade , Vigilância de Evento Sentinela , Estados Unidos , Organização Mundial da Saúde
4.
MMWR Morb Mortal Wkly Rep ; 65(47): 1343-1348, 2016 Dec 02.
Artigo em Inglês | MEDLINE | ID: mdl-27906905

RESUMO

Congenital Zika virus infection can cause microcephaly and severe brain abnormalities (1). Congenital Zika syndrome comprises a spectrum of clinical features (2); however, as is the case with most newly recognized teratogens, the earliest documented clinical presentation is expected to be the most severe. Initial descriptions of the effects of in utero Zika virus infection centered prominently on the finding of congenital microcephaly (3). To assess the possibility of clinical presentations that do not include congenital microcephaly, a retrospective assessment of 13 infants from the Brazilian states of Pernambuco and Ceará with normal head size at birth and laboratory evidence of congenital Zika virus infection was conducted. All infants had brain abnormalities on neuroimaging consistent with congenital Zika syndrome, including decreased brain volume, ventriculomegaly, subcortical calcifications, and cortical malformations. The earliest evaluation occurred on the second day of life. Among all infants, head growth was documented to have decelerated as early as 5 months of age, and 11 infants had microcephaly. These findings provide evidence that among infants with prenatal exposure to Zika virus, the absence of microcephaly at birth does not exclude congenital Zika virus infection or the presence of Zika-related brain and other abnormalities. These findings support the recommendation for comprehensive medical and developmental follow-up of infants exposed to Zika virus prenatally. Early neuroimaging might identify brain abnormalities related to congenital Zika infection even among infants with a normal head circumference (4).


Assuntos
Microcefalia/epidemiologia , Infecção por Zika virus/congênito , Infecção por Zika virus/diagnóstico , Zika virus/isolamento & purificação , Brasil/epidemiologia , Feminino , Humanos , Lactente , Recém-Nascido , Masculino , Gravidez , Complicações Infecciosas na Gravidez , Estudos Retrospectivos
5.
Pediatr Infect Dis J ; 35(5): 488-93, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-26766145

RESUMO

BACKGROUND: In 2012, Oregon observed its highest numbers of reported pertussis cases since 1953. The greatest morbidity occurred among infants <6 months of age, with higher rates among Hispanics than non-Hispanics. To explain this disparity, we analyzed pertussis surveillance data. METHODS: An analysis was conducted among infants <6 months of age in the Portland metropolitan area during 2010-2012. Characteristics examined were ethnicity (Hispanic or non-Hispanic), household size (>4 or ≤4 persons), pertussis vaccination status (upto-date or not up-to-date for age), child care center attendance (yes or no), infant birth weight (<2500 or ≥2500 g) and maternal age (<20 or ≥20 years). RESULTS: Eighty-two infants <6 months of age with pertussis were identified. Twenty-eight case-infants (34%) were Hispanic, and 54 (66%) were non-Hispanic. By ethnicity, infants with pertussis were similar in illness confirmation method, sex, age, hospitalization status, vaccination status, child care center attendance, infant birth weight and maternal age. Hispanic infants were more likely than non-Hispanic infants to live in households with >4 persons. Univariate analysis showed Hispanic infants had approximately 2.3 times the risk for pertussis, compared with non-Hispanic infants, and infants living in households >4 persons had approximately 2.4 times the risk for illness, compared with those in households with <4 persons; stratified risk ratios did not differ between Hispanic (2.4; confidence interval: 1.0-5.7]) and non-Hispanic infants (2.0; confidence interval: 1.2-3.5). CONCLUSIONS: A household size of >4 persons is a potential risk factor for pertussis; the magnitude of this risk is similar for Hispanic and non-Hispanic infants.


Assuntos
Hispânico ou Latino , Coqueluche/epidemiologia , Adulto , Feminino , Humanos , Lactente , Recém-Nascido , Masculino , Oregon/epidemiologia , Medição de Risco , Fatores de Risco , População Urbana , Adulto Jovem
6.
MMWR Morb Mortal Wkly Rep ; 64(25): 685-9, 2015 Jul 03.
Artigo em Inglês | MEDLINE | ID: mdl-26135588

RESUMO

On October 27, 2014, CDC released guidance for monitoring and movement of persons with potential Ebola virus disease (Ebola) exposure in the United States. For persons with possible exposure to Ebola, this guidance recommended risk categorization, daily monitoring during the 21-day incubation period, and, for persons in selected risk categories, movement restrictions. The purpose of the guidance was to delineate methods for early identification of symptoms among persons at potential risk for Ebola so that they could be isolated, tested, and if necessary, treated to improve their chance of survival and reduce transmission. Within 7 days, all 50 states and two local jurisdictions (New York City [NYC] and the District of Columbia [DC]) had implemented the guidelines. During November 3, 2014-March 8, 2015, a total of 10,344 persons were monitored for up to 21 days with >99% complete monitoring. This public health response demonstrated the ability of state, territorial, and local health agencies to rapidly implement systems to effectively monitor thousands of persons over a sustained period.


Assuntos
Doença pelo Vírus Ebola/prevenção & controle , Vigilância da População , Doença pelo Vírus Ebola/epidemiologia , Humanos , Medição de Risco , Estados Unidos/epidemiologia
7.
Matern Child Health J ; 14(3): 373-81, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-19252975

RESUMO

OBJECTIVES: Given that approximately half of all pregnancies in the United States are unplanned, the authors sought to understand the relation between pregnancy intention and health behaviors. METHODS: Mothers of live-born infants without major birth defects were interviewed as part of the National Birth Defects Prevention Study. The interview assessed pregnancy intention as well as exposures to vitamins, alcohol, tobacco, illicit drugs, occupational hazards, exogenous heat (e.g., hot tubs and saunas) and caffeine. Crude odds ratios and 95% confidence intervals were calculated and stratified analyses were performed to assess interaction. Multiple logistic regression was used to calculate adjusted odds ratios. RESULTS: Both before and after the diagnosis of pregnancy, women with unintended pregnancies were more likely to use illicit drugs, smoke, be exposed to environmental smoke, and not take folic acid or multivitamins. The degree to which women altered behaviors after they realized they were pregnant was also associated with their pregnancy intention status. For certain behaviors, maternal age or parity altered the association between pregnancy intention and changing behaviors after awareness of pregnancy. CONCLUSION: Pregnancy intention status is a key determinant of pregnancy-related behavior. To improve reproductive outcomes, preconceptional and prenatal programs should consider a woman's desire for pregnancy.


Assuntos
Anormalidades Congênitas/prevenção & controle , Comportamentos Relacionados com a Saúde , Intenção , Testes de Gravidez/psicologia , Gestantes/psicologia , Medicina Reprodutiva , Estudos de Casos e Controles , Anormalidades Congênitas/epidemiologia , Anormalidades Congênitas/etiologia , Feminino , Humanos , Modelos Logísticos , Idade Materna , Exposição Materna/efeitos adversos , Exposição Materna/prevenção & controle , Exposição Materna/estatística & dados numéricos , Paridade , Gravidez , Complicações na Gravidez/epidemiologia , Complicações na Gravidez/psicologia , Gravidez não Planejada/psicologia , Gravidez não Desejada/psicologia , Autocuidado/métodos , Autocuidado/psicologia , Autocuidado/estatística & dados numéricos , Fumar/efeitos adversos , Fumar/epidemiologia , Fumar/psicologia , Transtornos Relacionados ao Uso de Substâncias/complicações , Transtornos Relacionados ao Uso de Substâncias/epidemiologia , Transtornos Relacionados ao Uso de Substâncias/psicologia , Inquéritos e Questionários , Estados Unidos/epidemiologia , Vitaminas/uso terapêutico
8.
Am J Med Genet A ; 140(8): 837-42, 2006 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-16528746

RESUMO

Investigators have reported that certain metabolic disorders (fatty acid oxidation (FAO) disorders and organic acidemias) contribute to unexpected early childhood deaths. We estimated the contribution of these metabolic disorders to a population-based sample of unexpected early childhood deaths. The study population included children less than 3 years of age who died during 1996-2001 and whose deaths were investigated by the Virginia Office of the Chief Medical Examiner (ME). Dried post-mortem blood on filter paper was sent to a reference laboratory for metabolic screening by tandem mass spectrometry. When molecular DNA analysis was available to identify known gene mutations, positive screens were confirmed. If molecular DNA analysis for a suspected disorder was not available, tandem mass spectrometry was performed on newborn blood spots when available. If DNA analysis was not available and newborn blood spots could not be obtained, an independent expert biochemical geneticist confirmed the post-mortem interpretation. We obtained screening results for 793 (88%) of 904 children examined. Eight children had a positive screen for FAO disorders or organic acidemias. One child would not have benefited from identification in the newborn period. However, seven children's outcomes might have been improved had they been identified during the newborn period and effectively treated. Post-mortem metabolic screening may identify a cause of death for about 1% of children who die unexpectedly before 3 years of age, allowing for identification and treatment of affected siblings. Identifying and treating affected children during the newborn period may offer an opportunity to reduce early childhood mortality.


Assuntos
Morte Súbita/epidemiologia , Doenças Metabólicas/diagnóstico , Doenças Metabólicas/mortalidade , Espectrometria de Massas em Tandem , Acil-CoA Desidrogenase/deficiência , Acil-CoA Desidrogenase/genética , Pré-Escolar , Humanos , Lactente , Recém-Nascido , Doenças Metabólicas/genética
9.
J Midwifery Womens Health ; 50(4): 296-300, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-15973266

RESUMO

Afghanistan has one of the highest maternal and perinatal mortality rates in the world. Lack of a health information system presented obstacles to efforts to improve the quality of care and reduce mortality. To rapidly overcome this deficit in a large women's hospital, staff implemented a facility-based maternal and perinatal surveillance system known as "BABIES," which is specially designed for intervention and evaluation in low-resource settings. During a 12-month period, 15,509 deliveries resulted in 28 maternal deaths and a perinatal mortality rate of 56 per 1000 births. When stratified by birth weight and perinatal period of death, fetuses weighing at least 2500 g who died during the antepartum period contributed the most cases of perinatal death. This finding suggests that the greatest reduction in perinatal mortality would be realized by increasing access to high-quality antepartum care. Among fetuses weighing at least 2500 g, 93 deaths occurred during the intrapartum period. These deaths will continue to be monitored to ensure that the chosen interventions are improving intrapartum care for mothers and newborns. Because of its simplicity, flexibility, and ability to identify interventions, BABIES is a valuable tool that enables clinicians and program managers to prioritize resources.


Assuntos
Atenção à Saúde/organização & administração , Maternidades/organização & administração , Vigilância da População/métodos , Desenvolvimento de Programas/métodos , Afeganistão/epidemiologia , Feminino , Maternidades/estatística & dados numéricos , Humanos , Mortalidade Infantil , Recém-Nascido de Baixo Peso , Recém-Nascido , Mortalidade Materna , Avaliação de Processos e Resultados em Cuidados de Saúde/métodos , Gravidez , Complicações na Gravidez/mortalidade , Complicações na Gravidez/prevenção & controle , Avaliação de Programas e Projetos de Saúde
10.
Birth Defects Res A Clin Mol Teratol ; 67(4): 261-7, 2003 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12854661

RESUMO

BACKGROUND: Congenital diaphragmatic hernia affects about 1000 United States infants a year. In most cases, the etiology of this condition is unknown. Treatment strategies have changed in recent years. We sought to calculate the birth prevalence, determine risk factors, examine associated defects, and assess trends in survival. METHODS: We conducted a population-based cohort study of all infants born during 1968-99 whose mothers resided in the five-county metropolitan Atlanta area (n = 1,029,143). Infants with congenital diaphragmatic hernia were identified using the Metropolitan Atlanta Congenital Defects Program. To document vital status, we used data from hospital records, Georgia vital records, and the National Death Index. RESULTS: The birth prevalence of congenital diaphragmatic hernia was 2.4 per 10,000 births. Infants with isolated congenital diaphragmatic hernia were more likely to be premature, macrosomic, and male than their birth cohort. About one-third of affected infants had additional major defects. Of infants with congenital diaphragmatic hernia, 8% had known syndromes, most commonly chromosomal abnormalities. During the study period, the percentage of infants with congenital diaphragmatic hernia who survived to 1 year of age increased from 19% (1968-71) to about 54% (1996-99). During the last 10 years of the study, infants who were of low birth weight, had a syndrome, or were prenatally diagnosed were more likely to die than other infants with congenital diaphragmatic hernia. CONCLUSIONS: Despite new treatments, the death rate from congenital diaphragmatic hernia remains substantial, highlighting the need to identify mechanisms for primary prevention.


Assuntos
Hérnia Diafragmática/mortalidade , Hérnias Diafragmáticas Congênitas , Adulto , Estudos de Coortes , Feminino , Georgia/epidemiologia , Humanos , Recém-Nascido , Masculino , Idade Materna , Triagem Neonatal , Gravidez , Prevalência , Fatores de Risco , Taxa de Sobrevida
11.
Arch Pediatr Adolesc Med ; 157(4): 341-7, 2003 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12695229

RESUMO

BACKGROUND: Infantile cataract is an important cause of childhood visual impairment. Surgery before 6 weeks of age is recommended for optimal visual outcome. Description of the epidemiologic characteristics of cataracts is important for an improved understanding of the condition. OBJECTIVES: To identify at-risk populations and facilitate successful treatment of patients with infantile cataracts. METHODS: Infants with cataracts diagnosed in the first year of life were identified using the Metropolitan Atlanta Congenital Defects Program, a birth defects surveillance program with active methods of case ascertainment, for the years 1968-1998. Several factors were analyzed, including year of birth, sex, race, maternal age, plurality (single vs multiple gestation), gestational age, birth weight, laterality, seasonality, and age at diagnosis. RESULTS: A total of 199 infants with cataracts were identified, for a rate of 2.03 per 10 000 births. In 117 infants (59%), cataracts occurred as an isolated defect; in 43 infants (22%), cataracts occurred as part of a syndrome; and in 39 infants (20%), additional, unrelated, major birth defects were also present. Rates were higher for low-birth-weight infants (those weighing <1500 g; risk ratio [RR], 6.01; 95% confidence interval [CI], 3.83-9.43) and preterm infants (RR, 1.70; 95% CI, 1.21-2.40). Of the cases that occurred as an isolated defect, 38% were diagnosed after 6 weeks. CONCLUSIONS: This population-based study provides 31 years of data from a diverse US population and allows identification of risk factors for infantile cataracts. The finding that a number of infants with cataracts continue to have their conditions diagnosed after 6 weeks of age emphasizes the need for direct ophthalmoscopic examination of the red reflex in the newborn period to facilitate early detection and improve outcomes.


Assuntos
Catarata/congênito , Catarata/epidemiologia , Anormalidades Múltiplas/epidemiologia , Catarata/diagnóstico , Catarata/etiologia , Feminino , Lateralidade Funcional , Georgia/epidemiologia , Humanos , Incidência , Lactente , Recém-Nascido , Masculino , Gravidez , Fatores de Risco , Síndrome
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