985 resultados para Child restraint system


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National Highway Traffic Safety Administration, Washington, D.C.

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National Highway Traffic Safety Administration, Washington, D.C.

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The purpose of this study was to determine the use and misuse of child safety seats among Mexican parents. Data were collected via personal interview and by use of the SAFE KIDS BUCKLE UP Child Safety Seat Checklist Form. This study used a descriptive comparative design. The convenience sample consisted of 63 Mexican mothers with at least one child under the age of four (index child). The findings showed that Mexican parents tend to misuse or not use child safety seats. Most parents were not aware of the misuse, and receiving prior information on the use of child safety seats had no bearing on its correct use. Factors influencing nonuse include lack of finances, driving short distances, leaving child safety seat at home, and being unaware of the Florida child restraint law. Findings of this study have implications for how nurses need to educate mothers on car safety and help reduce childhood injuries.

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This article draws attention to the importance of routinely collected administrative data as an important source for understanding the characteristics of the Northern Ireland child welfare system as it has developed since the Children (Northern Ireland) Order 1995 became its legislative base. The article argues that the availability of such data is a strength of the Northern Ireland child welfare system and urges local politicians, lobbyists, researchers, policy-makers, operational managers, practitioners and service user groups to make more use of them. The main sources of administrative data are identified. Illustration of how these can be used to understand and to ask questions about the system is provided by considering some of the trends since the Children Order was enacted. The “protection” principle of the Children Order provides the focus for the illustration. The statistical trends considered relate to child protection referrals, investigations and registrations and to children and young people looked after under a range of court orders available to ensure their protection and well-being.

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Dozens of countries have enacted mandatory reporting laws in various forms to respond to child abuse and neglect. Other countries including England are currently considering whether to introduce them, and if so in what form. It is important for policymakers, practitioners and researchers to understand these laws’ background, nature and purpose. This chapter outlines the origins and provenance of the first mandatory reporting laws; discusses their nature; describes major developments over time; and identifies some major effects and their consequences. It is shown that the laws are a heterogeneous, organic, flexible mechanism enabling social intervention where otherwise such intervention is severely compromised or impossible. Their primary function is to comprise but one aspect of a multifaceted child welfare system by identifying cases of serious maltreatment which would not otherwise come to light: sexual abuse and severe physical abuse are paradigm examples. The essential role of these laws is therefore primarily a tertiary aspect of a public health model, rather than a purely preventative strategy. Mandatory reporting laws are made by each specific jurisdiction according to its preferred design and function within its socio-political system. There is a spectrum of different approaches from which a jurisdiction can choose: they can apply to a broad or a narrow range of reporter groups, a broad or a narrow range of types of maltreatment, and a broad or a narrow range of instances where abuse or neglect occurs.

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Bone mass acquired during childhood is the primary determinant of adult bone mineral density (BMD) and osteoporosis risk. Bone accrual is subject to genetic influences. Activating and inactivating LRP5 gene mutations elicit extreme bone phenotypes, while more common LRP5 polymorphisms are associated with normal variation of BMD. Our aim was to test the hypothesis that LRP5 gene polymorphisms influence bone mass acquisition during childhood. The association between LRP5 gene polymorphisms and bone size and mineralization was examined in 819 unrelated British Caucasian children (n = 429 boys) aged 9 years. Height, weight, pubertal status (where available), total-body and spinal bone area, bone mineral content (BMC), BMD, and area-adjusted BMC (aBMC) were assessed. Dual-energy X-ray absorptiometry (DXA)-gene associations were assessed by linear regression, with adjustment for age, gender, pubertal status, and body size parameters. There were 140, 79, 12, and 2 girls who achieved Tanner stages I-IV, respectively, and 179 and 32 boys who achieved Tanner stages I and II, respectively. The rs2306862 (N740N) coding polymorphism in exon 10 of the LRP5 gene was associated with spinal BMD and aBMC (each P = 0.01) and total-body BMD and aBMC (P = 0.04 and 0.03, respectively). Adjusting for pubertal stage strengthened associations between this polymorphism and spinal BMD and aBMC (P = 0.01 and 0.002, respectively). Individuals homozygous for the T allele had greater spinal BMD and aBMC scores than those homozygous for the C allele. A dose effect was apparent as the mean spinal BMD and aBMC of heterozygous TC individuals were intermediate between those of their TT and CC counterparts. The N740N polymorphism in exon 10 of LRP5 was associated with spinal BMD and aBMC in pre- and early pubertal children. These results indicate that LRP5 influences volumetric bone density in childhood, possibly through effects on trabecular bone formation.

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Objectives: To describe longitudinal height, weight, and body mass index changes up to 15 years after childhood liver transplantation. Study design: Retrospective chart review of patients who underwent liver transplant from 1985-2004 was performed. Subjects were age <18 years at transplant, survived ≥5 years, with at least 2 recorded measurements, of which one was ≥5 years post-transplant. Measurements were recorded pre-transplant, 1, 5, 10, and 15 years later. Results: Height and weight data were available in 98 and 104 patients, respectively; 47% were age <2 years at transplant; 58% were Australian, and the rest were from Japan. Height recovery continued for at least 10 years to reach the 26th percentile (Z-score -0.67) 15 years after transplant. Australians had better growth recovery and attained 47th percentile (Z-score -0.06) at 15 years. Weight recovery was most marked in the first year and continued for 15 years even in well-nourished children. Growth impaired and malnourished children at transplant exhibited the best growth, but remained significantly shorter and lighter even 15 years later. No effect of sex or age at transplant was noted on height or weight recovery. Post-transplant factors significantly impact growth recovery and likely caused the dichotomous growth recovery between Australian and Japanese children; 9% (9/98) of patients were overweight on body mass index calculations at 10-15 years but none were obese. Conclusions: After liver transplant, children can expect ongoing height and weight recovery for at least 10-15 years. Growth impairment at transplant and post-transplant care significantly impact long-term growth recovery. Copyright © 2013 Mosby Inc. All rights reserved.

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Carers are at the frontline working with children in the care of the child protection system. This paper reports carer's views about key factors influencing the placement trajectories of children and young people living in out-of-home care in Queensland, Australia. The study sample included 21 foster and kinship carers with a minimum two-year experience in the carer role. Study data were from semi-structured telephone interviews in which carers shared their experiences of the factors impacting upon placement stability and placement movement. Carers' responses were analysed thematically. Data analysis yielded an overarching theme regarding placement trajectory: Carer engagement, and its three sub-themes; with the child; with the child protection system; and, with the caring role. Findings suggested that carer engagement and ‘fit’ are complex constructs that play critical influential roles in placement outcomes (stability or movement) for individual children in out-of-home care. It is argued that practice needs to be better grounded in these relational dynamics, and better aligned concerning the power differentials that exist.

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Children s participation has been a subject in the international research since past ten years. This research has explored participation from the standpoint of the UN s Convention of the Rights of the Child and focused mainly on schoolchildren or on the working youth s chances in developing countries to have impact on their own lives (eg. Sinclair, 2004 and Thomas, 2002). In Finland there has been less research about the children s rights while the main focus has been on the customers of the child welfare system. This study examines children s participation in Helsinki metropolitan area via the views and the practices of the personnel of early childhood education. The adopted viewpoint is Shier s level model of participation (2001), in which the children s participation process is building in phases, is observed via the everyday actions of the kindergarten personnel. Attention has been paid on the special characteristics of the Finnish early childhood education. This study was part of VKK-Metro s research project. The inquiry in May 2010 was directed to all working teams in the kindergartens of the Helsinki metropolitan area. Of these 56.59 % (1116 teams) answered. The quantitative data analyzed by principal component analysis gave four principal components, from which three were named after Shier s participation model. The fourth component included variables about rules and power. The level model of participation fit well to assess early childhood education in the Helsinki metropolitan area. The professionalism of the personnel became emphasized in the area of everyday interactions between the personnel and the children. Important aspects of the children s participation are to become heard, to get support in the play and in interaction and to be able to share both power and responsibility with personnel of the early childhood education.

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O presente trabalho se propõe a colocar em análise as relações de três famílias pobres com o Sistema de Garantia de Direitos (SGD), as quais, por fim, tiveram o seu poder familiar destituído, sob a perspectiva da moralização, da disciplina, da vigilância e do controle. As tramas e os caminhos tortuosos, as práticas sociais punitivas e penais, as relações de verdades e os poderes que se exercem e se atualizam, as resistências e os jogos de tensões e forças que se apresentam, tudo isso está posto e descrito nas linhas desta pesquisa, à luz de autores clássicos como Foucault (principalmente), Deleuze, Guattari, Lourau, Nietzche, Donzelot, bem como contribuições mais próximas de autores nacionais, que se debruçam em estudos e pesquisas sobre os temas acima e dialogam com as situações em análise nesta pesquisa. Desnaturalizar os lugares constituídos à luz da moral, das produções subjetivas contemporâneas, dos costumes higienistas e correcionais, das tentativas de enquadramento das práticas familiares, de um jeito de ser pai e mãe, é um dos principais propósitos desta pesquisa. Trata-se de pensar e criar outras possibilidades, como um sopro de liberdade, de desconstrução de lugares, de outras perspectivas e práticas possíveis.

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O tema central da presente dissertação está focalizado na relação família-creche. Este estudo possui, como objetivo principal, analisar como essa relação foi compreendida em três creches públicas cariocas que desenvolveram as atividades do programa Primeira Infância Completa (PIC). Tal programa fez parte das políticas públicas educacionais do município do Rio de Janeiro de 2009 a 2013. Foi direcionado a crianças de até 3 (três) anos de idade que não obtiveram matrícula regular nas creches. As atividades do PIC aconteciam aos sábados com crianças e, para as famílias, eram desenvolvidos os encontros da Escola de Pais. A pesquisa analisa os documentos oficiais (decretos, portarias, resoluções, relatórios, projetos, outras publicações internas) de criação e ampliação do programa, incluindo aqueles referentes às consultorias da UNESCO realizadas em 2012. Foi desenvolvido um levantamento bibliográfico sobre os temas família e a relação família-creche, nas bibliotecas eletrônicas SciELO e Google Acadêmico, com artigos publicados entre 2005 e 2014. A investigação empírica se deu no diálogo com alguns atores do programa, participantes das três creches municipais, totalizando 122 sujeitos, entre gestoras, professoras, agentes auxiliares de creche e familiares. As estratégias metodológicas utilizadas foram entrevistas, grupos focais e oficinas Os dados da segunda consultoria da UNESCO serviram de base para a construção das questões centrais desta pesquisa. Os resultados nos apontam que, para os sujeitos que participaram do programa, os propósitos do mesmo nem sempre foram claros. Embora tenha acontecido no espaço físico das creches (portanto, da Educação), com uma intenção intersetorial, seus objetivos tinham um forte cunho assistencial, caracterizando-o como uma modalidade alternativa de atividades para crianças e familiares. As famílias viam no programa o caminho para a conquista da vaga semanal para as suas crianças e, quando isso não acontecia, ficavam frustrados e deixavam de participar. O esforço das gestoras para a realização do programa foi sua marca de qualidade. A experiência do PIC deixou de legado para as instituições novas formas de pensar a proposta pedagógica e de lidar com as famílias, crianças e funcionários na jornada semanal

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In the UK, The Munro Review of Child Protection (2010, 2011a, 2011b) has recently highlighted that among the failings in safeguarding children known to social services is the lack of meaningful relationships between social workers and children. In her final report, Munro (2011b) has made recommendations for a more child-centred system anchored on two themes – the child's journey and the United Nations Convention on the Rights of the Child (UNCRC). This article illustrates by way of practical examples how the UNCRC, together with the detailed advice and guidance contained in the UNCRC general comments numbers 5, 7 and 12, provides the best framework for developing effective social work relationships with, and safeguarding, young children.

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Aim: Intrauterine, early life and maternal exposures may have important consequences for cancer development in later life. The aim of this study was to examine perinatal and birth characteristics with respect to Cutaneous malignant melanoma (CMM) risk. Methods: The Northern Ireland Child Health System database was used to examine gestational age adjusted birth weight, infant feeding practices, parental age and socioeconomic factors at birth in relation to CMM risk amongst 447,663 infants delivered between January 1971 and December 1986. Follow-up of histologically verified CMM cases was undertaken from the beginning of 1993 to 31st December 2007. Multivariable adjusted unconditional logistic regression was used to calculate odds ratios (OR) and 95% confidence intervals (CI) of CMM risk. Results: A total of 276 CMM cases and 440,336 controls contributed to the final analysis. In reference to normal (gestational age-adjusted) weight babies, those heaviest at birth were twice as likely to develop CMM OR 2.4 (95% CI 1.1-5.1). Inverse associations with CMM risk were observed with younger (

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Chapter explores the complexity of implementing evidence-informed practice within the child welfare system in Ontario, Canada. The paper explores the work of Practice and Research Together (PART; www. partcanada.org)

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En réponse à la disproportion des familles de minorités visibles dans le système montréalais de la protection de la jeunesse, cette recherche explore, du point de vue de l'intervenant, le rôle de ses compétences culturelles et du soutien informel parental dans l’élaboration d'une relation de collaboration. L’analyse porte sur 24 entrevues individuelles, où 48 interventions sont racontées par des intervenants. Les résultats proposent une typologie, élaborée à partir de la collaboration des parents et de l’engagement de leur réseau informel dans l’intervention. Ils présentent ensuite une description des compétences culturelles et de leur utilisation auprès des dynamiques familiales comprises dans la typologie. La discussion aborde la résilience sociale, les stratégies d’intervention et le constructionnisme social. Trois principales idées sont évoquées : une conception de la collaboration qui inclut le réseau informel, une réflexion sur la notion de « compétences culturelles » et le développement d’une pratique réflexive.