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1.
Br J Dermatol ; 182(5): 1245-1252, 2020 05.
Artigo em Inglês | MEDLINE | ID: mdl-31420964

RESUMO

BACKGROUND: Childhood atopic dermatitis can often have a negative impact on quality of life for affected children and their caregivers. The condition contributes to increased healthcare costs and can pose heavy economic burdens on healthcare systems and societies. OBJECTIVES: The objective of this study is to provide a comprehensive estimate of the economic burden of childhood atopic dermatitis in a Singaporean sample and to investigate associated factors. METHODS: This cross-sectional cost-of-illness study applied a societal perspective. Data was collected between December 2016 and December 2017 in Singapore. Caregivers to children below 16 years of age with a physician-confirmed diagnosis of atopic dermatitis were recruited and sociodemographics, clinical characteristics, health service utilization data and time spent on caregiving were collected from all eligible participants. RESULTS: The average annual cost per child with atopic dermatitis was estimated at U.S. dollars (USD) 7943 (mild USD 6651, moderate USD 7935 and severe USD 14 335) in 2017 prices. The major cost was for informal caregiving (46% of the total cost) followed by out-of-pocket expenses (37%). Healthcare utilization contributed to 17% of the total cost of which 43% was for medications. CONCLUSIONS: Childhood atopic dermatitis imposes substantial costs with a large proportion arising from informal caregiving and out-of-pocket expenses. The costs related to atopic dermatitis are also strongly related to disease severity. This information is important for policy makers and other health planners when considering how to better support affected families. What's already known about the topic? Childhood atopic dermatitis is a costly disease for society. However, comprehensive cost estimations are lacking. Previous cost studies are old, based on small sample sizes or are healthcare-setting specific. What does this study add? This study comprises a health economic evaluation assessing different levels of care and includes various categories of costs. The result showed that informal caregiving was the most prominent cost for children with atopic dermatitis.


Assuntos
Dermatite Atópica , Criança , Efeitos Psicossociais da Doença , Estudos Transversais , Dermatite Atópica/epidemiologia , Custos de Cuidados de Saúde , Humanos , Qualidade de Vida , Singapura/epidemiologia
2.
Am J Ment Retard ; 105(2): 81-102, 2000 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10755173

RESUMO

The costs, nature, and benefits of residential supports were examined for 86 adults with mental retardation living in village communities, 133 adults living in newly built residential campuses, and 281 adults living in dispersed housing schemes (small community-based group homes and supported living). Results indicated that (a) the adjusted comprehensive costs of provision in dispersed housing schemes were 15% higher than in residential campuses and 20% higher than in village communities; (b) dispersed housing schemes and village communities offered a significantly greater quality of care than did residential campuses; and (c) there appeared to be distinct patterns of quality of life benefits associated with dispersed housing schemes and village communities, with both approaches offering a greater quality of life than did residential campuses.


Assuntos
Pessoas com Deficiência Mental/psicologia , Pessoas com Deficiência Mental/reabilitação , Qualidade de Vida/psicologia , Instituições Residenciais/economia , Instituições Residenciais/normas , Adulto , Análise de Variância , Antipsicóticos/uso terapêutico , Estudos Transversais , Uso de Medicamentos , Feminino , Lares para Grupos/economia , Humanos , Masculino , Pessoa de Meia-Idade , Vigilância da População , Apoio Social , Inquéritos e Questionários , Reino Unido
3.
Am J Ment Retard ; 106(5): 401-15, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11531460

RESUMO

Information was collected on 63 adults in supported living residences, 55 adults in small group homes, and 152 adults in large group homes. Results indicated that (a) there were no statistically significant differences in service costs once these had been adjusted to take account of participant characteristics; (b) compared with participants living in small group homes, those in supported living residences had greater choice, participated in more community-based activities, experienced fewer scheduled activities, were more likely to have had their home vandalized, and were considered at greater risk of exploitation; (c) compared with participants living in large group homes, those in small group homes had larger social networks, more people in their social networks who were not staff, not family, and did not have mental retardation. These residents were considered at less risk of abuse.


Assuntos
Lares para Grupos/economia , Deficiência Intelectual/economia , Garantia da Qualidade dos Cuidados de Saúde/economia , Instituições Residenciais/economia , Adulto , Análise Custo-Benefício , Estudos Transversais , Feminino , Humanos , Deficiência Intelectual/reabilitação , Masculino , Pessoa de Meia-Idade , Avaliação de Processos e Resultados em Cuidados de Saúde , Características de Residência , Reino Unido
4.
Autism ; 5(1): 7-22, 2001 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-11708392

RESUMO

Little is known about the economic impact of autism. This study estimated the economic consequences of autism in the United Kingdom, based on published evidence and on the reanalysis of data holdings at the Centre for the Economics of Mental Health (CEMH). With an assumed prevalence of 5 per 10,000, the annual societal cost for the UK was estimated to exceed l1 billion. The lifetime cost for a person with autism exceeded l2.4 million. The main costs were for living support and day activities. Family costs account for only 2.3 percent of the total cost, but a lack of relevant information limited our ability to estimate these costs. Minor improvements in life outcome for people with autism could substantially reduce costs over the lifetime.


Assuntos
Transtorno Autístico/economia , Medicina Estatal/economia , Transtorno Autístico/epidemiologia , Transtorno Autístico/reabilitação , Criança , Efeitos Psicossociais da Doença , Custos e Análise de Custo , Estudos Transversais , Intervenção Educacional Precoce/economia , Humanos , Equipe de Assistência ao Paciente/economia , Reino Unido/epidemiologia
5.
Scand J Public Health ; 27(1): 22-9, 1999 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10847667

RESUMO

There are substantial differences in the sales of benzodiazepines between Swedish regions. In order to determine whether there are consistent differences in the inclination of Swedish doctors to prescribe benzodiazepines depending on region and characteristics of the prescriber, a questionnaire was sent to a stratified random sample of physicians (116 family practitioners, 78 psychiatrists, and 96 private practitioners). The questionnaire contained six case studies in which benzodiazepine treatment was suggested and two case studies concerning change of benzodiazepine dosage. There were significant differences (p < 0.05) in the inclination to prescribe benzodiazepines depending on both region and the physician's age in two cases and the physician's speciality and gender in one case each. Psychiatrists and female physicians were, in general, less inclined to prescribe benzodiazepines. In spite of higher sales of benzodiazepines in Göteborg, physicians there had a lower inclination to prescribe benzodiazepines compared with physicians working in regions with lower prescription rates.


Assuntos
Ansiolíticos/administração & dosagem , Padrões de Prática Médica , Área de Atuação Profissional , Adulto , Fatores Etários , Idoso , Idoso de 80 Anos ou mais , Benzodiazepinas , Medicina de Família e Comunidade/estatística & dados numéricos , Feminino , Fidelidade a Diretrizes , Humanos , Modelos Logísticos , Masculino , Medicina , Pessoa de Meia-Idade , Guias de Prática Clínica como Assunto , Prática Privada/estatística & dados numéricos , Psiquiatria/estatística & dados numéricos , Fatores Sexuais , Especialização , Suécia
6.
J Intellect Disabil Res ; 46(Pt 5): 394-404, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12031022

RESUMO

BACKGROUND: In recent years, a growing volume of research evidence has been generated about the relative cost-effectiveness of various types of community-based residential supports for people with intellectual disability (ID) in the UK. However, few reliable data are available to inform planners, commissioners or service providers about the quality and costs of providing support within residential or village communities. METHODS: The evaluation described in the present paper aimed to fill some of the gaps in knowledge by examining the comparative costs of supporting people in village community settings, in National Health Service (NHS) residential campuses and in dispersed, community-based housing schemes. The complete service package received by each study participant was described and costed, and a series of statistical analyses was undertaken to identify factors associated with variations in the cost of support. The analyses reported in the present paper were based on comparisons of 86 people living in village communities, 133 in residential campuses and 281 in dispersed housing schemes. RESULTS: Wide variations in cost were found, not only between models of accommodation, but between individual organizations, settings and service users. Multivariate analysis revealed that higher costs were associated with supports for people with higher levels of ID and more severe challenging behaviour. The cost of support was affected by the size of the residential setting, with smaller facilities likely to be more expensive. Associations were also found between increased costs, and services for younger users, male users and people who had not moved from a NHS hospital. Generally, more sophisticated service processes within the setting were associated with higher costs; although systematic arrangements for supervision and training of staff had a negative effect on cost. CONCLUSIONS: The cost findings should be considered alongside evidence on outcomes. A comparison of village communities and dispersed housing schemes suggests that both models of provision appear be associated with particular benefits, although different types of setting are appropriate for different individuals and therefore, the continued development of a range of residential models is important.


Assuntos
Serviços Comunitários de Saúde Mental/economia , Habitação/economia , Deficiência Intelectual/economia , Deficiência Intelectual/terapia , Tratamento Domiciliar/economia , Adulto , Análise Custo-Benefício , Feminino , Humanos , Masculino , Reino Unido
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