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1.
Scand Cardiovasc J ; 51(6): 316-322, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29019280

RESUMO

AIM: Barriers to participation in cardiac rehabilitation (CR) may occur at three levels of the referral process (lack of information, declining to participate, and referral to appropriate CR programme). The aim is to analyse the impact of socioeconomic status on barriers to CR and investigate whether such barriers influenced the choice of referral. METHODS: The Rehab-North Register, a cross-sectional study, enrolled 5455 patients hospitalised at Aalborg University Hospital with myocardial infarction (MI) during 2011-2014. Patients hospitalised with ST-elevated MI and complicated non-ST-elevated MI were to be sent to specialized CR, whereas patients with uncomplicated non-ST-elevated MI and unstable angina pectoris were to be sent to community-based CR. Detailed selected socioeconomic information was gathered from statistical registries in Statistics Denmark. Data was assessed using logistic regression. RESULTS: Patients being retired, low educated, and/or with an annual gross income <27.000 Euro/yr were significantly less informed about cardiac rehabilitation programmes. Patients being older than 70 years, retired, low educated and/or with an annual gross income <27.000 Euro were significantly less willing to participate in CR. Further, this patient population were to a higher extent referred to community-based CR. CONCLUSION: Patients with low socioeconomic status received less information about and were less willing to participate in cardiac rehabilitation. The same patient population was to a higher extent referred to community-based CR. Knowledge about barriers at different levels and the impact of social inequality may help in tailoring a better approach in the referral process to CR.


Assuntos
Angina Instável/reabilitação , Reabilitação Cardíaca/métodos , Equidade em Saúde/organização & administração , Disparidades em Assistência à Saúde/organização & administração , Infarto do Miocárdio sem Supradesnível do Segmento ST/reabilitação , Avaliação de Processos em Cuidados de Saúde/organização & administração , Infarto do Miocárdio com Supradesnível do Segmento ST/reabilitação , Fatores Socioeconômicos , Acesso à Informação , Idoso , Idoso de 80 Anos ou mais , Angina Instável/diagnóstico , Serviços de Saúde Comunitária/organização & administração , Informação de Saúde ao Consumidor , Estudos Transversais , Dinamarca , Feminino , Hospitais Universitários , Humanos , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Infarto do Miocárdio sem Supradesnível do Segmento ST/diagnóstico , Razão de Chances , Cooperação do Paciente , Encaminhamento e Consulta/organização & administração , Sistema de Registros , Infarto do Miocárdio com Supradesnível do Segmento ST/diagnóstico , Inquéritos e Questionários , Fatores de Tempo
2.
Ugeskr Laeger ; 177(46): V05150378, 2015 Nov 09.
Artigo em Dinamarquês | MEDLINE | ID: mdl-26573950

RESUMO

The term "floppy infant" is used for describing children presenting with muscle hypotonia at or shortly after birth. These floppy infants are usually a diagnostic challenge due to the many rare and genetic causes of hypotonia. It is common to start by classifying the hypotonia as peripheral or central, but even from here the path to a diagnosis can be long. This article reviews the literature, mostly retrospective studies done on floppy infants and presents a new simplified algorithm to help guide the diagnostics of the hypotonic children.


Assuntos
Algoritmos , Hipotonia Muscular/diagnóstico , Humanos , Lactente
3.
Ugeskr Laeger ; 177(40): V05150380, 2015 Sep 28.
Artigo em Dinamarquês | MEDLINE | ID: mdl-26418712

RESUMO

The hypotone neonate, floppy infant, often proves to be a diagnostic challenge, as the causes of floppy infant syndrome are many and often rare. In this case story a floppy girl was diagnosed with the rare, autosomal recessive disease pontocerebellar hypoplasia type I. The tests for the most common causes of floppy infant syndrome showed nothing abnormal, but an array comparative genomic hybridization test gave information of loss of heterozygosity. This helped to narrow the list of plausible diagnoses and eventually led to the diagnosis of pontocerebellar hypoplasia type I.


Assuntos
Hipotonia Muscular/etiologia , Atrofias Olivopontocerebelares/complicações , Evolução Fatal , Feminino , Humanos , Lactente , Imageamento por Ressonância Magnética , Hipotonia Muscular/diagnóstico , Atrofias Olivopontocerebelares/diagnóstico , Doenças Raras
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