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1.
Scand Cardiovasc J ; 51(6): 316-322, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29019280

RESUMEN

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.


Asunto(s)
Angina Inestable/rehabilitación , Rehabilitación Cardiaca/métodos , Equidad en Salud/organización & administración , Disparidades en Atención de Salud/organización & administración , Infarto del Miocardio sin Elevación del ST/rehabilitación , Evaluación de Procesos, Atención de Salud/organización & administración , Infarto del Miocardio con Elevación del ST/rehabilitación , Factores Socioeconómicos , Acceso a la Información , Anciano , Anciano de 80 o más Años , Angina Inestable/diagnóstico , Servicios de Salud Comunitaria/organización & administración , Información de Salud al Consumidor , Estudios Transversales , Dinamarca , Femenino , Hospitales Universitarios , Humanos , Modelos Logísticos , Masculino , Persona de Mediana Edad , Infarto del Miocardio sin Elevación del ST/diagnóstico , Oportunidad Relativa , Cooperación del Paciente , Derivación y Consulta/organización & administración , Sistema de Registros , Infarto del Miocardio con Elevación del ST/diagnóstico , Encuestas y Cuestionarios , Factores de Tiempo
2.
Ugeskr Laeger ; 177(46): V05150378, 2015 Nov 09.
Artículo en Danés | MEDLINE | ID: mdl-26573950

RESUMEN

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.


Asunto(s)
Algoritmos , Hipotonía Muscular/diagnóstico , Humanos , Lactante
3.
Ugeskr Laeger ; 177(40): V05150380, 2015 Sep 28.
Artículo en Danés | MEDLINE | ID: mdl-26418712

RESUMEN

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.


Asunto(s)
Hipotonía Muscular/etiología , Atrofias Olivopontocerebelosas/complicaciones , Resultado Fatal , Femenino , Humanos , Lactante , Imagen por Resonancia Magnética , Hipotonía Muscular/diagnóstico , Atrofias Olivopontocerebelosas/diagnóstico , Enfermedades Raras
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