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Feldman, M. A.; Owen, F.; Andrews, A.; Hamelin, J.; Barber, R.; Griffiths, D. – Journal of Intellectual Disability Research, 2012
Background: People with intellectual disabilities (ID) have unequal access to health care. While systemic efforts are addressing health inequalities, there remains a need to demonstrate that persons with ID can increase their health self-advocacy skills. Method: A randomised control design with up to 6-month follow-up was used to evaluate the 3Rs…
Descriptors: Access to Health Care, Self Advocacy, Control Groups, Training
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Guest, J. F.; Bai, J. J.; Taylor, R. R.; Sladkevicius, E.; Lee, P. J.; Lachmann, R. H. – Journal of Intellectual Disability Research, 2013
Background: To quantify the costs and consequences of managing phenylketonuria (PKU) in the UK and to estimate the potential implications to the UK's National Health Service (NHS) of keeping patients on a phenylalanine-restricted diet for life. Methods: A computer-based model was constructed depicting the management of PKU patients over the first…
Descriptors: Foreign Countries, Diseases, Metabolism, Dietetics
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Brolan, C. E.; Boyle, F. M.; Dean, J. H.; Gomez, M. Taylor; Ware, R. S.; Lennox, N. G. – Journal of Intellectual Disability Research, 2012
Background: People with intellectual disability (ID) experience health inequity compared with the general population, a key contributing factor being disparities in social determinants of health. The enactment of the United Nations Convention on the Rights of Persons with Disabilities (CRPD) provides a platform for the progression and promotion of…
Descriptors: Parents, Advocacy, Caring, Mental Retardation
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Redley, M.; Prince, E.; Bateman, N.; Pennington, M.; Wood, N.; Croudace, T.; Ring, H. – Journal of Intellectual Disability Research, 2013
Background: Patients with intellectual disabilities (ID) receive health care by proxy. It is family members and/or paid support staff who must recognise health problems, communicate with clinicians, and report the benefits, if any, of a particular treatment. At the same time international and national statutes protect and promote the right of…
Descriptors: Parent Participation, Decision Making, Health Services, Mental Retardation
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Cobigo, V.; Ouellette-Kuntz, H.; Balogh, R.; Leung, F.; Lin, E.; Lunsky, Y. – Journal of Intellectual Disability Research, 2013
Background: Effective cancer screening must be available for all eligible individuals without discrimination. Lower rates of cervical and breast cancer screening have been reported in certain groups compared with women from the general population, such as women with intellectual and developmental disabilities (IDD). Research on the factors…
Descriptors: Cancer, Screening Tests, Access to Health Care, Females
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Robertson, J.; Roberts, H.; Emerson, E.; Turner, S.; Greig, R. – Journal of Intellectual Disability Research, 2011
Background: Health checks for people with intellectual disabilities (ID) have been recommended as one component of health policy responses to the poorer health of people with ID. This review summarises evidence on the impact of health checks on the health and well-being of people with ID. Methods: Electronic literature searches and email contacts…
Descriptors: Health Needs, Mental Retardation, Access to Health Care, Literature Reviews
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Werner, S.; Stawski, M.; Polakiewicz, Y.; Levav, I. – Journal of Intellectual Disability Research, 2013
Background: Psychiatrists are responsible for providing proper care for people with intellectual disability who have psychiatric disorders. This study examined psychiatrists' perceptions of their own training, knowledge and therapeutic skills, as well as their attitudes towards this population. Methods: Questionnaires were distributed to 679…
Descriptors: Foreign Countries, Psychiatry, Mental Retardation, Questionnaires
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Lin, E.; Balogh, R.; Cobigo, V.; Ouellette-Kuntz, H.; Wilton, A. S.; Lunsky, Y. – Journal of Intellectual Disability Research, 2013
Background: Individuals with intellectual and developmental disabilities (IDD) experience high rates of physical and mental health problems; yet their health care is often inadequate. Information about their characteristics and health services needs is critical for planning efficient and equitable services. A logical source of such information is…
Descriptors: Mental Retardation, Developmental Disabilities, Disability Identification, Data Analysis
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Balogh, R. S.; Ouellette-Kuntz, H.; Brownell, M.; Colantonio, A. – Journal of Intellectual Disability Research, 2013
Background: Hospitalisations for ambulatory care-sensitive (ACS) conditions are used as an indicator of access to, and the quality of, primary care. The objective was to identify factors associated with hospitalisations for ACS conditions among adults with an intellectual disability (ID) in the context of a publicly insured healthcare system.…
Descriptors: Mental Retardation, Hospitals, Access to Health Care, Primary Health Care
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Jensen, K. M.; Taylor, L. C.; Davis, M. M. – Journal of Intellectual Disability Research, 2013
Background: Due to significant medical improvements, persons with Down syndrome now live well into adulthood. Consequently, primary care for adults with Down syndrome needs to incorporate routine care with screening for condition-specific comorbidities. This study seeks to evaluate the adherence of primary care physicians to age- and…
Descriptors: Adults, Down Syndrome, Access to Health Care, Medical Services
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Gobrial, E. – Journal of Intellectual Disability Research, 2012
Background: Children with intellectual disabilities (IDs) have the same human value as other children and are entitled to their basic human rights. And yet, in developing countries they face many barriers to accessing these rights. This study focuses on children with IDs in Egypt. Method: A new measure, the Human Rights of children with…
Descriptors: Access to Education, Access to Health Care, Foreign Countries, Mental Retardation
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Cooper, S. A.; McConnachie, A.; Allan, L. M.; Melville, C.; Smiley, E.; Morrison, J. – Journal of Intellectual Disability Research, 2011
Background: Adults with intellectual disabilities (IDs) experience health inequalities and are more likely to live in deprived areas. The aim of this study was to determine whether the extent of deprivation of the area a person lives in affects their access to services, hence contributing to health inequalities. Method: A cross-sectional study…
Descriptors: Accidents, Health Promotion, Mental Retardation, Disadvantaged
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Brown, M.; MacArthur, J.; McKechanie, A.; Mack, S.; Hayes, M.; Fletcher, J. – Journal of Intellectual Disability Research, 2012
Background: There have been significant concerns about the care and treatment of people with intellectual disabilities (ID) when attending general hospitals, which have led to inquiries that highlight service and systems failures. One response has been the development of Learning Disability Liaison Nursing (LDLN) Services across the UK that aim to…
Descriptors: Nursing, Health Needs, Program Effectiveness, Stakeholders
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Chaplin, R. – Journal of Intellectual Disability Research, 2009
Background: There are a variety of models for the mental health care of adults with comorbid intellectual disability (ID) and mental illness. There has been a long-running debate as to whether this should be provided by general psychiatric or specialised ID services. A previous review concluded that there was no clear evidence to support either…
Descriptors: Psychiatric Services, Mental Retardation, Mental Disorders, Adults
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Taggart, L.; Truesdale-Kennedy, M.; McIlfatrick, S. – Journal of Intellectual Disability Research, 2011
Background: Women with intellectual disability (ID) are surviving to the age group at greatest risk of developing breast cancer (50-69 years). These women are more likely to experience a greater number of risk factors placing them at an advanced threat of developing breast cancer. However, as a result of cognitive deficits and communication…
Descriptors: Health Promotion, Females, Mental Retardation, Nurses
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