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Patricia M Wilson

Biographic Data

ID198214
NAMEPatricia M Wilson
GIVEN NAMESPatricia M
FAMILY NAMEWilson
SIGNATUREWILSON P M
AFFILIATIONSArizona State University
VERIFIEDNo
TOTAL WORKS4
TOTAL CITATIONS26
AUTHOR COUNT4
EDITOR COUNT0
FIRST PUBLICATION YEAR1992
LATEST PUBLICATION YEAR2015
H-INDEX2
  • You Cannot Choose Your Family

    Open Access•Patricia M Wilson, Patricia Wilson et al.•ARTICLE•Qualitative Health Research•2015•References: 35

    Living with end-stage renal disease is challenging and requires a great deal of self-management, but little is known about the experiences of patients and staff around the subject. We held six focus groups in three hemodialysis units, each unit hosting 1 staff and 1 patient focus group. A total of 15 staff members and 15 patients participated. We employed thematic analysis using a priori and emerging codes. Five key themes emerged: challenges, en…

  • The Expert Patients Programme

    Open Access•Patricia M Wilson, Patricia Wilson et al.•ARTICLE•Health & Social Care in the…•2007•Cited by: 18•References: 15

    Self-care is seen as a key element in managing resource demand in chronic disease and is also perceived as an empowering right for patients. The Chronic Disease Self-Management Programme developed in the USA has been adopted in a number of countries and in the UK has been as adapted as the Expert Patients Programme. However, despite its potential as a lay-led empowering initiative, the Expert Patients Programme has been criticised as perpetuating…

  • A policy analysis of the Expert Patient in the United Kingdom

    Open Access•Patricia M Wilson, Patricia Wilson•ARTICLE•Health & Social Care in the…•2001

    The rise in chronic illness and comorbidity in Western society has resulted in an increasing emphasis on self-care initiatives. In the United Kingdom this is exemplified by the Expert Patient policy. This paper discusses the Expert Patient initiative as an example of the State's third way approach to public health. The extent to which this policy challenges conventional power relationships between professional and patient, and fosters equal partn…

  • Environmental Influences on Adolescent Educational Aspirations

    Open Access•Patricia M Wilson, Patricia Wilson et al.•ARTICLE•Youth & Society•1992•Cited by: 8•References: 20

  • The Expert Patients Programme

    Open Access•Patricia M Wilson, Patricia Wilson et al.•ARTICLE•Health & Social Care in the…•2007•Cited by: 18•References: 15

    Self-care is seen as a key element in managing resource demand in chronic disease and is also perceived as an empowering right for patients. The Chronic Disease Self-Management Programme developed in the USA has been adopted in a number of countries and in the UK has been as adapted as the Expert Patients Programme. However, despite its potential as a lay-led empowering initiative, the Expert Patients Programme has been criticised as perpetuating…

  • Environmental Influences on Adolescent Educational Aspirations

    Open Access•Patricia M Wilson, Patricia Wilson et al.•ARTICLE•Youth & Society•1992•Cited by: 8•References: 20

  • Environmental Influences on Adolescent Educational Aspirations

    Open Access•Patricia M Wilson, Patricia Wilson et al.•ARTICLE•Youth & Society•1992•Cited by: 8•References: 20

  • A policy analysis of the Expert Patient in the United Kingdom

    Open Access•Patricia M Wilson, Patricia Wilson•ARTICLE•Health & Social Care in the…•2001

    The rise in chronic illness and comorbidity in Western society has resulted in an increasing emphasis on self-care initiatives. In the United Kingdom this is exemplified by the Expert Patient policy. This paper discusses the Expert Patient initiative as an example of the State's third way approach to public health. The extent to which this policy challenges conventional power relationships between professional and patient, and fosters equal partn…

  • The Expert Patients Programme

    Open Access•Patricia M Wilson, Patricia Wilson et al.•ARTICLE•Health & Social Care in the…•2007•Cited by: 18•References: 15

    Self-care is seen as a key element in managing resource demand in chronic disease and is also perceived as an empowering right for patients. The Chronic Disease Self-Management Programme developed in the USA has been adopted in a number of countries and in the UK has been as adapted as the Expert Patients Programme. However, despite its potential as a lay-led empowering initiative, the Expert Patients Programme has been criticised as perpetuating…

  • You Cannot Choose Your Family

    Open Access•Patricia M Wilson, Patricia Wilson et al.•ARTICLE•Qualitative Health Research•2015•References: 35

    Living with end-stage renal disease is challenging and requires a great deal of self-management, but little is known about the experiences of patients and staff around the subject. We held six focus groups in three hemodialysis units, each unit hosting 1 staff and 1 patient focus group. A total of 15 staff members and 15 patients participated. We employed thematic analysis using a priori and emerging codes. Five key themes emerged: challenges, en…

Sociology (4 works) · Medicine (3 works) · Mental Health and Patient Involvement (3 works) · Nursing (3 works) · Psychology (3 works) · Focus group (2 works) · Political science (2 works) · Qualitative research (2 works) · Social Psychology (2 works) · Social science (2 works)

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