Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Andrew Carson‐Stevens

Biographic Data

ID8979888
NAMEAndrew Carson‐Stevens
GIVEN NAMESAndrew
FAMILY NAMECarson‐Stevens
SIGNATURESTEVENS A C
AFFILIATIONSDivision of Population Medicine, School of Medicine, College of Biomedical and Life Sciences Cardiff University and PRIME Centre Wales Cardiff UK
VERIFIEDNo
TOTAL WORKS3
TOTAL CITATIONS0
AUTHOR COUNT3
EDITOR COUNT0
FIRST PUBLICATION YEAR2016
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Recommendations for a Communication Strategy to Support Informed Decision‐Making About Self or Clinician Sampling for Cervical Screening in the UK

    Open Access•Denitza Williams, Eleanor Clarke et al.•ARTICLE•Health Expectations•2025

    BACKGROUND: Cervical screening for high-risk Human Papillomavirus subtypes is offered to those eligible in the UK via the NHS cervical screening programmes. However, uptake of cervical screening continues to remain below the national target of 80%. Groups less likely to participate include people from low socioeconomic groups, ethnic minority backgrounds, younger/older age and/or LGBTQ group identity. The cervical screening-eligible population co…

  • End‐of‐life care decisions for haemodialysis patients – ‘We only tend to have that discussion with them when they start deteriorating’

    Open Access•Sophia Lazenby, Adrian Edwards et al.•ARTICLE•Health Expectations•2017

    BACKGROUND: Haemodialysis patients receive very little involvement in their end-of-life care decisions. Issues relating to death and dying are commonly avoided until late in their illness. This study aimed to explore the experiences and perceptions of doctors and nurses in nephrology for involving haemodialysis patients in end-of-life care decisions. METHODS: A semi-structured qualitative interview study with 15 doctors and five nurses and themat…

  • Doctors’ perspectives of informed consent for non‐emergency surgical procedures

    Open Access•Fiona Wood, Sean M Martin et al.•ARTICLE•Health Expectations•2016

    BACKGROUND: The need to involve patients more in decisions about their care, the ethical imperative and concerns about ligation and complaints has highlighted the issue of informed consent and how it is obtained. In order for a patient to make an informed decision about their treatment, they need appropriate discussion of the risks and benefits of the treatment. OBJECTIVES: To explore doctors' perspectives of gaining informed consent for routine …

No prominent works on this page.

  • Doctors’ perspectives of informed consent for non‐emergency surgical procedures

    Open Access•Fiona Wood, Sean M Martin et al.•ARTICLE•Health Expectations•2016

    BACKGROUND: The need to involve patients more in decisions about their care, the ethical imperative and concerns about ligation and complaints has highlighted the issue of informed consent and how it is obtained. In order for a patient to make an informed decision about their treatment, they need appropriate discussion of the risks and benefits of the treatment. OBJECTIVES: To explore doctors' perspectives of gaining informed consent for routine …

  • End‐of‐life care decisions for haemodialysis patients – ‘We only tend to have that discussion with them when they start deteriorating’

    Open Access•Sophia Lazenby, Adrian Edwards et al.•ARTICLE•Health Expectations•2017

    BACKGROUND: Haemodialysis patients receive very little involvement in their end-of-life care decisions. Issues relating to death and dying are commonly avoided until late in their illness. This study aimed to explore the experiences and perceptions of doctors and nurses in nephrology for involving haemodialysis patients in end-of-life care decisions. METHODS: A semi-structured qualitative interview study with 15 doctors and five nurses and themat…

  • Recommendations for a Communication Strategy to Support Informed Decision‐Making About Self or Clinician Sampling for Cervical Screening in the UK

    Open Access•Denitza Williams, Eleanor Clarke et al.•ARTICLE•Health Expectations•2025

    BACKGROUND: Cervical screening for high-risk Human Papillomavirus subtypes is offered to those eligible in the UK via the NHS cervical screening programmes. However, uptake of cervical screening continues to remain below the national target of 80%. Groups less likely to participate include people from low socioeconomic groups, ethnic minority backgrounds, younger/older age and/or LGBTQ group identity. The cervical screening-eligible population co…

Family medicine (3 works) · Medicine (3 works) · Nursing (3 works) · Psychology (3 works) · Qualitative research (3 works) · Alternative medicine (2 works) · Patient-Provider Communication in Healthcare (2 works) · Advance care planning (1 works) · Cervical cancer (1 works) · Cervical Cancer and HPV Research (1 works)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae