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Jeannine Stairmand

Biographic Data

ID179258
NAMEJeannine Stairmand
GIVEN NAMESJeannine
FAMILY NAMEStairmand
SIGNATURESTAIRMAND J
AFFILIATIONSUniversity of Otago
ORCID0000-0002-1754-902X
VERIFIEDYes
TOTAL WORKS9
TOTAL CITATIONS7
AUTHOR COUNT9
EDITOR COUNT0
FIRST PUBLICATION YEAR2015
LATEST PUBLICATION YEAR2025
H-INDEX2
  • The undercounting of Indigenous Māori imprisoned by the New Zealand carceral state: A national record study

    Open Access•Paula Toko King, Frederieke Sanne Petrović-Van Der Deen et al.•ARTICLE•Health & Justice•2025

    BACKGROUND: Indigenous Māori are imprisoned on a mass scale by the nation-state currently known as New Zealand, driven by racialised inequities that occur across the criminal legal system and a rapidly expanding carceral state. Lack of reliable data limits the ability to monitor and evaluate the health and disability impacts of imprisonment on Māori. We examined ethnicity data quality; specifically, potential miscounting of Māori in prison. All i…

  • Health in justice or health injustice? Indigenous Māori experiences of primary care following release from New Zealand prisons: A National Record Study

    Open Access•Paula Toko King, Frederieke Sanne Petrović-Van Der Deen et al.•ARTICLE•Social Science & Medicine•2025•References: 38

    Whilst our findings indicate that Māori released from prisons access primary care, there are financial barriers to access. We also found (across a range of access and quality measures) that primary care services are not meeting their high health needs, demonstrating governmental breach of Indigenous rights to health. High-quality primary care is critical to successful community re-entry and to preventing adverse outcomes. There is an urgent requi…

  • It’s more than just physical: Experiences of pain and pain management among Māori with cancer and their whānau

    Open Access•Virginia Signal, Rhiannon Jones et al.•ARTICLE•International Journal of…•2023

    This study investigated the experiences of pain and pain management among Māori with cancer in Aotearoa New Zealand. Using a qualitative study design underpinned by kaupapa Māori research principles, focus group hui and interviews were held with Māori with cancer and their whānau (n=24). We identified themes relating to holistic experiences of pain and pain management, the importance of appropriate support and good communication, and intertwined …

  • Palliative care and quality of life needs and outcomes for Māori with cancer: What do we know

    Open Access•R M Jones, Virginia Signal et al.•ARTICLE•AlterNative An International…•2023

    There are access, treatment and morbidity inequities for Māori (Indigenous people of New Zealand) with cancer in Aotearoa (New Zealand). This includes inequities in quality of life and experiences of the palliative care setting for Māori. This review included 20 papers that were identified through a combination of our literature review and key informant surveys. In this review, we consider the context of palliative care and cancer quality of care…

  • A kia ora, a wave and a smile: An urban marae-led response to Covid-19, a case study in manaakitanga

    Open Access•Cheryl Davies, Carmen Timu-Parata et al.•ARTICLE•International Journal for Equity…•2022

    Māori health providers are well placed to respond effectively in a public-health crisis when resourced appropriately and trusted to deliver. We propose a number of recommendations based on the insights generated from the researchers, kaimahi, and whānau. These are that: Māori be included in pandemic planning and decision-making, Māori-led initiatives and organisations be valued and adequately resourced, and strong communities with strong networks…

  • Ascertaining patients' understandings of their condition: A Conversation Analysis of Contradictory Norms in Cancer Specialist Consultations

    Kelsi Dew, Josh Barton et al.•ARTICLE•Health Sociology Review•2019•Cited by: 1•References: 31

    Patient-centred care requires patients to be active participants in decision-making in consultations. Decision-making participation requires patients to understand their condition and to be able to convey their health literacy to medical specialists they encounter. Based on conversation analysis of 18 audio-recorded consultations between cancer patients and a range of cancer care specialists, this article analyses the ways cancer specialists atte…

  • Cancer care decision-making and treatment consent: An observational study of patients' and clinicians' rights

    Open Access•Kelsi Dew, Louise Signal et al.•ARTICLE•Journal of Sociology•2019•Cited by: 2•References: 21

    This study identified ways in which patients and medical specialists negotiated decisions about cancer treatment by observing decision-making discussion in situ. Audio-recordings of cancer care consultations with 18 patients, their support people, and their medical specialists, including medical oncologists, radiation oncologists and surgeons were collected in different regions of New Zealand. Patients were followed up with interviews and special…

  • Cancer Care Decision Making in Multidisciplinary Meetings

    Open Access•Kelsi Dew, Kevin Dew et al.•ARTICLE•Qualitative Health Research•2015

    Little research has been undertaken on the actual decision-making processes in cancer care multidisciplinary meetings (MDMs). This article was based on a qualitative observational study of two regional cancer treatment centers in New Zealand. We audiorecorded 10 meetings in which 106 patient cases were discussed. Members of the meetings categorized cases in varying ways, drew on a range of sources of authority, expressed different value positions…

  • Dissonant roles: The experience of Māori in cancer care

    Open Access•Kelsi Dew, Kevin Dew et al.•ARTICLE•Social Science & Medicine•2015•Cited by: 4•References: 19

  • Dissonant roles: The experience of Māori in cancer care

    Open Access•Kelsi Dew, Kevin Dew et al.•ARTICLE•Social Science & Medicine•2015•Cited by: 4•References: 19

  • Cancer care decision-making and treatment consent: An observational study of patients' and clinicians' rights

    Open Access•Kelsi Dew, Louise Signal et al.•ARTICLE•Journal of Sociology•2019•Cited by: 2•References: 21

    This study identified ways in which patients and medical specialists negotiated decisions about cancer treatment by observing decision-making discussion in situ. Audio-recordings of cancer care consultations with 18 patients, their support people, and their medical specialists, including medical oncologists, radiation oncologists and surgeons were collected in different regions of New Zealand. Patients were followed up with interviews and special…

  • Ascertaining patients' understandings of their condition: A Conversation Analysis of Contradictory Norms in Cancer Specialist Consultations

    Kelsi Dew, Josh Barton et al.•ARTICLE•Health Sociology Review•2019•Cited by: 1•References: 31

    Patient-centred care requires patients to be active participants in decision-making in consultations. Decision-making participation requires patients to understand their condition and to be able to convey their health literacy to medical specialists they encounter. Based on conversation analysis of 18 audio-recorded consultations between cancer patients and a range of cancer care specialists, this article analyses the ways cancer specialists atte…

  • Cancer Care Decision Making in Multidisciplinary Meetings

    Open Access•Kelsi Dew, Kevin Dew et al.•ARTICLE•Qualitative Health Research•2015

    Little research has been undertaken on the actual decision-making processes in cancer care multidisciplinary meetings (MDMs). This article was based on a qualitative observational study of two regional cancer treatment centers in New Zealand. We audiorecorded 10 meetings in which 106 patient cases were discussed. Members of the meetings categorized cases in varying ways, drew on a range of sources of authority, expressed different value positions…

  • Dissonant roles: The experience of Māori in cancer care

    Open Access•Kelsi Dew, Kevin Dew et al.•ARTICLE•Social Science & Medicine•2015•Cited by: 4•References: 19

  • Ascertaining patients' understandings of their condition: A Conversation Analysis of Contradictory Norms in Cancer Specialist Consultations

    Kelsi Dew, Josh Barton et al.•ARTICLE•Health Sociology Review•2019•Cited by: 1•References: 31

    Patient-centred care requires patients to be active participants in decision-making in consultations. Decision-making participation requires patients to understand their condition and to be able to convey their health literacy to medical specialists they encounter. Based on conversation analysis of 18 audio-recorded consultations between cancer patients and a range of cancer care specialists, this article analyses the ways cancer specialists atte…

  • Cancer care decision-making and treatment consent: An observational study of patients' and clinicians' rights

    Open Access•Kelsi Dew, Louise Signal et al.•ARTICLE•Journal of Sociology•2019•Cited by: 2•References: 21

    This study identified ways in which patients and medical specialists negotiated decisions about cancer treatment by observing decision-making discussion in situ. Audio-recordings of cancer care consultations with 18 patients, their support people, and their medical specialists, including medical oncologists, radiation oncologists and surgeons were collected in different regions of New Zealand. Patients were followed up with interviews and special…

  • A kia ora, a wave and a smile: An urban marae-led response to Covid-19, a case study in manaakitanga

    Open Access•Cheryl Davies, Carmen Timu-Parata et al.•ARTICLE•International Journal for Equity…•2022

    Māori health providers are well placed to respond effectively in a public-health crisis when resourced appropriately and trusted to deliver. We propose a number of recommendations based on the insights generated from the researchers, kaimahi, and whānau. These are that: Māori be included in pandemic planning and decision-making, Māori-led initiatives and organisations be valued and adequately resourced, and strong communities with strong networks…

  • It’s more than just physical: Experiences of pain and pain management among Māori with cancer and their whānau

    Open Access•Virginia Signal, Rhiannon Jones et al.•ARTICLE•International Journal of…•2023

    This study investigated the experiences of pain and pain management among Māori with cancer in Aotearoa New Zealand. Using a qualitative study design underpinned by kaupapa Māori research principles, focus group hui and interviews were held with Māori with cancer and their whānau (n=24). We identified themes relating to holistic experiences of pain and pain management, the importance of appropriate support and good communication, and intertwined …

  • Palliative care and quality of life needs and outcomes for Māori with cancer: What do we know

    Open Access•R M Jones, Virginia Signal et al.•ARTICLE•AlterNative An International…•2023

    There are access, treatment and morbidity inequities for Māori (Indigenous people of New Zealand) with cancer in Aotearoa (New Zealand). This includes inequities in quality of life and experiences of the palliative care setting for Māori. This review included 20 papers that were identified through a combination of our literature review and key informant surveys. In this review, we consider the context of palliative care and cancer quality of care…

  • The undercounting of Indigenous Māori imprisoned by the New Zealand carceral state: A national record study

    Open Access•Paula Toko King, Frederieke Sanne Petrović-Van Der Deen et al.•ARTICLE•Health & Justice•2025

    BACKGROUND: Indigenous Māori are imprisoned on a mass scale by the nation-state currently known as New Zealand, driven by racialised inequities that occur across the criminal legal system and a rapidly expanding carceral state. Lack of reliable data limits the ability to monitor and evaluate the health and disability impacts of imprisonment on Māori. We examined ethnicity data quality; specifically, potential miscounting of Māori in prison. All i…

  • Health in justice or health injustice? Indigenous Māori experiences of primary care following release from New Zealand prisons: A National Record Study

    Open Access•Paula Toko King, Frederieke Sanne Petrović-Van Der Deen et al.•ARTICLE•Social Science & Medicine•2025•References: 38

    Whilst our findings indicate that Māori released from prisons access primary care, there are financial barriers to access. We also found (across a range of access and quality measures) that primary care services are not meeting their high health needs, demonstrating governmental breach of Indigenous rights to health. High-quality primary care is critical to successful community re-entry and to preventing adverse outcomes. There is an urgent requi…

Medicine (7 works) · Nursing (6 works) · Political science (6 works) · Psychology (6 works) · Sociology (5 works) · Health care (4 works) · Law (4 works) · Aotearoa (3 works) · Family medicine (3 works) · Indigenous (3 works)

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