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Eline M Bunnik

Dados Biográficos

ID9210397
NOMEEline M Bunnik
PRENOMESEline M
SOBRENOMEBunnik
ASSINATURABUNNIK E M
AFILIAÇÕESErasmus MC
ORCID0000-0003-1481-6222
VERIFICADOSim
TOTAL DE OBRAS12
TOTAL DE CITAÇÕES2
TOTAL COMO AUTOR12
TOTAL COMO EDITOR0
PRIMEIRO ANO DE PUBLICAÇÃO2018
ANO MAIS RECENTE DE PUBLICAÇÃO2026
ÍNDICE H1
  • Changing the Child

    Open Access•Sietske A L van Till, Maartje H N Schermer et al.•ARTICLE•Bioethics•2026

    Scientific advancements offer new possibilities for developing novel treatments for children with monogenic neurodevelopmental disorders (mNDDs), targeting the underlying effects of their condition. Although, in qualitative studies, parents of children with mNDDs have predominantly positive attitudes towards the development of novel treatments, a few parents express concerns about whether treatments could change who their child is . Existing lite…

  • ‘Empathy counterbalancing’ to mitigate the ‘identified victim effect’? Ethical reflections on cognitive debiasing strategies to increase support for healthcare priority setting

    Jilles Smids, Charlotte H C Bomhof et al.•ARTICLE•Journal of Medical Ethics•2025

    Priority setting is inevitable to control expenditure on expensive medicines, but citizen support is often hampered by the workings of the ‘identified victim effect’, that is, the greater willingness to spend resources helping identified victims than helping statistical victims. In this paper we explore a possible cognitive debiasing strategy that is being employed in discussions on healthcare priority setting, which we call ‘empathy counterbalan…

  • Access to Non‐reimbursed Expensive Cancer Treatments

    Open Access•Jilles Smids, Eline M Bunnik•ARTICLE•Journal of Applied Philosophy•2024

    When the cost‐effectiveness of newly approved cancer treatments is insufficient or unclear, they may not (immediately) be eligible for reimbursement through basic health insurance in publicly funded healthcare systems. Patients may seek access to non‐reimbursed treatment through other channels, including individual funding requests made to hospitals, health insurers, or pharmaceutical companies. Alternatively, they may try to pay out of pocket fo…

  • Vulnerable person investigation plan (VIP) to optimise inclusion in clinical trials

    Ilana C Raburn, Eline M Bunnik et al.•ARTICLE•Journal of Medical Ethics•2023

    TEST 02 - Elsevier's Scopus, the largest abstract and citation database of peer-reviewed literature. Search and access research from the science, technology, medicine, social sciences and arts and humanities fields

  • Access to effective but expensive treatments

    Open Access•Sietske A L van Till, Jilles Smids et al.•ARTICLE•Bioethics•2023

    The development of new effective but expensive medical treatments leads to discussions about whether and how such treatments should be funded in solidarity‐based healthcare systems. Solidarity is often seen as an elusive concept; it appears to be used to refer to different sets of concerns, and its interrelations with the concept of justice are not well understood. This paper provides a conceptual analysis of the concept of solidarity as it is us…

  • The ‘false hope’ argument in discussions on expanded access to investigational drugs

    Open Access•Marjolijn Hordijk, Stefan F Vermeulen et al.•ARTICLE•Medicine Health Care and Philosophy•2022

    When seriously ill patients reach the end of the standard treatment trajectory for their condition, they may qualify for the use of unapproved, investigational drugs regulated via expanded access programs. In medical-ethical discourse, it is often argued that expanded access to investigational drugs raises ‘false hope’ among patients and is therefore undesirable. We set out to investigate what is meant by the false hope argument in this discourse…

  • Factors of feasibility

    Open Access•Stefan F Vermeulen, Marjolijn Hordijk et al.•ARTICLE•Humanities and Social Sciences…•2021

    Seriously ill patients who have exhausted all approved treatment regimens and who cannot be enrolled in clinical trials may resort to expanded access programmes in order to gain access to unapproved, investigational drugs. It seems that in some countries, expanded access to investigational drugs is offered in clinical practice on a more routine basis than in other countries. This study is the first to investigate the experiences of physicians wit…

  • Prevention in the age of personal responsibility

    Open Access•Ineke Bolt, Eline M Bunnik et al.•ARTICLE•Journal of Medical Ethics•2021

    Epigenetic markers could potentially be used for risk assessment in risk-stratified population-based cancer screening programmes. Whereas current screening programmes generally aim to detect existing cancer, epigenetic markers could be used to provide risk estimates for not-yet-existing cancers. Epigenetic risk-predictive tests may thus allow for new opportunities for risk assessment for developing cancer in the future. Since epigenetic changes a…

  • The Impact of Incidental Findings Detected During Brain Imaging on Research Participants of the Rotterdam Study

    Open Access•Charlotte H C Bomhof, LISA VAN BODEGOM et al.•ARTICLE•Cambridge Quarterly of Healthcare…•2020

    This interview study investigates the short- and long-term implications of incidental findings detected through brain imaging on research participants’ lives and their surroundings. For this study, nine participants of the Rotterdam Scan Study with an incidental finding were approached and interviewed. When examining research participants’ narratives on the impact of the disclosure of incidental findings, the authors identified five sets of tensi…

  • Why Nipt should be publicly funded

    Open Access•Eline M Bunnik, Adriana Kater‐Kuipers et al.•ARTICLE•Journal of Medical Ethics•2020

    Asking pregnant women to (co)pay for non-invasive prenatal testing (NIPT) out of pocket leads to unequal access across socioeconomic strata. To avoid these social justice issues, first-trimester prenatal screening should be publicly funded in countries such as the Netherlands, with universal coverage healthcare systems that offer all other antenatal care services and screening programmes free of charge. In this reply, we offer three additional re…

  • Rethinking counselling in prenatal screening

    Open Access•Adriana Kater‐Kuipers, Inez D de Beaufort et al.•ARTICLE•Bioethics•2020

    Informed consent is a key condition for prenatal screening programmes to reach their aim of promoting reproductive autonomy. Reaching this aim is currently being challenged with the introduction of non‐invasive prenatal testing (NIPT) in first‐trimester prenatal screening programmes: amongst others its procedural ease—it only requires a blood draw and reaches high levels of reliability—might hinder women’s understanding that they should make a pe…

  • At, with and beyond risk

    Open Access•Richard Milne, Ana Díaz et al.•ARTICLE•Sociology of Health & Illness•2018•Citada por: 2•Referências: 71

    Biomedical research aimed at the development of therapies for chronic and late-onset conditions increasingly concentrates on the early treatment of symptom-less disease. This broad trend is evidenced in prominent shifts in contemporary dementia research. Revised diagnostic criteria and new approaches to clinical trials propose a focus on earlier stages of disease and prompt concerns about the implications of communicating test results associated …

  • At, with and beyond risk

    Open Access•Richard Milne, Ana Díaz et al.•ARTICLE•Sociology of Health & Illness•2018•Citada por: 2•Referências: 71

    Biomedical research aimed at the development of therapies for chronic and late-onset conditions increasingly concentrates on the early treatment of symptom-less disease. This broad trend is evidenced in prominent shifts in contemporary dementia research. Revised diagnostic criteria and new approaches to clinical trials propose a focus on earlier stages of disease and prompt concerns about the implications of communicating test results associated …

  • At, with and beyond risk

    Open Access•Richard Milne, Ana Díaz et al.•ARTICLE•Sociology of Health & Illness•2018•Citada por: 2•Referências: 71

    Biomedical research aimed at the development of therapies for chronic and late-onset conditions increasingly concentrates on the early treatment of symptom-less disease. This broad trend is evidenced in prominent shifts in contemporary dementia research. Revised diagnostic criteria and new approaches to clinical trials propose a focus on earlier stages of disease and prompt concerns about the implications of communicating test results associated …

  • The Impact of Incidental Findings Detected During Brain Imaging on Research Participants of the Rotterdam Study

    Open Access•Charlotte H C Bomhof, LISA VAN BODEGOM et al.•ARTICLE•Cambridge Quarterly of Healthcare…•2020

    This interview study investigates the short- and long-term implications of incidental findings detected through brain imaging on research participants’ lives and their surroundings. For this study, nine participants of the Rotterdam Scan Study with an incidental finding were approached and interviewed. When examining research participants’ narratives on the impact of the disclosure of incidental findings, the authors identified five sets of tensi…

  • Why Nipt should be publicly funded

    Open Access•Eline M Bunnik, Adriana Kater‐Kuipers et al.•ARTICLE•Journal of Medical Ethics•2020

    Asking pregnant women to (co)pay for non-invasive prenatal testing (NIPT) out of pocket leads to unequal access across socioeconomic strata. To avoid these social justice issues, first-trimester prenatal screening should be publicly funded in countries such as the Netherlands, with universal coverage healthcare systems that offer all other antenatal care services and screening programmes free of charge. In this reply, we offer three additional re…

  • Rethinking counselling in prenatal screening

    Open Access•Adriana Kater‐Kuipers, Inez D de Beaufort et al.•ARTICLE•Bioethics•2020

    Informed consent is a key condition for prenatal screening programmes to reach their aim of promoting reproductive autonomy. Reaching this aim is currently being challenged with the introduction of non‐invasive prenatal testing (NIPT) in first‐trimester prenatal screening programmes: amongst others its procedural ease—it only requires a blood draw and reaches high levels of reliability—might hinder women’s understanding that they should make a pe…

  • Factors of feasibility

    Open Access•Stefan F Vermeulen, Marjolijn Hordijk et al.•ARTICLE•Humanities and Social Sciences…•2021

    Seriously ill patients who have exhausted all approved treatment regimens and who cannot be enrolled in clinical trials may resort to expanded access programmes in order to gain access to unapproved, investigational drugs. It seems that in some countries, expanded access to investigational drugs is offered in clinical practice on a more routine basis than in other countries. This study is the first to investigate the experiences of physicians wit…

  • Prevention in the age of personal responsibility

    Open Access•Ineke Bolt, Eline M Bunnik et al.•ARTICLE•Journal of Medical Ethics•2021

    Epigenetic markers could potentially be used for risk assessment in risk-stratified population-based cancer screening programmes. Whereas current screening programmes generally aim to detect existing cancer, epigenetic markers could be used to provide risk estimates for not-yet-existing cancers. Epigenetic risk-predictive tests may thus allow for new opportunities for risk assessment for developing cancer in the future. Since epigenetic changes a…

  • The ‘false hope’ argument in discussions on expanded access to investigational drugs

    Open Access•Marjolijn Hordijk, Stefan F Vermeulen et al.•ARTICLE•Medicine Health Care and Philosophy•2022

    When seriously ill patients reach the end of the standard treatment trajectory for their condition, they may qualify for the use of unapproved, investigational drugs regulated via expanded access programs. In medical-ethical discourse, it is often argued that expanded access to investigational drugs raises ‘false hope’ among patients and is therefore undesirable. We set out to investigate what is meant by the false hope argument in this discourse…

  • Vulnerable person investigation plan (VIP) to optimise inclusion in clinical trials

    Ilana C Raburn, Eline M Bunnik et al.•ARTICLE•Journal of Medical Ethics•2023

    TEST 02 - Elsevier's Scopus, the largest abstract and citation database of peer-reviewed literature. Search and access research from the science, technology, medicine, social sciences and arts and humanities fields

  • Access to effective but expensive treatments

    Open Access•Sietske A L van Till, Jilles Smids et al.•ARTICLE•Bioethics•2023

    The development of new effective but expensive medical treatments leads to discussions about whether and how such treatments should be funded in solidarity‐based healthcare systems. Solidarity is often seen as an elusive concept; it appears to be used to refer to different sets of concerns, and its interrelations with the concept of justice are not well understood. This paper provides a conceptual analysis of the concept of solidarity as it is us…

  • Access to Non‐reimbursed Expensive Cancer Treatments

    Open Access•Jilles Smids, Eline M Bunnik•ARTICLE•Journal of Applied Philosophy•2024

    When the cost‐effectiveness of newly approved cancer treatments is insufficient or unclear, they may not (immediately) be eligible for reimbursement through basic health insurance in publicly funded healthcare systems. Patients may seek access to non‐reimbursed treatment through other channels, including individual funding requests made to hospitals, health insurers, or pharmaceutical companies. Alternatively, they may try to pay out of pocket fo…

  • ‘Empathy counterbalancing’ to mitigate the ‘identified victim effect’? Ethical reflections on cognitive debiasing strategies to increase support for healthcare priority setting

    Jilles Smids, Charlotte H C Bomhof et al.•ARTICLE•Journal of Medical Ethics•2025

    Priority setting is inevitable to control expenditure on expensive medicines, but citizen support is often hampered by the workings of the ‘identified victim effect’, that is, the greater willingness to spend resources helping identified victims than helping statistical victims. In this paper we explore a possible cognitive debiasing strategy that is being employed in discussions on healthcare priority setting, which we call ‘empathy counterbalan…

  • Changing the Child

    Open Access•Sietske A L van Till, Maartje H N Schermer et al.•ARTICLE•Bioethics•2026

    Scientific advancements offer new possibilities for developing novel treatments for children with monogenic neurodevelopmental disorders (mNDDs), targeting the underlying effects of their condition. Although, in qualitative studies, parents of children with mNDDs have predominantly positive attitudes towards the development of novel treatments, a few parents express concerns about whether treatments could change who their child is . Existing lite…

Medicine (9 obras) · Political science (7 obras) · Psychology (7 obras) · Law (6 obras) · Health Systems, Economic Evaluations, Quality of Life (5 obras) · Alternative medicine (4 obras) · Health care (4 obras) · Public relations (4 obras) · Biomedical Ethics and Regulation (3 obras) · Computer Science (3 obras)

Ethnos_APP • Projeto Open Source • Licença MIT • Frontend v2.0.0 • Privacidade e Cookies • Documentação da API: api.ethnos.app/docs • Código da API: GitHub • DOI: 10.5281/zenodo.17049435 • Código do Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae