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Ian Kerridge

Biographic Data

ID197628
NAMEIan Kerridge
GIVEN NAMESIan
FAMILY NAMEKerridge
SIGNATUREKERRIDGE I
AFFILIATIONSThe University of Sydney
ORCID0000-0001-7445-4660
VERIFIEDYes
TOTAL WORKS42
TOTAL CITATIONS61
AUTHOR COUNT42
EDITOR COUNT0
FIRST PUBLICATION YEAR2005
LATEST PUBLICATION YEAR2026
H-INDEX5
  • Evolution or erosion? Promissory discourses in ‘accelerated’ regulatory approval of health technologies

    Open Access•Sara Attinger, Ian Kerridge et al.•ARTICLE•BioSocieties•2026

    In recent years, regulatory processes governing the approval of new health technologies have undergone changes aimed at expediting access. Some of these changes involve the adaptation of established standards of evidence for safety and efficacy, which we refer to as evidence-adapted regulatory pathways (EARPs). While EARPs have provided more timely access to potentially beneficial interventions, critics argue that reducing evidentiary thresholds …

  • Paediatric Nurses’ Decision-Making About CPR in Challenging Clinical Scenarios: Insights From a Cross-Sectional Survey

    Open Access•Suzanne Bowdler, Judeil K Teus et al.•ARTICLE•Journal of Bioethical Inquiry•2026

    This study explored paediatric nurses’ decision-making regarding resuscitation in patients with unequivocal signs of death and no Do Not Resuscitate (DNR) order. A cross-sectional survey was conducted between October 2023 and April 2024 across the paediatric wards of four Australian hospitals. Participants were asked to respond to two hypothetical clinical scenarios involving a three-year-old boy and a twelve-year-old girl, both clearly deceased—…

  • Stakeholder perspectives regarding single participant research in oncology

    Open Access•Sarah Heynemann, Wendy Lipworth et al.•ARTICLE•Research Ethics•2026

    The term ‘N-of-1 trial’ has traditionally referred to a specific, well-defined, clinical trial methodology, involving evaluation of an intervention (or interventions) in a single individual, with alternating periods ‘on’ and ‘off’ an intervention. Given methodological constraints, such trials are best suited to the study of chronic, stable conditions, and so have had a limited role in progressive conditions like cancer. According to evidence-base…

  • The ‘power of 1’: The ethics and epistemology of ‘N-of-1 trials’ in oncology

    Open Access•Sarah Heynemann, Wendy Lipworth et al.•ARTICLE•Research Ethics•2026

    Conduct of clinical research involving single patient subjects has a relatively long history. The notion of ‘N-of-1 trials’ first emerged in the 1980s, introducing a method for evaluating the impact of alternately exposing individuals ‘on’ and ‘off’ a particular treatment. In the years since, interest in conventional, randomised, ‘N-of-1 trials’ has fluctuated, though recent advancements in data science, remote monitoring technologies and, more b…

  • Understanding “interests”: Historical insights for managing conflicts of interest in healthcare and biomedical science

    Open Access•Miriam Wiersma, Ian Kerridge et al.•ARTICLE•Medicine Health Care and Philosophy•2025

    Conflicts of interest are widely regarded as being morally, socially, and scientifically problematic in the many sectors, including in the health sector. There has been considerable attention paid to managing conflicts of interest in clinical practice, medical research and health policy through strategies such as recusal, disinvestment, and disclosure. While these efforts have been important, they are often based on a superficial account of “inte…

  • Attitudes to End-of-Life Care and Voluntary Assisted Dying Amongst Members of the Australian Jewish community

    Open Access•Eli W Janover, Camille La Brooy et al.•ARTICLE•Journal of Religion and Health•2025

    The implementation of voluntary assisted dying (VAD) in the Australian State of Victoria in 2019 has stimulated discussions about end-of-life care and dying in many communities. Various attempts have been made to represent the attitudes of the Jewish community, a distinct culturally and linguistically diverse (CALD) group, in terms that suggest a unified set of opinions that opposes VAD policies. This research aimed to explore attitudes to VAD in…

  • Therapeutic misunderstandings in modern research

    Open Access•Sarah Heynemann, Wendy Lipworth et al.•ARTICLE•Bioethics•2024

    Clinical trials play a crucial role in generating evidence about healthcare interventions and improving outcomes for current and future patients. For individual trial participants, however, there are inevitably trade‐offs involved in clinical trial participation, given that trials have traditionally been designed to benefit future patient populations rather than to offer personalised care. Failure to understand the distinction between research an…

  • Choreographing a good death: Carers' experiences and practices of enacting assisted dying

    Open Access•Sophie Lewis, Camille La Brooy et al.•ARTICLE•Sociology of Health & Illness•2024•Cited by: 5•References: 9

    The proliferation of assisted dying legislative reforms globally is a significant change in the social and medico-legal landscape of end-of-life care. Understanding the impacts of these legislative reforms on family members who care for a dying person is vital, yet under-theorised in research. In this article, drawing on semi-structured interviews with 42 carers for a person who has sought assisted dying in Australia, and extending ideas of ontol…

  • Clinical innovation ethics frameworks: A systematic narrative review

    Open Access•Miriam Wiersma, Ian Kerridge et al.•ARTICLE•Health Policy•2023

  • The silent world of assisted reproduction: A qualitative account of communication between doctors and patients undergoing in vitro fertilisation in Australia

    Open Access•Louis Taffs, Ian Kerridge et al.•ARTICLE•Health Expectations•2023

    CONTEXT: In vitro fertilisation (IVF) is now a common assisted reproductive technology (ART) procedure globally, with 8 million children alive today having been conceived utilising IVF. For many patients, IVF is a difficult experience with many discontinuing treatment because of emotional, relationship and financial stress, or intolerable physical side effects of hormone treatments. DESIGN AND PARTICIPANTS: A qualitative study, in which 31 profes…

  • Predictors of post traumatic growth in allogeneic hematopoietic stem cell transplantation survivors: A cross-sectional survey

    Open Access•Gemma McErlean, Caley Tapp et al.•ARTICLE•BMC Psychology•2023

    In this study - the largest study of PTG in long-term allogeneic HSCT survivors - we found that growth appears ubiquitous, with 99% of survivors reporting some degree of PTG and 67% reporting moderate-high levels of PTG. Importantly, we found no association with GVHD or chronic physical post-HSCT morbidity, or adverse financial, occupational or sexual impacts. This suggests that it is the necessity for and experience of, HSCT itself that foments …

  • Raising the Dead? Limits of CPR and Harms of Defensive Practices

    Open Access•George Skowronski, Ian Kerridge et al.•ARTICLE•The Hastings Center Report•2022

    We describe the case of an eighty‐four‐year‐old man with disseminated lung cancer who had been receiving palliative care in the hospital and was found by nursing staff unresponsive, with clinically obvious signs of death, including rigor mortis. Because there was no documentation to the contrary, the nurses commenced cardiopulmonary resuscitation and called a code blue, resulting in resuscitative efforts that continued for around twenty minutes. …

  • Are my religious beliefs anyone’s business? A framework for declarations in health and biomedicine

    Narcyz Ghinea, Miriam Wiersma et al.•ARTICLE•Journal of Medical Ethics•2021

    Conflicts of interests (COI) are typically divided into those that are financial and those that are not. While there is general agreement that financial COIs have a significant impact on decisions and need to be declared and managed, the status of non-financial COIs continues to be disputed. In a recent BMJ feature article it was proposed that religious beliefs should be routinely declared as an interest. The article generated over 41 responses f…

  • A survey of Australian public attitudes towards funding of high cost cancer medicines

    Open Access•Narcyz Ghinea, Christine Critchley et al.•ARTICLE•Health Policy•2021

  • Examining diversity in public willingness to participate in offshore human biobanking: An Australian mixed methods study

    Open Access•Christine Critchley, Miriam Wiersma et al.•ARTICLE•Public Understanding of Science•2020

    To ensure their sustainability and scientific utility, human biobanks are networking internationally. Sharing biospecimens and associated data across jurisdictions raise a number of practical, ethical, legal and social challenges that could reduce the publics’ willingness to donate their much needed tissue for research purposes. This research aims to identify the impact of biobank location on willingness to donate through a national quantitative …

  • Treat them into the grave: Cancer Physicians' Attitudes Towards the Use of High-Cost Cancer Medicines at the End of Life

    Open Access•Miriam Wiersma, Narcyz Ghinea et al.•ARTICLE•Sociology of Health & Illness•2019•Cited by: 2•References: 55

    The prescribing of high-cost cancer medicines at the end of life has become a focus of criticism, due primarily to concerns about the safety, efficacy and cost-effectiveness of these medicines in this clinical context. In response to these concerns, a number of interventions have been proposed - frequently focused on improving physician-patient communication at the end of life. Underpinning these strategies is the assumption that the prescribing …

  • Religious Perspectives on Human Suffering: Implications for Medicine and Bioethics

    Open Access•Scott J Fitzpatrick, Ian Kerridge et al.•ARTICLE•Journal of Religion and Health•2016

  • Conflicts of interest in neoliberal times: Perspectives of Australian medical students

    C Mayes, Ian Kerridge et al.•ARTICLE•Health Sociology Review•2016•References: 44

    In this paper we report on the findings from six focus groups conducted with Australian medical students. The focus groups discussed students’ perceptions of conflicts of interest and the influence of commercial values in health care and medical education. Our research revealed that students were aware of a number of structural influences that affected the medical education they received and that had the potential to shape their attitudes and pra…

  • Overcoming Entrenched Disagreements: The Case of Misoprostol for Post‐Partum Haemorrhage

    Open Access•Narcyz Ghinea, Wendy Lipworth et al.•ARTICLE•Developing World Bioethics•2015

    The debate about whether misoprostol should be distributed to low resource communities to prevent post‐partum haemorrhage ( PPH ), recognised as a major cause of maternal mortality, is deeply polarised. This is in spite of stakeholders having access to the same evidence about the risks and benefits of misoprostol. To understand the disagreement, we conducted a qualitative analysis of the values underpinning debates surrounding community distribut…

  • Implementing a One Health approach to emerging infectious disease: Reflections on the socio-political, ethical and legal dimensions

    Open Access•Chris Degeling, Jane Johnson et al.•ARTICLE•BMC Public Health•2015

    Based on the philosophical review and critical analysis of scholarship around the theory and practice of One Health it is clear that EID events are not simply about pathogens jumping species barriers; they are comprised of complex and contingent sets of relations that involve socioeconomic and socio-political drivers and consequences with the latter extending beyond the impact of the disease. Therefore, the effectiveness of policies based on One …

  • Manifesto on Art, Design and Social Science—Method as Speculative Event

    Mike Michael, Brigid Costello et al.•ARTICLE•Leonardo•2015•References: 3

    The authors propose that techniques from art and design can be used within social science research as part of a speculative methodology and provide a set of heuristic principles for speculative method, characterizing it as processual, performative, playful, promising and propositional

  • Liminal Reproductive Experiences After Therapies for Hematological Malignancy

    Open Access•Lesley E Halliday, Lesley Halliday et al.•ARTICLE•Qualitative Health Research•2015•Cited by: 5•References: 41

    In this article, we discuss the psychosocial health of young women related to fertility, pregnancy, and motherhood after therapies for hematological malignancies. We utilized a hermeneutical phenomenological approach to conduct in-depth interviews with 12 women who had previously received treatment for a hematological malignancy and had experienced uncertainty surrounding their ability to start or extend their biological family. Our presented fin…

  • Ethics & Evidence in Medical Debates: The Case of Recombinant Activated Factor VII

    Open Access•Narcyz Ghinea, Wendy Lipworth et al.•ARTICLE•The Hastings Center Report•2014

    While ethics and evidence‐based medicine are often viewed as separate domains of inquiry and practice, what we know influences what we can ethically justify doing, and what we see as our moral obligations shapes the way we interpret evidence. The boundaries between the moral and epistemic spheres become particularly blurred when the health of people is at stake and even more so when no “officially” recommended medical intervention is available to…

  • Religious Perspectives on the Use of Psychopharmaceuticals as an Enhancement Technology

    Open Access•Scott J Fitzpatrick, Christopher F C Jordens et al.•ARTICLE•Journal of Religion and Health•2014

  • Manifesto on Art, Design and Social Science - Method as Speculative Event

    Mike Michael, Brigid Costello et al.•ARTICLE•Leonardo•2014•References: 3

    The authors propose that techniques from art and design can be used within social science research as part of a speculative methodology and provide a set of heuristic principles for speculative method, characterizing it as processual, performative, playful, promising and propositional

Next
  • From altruism to monetisation: Australian women's ideas about money, ethics and research eggs

    Open Access•Catherine Waldby, Ian Kerridge et al.•ARTICLE•Social Science & Medicine•2013•Cited by: 10•References: 26

  • Evidence, Ethics, and Values: A Framework for Health Promotion

    Stacy M Carter, Lucie Rychetnik et al.•ARTICLE•American Journal of Public Health•2011•Cited by: 10•References: 65

    We propose a new approach to guide health promotion practice. Health promotion should draw on 2 related systems of reasoning: an evidential system and an ethical system. Further, there are concepts, values, and procedures inherent in both health promotion evidence and ethics, and these should be made explicit. We illustrate our approach with the exemplar of intervention in weight, and use a specific mass-media campaign to show the real-world dang…

  • Hendra in the news: Public policy meets public morality in times of zoonotic uncertainty

    Open Access•Chris Degeling, Ian Kerridge•ARTICLE•Social Science & Medicine•2013•Cited by: 7•References: 28

  • Rules of engagement: Journalists’ attitudes to industry influence in health news reporting

    Open Access•Bronwen Morrell, Rowena Forsyth et al.•ARTICLE•Journalism•2014•Cited by: 6•References: 18

    Health-related industries use a variety of methods to influence health news, including the formation and maintenance of direct relationships with journalists. These interactions have the potential to subvert news reporting such that it comes to serve the interests of industry in promoting their products, rather than the public interest in critical and accurate news and information. Here, we report the findings of qualitative interviews conducted …

  • Empirical uncertainty and moral contest: A qualitative analysis of the relationship between medical specialists and the pharmaceutical industry in Australia

    Open Access•Evan Doran, Ian Kerridge et al.•ARTICLE•Social Science & Medicine•2006•Cited by: 6•References: 14

  • Choreographing a good death: Carers' experiences and practices of enacting assisted dying

    Open Access•Sophie Lewis, Camille La Brooy et al.•ARTICLE•Sociology of Health & Illness•2024•Cited by: 5•References: 9

    The proliferation of assisted dying legislative reforms globally is a significant change in the social and medico-legal landscape of end-of-life care. Understanding the impacts of these legislative reforms on family members who care for a dying person is vital, yet under-theorised in research. In this article, drawing on semi-structured interviews with 42 carers for a person who has sought assisted dying in Australia, and extending ideas of ontol…

  • Liminal Reproductive Experiences After Therapies for Hematological Malignancy

    Open Access•Lesley E Halliday, Lesley Halliday et al.•ARTICLE•Qualitative Health Research•2015•Cited by: 5•References: 41

    In this article, we discuss the psychosocial health of young women related to fertility, pregnancy, and motherhood after therapies for hematological malignancies. We utilized a hermeneutical phenomenological approach to conduct in-depth interviews with 12 women who had previously received treatment for a hematological malignancy and had experienced uncertainty surrounding their ability to start or extend their biological family. Our presented fin…

  • Journal peer review in context: A qualitative study of the social and subjective dimensions of manuscript review in biomedical publishing

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Social Science & Medicine•2011•Cited by: 4•References: 3

  • Pragmatic pluralism: Mutual tolerance of contested understandings between orthodox and alternative practitioners in autologous stem cell transplantation

    Open Access•Miles Little, Christopher F C Jordens et al.•ARTICLE•Social Science & Medicine•2007•Cited by: 3•References: 29

  • Treat them into the grave: Cancer Physicians' Attitudes Towards the Use of High-Cost Cancer Medicines at the End of Life

    Open Access•Miriam Wiersma, Narcyz Ghinea et al.•ARTICLE•Sociology of Health & Illness•2019•Cited by: 2•References: 55

    The prescribing of high-cost cancer medicines at the end of life has become a focus of criticism, due primarily to concerns about the safety, efficacy and cost-effectiveness of these medicines in this clinical context. In response to these concerns, a number of interventions have been proposed - frequently focused on improving physician-patient communication at the end of life. Underpinning these strategies is the assumption that the prescribing …

  • Risk, rationality, and regret: Responding to the uncertainty of childhood food anaphylaxis

    Wendy Hu, Ian Kerridge et al.•ARTICLE•Medical Humanities•2005•Cited by: 2•References: 6

    Risk and uncertainty are unavoidable in clinical medicine. In the case of childhood food allergy, the dysphoric experience of uncertainty is heightened by the perception of unpredictable danger to young children. Medicine has tended to respond to uncertainty with forms of rational decision making. Rationality cannot, however, resolve uncertainty and provides an insufficient account of risk. This paper compares the medical and parental accounts of…

  • Cancergazing? CA125 and post-treatment surveillance in advanced ovarian cancer

    Open Access•Christopher F C Jordens, Bronwen Morrell et al.•ARTICLE•Social Science & Medicine•2010•Cited by: 1•References: 5

  • Religious perspectives on withdrawal of treatment from patients with multiple organ failure

    Open Access•Rachel A Ankeny, Christopher F C Jordens et al.•ARTICLE•The Medical Journal of Australia•2005

    Religious or spiritual values often influence health care decision-making by patients and their families, particularly in times of crisis. Though religious values might seem to be irrelevant where continuing treatment is judged to be "futile", such clinical assessments should instead serve to open a dialogue about values and beliefs. The six major religious traditions in Australia have some similar values and principles about death and provision …

  • Risk, rationality, and regret: Responding to the uncertainty of childhood food anaphylaxis

    Wendy Hu, Ian Kerridge et al.•ARTICLE•Medical Humanities•2005•Cited by: 2•References: 6

    Risk and uncertainty are unavoidable in clinical medicine. In the case of childhood food allergy, the dysphoric experience of uncertainty is heightened by the perception of unpredictable danger to young children. Medicine has tended to respond to uncertainty with forms of rational decision making. Rationality cannot, however, resolve uncertainty and provides an insufficient account of risk. This paper compares the medical and parental accounts of…

  • Taking the Oath in the Twenty-First Century

    Open Access•Ian Kerridge•ARTICLE•Metascience•2006

  • Empirical uncertainty and moral contest: A qualitative analysis of the relationship between medical specialists and the pharmaceutical industry in Australia

    Open Access•Evan Doran, Ian Kerridge et al.•ARTICLE•Social Science & Medicine•2006•Cited by: 6•References: 14

  • Pragmatic pluralism: Mutual tolerance of contested understandings between orthodox and alternative practitioners in autologous stem cell transplantation

    Open Access•Miles Little, Christopher F C Jordens et al.•ARTICLE•Social Science & Medicine•2007•Cited by: 3•References: 29

  • Religious Perspectives on Abortion and a Secular Response

    Open Access•Moira Stephens, Christopher F C Jordens et al.•ARTICLE•Journal of Religion and Health•2010

  • Cancergazing? CA125 and post-treatment surveillance in advanced ovarian cancer

    Open Access•Christopher F C Jordens, Bronwen Morrell et al.•ARTICLE•Social Science & Medicine•2010•Cited by: 1•References: 5

  • Tissue donation to biobanks: A review of sociological studies

    Open Access•Wendy Lipworth, Claudio Corvino et al.•ARTICLE•Sociology of Health & Illness•2011

    Collections of human tissue (biobanks) are thought to be an essential resource for biomedical research. Biobanks have, however, been a source of debate in both bioethics and sociology. In recent years this theorising has been supplemented with empirical research, including a significant body of qualitative research, into donors’ experiences and attitudes. To date, this literature has not been synthesised. We report the findings of a review of qua…

  • Journal peer review in context: A qualitative study of the social and subjective dimensions of manuscript review in biomedical publishing

    Open Access•Wendy L Lipworth, Wendy Lipworth et al.•ARTICLE•Social Science & Medicine•2011•Cited by: 4•References: 3

  • Evidence, Ethics, and Values: A Framework for Health Promotion

    Stacy M Carter, Lucie Rychetnik et al.•ARTICLE•American Journal of Public Health•2011•Cited by: 10•References: 65

    We propose a new approach to guide health promotion practice. Health promotion should draw on 2 related systems of reasoning: an evidential system and an ethical system. Further, there are concepts, values, and procedures inherent in both health promotion evidence and ethics, and these should be made explicit. We illustrate our approach with the exemplar of intervention in weight, and use a specific mass-media campaign to show the real-world dang…

  • Cancer as Rubbish: Donation of Tumor Tissue for Research

    Open Access•Bronwen Morrell, Wendy Lipworth et al.•ARTICLE•Qualitative Health Research•2011•References: 37

    Tissue banking (or biobanking), thought by many to be an essential form of medical research, has raised a number of ethical issues that highlight a need to understand the beliefs and values of tissue donors, including the motivations underlying consent or refusal to donate. Data from our qualitative study of the legal, social, and ethical issues surrounding tumor banking in New South Wales, Australia, show that participants' attitudes to donation…

  • Decision Making in a Crowded Room: The Relational Significance of Social Roles in Decisions to Proceed With Allogeneic Stem Cell Transplantation

    Open Access•Rowena Forsyth, Camilla Scanlan et al.•ARTICLE•Qualitative Health Research•2011•References: 41

    Researchers studying health care decision making generally focus on the interaction that unfolds between patients and health professionals. Using the example of allogeneic bone marrow transplant, in this article we identify decision making to be a relational process concurrently underpinned by patients' engagement with health professionals, their families, and broader social networks. We argue that the person undergoing a transplant simultaneousl…

  • Rhetoric, power and legitimacy: A critical analysis of the public policy disputes surrounding stem cell research in Australia (2005–6)

    Open Access•Tamra Lysaght, Ian Kerridge•ARTICLE•Public Understanding of Science•2012

    In December 2006, the Australian Parliament liberalized regulation governing stem cell research. This decision and preceding legislative review generated considerable public debate, which centred on objections to the deliberate creation and destruction of human embryos for research purposes. This paper draws on qualitative research conducted on the public debate surrounding this policy episode. The aim of this research was to examine how science …

  • Mothering and Self-Othering: The Impact of Uncertain Reproductive Capability in Young Women After Hematological Malignancy

    Lesley E Halliday, Lesley Halliday et al.•ARTICLE•Health Care For Women International•2013

    We explored the experiences of uncertain fertility, pregnancy, and motherhood in 12 young women treated for hematological malignancy during their reproductive years. It is demonstrated how, through interpretations of the women's own words, these women lived and coped with a sense of "otherness" in relation to their peers. The concept of otherness is described and discussed in relation to relevant existing literature and it is concluded that, rega…

  • Hendra in the news: Public policy meets public morality in times of zoonotic uncertainty

    Open Access•Chris Degeling, Ian Kerridge•ARTICLE•Social Science & Medicine•2013•Cited by: 7•References: 28

  • From altruism to monetisation: Australian women's ideas about money, ethics and research eggs

    Open Access•Catherine Waldby, Ian Kerridge et al.•ARTICLE•Social Science & Medicine•2013•Cited by: 10•References: 26

  • Ethics & Evidence in Medical Debates: The Case of Recombinant Activated Factor VII

    Open Access•Narcyz Ghinea, Wendy Lipworth et al.•ARTICLE•The Hastings Center Report•2014

    While ethics and evidence‐based medicine are often viewed as separate domains of inquiry and practice, what we know influences what we can ethically justify doing, and what we see as our moral obligations shapes the way we interpret evidence. The boundaries between the moral and epistemic spheres become particularly blurred when the health of people is at stake and even more so when no “officially” recommended medical intervention is available to…

  • Religious Perspectives on the Use of Psychopharmaceuticals as an Enhancement Technology

    Open Access•Scott J Fitzpatrick, Christopher F C Jordens et al.•ARTICLE•Journal of Religion and Health•2014

  • Manifesto on Art, Design and Social Science - Method as Speculative Event

    Mike Michael, Brigid Costello et al.•ARTICLE•Leonardo•2014•References: 3

    The authors propose that techniques from art and design can be used within social science research as part of a speculative methodology and provide a set of heuristic principles for speculative method, characterizing it as processual, performative, playful, promising and propositional

  • Rules of engagement: Journalists’ attitudes to industry influence in health news reporting

    Open Access•Bronwen Morrell, Rowena Forsyth et al.•ARTICLE•Journalism•2014•Cited by: 6•References: 18

    Health-related industries use a variety of methods to influence health news, including the formation and maintenance of direct relationships with journalists. These interactions have the potential to subvert news reporting such that it comes to serve the interests of industry in promoting their products, rather than the public interest in critical and accurate news and information. Here, we report the findings of qualitative interviews conducted …

  • Overcoming Entrenched Disagreements: The Case of Misoprostol for Post‐Partum Haemorrhage

    Open Access•Narcyz Ghinea, Wendy Lipworth et al.•ARTICLE•Developing World Bioethics•2015

    The debate about whether misoprostol should be distributed to low resource communities to prevent post‐partum haemorrhage ( PPH ), recognised as a major cause of maternal mortality, is deeply polarised. This is in spite of stakeholders having access to the same evidence about the risks and benefits of misoprostol. To understand the disagreement, we conducted a qualitative analysis of the values underpinning debates surrounding community distribut…

  • Implementing a One Health approach to emerging infectious disease: Reflections on the socio-political, ethical and legal dimensions

    Open Access•Chris Degeling, Jane Johnson et al.•ARTICLE•BMC Public Health•2015

    Based on the philosophical review and critical analysis of scholarship around the theory and practice of One Health it is clear that EID events are not simply about pathogens jumping species barriers; they are comprised of complex and contingent sets of relations that involve socioeconomic and socio-political drivers and consequences with the latter extending beyond the impact of the disease. Therefore, the effectiveness of policies based on One …

  • Manifesto on Art, Design and Social Science—Method as Speculative Event

    Mike Michael, Brigid Costello et al.•ARTICLE•Leonardo•2015•References: 3

    The authors propose that techniques from art and design can be used within social science research as part of a speculative methodology and provide a set of heuristic principles for speculative method, characterizing it as processual, performative, playful, promising and propositional

  • Liminal Reproductive Experiences After Therapies for Hematological Malignancy

    Open Access•Lesley E Halliday, Lesley Halliday et al.•ARTICLE•Qualitative Health Research•2015•Cited by: 5•References: 41

    In this article, we discuss the psychosocial health of young women related to fertility, pregnancy, and motherhood after therapies for hematological malignancies. We utilized a hermeneutical phenomenological approach to conduct in-depth interviews with 12 women who had previously received treatment for a hematological malignancy and had experienced uncertainty surrounding their ability to start or extend their biological family. Our presented fin…

  • Religious Perspectives on Human Suffering: Implications for Medicine and Bioethics

    Open Access•Scott J Fitzpatrick, Ian Kerridge et al.•ARTICLE•Journal of Religion and Health•2016

Political science (26 works) · Medicine (25 works) · Psychology (24 works) · Law (20 works) · Sociology (19 works) · Public relations (13 works) · Social Psychology (11 works) · Nursing (10 works) · Ethics in medical practice (8 works) · Business (7 works)

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