ORCID Profile
0000-0002-0784-3954
Current Organisations
Queensland University of Technology
,
Queensland University of Technology Faculty of Law
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Medical Devices | Biomaterials | Biomedical Engineering |
Manufacturing not elsewhere classified | Expanding Knowledge in the Medical and Health Sciences
Publisher: Oxford University Press
Date: 04-2019
DOI: 10.1093/MED/9780190851361.001.0001
Abstract: This volume brings together original essays exploring the intersections of clinical practice, policy, and bioethics in women’s healthcare. Including but moving beyond the familiar theme of reproduction, it aims to both broaden areas of scholarship in feminist bioethics and to respond to ethical challenges that many women experience in accessing healthcare. Some of the contributions overlap with concerns that feminist scholars have voiced in the past, such as the medicalization of women’s bodies, but address new procedures (e.g., female cosmetic genital surgery). Other chapters expand into new fields that are underexplored in the bioethics literature, such as ethical issues concerning the care of Indigenous women, uninsured refugees and immigrants, women engaged in sex work, and those with HIV and perinatal mental health disorders. The richness of the collection lies in the multitude of disciplines represented. Contributors range from those who are in active clinical practice—medicine, nursing, and ethics—to philosophers contemplating new conceptual issues. Topical and contemporary, this book provides a valuable resource for physicians, nurses, clinical ethicists, and researchers working in the areas of women’s health and applied ethics.
Publisher: SAGE Publications
Date: 06-04-2023
DOI: 10.1177/0067205X231165872
Abstract: Legal and political battles about health policy in the immediate post-war years have cast a long shadow in Australia. The ‘civil conscription’ sub-provision in s 51(xxiiiA) (health and welfare power) of the Australian Constitution is still cited as a major barrier to developing health policy. But long after the High Court moved on from a very restrictive interpretation of Commonwealth powers, policymakers appear to be cautious about testing whether the Commonwealth has power to make laws about medical services to pursue a bold agenda about access, quality, and efficiency of medical care. In this article we will first describe the origin and phrasing of s 51(xxiiiA), the main head of power, then trace the development of the interpretation of the civil conscription sub-provision, and finally discuss whether politically realistic policy options are likely to founder on the shoals of High Court interpretation. We argue that the civil conscription limitation in s 51 (xxiiiA) in the Constitution looms larger as a policy constraint on regulation of health care by the Commonwealth government in the minds of decision-makers, and as a weapon in the hands of stakeholders, than contemporary analysis of it warrants.
Publisher: Elsevier BV
Date: 05-2018
DOI: 10.1016/J.IJLP.2018.04.001
Abstract: Since the introduction of the Convention on the Rights of Persons with Disabilities (2006) (CRPD), there have been calls to establish standards to measure compliance of domestic mental health laws with the human rights outlined in the CRPD. This article aims to address this gap by proposing a tool: the Analysis Instrument for Mental health (AIM). In particular, the tool's purpose is to enable states and civil society to assess the compliance of non-forensic domestic mental health laws with Article 12 of the CRPD. It responds to Dawson's (2015) call for a mechanism designed to provide clear and measurable standards for which to undertake this exercise. The content of AIM draws directly from the authoritative interpretation of Article 12 provided by the United Nations Committee on the Rights of Persons with Disabilities (the Committee) in its General Comment, as well as the substantial body of academic and other literature about Article 12.
Publisher: Informa UK Limited
Date: 02-01-2016
Publisher: Springer International Publishing
Date: 2017
Publisher: SAGE Publications
Date: 09-2023
Publisher: AMPCo
Date: 22-02-2021
DOI: 10.5694/MJA2.50952
Publisher: WHO Press
Date: 12-05-2017
Publisher: Queensland University of Technology
Date: 11-03-2016
Abstract: style="margin: 0cm 0cm 10pt text-align: justify line-height: normal " span style="font-family: 'Times New Roman',serif font-size: 12pt mso-bidi-font-size: 11.0pt " lang="EN-AU" em The International Conference on End of Life: Law, Ethics, Policy and Practice was held at Queensland University of Technology, Brisbane, Australia in August 2014. It was co-hosted by the Australian Centre for Health Law Research, the Dalhousie Health Law Institute (Canada) and the Tsinghua Health Law Research Center (China). The conference attracted almost 350 delegates from 26 countries and included representation from over a dozen different disciplines with an interest in end of life care. /em /span
Publisher: Springer Science and Business Media LLC
Date: 12-2015
Publisher: Springer Singapore
Date: 26-11-2022
Publisher: Informa UK Limited
Date: 07-2012
Publisher: Elsevier BV
Date: 06-2019
Publisher: Mary Ann Liebert Inc
Date: 06-2010
Publisher: Cambridge University Press (CUP)
Date: 06-04-2020
DOI: 10.1017/DMP.2020.37
Abstract: Disasters may impact air quality through the generation of high levels of potentially pathogenic particulate matter (PM), for ex le, in a volcanic eruption. Depending on the concentrations of particles in the air, their size and composition, and the duration of exposure, high levels of PM can create significant public health issues. It has been argued that air pollution, in and of itself, is a public health crisis. One possible intervention to reduce exposure to high levels of PM during an air pollution disaster (APD) is using facemasks. However, agencies may be reluctant to recommend or distribute facemasks for community use during APDs for a variety of reasons, including concerns about liability. There has been no analysis of these concerns. This paper analyzes whether agencies may have a legal duty of care in negligence to provide warnings about the health risks associated with APDs and/or to recommend facemasks as a protective mechanism for community use to reduce exposure to PM. It is also the first to examine the potential for liability in negligence, when a decision is made to distribute facemasks for community use during an APD and the receiver alleges that they sustained a personal injury and seeks compensation.
Publisher: Routledge
Date: 21-02-2021
Publisher: Mary Ann Liebert Inc
Date: 10-2020
Publisher: Springer Science and Business Media LLC
Date: 16-02-2016
DOI: 10.1007/S11673-016-9708-2
Abstract: Whilst the nature of human illness is not determined by time of day or day of week, we currently structure health service delivery around a five-day delivery model. At least one country is endeavouring to develop a systems-based approach to planning a transition from five- to seven-day healthcare delivery models, and some services are independently instituting program reorganization to achieve these ends as research, amongst other things, highlights increased mortality and morbidity for weekend and after-hours admissions to hospitals. In this article, we argue that this issue does not merely raise instrumental concerns but also opens up a normative ethical dimension, recognizing that clinical ethical dilemmas are impacted on and created by systems of care. Using health policy ethics, we critically examine whether our health services, as currently structured, are at odds with ethical obligations for patient care and broader collective goals associated with the provision of publicly funded health services. We conclude by arguing that a critical health policy ethics perspective applying relevant ethical values and principles needs to be included when considering whether and how to transition from five-day to seven-day models for health delivery.
Publisher: Mary Ann Liebert Inc
Date: 08-2019
Abstract: How do postgenomic innovations emerge and become legitimate? Proteomics, a frequently utilized postgenomic technology, provides a valuable case study of the sociotechnical strategies used by an emergent scientific field to establish its legitimacy and assert political power. Chief among these strategies is standard making, an inherently political process that requires examination through a critical social science lens. We report in this study an original case study from interviews with proteomics scientists and observations at conferences of the Human Proteome Organization and Australasian Proteomics Society over a 5-year period (2011-2015). The study contributes new knowledge on how an emerging postgenomic science uses standard-setting practices to politically legitimize a hitherto contested technology. Drawing on legitimacy theory, we show how proteomics scientists and organizations used standards as strategic tools to establish the legitimacy of this postgenomic field and affirm that proteomics can generate verifiable and reproducible results, thereby establishing it as a legitimate scientific field. Notably, legitimacy can be leveraged, at the same time, to maximize political power vis-à-vis other fields of science and as such embodies power relationships. These data collectively inform the broader context, in which postgenomic innovations emerge and legitimize, both technically and politically, through standards making. These findings have relevance for the design of next generation technology policies by demonstrating that standards are not "just" standards or neutral constructs but also tools to leverage political power of and by science and innovation actors, as shown in this case study of the emerging early phase of proteomics from 2011 to 2015.
Publisher: Springer Science and Business Media LLC
Date: 02-03-2023
DOI: 10.1007/S11673-023-10237-8
Abstract: Ethical perspectives on regional, rural, and remote healthcare often, understandably and importantly, focus on inequities in access to services. In this commentary, we take the opportunity to examine the implications of normalizing metrocentric views, values, knowledge, and orientations, evidenced by the recent (2022) New South Wales inquiry into health outcomes and access to hospital and health services in regional, rural and remote New South Wales, for contemporary rural governance and justice debates. To do this, we draw on the feminist inspired approach to rural health ethics involving analysis of power relationships developed by Simpson and McDonald and related ideas from critical health sociology. In presenting this analysis, we extend contemporary thought about spatial health inequities and structural violence.
Publisher: UPT Penerbitan Universitas Jember
Date: 27-06-2020
DOI: 10.19184/JSEAHR.V4I1.14088
Abstract: The right to health is included in United Nations (UN) Sustainable Development Goals (SDG) number 3, “Good health and well-being”. This goal aims to ensure healthy life and to promote well-being for all, at all ages. The SDGs, which build on the Millennial Development Goals (MDGs), provide a significant expansion to the development agenda. Inclusive development is part and parcel of the SDGs. Evidence-based policymaking studies provide explanations of normative and legitimate expectations for policymakers, namely, to use scientific evidence and specific indicators in their policymaking process. The right to health, as constructed, in evidence-based policymaking discourse is in contention. This paper addresses the various types of meaning Indonesian policymakers attach to the right to health through their discourses in norms of health policy. This study provides an analysis of discourses, regulatory analysis, and historical narratives (based on analysis of health regulations and newspaper articles) pertaining to evidence-informed policy in the health sector in Indonesia from 2009-2017. Our findings elucidate how the right to health manifests in the processes of evidence-based policymaking. We do so by way of a two-pronged analysis, i) discourse analysis at the macro level in Indonesia about the right to health as a norm and ii) health policymaking at the micro level, in the Indonesian district of Gunungkidul,within the region of Yogyakarta.
Publisher: Wiley
Date: 18-02-2021
Abstract: The role of local government in improving public health has been given legislative recognition in some Australian states. There is growing evidence of the positive role this statutory recognition has given to align local government efforts with state government health policy. Health in All Policies (HiAP) is a comprehensive approach to integrating public health, promoting components into a range of traditional local policies such as those relating to housing, transport and water. While much of the work internationally in HiAP has focused on urban populations, we argue that there are opportunities for rural and remote Australian local governments to use HiAP to respond to disparities in health outcomes amongst rural and remote Australian communities. We examine the Australian experiences with HiAP, the role for local governments and the future challenges and opportunities around the use of a HiAP approach to improve community health outcomes in rural and remote Australian communities.
Publisher: Springer Science and Business Media LLC
Date: 06-2008
Publisher: Maad Rayan Publishing Company
Date: 22-11-2018
Publisher: Mary Ann Liebert Inc
Date: 06-2016
Abstract: Proteomics is one of the pivotal next-generation biotechnologies in the current "postgenomics" era. Little is known about the ways in which innovative proteomics science is navigating the complex socio-political space between laboratory and society. It cannot be assumed that the trajectory between proteomics laboratory and society is linear and unidirectional. Concerned about public accountability and hopes for knowledge-based innovations, funding agencies and citizens increasingly expect that emerging science and technologies, such as proteomics, are effectively translated and disseminated as innovation in society. Here, we describe translation strategies promoted in the knowledge translation (KT) and science communication literatures and examine the use of these strategies within the field of proteomics. Drawing on data generated from qualitative interviews with proteomics scientists and ethnographic observation of international proteomics conferences over a 5-year period, we found that proteomics science incorporates a variety of KT strategies to reach knowledge users outside the field. To attain the full benefit of KT, however, proteomics scientists must challenge their own normative assumptions and approaches to innovation dissemination-beyond the current paradigm relying primarily on publication for one's scientific peers within one's field-and embrace the value of broader (interdisciplinary) KT strategies in promoting the uptake of their research. Notably, the Human Proteome Organization (HUPO) is paying increasing attention to a broader range of KT strategies, including targeted dissemination, integrated KT, and public outreach. We suggest that increasing the variety of KT strategies employed by proteomics scientists is timely and would serve well the omics system sciences community.
Location: Australia
Start Date: 03-2017
End Date: 09-2021
Amount: $3,722,989.00
Funder: Australian Research Council
View Funded Activity