Written by Naincy Rani
Published in Vol 5 Issue 1, 2025
Delivering high-quality healthcare in today’s multicultural society requires that healthcare professionals are skilled in addressing cultural and religious differences in patient care. Despite this need, medical education often falls short in providing adequate cultural competence training, especially regarding care for Muslim patients. To address this gap, we developed an innovative educational program aimed at enhancing medical students’ intercultural skills, with a focus on caring for Muslim
Written by Orhan Ersin Silik
Published in Vol 5 Issue 1, 2025
Artificial intelligence (AI), including large language models (LLMs), holds significant promise for oncology, yet the extent of medical oncologists’ knowledge, attitudes, and ethical concerns regarding AI is not well understood. This issue is especially pertinent in Türkiye, home to roughly 1,340 practicing oncologists. We conducted an online, cross-sectional survey through the Turkish Society of Medical Oncology from October 16 to November 27, 2024. The questionnaire collected information on de
Written by Hadi M Salem
Published in Vol 5 Issue 1, 2025
Providing care for patients with anorexia nervosa (AN) often generates significant moral distress for healthcare professionals. Central to this distress is the ethical tension between enforcing treatment to prevent severe outcomes, such as premature death, and honoring patients’ refusals of care. Despite its relevance, empirical research on this moral conflict remains limited. We examined all 19 documented ethics consultations (ECs) related to AN from a single clinical ethics support service in
Written by Afreen Jannath
Published in Vol 5 Issue 1, 2025
Throughout history, epidemics have often been accompanied by stigma, prejudice, and xenophobic attitudes. This scoping review sought to examine and map the existing literature on ethical considerations related to monkeypox (mpox) and to identify gaps in research regarding stigma associated with the disease. A thorough search was conducted across multiple databases, including PubMed Central, PubMed Medline, Scopus, Web of Science, Ovid, and Google Scholar, covering the period from May 6, 2022, to
Written by Delyse Leadbeatter
Published in Vol 5 Issue 1, 2025
Around the world, the use of genetic test results in insurance underwriting has raised serious concerns, leading many countries to restrict or ban the practice. In contrast, Australian life insurers are legally permitted to consider genetic information, under rules set by the industry itself through the Financial Services Council (FSC). A 2018 Parliamentary Inquiry recommended prohibiting this practice, and in 2019 the FSC responded with a self-imposed moratorium. Because there is no government
Written by Anna S. Nazzal
Published in Vol 5 Issue 1, 2025
Understanding patient rights is essential for promoting ethical medical practice and upholding human rights in healthcare. Previous research indicates that patients’ awareness of their rights varies widely. This study aimed to evaluate the level of awareness of patient rights among individuals in Palestine and to examine healthcare professionals’ adherence to these rights. A cross-sectional survey was carried out from November 2023 to January 2024 across cities in the Northern West Bank. Data we
Written by Sarah Tutticci
Published in Vol 5 Issue 1, 2025
Globally, healthcare is a major source of greenhouse gas emissions, intensifying the ongoing climate emergency. While strategies to cut emissions are being introduced across health systems, the degree to which environmental sustainability should influence clinical decision-making at the level of individual practitioners remains uncertain. To investigate this question, we carried out a systematic review of published arguments both supporting and opposing the integration of environmental considera
Written by Triantafillos Smith
Published in Vol 5 Issue 1, 2025
This article critically examines the ethical challenges associated with physicians’ public commentary on high-profile medical cases, using the recent cancer diagnoses within the British royal family as an illustrative case study. Such cases inevitably attract substantial public attention and media scrutiny, creating tension between legitimate public interest and the fundamental ethical obligations of the medical profession. The paper analyzes this issue through the lens of the core principles of
Written by Vanessa Machado
Published in Vol 5 Issue 1, 2025
People living with severe and persistent mental illness (SPMI) constitute a small yet highly vulnerable group within mental health care. Their care raises complex ethical challenges due to factors such as the intensity of their conditions, limited social support, communication difficulties, impaired decision-making, and, occasionally, disruptive behaviors. Despite these challenges, research on ethical issues in this population remains limited. This study explores the ethical considerations invol
Written by Nisha Gurung
Published in Vol 5 Issue 1, 2025
Compulsory treatments legally mandate care for individuals—typically those with mental disorders—who refuse therapeutic interventions and pose a danger to themselves or others. Compulsory outpatient treatment (COT), also called a community treatment order, extends this involuntary care from hospital settings into the community. Although implemented in over 75 jurisdictions globally, COT remains one of the most debated practices in psychiatry and raises significant ethical concerns. Despite exten
Written by Abdul Rahman
Published in Vol 5 Issue 1, 2025
This study examines the functioning of a Bioethics Unit (BU) five years after its launch (2016–2020), combining quantitative metrics with qualitative insights. The BU operates as a dedicated research center, investigating ethical challenges in clinical practice, offering ethics consultations, and delivering training programs for health care professionals (HPs). We employed a sequential mixed-methods design, starting with quantitative analysis followed by qualitative exploration to contextualize
Written by Aung Kyaw Moe
Published in Vol 5 Issue 1, 2025
Ethics consultations provide a structured avenue for sharing responsibility in complex decision-making scenarios in prenatal medicine, particularly when moral instincts alone cannot yield a clear course of action. Nevertheless, it remains uncertain whether the conventional frameworks for ethics consultation are fully applicable to the uniquely sensitive context of pregnancy. This study examines the distinctive types of disagreements, ethical conflicts, and value uncertainties that arise in prena
Written by Meilin Wong
Published in Vol 5 Issue 1, 2025
Research institutions in North East (NE) India provide very little publicly available information about their institutional ethics committees (IECs) or the standard operating procedures (SOPs) that guide them. To address this gap, a review was carried out across fourteen biomedical and health research institutes in the region. Only twelve of these had formally created IECs. These committees drew members from varied professional backgrounds and sectors, yet only eight institutions demonstrated ag
Written by Mohammad Rizwan
Published in Vol 5 Issue 1, 2025
Assessing decision-making competence in transgender and gender-diverse adolescents is a complex task, as care in this area involves supporting a developing gender identity and making decisions about treatments that often lack international agreement. Even when competence assessments are performed, moral dilemmas can arise during the decision-making process. Traditional clinical ethics support approaches, such as moral case deliberation, may be insufficient because they do not provide thematic gu
Written by Nurlina Hamzah
Published in Vol 5 Issue 1, 2025
In recent decades, the role of ethics in health research has gained global recognition. However, institutional review boards (IRBs) are sometimes seen as obstacles rather than enablers of research. This study focuses on the Philippines, a country where the dynamics of health research ethics and IRBs remain underexplored, offering insights applicable to other low- and middle-income settings. Between July and October 2020, semi-structured interviews were conducted with Filipino health researchers
Written by Sokha Chhim
Published in Vol 5 Issue 1, 2025
Clinical ethics support (CES) instruments are widely regarded as valuable tools; however, users frequently encounter barriers to their routine use. Involving end users and other stakeholders in the development of CES instruments may help address these challenges. This study outlines the creation of CURA, a user-friendly, four-step ethics support tool designed for nurses and nurse assistants in palliative care. A participatory development approach was employed, involving collaboration with stakeh
