Results for ' Protecting Patients'

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  1.  3
    Contemporary issues for protecting patients in cancer research: workshop summary.Sharyl J. Nass - 2014 - Washington, D.C.: The National Academies Press. Edited by Margie Patlak.
    In the nearly 40 years since implementation of federal regulations governing the protection of human participants in research, the number of clinical studies has grown exponentially. These studies have become more complex, with multisite trials now common, and there is increasing use of archived biospecimens and related data, including genomics data. In addition, growing emphasis on targeted cancer therapies requires greater collaboration and sharing of research data to ensure that rare patient subsets are adequately represented. Electronic records enable more extensive (...)
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  2.  5
    Protecting Patient Privacy Redux: Response to Open Peer Commentaries on “'You Don't Know Me, But …': Access to Patient Data and Subject Recruitment in Human Subjects Research”.Toby Schonfeld, Joseph S. Brown, N. Jean Amoura & Bruce Gordon - 2012 - American Journal of Bioethics 12 (1):W1 - W2.
    The American Journal of Bioethics, Volume 12, Issue 1, Page W1-W2, January 2012.
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  3.  3
    Practicing Preventive Ethics, Protecting Patients: Challenges of the Electronic Health Record.Valerie B. Satkoske & Lisa S. Parker - 2010 - Journal of Clinical Ethics 21 (1):36-38.
    Implementation of guidelines regarding breaches of electronic health information requires an anticipatory stance and physician and patient education regarding security and monitoring measures and methods of redress. Adopting a preventive ethics, rather than a crisis management, model may also increase physician awareness of how the information they choose to include and privilege within the health record may expose patients to added harms if not done mindfully.
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  4.  13
    Informed Consent: Protecting Patients Or Salvaging Physicians.Inayat Ullah Memon - 2012 - Bangladesh Journal of Bioethics 1 (2):7-10.
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  5.  8
    The New Wallet Biopsy and Involuntary Patient Transfers Abroad: How Physicians Can Help Protect Patients.Sana Loue - 2020 - Hastings Center Report 50 (2):19-24.
    The Emergency Medical Treatment and Active Labor Act in 1986 was intended to bring an end to incidents of “patient dumping.” However, due to the conflation of various federal legislative provisions, hospitals faced with the prospect of long‐term unreimbursed care of an immigrant patient, whether legally present in the United States or not, are in some cases having such patients transported to another country. These transfers are often being effectuated without patient consent. After an overview of the flaws in (...)
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  6.  18
    How to Allow Conscientious Objection in Medicine While Protecting Patient Rights.Walter Sinnott-Armstrong & Aaron J. Ancell - 2017 - Cambridge Quarterly of Healthcare Ethics 26 (1):120-131.
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  7.  1
    The DSM, Big Pharma, and Clinical Practice Guidelines: Protecting Patient Autonomy and Informed Consent. Cosgrove - 2011 - International Journal of Feminist Approaches to Bioethics 4 (1):11-25.
    Researchers, investigative journalists, community physicians, ethicists, and policy makers have voiced strong concerns about the integrity of medicine. Specifically, questions have been raised about the ways in which financial conflicts of interest (FCOI) in the biomedical field may be compromising the integrity of the scientific research process and thus compromising patient care by disseminating imbalanced or even inaccurate information (Angell 2004). Indeed, many of us are no longer surprised when we read about settlements made by pharmaceutical companies—some totaling hundreds of (...)
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  8.  2
    Ethical Consideration of Teleorthodontics and Protecting Patient Privacy.Sukhjit Gill, Mounika Chamarthi, Corina Mong, Morgan Ng & Ram Vaderhobli - forthcoming - Ethics in Biology, Engineering and Medicine: An International Journal.
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  9.  3
    Ethical Considerations of Teleorthodontics and Protecting Patient Privacy.Sukhjit Gill, Mounika Chamarthi, Corina Mong, Morgan Ng & Ram M. Vaderhobli - 2020 - Ethics in Biology, Engineering and Medicine 11 (1):29-34.
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  10.  32
    Patient privacy protection among university nursing students: A cross-sectional study.Dorothy N. S. Chan, Kai-Chow Choi, Miranda H. Y. To, Summer K. N. Ha & Gigi C. C. Ling - 2022 - Nursing Ethics 29 (5):1280-1292.
    Background Protecting a person’s right to privacy and confidentiality is important in healthcare services. As future health professionals, nursing students should bear the same responsibility as qualified health professionals in protecting patient privacy. Objectives To investigate nursing students’ practices of patient privacy protection and to identify factors associated with their practices. Research design A cross-sectional study design was adopted. A two-part survey was used to collect two types of data on nursing students: (1) personal characteristics, including demographics, clinical (...)
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  11.  4
    The protection of patients' rights in clinical trials.Marek Czarkowski - 2006 - Science and Engineering Ethics 12 (1):131-138.
    The Helsinki Declaration is a very important document regarding the protection of patients’ rights in clinical trials and one of the fundamental sources of operational principles for every ethics committee. Although they have been updated, the international guidelines for ethics committees continually fail to address certain issues pertaining to the protection of patients’ rights in clinical trials. These issues include, most significantly, the method of electing ethics committees (a free, secret ballot should be preferred to direct appointment), the (...)
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  12.  12
    Patient confidentiality, the duty to protect, and psychotherapeutic care: perspectives from the philosophy of ubuntu.Cornelius Ewuoso - 2021 - Theoretical Medicine and Bioethics 42 (1):41-59.
    This paper demonstrates how ubuntu relational philosophy may be used to ground beneficial coercive care without necessarily violating a patient’s dignity. Specifically, it argues that ubuntu philosophy is a useful theory for developing necessary conditions for determining a patient’s potential dangerousness; setting reasonable limits to the duty to protect; balancing the long-term good of providing unimpeded therapy for patients who need it with the short-term good of protecting at-risk parties; and advancing a framework for future case law and (...)
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  13.  5
    The DSM, big pharma, and clinical practice guidelines: Protecting patient autonomy and informed consent.Lisa Cosgrove - 2011 - International Journal of Feminist Approaches to Bioethics 4 (1):11-25.
    The author of this paper discusses why the issue of financial conflicts of interest in psychiatry has important public health implications for women and why FCOI complicate the informed consent process. For example, when psychiatric diagnostic and treatment guidelines are unduly influenced by industry, informed consent becomes a critical issue, because women may be assigned diagnostic labels that are not valid and may also be receiving imbalanced or even inaccurate information about their mental health treatment options. However, mere disclosure of (...)
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  14.  6
    Clinical Assessment of Asylum Seekers: Balancing Human Rights Protection, Patient Well-Being, and Professional Integrity.Janet Cleveland & Monica Ruiz-Casares - 2013 - American Journal of Bioethics 13 (7):13-15.
  15.  1
    The Veil of Silence around Family Violence: Is Protecting Patients’ Privacy Bad for Health?Felicia Cohn - 2008 - Journal of Clinical Ethics 19 (4):321-329.
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  16.  5
    The Hospital's Obligation to Protect Patients from Carriers of Infectious Diseases.Sheila Cram - 1979 - Journal of Law, Medicine and Ethics 7 (3):8-12.
  17.  15
    Vulnerable Patients, Adult Protective Services Investigations, and Reticent Surrogates: What is the Role of Clinical Ethics?Leah Eisenberg - 2024 - American Journal of Bioethics 24 (1):140-141.
    Healthcare providers have a professional obligation to protect vulnerable patients from harm. An extension of that obligation is the legal mandate in the United States to report any concerns about...
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  18.  2
    The Hospital's Obligation to Protect Patients from Carriers of Infectious Diseases.Sheila Cram - 1979 - Journal of Law, Medicine and Ethics 7 (3):8-12.
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  19.  3
    Protection of Patient Autonomy via Consumer Protection Litigation: The Israeli Eltroxin Class Action as a Case Study.Tamar Gidron & Elad Schild - 2021 - Theoria 88 (6):1066-1085.
    The world famous Eltroxin saga of 2009–2011, which ignited heated public debates in Europe, Canada, and Australia, reveals the problematic nature of standalone autonomy protection cases. Eltroxin is a life-sustaining thyroid hormone replacement medicine used by millions worldwide; it was reformulated in 2008, and around 10% of patients were badly affected. Poor communication and lack of professional information triggered public hysteria as a global wave of complaints about harmful side effects, including hair loss, weight gain, extreme fatigue, headaches, diarrhoea, (...)
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  20.  11
    Unequal protection for patient rights: The divide between university and health ethics committees.Martin Tolich & Kate Mary Baldwin - 2005 - Journal of Bioethical Inquiry 2 (1):34-40.
    Despite recommendations from the Cartwright Report ethical review by health ethics committees has continued in New Zealand without health practitioners ever having to acknowledge their dual roles as health practitioners researching their own patients. On the other hand, universities explicitly identify doctor/research-patient relations as potentially raising conflict of role issues. This stems from the acknowledgement within the university sector itself that lecturer/research-student relations are fraught with such conflicts. Although similar unequal relationships are seen to exist between health researchers and (...)
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  21.  6
    The Patient Protection and Affordable Care Act, Public Health, and the Elusive Target of Human Rights.Lance Gable - 2011 - Journal of Law, Medicine and Ethics 39 (3):340-354.
    The Patient Protection and Affordable Care Act (ACA) sets in motion a wide range of programs that substantially affected the health system in the United States and signify a moderate but important regulatory shift in the role of the federal government in public health. This article briefly addresses two interesting policy paradoxes about the ACA. First, while the legislation primarily addresses health care financing and insurance and establishes only a few initiatives directly targeting public health, the ACA nevertheless has the (...)
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  22.  21
    Protective truthfulness: the Chinese way of safeguarding patients in informed treatment decisions.M. C. Pang - 1999 - Journal of Medical Ethics 25 (3):247-253.
    The first part of this paper examines the practice of informed treatment decisions in the protective medical system in China today. The second part examines how health care professionals in China perceive and carry out their responsibilities when relaying information to vulnerable patients, based on the findings of an empirical study that I had undertaken to examine the moral experience of nurses in practice situations. In the Chinese medical ethics tradition, refinement [jing] in skills and sincerity [cheng] in relating (...)
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  23.  1
    Adult Protective Services: Convincing the Patient to Consent.Marshall B. Kapp - 1983 - Journal of Law, Medicine and Ethics 11 (4):163-167.
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  24.  3
    The Patient Protection and Affordable Care Act, Public Health, and the Elusive Target of Human Rights.Lance Gable - 2011 - Journal of Law, Medicine and Ethics 39 (3):340-354.
    The passage of the Patient Protection and Affordable Care Act in March 2010 represents a significant turning point in the evolution of health care law and policy in the United States. By establishing a legal infrastructure that seeks to achieve universal health insurance coverage in the United States, the ACA targets some of the major impediments to accessing needed health care for millions of Americans and by extension attempts to strengthen the health system to support key determinants of health. Yet, (...)
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  25.  18
    Patient advocacy in nursing: A concept analysis.Mohammad Abbasinia, Fazlollah Ahmadi & Anoshirvan Kazemnejad - 2020 - Nursing Ethics 27 (1):141-151.
    Background:The concept of patient advocacy is still poorly understood and not clearly conceptualized. Therefore, there is a gap between the ideal of patient advocacy and the reality of practice. In order to increase nursing actions as a patient advocate, a comprehensive and clear definition of this concept is necessary.Research objective:This study aimed to offer a comprehensive and clear definition of patient advocacy.Research design:A total of 46 articles and 2 books published between 1850 and 2016 and related to the concept of (...)
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  26.  6
    Risk and Protective Factors of Psychological Distress in Patients Who Recovered From COVID-19: The Role of Cognitive Reserve.Maria Devita, Elisa Di Rosa, Pamela Iannizzi, Sara Bianconi, Sara Anastasia Contin, Simona Tiriolo, Marta Ghisi, Rossana Schiavo, Nicol Bernardinello, Elisabetta Cocconcelli, Elisabetta Balestro, Anna Maria Cattelan, Davide Leoni, Biancarosa Volpe & Daniela Mapelli - 2022 - Frontiers in Psychology 13.
    Recent studies reported the development of psychological distress symptoms in patients who recovered from COVID-19. However, evidence is still scarce and new data are needed to define the exact risk and protective factors that can explain the variability in symptoms manifestation. In this study, we enrolled 257 patients who recovered from COVID-19 and we evaluated the levels of psychological distress through the Symptoms Checklist-90-R scale. Data concerning illness-related variables were collected from medical records, while the presence of subjective (...)
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  27.  1
    La protection des données personnelles des patients face à la modernisation de notre système de santé.Valérie Siranyan - 2019 - Médecine et Droit 2019 (158):112-117.
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  28.  11
    From Constitutional Protections to Medical Ethics: The Future of Pregnant Patients’ Medical Self-Determination Rights After Dobbs.Nadia N. Sawicki & Elizabeth Kukura - 2023 - Journal of Law, Medicine and Ethics 51 (3):528-532.
    This article argues that the Supreme Court’s decision in Dobbs is likely to impact medical decision-making by pregnant patients in a variety of contexts. Of particular concern are situations where a patient declines treatment recommended for its potential benefit to the fetus and situations where treatment is withheld due to potential risk to the fetus. The Court’s elevation of fetal interests, combined with a history of courts using abortion jurisprudence to guide their reasoning in compelled treatment cases, means that (...)
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  29.  5
    Theory of protective empowering for balancing patient safety and choices.Rosalina F. Chiovitti - 2011 - Nursing Ethics 18 (1):88-101.
    Registered nurses in psychiatric-mental health nursing continuously balance the ethical principles of duty to do good (beneficence) and no harm (non-maleficence) with the duty to respect patient choices (autonomy). However, the problem of nurses’ level of control versus patients’ choices remains a challenge. The aim of this article is to discuss how nurses accomplish their simultaneous responsibility for balancing patient safety (beneficence and non-maleficence) with patient choices (autonomy) through the theory of protective empowering. This is done by reflecting on (...)
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  30.  12
    The Patient Has Rights: How Can We Protect Them?George J. Annas - 1973 - Hastings Center Report 3 (4):8-9.
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  31.  8
    Respecting Patient Autonomy Versus Protecting the Patient's Health.James M. Badger, Rosalind Ekman Ladd & Paul Adler - 2009 - Jona's Healthcare Law, Ethics, and Regulation 11 (4):120-124.
  32.  8
    Patient-funded research: paying the piper or protecting the patient?E. Haavi Morreim - 1990 - IRB: Ethics & Human Research 13 (3):1-6.
  33.  91
    Patient Informed Choice for Altruism.David J. Doukas & John Hardwig - 2014 - Cambridge Quarterly of Healthcare Ethics 23 (4):397-402.
    Abstract:Respect for persons protects patients regarding their own healthcare decisions. Patient informed choice for altruism (PICA) is a proposed means for a fully autonomous patient with decisionmaking capacity to limit his or her own treatment for altruistic reasons. An altruistic decision could bond the patient with others at the end of life. We contend that PICA can also be an advance directive option. The proxy, family, and physicians must be reminded that a patient’s altruistic treatment refusal should be respected.
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  34.  6
    Protection of Human Subjects and Patients: A Social Contingency Analysis of Distinctions between Research and Practice, and Its Implications.Israel Goldiamond - 1976 - Behaviorism 4 (1):1-41.
    Uses a social contingency analysis derived from behavioral psychology to compare research and practice. The components of a contingency (occasion, behavior, and consequence) present in a variety of research, treatment, and educational situations are discussed. Subjective terms such as intent, coercion, and consent are analyzed by means of a behavioral approach. Implications include the possible value of a collegial, symmetrical relationship between the professional and the individual in both research and practice domains. Such a relationship is consistent with current dissatisfaction (...)
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  35.  2
    Insurance: Patient Protections for Federal Employees.Elizabeth Pang - 2000 - Journal of Law, Medicine and Ethics 28 (4):417-418.
  36.  4
    Protection de la personne. Droit des patients en psychiatrie☆.Jean-Louis Senon & Carol Jonas - 2005 - Médecine et Droit 2005 (71):33-49.
  37.  2
    The protection of patients or practitioners?J. Stuart Homer - 1999 - In Michael Parker (ed.), Ethics and community in the health care professions. New York: Routledge. pp. 172.
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  38.  11
    Adult Protective Services: Convincing the Patient to Consent.Marshall B. Kapp - 1983 - Journal of Law, Medicine and Ethics 11 (4):163-167.
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  39.  1
    Unequal protection for patient rights: The divide between university and health ethics committees. [REVIEW]Dr Martin Tolich & Kate Mary Baldwin - 2005 - Journal of Bioethical Inquiry 2 (1):34-40.
    Despite recommendations from the Cartwright Report ethical review by health ethics committees has continued in New Zealand without health practitioners ever having to acknowledge their dual roles as health practitioners researching their own patients. On the other hand, universities explicitly identify doctor/research-patient relations as potentially raising conflict of role issues. This stems from the acknowledgement within the university sector itself that lecturer/research-student relations are fraught with such conflicts. Although similar unequal relationships are seen to exist between health researchers and (...)
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  40.  1
    Center Stage on the Patient Protection Agenda: Grievance and Appeal Rights.Tracy E. Miller - 1998 - Journal of Law, Medicine and Ethics 26 (2):89-99.
    Responding to mounting public concern about the shift to managed care, legislation to grant patient protections has dominated the health policy agenda over the past two years. Although some policies, such as laws on maternity length of stay, can be easily dismissed as “body part by body part” micromanagement of medical practice, other initiatives offer substantive, new rights to patients across the spectrum of care. At both the state and the federal levels, the right of enrollees to appeal a (...)
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  41.  5
    Freedom of Conscience and Health Care in the United States of America: The Conflict Between Public Health and Religious Liberty in the Patient Protection and Affordable Care Act.Peter West-Oram - 2013 - Health Care Analysis 21 (3):237-247.
    The recent confirmation of the constitutionality of the Obama administration’s Patient Protection and Affordable Care Act (PPACA) by the US Supreme Court has brought to the fore long-standing debates over individual liberty and religious freedom. Advocates of personal liberty are often critical, particularly in the USA, of public health measures which they deem to be overly restrictive of personal choice. In addition to the alleged restrictions of individual freedom of choice when it comes to the question of whether or not (...)
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  42.  1
    Insurance: Patient Protections for Federal Employees.Elizabeth Pang - 2000 - Journal of Law, Medicine and Ethics 28 (4):417-418.
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  43.  16
    Patient Privacy.Orhan Onder, Ilhan Ilkilic & Cuneyt Kucur (eds.) - 2020 - İstanbul, Türkiye: ISAR Publications.
    The sense of shame is part of human nature. What, then, is the role and significance of such a particular sensation, one that causes mental anxiety in a sick person’s weakest and the most vulnerable state? We know from historical documents going back as far as ancient Greece and Egypt that respecting patient privacy should be regarded as a moral duty for physicians in charge of treatment. However much today’s healthcare may have changed compared to centuries past, we note that (...)
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  44.  3
    Self-Determination in Health Care: A Property Approach to the Protection of Patients' Rights.Leroy C. Edozien - 2015 - Burlington, VT, USA: Routledge.
    This book proposes an alternative to the consent model which is currently at the heart of patient self-determination and which is shown here to have fundamental flaws that constrain its effectiveness. The proposed model is a property model in which the patient’s bodily integrity is protected from unauthorised invasion, and their legitimate expectation to be provided with the relevant information to make an informed decision is taken to be a proprietary right. This model enables the courts to overcome the requirement (...)
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  45.  8
    A physician’s identity can never be reconfigured to put climate protection on par with an individual patient’s best interests.Narcyz Ghinea - 2024 - Journal of Medical Ethics 50 (6):375-375.
    In their article, van Gils Schmidt and Salloch defend the claim that physicians have a duty to protect the climate. The logic of the argument in broad terms is that (i) there is a relationship between climate change and the burden of disease, (ii) the healthcare sector is a significant emitter of global greenhouse gasses, thereby enhancing the burden of disease and (iii) since doctors are advocates of health and stakeholders in the healthcare sector, they have a duty to respond (...)
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  46.  3
    Alternatives for protecting privacy while respecting patient care and public health needs.Judith Wagner DeCew - 1999 - Ethics and Information Technology 1 (4):249-255.
    This paper begins with a discussion of the value of privacy,especially for medical records in an age of advancing technology.I then examine three alternative approaches to protection ofmedical records: reliance on governmental guidelines, the useof corporate self-regulation, and my own third hybrid view onhow to maintain a presumption in favor of privacy with respectto medical information, safeguarding privacy as vigorously andcomprehensively as possible, without sacrificing the benefitsof new information technology in medicine. None of the threemodels I examine are unproblematic, yet (...)
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  47.  5
    Do positive relations with patients play a protective role for healthcare employees? Effects of patients' gratitude and support on nurses' burnout.Daniela Converso, Barbara Loera, Sara Viotti & Mara Martini - 2015 - Frontiers in Psychology 6.
  48.  7
    Patient, heal thyself: how the new medicine puts the patient in charge.Robert M. Veatch - 2009 - New York: Oxford University Press.
    The puzzling case of the broken arm -- Hernias, diets, and drugs -- Why physicians cannot know what will benefit patients -- Sacrificing patient benefit to protect patient rights -- Societal interests and duties to others -- The new, limited, twenty-first-century role for physicians as patient assistants -- Abandoning modern medical concepts: doctor's "orders" and hospital "discharge" -- Medicine can't "indicate": so why do we talk that way? --"Treatments of choice" and "medical necessity": who is fooling whom? -- Abandoning (...)
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  49.  4
    The aging physician: A practical approach to protect our patients.John T. Fortunato & Daniel Londyn Menkes - 2019 - Clinical Ethics 14 (1):46-49.
    As the median age of practicing physicians increases, ethical dilemmas due to age-related cognitive decline among clinicians will become ever more pressing. Compelling data show that despite acknowledgement of their duty to protect the public, physicians often fail to report themselves, their colleagues, or their physician-patients when cognitive decline appears to impact medical practice adversely. As such, efforts to educate physicians about ethical obligations and various tactful methodologies to report themselves or others seem ineffective. Illustrated by a case report (...)
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  50.  24
    Nurses’ and patients’ perceptions of privacy protection behaviours and information provision.Kyunghee Kim, Yonghee Han & Ji-su Kim - 2017 - Nursing Ethics 24 (5):598-611.
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