Results for 'Caregivers '

982 found
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  1.  23
    Caregiving for ageing parents: A literature review on the experience of adult children.Ina Luichies, Anne Goossensen & Hanneke van der Meide - 2021 - Nursing Ethics 28 (6):844-863.
    Background: More and more adults in their fifties and sixties are confronted with the need to support their ageing parents. Although many aspects of filial caregiving have been researched, a well-documented and comprehensive overview of the caregiving experience is lacking. Aim: This study aims for a better understanding of the caregiving experience of adult children by generating an overview of main themes in international research. Method: A literature review of qualitative studies, focusing on the experiences of adult children caring for (...)
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  2. Caregiving and role conflict distress.Jordan MacKenzie - 2024 - Clinical Ethics 19 (2):136-142.
    When our nearest and dearest experience medical crises, we may need to step into caregiving roles. But in doing so, we may find that our new caregiving relationship is actually in tension with the loving relationship that motivated us towards care. What we owe and are entitled to as friends, spouses, and family members, can be different from what we owe and are entitled to as caregivers. For this reason, caregiving carries with it the risk of a type of (...)
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  3.  1
    Family caregivers’ role in dignity of people with schizophrenia: A qualitative study.Elham Amiri, Hossein Ebrahimi, Hossein Habibzadeh & Rahim Baghaei - forthcoming - Nursing Ethics.
    Background: When patients with schizophrenia feel a lack of dignity, their sense of worth is weakened and they are more likely to feel like a burden to their family. In this regard, families play a vital role in supporting the patient, who can effectively contribute to preserving their dignity. The concept of understanding the role of families in the patients’ dignity is influenced by various factors. Still, there is limited knowledge in this domain in the sociocultural context of Iran. Aim: (...)
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  4.  37
    Caregivers’ perception of dignity in teenagers with autism spectrum disorder.Fatemeh Mohammadi, Mahnaz Rakhshan, Zahra Molazem, Najaf Zareh & Mark Gillespie - 2019 - Nursing Ethics 26 (7-8):2035-2046.
    Introduction: Maintaining dignity is one of patients is one of the main ethical responsibilities of caregivers. However, in many cases, the dignity of patients, especially autistic teenagers is not maintained. The extent to which dignity needs are met for this group within the Iranian care system is difficult to determine as dignity is an abstract concept, and there are few related research studies reported. Objectives: The objective of this study is to find out caregivers perspectives on dignity in (...)
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  5.  28
    Caregivers’ Sensemaking of Children’s Hereditary Angioedema: A Semiotic Narrative Analysis of the Sense of Grip on the Disease.Maria Francesca Freda, Livia Savarese, Pasquale Dolce & Raffaele De Luca Picione - 2019 - Frontiers in Psychology 10.
    Background and aims. In pediatrics receiving a diagnosis of a chronic condition is a matter that involves caregivers at first. Beyond the basic issues of caring for the physical body of the ill child, caregivers’ manners of facing and making sense of the disease orient and co-construct their children’s sensemaking processes of the disease itself. The aim of this article is to explore the experience of a rare chronic illness, Hereditary Angioedema (HAE), in pediatrics, from the caregivers (...)
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  6.  37
    Caregiving and Moral Distress for Family Caregivers during Early-Stage Alzheimer’s Disease.Chris Weigel - 2019 - International Journal of Feminist Approaches to Bioethics 12 (2):74-91.
    As the global prevalence of Alzheimer’s disease increases, the need to understand family caregiving becomes increasingly pressing. I argue that there is an under-recognized form of caregiving for people with early to mid-stage Alzheimer’s disease. This type of caregiving involves, roughly, helping people reason through their values. It arises along with the loss of the capacity for executive functioning. Moreover, it is prone to give rise to moral distress, which is an under-recognized vulnerability in family caregiving. Categories of family caregiving (...)
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  7.  23
    Caregivers of persons with a brain tumor: a conceptual model.Paula Sherwood, Barbara Given, Charles Given, Rachel Schiffman, Daniel Murman & Mary Lovely - 2004 - Nursing Inquiry 11 (1):43-53.
    Researchers have documented negative physical and emotional consequences for both family caregivers of persons with cancer as well as caregivers of persons with a neurologic disorder. However, there is a unique subset of caregivers who must provide care for someone who may suffer from both a short, terminal trajectory of disease, as well as neurological and neuropsychiatric sequelae — the caregiver of a person with a primary malignant brain tumor. The purpose of this article was to describe (...)
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  8.  36
    Caregivers’ perception of women’s dignity in the delivery room: A qualitative study.Fateme Mohammadi, Hadise Sadate Tabatabaei, Farzaneh Mozafari & Mark Gillespie - 2020 - Nursing Ethics 27 (1):116-126.
    Introduction: Dignified care is one of the moral responsibilities of professional caregivers. However, in many cases the dignity of hospitalized patients, especially women in the delivery room, is not maintained. Dignity is an abstract concept and there has been no previous research exploring the dignity of pregnant women in the delivery room in Iran. Objectives: The objective of this study is to define and explain the concept of dignity for pregnant women in the delivery room from the perspectives of (...)
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  9.  96
    Caregiver decision-making concerning involuntary treatment in dementia care at home.Vincent R. A. Moermans, Angela M. H. J. Mengelers, Michel H. C. Bleijlevens, Hilde Verbeek, Bernadette Dierckx de Casterle, Koen Milisen, Elizabeth Capezuti & Jan P. H. Hamers - 2022 - Nursing Ethics 29 (2):330-343.
    Background: Dementia care at home often involves decisions in which the caregiver must weigh safety concerns with respect for autonomy. These dilemmas can lead to situations where caregivers provide care against the will of persons living with dementia, referred to as involuntary treatment. To prevent this, insight is needed into how family caregivers of persons living with dementia deal with care situations that can lead to involuntary treatment. Objective: To identify and describe family caregivers’ experiences regarding care (...)
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  10.  34
    Family Caregiving and the Intergenerational Transmission of Poverty.Richard L. Kaplan - 2018 - Journal of Law, Medicine and Ethics 46 (3):629-635.
    The United States relies on uncompensated family caregivers to provide most of the long-term care required by older adults as they age. But such care comes at a significant financial cost to these caregivers in the form of lower lifetime earnings and diminished Social Security retirement benefits, ineligibility for Medicare coverage of their healthcare costs, and minimal retirement savings. To reduce the impact of uncompensated caregiving on the intergenerational transmission of poverty, this paper discusses three possible mechanisms of (...)
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  11.  15
    Professional Caregivers: Stress and Coping in the Face of Loss and Trauma.D. Machando, V. Maasdorp, C. Wogrin, G. Javangwe & K. C. Muchena - 2019 - Indo-Pacific Journal of Phenomenology 19 (2):81-90.
    Professional caregivers who work with the trauma and suffering of others, such as doctors, nurses and psychologists, may face significant challenges along with the risk of adverse, long-term mental and physical health problems. Caregivers with responsibility for dependants outside their professional work reported more stress. This finding is of particular relevance in respect of caregivers in under-developed countries such as Zimbabwe, where many households have taken in additional children who have been orphaned, whose parents are ill, or (...)
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  12.  22
    Caregiving, Self‐Care, and Contemplation: Resources from Thomas Aquinas.Emily Dubie - 2021 - New Blackfriars 102 (1099):384-400.
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  13.  19
    Caregiving and the Abuse of Power.Joseph Walsh - 2019 - Feminist Philosophy Quarterly 5 (3).
    Caregiving relationships are often characterized by an imbalance of power between the caregiver and her cared-for. The danger that this power will be abused is a source of serious moral concern. In this article, I argue that the risk of an abuse of power sometimes stems not from the possession of power itself, but from the very nature of caring relationships. This is because carers must be prepared to exercise non-minimal amounts of power over their cared-fors, even if doing so (...)
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  14.  20
    Caregivers’ Grief in Acquired Non-death Interpersonal Loss (NoDIL): A Process Based Model With Implications for Theory, Research, and Intervention.Einat Yehene, Alexander Manevich & Simon Shimshon Rubin - 2021 - Frontiers in Psychology 12.
    The number of family members caring and caregiving for a loved one undergoing physical and mental changes continues to increase dramatically. For many, this ongoing experience not only involves the “burden of caregiving” but also the “burden of grief” as their loved-one’s newfound medical condition can result in the loss of the person they previously knew. Dramatic cognitive, behavioral, and personality changes, often leave caregivers bereft of the significant relationship they shared with the affected person prior to the illness (...)
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  15.  25
    Gendered caregiving and structural constraints: An empirical ethical study.Xiang Zou, Jing-Bao Nie & Ruth Fitzgerald - 2021 - Nursing Ethics 28 (3):387-401.
    Background: The pressing issue of aged care has made gendered caregiving a growing subject of feminist bioethical enquiry. However, the impact of feminism on empirical studies in the area of gendered care in Chinese sociocultural contexts has been less influential. Objectives: To examine female members’ lived experiences of gendered care in rural China and offer proper normative evaluation based on their experiences. Research design: This article adopted an empirical ethical approach that integrates ethnographical investigation and feminist ethical inquiry. Participants and (...)
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  16.  56
    Caregivers’ Role in Maternal–Fetal Conflict.Ercan Avci - 2015 - Narrative Inquiry in Bioethics 5 (1):67-76.
    The case, which occurred in a public hospital in Turkey in 2005, exhibits a striking dilemma between a mother’s and her fetus’ interests. For a number of reasons, the mother refused to cooperate with the midwives and obstetrician in the process of giving birth, and wanted to leave the hospital. The care providers evaluated the case as a matter of maternal autonomy and asked the mother to give her consent to be discharged from the hospital, which she did despite the (...)
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  17.  39
    Kin Relationships and the Caregiving Biases of Grandparents, Aunts, and Uncles.Alexander Pashos & Donald H. McBurney - 2008 - Human Nature 19 (3):311-330.
    Paternity certainty and matrilineal family ties have been used to explain the asymmetric caregiving of grandparents and aunts and uncles. The proximate mechanisms underlying biased kin investment, however, remain unclear. A central question of the study presented here was whether the parent-kin relationship is an important link in the caregiving. In a two-generational questionnaire study, we asked subjects to estimate the intensity of their relationships to parents, grandparents, aunts, and uncles (emotional closeness, investment received in childhood). In addition, the subjects’ (...)
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  18.  35
    Caregiving relationships as evolutionary and developmental bases of obligation.Rachna B. Reddy & Henry M. Wellman - 2020 - Behavioral and Brain Sciences 43.
    Obligation as defined by Tomasello requires mutually capable parties, but one-sided caregiver relationships reveal its developmental and evolutionary precursors. Specifically, “coercive” emotions may prompt protective action by caregivers toward infant primates, and infants show distress toward caregivers when they appear to violate expectations in their relationships. We argue that these early social-relational expectations and emotions may form the base of obligation.
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  19. Robot caregivers: harbingers of expanded freedom for all? [REVIEW]Yvette Pearson - 2010 - Ethics and Information Technology 12 (3):277-288.
    As we near a time when robots may serve a vital function by becoming caregivers, it is important to examine the ethical implications of this development. By applying the capabilities approach as a guide to both the design and use of robot caregivers, we hope that this will maximize opportunities to preserve or expand freedom for care recipients. We think the use of the capabilities approach will be especially valuable for improving the ability of impaired persons to interface (...)
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  20.  11
    Caregiving, Cultural, and Cognitive Perspectives on Secure-base Behavior and Working Models: New Growing Points of Attachment Theory and Research.John H. Flavell, Janet W. Astington, Paul L. Harris, Eleanor R. Flavell & Frances L. Green - 1995
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  21.  3
    A Case for Caregiver Testimony about the Cognitively Disabled.Sara Chan - forthcoming - Episteme:1-15.
    It is common for caregivers of the cognitively disabled to speak on behalf of their charges who cannot speak for themselves. Their testimony, however, is often dismissed either because of doubt about their having relevant expertise or because of worries that they are blinded by love. This paper is positioned against such dismissals. I argue that good caregivers are uniquely positioned to offer reliable and often insightful testimony about the well-being of their charges and so ought to be (...)
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  22.  42
    Caregiving, emotion, and concern for others.Carolyn Zahn-Waxler - 2001 - Behavioral and Brain Sciences 25 (1):48-49.
    Few individuals are constitutionally incapable of showing concern for others at an early age, and malleability is possible. Individual variations will be best understood through study of the representational prerequisites of empathy in close conjunction with caregiving environments and affective underpinnings.
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  23.  23
    Caregiver burden and the medical ethos.Karsten Witt, Johanne Stümpel & Christiane Woopen - 2017 - Medicine, Health Care and Philosophy 20 (3):383-391.
    Are physicians sometimes morally required to ease caregiver burden? In our paper we defend an affirmative answer to this question. First, we examine the well-established principle that medical care should be centered on the patient. We argue that although this principle seems to give physicians some leeway to lessen caregivers' suffering, it is very restrictive when spelled out precisely. Based on a critical analysis of existing cases for transcending patient-centeredness we then go on to argue that the medical ethos (...)
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  24.  26
    Levinasian Caregiving.Jonathan Yahalom - 2017 - Philosophy in the Contemporary World 24 (1):51-62.
    This article reviews the work of philosopher Emmanuel Levinas to explore caregiving for dementia. It defends a dual thesis whereby it first articulates how Levinas provides a phenomenological description to account for why caregiving is subjectively dreadful and, second, how caregiving invites a fresh re-reading of Levinasian thought. The article introduces two different forms of otherness represented by death and dementia, respectively. This re-reading shows how dementia forces us to more immediately reckon with the intensity Levinas attributes to the nature (...)
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  25.  23
    Acknowledging caregivers’ vulnerability in the managment of challenging behaviours to reduce control measures in psychiatry.Jean Lefèvre-Utile, Marjorie Montreuil, Amélie Perron, Aymeric Reyre & Franco Carnevale - 2022 - Nursing Ethics 29 (3):758-779.
    Background: The management of challenging behaviours in inpatient with intellectual disability and/or autism spectrum disorders can lead to an escalation of control measures. In these complex situations where patients have an intellectual disability/autism spectrum disorder accompanied by a psychiatric comorbidity, the experiences of caregivers related to the crisis management have rarely been studied. Purpose: This study examined the moral experiences of caregivers related to challenging behaviours’ management and alternatives to control measures. Research design: Using Charles Taylor’s hermeneutic framework, (...)
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  26.  30
    Informal Caregivers of Patients with Disorders of Consciousness: a Qualitative Study of Communication Experiences and Information Needs with Physicians.Karoline Boegle, Marta Bassi, Angela Comanducci, Katja Kuehlmeyer, Philipp Oehl, Theresa Raiser, Martin Rosenfelder, Jaco Diego Sitt, Chiara Valota, Lina Willacker, Andreas Bender & Eva Grill - 2022 - Neuroethics 15 (3):1-19.
    Due to improvements in medicine, the figures of patients with disorders of consciousness (DoC) are increasing. Diagnostics of DoC and prognostication of rehabilitation outcome is challenging but necessary to evaluate recovery potential and to decide on treatment options. Such decisions should be made by doctors and patients’ surrogates based on medico-ethical principles. Meeting information needs and communicating effectively with caregivers as the patients´ most common surrogate-decision makers is crucial, and challenging when novel tech-nologies are introduced. This qualitative study aims (...)
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  27.  14
    Caregiver Report of Executive Functioning in Adolescent Females With Anorexia Nervosa or Autism Spectrum Disorder.C. Alix Timko, John D. Herrington, Anushua Bhattacharya, Emily S. Kuschner & Benjamin E. Yerys - 2021 - Frontiers in Psychology 11.
    Current literature suggesting a shared endophenotype between individuals with anorexia nervosa and autism spectrum disorder related to executive functioning has several limitations: performance-based instead of ecologically valid measures of set-shifting are used, lack of comparisons between same-sex groups, and reliance on adult samples only. This was the first study directly comparing female youth with ASD to female youth with AN using an ecologically valid measure of EF. A secondary data analysis combined caregiver-reported EF on the Behavior Rating Inventory of Executive (...)
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  28.  44
    Informal caregivers – A missing voice in clinical ethics.Aleksandra Glos - 2024 - Clinical Ethics 19 (2):143-149.
    This paper argues that the missing voice in clinical ethics is that of informal caregivers. Despite their substantial contribution to care provided to individuals with disabilities, chronic illness or dementia, informal caregivers are rarely thought of as members of the healthcare team and their narratives are rarely listened to and included in clinical and ethical decisions. Addressing this gap, this paper discusses the reasons for the systemic misrecognition of informal caregivers in healthcare systems and argues for their (...)
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  29.  27
    Information disclosure to family caregivers: Applying Thiroux's framework.John Rowe - 2010 - Nursing Ethics 17 (4):435-444.
    In the UK, community care has led to more complex relationships for mental health nurses. They need to respect the rights of service users to confidentiality while also respecting the rights of family caregivers to information that directly affects them. An unsatisfactory situation has arisen in which utilitarian and legally driven motives have seen family caregivers’ interests become subsidiary to those of service users and providers. An ethical case is made for sharing information with family caregivers, even (...)
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  30.  54
    Caregivers’ perception of teenagers’ dignity in end of life stages: A phenomenological study.Fateme Mohammadi, Khodayar Oshvandi, Masoud Khodaveisi, Fatemeh Cheraghi, Tayebeh Hasan Tehrani, Arash Khalili & Hazel Kyle - 2023 - Nursing Ethics 30 (1):121-132.
    Introduction: Maintaining patient dignity in a caregiving environment is one of the most important moral responsibilities for caregivers. Nonetheless, there are vulnerable groups, specifically teenagers, who in their final stages of life are prone to their dignity being threatened. Moreover, dignity is an abstract concept and there is no studies done on teenagers’ dignity in the final stages of life available in Iran.Purpose: The purpose of this study is to describe the caregivers’ experiences regarding teenagers’ dignity in the (...)
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  31.  55
    Just Caring for Caregivers: What Society and the State Owe to Those Who Render Care.Alison Reiheld - 2015 - Feminist Philosophy Quarterly 1 (2):1-24.
    Traditional considerations of justice for those who require caregiving have centered on what is due to the dependent person. However, considerations of justice also bear strongly on what is due to the caregiver. I focus on unpaid dependency work, too long treated as a private matter rather than a public concern. More is owed to those who render care: the division of labor is unjust, the nature of dependency work creates vulnerabilities for caregivers, and unpaid caregivers are disadvantaged (...)
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  32.  42
    Testimonial injustice: considering caregivers in paediatric behavioural healthcare.Michelle Trang Pham, Eric A. Storch & Gabriel Lázaro-Muñoz - 2021 - Journal of Medical Ethics 47 (11):738-739.
    Harcourt argues that in clinical contexts, children and young people with mental health illness can experience epistemic, specifically testimonial, injustice when their perspectives are unjustifiably discounted by health service providers.1 Our goal in this commentary was to illustrate how caregivers, a critical component of CYP treatment triad, can also engage in testimonial injustice towards CYP patients. Testimonial injustice occurs when one suffers a credibility deficit and that credibility deficit is based on prejudice.2 Harcourt expands Fricker’s account of testimonial injustice (...)
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  33.  36
    Caregivers’ Understanding of Informed Consent in a Randomized Control Trial.Dorothy Helen Boyd, Yinan Zhang, Lee Smith, Lee Adam, L. Foster Page & W. M. Thomson - 2021 - Journal of Bioethical Inquiry 18 (1):141-150.
    There are differences in caregivers’ literacy and health literacy levels that may affect their ability to consent to children participating in clinical research trials. This study aimed to explore the effectiveness, and caregivers’ understandings, of the process of informed consent that accompanied their child’s participation in a dental randomized control trial (RCT). Telephone interviews were conducted with a convenience sample of ten caregivers who each had a child participating in the RCT. Pre-tested closed and open-ended questions were (...)
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  34.  21
    Caregiving In Transnational Context: “My Wings Have Been Cut; Where Can I Fly?”.Miriam Stewart, Karen Hughes, Margaret Harrison, Anne Neufeld & Denise Spitzer - 2003 - Gender and Society 17 (2):267-286.
    Migration often requires the renegotiation of familial and gender roles as immigrants encounter potentially competing values and demands. Employing ethnographic methods and including in-depth interviewing and participant observation, the authors explore the experiences of 29 South Asian and Chinese Canadian female family caregivers. Caregiving was central to their role as women and members of their ethnocultural community. The women were often engaged in paid labor that compressed the time available to fulfill their duties as caregivers. Women’s role in (...)
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  35.  25
    Why caregivers have no autonomy‐based reason to respect advance directives in dementia care.Sigurd Lauridsen, Anna P. Folker & Martin M. Andersen - 2023 - Bioethics 37 (4):399-405.
    Advance directives (ADs) have for some time been championed by ethicists and patient associations alike as a tool that people newly diagnosed with dementia, or prior to onset, may use to ensure that their future care and treatment are organized in accordance with their interests. The idea is that autonomous people, not yet neurologically affected by dementia, can design directives for their future care that caregivers are morally obligated to respect because they have been designed by autonomous individuals. In (...)
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  36.  25
    Experiences of Caregivers and Relatives in Public Nursing Homes.Elisabeth Häggström & Annica Kihlgren - 2007 - Nursing Ethics 14 (5):691-701.
    The aim of the present study was, by means of discussion highlighting ethical questions and moral reasonings, to increase understanding of the situations of caregivers and relatives of older persons living in a public nursing home in Sweden. The findings show that these circumstances can be better understood by considering two different perspectives: an individual perspective, which focuses on the direct contact that occurs among older people, caregivers and relatives; and a societal perspective, which focuses on the norms, (...)
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  37.  24
    Caregivers blinded by the care: A qualitative study of physical restraint in pediatric care.Bénédicte Lombart, Carla De Stefano, Didier Dupont, Leila Nadji & Michel Galinski - 2020 - Nursing Ethics 27 (1):230-246.
    Background: The phenomenon of forceful physical restraint in pediatric care is an ethical issue because it confronts professionals with the dilemma of using force for the child’s best interest. This is a paradox. The perspective of healthcare professional working in pediatric wards needs further in-depth investigations. Purpose: To explore the perspectives and behaviors of healthcare professionals toward forceful physical restraint in pediatric care. Methods: This qualitative ethnographic study used focus groups with purposeful sampling. Thirty volunteer healthcare professionals (nurses, hospital aids, (...)
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  38.  9
    Family caregivers and the ethical relevance of moral identity.Mario Kropf & Martina Schmidhuber - 2024 - Nursing Inquiry 31 (4):e12670.
    Many people want to spend the last stages of their lives at home, in familiar surroundings, and possibly with people they know. However, this increasing desire on the part of older, ill, or even dying people also makes support from other people unavoidable, which in many cases involves family members, loved ones, or even friends. These family caregivers care for the person concerned, even though they lack the professional skills of nursing staff, for example, and have usually not been (...)
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  39.  9
    Caregivers' perspectives on good care for nursing home residents with Korsakoff syndrome.Ineke J. Gerridzen, Cees M. P. M. Hertogh, Karlijn J. Joling, Ruth B. Veenhuizen, Els M. L. Verschuur, Tjeu Janssen & Marja F. Depla - 2021 - Nursing Ethics 28 (3):358-371.
    Background: In the Netherlands, people with severe cognitive deficits due to Korsakoff syndrome are generally admitted to a specialized nursing home. Professional caregivers experience that these residents are often not aware of their deficits, and consequently, their willingness to accept care is relatively low. However, these residents need permanent support when performing daily tasks due to severe cognitive deficits. The combination of objective care needs and low subjective responsiveness makes caring for people with Korsakoff syndrome a complex undertaking. It (...)
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  40.  54
    Views of Caregivers on the Ethics of Assistive Technology Used for Home Surveillance of People Living with Dementia.Maurice Mulvenna, Anton Hutton, Vivien Coates, Suzanne Martin, Stephen Todd, Raymond Bond & Anne Moorhead - 2017 - Neuroethics 10 (2):255-266.
    This paper examines the ethics of using assistive technology such as video surveillance in the homes of people living with dementia. Ideation and concept elaboration around the introduction of a camera-based surveillance service in the homes of people with dementia, typically living alone, is explored. The paper reviews relevant literature on surveillance of people living with dementia, and summarises the findings from ideation and concept elaboration workshops, designed to capture the views of those involved in the care of people living (...)
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  41.  25
    Situated Personhood: Insights from Caregivers of Minimally Communicative Individuals.Johnny Brennan, Molly Kelleher, Rossio Motta-Ochoa, Stefanie Blain-Moraes & Laura Specker Sullivan - 2023 - International Journal of Feminist Approaches to Bioethics 16 (2):64-94.
    For caregivers of minimally communicative individuals, providing support in the absence of clearly meaningful responses is ethically fraught. We conducted a secondary analysis of qualitative data from caregivers of individuals who are minimally communicative, including persons with advanced dementia and individuals in disorders of consciousness. Our analysis led to two central claims: (1) Personhood is a threshold concept that is situated, relational, and dynamic and (2) in circumstances in which personhood is difficult to judge, caregivers can “fill (...)
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  42.  22
    Caregiver Choice and Caregiver Outcomes: A Longitudinal Study of Irish Spousal Dementia Caregivers.Maria M. Pertl, Aditi Sooknarine-Rajpatty, Sabina Brennan, Ian H. Robertson & Brain A. Lawlor - 2019 - Frontiers in Psychology 10.
  43.  29
    Exploring Caregiver Perspectives of Social and Motor Skills in Children With Autism Spectrum Disorder and the Impact on Participation.P. Camila Rios & Sara M. Scharoun Benson - 2020 - Frontiers in Psychology 11.
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  44.  78
    (1 other version)Caregiver–chimpanzee interactions with species-specific behaviors.Mary Lee A. Jensvold, Jacquelyn C. Buckner & Gina B. Stadtner - 2010 - Interaction Studies 11 (3):396-409.
    The relationships between captive primates and their caregivers are critical ones and can affect animal welfare. This study tested the effect of caregivers using chimpanzee behaviors or not, in daily interactions with captive chimpanzees. In the Chimpanzee Behavior condition the caregiver presented chimpanzee behaviors. In the Human Behavior condition the caregiver avoided using chimpanzee behaviors. The chimpanzees had individual patterns of response and had significant differences in their responses to each condition. These data are compared to a similar (...)
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  45.  25
    Caregivers’ perceptions of compulsory treatment of physical illness in involuntarily psychiatric hospitalization.Sophie Joury, Oren Asman & Azgad Gold - 2023 - Nursing Ethics 30 (3):423-436.
    Background Physical morbidity is rife among patients with serious mental illness. When they are involuntarily hospitalized and even treated, they may still refuse treatment for physical illness leading clinicians to wonder about the ethics of coercing such treatments. Research aim This survey study explored psychiatric caregivers’ perceptions on whether compulsory treatment of physical illness is legal and whether it is justifiable in patients with serious mental illness and under what circumstances. Research design A questionnaire that included two case vignettes (...)
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  46.  29
    The Caregiving Experiences of Fathers and Mothers of Children With Rare Diseases in Italy: Challenges and Social Support Perceptions.Paola Cardinali, Laura Migliorini & Nadia Rania - 2019 - Frontiers in Psychology 10.
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  47.  16
    Untangling Caregiving Role From Parent Gender in Coparenting Research: Insights From Gay Two-Father Families.Nicola Carone & Vittorio Lingiardi - 2022 - Frontiers in Psychology 13.
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  48.  26
    When do caregivers ignore the veil of ignorance? An empirical study on medical triage decision–making.Azgad Gold, Binyamin Greenberg, Rael Strous & Oren Asman - 2021 - Medicine, Health Care and Philosophy 24 (2):213-225.
    In principle, all patients deserve to receive optimal medical treatment equally. However, in situations in which there is scarcity of time or resources, medical treatment must be prioritized based on a triage. The conventional guidelines of medical triage mandate that treatment should be provided based solely on medical necessity regardless of any non-medical value-oriented considerations (“worst-first”). This study empirically examined the influence of value-oriented considerations on medical triage decision–making. Participants were asked to prioritize medical treatment relating to four case scenarios (...)
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  49.  27
    Caregiver reactions to neuroimaging evidence of covert consciousness in patients with severe brain injury: a qualitative interview study.Charles Weijer, Adrian M. Owen, Sarah Munce, Laura Elizabeth Gonzalez-Lara, Fiona Webster & Andrew Peterson - 2021 - BMC Medical Ethics 22 (1):1-13.
    BackgroundSevere brain injury is a leading cause of death and disability. Diagnosis and prognostication are difficult, and errors occur often. Novel neuroimaging methods can improve diagnostic and prognostic accuracy, especially in patients with prolonged disorders of consciousness (PDoC). Yet it is currently unknown how family caregivers understand this information, raising ethical concerns that disclosure of neuroimaging results could result in therapeutic misconception or false hope.MethodsTo examine these ethical concerns, we conducted semi-structured interviews with caregivers of patients with PDoC (...)
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  50.  20
    Caregiver influence on looking behavior and brain responses in prelinguistic development.Heather L. Ramsdell-Hudock - 2014 - Frontiers in Psychology 5.
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