Liminality as a conceptual frame for understanding the family caregiving rite of passage: an integrative review.
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[1] C. Hatton,et al. The impacts of short break provision on families with a disabled child: an international literature review. , 2011, Health & social care in the community.
[2] L. Williams. Whatever it takes: informal caregiving dynamics in blood and marrow transplantation. , 2007, Oncology nursing forum.
[3] P. Kulhara,et al. Positive aspects of caregiving in schizophrenia: A review. , 2012, World journal of psychiatry.
[4] Tzu-Ting Huang,et al. Role adaptation of family caregivers for ventilator-dependent patients: transition from respiratory care ward to home. , 2010, Journal of clinical nursing.
[5] R. Woods,et al. The impact of motivations and meanings on the wellbeing of caregivers of people with dementia: a systematic review , 2009, International Psychogeriatrics.
[6] K. Thompson. Liminality as a Descriptor for the Cancer Experience , 2007 .
[7] O. Söderhamn,et al. Experiences of Living in a Disrupted Situation as Partner to a Man With Testicular Cancer , 2009, American journal of men's health.
[8] Margarete Sandelowski,et al. Handbook for Synthesizing Qualitative Research , 2006 .
[9] K. Segesten,et al. Relations governed by uncertainty: part of life of families of a child with asthma. , 2004, Journal of pediatric nursing.
[10] A. Sheikh,et al. Archetypal trajectories of social, psychological, and spiritual wellbeing and distress in family care givers of patients with lung cancer: secondary analysis of serial qualitative interviews , 2010, BMJ : British Medical Journal.
[11] S. Fowler-Kerry,et al. Impact of caregiving: listening to the voice of informal caregivers. , 2003, Journal of psychiatric and mental health nursing.
[12] B. Ferrell,et al. Deriving meaning and faith in caregiving. , 2012, Seminars in oncology nursing.
[13] R. Adelman,et al. Caregiver burden: a clinical review. , 2014, JAMA.
[14] G J Acton,et al. Self-Transcendence and Family Caregivers of Adults with Dementia , 2000, Journal of holistic nursing : official journal of the American Holistic Nurses' Association.
[15] D. Angus,et al. Informal caregiver burden among survivors of prolonged mechanical ventilation. , 2007, American journal of respiratory and critical care medicine.
[16] R. Barbour,et al. Ambiguity and uncertainty: the ongoing concerns of male partners of women treated for breast cancer. , 2008, European journal of oncology nursing : the official journal of European Oncology Nursing Society.
[17] G. Ahlström,et al. Quality of Life in Spite of an Unpredictable Future: The Next of Kin of Patients With Multiple Sclerosis , 2010, The Journal of neuroscience nursing : journal of the American Association of Neuroscience Nurses.
[18] Judith E Hupcey,et al. A Model of Caregiving Through the End of Life , 2012, Western journal of nursing research.
[19] A. Kelly. Living loss: an exploration of the internal space of liminality , 2008 .
[20] E. Bocchi,et al. Caring for heart transplant recipients: The lived experience of primary caregivers. , 2013, Heart & lung : the journal of critical care.
[21] A. Thinnes,et al. Effect of educational and supportive strategies on the ability of caregivers of people with dementia to maintain participation in that role. , 2011, The American journal of occupational therapy : official publication of the American Occupational Therapy Association.
[22] A. Koivisto,et al. Life orientation in Finnish family caregivers' of persons with Alzheimer's disease: a diary study. , 2012, Nursing & health sciences.
[23] C. L. Callahan,et al. The quality of life. , 1970, Nursing outlook.
[24] M. Bakitas,et al. Cancer family caregivers: a new direction for interventions. , 2012, Journal of palliative medicine.
[25] K. Adams. The Transition to Caregiving , 2006, Journal of gerontological social work.
[26] C. Mwaria. The concept of self in the context of crisis: a study of families of the severely brain-injured. , 1990, Social science & medicine.
[27] P. Vitaliano,et al. Is caregiving hazardous to one's physical health? A meta-analysis. , 2003, Psychological bulletin.
[28] K. Cox,et al. Liminality as a framework for understanding the experience of cancer survivorship: a literature review. , 2012, Journal of advanced nursing.
[29] Christina Jones,et al. Sources of Uncertainty: Experiences of Alzheimer's Disease , 2009, Issues in mental health nursing.
[30] P. Ubel,et al. Caregiving Behavior Is Associated With Decreased Mortality Risk , 2009, Psychological science.
[31] M. Brown,et al. AIDS Family Caregiving: Transitions Through Uncertainty , 1991, Nursing research.
[32] Cornelia M Ruland,et al. Review of the literature on the effects of caring for a patient with cancer , 2010, Psycho-oncology.
[33] P. Donnelly. Korean American Family Experiences of Caregiving for their Mentally Ill Adult Children: An Interpretive Inquiry , 2001, Journal of transcultural nursing : official journal of the Transcultural Nursing Society.
[34] Valentina Mazzoni,et al. Becoming a caregiver: new family carers' experience during the transition from hospital to home. , 2012, Journal of clinical nursing.
[35] R. Wiechula,et al. Women's experience of becoming caregivers to their ill partners: Gadamerian hermeneutics. , 2011, Australian journal of primary health.
[36] L. Todres,et al. The intimate mediator: a carer's experience of Alzheimer's. , 2005, Scandinavian journal of caring sciences.
[37] Anne Bruce,et al. Stories of Liminality , 2014, Journal of holistic nursing : official journal of the American Holistic Nurses' Association.
[38] Margaret C. Harrell,et al. Military Caregivers: Cornerstones of Support for Our Nation's Wounded, Ill, and Injured Veterans. , 2013, Rand health quarterly.
[39] Wright Professor Stephen,et al. Rites of Passage , 2010 .
[40] A. Strauss,et al. THE PURPOSE AND CREDIBILITY OF QUALITATIVE RESEARCH , 1966, Nursing research.
[41] H. Peyrovi,et al. Lived experiences of Iranian family member caregivers of persons with Alzheimer's disease: caring as 'captured in the whirlpool of time'. , 2012, Journal of clinical nursing.
[42] M. Littrell,et al. The influence of orphan care and other household shocks on health status over time: a longitudinal study of children's caregivers in rural Malawi , 2011, AIDS care.
[43] J. Kornfield. The Wise Heart: A Guide to the Universal Teachings of Buddhist Psychology , 2008 .
[44] M. Patton,et al. Enhancing the quality and credibility of qualitative analysis. , 1999, Health services research.
[45] M. Burman. Family caregiver expectations and management of the stroke trajectory. , 2001, Rehabilitation nursing : the official journal of the Association of Rehabilitation Nurses.
[46] R. Whittemore,et al. The integrative review: updated methodology. , 2005, Journal of advanced nursing.
[47] P. Munhall. In women's experience , 1994 .
[48] J. Penrod. Living with uncertainty: concept advancement. , 2007, Journal of advanced nursing.
[49] R. Schulz,et al. Spousal suffering and partner's depression and cardiovascular disease: the Cardiovascular Health Study. , 2009, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.
[50] Laura K M Donorfio,et al. Filial Responsibility and Transitions Involved: A Qualitative Exploration of Caregiving Daughters and Frail Mothers , 2006 .
[51] N. Greenwood,et al. Positive experiences of caregiving in stroke: a systematic review , 2012, Disability and rehabilitation.
[52] Tzu-Ying Lee,et al. Living experiences of male spouses of patients with metastatic cancer in Taiwan. , 2013, Asian Pacific journal of cancer prevention : APJCP.
[53] Richard Schulz,et al. Linguistic markers of emotion regulation and cardiovascular reactivity among older caregiving spouses. , 2012, Psychology and aging.
[54] Lixin Song,et al. Interventions with Family Caregivers of Cancer Patients: Meta‐Analysis of Randomized Trials , 2010, CA: a cancer journal for clinicians.
[55] C. Bulley,et al. Carer experiences of life after stroke – a qualitative analysis , 2010, Disability and rehabilitation.
[56] A. Loke,et al. The positive aspects of caregiving for cancer patients: a critical review of the literature and directions for future research , 2013, Psycho-oncology.
[57] Shalini Grover. Lived experiences , 2009 .
[58] B. Mausbach,et al. A Review of the Psychobiology of Dementia Caregiving: A Focus on Resilience Factors , 2011, Current psychiatry reports.
[59] Reg C Morris,et al. The experience of partners of young stroke survivors , 2009, Disability and rehabilitation.
[60] L. Johnston. Surviving Critical Illness: A Case Study in Ambiguity , 2011, Journal of social work in end-of-life & palliative care.
[61] S. Söderberg,et al. Transition as Experienced by Close Relatives of People With Traumatic Brain Injury , 2011, The Journal of neuroscience nursing : journal of the American Association of Neuroscience Nurses.
[62] N. Greenwood,et al. Managing uncertainty in life after stroke: a qualitative study of the experiences of established and new informal carers in the first 3 months after discharge. , 2009, International journal of nursing studies.
[63] C. McAiney,et al. Uncertainty and alternate level of care: a narrative study of the older patient and family caregiver experience. , 2013, The Canadian journal of nursing research = Revue canadienne de recherche en sciences infirmieres.