Citations (47)
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Brian Matthews & Jamie Daigle. (2020) Connecting the dots between caregiver expectations and perceptions during the hospice care continuum: Lessons for interdisciplinary teams. International Journal of Healthcare Management 13:sup1, pages 120-132.
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DeborahP. Waldrop & ElaineS. Rinfrette. (2009) Making the Transition to Hospice: Exploring Hospice Professionals' Perspectives. Death Studies 33:6, pages 557-580.
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Gary
E Myers. (2003) Restoration or transformation? Choosing ritual strategies for end-of-life care. Mortality 8:4, pages 372-387.
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Sandra L. Ragan, Elaine Wittenberg & Harry T. Hall. (2003) The Communication of Palliative Care for the Elderly Cancer Patient. Health Communication 15:2, pages 219-226.
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Sherri Roff. (2001) Analyzing End-of-Life Care Legislation. Social Work in Health Care 33:1, pages 51-68.
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Robert W Buckingham & Edward A Meister. (2001) Hospice care for the child with AIDS. The Social Science Journal 38:3, pages 461-467.
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Brandi R. Newsome, George E. Dickinson. (2000) DEATH EXPERIENCES AND HOSPICE: PERCEPTIONS OF COLLEGE STUDENTS. Death Studies 24:4, pages 335-341.
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Articles from other publishers (40)
Elie K Mehanna, Paul J Catalano, Daniel N Cagney, Daphne A Haas-Kogan, Brian M Alexander, James A Tulsky & Ayal A Aizer. (2020) Hospice Utilization in Elderly Patients With Brain Metastases. JNCI: Journal of the National Cancer Institute 112:12, pages 1251-1258.
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Channing E. Tate, Grace Venechuk, Elinor J. Brereton, Pilar Ingle, Larry A. Allen, Megan A. Morris & Daniel D. Matlock. (2019) “It’s Like a Death Sentence but It Really Isn’t” What Patients and Families Want to Know About Hospice Care When Making End-of-Life Decisions. American Journal of Hospice and Palliative Medicine® 37:9, pages 721-727.
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Mary Ann Meeker, Jacqueline M. McGinley & Mary Ann Jezewski. (2019) Metasynthesis: Dying adults’ transition process from cure‐focused to comfort‐focused care. Journal of Advanced Nursing 75:10, pages 2059-2071.
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Carey Candrian, Channing Tate, Kirsten Broadfoot, Alexandra Tsantes, Daniel Matlock & Jean Kutner. (2017) Designing Effective Interactions for Concordance around End-of-Life Care Decisions: Lessons from Hospice Admission Nurses. Behavioral Sciences 7:4, pages 22.
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Stephen Claxton-Oldfield & Hayley Marrison-Shaw. (2013) Perceived Barriers and Enablers to Referrals to Community-Based Hospice Palliative Care Volunteer Programs in Canada. American Journal of Hospice and Palliative Medicine® 31:8, pages 836-844.
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Laura Foran Lewis. (2014) Caregivers’ Experiences Seeking Hospice Care for Loved Ones With Dementia. Qualitative Health Research 24:9, pages 1221-1231.
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Emma Kirby, Alex Broom, Phillip Good, Julia Wootton & Jon Adams. (2014) Medical specialists’ motivations for referral to specialist palliative care: a qualitative study. BMJ Supportive & Palliative Care 4:3, pages 277-284.
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Melissa D. Aldridge & Jean S. Kutner. 2014. Meeting the Needs of Older Adults with Serious Illness. Meeting the Needs of Older Adults with Serious Illness
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M. Encarlita Tee, Gayle Z. Balmaceda, Myra A. Granada, Clara S. Fowler & Judith K. Payne. (2013) End-of-Life Decision Making in Hematopoietic Cell Transplantation Recipients. Clinical Journal of Oncology Nursing 17:6, pages 640-646.
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Jissy Vijo Poulose, Young Kyung Do & Patricia Soek Hui Neo. (2013) Association Between Referral-to-Death Interval and Location of Death of Patients Referred to a Hospital-Based Specialist Palliative Care Service. Journal of Pain and Symptom Management 46:2, pages 173-181.
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Rebecca E. Colman, J. Randall Curtis, Judith E. Nelson, Linda Efferen, Denis Hadjiliadis, Deborah J. Levine, Keith C. Meyer, Maria Padilla, Mary Strek, Basil Varkey & Lianne G. Singer. (2013) Barriers to Optimal Palliative Care of Lung Transplant Candidates. Chest 143:3, pages 736-743.
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Alex BroomEmma KirbyPhillip GoodJulia WoottonJon Adams. (2012) Specialists' Experiences and Perspectives on the Timing of Referral to Palliative Care: A Qualitative Study. Journal of Palliative Medicine 15:11, pages 1248-1253.
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Ching-Ye HongGuat Ngoo Ng, Jissy Poulose, Nelson Jianli Lin & Cynthia Ruth Goh. (2018) Attitude of Doctors in An Asian Oncology Centre towards Referral to Palliative Care. Journal of Palliative Care 27:2, pages 157-163.
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Todd M. JenkinsKathryn L. Chapman, Christine S. Ritchie, Donna K. Arnett, Gerald McGwinJrJr, Stacey S. Cofield & H. Micheal Maetz. (2010) Barriers to Hospice Care in Alabama: Provider-Based Perceptions. American Journal of Hospice and Palliative Medicine® 28:3, pages 153-160.
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Cecile N. YancuDeborah F. Farmer & Dee Leahman. (2009) Barriers to Hospice Use and Palliative Care Services Use by African American Adults. American Journal of Hospice and Palliative Medicine® 27:4, pages 248-253.
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Kelly K. Hill & Eileen D. Hacker. (2010) Helping Patients With Cancer Prepare for Hospice. Clinical Journal of Oncology Nursing 14:2, pages 180-188.
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Christina S. Melvin & Lynn Oldham. (2009) When to Refer Patients to Palliative Care. Journal of Hospice & Palliative Nursing 11:5, pages 291-301.
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Stephen Claxton-OldfieldJane Claxton-Oldfield. (2008) Some Common Problems Faced by Hospice Palliative Care Volunteers. American Journal of Hospice and Palliative Medicine® 25:2, pages 121-126.
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Melissa D.A. CarlsonR. Sean MorrisonElizabeth H. Bradley. (2008) Improving Access to Hospice Care: Informing the Debate. Journal of Palliative Medicine 11:3, pages 438-443.
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Makiko Sanjo, Mitsunori Miyashita, Tatsuya Morita, Kei Hirai, Masako Kawa, Tomoko Ashiya, Tatsuhiko Ishihara, Izuru Miyoshi, Tatsuhiro Matsubara, Toshimichi Nakaho, Nobuaki Nakashima, Hideki Onishi, Taketoshi Ozawa, Kazuyuki Suenaga, Tsukasa Tajima, Takayuki Hisanaga & Yosuke Uchitomi. (2008) Perceptions of Specialized Inpatient Palliative Care: A Population-Based Survey in Japan. Journal of Pain and Symptom Management 35:3, pages 275-282.
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Mitsunori Miyashita, Kei Hirai, Tatsuya Morita, Makiko Sanjo & Yosuke Uchitomi. (2007) Barriers to referral to inpatient palliative care units in Japan: a qualitative survey with content analysis. Supportive Care in Cancer 16:3, pages 217-222.
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C.E. JohnsonA. Girgis, C.L. Paul & D.C. Currow. (2008) Cancer specialists' palliative care referral practices and perceptions: results of a national survey. Palliative Medicine 22:1, pages 51-57.
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Verna L Hendricks-Ferguson. (2007) Parental perspectives of initial end-of-life care communication. International Journal of Palliative Nursing 13:11, pages 522-531.
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Dorry McLaughlin, Kate Sullivan & Felicity Hasson. (2006) Hospice at Home service: the carer’s perspective. Supportive Care in Cancer 15:2, pages 163-170.
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Elaine M. Wittenberg-Lyles & Sharlene Thompson. (2016) Understanding Enrollment Conversations: The Role of the Hospice Admissions Representative. American Journal of Hospice and Palliative Medicine® 23:4, pages 317-322.
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Inga Lill Kallstrom Karlsson, Margareta Ehnfors & Britt-Marie Ternestedt. (2006) Patient characteristics of women and men cared for during the first 10 years at an inpatient hospice ward in Sweden. Scandinavian Journal of Caring Sciences 20:2, pages 113-121.
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Elizabeth K. Vig, Helene Starks, Janelle S. Taylor, Elizabeth K. Hopley, Kelly Fryer-Edwards & Robert A. Pearlman. (2016) How do surrogate decision makers describe hospice? Does it matter?. American Journal of Hospice and Palliative Medicine® 23:2, pages 91-99.
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Lori A. Roscoe & Ronald S. Schonwetter. (2019) Improving Access to Hospice and Palliative Care for Patients near the End of Life: Present Status and Future Direction. Journal of Palliative Care 22:1, pages 46-50.
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Deborah P. Waldrop. (2006) At the Eleventh Hour: Psychosocial Dynamics in Short Hospice Stays. The Gerontologist 46:1, pages 106-114.
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Deborah P. WaldropBetty J. KramerJudith A. SkretnyRobert A. MilchWilliam Finn. (2005) Final Transitions: Family Caregiving at the End of Life. Journal of Palliative Medicine 8:3, pages 623-638.
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N Ahmed, J E Bestall, S H Ahmedzai, S A Payne, D Clark & B Noble. (2016) Systematic review of the problems and issues of accessing specialist palliative care by patients, carers and health and social care professionals. Palliative Medicine 18:6, pages 525-542.
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Charlene L. Taylor. (2004) Improving referral of patients to hospice through community physician outreach. Journal of Pain and Symptom Management 28:3, pages 294-295.
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Leslea BricknerKate ScannellStephanie Marquet & Lynn Ackerson. (2004) Barriers to Hospice Care and Referrals: Survey of Physicians' Knowledge, Attitudes, and Perceptions in a Health Maintenance Organization. Journal of Palliative Medicine 7:3, pages 411-418.
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Brenda S. Sanders, Tracy L. Burkett, George E. Dickinson & Robert E. Tournier. (2016) Hospice referral decisions: The role of physicians. American Journal of Hospice and Palliative Medicine® 21:3, pages 196-202.
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Susan C. Miller, Sherry Weitzen & Barrt Kinzbrunner. (2003) Factors Associated with the High Prevalence of Short Hospice Stays. Journal of Palliative Medicine 6:5, pages 725-736.
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Richard D. Brumley, Susan Enguidanos & David A. Cherin. (2003) Effectiveness of a Home-Based Palliative Care Program for End-of-Life. Journal of Palliative Medicine 6:5, pages 715-724.
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George R. Wilson & Gary M. Reisfield. (2016) More patients served by hospice, but still a last resort. American Journal of Hospice and Palliative Medicine® 20:3, pages 173-174.
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JAMES L. WERTHJr.Jr. & DEAN BLEVINS. (2016) Public Policy and End-of-life Care. American Behavioral Scientist 46:3, pages 401-417.
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Chris Bailey, Katherine Froggatt, David Field & Meinir Krishnasamy. (2002) The nursing contribution to qualitative research in palliative care 1990–1999: a critical evaluation. Journal of Advanced Nursing 40:1, pages 48-60.
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Maria J. Friedrichsen, Peter M. Strang & Maria E. Carlsson. (2019) Receiving Bad News: Experiences of Family Members. Journal of Palliative Care 17:4, pages 241-247.
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