“Going Home [Is] Just a Feel-Good Idea With No Structure”: A Qualitative Exploration of Patient and Family Caregiver Needs When Transitioning From Hospital to Home in Palliative Care

This publication has 32 references indexed in Scilit:

• Preferred place of death for children and young people with life-limiting and life-threatening conditions: A systematic review of the literature and recommendations for future inquiry and policy
  Palliative Medicine, 2013
• Heterogeneity and changes in preferences for dying at home: a systematic review
  BMC Palliative Care, 2013
• Japanese People’s Preference for Place of End-of-Life Care and Death: A Population-Based Nationwide Survey
  Journal of Pain and Symptom Management, 2011
• End-of-Life Transitions among Nursing Home Residents with Cognitive Issues
  New England Journal of Medicine, 2011
• Discharge Planning for Palliative Care Patients: A Qualitative Analysis
  Journal of Palliative Medicine, 2011
• Part 2: Home-based family caregiving at the end of life: a comprehensive review of published qualitative research (1998-2008)
  Palliative Medicine, 2010
• Bereaved Hospice Caregivers' Views of the Transition to Hospice
  Social Work in Health Care, 2010
• Rehospitalizations among Patients in the Medicare Fee-for-Service Program
  New England Journal of Medicine, 2009
• A practical instrument to explore patients' needs in palliative care: the Problems and Needs in Palliative Care questionnaire — short version
  Palliative Medicine, 2007
• Preparing Patients and Caregivers to Participate in Care Delivered Across Settings: The Care Transitions Intervention
  Journal of the American Geriatrics Society, 2004