171 results on '"Bandini, Julia"'
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2. Impact of group visits for older patients with heart failure on advance care planning outcomes: Preliminary data
3. Feasibility of Group Visits for Advance Care Planning Among Patients with Heart Failure and Their Caregivers.
4. ‘You just don’t feel like your work goes recognised’: healthcare worker experiences of tension related to public discourse around the COVID-19 pandemic
5. Experience with a Revised Hospital Policy on Not Offering Cardiopulmonary Resuscitation
6. Incorporating the Patient and Caregiver Voice in Palliative Care Quality Measure Development
7. Encountering the social determinants of health on a COVID-19 ICU: Frontline providers’ perspectives on inequality in a time of pandemic
8. Understanding Multilevel Factors Related to Retention Among the Direct Care Workforce: Incorporating Lessons Learned in Considering Innovative Interventions
9. Individual, interpersonal, and health care factors associated with informal and formal advance care planning in a nationally-representative sample of midlife and older adults
10. Ethics Consultation for Adult Solid Organ Transplantation Candidates and Recipients: A Single Centre Experience
11. Ethics Consultations Related to Opioid Use Disorder
12. “It Haunts Me”: Impact of COVID-19 Deaths on Frontline Clinicians In Acute Care Settings—A Qualitative Study
13. MACRA Palliative Care Quality Measure Development: Summary Report of Alpha Testing
14. The role of religious beliefs in ethics committee consultations for conflict over life-sustaining treatment
15. Assessing Learning in a Sociology Department: What Do Students Say That They Learn?
16. An Evaluation of a Multisite, Health Systems–Based Direct Care Worker Retention Program: Key Findings and Recommendations
17. Developing a Medical School Curriculum for Psychological, Moral, and Spiritual Wellness: Student and Faculty Perspectives
18. Low Tech, High Potential: Using Technology to Improve Communication across Home Care Workers
19. Illness and the Internet : From Private to Public Experience
20. Religion, Spirituality, and the Hidden Curriculum: Medical Student and Faculty Reflections
21. Letter to the Editor: Tele-Palliative Care among Underserved Patients: Considerations for Future Research to Ensure Equity for All Patients
22. MACRA Palliative Care Quality Measure Development—Testing Summary Report: Measure Name: Receiving Desired Help for Pain
23. “Palliative Care Is the Only Medical Field That I Feel Like I'm Treated As a Person, Not As a Black Person”: A Mixed-Methods Study of Minoritized Patient Experiences with Palliative Care
24. Experiences with Telehealth for Outpatient Palliative Care: Findings from a Mixed-Methods Study of Patients and Providers across the United States
25. Experiences of moral distress in a COVID‐19 intensive care unit: A qualitative study of nurses and respiratory therapists in the United States
26. Clinician Perspectives on Group Visits for Advance Care Planning Among Caregivers and Older Adult Patients with Heart Failure (GP718)
27. Low Tech, High Potential: Using Technology to Improve Communication across Home Care Workers.
28. Journaling among home care workers during the COVID-19 pandemic: A promising method for qualitative data collection.
29. The Evolution of Spiritual Assessment Tools in Healthcare
30. Clinical Ethics Consultation During the First COVID-19 Pandemic Surge at an Academic Medical Center: A Mixed Methods Analysis
31. Supplemental Material - Low Tech, High Potential: Using Technology to Improve Communication across Home Care Workers
32. Student and Faculty Reflections of the Hidden Curriculum: How Does the Hidden Curriculum Shape Students’ Medical Training and Professionalization?
33. "Palliative Care Is the Only Medical Field That I Feel Like I'm Treated As a Person, Not As a Black Person": A Mixed-Methods Study of Minoritized Patient Experiences with Palliative Care.
34. Experiences of moral distress in a COVID‐19 intensive care unit: A qualitative study of nurses and respiratory therapists in the United States.
35. Patient-Reported Experiences Measure
36. Patient, Family Caregiver, and Provider Perceptions on Self-Assessment Screening for Cognitive Impairment in Primary Care: Findings From a Qualitative Study
37. Journaling among home care workers during the COVID-19 pandemic: A promising method for qualitative data collection
38. Mental Illness as a Form of Deviance
39. Family Economic Impact of Nontraumatic Deaths in the San Francisco Bay Area
40. Racial Differences in End-of-Life Care Quality between Asian Americans and Non-Hispanic Whites in San Francisco Bay Area
41. Bereaved Family More Likely to Report “Too Little” Care than “Too Much” Care at the End of Life
42. Intensive care unit nurses living through COVID‐19: A qualitative study
43. “If We Turned Our Backs, They Would Ignore Our Wishes”: Bereaved Family Perceptions of Concordance of Care at the End of Life
44. Clinician Perspectives on Group Visits for Advance Care Planning Among Caregivers and Older Adult Patients With Heart Failure
45. Beyond the hour of death: Family experiences of grief and bereavement following an end-of-life hospitalization in the intensive care unit.
46. Home Care Aide Safety Concerns and Job Challenges During the COVID-19 Pandemic
47. Experience with a Revised Hospital Policy on Not Offering Cardiopulmonary Resuscitation
48. Beyond the hour of death: Family experiences of grief and bereavement following an end-of-life hospitalization in the intensive care unit
49. Negotiating the ‘buffet’ of choice: advances in technology and end‐of‐life decision‐making in the intensive care unit setting
50. Interprofessional Spiritual Care Training for Geriatric Care Providers
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