447 results on '"Kaye, Erica C."'
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2. Full Collection of Personal Narratives
3. Exploring treatment decision-making at diagnosis for children with advanced cancer in low- and middle-income countries
4. Parent and oncologist perspectives on prognostic disclosure in advanced childhood cancer: communication pearls and pitfalls
5. Narrative medicine interventions for oncology clinicians: a systematic review
6. Publicly available information about fertility benefits for trainees at medical schools in the US
7. Questions to promote child-centered care in racially discordant interactions in pediatric oncology
8. Supporting Disclosure of Unmet Mental Health Needs among Parents of Critically Ill Infants
9. Pediatric Palliative Care Program Implementation in LMICs: A Systematic Review using SWOT Analysis
10. The Landscape of Outpatient Pediatric Palliative Care: A National Cross-Sectional Assessment
11. Approaches for Discussing Clinical Trials with Pediatric Oncology Patients and Their Families
12. Novel approaches to communication skills development: The untapped potential of qualitative research immersion
13. Medical experts and trusted confidants: parent perceptions of the clinician-parent relationship in childhood cancer
14. Oncologist approaches to communicating uncertain disease status in pediatric cancer: a qualitative study
15. The ALIGN Framework: A Parent-Informed Approach to Prognostic Communication for Infants With Neurologic Conditions
16. Storytelling to support legacy making for bereaved parents of children with cancer.
17. Narrative Medicine in Hospice and Palliative Care: A Longitudinal Fellowship Curriculum Pilot.
18. Conflicting goals and obligations: Tensions affecting communication in pediatric oncology
19. “Still Caring for the Family”: Condolence Expression Training for Pediatric Residents
20. The Power of Story
21. Global Experiences of Pediatric Palliative Care Teams During the First 6 Months of the SARS-CoV-2 Pandemic
22. Communication around palliative care principles and advance care planning between oncologists, children with advancing cancer and families
23. Communication of Early Integration of Palliative Care for Children With Cancer in Latin America: The Care as a Vessel Metaphor
24. The Impact of Specialty Palliative Care in Pediatric Oncology: A Systematic Review
25. Investigation of Modifiable Variables to Increase Hospice Nurse Comfort With Care Provision to Children and Families in the Community: A Population-Level Study Across Tennessee, Mississippi, and Arkansas
26. Language to Support Dignity for Children With Advanced Cancer and Their Families.
27. Access to legacy‐oriented interventions at end of life for pediatric oncology patients: A decedent cohort review.
28. Opportunities for Palliative Care in Patients With Burn Injury—A Systematic Review
29. End-of-Life Care, Palliative Care Consultation, and Palliative Care Referral in the Emergency Department: A Systematic Review
30. you leave a hole
31. Understanding treatment recommendations at diagnosis of advanced cancer in pediatric oncology: The need to explore decision‐making challenges globally
32. Equitable communication for pediatric cancer patients and families who speak languages other than English
33. Questions to promote child-centered care in racially discordant interactions in pediatric oncology
34. Opportunities to Improve Utilization of Palliative Care Among Adults With Cystic Fibrosis: A Systematic Review
35. Thoughts from the threshold: patient and family hopes, fears, values, and goals at the onset of pediatric hematopoietic cell transplantation
36. Communication with Children with Cancer and Their Families Throughout the Illness Journey and at the End of Life
37. Palliative Care Opportunities Among Adults With Congenital Heart Disease—A Systematic Review
38. Palliative Care Transitions From Acute Care to Community-Based Care—A Systematic Review
39. Introduction to a New Special Series for the Journal of Pain and Symptom Management—Science in Action: Evidence and Opportunities for Palliative Care Across Diverse Populations and Care Settings
40. Translating Research to Action: The Development of a Pediatric Palliative Cancer Care Advocacy Tool in Eurasia
41. Provision of Palliative and Hospice Care to Children in the Community: A Population Study of Hospice Nurses
42. Factors influencing parents' choice of palliative treatment goals for children with relapsed or refractory neuroblastoma: A multi‐site longitudinal survey study.
43. Equitable communication for pediatric cancer patients and families who speak languages other than English.
44. CritCom: assessment of quality of interdisciplinary communication around deterioration in pediatric oncologic patients
45. Longitudinal Impact of a Novel Condolence Expression Curriculum
46. Factors influencing treatment decision‐making for cancer patients in low‐ and middle‐income countries: A scoping review
47. A new measure for multi-professional medical team communication: design and methodology for multilingual measurement development
48. Productivity in Pediatric Palliative Care: Measuring and Monitoring an Elusive Metric
49. Empowering Bereaved Parents Through the Development of a Comprehensive Bereavement Program
50. Factors Influencing Pediatric Oncologists' Decision-Making when Balancing Curative and Non-Curative Treatment Options at Diagnosis in Low- and Middle-Income Countries (Sch429)
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