443 results on '"Kaye, Erica C."'
Search Results
2. Full Collection of Personal Narratives
3. Parent and oncologist perspectives on prognostic disclosure in advanced childhood cancer: communication pearls and pitfalls
4. Narrative medicine interventions for oncology clinicians: a systematic review
5. Questions to promote child-centered care in racially discordant interactions in pediatric oncology
6. Publicly available information about fertility benefits for trainees at medical schools in the US
7. Dignity in the Pediatric Population: A Systematic Review
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. Medical experts and trusted confidants: parent perceptions of the clinician-parent relationship in childhood cancer
12. The Power of Story
13. Approaches for Discussing Clinical Trials with Pediatric Oncology Patients and Their Families
14. Novel approaches to communication skills development: The untapped potential of qualitative research immersion
15. Oncologist approaches to communicating uncertain disease status in pediatric cancer: a qualitative study
16. The ALIGN Framework: A Parent-Informed Approach to Prognostic Communication for Infants With Neurologic Conditions
17. Conflicting goals and obligations: Tensions affecting communication in pediatric oncology
18. Language to Support Dignity for Children With Advanced Cancer and Their Families.
19. Access to legacy‐oriented interventions at end of life for pediatric oncology patients: A decedent cohort review.
20. Communication of Early Integration of Palliative Care for Children With Cancer in Latin America: The Care as a Vessel Metaphor
21. Communication around palliative care principles and advance care planning between oncologists, children with advancing cancer and families
22. “Still Caring for the Family”: Condolence Expression Training for Pediatric Residents
23. you leave a hole
24. Understanding treatment recommendations at diagnosis of advanced cancer in pediatric oncology: The need to explore decision‐making challenges globally
25. Global Experiences of Pediatric Palliative Care Teams During the First 6 Months of the SARS-CoV-2 Pandemic
26. The Impact of Specialty Palliative Care in Pediatric Oncology: A Systematic Review
27. Narrative Medicine in Hospice and Palliative Care: A Longitudinal Fellowship Curriculum Pilot.
28. 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
29. Factors influencing parents' choice of palliative treatment goals for children with relapsed or refractory neuroblastoma: A multi‐site longitudinal survey study.
30. Opportunities for Palliative Care in Patients With Burn Injury—A Systematic Review
31. End-of-Life Care, Palliative Care Consultation, and Palliative Care Referral in the Emergency Department: A Systematic Review
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. CritCom: assessment of quality of interdisciplinary communication around deterioration in pediatric oncologic patients
35. Opportunities to Improve Utilization of Palliative Care Among Adults With Cystic Fibrosis: A Systematic Review
36. Palliative Care Opportunities Among Adults With Congenital Heart Disease—A Systematic Review
37. Palliative Care Transitions From Acute Care to Community-Based Care—A Systematic Review
38. Translating Research to Action: The Development of a Pediatric Palliative Cancer Care Advocacy Tool in Eurasia
39. Thoughts from the threshold: patient and family hopes, fears, values, and goals at the onset of pediatric hematopoietic cell transplantation
40. Communication with Children with Cancer and Their Families Throughout the Illness Journey and at the End of Life
41. 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
42. Provision of Palliative and Hospice Care to Children in the Community: A Population Study of Hospice Nurses
43. Equitable communication for pediatric cancer patients and families who speak languages other than English.
44. Longitudinal Impact of a Novel Condolence Expression Curriculum
45. Factors influencing treatment decision‐making for cancer patients in low‐ and middle‐income countries: A scoping review
46. A new measure for multi-professional medical team communication: design and methodology for multilingual measurement development
47. Factors Influencing Pediatric Oncologists' Decision-Making when Balancing Curative and Non-Curative Treatment Options at Diagnosis in Low- and Middle-Income Countries (Sch429)
48. A Descriptive Analysis of Outpatient Pediatric Palliative Care Clinic Structure and Workflow in the United States (Sch404)
49. Disparate Access to Fertility Preservation in Youth: A Call for Advocacy to Close the Gap
50. Productivity in Pediatric Palliative Care: Measuring and Monitoring an Elusive Metric
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