86 results on '"Miyashita, Mitsunori"'
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2. Cancer Pain Management in Patients Receiving Inpatient Specialized Palliative Care Services
3. Validity and reliability of the Japanese version of the Patient Satisfaction Questionnaire (PSQ-J) for evaluating oncologist consultations
4. The Impact of Stressful Life Events after Bereavement: A Nationwide Cross-sectional Survey
5. Factors related to suicidal ideation among bereaved family members of patients with cancer: Results from a nationwide bereavement survey in Japan
6. Experience of the temporary discharge from the inpatient palliative care unit: A nationwide post-bereavement survey for end-of-life cancer patients
7. Caregiver experience with decision-making difficulties in end-of-life care for patients with cardiovascular diseases
8. Quality Indicators in Palliative Radiation Oncology: Development and Pilot Testing
9. Attitudes of Physicians toward Palliative Care in Intensive Care Units: A Nationwide Cross-Sectional Survey in Japan
10. The Association of Family Functioning With Possible Major Depressive Disorders and Complicated Grief Among Bereaved Family Members of Patients With Cancer: Results From the J-HOPE4 Study, a Nationwide Cross-Sectional Follow-Up Survey in Japan
11. The prevalence of artificially administered nutrition and hydration in different age groups among patients with advanced cancer admitted to palliative care units
12. Developing an instrument to assess the readiness for advance care planning
13. Physician's Communication in Code Status Discussions for Terminally Ill Cancer Patients in Inpatient Hospice/Palliative Care Units in Japan: A Nationwide Post-Bereavement Survey
14. How Successful Is Parenteral Oxycodone for Relieving Terminal Cancer Dyspnea Compared With Morphine? A Multicenter Prospective Observational Study
15. Growth and Challenges in Hospital Palliative Cancer Care Services: An Analysis of Nationwide Surveys Over a Decade in Japan
16. Care Associated With Satisfaction of Bereaved Family Members of Terminally Ill Cancer Patients With Dyspnea: A Cross-sectional Nationwide Survey
17. Effects of enteral nutrition and parenteral nutrition on survival in patients with advanced cancer cachexia: Analysis of a multicenter prospective cohort study
18. A Population-Based Mortality Follow-Back Survey Evaluating Good Death for Cancer and Noncancer Patients: A Randomized Feasibility Study
19. Rehabilitation for Cancer Patients in Inpatient Hospices/Palliative Care Units and Achievement of a Good Death: Analyses of Combined Data From Nationwide Surveys Among Bereaved Family Members
20. Insomnia and changes in alcohol consumption: Relation between possible complicated grief and depression among bereaved family caregivers
21. Beliefs and Perceptions About Parenteral Nutrition and Hydration by Family Members of Patients With Advanced Cancer Admitted to Palliative Care Units: A Nationwide Survey of Bereaved Family Members in Japan
22. Quality indicators of palliative care for acute cardiovascular diseases
23. Difference in Opinions About Continuous Deep Sedation Among Cancer Patients, Bereaved Families, and Physicians
24. Communication Disparity Between the Bereaved and Others: What Hurts Them and What Is Unhelpful? A Nationwide Study of the Cancer Bereaved
25. Editorial Special Issue: Pain Management
26. Communication Disparity Between the Bereaved and Others: What Hurts Them and What Is Unhelpful? A Nationwide Study of the Cancer Bereaved
27. Changes in Nurses' Knowledge, Difficulties, and Self-reported Practices Toward Palliative Care for Cancer Patients in Japan: An Analysis of Two Nationwide Representative Surveys in 2008 and 2015
28. Which Research Questions Are Important for the Bereaved Families of Palliative Care Cancer Patients? A Nationwide Survey
29. Acculturation and Perceptions of a Good Death Among Japanese Americans and Japanese Living in the U.S.
30. Talking About Death With Terminally-Ill Cancer Patients: What Contributes to the Regret of Bereaved Family Members?
31. Psychological and psychiatric symptoms of terminally ill patients with cancer and their family caregivers in the home-care setting: A nation-wide survey from the perspective of bereaved family members in Japan
32. Unfinished Business in Families of Terminally Ill With Cancer Patients
33. Variations in Denominators and Cut-off Points of Pain Intensity in the Pain Management Index: A Methodological Systematic Review
34. Potential palliative care quality indicators in heart disease patients: A review of the literature
35. Meaningful Communication Before Death, but Not Present at the Time of Death Itself, Is Associated With Better Outcomes on Measures of Depression and Complicated Grief Among Bereaved Family Members of Cancer Patients
36. Effects of End-of-Life Discussions on the Mental Health of Bereaved Family Members and Quality of Patient Death and Care
37. Decision Making Regarding the Place of End-of-Life Cancer Care: The Burden on Bereaved Families and Related Factors
38. P196 Does Negative PMI Indicate a Need for Further Pain Treatment? Concordance Between PMI and Other Indicators
39. Changes in Relatives' Perspectives on Quality of Death, Quality of Care, Pain Relief, and Caregiving Burden Before and After a Region-Based Palliative Care Intervention
40. Nationwide Japanese Survey About Deathbed Visions: “My Deceased Mother Took Me to Heaven”
41. Evaluation of care for leukemia and lymphoma patients during their last hospitalization from the perspective of the bereaved family
42. Development and validation of scales for attitudes, self-reported practices, difficulties and knowledge among home care nurses providing palliative care
43. Association Between Bereaved Families' Sense of Security and Their Experience of Death in Cancer Patients: Cross-Sectional Population-Based Study
44. Population-Based Quality Indicators for Palliative Care Programs for Cancer Patients in Japan: A Delphi Study
45. Improvements in Physicians' Knowledge, Difficulties, and Self-Reported Practice After a Regional Palliative Care Program
46. A Nationwide Survey of Quality of End-of-Life Cancer Care in Designated Cancer Centers, Inpatient Palliative Care Units, and Home Hospices in Japan: The J-HOPE Study
47. Independent Validation of the Japanese Version of the EORTC QLQ-C15-PAL for Patients With Advanced Cancer
48. Why People Accept Opioids: Role of General Attitudes Toward Drugs, Experience as a Bereaved Family, Information From Medical Professionals, and Personal Beliefs Regarding a Good Death
49. Changes in Quality of Care and Quality of Life of Outpatients With Advanced Cancer After a Regional Palliative Care Intervention Program
50. A Survey of the Influence of Patients' Residential Areas on Satisfaction Levels in Cancer Care at Designated Hospitals
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