Family consent, communication, and advance directives for cancer disclosure: a Japanese case and discussion.
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Perspectives on advance directives in Japanese society: A population-based questionnaire surveyDisclosure of cancer diagnosis and prognosis: a survey of the general public's attitudes toward doctors and family holding discretionary powersMeasuring motivation for medical treatment: confirming the factor structure of the Achievement Motivation Index for Medical Treatment (AMI-MeT)Breaking bad news: a Chinese perspective.Acculturation of attitudes toward end-of-life care: a cross-cultural survey of Japanese Americans and JapaneseEthical dilemmas in oncofertility: an exploration of three clinical scenariosShould cancer patients be informed about their diagnosis and prognosis? Future doctors and lawyers differ.Evaluation of end of life care in cancer patients at a teaching hospital in JapanDisclosure preferences regarding cancer diagnosis and prognosis: to tell or not to tell?Conceptualizing the Pathways and Processes Between Language Barriers and Health Disparities: Review, Synthesis, and Extension.Bioethics in and from Asia.Truth-telling in discussing prognosis in advanced life-limiting illnesses: a systematic review.Applicability of the principle of respect for autonomy: the perspective of Turkey.Identification of quality indicators of end-of-life cancer care from medical chart review using a modified Delphi method in Japan.Treatment initiatives for patients with Alzheimer's disease.Truth telling for patients with esophageal squamous cell carcinoma in Henan, China.End-of-life communication in Korean older adults: With focus on advance care planning and advance directives.Korean nurses' attitudes to good and bad death, life-sustaining treatment and advance directives.End-of-life decision-making of terminally ill cancer patients in a tertiary cancer center in Shanghai, China.The emerging need for family-centric initiatives for obtaining consent in personal genome research.The evaluation of the relationship between the level of disclosure of cancer in terminally ill patients with cancer and the quality of terminal care in these patients and their families using the Support Team Assessment Schedule.Evolving legal responses to dependence on families in New Zealand and Singapore healthcare.What and when Korean American older adults want to know about serious illness.The current status of bereavement follow-up in hospice and palliative care in Japan.Physician-patient end-of-life care discussions: correlates and associations with end-of-life care preferences of cancer patients-a cross-sectional survey study.Congruence of knowledge, experiences, and preferences for disclosure of diagnosis and prognosis between terminally-ill cancer patients and their family caregivers in Taiwan.Surrogate decision-making in Korean patients with advanced cancer: a longitudinal studyResponse to Open Peer Commentaries on “Informed Consent Revisited: Japan and the US”Informed Consent Revisited: Japan and the U.S.
P2860
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P2860
Family consent, communication, and advance directives for cancer disclosure: a Japanese case and discussion.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Family consent, communication, ...... Japanese case and discussion.
@ast
Family consent, communication, ...... Japanese case and discussion.
@en
type
label
Family consent, communication, ...... Japanese case and discussion.
@ast
Family consent, communication, ...... Japanese case and discussion.
@en
prefLabel
Family consent, communication, ...... Japanese case and discussion.
@ast
Family consent, communication, ...... Japanese case and discussion.
@en
P2093
P2860
P356
P1476
Family consent, communication, ...... Japanese case and discussion.
@en
P2093
Akabayashi A
Fetters MD
P2860
P304
P356
10.1136/JME.25.4.296
P577
1999-08-01T00:00:00Z