Definition and recommendations of advance care planning : a Delphi study in five Asian sectors

Article indépendant

MORI, Masanori | CHAN, Helen Y. L. | LIN, Cheng-Pei | KIM, Sun-Hyun | NG HAN LIP, Raymond | MARTINA, Diah | YUEN, Kwok Keung | CHENG, Shao-Yi | TAKENOUCHI, Sayaka | SUH, Sang-Yeon | MENON, Sumytra | KIM, Jungyoung | CHEN, Ping-Jen | IWATA, Futoshi | TASHIRO, Shimon | KWOK, Oi Ling Annie | PENG, Jen-Kuei | HUANG, Hsien-Liang | MORITA, Tatsuya | KORFAGE, Ida J. | RIETJENS, Judith A. C. | KIZAWA, Yoshiyuki

BACKGROUND: In Confucian-influenced Asian societies, explicit end-of-life conversations are uncommon and family involvement in decision-making is crucial, which complicates the adoption of culturally sensitive advance care planning. AIM: To develop a consensus definition of advance care planning and provide recommendations for patient-centered and family-based initiatives in Asia. DESIGN: A five-round Delphi study was performed. The rating of a definition and 84 recommendations developed based on systematic reviews was performed by experts with clinical or research expertise using a 7-point Likert scale. A median = 1 and an inter-quartile range = 0–1 were considered very strong agreement and very strong consensus, respectively. SETTING/PARTICIPANTS: The Delphi study was carried out by multidisciplinary experts on advance care planning in five Asian sectors (Hong Kong/Japan/Korea/Singapore/Taiwan). RESULTS: Seventy-seven of 115 (67%) experts rated the statements. Advance care planning is defined as "a process that enables individuals to identify their values, to define goals and preferences for future medical treatment and care, to discuss these values, goals, and preferences with family and/or other closely related persons, and health-care providers, and to record and review these preferences if appropriate." Recommendations in the domains of considerations for a person-centered and family-based approach, as well as elements, roles and tasks, timing for initiative, policy and regulation, and evaluations received high levels of agreement and consensus. CONCLUSIONS: Our definition and recommendations can guide practice, education, research, and policy-making in advance care planning for Asian populations. Our findings will aid future research in crafting culturally sensitive advance care planning interventions, ensuring Asians receive value-aligned care.

http://dx.doi.org/10.1177/02692163241284088

Voir la revue «PALLIATIVE MEDICINE»

Autres numéros de la revue «PALLIATIVE MEDICINE»

Consulter en ligne

Suggestions

Du même auteur

Definition and recommendations of advance car...

Article indépendant | MORI, Masanori | PALLIATIVE MEDICINE

BACKGROUND: In Confucian-influenced Asian societies, explicit end-of-life conversations are uncommon and family involvement in decision-making is crucial, which complicates the adoption of culturally sensitive advance care plannin...

Improved symptom change enhances quality of d...

Article indépendant | HUANG, Hsien-Liang | The oncologist

Background: Symptom burdens tend to increase for patients with cancer and their families over the disease trajectory. There is still a lack of evidence on the associations between symptom changes and the quality of dying and death...

Association between the amount of artificial ...

Article | WU, Chien-Yi | Cancer

BACKGROUND: Artificial hydration (AH) is a challenging issue in terminally ill patients with cancer, because it influences patients' symptoms control, quality of life, and quality of dying (QOD). To date, it is not clear how much ...

De la même série

Posttraumatic growth in palliative care setti...

Article indépendant | AUSTIN, Philip D. | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: Posttraumatic growth refers to positive psychological change following trauma. However, there is a need to better understand the experience of posttraumatic growth in the palliative care setting as well as the availabi...

The perspectives of people with dementia and ...

Article indépendant | MONNET, Fanny | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: Advance care planning has been defined in an international consensus paper, supported by the European Association for Palliative Care. There are concerns that this definition may not apply to dementia. Moreover, it is ...

A palliative care goals model for people with...

Article indépendant | NISHIMURA, Mayumi | PALLIATIVE MEDICINE | n°4 | vol.38

BACKGROUND: Advance care planning in dementia includes supporting the person and their family to consider important goals of care. International research reports the importance of psycho-social-spiritual aspects towards end of lif...

Death education interventions for people with...

Article indépendant | WANG, Tong | PALLIATIVE MEDICINE | n°4 | vol.38

BACKGROUND: People with life-threatening diseases and their family caregivers confront psychosocial and spiritual issues caused by the persons' impending death. Reviews of death education interventions in the context of life-threa...

Research methods in palliative care

Article indépendant | DELIENS, Luc | PALLIATIVE MEDICINE | n°6 | vol.38

Research in palliative care is challenging and complex and it uses a range of research designs and research methods, derived from many different scientific disciplines: from medicine and nursing over health sciences, communication...

Chargement des enrichissements...