|Ahead of print publication
Definition and recommended cultural considerations for advance care planning in Japan: A systematic review
Ai Chikada1, Sayaka Takenouchi1, Kazuko Nin1, Masanori Mori2
1 Department of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan
2 Palliative and Supportive Care Division, Seirei Mikatahara General Hospital, Hamamatsu, Japan
|Date of Submission||10-May-2021|
|Date of Acceptance||19-Jul-2021|
|Date of Web Publication||15-Sep-2021|
PhD, RN. Department of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto
Source of Support: None, Conflict of Interest: None
Although Delphi studies in Western countries have provided a consensus for practices pertaining to advance care planning (ACP), their findings may not be applicable to Asian countries with distinct, family-oriented cultures. This systematic review aimed to synthesize the definitions of and evidence for ACP and analyze recommended practices in Japan. We conducted a systematic review using narrative synthesis in December 2018. Key words were searched from Ichushi-Web by NPO Japan Medical Abstracts Society, Citation Information by the National Institute of Informatics, and Japanese Institutional Repositories Online databases. In addition, in August 2019, we conducted hand searching using Google Scholar and Google. We included original Japanese articles that addressed factors regarding ACP (e.g. definitions, elements, roles and tasks, and timing of ACP). Data were synthesized using thematic analysis. The study protocol was registered prospectively (PROSPERO: CRD42020152391). Of the 3512 studies screened, 27 were included: 22 quantitative and 5 qualitative. Five-position statements/guidelines were added by hand searching. Definitions and several distinct practice patterns of ACP and the importance of families' roles were identified. Unique recommendations addressed the importance of properly eliciting patients' preferences that are the best for both patients and families, engaging the public to raise awareness of ACP, and developing policies and guidelines for ACP. We identified the definition of and unique recommendations for ACP based on Japanese cultural values and norms. Further research is needed to evaluate the recommendations provided in this systematic review.
Keywords: Advance care planning, advance directives, culturally competent care, end-of-life care, systematic review
|How to cite this URL:|
Chikada A, Takenouchi S, Nin K, Mori M. Definition and recommended cultural considerations for advance care planning in Japan: A systematic review. Asia Pac J Oncol Nurs [Epub ahead of print] [cited 2021 Sep 20]. Available from: https://www.apjon.org/preprintarticle.asp?id=326078
| Introduction|| |
Advance care planning (ACP) enables individuals to define goals and preferences for future medical treatment and care, discuss these goals and preferences with family and healthcare providers (HCPs), and record and review them, if appropriate. Several international Delphi studies in western countries have recently provided a consensus regarding the definition and practice of ACP., Further, the national framework regarding ACP has been provided in Canada, the UK, and Australia.
In Japan, the concept of ACP has gradually become better known. The Guidelines for the Decision-Making Process in End-of-Life Care were developed by the Japanese government in 2007, after a case at Imizu City Hospital in Toyama prefecture, in which a ventilator was removed by physicians from an unconscious patient at the end of life (EOL), without the patient's wishes being made clear previously. These guidelines have incorporated the concept of ACP, such as the importance of providing and explaining appropriate information for patients and families and decision-making by patients themselves based on discussions with patients, families, and HCPs.
Owing to the recent progression of an aging society in Japan, demand for community-based treatment and care has increased, and the construction of community-based integrated care systems has been promoted. Thus, in March 2018, the guidelines were revised to place greater emphasis on the concepts of ACP, such as the importance of repetitive discussion and advance directives (AD), including designating a healthcare proxy.
However, in Japan, it remains unclear how ACP should be defined and implemented in actual clinical practice. Therefore, HCPs struggle to determine the most suitable way to practice ACP. Although the number of ACP studies in Japan has increased dramatically since 2010, it has been pointed out that many of them are commentaries that only highlight the importance of ACP, without concrete implications.
Unlike in western countries where ACP is developed with an emphasis on an individual's right to self-determination, Japan has unique values and family relationships which emphasize harmony for patients and families., Furthermore, Japan has its own cultural background, healthcare system, legal system, and social issues related to having the largest rapidly aging population worldwide. Therefore, it is necessary to consider Japanese cultural and social aspects when introducing ACP to Japan.
Sumita conducted a literature review on Japanese-language articles published between 1983 and 2014 to assess the content of studies published in Japan on ACP and to identify the elements that constitute ACP. However, specific clinical implications still need to be addressed. Additionally, Tanimoto, Akuta, and Shigeta conducted an integrative literature review of ACP research in Japan limited to 2011_2017 and reported a lack of detailed information regarding the definition of and strategies for ACP in a Japanese context. In these two review studies, “advance care planning” was used as a keyword in the searches, and no search terms strongly associated with ACP were used, such as “advance directive,” “end of life discussion,” and “do not attempt resuscitation (DNAR).” Therefore, it remains unclear whether the concept of ACP was comprehensively searched. Furthermore, the above two studies were limited to literature reviews rather than systematic reviews.
Thus, the main purpose of this systematic review was to synthesize definitions of and evidence for ACP regarding elements of ACP, roles and tasks, the timing of ACP, elements of policy and regulation, and evaluations of ACP, and analyze recommended practices for Japan. The secondary purpose was to obtain insight into Japanese cultural aspects related to ACP.
| Methods|| |
This study's protocol has been registered in the International Prospective Register of Systematic Reviews (PROSPERO: CRD42020152391). The Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement was used for reporting.
Regardless of the study design, all original articles exploring perspectives on ACP definitions and recommendations reported in Japanese were included in this study. A systematic review of the English-language articles on ACP in Asia including Japan, available on Embase, MEDLINE, Web of Science, and Google Scholar, has been reported. The findings were integrated using a narrative synthesis because it has the distinction of being able to adopt a textual approach to the process of integration to “tell the story” of the findings from the studies it contains, as well as being able to involve the manipulation of statistical data.
The selected search strategy was developed in cooperation with a healthcare librarian. The search was conducted in December 2018 using the three most major bibliographic databases in Japan: Ichushi-Web by NPO Japan Medical Abstracts Society, Citation Information by National Institute of Informatics (CiNii), and Japanese Institutional Repositories Online (JAIRO, known as Institutional Repositories DataBase [IRDB] since April 2019). The databases were searched using keywords and MeSH headings, translated from each database's associated thesaurus. Additionally, in August 2019, we conducted hand searching using Google Scholar and Google. The keywords were “advance care planning,” “living will,” “advance directive,” “do-not-resuscitate order,” and “end-of-life discussions.”
We included original articles written in Japanese on ACP from peer-reviewed journals that addressed definitions, elements of ACP, roles and tasks, timing of ACP, elements of policy and regulation, and evaluations of ACP. Each domain used was from the Delphi study of the European Association for Palliative Care.
Studies that included patients with decision-making capacity, families, and HCPs were included in our review.
Based on the discussion and agreement by the research team, articles referring to decisions involving only family members were excluded in addition to case reports, reviews, systematic reviews, proceedings, quantitative studies with fewer than 100 participants, and qualitative studies involving fewer with 10 participants.
Studies conducted with trainee (unqualified) HCPs, children/adolescents (<18 years old), individuals with psychiatric illnesses, and general populations were excluded.
After integrating the search results from each database, duplicate articles were excluded. Two reviewers (AC and ST) excluded literature from nonmedical fields, journal features, reviews, case reports, and nonJapanese studies. Two reviewers (AC and MM) independently screened titles and abstracts against eligibility criteria. Then, all potentially relevant articles were retrieved, followed by an independent assessment/screening of full-text articles before data extraction and synthesis. Any disputes were resolved through discussion with all three reviewers (AC, MM, and ST).
An extraction form was developed, and data were extracted using this form of study characteristics judged to be important for addressing this review's aims. Characteristics included source, eligibility, context (e.g., research setting), methods, results (e.g., the total number of participants, definitions, elements of ACP, roles and tasks, timing of ACP, elements of policy and regulation, evaluations of ACP, and conclusions), and quality assurance for each study. In addition, Japanese cultural characteristics affecting ACP were identified. Data were extracted and reviewed for accuracy by three authors (AC, ST, and MM) through discussion.
Risk of bias (quality) assessment
We assessed the quality of each study using an appraisal tool for systematic reviews and each reviewer assessed the accepted empirical studies independently with clear criteria of “good,” “fair,” “poor,” and “very poor.” Studies were not excluded depending on methodological quality.
Strategy for data synthesis
We used narrative synthesis for the data, utilizing several tools suggested by Popay et al. The steps were as follows:
- Textual description: Summarize the findings by focusing on discoveries that are unusual or related to a novel theme
- Tabulation: Provide details of the study design, results of the study quality assessment, outcome measures, and other results visually on the extraction form
- Thematic analysis: Based on the review question, systematically identify the main, frequent, and/or most important themes and/or concepts across multiple studies and explore similarities and differences between studies. More specifically, the extracted data were repeatedly read, and characteristic descriptions related to elements, roles and tasks, timing, elements of policy and regulations, and evaluation of ACP, and Japanese characteristics regarding ACP (decision-making process) were coded. Second, codes were classified based on similarities and differences; similar codes were integrated, and subcategories representing characteristics of the meaning of the group were extracted. Third, by comparing and examining the relationships between subcategories, the level of abstraction was further raised, and categories representing the characteristics of the meaning of the collection of subcategories were extracted. Finally, we explored relationships between the extracted categories
- Assessing the robustness of the synthesized product: we reflected critically on the synthesis process.
| Results|| |
Out of 3,512 studies screened, 32 were included, with 22 quantitative studies, five qualitative studies, and five-position statements/guidelines added by hand searching [Figure 1]. Characteristics of included studies are shown in [Supplementary Table 1].
|Figure 1: Preferred Reporting Items for Systematic Reviews and Meta-Analyses flow diagram|
Click here to view
Definition of advance care planning
We summarized definitions of ACP from previous studies [Table 1]. Seven out of 32 studies included definitions for ACP.,,,,,, Two studies directly referenced definitions from studies published in Western countries, two studies used operational definitions, and three guidelines used original definitions.,, The elements of the definitions were extracted as 14 codes from the descriptions and definitions of ACP in those studies. As a result, two themes were identified: “specific definition of ACP (i.e. meaning, purpose, and method of ACP)” and “goals for ACP.” The integrated definition's key point is that ACP is a process of continuous discussions regarding future medical care based on the patient's values and preferences. The definition also includes realizing the patient's wishes and preferences regarding treatment to safeguard the dignity of a patient with a serious illness.
ACP is a process in which adult patients (individuals) repeatedly discuss future medical care with family and/or other closely related people and their healthcare team, so they can identify future medical care based on their values and preferences, should they, at some point, be unable to make their own decisions. ACP helps make decisions that ensure patients' dignity at the end of life.
Recommended elements of advance care planning
This domain included 15 sub-themes and six themes extracted from 233 codes [Table 2]. Recommendations regarding the elements of ACP included ensuring patients understand their current medical conditions and prospects by providing sufficient information and explanations.,,,,,,,,,, ACP should also include clarification of patients' preferences for EOL medical treatment and care.,,,,,,,,,,,, In addition, it is recommended that coordination between patients and their families be repeated, and the best EOL plan for both the patients and their families be explored as elements of ACP.,,,,,,,,,,,, ACP involves having repeated conversations that aim to build a consensus through shared decision-making using a patient-centered approach that includes families.,,,,,,,,,, Where appropriate, ACP includes encouraging patients to provide their families and HCPs with a copy of their AD.,,,,,,,,,,, Finally, ACP aims to help patients achieve “a good death” by providing medical care at the EOL that is consistent with patients' preferences.,,,,,,,,,,,
Recommended roles and tasks
This domain included 13 sub-themes and six themes extracted from 121 codes [Table 3]. HCPs are recommended to support patient engagement in the ACP process by developing a rapport with them, ensuring their basic needs are met, and addressing symptoms.,,,, This can increase patients' willingness to participate in ACP. HCPs should provide patients and families with sufficient information (e.g. diagnosis, prospects for future mental and physical changes, and the benefits and risks of all available treatment and care options) and explanations while considering their feelings and assessing their understanding.,,,,,,,,, In addition, HCPs should obtain information about patients' life histories and values through everyday conversations and aim to understand the reasons behind patients' expressed preferences.,,,,,,, Interdisciplinary teams should also collaborate and make efforts to support patients' decision-making, which includes improvement of ethics and training designed to create a sense of responsibility to fulfill one's role as a team member involved in ACP.,,,,, Furthermore, HCPs should facilitate and coordinate conversations and resolve any differences between patients and families so that patients' preferences are respected.,,,,,,,, Finally, HCPs should regularly update patients' preferences through conversations, as well as documents, and share those conversations with the interdisciplinary team.,,,,,,,,,
Recommended timing of advance care planning
This domain included six sub-themes and three themes, extracted from 26 codes [Table 4]. We identified the recommended timing for starting ACP discussions and for repeating the discussions. It is recommended that older patients receiving any medical care or patients with an incurable disease immediately engage in ACP, in case they lose their decision-making capacity.,,,,,, It is also recommended that discussions focusing on EOL care and preferred place of death should be initiated at the introduction of integrated community-based care or upon transition of care.,,, In addition, ACP conversations should be repeated among patients, families, and HCPs,,,, keeping in mind that individuals' feelings and preferences can change.
Recommended elements of policy and regulations
This domain included eight sub-themes and five themes extracted from 50 codes [Table 5]. Standardizing the documentation of the ACP process (AD) and integrating it into the municipality unit are recommended to make it easy to share and transfer within the communities the patients live in.,,,, Further, it is recommended that the government enact a healthcare proxy law, as the current adult guardianship system in Japan does not authorize such guardians to make medical decisions, and there is no legally approved process for selecting a medical representative to make these decisions., The government should also develop laws and systems regarding medical care and decision-making at EOL, as there are currently no laws in Japan regarding AD, including death with dignity or the designation of medical representatives, making the related legal implications unclear.,,,,,, Furthermore, it is recommended that a collaborative support system should be developed,,,,,,, in which opportunities for interdisciplinary HCP training are enhanced so that interdisciplinary team members can deepen their understanding of each occupation through training.,, Finally, the government should make efforts to raise public awareness of EOL care, ACP, and AD.,,,,,
Recommended evaluation of advance care planning
This domain included three sub-themes and two themes, extracted from seven codes [Table 6]. Regarding the quality of medical treatment and care at EOL, it was suggested that the ACP conversation should reach a consensus among patients, families, and HCPs regarding medical treatment,, with early initiation of the phase of disease trajectory creating a higher quality of EOL care. It was further suggested that a place of death consistent with the patients' preference, is an outcome related to the quality of EOL care. Opportunities to consider EOL treatment and care could also be recommended as an endpoint.
Japanese cultural characteristics affecting the advance care planning process
This domain included five sub-themes and four themes extracted from 21 codes [Table 7]. The first characteristic was that Japanese people tend to avoid the explicit expression of their own preferences and expect “heart to heart communication” (i.e. nonverbal communication) owing to the high-context nature of Japanese culture., Second, although many Japanese people consider AD and EOL care to be necessary, they are not comfortable thinking about death and tend to defer decision-making., Third, families' preferences tend to be valued over patients' own owing to Japan's family-centered culture.,,, Finally, Japanese people tend to refrain from assertive decision-making and view harmony with others as more important than the wish of individuals.,,,
|Table 7: Japanese characteristics affecting advance care planning process|
Click here to view
| Discussion|| |
To our knowledge, this study is the first to summarize culturally sensitive recommendations for ACP, by systematically dividing them into multiple domains used in a large international Delphi study and clarifying Japanese cultural characteristics. Definitions of ACP were also summarized based on literature extracted from the systematic review. Our findings provide insight on ACP in the context of Eastern culture, which respects the harmony between patients and families in patient-centered decision-making support.
Both our study and the Western Delphi study emphasized the process of conversing with patients, family members, and HCPs. However, our results suggest that the ACP process should include building trust with patients before the conversation itself. Moreover, the ACP process in Japan should elicit patients' true feelings through daily care and by focusing on frequent communication, which can clarify the patients' goals and preferences, as well as the families'. Furthermore, although the Western Delphi study reported that laws should respect the results of an ACP process, Japan emphasized that the government should improve public awareness about the importance of ACP to develop laws regarding ACP and AD. Our overall findings indicate the importance of family involvement in and public awareness of ACP. Therefore, our systematic review offers two proposals for the implementation of the recommendations for ACP practices in Japan.
The first proposal is to include families in a patient-centered approach to ACP. Many studies mentioned the relationship between patients and families. For example, one element of ACP is having repetitive conversations using a patient-centered approach, including families, with the aim of creating a consensus through shared decision-making.,,,,,,,,,,,,,,,,, Thus, in Japan, families are treated as full participants in medical consultations from the very start. We observed, however, differences between Japan and some western countries. In some western countries, HCPs adopt a person-centered approach when engaging in ACP conversations with patients and if the patient wishes, their family., ACP may include choosing and preparing trusted person (s), and whether or not families are included depends largely on the patient's wishes. Such a framework in western countries places emphasis on a patient-centered approach. In Japan, emphasis is placed on creating the best goals for both patients and families. A cultural anthropological perspective shows that in many Asian cultures, emphasis is placed on attending to others, fitting in, and achieving harmonious interdependence with team members. According to findings regarding how Japanese cultural characteristics affect the ACP process, Japanese patients expressed preferences that consider their families rather than their own preferences alone. Patient autonomy is reported to be subordinate to family values, while physician authority in most East Asian countries is influenced by Confucianism. In the West, where individualism is emphasized, patient autonomy is respected. While in East Asia, including Japan, relational autonomy, which is a concept of autonomy that places the individual in a socially embedded network of others, is favored. Thus, families may either be a facilitator or a barrier to ACP, especially in a family-oriented culture like Japan. Given that Japanese patients tend to care about their families' opinions and potential burdens in decision-making, family engagement in ACP is imperative. Therefore, while HCPs should value the patient-centered approach, they should likewise ensure that family harmony is maintained. To implement ACP in clinical practice, HCPs need to be educated with the necessary communication skills to facilitate ACP discussions among patients and families. Several communication training programs have recently been developed and introduced in Japan, which include SHARE (http://www.share-cst.jp/), Education For Implementing End of Life Discussion (E-FIELD) (https://square.umin.ac.jp/endoflife/2019/general.html), VitalTalk Japan (https://www.facebook.com/vitaltalk.jp/), and Serious Illness Care Program (https://portal. ariadnelabs.org/).
The second proposal is to raise public awareness by disseminating and implementing existing guidelines to support ACP.,,,, Several studies pointed out the lack of laws and concrete guidelines and consequently recommended creating new models for implementing ACP conversations, as well as raising public awareness regarding the lack of laws, systems, and knowledge with respect to the ACP process and AD.,,,,,,, Additionally, Japanese people tend to defer decision-making and also value their families' preferences over their own. Our results are consistent in that Japanese physicians and patients relied more on family and physician authority and placed less emphasis on patient autonomy, unlike in the US. Therefore, AD has no weight in Japan, as it does not always guarantee that patients' preferences will be respected. The United States and many European countries have laws regulating ACP and AD, as do some Asian countries, such as the Act on decisions on Life-Sustaining Treatment for patients in hospice and palliative care or at the end of life, in Korea, and The Mental Capacity Act, in Singapore. It was reported that public awareness and prevalence of ACP have improved after legislation in Taiwan and South Korea. Umezawa et al. found that Japanese patients with advanced cancer prefer that their HCPs not give sole preference or priority to their families and that patients want to participate in the decision-making process, even in situations of disease progression. Thus, public awareness of ACP should be increased, including its aims and content, legal policy, and its accessibility by approaching governments and municipalities to undertake promotional activities and to develop laws. Promotional activities using brochures, posters, websites, and educational curriculum may be effective. Further, we should continue to present the evidence regarding the ACP process and deliver the voice of clinical settings.
Of note, none of the reviewed literature examined the influence of religious beliefs and practices on ACP. These literatures, including those in the field of sociology, cultural anthropology, and philosophy, may not have been found because they were excluded pursuant to the exclusion criteria. This may have contributed to the lack of literature focusing on religiosity. In the West, religiousness often influences EOL decisions. Previous studies that explored the difference in the physician-perceived importance of religion for a patient's “good death” in three East Asian countries, including Japan, reported that Japanese physicians had significantly lower awareness of the importance of religion for a patient's good death, as compared to Taiwan and Korea. There was also a correlation with the physician's own religiosity. It is possible that religious beliefs are not only the waning importance of religion in modern Japanese culture but also relatively not important for HCPs in clinical settings in Japan. In addition, understanding the characteristics of the cultural background presented in the results makes it easier to understand the values of individuals. However, HCPs must be aware that the four Japanese cultural characteristics may not necessarily reflect the value of all individuals and families in Japanese culture. Thus, it is important to respect individual values rather than taking a stereotypical approach.
Our study had strengths and several limitations. One of the strengths is that this study conducted a systematic review of ACP in Japan, whereas previous studies were limited to literature reviews. In addition, while “advance care planning” was the only keyword used in these previous studies, this study involved a comprehensive search that included keywords such as “advance directive,” “end of life discussion,” and “do not attempt resuscitation.” Furthermore, our framework was based on the international Delphi study. Our study carefully examined the recommendations for ACP in Japan by integrating results from both quantitative and qualitative studies.
Regarding limitations, first, most studies were published before 2018, but the Ministry of Health, Labour and Welfare in Japan only first mentioned ACP in 2018. Thus, recommendations may change with future research, although aspects relating to Japanese culture remain. Second, the number of articles was limited and some lacked methodological rigor, with only a few having undertaken interventional studies. Further studies are needed to develop ACP intervention programs based on cultural norms in Japan. Third, since the extracted studies were written in Japanese, results from studies in other languages were not reflected. Finally, according to the agreement of the research team, we excluded quantitative studies with fewer than 100 participants and qualitative studies with fewer than 10 participants. The inclusion of this criterion may have resulted in the exclusion of a small number of high-quality studies.
In conclusion, this systematic review provided a definition of and recommendations for ACP based on cultural norms in Japan, integrating published literature with currently available evidence by including both quantitative and qualitative studies. The recommendations in this study reflect an ACP process in Japan that is focused on the exploration of the best decision for patients and their families. Future research should evaluate the implementation of these recommendations in clinical practice.
The authors would like to thank Toshiyuki Swa, who is an information specialist, for his support in developing the search strategy.
Financial support and sponsorship
This study was supported by JSPS KAKENHI (Grant No. JP 20K23223) (Grant-in-Aid for Research Activity Start-up).
Conflicts of interest
There are no conflicts of interest.
| References|| |
Rietjens JA, Sudore RL, Connolly M, van Delden JJ, Drickamer MA, Droger M, et al
. Definition and recommendations for advance care planning: An international consensus supported by the European Association for Palliative Care. Lancet Oncol 2017;18:e543-51.
Sudore RL, Lum HD, You JJ, Hanson LC, Meier DE, Pantilat SZ, et al
. Defining advance care planning for adults: A consensus definition from a multidisciplinary Delphi panel. J Pain Symptom Manage 2017;53:821-32.e1.
Bagheri A. Medical Futility: A Cross-National Study. London, UK: Imperial College Press; 2013.
Tanimoto M, Akuta Y, Shigeta I. Integrative review of advance care planning research in Japan. Palliat Care Res 2018;13:341-55.
Beck ER, McIlfatrick S, Hasson F, Leavey G. Health care professionals' perspectives of advance care planning for people with dementia living in long-term care settings: A narrative review of the literature. Dementia (London) 2017;16:486-512.
Sumita M. The present state of advance care planning in Japan. Jpn Assoc Bioeth 2015;25:57-68.
Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. BMJ 2009;339:b2535.
Martina D, Lin CP, Kristanti MS, Bramer WM, Mori M, Korfage IJ, et al
. Advance care planning in Asia: A systematic narrative review of healthcare professionals' knowledge, attitude, and experience. J Am Med Dir Assoc 2021;22:349.e1-28.
Popay J, Arai L, Britten N. Guidance on the Conduct of Narrative Synthesis in Systematic Reviews: A Product from the ESRC Methods Programme. Lancaster, UK: Lancaster University; 2006. [doi: 10.13140/2.1.1018.4643].
Hawker S, Payne S, Kerr C, Hardey M, Powell J. Appraising the evidence: Reviewing disparate data systematically. Qual Health Res 2002;12:1284-99.
Boyatzis RE. Transforming Qualitative Information: Thematic Analysis and Code Development. Thousand Oaks, CA: Sage Publications; 1998.
Omomo M, Tsuruwaka M. Factors promoting ACP and factors hindering ACP: An analysis of the care process and specific support of home care nurses for elderly people living alone. J Jpn Assoc Bioeth 2018;28:11-21.
Ishikawa T, Fukui S, Okamoto Y. Association between advance care planning by a visiting nurse and achieving the desired place of death for patients with end-stage cancer. J Jpn Acad Nurs Sci 2017;37:123-31.
Komatsu M, Shimatani T. Recognition of general ward nurses on advance care planning (ACP) for cancer patient in palliative care. Palliat Care Res 2017;12:701-7.
Naito SA, Morita T, Yamaguchi T, Yokomichi N, Odagiri T, Imai K, et al
. Preferences of patients with advanced cancer for advance care planning Akemi. Palliat Care Res 2016;11:101-8.
Watanabe Y, Hirakata H, Okada K, Yamamoto H, Tsuruya K, Sakai K, et al
. Proposal for the shared decision-making process regarding initiation and continuation of maintenance hemodialysis. Ther Apher Dial 2015;19 Suppl 1:108-17.
Matsushita S, Inamatsu T, Hashimoto H, Takahashi R, Takahashi T, Mori M, et al
. Elderly outpatients' attitudes toward care in terminal stage disease. Nihon Ronen Igakkai Zasshi 1999;36:45-51.
Watanabe M, Chiba M, Hosoda E, Matsuzawa Y, Sone C. The nursing homes' difficulties and terminal care practice for individuals with dementia – Comparison by taking care ratio of death in nursing home. J Jpn Soc Study Nurs Soc Work 2010;15:99-110.
Kobayashi M, Matsushima E, Noguchi W, Matsushita T, Hirasawa H. Death with dignity in geriatric intermediate care facilities – Its current situation and real problems. Jpn Bull Soc Psychiatry 2008;16:255-62.
Kajiyama M, Yoshioka S. Characteristics of and factors related to nurses' decision-making support for transition to home care settings for end-stage cancer patients. Palliat Care Res 2018;13:99-108.
Sato T, Makigami K. Terminal care education and consultation activities in advance of the critical stage of disease by attending physicians at a rehabilitation unit. Nihon Ronen Igakkai Zasshi 2008;45:401-7.
Arita K, Funaki H, Hashimoto K, Furutama J, Ikegami Y, Yamasaki M. Thought patterns of patients with non-malignant respiratory disease and lung cancer in relation to advanced directives in the terminal stage. Jpn J Chest Dis 2015;74:211-9.
The Japanese Society of Intensive Care Medicine. The Japanese Association for Acute Medicine, The Japanese Circulation Society. Guidelines for end-of-life care in emergency and intensive medicine – Proposals from three academic societies. 2014. p. 1-4. Available from: https://www.jsicm.org/pdf/1guidelines1410.pdf
.[Last accessed on 2020 Jan 31]
Fukaura A, Tazawa H, Sato I, Arai T, Sano H, Hirose T, et al
. Survey of the physicians consciousness about D. N. R. (do not resuscitate) orders in treatment of patients with terminal lung cancer in Japan – Nationwide questionnaire. J Jpn Soc Cancer Ther 1994;29:1696-708.
Ohira S, Sugisaki H, Yamazaki C. Investigation of physicians' attitudes about terminal care for dialysis patients. J Jpn Soc Dial Ther 2006;21:442-60.
Sato H. Nurses' support for self-determination of terminally ill cancer patients. Nihon Kango Gakkai Ronbunnsyu Kango Sogo 2014;44:174-7.
Mayumi T, Takemura H, Shimizu K, Hirabayashi S, Iede K, Shunsuke N, et al
. The present conditions of the transportation of the cardiac arrest case in the end-of-life similar state. Jpn Soc Emerg Med 2017;20:10-7.
Shimada C, Nakazato K, Arai K, Aita K, Shimizu T, Tsuruwaka M, et al
. Communication with important others regarding their preferences for end-of-life care. Jpn J Geriatr 2015;52:79-85.
Soga I, Ochi G, Kohno N, Sasaki T, Ohhoshi M, Nezu K. The present situation and problems with DNAR (Do-Not-Attempt-Resuscitation) requests in the Nan-Yo Area of Ehime Prefecture. Nan Yo Med J 2017;18:23-31.
Fukuda T. DNAR in out-of-hospital cardiopulmonary arrest. J Jpn Assoc Acute Med 2012;23:101-8.
Kuriaki S, Kamimura T. Retrospective study of decision-making regarding end-of-life care near death for terminally ill cancer patients. Palliat Care Res 2014;9:118–123.
Takahashi M, Fuse J. The visiting nurses' identification of core information in regards to homebound seniors' preferences on their end-of-life care. Jpn J Nurs Res 2014;37:49-60.
Sato T, Sato K, Sato A. Confirmation of intention by signature regarding terminal care treatment in elderly people. Jpn J Geriatr 2011;48:524-9.
Koshiishi M, Ide H, Sagara M, Fukushima A, Yanagizawa C. Changing awareness of decision -making support in nurses and care managers after using the advance care planning (ACP) sheet. Nihon Kango Gakkai Ronbunnsyu Manseikikango 2018;48:163-6.
Kawamoto T, Sunada S, Shigematsu K, Tamura R, Matsuda M, Hatanaka N, et al
. Comparison of the registration of living will and advance directives between cancer and non-cancer patients in electronic medical records. Iryo 2014;68:392-8.
Arita K, Ikegami Y. Clinicians' opinions on receiving the advance directives of terminal-stage patients vary according to the age of respondents. Nihon Ronen Igakkai Zasshi 2012;49:318-24.
Okada K, Imada A, Kaizu K, Kawanishi H, Sugawara G, Suzuki M, et al
. Questionnaire to nephrologists: Withdrawal from hemodialysis in a patient in the terminal stage of malignancy. Nihon Toseki Igakkai Zasshi 2003;36:1315-26.
Iwabuchi M, Sato K, Miyashita M, Morita T, Kinoshita H. Factors that influence the decision maker regarding end-of-life care. Palliat Care Res 2016;11:189-200.
Ikegami A, Sakamoto I, Numata M, Ouchi H, Teramoto K. Impact of timing of end-of-life discussion on quality of end-of-life care in gynecologic cancer. Jpn J Gynecol Oncol 2016;34:8-13.
Suzuki Y. Causes of emergency ambulance transport in terminal cancer patients with do not attempt resuscitation (DNAR) decisions. J Japan Prim Care Assoc 2015;38:121-6.
Markus HR, Kitayama S. Culture and the self: Implications for cognition, emotion, and motivation. Psychol Rev 1991;98:224-53.
Cheng SY, Lin CP, Chan HY, Martina D, Mori M, Kim SH, et al
. Advance care planning in Asian culture. Jpn J Clin Oncol 2020;50:976-89.
Dove ES, Kelly SE, Lucivero F, Machirori M, Dheensa S, Prainsack B. Beyond individualism: Is there a place for relational autonomy in clinical practice and research? Clin Ethics 2017;12:150-65.
Johnson S, Butow P, Kerridge I, Tattersall M. Advance care planning for cancer patients: A systematic review of perceptions and experiences of patients, families, and healthcare providers. Psychooncology 2016;25:362-86.
Ruhnke GW, Wilson SR, Akamatsu T, Kinoue T, Takashima Y, Goldstein MK, et al
. Ethical decision making and patient autonomy: a comparison of physicians and patients in Japan and the United States. Chest 2000;118:1172-82.
Chu D, Yen YF, Hu HY, Lai YJ, Sun WJ, Ko MC, et al
. Factors associated with advance directives completion among patients with advance care planning communication in Taipei, Taiwan. Malhotra C, editor. PLoS One 2018;13:E0197552.
Park HY, Kim YA, Sim JA, Lee J, Ryu H, Lee JL, et al
. Attitudes of the general public, cancer patients, family caregivers, and physicians toward advance care planning: A nationwide survey before the enforcement of the life-sustaining treatment decision-making act. J Pain Symptom Manage 2019;57:774-82.
Umezawa S, Fujimori M, Matsushima E, Kinoshita H, Uchitomi Y. Preferences of advanced cancer patients for communication on anticancer treatment cessation and the transition to palliative care. Cancer 2015;121:4240-9.
Steinberg S. Cultural and religious aspects of palliative care. Int J Crit Illn Inj Sci 2011;1:154.
] [Full text]
Morita T, Oyama Y, Cheng SY, Suh SY, Koh SJ, Kim HS, et al
. Palliative care physicians' attitudes toward patient autonomy and a good death in East Asian countries. J Pain Symptom Manage 2015;50:190-9.e1.
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6], [Table 7]