Sage Journals: Discover world-class research

Abstract

Background:

People of Black and minority ethnic heritage are more likely to die receiving life supporting measures and less likely to die at home. End-of-life care decision making often involves adult children as advance care planning is uncommon in these communities. Physicians report family distress as being a major factor in continuing with futile care.

Aim:

To develop a deeper understanding of the perspectives of elders of Black and minority ethnic heritage and their children, about end-of-life conversations that take place within the family, using a meta-ethnographic approach

Design:

Systematic interpretive exploration using the process of meta-ethnography was utilised.

Data sources:

CINAHL, MEDLINE, PubMed and PsycINFO databases were searched. Inclusion criteria included studies published between 2005 and 2019 and studies of conversations between ethnic minority elders and family about end-of-life care. Citation snowballing was used to ensure all appropriate references were identified. A total of 13 studies met the inclusion criteria and required quality level using Critical Appraisal Skills Programme.

Results:

The following four storylines were constructed: ‘My family will carry out everything for me; it is trust’; ‘No Mum, don’t talk like that’; ‘I leave it in God’s hands’; and ‘Who’s going to look after us?’ The synthesis reflected the dichotomous balance of trust and burden avoidance that characterises the perspectives of Black and minority ethnic elders to end-of-life care planning with their children.

Keywords

Attitude to death decision making adult children meta-ethnography terminal care end-of-life conversations race

What is already known about the topic?

Conversations around treatment decisions near the end of life are distressing for both health care professionals and families.

Physicians avoid discussions about limiting treatments at end of life due to the distress; this has been found to be exacerbated in families of Black and minority ethnic heritage.

Adult children play a major role as end-of-life decisions makers for their parents of Black and minority ethnic heritage. However, few adult children have had conversations with their parents about end-of-life preferences.

What this paper adds?

Elders of Black and minority ethnic heritage avoid end-of-life planning conversations with their children to protect them from distressing conversations.

Adult children block attempts by their parents to have end-of-life conversations with them.

Elders of Black and minority ethnic heritage express a preference for end-of-life decisions to be made by family proxies acknowledging that these decisions may not reflect their own preferences.

Implications for practice, theory or policy

Focus is needed on the role played by adult children about their perspectives on having end-of-life conversations with their parents. This could lead the way for innovative community engagement in the development of public health palliative care that may result in more effective end-of-life care planning and engagement with palliative care provision.

Introduction

Conversations around treatment decisions near the end of life are distressing for both health care professionals and families.^1,2 In Western societies, autonomous decision-making models for health matters are favoured. However, at the end of life, without early conversations having taken place, decision making is often left to family members, many of whom have little awareness of the preferences of the older person who is now dying.³ In situations involving people of Black and minority ethnic heritage, formal end-of-life planning has been found to be low.^4,5 The aim of this synthesis is to develop a better understanding of the experiences and preferences of elders of Black and minority ethnic heritage and their children around end-of-life care conversations within their families. This may inform ways of facilitating earlier family-based conversations around illness progression and potential outcomes and perhaps provide a first step towards improving the difficult conversations that need to happen when someone is dying.⁶

Background

Impact of conversations on decision making at end of life

Many people receive treatments that do not prolong life nor provide a relief from suffering so are considered to be non-beneficial or futile in the last 6 months of their lives.⁴ While improving the quality of the dying experience is an issue that is faced by all communities, people of Black and minority ethnic heritage are more likely to die receiving life supporting measures⁵ and least likely to die at home.⁷ One of the main drivers leading to the instigation of futile treatments is families’ insistence.^8,9 The difficulties clinicians have in conducting potentially distressing conversations with Black and minority ethnic families about limiting treatment is often a deterrent to engaging in them at all.⁹ Research with people of Black and minority ethnic heritage illustrate poor communication between health care professionals and families, and a lack of culturally competent end-of-life skills among these professionals when dealing with matters at the end of life.¹⁰

In part, difficult conversations at the end of life arise when family conversations about the end-of-life wishes of the dying person have not taken place and cannot now be elucidated due to their deteriorating condition.² Many older people feel they do not need to discuss their end-of-life preferences with their families because their children will know what they would want.^1,11 In general, older people do not want to live a long lingering existence and White majority populations find doing some kind of advance care planning is a comfort.¹¹ However with people of Black and minority ethnic heritage, discussing dying is thought to be taboo more often than in the White majority population which results in much lower levels of evidence of end-of-life family conversations.^8,11,12 These geographical differences in the way communities discuss dying are illustrated and explored in some recent studies which show greater levels of end-of-life planning conversations taking place in societies that favour autonomous models of decision making over more collective societal and family-based decision-making norms.^13–15

Research exploring end-of-life conversations and decision making in a variety of Black and minority ethnic communities reveals high levels of fear,^16–18 worry or anxiety about dying which can inhibit a desire for palliative care. Fear can also inhibit discussions within communities or families about the potential death of a family member.^8,12,19,20 Anxieties around end-of-life care are complicated by a prevailing distrust of written advance care plans and a lack of expression of preferences by the elders themselves.^21–23 All these factors contribute to the difficulties encountered both by families and by health care teams when end-of-life care decision making is required in health care settings.

There is also a consistent desire by elders of Black and minority ethnic heritage and families for family-based decision making around health care decisions that can be in conflict with the prevailing model of individual autonomy.^8,24 Many elders of Black and minority ethnic heritage express trust that their family, in the majority of cases this being their adult children, will make the right decisions when needed.^12,19,20 However, poor congruency between the wishes of these elders and those of their children around end-of-life treatment preferences has been demonstrated.^3,25 Assumptions that elders of Black and minority ethnic heritage have a preference for continued interventions have not been supported by research.⁸

The complexities involved in achieving good dying among diverse populations has received much international attention over the past 15 years; however, the nature of the interactions and conversations that take place between elders and their adult children and the impact this has on subsequent end-of-life decision making has not been considered in depth.¹

Definitions

To ensure consistency with public body work in the United Kingdom and contemporary culture as portrayed by the main stream media, the term people of Black and minority ethnic heritage has been used in this work, however, with an acknowledgement of the limitations of such terms. One of the risks that need to be overcome when undertaking research with ethnic minorities is that assumptions about homogeneity may be made.²⁶ Ideas of identity are complex ones and there is now a greater respect for the issues it can bring for people labelled by others.²⁷

Over the last decade, there has been an increasing debate over the best way to define care given to improve the way people die, with particular disparities around the terms palliative and end of life.^28,29 For the purpose of this review, end of life was defined as the time when people are considered to be in the last 6 months of life, acknowledging this timing can be difficult to predict. End-of-life conversations refer to conversations regarding preferences around place of care, decisions about end-of-life care interventions and important end-of-life rituals. Care decision making can refer to decisions made by people for themselves or made by proxy decision makers when that person has lost the capacity to make decisions for themselves due to their deteriorating ill health.³⁰

The review

Selecting meta-ethnography and getting started

The aim of this review was to explore the views articulated by elders of Black and minority ethnic heritage and their children about having end-of-life conversations within the family. Meta-ethnography was chosen as the method to enable an in-depth exploration and greater understanding of prospective family conversations around end of life. The process of meta-ethnography aims to facilitate a greater understanding of a social phenomenon by synthesising the findings of qualitative studies retaining the rich context of the data through a seven-stage synthesis process (Table 1).^31,32 It is designed to develop new overarching concepts and theories with an emphasis on preserving original contexts within the synthesis of data from multiple studies.³³

Table 1.

Process of meta-ethnography.

Phase 1: Getting started	A scoping literature search identified adult children as an inhibiting factor in the end-of-life planning of Black and minority elders.
Phase 2: Defining the area that is relevant to the initial interest	A systematic and purposive search was undertaken using a variety of searching techniques.
Phase 3 Reading the studies	Deep inspection of the literature was conducted first and second constructs were identified using QSR International’s NVivo 11 Software for coding. Metaphors identified.
Phase 4 Deciding how the studies are related	Consensus on how studies related to each other and which key metaphors in each stage would be chosen was discussed by team.
Phase 5. Translating the studies into each other	Re-reading and discussion were used to explore each study in relation to the others with a focus on the key metaphors. Reciprocal translations and refutational translations were noted.
Phase 6 Synthesising translations	Reinterpretation of metaphors and generation of cohesive storylines
Phase 7 Expressing the synthesis	The four storylines that were created are discussed in this article.

The data in existing studies consist of two forms: first- and second-order metaphors (see Table 2 for definition). A collaborative process of discussion of these metaphors was undertaken by the review team to seek links and translations between the studies being explored. The final stage involved developing overarching lines of understanding called lines of argument or storylines as a review team with an overall aim to develop new understanding rather than new knowledge.^34,35

Table 2.

Definition of terms.

Metaphors	These are ways of communicating knowledge about a concept that is symbolic of the interpretation the writer has given to the concept. Metaphors are therefore knowledge that is again open to reinterpretation.
First-order constructs/metaphors	Quotations from primary study participants as reported by study authors.
Second-order constructs/metaphors	Interpretation of those findings made by authors of the original study.
Reciprocal and refutational translations	Process by which studies are read comparatively seeking insights from one study that help to illuminate aspects of another. Reciprocal translations occur when similar metaphors are found and assimilated. Refutational translations occur when the metaphors in one study contradict the metaphors in another.
Storylines (third-order constructs or lines of argument)	Interpretations of the synthesis team undertaking the meta-ethnography which have been drawn together to form a new interpretation.

This collaboration aims to be reflexive with an acknowledgement of the inherent culturally laden assumptions that each reviewer brings to the process of interpretation. The interpretations are open to further discussion and debate by the reader.³⁴

The main purpose of this review is to increase the understanding of the ways some families of Black and minority ethnic heritage operate around end-of-life conversations. It is hoped that the findings of the review will help to identify ways of engaging people of Black and minority ethnic heritage to think about strategies to enable better awareness of each other’s preferences at end of life. An additional purpose of this review is to increase professionals’ understanding of end-of-life communication in and with Black and ethnic minority families. The following aim and review questions were formulated.

Review aim

The aim of this study was to develop a deeper understanding of the perspectives of elders of Black and minority ethnic heritage and their children, about end-of-life conversations that take place within the family, using a meta-ethnographic approach.

Review questions

How do older people of Black and minority ethnic heritage describe their experiences of having end-of-life conversations with their adult children?

How do children of elders of Black and minority ethnic heritage describe their experiences of having end-of-life conversations with their parents?

What influences do these experiences have on the way these elders feel and think about initiating discussions about their end-of-life preferences?

Deciding what is relevant

Search strategy

CINAHL, MEDLINE, PubMed and PsycINFO databases were searched for articles from 2005 to 2019; 2005 was used as a starting point as Jones³⁶ in the United Kingdom and Kwak and Haley³⁷ in the United States both published reviews of the current state of literature exploring ethnic differences in end-of-life experiences. Key words were matched to MeSH terms (Table 3). Seven studies were identified.

Table 3.

Search terms – facet analysis.

Search 1
1. Cultur*,
MESH terms: culture, cross cultural, ethnography,
OR Race MESH: Black, White, Asian, Hispanics
OR Black and Asian Minority Ethnic OR Ethnic* OR race
AND
2. end-of-life
End of life OR palliat* to include MESH terms: palliative care, terminal Care, terminal care ( Saba) Or attitudes to death OR death
AND
3. Conversations
MESH terms: advance care plan* OR advance directive* OR decision making OR expression of wish* OR communication

Generating a useful search was complex with search terms such as ‘adult children’ and minority generating large volumes of irrelevant hits. We found the most effective ways of choosing ethnicities to search was to use the term RACE which gave the MeSH headings of Black, White and Asian. We also included Hispanics as so many studies are done in the United States with this group. An analysis of all the MeSH terms linked to the initial 14 studies found by all types of searching was conducted; however, this identified that the chosen studies did not share any MeSH identifiers beyond generic terms such as human.^31,38 Two of the main studies in this area^39,40 had no MeSH headings associated with ethnicity, and Yonachiro-Cho had no end-of-life MeSH terms. Qualitative studies are not always identified by traditional search methods such as MeSH identifiers. Creative and purposeful searching is required. Citation snowballing⁴¹ and information foraging⁴² including Google Scholar searching were also employed to identify a further eight studies that fitted the inclusion criteria (PRISMA flow diagram; Figure 1). In total, 15 studies were selected for quality appraisal.

Figure 1.

PRISMA 2009 flow diagram.

Study selection

Studies that had a focus on conversations about end-of-life planning between elders and their adult children were included. Inclusion and exclusion criteria were applied (Table 4).

Table 4.

Inclusion and exclusion criteria.

Inclusion	Exclusion
1. Empirical research 2. Published in English 3. Published in peer reviewed journals 4. Published between 2005 and 2019 5. Data that were specifically attributable to people from Black and minority ethnic groups living in higher income countries which have established palliative care provision. 6. Involving community dwelling elders over the age of 60 7. Studies where discussions about end-of-life between elders and family members are discussed	1. Systematic reviews and quantitative studies 2. Studies focused on people with an established life-threatening condition where end-of-life care planning is specifically linked with deteriorating illness 3. Studies where language was a significant barrier 4. Studies where study questions relate to advance care planning initiatives or advance care planning tools

Inclusion

Exclusion

1. Empirical research
2. Published in English
3. Published in peer reviewed journals
4. Published between 2005 and 2019
5. Data that were specifically attributable to people from Black and minority ethnic groups living in higher income countries which have established palliative care provision.
6. Involving community dwelling elders over the age of 60
7. Studies where discussions about end-of-life between elders and family members are discussed

1. Systematic reviews and quantitative studies
2. Studies focused on people with an established life-threatening condition where end-of-life care planning is specifically linked with deteriorating illness
3. Studies where language was a significant barrier
4. Studies where study questions relate to advance care planning initiatives or advance care planning tools

Assessment of quality

The papers selected were assessed for quality using the critical synthesis form for qualitative studies, which is an adapted form of Critical Appraisal Skills Programme (CASP);⁴³ the scores were included in the data analysis table (Table 5).⁵² Two UK-based studies were excluded at this point as they were written up as reports and did not contain enough details on methodology or results to be assessed and used.^53,54 Thirteen studies were included in the synthesis.

Table 5.

Included studies.

Study details	Aim	Participants	Study design/method	Key findings	CASP score/13
Bullock et al.⁴⁴ USA	To identify themes that characterise what matters to African American elders who are faced with issues of death, dying and end-of-life care	African American elders (22) Median age 64 15 females 7 males All Christian Community dwelling	Grounded theory: Purposeful sampling Focus groups	Spirituality; burden on family members; trust; health insurance coverage; cultural concerns	11
Gutheil and Heyman⁴⁰ USA	To understand Hispanic elders’ and adult children’s concerns about end-of-life planning	Hispanic elders (10) Median age 66 Children (10) All female All Christian Community dwelling	Grounded theory (Strauss and Corbin): Focus groups	Communication; control; burden; spirituality; religious issues; importance of family relationships; communication regarding end-of-life planning	13
Glass and Nahapetyan³⁹ USA	To explore informal family communication about end-of-life preparation and preferences	Elders (15) Median age 78.6 Adult children (15) 13 White, 4 Black, 1 Asian All female Religion not detailed Community dwelling	Constructivist Open end interviews	Protection of the children; trust in others to make the decisions; preferences unknown; family rarely together; fear of death.	12
Ott⁴⁵ USA	To give voice to a culturally specific group by learning about their attitudes, opinions and experiences with living will documents	African American Elders (28) Median age 76.2 63% female 37% male Christian ( 26) No religion (2) Nursing home residents	Exploratory descriptive Focus groups	The value of artiﬁcial life supporting treatments; communication about end-of-life preferences; involvement of family members in end-of-life decisions; physician involvement in end-of-life decisions; the value of a living will	12
Cohen et al.⁴⁶ USA	To explore knowledge and attitudes and barriers to advance directives	Latino (20) Cambodian (19) Age mean 58.4 Religion not detailed Community dwelling	Exploratory Open ended Focus group Thematic analysis	Integration of belief systems: (a) religion, (b) destiny, (c) ideas about suffering; importance of quality of life; processes/preferences regarding decision-making: (a) family roles, (b) providers roles, (c) confusion/uncertainty regarding ACD and (d) openness to ACD	12
Ko and Berkman²¹ USA	To examine the role of adult children in end-of-life decision making among Korean American older adults and how culture affects this process	Korean elders (23) >65 years Christian 17 Buddhist 3 No religion 1 Community dwelling	Grounded theory (Strauss and Corbin): Individual interviews and focus groups conducted in Korean	Diversity of opinion among participants: (a) Are children resistant or receptive to discussing parents’ end-of-life treatment preferences; (b) whether older adults or their children should make decisions about end-of-life treatment; (c) whether decision making should be the responsibility of the eldest son or of all the children; (d) whether children would implement the parent’s preferences for end-of-life treatment	12
Bullock²² USA	Promote cultural competency in end-of-life care inclusive of extended family networks (part of a larger study)	African American elders (102) 84 females 15 males 98% Christian White elders (100) 75 females 25 males 98% Christian All over 55 Community dwelling	Exploratory mixed methods study Demographic questionnaire Focus groups with follow-up interviews Thematic analysis	African American compared to White; lack of trust in Dr decisions more; palliative care not enticing as corresponds with reducing life sustaining treatments; collective approach to decision making; fatalism; to plan or hasten death seen as anti-Christian	11
Crump⁴⁷ USA	Exploring African American seniors’ perspectives to inform health care professionals of decision making for patients who are seriously ill	African American elders 45 females 7 males All Christian Community dwelling	Community-based participatory research with focus groups with video prompted discussion	Primary themes: Trust; fear; relationships; lack of information/knowledge Secondary Themes: Deterioration of family/community; past discrimination; experiences; self-fulfilling prophecy; religion	11
Sharma et al.⁴⁸ USA	To examine the perspectives of South Asians living in the United States regarding end-of-life care	Asian Indian elders (12) 41–76 years 6 females 6 males Children (15) 23–36 years 7 femlaes 4 males Hindu (25) No religion stated ( 2) Christians and Muslims excluded	Thematic analysis Focus groups followed by demographical questionnaire	Attitudes towards death: Indian culture more accepting of death than US culture; family duty; preferences for information disclosure and decision making illustrated changes in societal structures; less reliance on children in terms of expectations but still looking for a family-based communication model	13
Venkatasalu et al.⁴⁹ UK	The perspectives of older South Asians towards talking about death and dying	South East Asian elders (55) 52–78 years 12 Muslim 3 Sikh 12 Hindu 5 Christian 1 non-religion 21 not detailed Community dwelling	Grounded theory (Charmaz): Focus groups followed by interviews	Avoidance as a cultural norm; avoidance as protection; assumption children will talk but not wanting to have conversations as it would upset them	12
Yonachiro Cho et al.⁵⁰ 2016 USA	To explore the knowledge, attitudes and preferences of Chinese Americans towards ACP.	Chinese American elders ( 34) 22 females 12 males 9 < 65, 25 > 65 Religion not specified Community dwelling	Grounded theory (Strauss and Corbin): Focus groups	Knowledge of advance directives; health as a factor in end-of-life decision making and communication; communication of end-of-life care preferences	13
Biondo et al.⁵¹ Canada	To gain an understanding of the barriers and facilitators to participating in ACP and to determine the ways this community would like to engage in ACP	South Asian community members (57) 22–82 years 28 females 10 males Sikh, Muslim, Hindu Numbers not specified	PACER Co-design method Narrative synthesis using story analysis	Concept of ACP – foreign to this community – associated with organ donation and estate planning; barriers to participation in ACP – cultural aspects, religious beliefs and immigration challenges; eager to learn about ACP	13
Boucher⁵² USA	How cross culturally shared characteristics of family involvement in health decisions, respect and duty, religiosity and fatalism might influence attitudes towards planning and decision making related to death and dying	Dominican elders (23) Puerto Rican elders (28) 38 females 13 males Largely identified as Catholic Community dwelling	Grounded theory (Charmaz and Sabrani): Semi-structured interviews	No significant differences found with apriori themes which included the following: Family involvement in health decisions/filial piety; religiosity/spirituality/fatalism; accessing/using end-of-life care; autonomy; influence of death/dying on own future care decisions; death/dying is a private matter. Stronger evidence of death denial than in previous findings	13

ACD: advance care directives; ACP: advance care planning; PACER: Patient and Community Engagement Research.

Reading the studies

Data extraction and synthesis

A data extraction form informed by the work of Campbell et al.³¹ was used and results tabulated in chronological order (Table 5). Noblit and Hare³⁴ suggest reading should be in the form of deep introspection of the literature, exploring both the narrative patterns and also the meanings that are created in the mind of the reader. A more detailed data extraction table of the first- and second-order metaphors, using QSR International’s NVivo 11 Software,⁵⁵ was conducted by J.D.S. and developed through discussion between the members of the review team (Supplemental Table 7).

Determining how the studies are related

A decision was taken to focus on the first-order metaphors (direct reports from study participants) to explore the conversations and experiences expressed in the studies as they offered rich insights into the experiences of the participants.⁵² First-order metaphors had been widely used to illustrate the findings of the original studies by the study authors, as a result there were limited second-order metaphors (author interpretations) developed. The second-order metaphors were included where they offered further insights.

Translating the studies into each other

Review team discussions, using a concept mapping process, enabled the process of translations. Contextual notations helped to elucidate patterns that were more represented by particular ethnic groups or in particular geographical locations. An example of this was the difference in attitude towards healthcare professional instigated advance care planning. There was more distrust of the system in the United States than in other countries, and attitudes towards advance planning were more positive in south East Asian heritage in the United States and Canada where educational levels were higher. These differences allowed for both reciprocal translations and refutable translations to take place (Supplemental Table 7).

Findings

Synthesising translations

Following the process of translation, overarching lines of argument or storylines were suggested by members of the review team. The studies were re-read as whole to consider what new interpretations were congruent with the primary data. Noblit³⁵ describes these as a new storyline which offers a new overarching interpretation of what is being related by the original study participants. Final extrapolation of the storylines took place following further discussion by the review team (Table 6).

Table 6.

Storylines.

Storyline 1	‘My family will carry out everything for me; it is trust’: trust, dependence and importance of family
Storyline 2.	‘No Mum, don’t talk like that’: burden and protection
Storyline 3	‘I leave it in God’s hands’: spiritual reassurance
Storyline 4	‘Who’s going to look after us?’ ambiguity and change

The storylines

The storylines illustrated first the role elders envisioned their children will play in end-of-life decision making ‘My family will carry out everything for me; it is trust’. The second aspect was the perception that adult children inhibit end-of-life planning conversations: ‘No Mum, don’t talk like that’. The third was the sense of fatalism often associated with religious beliefs: ‘I leave it in God’s hands’. The fourth is the recognition of change and realisation that things may need to be done differently: ‘Who’s going to look after us?’ These storylines are explored below.

Storyline 1 ‘My family will carry out everything for me; it is a trust’: trust, dependence and importance of family

Elders in all of the studies expressed perceptions of the centrality of family in end-of-life decisions. The metaphor – ‘my family will do right by me’ – captured the sense of trust these elders had in their children’s role as carers and decision makers for them at the end of life and the assumption that their children would be proxy decision makers for them ‘when the time comes’. There was often no mention of spouses playing this decision-making role.⁸ This sense of trust was linked to the metaphor ‘Basically, you have to take care of me’. It came from traditionally held views that as they had cared for their parents, their children would do the same:

Yo te pari y tu tiene que cuidame a mi . . . basically, you have to take care of me. (Puerto Rican elder,⁵² p. 360)

This sense of responsibility being taken to the point of complete dependence and a reluctance to accept outside carers is a feature found in other studies of Black and minority ethnic elders coping with severe illness:

There was a common understanding among families that if a family member became sick, . . ., the family/children would naturally take care of them: I told my doctor that I have kids who will take care of me and I am comfortable with them . . . I don’t need home care. (Canadian South East Asian elder,⁵¹ p. 916)

In the studies of African American communities, there was less notion of familial responsibility, but more emphasis on community:

There was a sense of comfort in knowing that there would be people of their own race or ethnic group available to care for them during the time of death and dying. ‘Usually black people are all one . . . if you don’t belong to a church, then you have a friend’. (African American elder,⁴⁴ p. 12)

A sense that the children would know the right thing to do without any prior discussions was expressed both as first- and as second-order metaphors:

‘I did not have a speciﬁc conversation with them, but they know what I want’. ‘My people will take care of me. They know’. (African American elder,⁴⁵ p. 120)

On questioning, we found many of them did not have a conversation with their families about their own wishes:

Leader: Well, have you talked to them?

No, but they know what is best for me. (Canadian South East Asian elder,⁴⁵ p. 120)

When anyone in the family is faced with a difficult situation, everyone intuitively knows what their role is and what to do, and then right decisions are just made without us planning ahead. (Canadian South East Asian elder,⁵¹ p. 915)

This lack of discussion was a form of protection practised by both parties:

I don’t think people ask where you die. I think the family makes that decision, family would come forward to take responsibility and make any necessary decisions on behalf of their older relatives, and thus shelter their older relatives from topics perceived to be unpleasant. (Asian elder,⁴⁹ p. 399)

For some, this felt secure because it was in fitting with cultural expectations. However, what appears clear is these decisions by family members may be incongruent with the preferences of the elders themselves. Elders in seven of the studies expressed a preference for limiting life sustaining therapies at the end of life:

I don’t want those machines . . . if I am sick. (Hispanic elder,⁴⁰ p. 62)

Storyline 2. ‘No Mum, don’t talk like that’: burden and protection

This storyline offers insights from the experiences of these elders of the conversational dance that goes on between elders and their adult children, each looking to protect the other from what they perceive to be difficult burdens. There was an interesting mix of some elders not wishing to burden their children with end-of-life conversations and those not wanting to burden them with end-of-life decisions. In the two studies which included adult children’s perspectives,^39,40 the children spoke of not wanting the burden of their parent’s end-of-life decision making. Several of the study authors,^{21,40,44,47,49,52} discussed this notion of burden and protection to be one of the most influential factors in conversations with children about end-of-life care planning.

A resonating metaphor in this storyline of protection and burden was the role adult children play, in limiting conversations about dying initiated by their elders or by others.^{3,21,22,40,39,57} Although Hispanic elders were comfortable to discuss end-of-life issues with their children, the responses they met was illustrated by the following:

They don’t want to hear us. (Hispanic elder,⁴⁰ p. 62)

This culture of inhibiting conversations was prevalent in many of the studies, across different ethnic groups:

When I tried to talk about this topic, my children were not willing to listen to me. They said, ‘Mom, please do not talk about such things. They get angry when they hear me saying such things’. (Korean elder,²¹ p. 170)

When I anticipate any unfortunate scenario, I am immediately told to shut up and not to dwell upon it. (Canadian South East Asian elder,⁵¹ p. 916)

The elders felt the children did not want to have the conversations their parents were hoping for. An elder reported their child had expressly said,

No Mom don’t talk like that. (Hispanic adult child,⁴⁰ p. 62)

The child explained that it came from a fear of losing their parents:

We’re all educated, but we don’t want to talk about that [end of life] . . . Mom and Dad are not going to die. (Hispanic adult child,⁴⁰ p. 64)

One child suggested this reluctance to discuss dying was not just about facing the death of her parents but also linked to a cultural norm of avoiding conversations about dying:

may be a taboo across the generations. (Hispanic adult child,⁴⁰ p. 65)

This is classic of the Latino family, the hiding. (Hispanic elder,⁴⁰ p. 62)

Adult children are not the only people reluctant to talk about dying to protect others from burden. The first-order metaphor ‘if I talk about this they will suffer’ was identified by elders in nine of the studies who spoke about not wanting to burden their children. Some elders were concerned that they were creating suffering and burden merely by discussing end-of-life issues. This was described by an elder:

If I tell them, they’re going to suffer; then I would suffer more seeing them suffer. (Hispanic elder,⁴⁰ p. 61)

This element of protection seemed to stem from three orientations. Avoidance as protection,⁴⁹ where the issue is protecting the children from having to think of these difficult things; avoidance as a cultural norm;⁴⁹ and finally a reluctance to play the role of a God who is viewed as the one who can give or take life and whose will cannot be known in advance.

In all nine of the studies where personal preferences regarding decision control were raised, elders felt that end-of-life decisions should be made by the patient. However, several participants based this preference on a desire to spare family members the emotional burden of having to make difficult end-of-life decisions rather than on a desire to promote patient self determination.

Storyline 3. ‘I leave it in God’s hands’: spiritual reassurance

When exploring what elders said about end-of-life decision-making responsibilities, many referred to their religious faith.^{22,39,40,44,46,51,52} African American, Hispanic and Cambodian elders frequently used spiritual references to characterise how they cope with illness and death.^{22,39,44,47,48} Their sense of faith was pervasive in their conversations:

You just have to put your faith in the Lord. (Hispanic elder,⁴⁴ p. 9)

For many, this was intertwined with a sense of divine control illustrated by this quote:

God would ‘take care of everything’. (Canadian South East Asian elder,⁵¹ p. 916)

Some people expressed a more fatalistic view that life and death matters were beyond people’s own control so necessitated little formal decision making regarding the future:

I live in life’s terms. If it happens, it happens. (Latino elder,⁵² p. 359)

Storyline 4. ‘Who’s going to look after us?’ Ambiguity and change

As part of the process of meta-ethnography, it is important to consider the metaphors that contradict the emergent storylines. These may be in the form of first-order metaphors or the more interpretive second-order metaphors. This final storyline resonated against the general themes of the others. While elders talked of trust and faith in their children as their decision markers, in some cases there was an open acknowledgement that the children may not respect their wishes:

Even if I make a will indicating not to use life-sustaining treatment, there will be no one who will follow my will. Even if there is a will, they will all gather and discuss it together. (Korean elder,²³ p. 174)

One elder explains how this incongruence was not a major problem:

I don’t think we can force them to simply follow what we wish just because we want them to. We also have to consider their wishes. If children try their best, but parents die, there is nothing they can do about it. However, if we die because they turned the ventilator off because we asked them to do it, I think they will regret what they did after we die. They might think, I should have made more efforts to save my parents’ lives. (Korean elder,²¹ p. 175)

An awareness of the complexity of reasons that wishes maybe questioned is captured by this second-order story:

One elder said her sister blamed her brother for carrying out their father’s wishes. Her sister went all the way to their brother’s house ‘saying that he killed our father’. (Hispanic elder,⁴⁰ p. 64)

These elders demonstrate a clear awareness of the complexities of this difficult work of end-of-life decision making and many seemed comfortable with this potential incongruence with their own stated wishes.

In most studies, an awareness that immigration and changing times might change cultural traditions was apparent. This was strongest in the South Asian heritage where there was more of an awareness of the cultural assimilation that was taking place. These populations had higher levels of tertiary education so this may be an influencing factor.⁵¹ In the earlier studies, there is a brief acknowledgement of why things are changing with geographical reasons for the families not living so close to each other:

Family rarely together. (African American elder, p. 4)

They’re not around much, but I told them. (African American elder living in a care home,⁴⁵ p. 120)

In the later studies, it is discussed more descriptively:

But then we have also expectations when we grow old and if we are in that situation. ‘Who’s going to look after us?’ It’s very selfish for us to expect that our children will come or move closer to us just to take care of us. At the same time, we expect that they should be there when we need them. So it’s more like an issue of moving from India to the US. Like those questions will never come to my mind if I was in India. (Canadian Asian Indian elder,⁴⁸ p. 314)

‘Kids are different now’ and ‘they have their own lives’. (Latino elder,⁵² p. 360)

Others acknowledged that they themselves need to change and adapt, but that this may be difficult:

It’s very selfish for us to expect that our children will come or move closer to us just to take care of us. At the same time, we expect that they should be there when we need them. (Latino elder,⁴⁸ p. 315)

There was a growing receptivity to planning around end-of-life decision making particularly as a result of having been exposed to a culturally sensitive explanation or demonstration of advanced care planning. Many of them had a wealth of ideas of how perhaps culturally sensitive advanced care planning education could reach people in these diverse communities:

Such a great thing we are doing by bringing this awareness and that more should be done. (Canadian South East Asian elder researcher,⁵¹ p. 917)

Maybe you can have . . . like you have diabetes class, maybe you want to have a class for this [advance care directives] where you get ten or twenty people in the same place with somebody who’s knowledgeable. (Cambodian elder,⁴⁶ p. 1430)

Discussion

Expressing the synthesis

The aim of this review was to gain a deeper understanding into the perspectives of elders of Black and minority ethnic heritage and their children about having family conversations around end-of-life issues. Although the review sought the views of both elders and their children, most of the studies found reflected the views of the elders. From their responses, four storylines were constructed. The storylines illustrated the dependence and desire to rely on family proxies for end-of-life decision making with an understanding that proxy decisions may not reflect elders’ own preferences: ‘My family will carry out everything for me; it is trust’. The second aspect was the role adult children play in inhibiting end-of-life planning conversations: ‘No Mum, don’t talk like that’. The third was a continued relationship with a spiritual sense of fatalism often associated with religious beliefs: ‘I leave it in God’s hands’. The fourth is the recognition of change and potential desire for doing things differently: ‘Who’s going to look after us?’

The storylines around the importance of family, the preference for informal rather than formal end-of-life planning and thoughts of planning being linked to religious views about God’s timing are themes that had been identified in previous systematic reviews.^8,12,20,58 Reliance on and expectation of adult children to play a major role in end-of-life decision making is perhaps cross cultural.^1,11 However, in these studies of elders of Black and minority ethnic heritage, the absence of demonstrable involvement of spouses may reflect a phenomenon found in some studies where children born in the host culture hold a better understanding of the underlying cultural language and rules and so become the cultural interpreter and tour guide through not only the health system but also other societal processes. Facilitating more family-based conversational processes may need to be more creative than only occurring when family members can attend face-to-face health care appointments.

Protection is a major factor identified by elders of Black and minority ethnic heritage in these studies that prevents early end-of-life conversations. Elders want to protect their children from having to think about these difficult things such as the idea of their parent dying. In many cases, this is not an unfounded worry as when they raise the topic of their lives coming to an end with their children, they report the authoritative manner in which the children themselves close down those conversations. The interactions taking place here and the perspectives of both elders and children have been only sparsely explored with only one study indicating the burden this can then become for the children concerned.³⁹ Further research work is needed in this area in different cultural contexts to explore how anxiety around end-of-life conversations can be reduced.

Religiosity is a complex factor in relation to preparation for dying. In her review, Johnson et al.⁵⁹ found significant emotional distress regarding the acceptance of death in spiritual leaders and parish visitors in African American communities in the United States and suggest that ‘health care providers should not be surprised when the same person views death as a transition to a better life and as something to be avoided by obtaining medical interventions’ (p. 146). Spiritual fatalism that is accompanied by limited health literacy – particularly around serious illness and palliative care – plays alongside a sense that God is in control and will provide the support that is needed negating the need for anticipatory conversations.⁶⁰ Further research is needed to understand how religious communities explore end-of-life preparation and how work with leaders in these communities can be used to build better dying, rather than faith practices acting as barriers.

The fourth storyline captures a refutable metaphor.³⁴ This storyline of ‘Who’s going to look after us?’ changes direction from ideas expressed in the majority of studies and offers a sense of change in the perspectives of elders as they undergo a process of acculturation⁶¹ into the prevailing majority cultures and start to see the role the children will play in their future care changing. This is a theme starting to emerge in many of the studies particularly in South East Asian cultures.^11,62 The storyline of an expectation of children caring for their parents fully as they age is changing to being one where parents are becoming concerned about the burden this may place on those children and one, they want to avoid. Gott et al.⁶³ in their quantitative study with older people from a Maori heritage raises the need for a greater understanding of this changing storyline and for the development of culturally appropriate end-of-life care planning support.

People from Black and minority ethnic heritage appear to respond poorly to generic end-of-life planning initiatives through the media or governmental institutions. However, those who had been exposed to specifically targeted culturally adapted education demonstrated a desire for engaging with more formal ways of documenting preferences and initiating discussions.^48,51,52,55 There is a need to develop a more co-operative and culturally resonant way of approaching the subject of end-of-life and how communities understand the challenges and opportunities and would wish to respond in ways that may be most effective for them.⁶⁴

What this synthesis adds

This synthesis offers an insight into the background of the prevailing preferences held by elders of Black and minority ethnic heritage and what appears to be a reluctance to discuss end-of-life issues within the family. A complex interplay between avoidance as protection⁴⁹ and a spiritual assurance of a world view that one’s children will be there to make the right decisions and that God has a plan shape the resultant silence. This insight can guide a more culturally sensitive approach to how to empower elders of Black and minority ethnic heritage and their adult children to engage in end-of-life conversations prior to situations where a serious deteriorating illness makes these types of conversations often more emotionally difficult.

The role that adult children play in shaping end-of-life conversations with their elders has emerged as a significant factor that merits further exploration. Understanding these dynamics is an important priority in helping to improve the current inequalities that existing in the achievement of enabling good dying across all communities.

Finally, the synthesis provides a clearer picture of the increasing receptivity of elders of Black and minority ethnic heritage to education initiatives around advance care planning as they recognise the need to be more self reliant as they age and face end-of-life issues.^54,55

Limitations of the review

Methodologically, the literature searching for qualitative studies has been demonstrated to be challenging using online databases.^42,44,53 Although multiple searches were conducted, some studies may have been missed. In addition, the processes of translation of studies are complex⁶⁵ and reflexive. As this is an iterative and interpretive piece of work, the studies chosen and the ways in which metaphors were selected are reflective of the interests of primarily the first reviewer who led the process but moderated by the review team.³⁴ Evaluating the integrity and reliability of meta-ethnographies has been limited so far. The use of EMERGE reporting guidelines for metathnographies⁶⁶ should help to enhance clarity of reporting and inclusion of the aspects important to the process. These guidelines were considered in the writing up of this meta-ethnography.

Conclusion

This meta-ethnography indicates the potentially inhibitory influence of adult children in the preparatory end-of-life decision making of their parents, particularly in Black and minority ethnic communities. It demonstrates the complexities of this influence when those children become the primary decision makers for their parents who are dying. It has explored a number of the reasons why there has been little discussion of the older person’s preferences, and the whole situation invokes a high level of anxiety for those adult children. Culturally curated education has been found to be helpful. Further exploration of what this might look like is needed, and how this may be also targeted at a range of family members. Understanding the perspectives and experiences of adult children of people from Black and minority ethnic heritage about having end-of-life conversations may be a useful next step in developing this work.

Supplemental Material

table_7 – Supplemental material for Perspectives of elders and their adult children of Black and minority ethnic heritage on end-of-life conversations: A meta-ethnography

Supplemental material, table_7 for Perspectives of elders and their adult children of Black and minority ethnic heritage on end-of-life conversations: A meta-ethnography by Joanna De Souza, Karen Gillett, Katherine Froggatt and Catherine Walshe in Palliative Medicine

Footnotes

Authors’ contribution

This expression of synthesis was written by JDS with contributions from the review team, KG, CW and KF. All authors have made a substantial contribution to the synthesis process and to the construction and review of this paper.

Data sharing

All the data used were from published studies that had themselves obtained ethical approval for their study dissemination.

Declaration of conflicting interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship and/or publication of this article.

Funding

The author(s) disclosed receipt of the following financial support for the research, authorship and/or publication of this article: This review was completed as part of a PhD at the Lancaster University, which has been supported by a Florence Nightingale Foundation Research Scholarship.

ORCID iDs

Joanna De Souza

Catherine Walshe

Supplemental material

Supplemental material for this article is available online.

References

Wallace

CL.

Family communication and decision making at the end of life: a literature review. Palliat Support Care 2015; 13(3): 815–825.

Clarke

Seymour

‘At the foot of a very long ladder’: discussing the end of life with older people and informal caregivers. J Pain Symptom Manage 2010; 40(6): 857–869.

Parks

Winter

Santana

, et al. Family factors in end-of-life decision-making: family conflict and proxy relationship. J Palliat Med 2011; 14(2): 179–184.

Cardona-Morrell

Kim

Turner

, et al. Non-beneficial treatments in hospital at the end of life: a systematic review on extent of the problem. Int J Qual Health Care 2016; 28(4): 456–469.

Barnato

Anthony

Skinner

, et al. Racial and ethnic differences in preferences for end-of-life treatment. J Gen Intern Med 2009; 24(6): 695–701.

Samanta

Exploring cultural values that underpin the ethical and legal framework of end-of-life care: a focus group study of South Asians. J Med Law Ethics 2013; 1: 63–74.

Koffman

Davies

, et al. Does ethnicity affect where people with cancer die? A population-based 10 year study. PLoS ONE 2014; 9(4): e95052.

Sanders

Robinson

Block

SD.

Factors impacting advance care planning among African Americans: results of a systematic integrated review. J Palliat Med 2016; 19(2): 202–227.

Willmott

White

Gallois

, et al. Reasons doctors provide futile treatment at the end of life: a qualitative study. J Med Ethics 2016; 42(8): 496–503.

10.

Cooper-Kazaz

Friedlander

Steinberg

, et al. Longitudinal changes in attitudes of offspring concerning life-sustaining measures for their terminally ill parents. J Am Geriatr Soc 1999; 47(11): 1337–1341.

11.

L-S

Huang

W-Y

, et al. Experiences and perspectives of older people regarding advance care planning: a meta-synthesis of qualitative studies. Palliat Med 2017; 31(5): 394–405.

12.

Ladd

SC.

Systematic review of research literature on African Americans’ end-of-life healthcare preferences. J Afr Am Stud 2014; 18: 373–397.

13.

Evans

Pasman

Vega Alonso

, et al. End-of-life decisions: a cross-national study of treatment preference discussions and surrogate decision-maker appointments. PLoS ONE 2013; 8(3): e57965.

14.

Sinclair

Smith

Toussaint

, et al. Discussing dying in the diaspora: attitudes towards advance care planning among first generation Dutch and Italian migrants in rural Australia. Soc Sci Med 2014; 101: 86–93.

15.

Schwarz

Claros-Salinas

Streibelt

Meta-synthesis of qualitative research on facilitators and barriers of return to work after stroke. J Occupat Rehabilit 2018; 28: 28–44.

16.

Bowling

Iliffe

Kessel

, et al. Fear of dying in an ethnically diverse society: cross-sectional studies of people aged 65+ in Britain. Postgrad Med J 2010; 86(1014): 197–202.

17.

Depaola

Griffin

Young

, et al. Death anxiety and attitudes toward the elderly among older adults: the role of gender and ethnicity. Death Stud 2003; 27(4): 335–354.

18.

Neimeyer

Currier

Coleman

, et al. Confronting suffering and death at the end of life: the impact of religiosity, psychosocial factors, and life regret among hospice patients. Death Stud 2011; 35(9): 777–800.

19.

Evans

Menaca

Andrew

, et al. Systematic review of the primary research on minority ethnic groups and end-of-life care from the United Kingdom. J Pain Symptom Manage 2012; 43(2): 261–286.

20.

Dixon

King

Matosevic

, et al. Equity in the provision of palliative care in the UK: review of evidence. London: London School of Economics and Political Science, 2015.

21.

Berkman

CS.

Role of children in end-of-life treatment planning among Korean American older adults. J Soc Work End Life Palliat Care 2010; 6(3–4): 164–184.

22.

Bullock

The influence of culture on end-of-life decision making. J Soc Work End Life Palliat Care 2011; 7: 83–98.

23.

Sanders

Johnson

Cannady

, et al. From barriers to assets: rethinking factors impacting advance care planning for African Americans. Palliat Support Care 2018; 17: 306–313.

24.

Morrison

Meier

DE.

High rates of advance care planning in New York City’s elderly population. Arch Intern Med 2004; 164(22): 2421–2426.

25.

Piamjariyakul

Myers

Werkowitch

, et al. End-of-life preferences and presence of advance directives among ethnic populations with severe chronic cardiovascular illnesses. Eur J Cardiovasc Nurs 2014; 13(2): 185–189.

26.

Williams

Hewison

Wagstaff

, et al. ‘Walk with your head high’: African and African-Caribbean fatherhood, children’s mental well-being and social capital. Ethn Health 2012; 17(1-2): 89–103.

27.

Carr

Racial differences in end-of-life planning: why don’t Blacks and Latinos prepare for the inevitable. Omega (Westport) 2011; 63(1): 1–20.

28.

Hui

De La Cruz

Mori

, et al. Concepts and definitions for ‘supportive care’, ‘best supportive care’, ‘palliative care’, and ‘hospice care’ in the published literature, dictionaries, and textbooks. Support Care Cancer 2013; 21(3): 659–685.

29.

Hui

Nooruddin

Didwaniya

, et al. Concepts and definitions for ‘actively dying’, ‘end of life’, ‘terminally ill’, ‘terminal care’, and ‘transition of care’: a systematic review. J Pain Symptom Manage 2014; 47(1): 77–89.

30.

Department of Health. End of life care strategy – promoting high quality care for all adults at the end of life. London: The Stationary Office, 2008.

31.

Campbell

Pound

Morgan

, et al. Evaluating meta-ethnography: systematic analysis and synthesis of qualitative research. Health Technol Assess 2011; 15(43): 1–164.

32.

Britten

Campbell

Pope

, et al. Using meta ethnography to synthesise qualitative research: a worked example. J Health Serv Res Policy 2002; 7(4): 209–215.

33.

France

Cunningham

Ring

, et al. Improving reporting of meta-ethnography: the eMERGe reporting guidance. BMC Med Res Methodol 2019; 19: 25.

34.

Noblit

Hare

DR.

Meta-ethnography: synthesizing qualitative studies. Newbury Park, CA: SAGE, 1988.

35.

Noblit

How qualitative (or interpretive or critical) is qualitative synthesis and what we can do about this (A public lecture by Professor George W Noblit). Chapel Hill, NC: University of North Carolina at Chapel Hill, 2016.

36.

Jones

Diversities in approach to end-of-life: a view from Britain of the qualitative literature. J Res Nurs 2005; 10: 431–454.

37.

Kwak

Haley

WE.

Current research findings on end-of-life decision making among racially or ethnically diverse groups. Gerontologist 2005; 45: 634–641.

38.

Booth

Sutton

Papaioannou

Systematic approaches to a successful literature review. Thousand Oaks, CA: SAGE, 2016.

39.

Glass

Nahapetyan

Peer reviewed: discussions by elders and adult children about end-of-life preparation and preferences. Prev Chronic Dis 2008; 5: A08.

40.

Gutheil

Heyman

JC.

‘They don’t want to hear us’: Hispanic elders and adult children speak about end-of-life planning. J Soc Work End Life Palliat Care 2006; 2(1): 55–70.

41.

Greenhalgh

Wong

Training materials for meta-narrative reviews. London: Global Health Innovation and Policy Unit Centre for Primary Care and Public Health Blizard Institute, Queen Mary University of London, 2013.

42.

Pirolli

Information foraging theory: adaptive interaction with information. Oxford; New York: Oxford University Press, 2007.

43.

Critical Appraisal Skills Programme. CASP qualitative checklist, 2018. https://casp-uk.net/casp-tools-checklists

44.

Bullock

McGraw

Blank

, et al. What matters to older African Americans facing end-of-life decisions? A focus group study. J Soc Work End Life Palliat Care 2005; 1(3): 3–19.

45.

Ott

BB.

Views of African American nursing home residents about living wills. Geriatr Nurs 2008; 29(2): 117–124.

46.

Cohen

McCannon

Edgman-Levitan

, et al. Exploring attitudes toward advance care directives in two diverse settings. J Palliat Med 2010; 13(12): 1427–1432.

47.

Crump

SK.

African American seniors’ perspectives on advance care planning: a virtue ethics community-based participatory research approach. PhD Thesis, University of Minnesota, Minneapolis, MN, 2012.

48.

Sharma

Khosla

Tulsky

, et al. Traditional expectations versus US realities: first- and second-generation Asian Indian perspectives on end-of-life care. J Gen Intern Med 2012; 27(3): 311–317.

49.

Venkatasalu

Arthur

Seymour

Talking about end-of-life care: the perspectives of older South Asians living in East London. J Res Nurs 2013; 18: 394–406.

50.

Yonashiro-Cho

Cote

Enguidanos

Knowledge about and perceptions of advance care planning and communication of Chinese-American older adults. J Am Geriatr Soc. 2016; Sep;64(9):1884-1889.

51.

Biondo

Kalia

Khan

, et al. Understanding advance care planning within the South Asian community. Health Expect 2017; 20(5): 911–919.

52.

Boucher

NA.

Faith, family, filiality, and fate. J Appl Gerontol 2017; 36(3): 351–372.

53.

Atkins

Lewin

Smith

, et al. Conducting a meta-ethnography of qualitative literature: lessons learnt. BMC Med Res Methodol 2008; 8: 21.

54.

Smith

Moreno-Leguizamon

Grohmann

End of life practices and palliative care among Black and Minority Ethnic Groups (BME). London: Health Education Kent, Surrey and Sussex, 2012.

55.

CID. Tie your camel first: planning ahead for the end of life with the Somali community. London: CID, 2016.

56.

QSR. NVivo qualitative data analysis software (Version 11). Doncaster, VIC, Australia: QSR International, 2012.

57.

Moore

Sherman

SR.

Factors that influence elders’ decisions to formulate advance directives. J Gerontol Social Work 1999; 31: 21–39.

58.

Evans

Menaca

Andrew

, et al. Appraisal of literature reviews on end-of-life care for minority ethnic groups in the UK and a critical comparison with policy recommendations from the UK end-of-life care strategy. BMC Health Serv Res 2011; 11: 141.

59.

Johnson

Hayden

True

, et al. The impact of faith beliefs on perceptions of end-of-life care and decision making among African American Church members. J Palliat Med 2016; 19(2): 143–148.

60.

Koffman

Morgan

Edmonds

, et al. ‘I know he controls cancer’: the meanings of religion among Black Caribbean and White British patients with advanced cancer. Soc Sci Med 2008; 67(5): 780–789.

61.

Schwartz

Unger

Zamboanga

, et al. Rethinking the concept of acculturation: implications for theory and research. Am Psychol 2010; 65(4): 237–251.

62.

Koh

S-J

Kim

Park

, et al. Attitudes and opinions of elderly patients and family caregivers on end-of-life care discussion. Ann Geriatr Med Res 2017; 21: 49–55.

63.

Gott

Frey

Wiles

, et al. End of life care preferences among people of advanced age: LiLACS NZ. BMC Palliat Care 2017; 16(1): 76–10.

64.

Moss

Deutsch

Hollen

, et al. Understanding end-of-life decision-making terminology among African American older adults. J Gerontol Nurs 2018; 44(2): 33–40.

65.

Toye

Seers

Allcock

, et al. Meta-ethnography 25 years on: challenges and insights for synthesising a large number of qualitative studies. BMC Med Res Methodol 2014; 14: 80.

66.

eMERGe. eMERGe – meta-ethnography reporting guidance, 2018. http://emergeproject.org/

Supplementary Material

Please find the following supplemental material available below.

For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.

For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.

0.00 MB

0.02 MB