Behavioural and psychological symptoms of dementia (BPSD) such as agitation, aggression, calling out repeatedly, sleep-disturbance, wandering and apathy affect up to 90% of people with dementia, and are associated with poor outcomes such as distress in both the person with dementia and the carer, long-term hospital stay, misuse of medication and increased healthcare costs. Behaviour in dementia care can be described as ‘challenging’ when it causes distress to the person or others (such as the family carer), thus threatening the quality of life of one or both parties. The relationship between BPSD and quality of life varies from person to person, and common or frequent BPSD are not necessarily the most challenging for family carers. Reference Fauth and Gibbons1 Moreover, the carer's own characteristics, independent of dementia severity or other patient factors, can contribute to the development of aggressiveness. Reference Hamel, Gold, Andres, Reis, Dastoor and Grauer2 Carer responses to BPSD vary, and how carers accept their situation and manage dementia-related problems can influence the course of BPSD. Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens3 This may be why, even when families receive professional support, two-thirds indicate an unmet need associated with how to deal with BPSD. Reference Peeters, Van Beek, Meerveld, Spreeuwenberg and Francke4 A recent Cochrane review concerning the management of challenging behaviour in dementia noted that all eleven studies of effective interventions with family carers involved various psychotherapeutic or counselling approaches directed at the carer. Reference Moniz-Cook, Swift, James, Malouf, de Vugt and Verhey5 However, the nature and range of carer needs that are addressed within these individually tailored counselling interventions are not clear, thus making the type of support less easy to apply widely in the management of BPSD in family settings. Little is known about the particular psychosocial and emotional needs of family carers in dealing with BPSD. We reviewed the literature in order to understand why the impact of BPSD varies from carer to carer, and to consider how personalised interventions for family carers experiencing challenging behaviour in dementia could be improved.
Method
We systematically reviewed studies that used both qualitative and quantitative methods to describe family carer experiences and reports of BPSD. The meta-ethnographic approach was used to extract the richest possible data-set, Reference Noblit and Hare6 since this widely used method of synthesising closely related qualitative data has also been used with quantitative data. Reference Barley, Murray, Waters and Tylee7 The method is interpretative in nature, focusing on drawing out analogies and relationships between concepts and metaphors that may be hidden within individual studies, and translating these into a meta-ethnographical synthesis. Reference Noblit and Hare6 Meta-ethnography allows researchers to go beyond the purely summative findings associated with traditional narrative reviews. This method suited our particular research question, which was to have a better understanding of the nature of challenging behaviour in dementia in family settings; that is, to ascertain why some family carers might appraise behaviour as challenging, whereas others have less difficulty in coping.
Selection of studies
A search strategy combining medical subject headings and text words relating to dementia, BPSD, mental disorders and behaviours, behaviours, elder care, significant others, carers, family, daughters, aged, carer burden, carer strain, and cost of illness was devised and adapted for five electronic databases (see online supplement DS1). Studies were restricted to those in the English language published between 1980 and April 2012, and to those that had a family carer's account of BPSD and/or the reasons why they felt these BPSD were challenging. Spousal and non-spousal carers were included. Reviews, conference proceedings, conference abstracts, theses, supplements, reports, letters and non-peer-reviewed articles were excluded.
Quality appraisal
Three reviewers (A.F. and two assistants) assessed relevant papers for methodological quality; disagreements were resolved by discussion. The Critical Appraisal Skills Programme (CASP) checklist was used for qualitative and mixed-methods studies and the 27-item Downs & Black checklist for quantitative studies. 8,Reference Downs and Black9 Quality thresholds for high-quality studies were those used in previous systematic reviews: Reference Crellin, Orrell, McDermott and Charlesworth10,Reference Lawrence, Fossey, Ballard, Moniz-Cook and Murray11 70% or more on the CASP or 75% or more on the Downs & Black checklist. Agreement was measured using Cohen's κ weighted for closeness of scores.
Data extraction and meta-ethnographic synthesis
To determine why BPSD are appraised as challenging by families, the meta-ethnographic procedure described in supplement DS2 was followed. Reference Noblit and Hare6
Results
A total of 10 375 references were identified (Fig. 1); of the 70 studies that met the inclusion criteria prior to quality assessment, 45 were quantitative, 18 were qualitative and 7 were mixed methods. Twenty-five studies were graded as high quality, 39 as moderate quality (5–7 on the CASP; 50–75% on the Downs & Black checklist) and 6 as poor quality (<5 on the CASP; <50% on the Downs & Black checklist). Characteristics of the included studies are shown in online Table DS1. Two studies exclusively focused on participants with young-onset dementia (i.e. onset before age 65 years). Reference Allen, Oyebode and Allen12,Reference Bakker, de Vugt, Vernooij-Dassen, van Vliet, Verhey and Raymond13
Study selection process.
Quality assessment of included studies
Levels of agreement between the three independent reviewers ranged from moderate (κ = 0.52, 95% CI 0.07–0.97) to substantial (κ = 0.78, 95% CI 0.37–1.00). Reference Landis and Koch14 Lower agreement was noted for items on the qualitative appraisal CASP checklist which was also used for mixed-method studies (n = 11 studies).
Third-order constructs: synthesis
Our inclusion criteria allowed extraction of data on both qualitative and quantitative accounts of BPSD in family care settings, but some studies relied totally on a structured interview, such as the Neuropsychiatric Inventory, Reference Cummings, Mega, Gray, Rosenberg-Thompson, Carusi and Gornbein15 in reporting the accounts of family carers. Therefore, six studies could not contribute to the themes that emerged since neither participant-derived (first-order) nor author-derived (second-order) data offered an explanation for why behaviour was appraised as challenging. Reference Allegri, Sarasola, Serrano, Taragano, Arizaga and Butman16–Reference Riedijk, de Vugt, Duivenvoorden, Niermeijer, van Swieten and Verhey21 Two studies offered no data in the form of first-order constructs but did provide second-order data which supported our theme categories. Reference Chappell and Penning22,Reference Gaugler, Wall, Kane, Menk, Sarsour and Johnston23
We identified two third-order constructs that contributed to the understanding of why behaviours are appraised as challenging. The first, ‘feeling bereft’, included theme categories which in some way conditioned communication and the relationship. Themes associated with the second construct in some way reflected behaviours that were appraised as a transgression of social norms, where a carer failed to understand why the person with dementia behaved in certain ways. These provided a foundation for ‘misunderstandings about behaviour’ and carer interpretations of the meaning of their relative's communications (see Appendix). Conceptual groups identified from first- and second-order constructs were all supported by at least one high-quality study. Each theme was supported by data extracted from both qualitative and quantitative studies.
Feeling bereft
A strong sense of ‘feeling bereft’ was associated with changes in communication and the impact of BPSD on the relationship.
Changes in communication
Withdrawal behaviours described as ‘apathy’ Reference Allegri, Sarasola, Serrano, Taragano, Arizaga and Butman16–Reference Riello, Geroldi, Zanetti and Frisoni19,Reference Brækhus, Oksengard, Engedal and Laake24–Reference De Vugt, Riedijk, Aalten, Tibben, van Swieten and Verhey28 in studies that used (for example) the Neuropsychiatric Inventory were commonly distressing for families, Reference Nygaard18,Reference Riello, Geroldi, Zanetti and Frisoni19,Reference Rinaldi, Spazzafumo, Mastriforti, Mattioli, Marvardi and Polidori25,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27 where items such as ‘shows seldom or no interest in news about friends and relatives’ were endorsed. Reference Nygaard18 As lack of interest was noticed, Reference Hurt, Bhattacharyya, Burns, Camus, Liperoti and Marriott17,Reference Chappell and Penning22,Reference Siriopoulos, Brown and Wright26,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27 the range of shared pleasurable activities also declined:
‘She'd watch a hockey game with me and all of a sudden it seems to be gone and there's no interest’ (p. 82). Reference Siriopoulos, Brown and Wright26
Positive communication between people with dementia and their carers was also undermined by repetitive interactions, such as when repeated questioning resulted in the need for providing repeated information. Reference Bruce and Paterson29–Reference Gitlin, Winter, Dennis, Hodgson and Hauck32 The sense of declining conversation, ‘You can't have a discussion any more, not a real discussion’ (p. 81), Reference Siriopoulos, Brown and Wright26 exacerbated the distress associated with challenging behaviour in dementia:
‘Not being able to talk with your wife or communicate in any way is the most distressing part of it’ (p. 230). Reference Albinsson and Strang33
The contribution of BPSD to deteriorating communication with the relative, ‘It is awful to be around a man all day who doesn't communicate. I would rather talk to someone about unimportant or stupid things, than not talk at all’ (p. 153), Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27 combined with a developing sense of isolation, Reference Siriopoulos, Brown and Wright26 ‘You can somehow communicate with a dead person in a grave, and that's better than visiting a living dead person when there are no signs whatsoever of communication’ (p. 230), Reference Albinsson and Strang33 was distressing, difficult to cope with and therefore appraised as ‘challenging’ by family carers. Reference Brækhus, Oksengard, Engedal and Laake24,Reference Siriopoulos, Brown and Wright26,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Scott, Lewis, Loughlin and Chambers30,Reference Hepburn, Lewis, Narayan, Tornatore, Lindstrom-Bremer and Wexler-Schermnan31,Reference Albinsson and Strang33 The extracted first- and second-order constructs for this theme category can be seen in online Table DS2.
Changes in relationships
As conversation and shared activities declined there was a detrimental effect on the relationship, since the carer missed companionship, Reference Almberg, Grafstrom and Winblad34 ‘I miss my mother … It is difficult to explain how much one can miss someone’ (p. 687), Reference Almberg, Grafstrom and Winblad34 and reciprocal interactions, ‘You can try everything, but you get no response at all. That is very difficult for me’ (p. 153). Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27 The ongoing struggle to live with a changed relationship left some with a sense of rejection: Reference Allen, Oyebode and Allen12,Reference Siriopoulos, Brown and Wright26,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Almberg, Grafstrom and Winblad34,Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35
‘I've always been able to trust my mother to support me one hundred per cent, but little by little all her support has vanished. Before I could phone her and ask her things or tell her about everything that was happening and I always got an honest answer. I could phone and complain and things like that’ (p. 230). Reference Albinsson and Strang33
Others no longer felt loved:
‘I miss the love between us. That is the most important problem. I miss his arm around me when I am cooking dinner’ (p. 153). Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27
This sense of loss, or ‘slipping away’, Reference Allen, Oyebode and Allen12 of the person they once knew became acute and in some cases resulted in grief, Reference Almberg, Grafstrom and Winblad34 particularly when carers appraised their loved one as ‘not knowing or recognising them.’ Reference Allen, Oyebode and Allen12,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Albinsson and Strang33,Reference Almberg, Grafstrom and Winblad34,Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35 The changed role and new responsibilities, such as role reversal from provider to dependant, Reference Allen, Oyebode and Allen12,Reference Albinsson and Strang33,Reference Almberg, Grafstrom and Winblad34 and from that of protection and nurturing to having to provide care: Reference Almberg, Grafstrom and Winblad34 ‘I don't want to be a mother for my mother …’ (p. 687), Reference Almberg, Grafstrom and Winblad34 engendered for some a sense of role captivity Reference Scott, Lewis, Loughlin and Chambers30 and strain. Reference Allen, Oyebode and Allen12,Reference Bakker, de Vugt, Vernooij-Dassen, van Vliet, Verhey and Raymond13,Reference Siriopoulos, Brown and Wright26,Reference Almberg, Grafstrom and Winblad34–Reference Tan, Wong and Allen36
The impact of BPSD on the relationship between the person with dementia and some family carers was the loss of the emotional bond of love Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Almberg, Grafstrom and Winblad34,Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35 and nurture resulting in isolation, Reference Siriopoulos, Brown and Wright26,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Almberg, Grafstrom and Winblad34 feelings of rejection, Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27 and even grief. Reference Allen, Oyebode and Allen12,Reference Almberg, Grafstrom and Winblad34
Misunderstandings about behaviour
The theme of misunderstandings about behaviour reflected the perception that the relative had transgressed social norms and was associated with the carer's personal or sociocultural expectations.
Personal expectations
Although families were aware that their relative had dementia, some had difficulty in understanding the ‘meaning’ of their relative's communicated behaviour, particularly when this was appraised as ‘out of character’, Reference Allen, Oyebode and Allen12,Reference Almberg, Grafstrom and Winblad34 or within their relative's control. Reference Chappell and Penning22 Thus repeated questioning about ‘forgotten’ tasks or activities that might be worrying the person with dementia, Reference Bruce and Paterson29,Reference Hepburn, Lewis, Narayan, Tornatore, Lindstrom-Bremer and Wexler-Schermnan31,Reference Gitlin, Winter, Dennis, Hodgson and Hauck32 requiring the carer to constantly repeat requests to no end, becomes challenging:
‘Well, I think it's very stressful and it's the repeating, repeating and repeating, and you expect him to remember something and then he doesn't … it is stressful’ (p. 221). Reference Hepburn, Lewis, Narayan, Tornatore, Lindstrom-Bremer and Wexler-Schermnan31
Accusations of stealing made by a person with dementia who has misplaced valued items become troublesome when interpreted as personally offensive, Reference Riello, Geroldi, Zanetti and Frisoni19,Reference Rinaldi, Spazzafumo, Mastriforti, Mattioli, Marvardi and Polidori25,Reference Nagarantnam, Lewis-Jones, Scott and Palazzi37 and when frustration in a relative with dementia is interpreted as aggression, the behaviour becomes stressful. This undermines the carer's efficacy in coping with BPSD, and the relative's behaviour is therefore appraised as challenging, Reference Allen, Oyebode and Allen12,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Riello, Geroldi, Zanetti and Frisoni19–Reference Chappell and Penning22,Reference Rinaldi, Spazzafumo, Mastriforti, Mattioli, Marvardi and Polidori25,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference De Vugt, Riedijk, Aalten, Tibben, van Swieten and Verhey28,Reference Scott, Lewis, Loughlin and Chambers30,Reference Almberg, Grafstrom and Winblad34–Reference Nagarantnam, Lewis-Jones, Scott and Palazzi37 since the carer feels unable to respond effectively: ‘She thinks I have met someone else. It isn't true and I don't know how to handle it’ (p. 687); Reference Almberg, Grafstrom and Winblad34 consequently the caregiving situation can deteriorate. This may also be the case with newly occurring behaviours as the carer may not yet know or feel confident in how to respond effectively. Reference Gaugler, Wall, Kane, Menk, Sarsour and Johnston23
Understanding helped some carers, but levels of understanding and thresholds of carer tolerance of their relatives' communications of distress or discomfort can vary, Reference Allen, Oyebode and Allen12,Reference Almberg, Grafstrom and Winblad34 even within families:
‘ … try to explain them [behaviours] to my mum. She does understand them but it is hard for her to keep them in mind’ (p. 465). Reference Allen, Oyebode and Allen12
The personal expectations of carers, such as the level of care they wish to provide, and their own need for care due to advanced age and disabilities, can also affect thresholds of tolerance of the relative's behaviour, and the efficacy of the carer to respond effectively to BPSD. Reference Rinaldi, Spazzafumo, Mastriforti, Mattioli, Marvardi and Polidori25,Reference De Vugt, Riedijk, Aalten, Tibben, van Swieten and Verhey28,Reference Hepburn, Lewis, Narayan, Tornatore, Lindstrom-Bremer and Wexler-Schermnan31,Reference Lim, Son, Song and Beattie38
Sociocultural expectations
Gender and sociocultural expectations can trigger embarrassment and shame for the carer, Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35,Reference Tan, Wong and Allen36 when BPSD such as disinhibition transgress expectations in public. Reference Allen, Oyebode and Allen12,Reference Bakker, de Vugt, Vernooij-Dassen, van Vliet, Verhey and Raymond13,Reference De Vugt, Riedijk, Aalten, Tibben, van Swieten and Verhey28 Although carers can use strategies to manage BPSD, strongly held expectations can also lead to distress and perceptions of challenging behaviour:
‘He did go to the toilet in the bed and I didn't know what to do the first time … I don't wanna clean it … I'm Italian … my mum still leaves my clothes on the bed in the morning … how am I supposed to clean an 80-year-old … I did and then I went outside and spewed my guts out’ (p. 293). Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35
The sometimes ‘expected submissive role’ of female carers in family subsystems can also undermine the ability of a carer to use strategies that require the provision of clear, firm instructions to assist the person with dementia. Reference Tan, Wong and Allen36
Line of argument synthesis
The sense that people with dementia inevitably lose their identity to the disorder was a key explanatory theme for challenging behaviour in family settings. Carer perceptions were anticipated: ‘Ummm, well if it gets worse and like he can't remember who me or my sister or anybody is then that would be hard to … not very nice’ (p. 473), Reference Allen, Oyebode and Allen12 or experienced: ‘I have come to terms with the fact that my dad is not my dad any more’ (p. 467), Reference Allen, Oyebode and Allen12 leading to a deconstruction of the person's ‘lived life’ associated with metaphors of decline to childhood, Reference Siriopoulos, Brown and Wright26,Reference Scott, Lewis, Loughlin and Chambers30,Reference Almberg, Grafstrom and Winblad34 ‘My mother is like a child’ (p. 687), Reference Almberg, Grafstrom and Winblad34 or worse. Reference Nagarantnam, Lewis-Jones, Scott and Palazzi37 Thus the common social construction about dementia – that is, the belief that the person would inevitably become ‘no longer human’ – can be seen in family carers who have difficulty in coping with BPSD:
‘It's an awful illness, because Mom no longer exists even though she's still there’ (p. 230). Reference Albinsson and Strang33
In accordance with this fear of dementia, the proposition of becoming dehumanised – of losing one's identity – is the construction that dementia is an invader which creeps up on people and steals them from themselves, resulting in metaphoric comparisons of people with dementia as the ‘living dead’. Reference Behuniak39
Discussion
We identified key constructs for the understanding and management of challenging behaviour in family care settings: namely, issues relating to changes in communication, companionship or reciprocity in relationships, and/or carer perceptions of transgressions against social norms. These are consistent with commentaries in which interpersonal, family and social contexts are noted as contributory factors in the development and course of BPSD. Reference Moniz-Cook, Swift, James, Malouf, de Vugt and Verhey5,Reference Siriopoulos, Brown and Wright26 The identified themes from this meta-ethnography provide a psychological understanding of unmet need in family carers who struggle to accept and adjust to their changed circumstances. Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35,Reference Tan, Wong and Allen36,Reference Diehl, Mayer, Kurz and Forstl40 For these carers emotions associated with loss of the relationship and perceptions of antisocial behaviour can act as barriers to their effective responses to BPSD. Underlying the experience of challenging behaviour were beliefs that the person with dementia would inevitably lose his or her identity to the disorder. Therefore for some family carers, metaphors of dementia as the ‘living dead’ appeared salient in undermining their effective responses to BPSD.
Unmet need in family carers
Difficulties arise for the carer when a behaviour that is appraised as being out of character for the relative is overgeneralised to indicate a complete change in the person, e.g. ‘All were mourning over the loved one who was no longer the person they had known’ (p. 448). Reference Diehl, Mayer, Kurz and Forstl40 Our findings suggest that underlying these perceptions is the carer's subtle but sustained distress resulting from loss of the emotional bond with the relative with dementia, and the carer's consequent own unmet need for nurture, care and emotional security.
Studies of attachment theory in dementia care describe why some carers adjust effectively to the changed circumstances associated with dementia and thus experience reduced challenging behaviour, whereas others do not. Reference Browne and Shlosberg41 For example, Ingebretsen & Solem noted that spouse carers' ability to cope with loss and changes was dependent on their own needs for emotional safety: secure attachments enabled adjustment, whereas those who did not cope well were seen as in need of high levels of support, empathy and individual care. Reference Ingebretsen and Solem42 Therefore, for carers who have difficulty in coping with BPSD, initial emotional support may enhance therapeutic engagement and their readiness to use BPSD management strategies. Reference Gitlin and Rose43 Carers who cope with BPSD through ‘emotional distancing’, Reference Reamy, Kyungmin, Zarit and Whitlach44 which can result in ‘deconstruction’ of the person with dementia, may then be unable to provide the support that is required by their relative, Reference Reamy, Kyungmin, Zarit and Whitlach44 including strategies to respond effectively to dementia-related problems. Examples of emotional distancing include the shift from an ‘us’ identity for spouses to a sense of ‘me and them’, Reference Davis, Gilliss, Deshefy-Longhi, Chestnutt and Molloy45 which at its worst reinforces fear and stigmatised beliefs, Reference Behuniak39 such as descriptions of the ‘living dead’ where the person with dementia is entirely ‘lost’ to the carer. Reference Albinsson and Strang33
Misunderstandings about the meaning of behaviours when these are perceived as transgressing interpersonal social norms and expectations can precipitate strong emotions that affect the carer's responses. For example, feelings of embarrassment and shame become barriers to help-seeking, Reference Dias, Samuel, Patel, Prince, Parameshwaran and Krishnamoorthy46 explaining why families feel ill-equipped in dealing with BPSD. Reference Peeters, Van Beek, Meerveld, Spreeuwenberg and Francke4 Although there are similarities in the experiences and perceptions of culturally and linguistically diverse family carers, there are also differences across groups. Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35 Therefore, interventions that take account of social and cultural factors that may contribute to variation in carer adjustment to changing circumstances, Reference Dias, Samuel, Patel, Prince, Parameshwaran and Krishnamoorthy46 and their approaches to BPSD, Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens3 can be helpful in bolstering some caregiving contexts.
Understanding and intervening
Consistent with the literature, Reference Braun, Mura, Peter-Wight, Hornung and Scholz47 our first explanatory construct for variation in carer responses to BPSD found noteworthy accounts of changes in communication due to dementia which appeared to reduce the quality of dyadic interactions, with a consequent declining relationship and a strong sense of loneliness: this we describe as the carer ‘feeling bereft’. Interventions to address the carer's need for understanding and managing changes in communication are at an early stage of development, Reference Liddle, Smith-Conway, Baker, Angwin, Gallois and Copland48 but one preliminary investigation reported reductions in BPSD and positive outcomes for the caring experience. Reference Liddle, Smith-Conway, Baker, Angwin, Gallois and Copland48 However, communication interventions are untested in caregiving contexts where there are known risk factors to carer adjustment to the changed circumstances associated with dementia, Reference Ablitt, Gregory and Muers49 or where role captivity may undermine meaning in the caregiving context. Reference Scott, Lewis, Loughlin and Chambers30,Reference Quinn, Clare and Woods50
Multicomponent interventions in family care settings have a developing evidence base for the management of challenging behaviour in dementia. Reference Allegri, Sarasola, Serrano, Taragano, Arizaga and Butman16 For example, one component of the intervention set out in the Seattle carer training protocols (STAR-C) focused on ‘increasing pleasant events’. Reference Logsdon, McCurry and Teri51 This has the potential to help adjustment to the changed circumstances and thus moderate the sense of ‘feeling bereft’ (see Appendix). An adaptation of this multicomponent programme to a UK setting also reduced BPSD and carer responses to behaviour, and improved carer mood. Reference Moniz-Cook, Elston, Gardiner, Agar, Silver and Win52 More recently, the Strategies for Relatives (START) psychoeducation programme, Reference Livingston, Barber, Rapaport, Knapp, Griffin and King53 which included an ‘understanding behaviour’ component, had a positive impact on family carer mood. This programme used cognitive–behavioural techniques to help carers identify unhelpful appraisals and identify more adaptive alternatives. Our review adds to this literature by suggesting that interventions should additionally target the carer's unmet need within each caregiving context by employing strategies to address the carer's underlying assumptions and core beliefs.
Strengths and limitations
Our study is the first, as far as we know, to review variation in family carer responses to BPSD. We used rigorous methods for systematic review, including a comprehensive search of five electronic databases and a selection of high-quality studies against predetermined criteria. Our review was inclusive in that it accessed both quantitative and qualitative studies which were heterogeneous in methodological design, relationship type, onset of dementia and country setting. There is a risk with meta-ethnography of compromising the integrity of the individual studies, but we made extra efforts to retain context and holism for the studies reviewed during each stage of the synthesis. Two experienced clinicians (G.C. and E.M.-C.) examined extracted data to ensure context and meaning from the original data (first-order constructs) were not lost during the synthesis. One disadvantage of our decision to include only high-quality studies was a loss of accounts from subthreshold studies, particularly qualitative and mixed-methods studies. To counter this we checked our findings against data from subthreshold studies to ensure completeness. Although additional theme categories from these studies were identified, they were in accordance with the data that shaped the current third-order constructs and subsequent line of argument. Caution is needed over the potential over-influence of two studies of caring experience in young-onset dementia. Reference Allen, Oyebode and Allen12,Reference Bakker, de Vugt, Vernooij-Dassen, van Vliet, Verhey and Raymond13 Our third-order construct ‘misunderstandings about behaviour’ was underpinned by perceived transgressions of social norms and qualitative accounts for ‘personal expectations’ (see Appendix), which drew heavily on one of these two studies. For this theme generalisation cannot be assumed, since disturbances in social behaviour are often a distinct feature of a dementia subtype that was present in some participants. Reference Allen, Oyebode and Allen12 A limitation to our findings was that six – almost a quarter – of the included studies did not offer data for synthesis on why carers might be distressed by BPSD. These studies reported quantitative or mixed-methods data. Reference Allegri, Sarasola, Serrano, Taragano, Arizaga and Butman16–Reference Riedijk, de Vugt, Duivenvoorden, Niermeijer, van Swieten and Verhey21 The information from these studies was weighted towards the structure of the questionnaire, for example the Neuropsychiatric Inventory, so it was not possible to extract first- or second-order constructs. Nevertheless, the synthesis has provided novel insight into how support programmes for family carers can be improved by understanding why some BPSD are experienced as challenging.
Implications for research and practice
The Cochrane review of an intervention for challenging behaviour noted that most successful programmes had elements of support for the family carer as well as addressing unmet need in the care recipient. Reference Moniz-Cook, Swift, James, Malouf, de Vugt and Verhey5 Interventions that focus on carer knowledge aim to reduce unrealistic expectations, increase feelings of competency, increase positive comparisons and thus reduce the number of behaviours that are perceived as challenging. However, our review suggests that attention to the wider caregiving context such as the carer's unmet psychological needs and negative feelings – feeling bereft and/or ashamed – are also important interventions for the management of challenging behaviour. It is possible that carers who can recognise the role of the illness in the loss of identity, and retain the conceptualisation of their relative with dementia as the person they have always known and loved, will continue to have a fulfilling relationship. Consequently, the companionship and feelings of care and nurture gained from the relationship will help to reduce carers' perception of behaviours as challenging, thus improving their ability to cope. Future interventions could also investigate the effect of helping family carers to redefine their new role in ways they find acceptable, identify new means of communicating with their relative, improve reciprocity with the dyadic relationship, and create more opportunities for shared activities. In order to support families these interventions should be studied early on in the illness, since aspects of our conceptualisation of the caregiving context can be understood independently of dementia severity or other patient characteristics.
Funding
This paper presents independent research funded by the National Institute for Health Research (NIHR) under its Programme Grants for Applied Research (RP-PG-0606-1067 and RP-PG-060-1083). The views expressed in this publication are those of the authors and not necessarily those of the National Health Service, the NIHR or the UK Department of Health.
Acknowledgements
We thank Dr Shaw, Dr Pound, Dr Malpass and Professor Britten for their advice and expertise on meta-ethnography, and William Pearson and Charlotte Stoner for assistance with reliability checking of the selected papers.
Appendix
Third-order constructs
Third-order constructs are listed with associated theme categories and themes for why behaviours are seen as challenging by family carers.
Feeling ‘bereft’
Changes in communication Reference Allen, Oyebode and Allen12,Reference Siriopoulos, Brown and Wright26,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Bruce and Paterson29–Reference Albinsson and Strang33,Reference Almberg, Grafstrom and Winblad34
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• repetitive interactions Reference Bruce and Paterson29–Reference Gitlin, Winter, Dennis, Hodgson and Hauck32
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• decline in conversation and isolation Reference Allen, Oyebode and Allen12,Reference Siriopoulos, Brown and Wright26,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Albinsson and Strang33,Reference Almberg, Grafstrom and Winblad34
Changes in relationships Reference Allen, Oyebode and Allen12,Reference Bakker, de Vugt, Vernooij-Dassen, van Vliet, Verhey and Raymond13,Reference Siriopoulos, Brown and Wright26,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Albinsson and Strang33,Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35,Reference Tan, Wong and Allen36
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• loss of care and nurture – ‘feeling unloved/rejected’ Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Albinsson and Strang33,Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35
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• loss of companionship Reference Siriopoulos, Brown and Wright26,Reference De Vugt, Stevens, Aalten, Lousberg, Jaspers and Winkens27,Reference Almberg, Grafstrom and Winblad34
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• role reversal/captivity Reference Allen, Oyebode and Allen12,Reference Bakker, de Vugt, Vernooij-Dassen, van Vliet, Verhey and Raymond13,Reference Albinsson and Strang33,Reference Almberg, Grafstrom and Winblad34,Reference Tan, Wong and Allen36
‘Misunderstandings about behaviour’ due to perceived transgressions against social norms
Personal expectations Reference Allen, Oyebode and Allen12,Reference Chappell and Penning22,Reference Gaugler, Wall, Kane, Menk, Sarsour and Johnston23,Reference Rinaldi, Spazzafumo, Mastriforti, Mattioli, Marvardi and Polidori25,Reference De Vugt, Riedijk, Aalten, Tibben, van Swieten and Verhey28,Reference Hepburn, Lewis, Narayan, Tornatore, Lindstrom-Bremer and Wexler-Schermnan31,Reference Boughtwood, Adams, Shanley, Santalucia and Kyriazopoulos35,Reference Almberg, Grafstrom and Winblad34–Reference Lim, Son, Song and Beattie38
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• understanding meaning and carer efficacy Reference Allen, Oyebode and Allen12,Reference Chappell and Penning22,Reference Gaugler, Wall, Kane, Menk, Sarsour and Johnston23,Reference Almberg, Grafstrom and Winblad34,Reference Nagarantnam, Lewis-Jones, Scott and Palazzi37
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• carer threshold/tolerance Reference Rinaldi, Spazzafumo, Mastriforti, Mattioli, Marvardi and Polidori25,Reference De Vugt, Riedijk, Aalten, Tibben, van Swieten and Verhey28,Reference Hepburn, Lewis, Narayan, Tornatore, Lindstrom-Bremer and Wexler-Schermnan31,Reference Lim, Son, Song and Beattie38
Sociocultural expectations
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