REVIEW ARTICLE |
Centre for Reviews and Dissemination, University of York, York
Centre for Suicide Research, University Department of Psychiatry, Warneford Hospital, Oxford
Centre for Reviews and Dissemination, University of York, York, UK
Correspondence: Dr Catriona McDaid, Centre for Reviews and Dissemination, University of York, York YO105 DD, UK. Email: cm36{at}york.ac.uk
None. Funding detailed in Acknowledgements.
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Promoting the mental health of people bereaved through suicide is a key aim of the National Suicide Prevention Strategy.
Aims
To evaluate the effects of interventions to support people bereaved through suicide.
Method
We conducted a systematic review of data from controlled studies of interventions for people bereaved through suicide. Studies were identified using systematic searches, the methodological quality of included studies was assessed and narrative synthesis conducted.
Results
Eight studies were identified. None was UK-based and all but one study had substantial methodological limitations. When compared with no intervention, there was evidence of some benefit from single studies of a cognitive–behavioural family intervention of four sessions with a psychiatric nurse; a psychologist-led 10-week bereavement group intervention for children; and 8-week group therapy for adults delivered by a mental health professional and volunteer. The findings from studies comparing two or more active interventions were more equivocal.
Conclusions
Although there is evidence of some benefit from interventions for people bereaved by suicide, this is not robust. Further methodologically sound evidence is required to confirm whether interventions are helpful and, if so, for whom.
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Sources of support for those bereaved through suicide include general practitioners, specialised therapists, self-help groups, specialised reading material and internet sites.5 However, little is known about the effects of providing support. We conducted a systematic review with the purpose of evaluating the effects of interventions to assist people bereaved by suicide in dealing with the impact of the death and the consequences for their well-being.
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Inclusion criteria
Any type of intervention targeted at adults or children bereaved through
suicide was eligible for inclusion, for example support groups, self-help and
volunteer-led groups, as well as therapeutic interventions delivered by health
professionals. There was no restriction on the relationship to the person who
had died: studies of people bereaved through a personal or professional
relationship were also eligible. All outcomes (qualitative and quantitative)
were considered relevant. The key restriction was that only randomised
controlled trials (RCTs) and studies with a control or comparison group
(including cohort studies) were eligible. This was viewed as particularly
important owing to the changing nature of grief over
time.3
Data extraction and quality assessment
Key study characteristics and outcomes were extracted and studies were
quality-assessed by one reviewer and checked for accuracy by a second.
Disagreements were resolved through consensus, and if necessary a third
reviewer was consulted. One French-language paper required translation. The
quality criteria (see Appendix) were based on the Centre for Reviews and
Disseminations guidance for undertaking systematic
reviews,8 and a
report on evaluating non-randomised
studies.9 In order
to assess the integrity of the intervention we drew on the Quality Assessment
Tool for Quantitative
Studies.10
Data synthesis
Given the diversity of the studies in terms of settings, interventions,
outcomes and outcome measures used, we undertook a narrative synthesis based
on recent
guidance.11,12
The primary study findings were interpreted, and similarities and differences
between the studies investigated. This included consideration of study design,
methodological quality, whether the study was appropriately powered,
intervention characteristics and delivery, participants and outcome measures.
Studies were grouped according to whether they had an active comparison
group.
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![]() View larger version (24K): [in a new window] [as a PowerPoint slide] |
Fig. 1 Study selection.
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The settings in which the interventions occurred were also diverse and included a school,13 the family home,20 the scene of the suicide,14 a laboratory at a university,16 and a suicide prevention centre.18,19 Two studies did not report any details about the setting.15,17 With the exception of one study,16 the interventions were delivered in a family or group context by mental health professionals15,17,19,20 or by mental health professionals in conjunction with volunteers who had themselves been bereaved by suicide.14,18
Quality
With the exception of the study by de Groot et
al,20
substantial methodological problems were identified in the studies. The key
threats to study validity are summarised in
Table 1; the full quality
appraisal is available from the authors.
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View this table: [in a new window] | Table 1 Summary of results: intervention v. no intervention |
Two of the RCTs were truly random,15,20 one was not (participants were assigned in alternating order),17 and one did not report how randomisation was carried out.16 One RCT attempted to conceal treatment allocation.20 There is therefore the risk that the effectiveness of the interventions was overestimated in the other studies, especially given that subjective outcome measures were used. The remaining studies used various methods to assign participants to the intervention and comparison groups, all of which had a high risk of selection bias. There were differences between groups at baseline in three studies,16–18 or it was unclear whether they were similar.13,15 None of the studies appeared to conduct a full intention-to-treat analysis including all allocated participants. In some situations this can lead to an overestimation of the treatment effect, but it is worth noting that in the study by de Groot et al those who dropped out had slightly more favourable scores at baseline for depression, complicated grief and self-blame.20
The studies were generally small and, with the exception of the de Groot et al study,20 it was unclear whether they were appropriately powered to detect an effect on all the outcomes measured. Four of the studies indicated (explicitly or implicitly) that the intervention was implemented based on a treatment protocol or manual.15–17,20 It was possible to assess the fidelity of the intervention in only one study, which measured consistency of delivery.17 Hence, there is the question of whether the intervention and comparison were delivered as planned, and in a consistent manner.
Study findings
Intervention v. no intervention
There was some evidence of a positive effect of interventions when compared
with no intervention (Table 1).
A 10-week bereavement group intervention for children, led by psychologists,
was more effective than no intervention at reducing anxiety and depression,
but not social adjustment and post-traumatic
stress.17 This was
a small study and it was unclear whether it was appropriately powered to
detect an effect on the outcomes measured. In addition, a fifth of the
comparison group sought other interventions, which might have diluted or
inflated the effect of the intervention. There were also differences between
the groups at baseline: children in the intervention group were younger, had
better social adjustment and the length of time since bereavement was
shorter.
An 8-week group therapy intervention delivered by a mental health professional and a volunteer was associated with a lessening in intensity of eight of nine emotions assessed compared with one of nine emotions for the control group.18 However, a statistical analysis was not reported for differences between groups, and at baseline the intervention group reported greater feelings of grief, shame and guilt than the comparison group. The reliability and validity of the outcome measure were unclear. The time lapse between bereavement and attending a crisis centre for assessment and treatment was shorter in those who had received an active outreach intervention at the scene of the suicide compared with those who had not;14 however, this outcome measure is based on the assumption that seeking help following the intervention is a positive outcome. In the absence of any information about individuals who received the outreach intervention but did not seek help at the crisis centre, it is unclear whether this was an appropriate assumption.
The third study was a cluster randomised trial of family-based cognitive–behavioural therapy (CBT), compared with usual care, for first-degree relatives and spouses.20 The intervention consisted of four sessions of CBT with a trained psychiatric nurse counsellor, 3–6 months following the bereavement. This was the best-quality study found: there was an adequate method of randomisation, an appropriate method was used to adjust for baseline differences and loss to follow-up was low. Thirteen months after the bereavement there was no beneficial effect on the primary outcome of self-reported complicated grief reaction (measured by the Inventory for Traumatic Grief) or on suicidal ideation or depression in the intervention group compared with controls. There was evidence, however, of fewer maladaptive grief reactions and less perception of being to blame for the suicide.20
Studies using an active comparator
The findings from the studies comparing two or more active interventions
were equivocal (Table 2). Among
undergraduates, writing therapy over a 2-week period which involved describing
the events and emotions around their loss had some marginal benefits compared
with a trivial writing
condition.16
However, participants in the profound writing group also had less severe grief
than the comparison group at baseline. In a school setting, implementation of
a crisis intervention involving first talk through and psychological
debriefing was associated with fewer pupils experiencing high-intensity grief,
but not stress response, than a less intense crisis
intervention.13 A
study comparing four professionally led, closed-group interventions of 2
months, 4 months, 6 months and 12 months duration reported a trend in all four
groups towards decreasing depression over the 12-month follow-up
period.19 There was
some variation between groups in the decrease in BDI score (least reduction in
the 2-month group and greatest in the 4-month group), although there was
considerable and unequal loss to follow-up across groups, and what appeared to
be baseline differences between the groups. In both these studies there was a
high risk of confounding due to indistinct
comparators.13,19
There was no benefit in participating in a health professional-led bereavement
group compared with a social group intervention for women bereaved by the
suicide of their spouse, although it was unclear whether this study was
appropriately powered to detect an
effect.13
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View this table: [in a new window] | Table 2 Summary of results: studies using an active comparator |
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Interpretation of results
Six of the eight studies showed some evidence of benefit for participants
receiving the intervention on at least one measure. However, because of the
differences between studies and the methodological limitations, considerable
care needs to be taken before accepting the assumption that some kind of
intervention is better than none. Some of the methodological limitations, such
as small sample size or the control group receiving support from elsewhere,
might have resulted in the treatment effect being underestimated. However, the
latter might also have led to an overestimation of the treatment effect if the
additional support was detrimental to the control group. Other limitations
such as non-randomised allocation of participants to intervention groups might
also have led to an overestimation. Despite positive findings from the study
with the lowest risk of bias, uncertainty remains, as there was no evidence of
benefit on the primary outcome of self-reported complicated grief. This
early-stage intervention has the benefit of being brief, although replication
and evidence of a stronger treatment effect would increase confidence in the
effectiveness of such an
intervention.20
Owing to the paucity of data it was not possible to explore whether the effects of interventions varied with age, gender, self-referral, characteristics of the deceased or the nature of the relationship between the bereaved and the deceased. Whether bereaved individuals benefit from an intervention may depend on whether or not they are experiencing complicated grief.6,21 However, it was not possible to explore this issue owing to the limited data available.
The review is limited by the small number of studies available, their diversity and general poor quality. This reflects the findings of a systematic review of bereavement care interventions for general population groups, where the authors reported considerable theoretical and clinical diversity, inadequate reporting of intervention procedures, methodological flaws, and few replication studies.22 The evidence for a positive effect of interventions for general bereaved populations is also weak.22–24 Our review did not address the question of whether interventions for people bereaved through suicide need to be different from those provided to people bereaved through other means. Given the limitations of the studies of general bereaved populations and populations bereaved through suicide, it is unlikely that data are currently available to address this question. However, it is an important issue that should be addressed.
Implications for practice and research
The evidence we have identified and appraised is not robust; clear
implications for practice therefore cannot be drawn. However, based on the
limited evidence available from single studies, the following tentative
suggestions are made: psychologist-led group therapy for children may reduce
anxiety and
depression,17 and
combined health professional- and volunteer-led group therapy for adults may
reduce feelings of anger towards the deceased and self, anxiety, depression,
grief, guilt, puzzlement and
shame.18 There is
also recent evidence that a brief CBT family intervention by a trained
psychiatric nurse counsellor resulted in fewer maladaptive grief reactions and
less self-blame.20
However, it remains unclear whether interventions are helpful and, if they
are, the best timing of such intervention. Similarly, it is unclear whether
they are helpful for all people bereaved through suicide or whether there are
specific individuals who might benefit most – for example those
experiencing complicated grief.
The views of participants were noticeably absent from the studies. Their views on the interventions received were generally not obtained and it was unclear whether the support given was viewed as helpful and appropriate to their needs. Obtaining the views of participants in future studies is vital to help identify the effective components of interventions and to establish what support is helpful to people bereaved by suicide. Grief can be culture-specific: consideration needs to be given to the generalisability of evidence to different ethnic groups. Research is required on the effectiveness of interventions in different ethnic groups as well as the potentially different responses of males and females, people of different ages and background as well as those experiencing complicated grief.
There is a pressing need for methodologically sound RCTs. Although this is a challenging study design to implement in this field, the recently published trial of CBT illustrates that it is possible. Sample size calculations need to take into account the need for analysis to investigate the impact of potentially important prognostic factors on outcome. It would aid meaningful comparison between studies if a core set of outcome measures could be used: consideration needs to be given to whether to use generic scales for anxiety and depression and/or grief specific measures.
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If it was described as an RCT, was the treatment allocation concealed?
Was the assignment of participants to treatments described?
Were the groups balanced at baseline in relation to potential confounders?
Were baseline differences adequately adjusted for in the design or in the analysis?
Were important confounders reported?
Was outcome assessment made masked to group allocation?
What proportion of participants completed the study?
Were withdrawal rates and reasons similar across intervention and control groups?
Were the data collection tools shown or known to be valid for the outcome?
Were the data collection tools shown or known to be reliable for the outcome?
Was the statistical analysis appropriate?
Did the analyses include an intention-to-treat analysis?
Was the consistency of the intervention measured?
If yes, was the intervention provided to all participants in the same way?
Is it likely that participants received an unintended co-intervention?
Is it likely that contamination might have influenced the results?
Was the length of follow-up long enough for the outcomes to occur?
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