| Literature DB >> 30700267 |
Karl Andriessen1,2, Karolina Krysinska1,3, Nicole T M Hill4, Lennart Reifels1, Jo Robinson4, Nicola Reavley1, Jane Pirkis5.
Abstract
BACKGROUND: Suicide bereavement is a risk factor for adverse outcomes related to grief, social functioning, mental health and suicidal behaviour. Consequently, suicide bereavement support (i.e., postvention) has been identified as an important suicide prevention strategy. However, little is known about its effectiveness. To redress this gap, this review aimed to assess the evidence of effectiveness of interventions for people bereaved by suicide, and appraise the quality of the research in this field.Entities:
Keywords: Bereavement; Effectiveness; Grief; Interventions; Postvention; Suicide; Systematic review
Mesh:
Year: 2019 PMID: 30700267 PMCID: PMC6354344 DOI: 10.1186/s12888-019-2020-z
Source DB: PubMed Journal: BMC Psychiatry ISSN: 1471-244X Impact factor: 3.630
Fig. 1PRISMA Flow Diagram
Effectiveness of suicide bereavement interventions: Summary of studies
| Author (year)/Location | Eligibility criteria | Sample size | Age (M, SD, range) | Male/female | Time since bereavement/Relationship to the deceased | Type of intervention/Setting | Characteristics of intervention | Duration/Frequency of contact | Outcome/Instrument/Timepoints | Main results |
|---|---|---|---|---|---|---|---|---|---|---|
| Battle (1984) USA [ | Intervention: suicide loss, help-seeking from a crisis centre | Intervention | Range 14–66 years | 22% /78% | 8 days – 11 years | Group | Support group with educational component | 1.5 h weekly sessions in first 4 months, followed by 2-weekly 1.5 h sessions | Psychosocial functioning incl. Problems, feelings, goals (self-constructed questions) | Participants are more emotional (more distress, pain, happiness, pleasure) than non-group controls); suicidal pain 50% vs 0%; perfect happiness: 67% vs 1%; more solutions to their problems than controls. |
| Constantino & Bricker (1996) USA [ | Widows whose spouse died by suicide | Intervention | M = 43 | Majority is female | Not reported | Group | Bereavement Group Postvention (BGP), i.e. group psycho therapy | 1.5 h weekly sessions, 8 weeks | Depression (BDI) | Reduction in depression and distress in both BGP and SGP groups (both |
| Constantino et al. (2001) USA [ | Widows whose spouse died by suicide | Range 24–70 yrs. | Male/female 10/37, | 1–27 months | Group | Bereavement Group Postvention (BGP), i.e. group psycho therapy | 1.5 h weekly sessions, 8 sessions | Depression (BDI) | N.s. differences between BGP and SGP groups on outcome variables at four timepoints. | |
| De Groot et al. (2007) The Netherlands [ | First-degree relatives or spouses bereaved by suicide | Intervention | Intervention M = 43, | Intervention Male/female 28/40, 41%/59% | 3–6 months after suicide | Group / family | Family-based cognitive behaviour counselling programme | 2 h, 2- -3 weekly sessions, 4 sessions | Grief (ITG, TRGR2L) | N.s. effect of intervention on complicated grief, depression, and suicidal ideation. |
| De Groot et al. (2010) The Netherlands [ | First-degree relatives or spouses bereaved by suicide | Total | Intervention M = 43, | Intervention Male/female 28/40, 41%/59% | 3–6 months after suicide | Group / family | Family-based cognitive behaviour counselling programme | 2 h, 2–3 weekly sessions, 4 sessions | Grief (ITG, TRGR2L) | Participant with suicidal ideation compared with non-ideators: |
| Farberow (1992) USA [ | Loss by suicide | Intervention | Range 18–60+ | Intervention Male/female 18/42, 30%/70% | Less than 3 to 24+ months | Group | Bereavement group with therapeutic and educational aspects | 1.5 h weekly sessions, 8 sessions, followed by open monthly sessions | Health, impact of loss, coping, major changes, feelings (self-constructed questions) | Intervention group: decreased scores from T1 to T2 to T3. |
| Hazell & Lewin (1993) Australia [ | Students selected by school staff on basis of close friendship with deceased student | Intervention | School A: M = 15.1 | Not reported | Within 7 days after suicide | Group | Group counselling and information | 1.5 h session | Behaviour (YSR) | N.s. differences between intervention and control group on internalizing |
| Kovac & Range (2000) USA [ | Undergraduate students who had a close person die by suicide in the past 2 years and were upset by the death | Total | Range 18–46 | Male/female 9/33, 21%/79% | Intervention M = 13.26 months, | Individual | Writing task: profound, death-related writing vs trivial writing | 15 min sessions, 4 sessions over 2 weeks | Grief (GRQ, GEQ) | Reduction in impact of grief ( |
| Pfeffer et al. (2002) USA [ | Families where child’s parent or sibling died by suicide | Total | Intervention M = 9.6, | Male/female | Within a year after death | Group / family | Manual based bereavement group intervention for children grouped by age | 1.5 h weekly sessions | Children: Posttraumatic stress symptoms (CPTSRI) | Children: |
| Sandor et al. (1994) USA [ | Members of a church-related youth group | Intervention | Intervention Range 14–17, M = 15.73 | Intervention Male/female 5/15, 33%/67%r | A few days after the death | Group | Supportive community intervention; Survivor Group (SG) vs Comparison Group (CG; no intervention) | 3 meetings: 2 h open session with youth and parents, after two days one closed psycho-educational session with youth, a day later a memorial service in church | Problem solving (APSA) | Greater self-efficacy at T2 and T3 compared to T1 in SG vs. CG group ( |
| Wittouck et al. (2014) Belgium [ | Suicide of a significant other 3–24 months before participation | Intervention | Intervention M = 49.3, | Intervention male/female 9/38, 19%/81% | Intervention 9.8 months, | Group / family | Cognitive-behavioral therapy-based psycho-educational intervention | 2 h sessions, 4 sessions | Depression BDI-II) | N.s. decrease in depression, hopelessness and grief in intervention vs. control group. |
| Zisook et al. (2018) USA [ | People bereaved by suicide SB), accident, homicide (A/H), and natural causes (NC) with ≥30 ITG score | Total | Range 18–95 | Male/female | Time since death | Individual | Manual-based structured Complicated Grief Therapy (CGT) | CGT: 16 sessions over 20 weeks | Grief (CG-CGI-I, GRAQ, ICG, SCI-CG, TBAQ) | Lower improvement on clinician-rated CG-CGI-I in SB vs. A/H and NC groups ( |
APSA: Adolescent Problem Solving Appraisal [60]; BDI: Beck Depression Inventory [48]; BHS: Beck Hopelessness Scale [61]; BSI: Brief Symptom Inventory [50]; CDI: Children’s Depression Inventory [62]; CES-D: Center for Epidemiological Studies Depression Scale [49]; CG-CGI-I: Complicated Grief Clinical Global Impressions Scale – Improvement [63]; CPTSRI: Childhood Posttraumatic Stress Reaction Index [64]; C-SSRS-r: Columbia Suicide Severity Rating Scale – Revised [52]; GCQ: Grief Cognitions Questionnaire [46]; GEI: Grief Experience Inventory [47]; GEQ: Grief Experience Questionnaire [65]; GRAQ: Grief-Related Avoidance Questionnaire [66]; GRQ: Grief Recovery Questions [57]; IES: Impact of Event Scale [67]; ITG: Inventory of Traumatic Grief [68]; PSI: Paykel’s Suicidality Items [69]; RBQ: Risk Behavior Questionnaire [70]; RCMAS: Revised Children’s Manifest Anxiety Scale [71]; SAICA: Social Adjustment Inventory for Children and Adolescents [72]; SAS: Social Adjustment Scale [51]; SCAN 2.1: Schedules for Clinical Assessment in Neuropsychiatry [73]; SCI-CG: Structured Clinical Interview for Complicated Grief [74]; SES: Self Efficacy Scale [75]; SPP: Self-Perception Profile for Adolescents [76]; TBQ: Typical Beliefs Questionnaire [77]; TRGR2L: Traumatic Grief Evaluation of Response to Loss [45]; UCL: Utrecht Coping List [78]; WSAS: Work and Social Adjustment Scale [79]; YSR: Youth Self Report Child Behavior Checklist [80]
Quality assessment
| Quality Criteria | Battle (1984) | Constantino & Bricker (1996) | Constantino et al. (2001) | De Groot et al. (2007; 2010) | Farberow (1992) USA [ | Hazell & Lewin (1993) | Kovac & Range (2000) | Pfeffer et al. (2002) | Sandor et al. (1994) | Wittouck et al. (2014) | Zisook et al. (2018) |
|---|---|---|---|---|---|---|---|---|---|---|---|
| A. Selection bias | |||||||||||
| Representativeness | Not likely | Not likely | Not likely | Somewhat likely | Somewhat likely | Somewhat likely | Somewhat likely | Somewhat likely | Can’t tell | Not likely | Not likely |
| Percentage agreed | Can’t tell | 80–100% | Can’t tell | < 60% | Can’t tell | 60–79% | 60–79% | 60–79% | Can’t tell | 80–100% | Can’t tell |
| Rating | Weak | Weak | Weak | Weak | Moderate | Moderate | Moderate | Moderate | Weak | Weak | Weak |
| B. Study design | |||||||||||
| Study design type | Other: 3 groups comparison | RCT | RCT | RCT | Cohort analytic | Case-control | RCT | RCT | Cohort analytic | RCT | RCT |
| Described as randomized? | No | Yes | Yes | Yes | No | No | Yes | Yes | No | Yes | Yes |
| Method of randomization described? | N.a. | No | Yes | Yes | N.a. | N.a. | No | Yes | N.a. | Yes | Yes |
| Method appropriate? | N.a. | No | Yes | Yes | N.a. | N.a. | No | Yes | N.a. | Yes | Yes |
| Rating | Weak | Strong | Strong | Strong | Moderate | Moderate | Strong | Strong | Moderate | Strong | Strong |
| C. Confounders | |||||||||||
| Pre-intervention differences? | Can’t tell | No | No | Yes | Yes | Yes | Yes | Yes | No | Yes | Yes |
| Percentage confounders controlled for | Can’t tell | N.a. | N.a. | 80–100% (most) | Can’t tell | 80–100% | 60–79% (some) | 80–100% (most) | 80–100% | 80–100% | < 60% (few or none) |
| Rating | Weak | Strong | Strong | Strong | Weak | Strong | Moderate | Strong | Strong | Strong | Weak |
| D. Blinding | |||||||||||
| Outcome assessors were blinded? | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell | No | Can’t tell | Yes | Can’t tell | No | Yes |
| Participants were blinded? | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Yes | Can’t tell | Can’t tell | Can’t tell | Yes |
| Rating | Weak | Weak | Weak | Weak | Weak | Weak | Moderate | Moderate | Weak | Weak | Strong |
| E. Data collection methods | |||||||||||
| Valid measures? | Can’t tell | Yes | Yes | Yes | Can’t tell | Yes | Yes | Yes | Yes | Yes | Yes |
| Reliable measures? | Can’t tell | Yes | Yes | Yes | Can’t tell | Can’t tell | Yes | Yes | Yes | Yes | Yes |
| Rating | Weak | Strong | Strong | Strong | Weak | Moderate | Strong | Strong | Strong | Strong | Strong |
| F. Withdrawals and drop-outs | |||||||||||
| Numbers and reasons reported per group? | Yes | Can’t tell | No | Yes | Can’t tell | No | No | No | Yes | Yes | No |
| Percentage completing study? | N.a. | 80–100% | 60–79% | 80–100% | Can’t tell | 80–100% | 60–79% | < 60% | 80–100% | 80–100% | < 60% |
| Rating | N.a. | Strong | Moderate | Strong | Weak | Weak | Weak | Weak | Strong | Strong | Weak |
| Total A-F: | WEAK | WEAK | WEAK | WEAK | WEAK | WEAK | MODERATE | MODERATE | WEAK | WEAK | WEAK |
| Number of ‘strong’ ratings | 0/6 | 4/6 | 3/6 | 4/6 | 0/6 | 1/6 | 2/6 | 3/6 | 3/6 | 4/6 | 3/6 |
| G. Intervention integrity | |||||||||||
| Percentage participants received intervention? | Can’t tell | 80–100% | 60–79% | 80–100% | 80–100% | 80–100% | 60–79% | 80–100% | Can’t tell | 80–100% | 60–79% |
| Intervention consistency measured? | Can’t tell | Yes | Yes | Yes | Yes | No | Yes | Yes | Can’t tell | Can’t tell | Yes |
| Confounding unintended intervention? | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell | Can’t tell |
| H. Analyses | |||||||||||
| Unit of allocation | Individual | Individual | Individual | Individual (family) | Individual | Individual | Individual | Individual (family) | Individual | Individual | Individual |
| Unit of analysis | Individual | Individual | Individual | Individual | Individual | Individual | Individual | Individual | Individual | Individual | Individual |
| Appropriate statistical methods? | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
| Analysis by intention-to-treat status | No | Can’t tell | No | Yes | No | Can’t tell | Can’t tell | No | Can’t tell | No | Can’t tell |