| Literature DB >> 31762949 |
Veerle Oosterbaan1, Milou L V Covers1, Iva A E Bicanic1, Rafaële J C Huntjens2, Ad de Jongh3,4,5,6.
Abstract
Objective: To review the safety and efficacy of early interventions after sexual assault in reducing or preventing posttraumatic stress disorder (PTSD). Method: Systematic searches were performed on studies (1980-2018) that examined the efficacy of interventions for PTSD within 3 months after sexual assault.Entities:
Keywords: Sexual assault; early intervention; meta-analysis; posttraumatic stress disorder; prevention; safety; • Seven studies have investigated early interventions post-rape.• The studies have a highly diverse design and a high risk of bias.• There is little data on safety and the prevention of posttraumatic stress disorder.• Early intervention can potentially reduce the severity of posttraumatic stress disorder.
Year: 2019 PMID: 31762949 PMCID: PMC6853210 DOI: 10.1080/20008198.2019.1682932
Source DB: PubMed Journal: Eur J Psychotraumatol ISSN: 2000-8066
Figure 1.Flow diagram of the study selection process. PTSD = Posttraumatic stress disorder. Adapted from ‘preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement’ (Moher, Liberati, Tetzlaff, Altman, & the PRISMA group, 2009).
Characteristics of included studies.
| Citation | Country | Setting | N in analysis | Participant characteristics | Main inclusion criteria | Main exclusion criteria | Interventions | Sessions |
|---|---|---|---|---|---|---|---|---|
| Echeburúaet al. ( | Spain | Seeking treatment at psychological counselling centres | 20 | Females | Sexual aggression < 3 months | Severe mental illness | Cognitive restructuring, coping skills training and progressive muscular relaxation training vs. progressive muscular relaxation training | 5 weekly |
| Resnicket al. ( | USA | Seeking forensic examination at an academic medical centre | 140 | Females | Sexual assault < 72 hours | Severe mental illness | Pre-examination video intervention vs. standard care | Single |
| Rothbaumet al. ( | USA | Public hospital emergency department | 47 | 65% females | Trauma < 72 hours | Intoxication | Modified prolonged exposure session vs. standard care | 3 weekly |
| Tarquinio et al. ( | France | Via research centre, family doctor or regional victim aid associations | 17a | Females | Sexual trauma 24–72 hours ago | Severe mental illness | Newly integrated EMDR protocol | Single |
| Tarquinio et al. ( | France | Referral via psychologists of regional victim aid associations | 6a | Females | Sexual assault 8–12 weeks ago | Severe mental illness | Standard EMDR treatment protocol according to Shapiro ( | 3–4 weekly |
| Milleret al. ( | USA | Via specialized nurse examiners at local hospital | 69–74b | Females | Sexual assault < 72 hours | Severe mental illness | Postexamination video intervention + standard care vs. standard care | Single |
| Nixonet al. ( | Australia | Seeking treatment at a rape and sexual assault crisis centre | 46c | Females | Rape or sexual assault < 1 month | Severe mental illness | Cognitive processing therapy vs. standard care | 6 weekly |
SD = standard deviation, NR = not reported, vs. = versus, DSM-III-R = Diagnostic and Statistical Manual of Mental Disorders third edition revised, ASD = acute stress disorder. a Initial sample size and drop-out rates not reported. b Depending on follow up. c Using multiple imputation by chained equations.
Figure 2.Risk of bias summary of included studies. The minus sign represents a high risk of bias, the plus sign a low risk of bias, and the question mark an unclear risk of bias. Produced using Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014.
Effects of interventions of included studies.
| Citation | Follow-up | Outcome measure | Within-group analysis in intervention group | Between-group analysis |
|---|---|---|---|---|
| Echeburúa et al. ( | Posttreatment | PSS-I | Significant decrease in PTSD scores in both cognitive restructuring and progressive muscular relaxation groups. | Significantly lower PTSD scores in the cognitive restructuring group than in the progressive muscular relaxation group. |
| Resnick et al. ( | 6 wks | PSS-SR | No significant difference in PTSD scores between the video intervention and standard care. | |
| Rothbaum et al. ( | 4, 12 wks | PSS-I | Significantly lower PTSD scores in the modified prolonged exposure session compared to assessment only. | |
| Tarquinio et al. ( | Pretreatment Posttreatment | IES | Significant decrease in PTSD scores in EMDR participants. | |
| Tarquinio et al. ( | Pretreatment | IES | Significant decrease in PTSD scores in EMDR participants. | |
| Miller et al. ( | Pretreatment | PSS-SR | Significant increase in PTSD scores at 2-wks follow-up, but not at 2-mth follow-up.a | No significant difference in PTSD scores between the video intervention and standard care. |
| Nixon et al. ( | Pretreatment | CAPS | Significant decrease in PTSD scores in the cognitive processing. | Between-group differences remained stable across treatment, indicating that there was no difference between cognitive processing therapy and standard care. |
mth = month(s), PSS-I = PTSD Symptom Scale Interview, PTSD = Posttraumatic Stress Disorder, wks = weeks, PSS-SR = PTSD Symptom Scale Self-Report, NR = not reported, IES = Impact of Events Scale, EMDR = Eye Movement Desensitization and Reprocessing, wk = week, CAPS = Clinician-Administered PTSD Scale. aWithin-group analysis calculated from reported means and standard deviations at pretreatment and follow-up assessments.
Figure 3.Forest plot of comparison: intervention versus standard care. Outcome: severity of PTSD symptoms at first follow-up. The first follow-up post-intervention was: for Resnick et al. (2007) six weeks, for Rothbaum et al. (2012) 4 weeks, for Miller et al. (2015) 2 weeks and for Nixon et al. (2016) 1 week. Produced using Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014.
Figure 4.Forest plot of comparison: intervention versus standard care. Outcome: severity of PTSD symptoms at latest follow-up. The latest follow-up was: for Resnick et al. (2007) 6-months post-intervention, for Rothbaum et al. (2012) 12 weeks, for Miller et al. (2015) 2 months and for Nixon et al. (2016) 1 year. Produced using Review Manager (RevMan) [Computer program]. Version 5.3. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2014.
Risk of bias of Echeburúa et al. (1996).
| Bias item | Authors’ judgement | Support for judgement |
|---|---|---|
| Random sequence generation | High risk | ‘in order of arrival’ (p.189) |
| Allocation concealment | High risk | Since allocation was based on order of arrival, there cannot have been allocation concealment. |
| Blinding of participants | High risk | No blinding. |
| Blinding of outcome assessment | High risk | The same therapist carried out therapy and assessment. |
| Incomplete outcome data | Low risk | No drop-outs or treatment changes. |
| Selective reporting | Low risk | All data seem to be reported. |
Risk of bias of Resnick et al. (2007).
| Bias item | Authors’ judgement | Support for judgement |
|---|---|---|
| Random sequence generation | High risk | Participants presenting on nonprime dates were assigned to the video condition, those on prime dates to the control group. |
| Allocation concealment | High risk | ‘Project assistants were aware of the designated study condition prior to recruiting participants.’ (p.2435) |
| Blinding of participants | High risk | No blinding. |
| Blinding of outcome assessment | Low risk | |
| Incomplete outcome data | High risk | As treated analysis, while 15 participants chose not to watch the video and 5 participants watched less than half after randomization. |
| Selective reporting | Low risk | All data seem to be reported. |
Risk of bias of Rothbaum et al. (2012).
| Bias item | Authors’ judgement | Support for judgement |
|---|---|---|
| Random sequence generation | Low risk | Computer-generated patient random assignments. |
| Allocation concealment | Low risk | |
| Blinding of participants | High risk | No blinding. |
| Blinding of outcome assessment | Low risk | ‘Blinded assessors administered’ (p.958) |
| Incomplete outcome data | Low risk | ‘Missing values for week 4 and week 12 were handled with multiple imputation’ (p.959) |
| Selective reporting | Low risk | All data seem to be reported. |
Risk of bias of Tarquinio et al. (2012a).
| Bias item | Authors’ judgement | Support for judgement |
|---|---|---|
| Random sequence generation | N/A | |
| Allocation concealment | N/A | |
| Blinding of participants | N/A | |
| Blinding of outcome assessment | N/A | |
| Incomplete outcome data | Uncertain risk | No data on participant selection and/or drop-outs. |
| Selective reporting | Low risk | All data seem to be reported. |
Risk of bias of Tarquinio et al. (2012b).
| Bias item | Authors’ judgement | Support for judgement |
|---|---|---|
| Random sequence generation | N/A | |
| Allocation concealment | N/A | |
| Blinding of participants | N/A | |
| Blinding of outcome assessment | N/A | |
| Incomplete outcome data | Uncertain risk | No data on participant selection and/or drop-outs. |
| Selective reporting | Low risk | All data seem to be reported. |
Risk of bias of Miller et al. (2015).
| Bias item | Authors’ judgement | Support for judgement |
|---|---|---|
| Random sequence generation | Uncertain risk | Randomization procedure not explained. |
| Allocation concealment | Uncertain risk | Allocation concealment not reported. |
| Blinding of participants | High risk | No blinding. |
| Blinding of outcome assessment | Low risk | ‘trained research assistants, blind to the study condition’ (p.132) |
| Incomplete outcome data | High risk | As treated analysis with 50–64% drop-out rates. |
| Selective reporting | High risk | Results are only reported according to previous assault status. |
Risk of bias of Nixon et al. (2016).
| Bias item | Authors’ judgement | Support for judgement |
|---|---|---|
| Random sequence generation | High risk | |
| Allocation concealment | High risk | Since allocation was sequential there cannot have been allocation concealment. |
| Blinding of participants | High risk | No blinding |
| Blinding of outcome assessment | Low risk | ‘Assessor … were unaware … of treatment condition’ (p.238) |
| Incomplete outcome data | Low risk | Many missing data, but imputed using appropriate methods. |
| Selective reporting | Low risk | All data seem to be reported. |