2012
DOI: 10.1001/archgenpsychiatry.2011.127
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Prevention of Posttraumatic Stress Disorder by Early Treatment

Abstract: Prolonged exposure, CT, and delayed PE effectively prevent chronic PTSD in recent survivors. The lack of improvement from treatment with escitalopram requires further evaluation. Trauma-focused clinical interventions have no added benefit to survivors with subthreshold PTSD symptoms. Trial Registration clinicaltrials.gov Identifier: NCT00146900.

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Cited by 238 publications
(105 citation statements)
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“…Two longitudinal studies included early interventions. The Jerusalem Trauma Outreach and Prevention Study (JTOPS) had 296 out of 1996 participants randomly assigned to treatment groups that included cognitive behavioural therapy, escitalopram, and placebo (Shalev et al, 2012). The Amsterdam oxytocin study (van Zuiden et al, 2017) evaluated the preventive effect of oxytocin, and data included in the ICPP consisted of that study’s placebo group.…”
Section: Methodsmentioning
confidence: 99%
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“…Two longitudinal studies included early interventions. The Jerusalem Trauma Outreach and Prevention Study (JTOPS) had 296 out of 1996 participants randomly assigned to treatment groups that included cognitive behavioural therapy, escitalopram, and placebo (Shalev et al, 2012). The Amsterdam oxytocin study (van Zuiden et al, 2017) evaluated the preventive effect of oxytocin, and data included in the ICPP consisted of that study’s placebo group.…”
Section: Methodsmentioning
confidence: 99%
“…Emergency departments in the USA, for example, evaluate over 30 million individuals with traumatic injuries every year (Bergen and National Center for Health Statistics (U.S.), 2008; Bonnie, Fulco, and Liverman, 1999; Cougle, Kiplatrick, and Resnick, 2012; Kilpatrick et al, 2013; McCaig, 1994; National Center for Injury Prevention, 2012; Rice, MacKenzie, Jones, and Associates, 1989); the prevalence of PTSD following acute care admissions is similar to that seen in survivors who are not brought to medical attention (Ameratunga, Tin, Coverdale, Connor, & Norton, 2009; Golding, 1999; Lipsky, Field, Caetano, & Larkin, 2005). PTSD longitudinal trajectories stabilize at 9–12 months after trauma exposure (Kessler, Sonnega, Bromet, Hughes, & Nelson, 1995), with symptoms at 9 and 12 months equally predicting symptoms at 2 and 6 years (Bryant, O’Donnell, Creamer, McFarlane, & Silove, 2013; Shalev et al, 2012; Shalev, Ankri, Peleg, Israeli-Shalev, & Freedman, 2011). Studying PTSD in acute care settings provides an opportunity to follow exposed individuals early on after traumatic events and therefore offers valuable longitudinal information difficult to obtain elsewhere.…”
Section: Introductionmentioning
confidence: 99%
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“…Experience from a previous large early intervention study (Shalev et al, 2012, 2011) informed many of our choices in this work. To facilitate the enrolment of participants at substantial risk of PTSD, we opted to employ skilled clinicians, thoroughly trained in the specific evaluation procedures.…”
Section: Methodsmentioning
confidence: 99%
“…Pharmacological interventions that target the acquisition and extinction of fear responses have generally failed to prevent PTSD (Cohen et al, 2011; Hoge et al, 2012; Pitman et al, 2002; Stein, Kerridge, Dimsdale, & Hoyt, 2007). Early cognitive behavioural interventions, although often effective (Roberts, Kitchiner, Kenardy, & Bisson, 2010), do not reach many symptomatic survivors (Hoge et al, 2004; Shalev et al, 2012, 2011), are costly, and are difficult to carry out in trauma-affected areas such as war and disaster zones. Devising novel interventions to prevent PTSD is a major public health need (Berg et al, 2008).…”
Section: Introductionmentioning
confidence: 99%