Evidence map›Paper›PMID 25885650›Full record

Trial reportBMC psychiatry2015

Escitalopram in the prevention of posttraumatic stress disorder: a pilot randomized controlled trial.

Sharain Suliman, Soraya Seedat, Janine Pingo, Taryn Sutherland, Joseph Zohar, Dan J Stein

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC psychiatry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00300313 (PTSD Prevention Using Escitalopram), which is not on this map. Cited by 10 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 4 pooled it
7.2field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00300313 nacompletednot on this map

PTSD Prevention Using Escitalopram

TypeinterventionalSponsorSheba Medical CenterRan2005 to 2009Enrolled450ConditionsPost-traumatic Stress DisorderArmsEscitalopram, Placebo
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 4 syntheses or guidelines pooled it, 36 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Sharain SulimanMRC Anxiety Disorders Unit, Department of Psychiatry, Stellenbosch University, Cape Town, South Africa. sharain@sun.ac.za.
Soraya SeedatMRC Anxiety Disorders Unit, Department of Psychiatry, Stellenbosch University, Cape Town, South Africa. sseedat@sun.ac.za.
Janine PingoMRC Anxiety Disorders Unit, Department of Psychiatry, Stellenbosch University, Cape Town, South Africa. j.pingo@hotmail.com.
Taryn SutherlandMRC Anxiety Disorders Unit, Department of Psychiatry, Stellenbosch University, Cape Town, South Africa. tarynsuth@hotmail.com.
Joseph ZoharDepartment of Psychiatry, Tel-Aviv University, Tel-Aviv, Israel. joseph.zohar@sheba.health.gov.il.
Dan J SteinMRC Anxiety Disorders Unit and Department of Psychiatry and Mental Health, University of Cape Town, Cape Town, South Africa. dan.stein@uct.ac.za.
Stellenbosch University · ZATel Aviv University · ILUniversity of Cape Town · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA small literature suggests that pharmacotherapy may be useful in the prophylaxis of posttraumatic stress disorder in patients presenting with major trauma. There is relatively little data, however, on the use of selective serotonin reuptake inhibitors (SSRIs) in this context.

methods24 week, double-blind placebo controlled study. 31 participants presenting immediately after trauma, and meeting diagnostic criteria for full or partial acute stress disorder were randomized to treatment with 10-20 mg of escitalopram or placebo daily for 24 weeks. 2 participants were excluded from the analysis due to early drop out, leaving 29 participants (escitalopram = 12, placebo = 17) for inclusion in an intent- to- treat analysis. Participants were followed up until 56 weeks, and assessed with the Clinician Administered PTSD Scale (CAPS). A mixed model repeated measures analysis of variance (RMANOVA) was undertaken to determine the efficacy of the intervention on the CAPS score.

resultsThere was a significant reduction in CAPS score over the course of treatment (F(7, 142) = 41. 58, p < 0.001) in both the escitalopram and placebo groups, with a greater reduction in CAPS score in the placebo group F(7, 142) = 2.12, p = 0.045. There were improvements on all secondary measures, including the Clinical Global Impressions scale, and scales assessing depression, anxiety and disability. Only functional disability outcomes (F(7, 141) = 2.13, p = .04), were significantly different between treatment and placebo groups. In the sample as a whole, improvement in scores were maintained at the 52 week follow-up. Side effects were comparable between the groups.

conclusionsThese data are consistent with other recent work indicating that the SSRIs may not be efficacious in the prevention of PTSD. Nevertheless, the small sample size and baseline differences between groups limit the explanatory power of the study. Although a consideration of the possibility of medication prophylaxis in PTSD remains important, both from conceptual and clinical perspectives, caution is needed with regards to the use of SSRIs until their efficacy can be proven.

trial registrationClinical Trials NCT00300313.

Indexed as

Stress Disorders, Post-TraumaticStress, PsychologicalAdultAnalysis of VarianceAnxietyCitalopramDepressionDouble-Blind MethodDrug MonitoringFemaleHumansMalePilot ProjectsPsychiatric Status Rating ScalesSelective Serotonin Reuptake InhibitorsTreatment OutcomeCitalopramSelective Serotonin Reuptake Inhibitors

Identifiers

PMID25885650
PMCPMC4337322
OpenAlexW2131315861

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.