APA's Practice Guideline
for the Treatment of Patients with Acute Stress Disorder and Posttraumatic
Stress Disorder was published in October 2004.
Since that time, a number of well-designed randomized controlled
trials of pharmacological and psychotherapeutic interventions for
posttraumatic stress disorder (PTSD) have been conducted in various
populations exposed to trauma. Numerous case reports, small case
series, and open trials have also been reported, but they will not
be the focus of this guideline watch. While early intervention studies
for acute stress disorder (ASD) are currently in progress, no major
research on the treatment of ASD has been completed since publication
of the 2004 guideline.
Factors predicting development of ASD or PTSD have still not
been established. A 2008 study by Bryant et al. (1) found that ASD
was a poorer predictor of getting PTSD than just having PTSD criteria
alone in the acute stage.
In response to increased attention on U.S. military veterans
returning from combat in Iraq and Afghanistan, the Institute of
Medicine has also reviewed and summarized the evidence supporting
treatment for PTSD (2). The 2007 report recognizes that there is
evidence for the pharmacological treatment of combat-related PTSD
but states that this evidence is not as strong as the evidence for
treatment of other trauma-related PTSD. In particular, the report
states that large randomized controlled trials, considered a standard
of evidence in other areas of medicine, are lacking from the evidence
base. The report concludes that existing evidence is sufficient
only to establish the efficacy of exposure-based psychotherapies
in the treatment of PTSD. However, there was disagreement among
the report authors about this conclusion, and the report includes
a dissenting opinion by one author about the strength of the evidence
for pharmacotherapy.
Our review concludes that the best evidence from recent studies
bolsters support for exposure-based psychotherapies as well as for
pharmacological intervention in many circumstances. Emerging evidence
suggests the potential for psychotherapy to be facilitated by at
least one recently identified pharmacological agent (d-cycloserine).
Recently published studies also suggest that in certain patient
populations new pharmacotherapeutic options, such as prazosin, may
be more effective than other widely prescribed medications (e.g.,
selective serotonin reuptake inhibitors [SSRIs])
indicated for PTSD.
As described in the 2004 guideline, the generalizability of findings
from available studies on treatments for PTSD is limited by small
numbers of subjects, variable inclusion criteria (e.g., patients
with treatment-resistant illness, patients receiving multiple treatments),
nonstandardized outcome measures, inadequate controls, and lack
of replication. These issues also limit meaningful comparison of
data for psychopharmacological versus psychotherapeutic approaches.
Specific recommendations to improve psychotherapy research for PTSD
have been put forward by Schottenbauer et al. (3).