Background: Posttraumatic stress disorder (PTSD) is typically associated wi
th a high degree of chronicity, comorbidity, and psychosocial disability. T
he efficacy of sertraline in the acute treatment of PTSD has been confirmed
based on the results of 2 large, placebo-controlled studies, but almost no
prospective long-term treatment studies have been reported.
Method: One hundred twenty-eight patients who completed 12 weeks of double-
blind, placebo-controlled, acute-phase treatment for DSM-III-R-defined PTSD
with sertraline were continued into a 24-week open-label continuation phas
e. Efficacy was evaluated using the endpoint change in the 17-item Clinicia
n Administered PTSD Scale Part 2 (CAPS-2) severity score, the 15-item patie
nt-rated Impact of Event Scale, and the Clinical Global Impressions-Improve
ment and -Severity of Illness scales as primary outcome measures. Treatment
response was defined as greater than or equal to 30% decrease in the CAPS-
2 total severity score (compared with acute-phase baseline score) and a Cli
nical Global Impressions-Improvement score of 1 or 2,
Results: Ninety-two percent of acute-phase responders maintained their resp
onse during the full 6 months of continuation treatment. In addition, 54% o
f acute-phase nonresponders converted to responder status during continuati
on therapy. Over the 36-week course of acute and continuation therapy, 20%
to 25% of the improvement in the CAPS-2 severity score occurred during the
continuation phase. Sertraline was well tolerated, with 8.6% of patients di
scontinuing due to adverse events. A high pretreatment CAPS-2 score (> 75)
predicted a longer time to response and a greater likelihood that response
occurred after 12 weeks of acute treatment.
Conclusion: The acute efficacy of sertraline is sustained in the vast major
ity of patients, and at least half of nonresponders to acute treatment will
eventually respond to continued treatment.