Background: Numerous studies have demonstrated the effectiveness of antidep
ressant medications in the treatment of dysthymia, or chronic mild depressi
on. Venlafaxine blocks reuptake of both serotonin and norepinephrine and ma
y produce a more complete antidepressant response than do single-mechanism
selective serotonin reuptake inhibitors. The purpose of this open label stu
dy was to provide preliminary data on the tolerability and effectiveness of
venlafaxine for patients with dysthymia.
Method: Twenty-two dysthymic subjects (DSM-III-R criteria) were enrolled in
this 10-week, open-label trial, and 5 dropped out prior to their second vi
sit. Seventeen subjects (77.3%) received more than 1 week of medication.
Results: Of these 17 subjects, 13 (76.5%) were treatment responders. Result
s of paired sample t tests were highly significant, indicating that, on ave
rage, there was significant improvement on all measures of symptomatology a
nd functioning, with mean +/- SD scores on the Hamilton Rating Scale for De
pression decreasing from 20.95 +/- 6.50 at baseline to 6.06 +/- 5.49 at wee
k 10. The mean +/- SD final dose was 178.68 +/- 70.80 mg/day. Side effects
were reported by 17 (85%) of the 20 subjects for whom tolerability was asse
ssed (the most common were fatigue, dry mouth, and nausea); 5 (22.7%) of 22
patients discontinued treatment because of side effects, primarily nausea
(N = 3).
Conclusion: These findings suggest the benefit of venlafaxine in the treatm
ent of chronic depression and the need for more rigorous studies.