Efficacy of fluvoxamine in the treatment of
major depression with comorbid
anxiety disorders
by
Sonawalla SB, Spillmann MK, Kolsky AR,
Alpert JE, Nierenberg AA, Rosenbaum
JF, Fava M
Depression Clinical and Research Program,
Massachusetts General Hospital and
Harvard Medical School,
Boston 02114, USA.
J Clin Psychiatry 1999 Sep; 60(9):580-3
ABSTRACT
BACKGROUND: Major depression with comorbid anxiety disorder is associated
with poor antidepressant outcome compared with major depression without comorbid
anxiety disorder. The purpose of our study was to assess changes in depressive
symptoms and anxiety levels in outpatients with major depression with comorbid
anxiety disorder following 12 weeks of open treatment with fluvoxamine. METHOD:
We enrolled 30 outpatients (mean +/- SD age = 39.4 +/- 11.3 years; 16 women and
14 men) with DSM-IV major depressive disorder accompanied by one or more current
comorbid DSM-IV anxiety disorders in our study. Patients were treated openly
with fluvoxamine initiated at 50 mg/day, with an upward titration to a maximum
of 200 mg/day (mean +/- SD dose = 143 +/- 45 mg/day). Efficacy assessments
included the 17-item Hamilton Rating Scale for Depression (HAM-D-17) and
Clinical Global Impressions-Severity of Illness (CGI-S) and Improvement (CGI-I)
scales for both depression and anxiety. Intent-to-treat analysis was used to
assess outcome. RESULTS: The mean +/- SD number of comorbid anxiety disorders
per patient was 2.1 +/- 1.1. Following fluvoxamine treatment, the mean +/- SD
HAM-D-17 score dropped from 20.2 +/- 3.3 to 1 1.0 +/- 7.0 (p < .0001). The
mean +/- SD depression CGI-S score dropped from 4.0 +/- 0.6 to 2.4 +/- 1.1 (p
< .0001), and the mean +/- SD anxiety CGI-S score decreased from 4.1 +/- 0.8
to 2.5 +/- 1.2 (p < .0001). Eighteen (60%) of the 30 patients had CGI-I
scores < or = 2 for both anxiety and depression at endpoint, with 53% showing
a > or = 50% reduction in HAM-D-17 scores at endpoint. CONCLUSION: Although
preliminary, our findings suggest that fluvoxamine is effective in treating
outpatients with major depression with comorbid anxiety disorder, having a
significant effect on both depression and anxiety symptoms. Further
double-blind, placebo-controlled trials are needed, in a larger sample, to
confirm our findings.
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