Drossman DA, Toner BB, Whitehead WE, et al.
Gastroenterology. 2003;125(1):19-31
Despite the fact that the use of antidepressants and
other psychologic strategies may seem intuitive in the setting of
moderate to severe functional bowel disease, conclusive data from
well-designed trials have been lacking.
In this setting, Drossman and colleagues have
conducted the largest randomized trial to evaluate the effectiveness of
desipramine, a tricyclic antidepressant, as well as cognitive-behavioral
therapy vs their control conditions (placebo and education,
respectively) in women with moderate to severe functional bowel
disorders. Additionally, these investigators assessed the clinical
benefits of the active treatment regimens (desipramine or
cognitive-behavioral therapy) in clinically meaningful patient subgroups
(ie, with/without history of depression; with/without history of sexual
or physical abuse; predominant diarrhea; predominant constipation;
moderate vs severe disease).
This randomized, comparator-controlled, multicenter
trial involved 431 adult women from the University of North Carolina and
the University of Toronto who had moderate to severe symptoms of
functional bowel disorders. Subjects received either psychologic
(cognitive-behavioral therapy vs education) or antidepressant (desipramine
vs placebo) therapy for a period of 12 weeks. Assessment of physiologic,
clinical, and psychosocial parameters were conducted before and after
end of therapy.
Overall, results suggest that the active psychologic
treatment (ie, cognitive-behavioral therapy) was effective for women
with functional bowel disorders, including irritable bowel syndrome,
whereas the active antidepressant treatment (desipramine) appeared to
only be effective in the management of those patients who were adherent
(ie, able to stay on their medication). Specifically, by
intention-to-treat analysis, cognitive-behavioral therapy was found to
be significantly more effective than its placebo condition (education;
P = .0001; responder rate, 70% vs 37%, respectively; number
needed to treat [NNT], 3.1). By contrast, desipramine did not
demonstrate significant efficacy vs placebo in the intention-to-treat
analysis (P = .016; responder rate, 60% vs 47%, respectively; NNT,
8.1) but did show a statistically significant benefit in the
per-protocol analysis (P = .01; responder rate, 73% vs 49%,
respectively; NNT, 5.2). The latter was especially significant when
subjects with nondetectable blood levels of desipramine were excluded.
Results of subgroup analyses demonstrated that
cognitive-behavioral therapy had benefit over its control condition for
all subgroups except those patients with depression. By contrast,
subgroup analyses indicated that active antidepressant therapy (desipramine)
was more beneficial than placebo for women with moderate vs severe
symptoms, a history of abuse, without comorbid depression, and with
predominant diarrhea.
The investigators highlighted several limitations
associated with this study that should be considered. First, at least
moderate side effects were observed in up to 25% of subjects taking
desipramine, and thus some participants may have become unblinded.
However, it should be noted that similar side effects occurred in up to
15% of participants receiving placebo as well. Additionally, dropouts
occurred in 23% of patients allocated to treatment; therefore, data that
anticipated treatment responses were "imputed" for several of these
individuals. Finally, the fact that all patients fulfilling Rome I or II
criteria for functional bowel disorders were included also warrants some
consideration. Overall, however, as the study authors emphasize, these
findings may be generalized to any patient who fulfills the selection
criteria used in this trial, who is treated by their standardized
psychologic protocol, or who is compliant in taking desipramine as
prescribed.
Thus for women with moderate to severe functional
bowel disorders, cognitive-behavioral therapy is effective and
desipramine may be effective when taken adequately. It is important to
note, however, that certain clinical subgroups are more or less amenable
to these relative treatments.
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