Background. Dysthymia is a common mental disorder, associated with consider
able disability and high co-morbidity. This review assessed the role of pha
rmacological treatment.
Methods. All randomized-controlled trials that compared active drug versus
placebo for dysthymic patients were included. Pooled relative risks (RR) an
d 95% confidence intervals (CI) were calculated with the Random Effect Mode
l method. Where possible, number needed to treat and number needed to harm
were estimated.
Results. Fifteen trials were included for the main comparisons. Similar res
ults were obtained in terms of efficacy for different groups of drugs, such
as tricyclic (TCA), selective serotonin reuptake inhibitors (SSRI), monoam
ine oxidase inhibitors (MAOI) and other drugs (sulpiride, amineptine, and r
itanserin). The pooled RR treatment response was 0.68 (95 % CI 0.59-0.78) f
or TCA, 0.64 (95% CI 0.55-0.74) for SSRIs, 0.59 (95% CI 0.48-0.71) for MAOI
s. Other drugs (amisulpride, amineptine and ritanserin) showed similar resu
lts. Patients treated on TCA were more likely to report adverse events, com
pared with placebo. There were no differences in response to active treatme
nt when dysthymia was compared to either dysthymia plus major depression or
briefer nonmajor depressive states.
Conclusions. Drug treatment appears to be effective in the short-term manag
ement of dysthymic disorder. The choice of drug should take into account sp
ecific side-effects profile of each drug.