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Author's reply

Published online by Cambridge University Press:  02 January 2018

T.T. Haug*
Affiliation:
University of Bergen, Department of Psychiatry, Section Haukeland University Hospital, N-5021 Bergen, Norway
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Abstract

Type
Columns
Copyright
Copyright © Royal College of Psychiatrists, 2004 

The primary efficacy measures from our paper about treatment effect at week 24 (Blomhoff et al, 2001) are reported in the method section of the paper about the follow-up study (Haug et al, 2003). In the pairwise comparisons, combined sertraline and exposure and sertraline alone were significantly superior to placebo, while a non-significant trend towards increased efficacy of exposure alone compared with placebo was reported.

The four study groups had a significant reduction in scores on all social phobia scales from baseline to follow-up. Furthermore, there was no significant difference in scores on primary efficacy measures between the active treatment groups in any of the time-point analyses between week 0 and week 24. In the follow-up analyses we were therefore mainly interested in the changes after cessation of treatment. For the exposure group and the placebo group there was a further improvement in scores on social phobia from week 24 to week 52 and the changes on several of the sub-scales were highly significant. On SF–36, which demonstrates changes in a more global functioning, there was a significant improvement for the exposure alone and the placebo groups, while there was a significant deterioration in both the sertraline-treated groups. Changes in scores on other social phobia scales for the sertraline-treated groups were non-significant, but there was a tendency towards deterioration (Tables 1 and 2, pp. 314–315). We agree that the changes in sertraline-treated groups during the follow-up period were marginal. However, contrasting these minimal changes with the significant improvement in the exposure-treated group, we find it appropriate to conclude that exposure therapy given alone seems to be more beneficial in the long term. Longer follow-up could have added valuable information to this issue. In all groups about 20% of the patients were treated with sertraline during the follow-up period so this could not explain the differences in scores between the groups at week 52.

References

Declaration of interest

Funding was provided by Pfizer, Inc.

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