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. 2017 Nov 15;1(4):bjgpopen17X101265.
doi: 10.3399/bjgpopen17X101265. eCollection 2018 Jan.

Withdrawal of unnecessary antidepressant medication: a randomised controlled trial in primary care

Affiliations

Withdrawal of unnecessary antidepressant medication: a randomised controlled trial in primary care

Rhona Eveleigh et al. BJGP Open. .

Abstract

Background: Antidepressant use has increased exponentially in recent decades, mostly due to long continuation.

Aim: To assess the effectiveness of a tailored recommendation to withdraw antidepressant treatment.

Design & setting: Randomised controlled trial in primary care (PANDA study) in the Netherlands.

Method: Long-term antidepressant users (≥9 months) were selected from GPs prescription databases. Patients were diagnosed with the Composite International Diagnostic Interview (CIDI). Long-term users without indication for maintenance treatment (overtreatment) were selected. The intervention consisted of disclosure of the current psychiatric diagnosis combined with a tailored treatment recommendation. Patients were followed for 12 months.

Results: The study included 146 participants from 45 family practices. Of the 70 patients in the intervention group, 34 (49%) did not comply with the advice to stop their antidepressant medication. Of the 36 (51%) patients who agreed to try, only 4 (6%) succeeded. These figures were consistent with the control group, where 6 (8%) of the 76 patients discontinued antidepressant use successfully. Patients who were recommended to discontinue their antidepressant medication reported a higher relapse rate than the control group (26% versus 13%, P = 0.05).

Conclusion: Changing inappropriate long-term antidepressant use is difficult.

Keywords: antidepressant agents; anxiety disorder; depressive disorder; general practice; inappropriate prescribing; primary care.

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Conflict of interest statement

The authors declare that no competing interests exist.

Figures

Figure 1.
Figure 1.. Flow diagram of practices and participants.aPost-randomisation patients did not meet inclusion criteria (human error during inclusion process). bPatients who did not complete follow-up interview. cPatients excluded with unknown primary outcome (due to dual primary outcome, excluded cases are less than patients lost to follow-up; that is, antidepressant use known via GP prescription database). dIntervention group restricted to patients with the intention to comply to recommendation and patients excluded with unknown primary outcome.
Figure 2.
Figure 2.. Patient flow and outcome in the overtreatment trial. In the intervention group 20/70 patients were lost to follow-up (12 in the group of patients with no intention to comply and 8 in the group with the intention to comply with the recommendation). In the control group 10/76 patients were lost to follow-up. AD = antidepressant.

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