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American Journal of Epidemiology Advance Access published online on June 4, 2009

American Journal of Epidemiology, doi:10.1093/aje/kwp142
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American Journal of Epidemiology © The Author 2009. Published by the Johns Hopkins Bloomberg School of Public Health. All rights reserved. For permissions, please e-mail: journals.permissions@oxfordjournals.org.

Original Contribution

Duration of Antidepressant Drug Treatment and Its Influence on Risk of Relapse/Recurrence: Immortal and Neglected Time Bias

Helga Gardarsdottir, Toine C. Egberts, Joost J. Stolker and Eibert R. Heerdink

Correspondence to Dr. Eibert R. Heerdink, Division of Pharmacoepidemiology and Pharmacotherapy, Faculty of Science, Utrecht University, PO Box 80 082, 3508 TB Utrecht, The Netherlands (e-mail: e.r.heerdink{at}uu.nl).

Received for publication October 5, 2008. Accepted for publication January 26, 2009.

Several observational studies have found a higher risk of recurrence/relapse of depression for patients who discontinue antidepressant use compared with those who continue. This study demonstrated that measurement of follow-up time can be subject to immortal and neglected time bias. Data were obtained from the 2001 Second Dutch National Survey of General Practice. The study population was composed of antidepressant users with a registered depression diagnosis, divided into early discontinuers and continuing users. Two methods were used to measure time to relapse/recurrence. Method 1, used in previously mentioned studies, measured the beginning of follow-up 6 months after starting antidepressant therapy. Method 2 constructed individual treatment episodes for each patient and measured follow-up from actual end-of-treatment episode. The Cox proportional hazards model produced a risk ratio of 1.58 (95% confidence interval: 1.02, 2.45) for method 1, suggesting a higher risk of relapse/recurrence for early discontinuers. In method 2, a statistically nonsignificant risk ratio of 0.77 (95% confidence interval: 0.49, 1.21) was produced, indicating no difference in risk of relapse/recurrence. The authors found the method used in previous studies subject to bias. Applying a different method, accounting for immortal and neglected time bias, eliminated the protective effects of longer treatments.

antidepressant agents; bias (epidemiology); depressive disorder; pharmacoepidemiology; recurrence

Abbreviations: DNSGP-2, Second Dutch National Survey of General Practice


Editor's note: An invited commentary on this article appears on page 000, and the authors’ response is published on page 000.


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