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Table of Contents
Vol. 82, No. 6, 2013
Issue release date: October 2013
Section title: Regular Article
Psychother Psychosom 2013;82:363-371
(DOI:10.1159/000351410)

Remission of Generalized Anxiety Disorder after 6 Months of Open-Label Treatment with Venlafaxine XR

Rickels K.a · Etemad B.a · Rynn M.A.c · Lohoff F.W.a · Mandos L.A.b · Gallop R.a
aMood and Anxiety Disorders Section, Department of Psychiatry, University of Pennsylvania School of Medicine, and bUniversity of the Sciences, Philadelphia, Pa., and cDepartment of Psychiatry, Columbia University, New York, N.Y., USA

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Article / Publication Details

First-Page Preview
Abstract of Regular Article

Received: October 13, 2012
Accepted: April 16, 2013
Published online: September 20, 2013
Issue release date: October 2013

Number of Print Pages: 9
Number of Figures: 3
Number of Tables: 5

ISSN: 0033-3190 (Print)
eISSN: 1423-0348 (Online)

For additional information: http://www.karger.com/PPS

Abstract

Background: Remission has become one of the leading outcome criteria in clinical trials. Data collected by this research group assessed the rate of remission after 6 months of treatment of generalized anxiety disorder (GAD) with venlafaxine XR, to search for predictors of remission and to define how early on in treatment later remission can be predicted. Method: Two hundred sixty-eight patients with a GAD diagnosis enrolled into an open-label 6-month-treatment trial with venlafaxine XR (75-225 mg/day). Remission was defined by a Hamilton anxiety scale total score ≤7. Logistic regression approaches were used to find out how early on in treatment later remission could be predicted, as well as to determine predictors of remission. In addition, adverse events were also followed over time. Results: While the total enrolled patient sample (n = 268) had a remission rate of 53%, 6-month completers (n = 159) had a remission rate of 79%. The only statistically significant predictor of remission, independent of baseline anxiety and depression levels, was a low Eysenck neuroticism score. The remission status outcome could best be predicted after 8 weeks of treatment when a CGI-I score of 1 or 2 predicted later remission with 78% accuracy and later nonremission with 91% accuracy. The incidence of adverse events decreased over the 6-month period, with sexual adverse events decreasing the least. Conclusion: The only significant predictor of remission was a low score on the Eysenck neuroticism scale. The earliest reliable prediction of later remission, based on improvement, could be made after 8 weeks of treatment with 91% accuracy.

© 2013 S. Karger AG, Basel


Article / Publication Details

First-Page Preview
Abstract of Regular Article

Received: October 13, 2012
Accepted: April 16, 2013
Published online: September 20, 2013
Issue release date: October 2013

Number of Print Pages: 9
Number of Figures: 3
Number of Tables: 5

ISSN: 0033-3190 (Print)
eISSN: 1423-0348 (Online)

For additional information: http://www.karger.com/PPS


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Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
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