Literature DB >> 10827885

Interruption of selective serotonin reuptake inhibitor treatment. Double-blind, placebo-controlled trial.

D Michelson1, M Fava, J Amsterdam, J Apter, P Londborg, R Tamura, R G Tepner.   

Abstract

BACKGROUND: Abrupt interruption of therapy with selective serotonin reuptake inhibitors (SSRIs) has been associated with somatic and psychological symptoms. AIMS: Systematically to assess symptoms and effects on daily functioning related to interruption of SSRI therapy.
METHOD: Patients treated with fluoxetine, setraline or paroxetine underwent identical five-day periods of treatment interruption and continued active treatment under double-blind, order-randomised conditions, with regular assessment of new symptoms.
RESULTS: Placebo substitution for paroxetine was associated with increases in the number and severity of adverse events following the second missed dose, and increases in functional impairment at five days. Placebo substitution for sertraline resulted in less pronounced changes, while interruption of fluoxetine was not associated with any significant increase in symptomatology.
CONCLUSIONS: Abrupt interruption of SSRI treatment can result in a syndrome characterised by specific physical and psychological symptoms. Incidence, timing and severity of symptoms vary among SSRIs in a fashion that appears to be related to plasma elimination characteristics.

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Year:  2000        PMID: 10827885     DOI: 10.1192/bjp.176.4.363

Source DB:  PubMed          Journal:  Br J Psychiatry        ISSN: 0007-1250            Impact factor:   9.319


  28 in total

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3.  A Randomized, Double-blind Study of the Efficacy and Tolerability of Extended Release Quetiapine Fumarate (Quetiapine XR) Monotherapy in Patients with Major Depressive Disorder.

Authors:  Gang Wang; Alexander McIntyre; Willie R Earley; Shane Raines; Hans Eriksson
Journal:  Psychopharmacol Bull       Date:  2012-02-15

4.  Efficacy and safety of long-term fluoxetine versus lithium monotherapy of bipolar II disorder: a randomized, double-blind, placebo-substitution study.

Authors:  Jay D Amsterdam; Justine Shults
Journal:  Am J Psychiatry       Date:  2010-04-01       Impact factor: 18.112

5.  Hypotension following cardiac surgery associated with paroxetine and mirtazapine withdrawal.

Authors:  Kimberly J Novak; William I Douglas; Robert J Kuhn
Journal:  J Pediatr Pharmacol Ther       Date:  2008-01

6.  Symptom-Onset Dosing of Sertraline for the Treatment of Premenstrual Dysphoric Disorder: A Randomized Clinical Trial.

Authors:  Kimberly A Yonkers; Susan G Kornstein; Ralitza Gueorguieva; Brian Merry; Kari Van Steenburgh; Margaret Altemus
Journal:  JAMA Psychiatry       Date:  2015-10       Impact factor: 21.596

7.  A pilot study of the pharmacodynamic impact of SSRI drug selection and beta-1 receptor genotype (ADRB1) on cardiac vital signs in depressed patients: a novel pharmacogenetic approach.

Authors:  Kelan L H Thomas; Vicki L Ellingrod; Jeffrey R Bishop; Michael J Keiser
Journal:  Psychopharmacol Bull       Date:  2010

8.  Predicting new molecular targets for known drugs.

Authors:  Michael J Keiser; Vincent Setola; John J Irwin; Christian Laggner; Atheir I Abbas; Sandra J Hufeisen; Niels H Jensen; Michael B Kuijer; Roberto C Matos; Thuy B Tran; Ryan Whaley; Richard A Glennon; Jérôme Hert; Kelan L H Thomas; Douglas D Edwards; Brian K Shoichet; Bryan L Roth
Journal:  Nature       Date:  2009-11-01       Impact factor: 49.962

Review 9.  Update on research and treatment of premenstrual dysphoric disorder.

Authors:  Joanne Cunningham; Kimberly Ann Yonkers; Shaughn O'Brien; Elias Eriksson
Journal:  Harv Rev Psychiatry       Date:  2009       Impact factor: 3.732

10.  The Comorbidity of Major Depression and Anxiety Disorders: Recognition and Management in Primary Care.

Authors:  Robert M. A. Hirschfeld
Journal:  Prim Care Companion J Clin Psychiatry       Date:  2001-12
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