Literature DB >> 12562113

Pharmacotherapy of generalized anxiety disorder.

Karl Rickels1, Moira Rynn.   

Abstract

Less than one third of people afflicted with generalized anxiety disorder (GAD) experience spontaneous remission, and the symptoms of GAD wax and wane throughout a person's life. The burden of GAD may be reduced with psychopharmacologic therapy. The medications with the most evidence of efficacy in GAD are the benzodiazepines, including a new long-acting formulation of alprazolam. These drugs have a low incidence of side effects but may cause physical dependence, withdrawal, and sedation. Antidepressants are also efficacious in GAD but act less quickly than benzodiazepines. Tricyclic antidepressants such as imipramine may substantially reduce symptoms of anxiety but are not considered a first-line therapy because of their side effects spectrum. The extended-release formulation of venlafaxine and selective serotonin reuptake inhibitors such as paroxetine and sertraline are also efficacious in GAD. While their association with sexual dysfunction may be intolerable for some adults, these drugs may be more appropriate than the benzodiazepines because their chronic use does not lead to dependence. Buspirone also significantly reduces symptoms of GAD and is associated with less sexual dysfunction than SSRIs and less sedation than benzodiazepines. Combining antidepressant and benzodiazepine therapy or medication treatment and psychotherapy may lead to an increase in improvement in patients not responding to 1 treatment approach alone. The most effective treatment for managing the recurrent symptoms of this chronic disorder will remain unknown until more long-term studies using both drug and nondrug therapies are conducted. Remission rates are still only about 40%, signifying the need for improved treatment interventions.

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Year:  2002        PMID: 12562113

Source DB:  PubMed          Journal:  J Clin Psychiatry        ISSN: 0160-6689            Impact factor:   4.384


  20 in total

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2.  Treatment of anxiety disorders in primary care practice: a randomised controlled trial.

Authors:  Christine A van Boeijen; Patricia van Oppen; Anton J L M van Balkom; Sako Visser; Pieter T Kempe; Nettie Blankenstein; Richard van Dyck
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3.  Differential behavioral effects of low efficacy positive GABAA modulators in combination with benzodiazepines and a neuroactive steroid in rhesus monkeys.

Authors:  Lance R McMahon; Charles P France
Journal:  Br J Pharmacol       Date:  2006-02       Impact factor: 8.739

4.  The Role of High-Potency Benzodiazepines in the Treatment of Panic Disorder.

Authors:  Jeffrey Susman; Brian Klee
Journal:  Prim Care Companion J Clin Psychiatry       Date:  2005

5.  Psychometric evaluation of a visual analog scale for the assessment of anxiety.

Authors:  Valerie S L Williams; Robert J Morlock; Douglas Feltner
Journal:  Health Qual Life Outcomes       Date:  2010-06-08       Impact factor: 3.186

Review 6.  Antiepileptic drugs in the treatment of anxiety disorders: role in therapy.

Authors:  Michael Van Ameringen; Catherine Mancini; Beth Pipe; Mark Bennett
Journal:  Drugs       Date:  2004       Impact factor: 9.546

7.  The neurotensin-1 receptor agonist PD149163 blocks fear-potentiated startle.

Authors:  Paul D Shilling; David Feifel
Journal:  Pharmacol Biochem Behav       Date:  2008-10       Impact factor: 3.533

8.  Stimulus-reinforcement-based decision making and anxiety: impairment in generalized anxiety disorder (GAD) but not in generalized social phobia (GSP).

Authors:  J DeVido; M Jones; M Geraci; N Hollon; R J R Blair; D S Pine; K Blair
Journal:  Psychol Med       Date:  2008-12-22       Impact factor: 7.723

9.  Response to emotional expressions in generalized social phobia and generalized anxiety disorder: evidence for separate disorders.

Authors:  Karina Blair; Jonathan Shaywitz; Bruce W Smith; Rebecca Rhodes; Marilla Geraci; Matthew Jones; Daniel McCaffrey; Meena Vythilingam; Elizabeth Finger; Krystal Mondillo; Madeline Jacobs; Dennis S Charney; R J R Blair; Wayne C Drevets; Daniel S Pine
Journal:  Am J Psychiatry       Date:  2008-05-15       Impact factor: 18.112

10.  The Kava Anxiety Depression Spectrum Study (KADSS): a randomized, placebo-controlled crossover trial using an aqueous extract of Piper methysticum.

Authors:  J Sarris; D J Kavanagh; G Byrne; K M Bone; J Adams; G Deed
Journal:  Psychopharmacology (Berl)       Date:  2009-05-09       Impact factor: 4.530

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