Literature DB >> 9329449

Biological therapies for posttraumatic stress disorder: an overview.

J R Davidson1.   

Abstract

Both core and secondary symptoms of posttraumatic stress disorder (PTSD) respond to medication, a valuable part of overall PTSD treatment. Treatment options include antidepressants, anxiolytics, anticonvulsants, and mood stabilizers. A growing data base of results from double-blind, placebo-controlled clinical trials supports the use of antidepressants, especially tricyclics, monoamine oxidase inhibitors (MAOIs), and serotonin selective reuptake inhibitors (SSRIs). Although heightened anxiety is characteristic of PTSD, benzodiazepines have not yet proved useful in controlled trials and may be associated with a rebound effect on discontinuation. The small, open studies of anticonvulsant drugs indicate moderate to good improvement with these agents. Tricyclic, SSRI, and MAOI antidepressants have demonstrated efficacy in larger, longer-term controlled trials. Drug/psychotherapy combinations may enhance the usefulness of psychotherapeutics in the management of PTSD. Studies with tricyclics and fluoxetine indicate that magnitude and type of trauma may determine the degree of response.

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Year:  1997        PMID: 9329449

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


  11 in total

1.  Autonomic reactivity and clinical severity in children with sickle cell disease.

Authors:  Sarah R Pearson; Abbey Alkon; Marsha Treadwell; Brian Wolff; Keith Quirolo; W Thomas Boyce
Journal:  Clin Auton Res       Date:  2005-12       Impact factor: 4.435

Review 2.  Post-traumatic stress disorder in children and adolescents: epidemiology, diagnosis and treatment options.

Authors:  Craig L Donnelly; Lisa Amaya-Jackson
Journal:  Paediatr Drugs       Date:  2002       Impact factor: 3.022

3.  Outcomes monitoring and the testing of new psychiatric treatments: work therapy in the treatment of chronic post-traumatic stress disorder.

Authors:  R Rosenheck; M Stolar; A Fontana
Journal:  Health Serv Res       Date:  2000-04       Impact factor: 3.402

Review 4.  [Disorders related to traumatic events. Screening and treatment].

Authors:  Stéphane Guay; Nicole Mainguy; André Marchand
Journal:  Can Fam Physician       Date:  2002-03       Impact factor: 3.275

5.  Chronic treatment with duloxetine is necessary for an anxiolytic-like response in the mouse zero maze: the role of the serotonin transporter.

Authors:  K B Troelsen; E Ø Nielsen; N R Mirza
Journal:  Psychopharmacology (Berl)       Date:  2005-09-29       Impact factor: 4.530

Review 6.  Pharmacotherapy for post traumatic stress disorder (PTSD).

Authors:  Taryn Williams; Nicole J Phillips; Dan J Stein; Jonathan C Ipser
Journal:  Cochrane Database Syst Rev       Date:  2022-03-02

7.  Differential effects of acute and repeated citalopram in mouse models of anxiety and depression.

Authors:  Cedric Mombereau; Tamar L Gur; Jennifer Onksen; Julie A Blendy
Journal:  Int J Neuropsychopharmacol       Date:  2009-12-14       Impact factor: 5.176

8.  Psychopharmacotherapy of posttraumatic stress disorder.

Authors:  Dragica Kozaric-Kovacic
Journal:  Croat Med J       Date:  2008-08       Impact factor: 1.351

Review 9.  Pharmacotherapy for post traumatic stress disorder (PTSD).

Authors:  D J Stein; J C Ipser; S Seedat
Journal:  Cochrane Database Syst Rev       Date:  2006-01-25

10.  Update on the epidemiology, diagnosis, and treatment of posttraumatic stress disorder.

Authors:  J Zohar; D Amital; H D Cropp; G Cohen-Rappaport; Y Zinger; Y Sasson
Journal:  Dialogues Clin Neurosci       Date:  2000-03       Impact factor: 5.986

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