Literature DB >> 14998877

Applying learning principles to the treatment of post-trauma reactions.

Barbara Olasov Rothbaum1, Michael Davis.   

Abstract

Posttraumatic stress disorder (PTSD) can be characterized as a failure of recovery caused, in part, by a failure of fear extinction after trauma. By studying the process of extinction, we can be informed regarding the etiology and maintenance of PTSD. The normal response to trauma in humans includes a set of predictable reactions including reexperiencing, avoidance, and hyperarousal that typically extinguish in the days and weeks after the trauma. In the majority of people exposed to trauma, these responses extinguish over time. However, in a substantial minority, extinction fails and these persisting responses become the symptoms of PTSD. Therefore, one of our fundamental hypotheses is that PTSD is a disorder caused in part by the failure of extinction of predictable posttraumatic physiological and psychological reactions. The most empirically validated treatments for PTSD involve exposure of the patient to trauma-related cues in the absence of danger that then lead to the extinction of these reexperiencing, avoidance, and arousal symptoms. There is also mounting evidence that individuals with PTSD are more resistant to extinction. Regarding early interventions with traumatized individuals, there is mounting evidence that some early one-time interventions actually may impede extinction, whereas interventions delivered in more than one session, at least several weeks after the trauma, to individuals continuing to experience above average reactions, generally are effective in preventing the development of PTSD. Thus, there appears to be an interaction between timing of the intervention, number of intervention sessions, and either arousal level and/or risk status in determining whether the intervention will be helpful, harmful, or neutral.

Entities:  

Mesh:

Year:  2003        PMID: 14998877     DOI: 10.1196/annals.1301.012

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  184 in total

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3.  Challenges and Successes in Dissemination of Evidence-Based Treatments for Posttraumatic Stress: Lessons Learned From Prolonged Exposure Therapy for PTSD.

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4.  Controlled cortical impact before or after fear conditioning does not affect fear extinction in mice.

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Journal:  Brain Res       Date:  2015-02-23       Impact factor: 3.252

5.  Treatment Outcome-Related White Matter Differences in Veterans with Posttraumatic Stress Disorder.

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Review 6.  From Pavlov to PTSD: the extinction of conditioned fear in rodents, humans, and anxiety disorders.

Authors:  Michael B VanElzakker; M Kathryn Dahlgren; F Caroline Davis; Stacey Dubois; Lisa M Shin
Journal:  Neurobiol Learn Mem       Date:  2013-12-07       Impact factor: 2.877

7.  Graded fear generalization enhances the level of cfos-positive neurons specifically in the basolateral amygdala.

Authors:  Abha K Rajbhandari; Ruoyan Zhu; Cora Adling; Michael S Fanselow; James A Waschek
Journal:  J Neurosci Res       Date:  2016-09-23       Impact factor: 4.164

8.  Controllable versus uncontrollable stressors bi-directionally modulate conditioned but not innate fear.

Authors:  M V Baratta; J P Christianson; D M Gomez; C M Zarza; J Amat; C V Masini; L R Watkins; S F Maier
Journal:  Neuroscience       Date:  2007-05-02       Impact factor: 3.590

9.  Beta-blockers may reduce intrusive thoughts in newly diagnosed cancer patients.

Authors:  Monica E Lindgren; Christopher P Fagundes; Catherine M Alfano; Stephen P Povoski; Doreen M Agnese; Mark W Arnold; William B Farrar; Lisa D Yee; William E Carson; Carl R Schmidt; Janice K Kiecolt-Glaser
Journal:  Psychooncology       Date:  2012-12-17       Impact factor: 3.894

10.  Vorinostat ameliorates impaired fear extinction possibly via the hippocampal NMDA-CaMKII pathway in an animal model of posttraumatic stress disorder.

Authors:  Yasutaka Matsumoto; Shigeru Morinobu; Shigeto Yamamoto; Tomoya Matsumoto; Shiro Takei; Yosuke Fujita; Shigeto Yamawaki
Journal:  Psychopharmacology (Berl)       Date:  2013-04-13       Impact factor: 4.530

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