Posttraumatic Stress Disorder: Practice Essentials, Background, Pathophysiology (original) (raw)

Practice Essentials

Posttraumatic stress disorder (PTSD) is a syndrome resulting from exposure to real or threatened serious injury or sexual assault. The signs and symptoms of PTSD appear to arise from complex interactions of psychological and neurobiological factors. Studies have found alterations in the amygdala, prefrontal cortex, hippocampus, and anterior cingulate, and corpus collosum as well as altered functioning of the hypothalamic pituitary axis (HPA).

Signs and symptoms

Symptoms of PTSD include the following:

One cannot diagnose PTSD until one month has passed since the traumatic incident. Acute stress disorder, which has similar symptoms, is diagnosed during the first month.

Diagnosis

Diagnosing PTSD in adults, adolescents, and children older than 6 years of age using the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) [1] requires a certain type and level of traumatic event, a combination of required symptoms, and the absence of exclusionary criteria.

A) Causation: The victim was exposed to actual or threatened death, serious injury or sexual violence in one of four ways:

B) The traumatic event is persistently re-experienced:

Children may re-experience the event through repetitive play.

C) Avoidance in one of two ways:

D) Negative alterations in cognition and mood. Two of the following:

E) Hyperarrousal: Two of the following:

F) The duration of symptoms is more than 1 month

G) Disturbance causes clinically significant distress or impairment in functioning

H) The disturbance is not attributable to the physiological effects of a substance or other medical condition

DSM-5-TR recognizes a “with dissociative symptom” specifier when the PTSD symptoms are accompanied by persistent or recurrent depersonalization or derealization.

The specifier “with delayed expression” should be included if the full criteria for PTSD are not met for more than 6 months following the trauma.

Children may have different reactions to trauma than do adults. Children aged 6–11 years may show extreme withdrawal, disruptive behavior, and/or an inability to pay attention. Regressive behaviors, nightmares, sleep problems, irrational fears, irritability, refusal to attend school, outbursts of anger, and fighting are also common. The child may have somatic complaints with no medical basis. Schoolwork often suffers. Depression, anxiety, feelings of guilt, and emotional numbing are often present. Adolescents aged 12–17 years generally have responses similar to those of adults. [2]

For children aged 6 years or younger, typical reactions to trauma can include regressive behavior, a fear of being separated from a parent, crying, whimpering, screaming, immobility and/or aimless motion, trembling, frightened facial expressions, and excessive clinging. Children are strongly affected by their parents' reactions to the traumatic event and their parents’ ability to provide support. [2] Special criteria for the diagnosis of PTSD in children 6 years of age and under are found in the DSM-5-TR. [1]

Management

Psychological First Aid (PFA) is very important in the immediate aftermath of a traumatic event. PFA includes psychoeducation that the patient's initial symptoms are a normal reaction to an abnormal event and do not mean the person is weak or "going crazy," and that the symptoms will subside with time. First aid also includes providing for the individual’s basic needs (shelter, food, and supportive relationships) and reassurance that support will continue. It is important to avoid making invalidating comments such as: "It's not that big a deal" or "Why are you so upset?"

Evidence-based therapies for PTSD include Trauma Focused Cognitive Behavioral Therapy (TF-CBT) Prolonged Exposure (PE), Cognitive Processing Therapy, and Eye Movement Desensitization and Reprocessing (EMDR). Psychotherapy is clearly more effective than medication. Certain medications may be helpful in increasing the effectivenenss of therapy. D-cycloserine, which enhances memory, may help with extinction learning. Inderal may help to decrease arousal during therapy and may make extinction learning more effective. However, inderal also impairs memory. [3]

The SSRI and SNRI antidepressants appear to be the most effective psychopharmacological interventions for the symptoms of PTSD in adults. Their efficacy in adolescents and children is certainly less and they may not have any efficacy at all. In addition, they carry Black Box warnings for suicidality. Guanfacine and clonidine can be helpful for agitation. Prazosin is sometimes helpful for decreasing trauma-related nightmares and insomnia. Use of inderal in the first few hours may decrease future hyperarrousal symptoms. Use of benzodiazepines has been shown to worsen the course of PTSD.

Playing a visually demanding game such as Tetris shortly after the traumatic event may help to interfere with consolidation of the memory and may decrease the risk of developing PTSD.

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Background

The psychological problems of soldiers in World War II, the Korean War, and the Vietnam War, along with the severe psychological impact of rape, fostered interest and research in the collection of symptoms that became known as posttraumatic stress disorder. PTSD was first included in the Diagnostic and Statistical Manual of Mental Disorders in 1980 when DSM-III was published. The diagnostic criteria have undergone significant revisions since then.

Under DSM-III one had to experience an event outside of normal human experience that would cause symptoms in almost anyone. In time, appreciation that the symptom cluster occurred as a result of common experiences, such as car accidents, led to a change in the criteria.

DSM-IV required that the individual respond to the trauma with “intense fear, helplessness, or horror.” Although the DSM-5-TR contains these as a possible manifestations of PTSD, the requirement for them was dropped. DSM-5-TR also moved PTSD from the "Anxiety Disorders" category to a new category of disorders referred to as "Trauma- and Stressor-Related Disorders."

Previous criteria focused on the clusters of re-experiencing, avoidance, and hyperarousal. This has been slightly modified in the DSM-5-TR, which now includes intrusive symptoms (similar to the older re-experiencing category), avoidance, negative changes to cognitions and emotions, and altered arousal and reactivity. [1]

Traumatic events had been limited to life-threatening occurrences such as natural disasters, personal assaults, war, or severe accidents.The DSM-5-TR included the possibility of developing PTSD following sexual violence even if there was no threat of death. For children, a developmentally inappropriate sexual experience may be considered a traumatic event, even though it may not have actually involved violence or physical injury.

The DSM-5-TR recognizes a new, dissociative subtype of PTSD, with clinical and neurobiological features that distinguish it from the non-dissociative form. This dissociative subtype is described as an over-modulation of affect, or a form of emotional dysregulation mediated by midline prefrontal inhibition of limbic regions. This subtype may require slight differences in treatment.

The DSM-5-TR now includes differing criteria for diagnosing PTSD in children 6 years of age and younger. Although the criteria are similar to those used in diagnosing PTSD in older populations, there are developmentally appropriate alterations. [1]

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Pathophysiology

In addition to the psychological impact of experiencing a traumatic event, posttraumatic stress disorder (PTSD) frequently leads to changes in the anatomy and neurophysiology of the brain. Reduced size of the hippocampus is probably both a predisposing factor and a result of trauma. The amygdala, which is involved in processing emotions and modulating the fear response, seems to be overly reactive in patients with PTSD. The medial prefrontal cortex (mPFC), which exhibits inhibitory control over the stress response and emotional reactivity of the amygdala, appears to be smaller and less responsive in individuals with PTSD. [4, 5, 6, 7]

Alterations in neurohormonal and neurotransmitter functioning have also been found. Individuals with PTSD tend to have normal to low circulating levels of cortisol despite their ongoing stress and elevated levels of Corticotropin Releasing Factor (CRF). Cortisol leads to decreased production of CRF. If cortisol is low then CRF continues to be high and stimulates norepinephrine release by the anterior cinculate cortex. Individuals with PTSD demonstrate hyperactivity of the sympathetic branch of the autonomic nervous system, as evidenced by changes in heart rate, blood pressure, skin conductance level, and other psychophysiological measures. They also have elevated noradrenergic reactivity to pharmacological challenges. A variety of other neurotransmitter systems, such as the serotonin, GABA, glutamate, neuropeptide Y, and endogenous opioids, show altered functioning in individuals with PTSD.

Further insight into the pathophysiology of PTSD may be found in the Dual Representational Theory. This understanding highlights the presence of two separate systems for memory. Verbally accessible memory (first recorded in the hippocampus and later in general brain memory storage) is able to be modified by reflection. This is characteristic of most non-traumatic memories. Situationally accessible memory, on the other hand, is non-verbal and associated with very strong emotions and the amygdala. Traumatic memories tend to be stored as situationally accessible memories, which are harder to process, are readily triggered by associations, and more likely to cause emotional distress when activated. Individuals may struggle to integrate these traumatic experiences with the rest of their life narrative thereby resulting in the traumatic memory having a significant impact on their views of the world and themselves. [8, 9]

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Etiology

The etiology of posttraumatic stress disorder (PTSD) is experiencing a serious threat of physical injury or death, or sexual assault. Children who suffer repeated child abuse are at risk for complex trauma. Chronic PTSD represents a failure to recover from the trauma, in part due to inadequate resilience. Considerable effort has been spent in an attempt to determine which individuals will have prolonged, maladaptive responses to trauma. Numerous risk factors have been determined. [1, 10]

Pre-existing factors

Pre-existing factors include the following:

Peritraumatic factors

Peritraumatic factors include the following:

Posttraumatic factors

Posttraumatic factors include the following:

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Epidemiology

Exposure to traumatic events is common. Among adults in the United States, as many as 50% of women and 60% of men have experienced a traumatic event. Most of these individuals will not develop posttraumatic stress disorder (PTSD).

The lifetime prevalence of PTSD in adults ranges from 6.1% to 9.2% in the United States and Canada. [11, 12] One-year prevalence rates range from 3.5% to 4.7%. [11] These rates vary considerably depending on the specific population being considered. [13]

In the United States, Native Americans living on reservations and refugees from countries where traumatic stress was endemic have higher rates of PTSD. [14] In a meta-analysis of 19 studies of mental disorders among Native Americans in the United States, Canada, and Latin America, indigenous peoples had 1.4 greater odds of lifetime PTSD compared with nonindigenous peoples with similar socio-demographic features. [15]

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Associated Concepts

Complex trauma and disorders of extreme stress not otherwise specified (DESNOS)

In the 1990s, Van Der Kolk and others began promoting the concept of “Complex PTSD.” It is also referred to as Disorder of Extreme Stress Not Otherwise Specified (DESNOS). DESNOS arises from severe, protracted abuse, most notably childhood sexual abuse, victims of torture, and living in a war zone. This type of trauma often leads to the use of primitive defense mechanisms (splitting and dissociation), which causes significant interpersonal problems and emotional struggles in addition to the standard symptoms of PTSD. Complex PTSD often leads to poor resilience, increased risk of depressive and anxiety disorders, and somatization. Numerous situations will trigger these individuals and lead to very strong adverse emotional reactions. The great majority of individuals who develop Borderline Personality Disorder or Dissociative Identity Disorder suffered complex trauma during childhood. Although many clinicians find this to be a useful conceptualization, it does not appear in the DSM-5-TR. [16]

Betrayal trauma

Freyd and others have developed the concept of betrayal trauma. Betrayal trauma does not fulfill the diagnostic criteria for PTSD because it does not entail a serious threat of injury or sexual assault. Nevertheless, betrayal, such as a spouse having an affair or abandonment by a parent can result in most of the same symptoms that PTSD can cause. [17, 18] Symonds argued that some of the symptoms we normally attribute to the initial traumatic event are actually the result of the individual feeling betrayed by those (s)he expected to provide support. Child abuse includes betrayal trauma because parents and teachers are supposed to protect children, not abuse them.

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Prognosis

Prognosis in posttraumatic stress disorder (PTSD) varies based on a number of factors including resilience, secondary stresses, level of support, prior traumatic experiences, ongoing injury, severity of the stressor, and so on.

The child's resilience is an important factor in prognosis. [10]

Three years after Hurricane Katrina, the prevalence of serious emotional disturbance for children in the area with high exposure (serious economic or housing problems, injury or death of someone close to them or victimization) was roughly one in three children. [13]

Child abuse and neglect predispose to personality disorders, affective disorders, substance abuse and medical problems. [19]

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Patient Education

Family members of those with posttraumatic stress disorder (PTSD) are also impacted by the trauma particularly through the detachment and irritability of the person with PTSD. Family members may desire to be supportive but are not clear what conversations to have or how best to show their concern and support. For many individuals with PTSD, comprehensive treatment includes involvement of the family in some form.

The following websites provide valuable information for patients and their families:

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  1. American Psychiatric Association. American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision. Washington, DC: 2022.
  2. National Institute of Mental Health. Helping Children and Adolescents Cope with Violence and Disasters. NIH Publication No. 01-3518. Bethesda, Md:. National Institute of Mental Health; 2001. [Full Text].
  3. Rothbaum, B. O., Price, M., Jovanovic, T., et al. A randomized, double-blind evaluation of d-cycloserine or alprazolam combined with virtual reality exposure therapy for posttraumatic stress disorder in Iraq and Afghanistan War Veterans. American Journal of Psychiatry, 171, 640-648. American Journal of Psychiatry. 2014. 171:640-648.
  4. Kasai K, Yamasue H, Gilbertson MW, Shenton ME, Rauch SL, Pitman RK. Evidence for acquired pregenual anterior cingulate gray matter loss from a twin study of combat-related posttraumatic stress disorder. Biol Psychiatry. 2008 Mar 15. 63(6):550-6. [QxMD MEDLINE Link]. [Full Text].
  5. LISA M. SHIN,SCOTT L. RAUCH,ROGER K. PITMAN. Amygdala, Medial Prefrontal Cortex, and Hippocampal Function in PTSD. Annals of the NY Academy of Sciences. 2006.
  6. Giacomo Ronzoni, Alberto del Arco1, Francisco Mora, Gregorio Segovia. nhanced noradrenergic activity in the amygdala contributes to hyperarousal in an animal model of PTSD. Psychoneuroendocrinology. 2016. 70:1-9.
  7. Bremner JD, Elzinga B, Schmahl C, & Vermetten E. Structural and functional plasticity of the human brain in posttraumatic stress disorder. . Progress in brain research. 2008. 167:171-86.
  8. Brewin CR, Dalgleish T and Joseph S. A dual representation theory of post-traumatic stress disorder. Psychological Review. 1996. 103:670-686.
  9. Brewin, Chris; Holmes, Emily. Psychological theories of posttraumatic stress disorder. Clinical Psychology Review. 2003. 23:339–376.
  10. Goldstein S & Brooks R. Handbook of Resilience in Children. Springer.; 2013.
  11. Goldstein RB, Smith SM, Chou SP, Saha TD, Jung J, Zhang H, et al. The epidemiology of DSM-5 posttraumatic stress disorder in the United States: results from the National Epidemiologic Survey on Alcohol and Related Conditions-III. Soc Psychiatry Psychiatr Epidemiol. 2016 Aug. 51 (8):1137-48. [QxMD MEDLINE Link].
  12. Van Ameringen M, Mancini C, Patterson B, Boyle MH. Post-traumatic stress disorder in Canada. CNS Neurosci Ther. 2008 Fall. 14 (3):171-81. [QxMD MEDLINE Link].
  13. McLaughlin, K, Fairbank, J, Gruber, M. Trends in Serious Emotional Disturbance among Youths Exposed to Hurricane Katrina. J of the Am Academy of Child Adolesc Psychiatry. 2010. 49(10):990-1000.
  14. Beals J, Belcourt-Dittloff A, Garroutte EM, Croy C, Jervis LL, Whitesell NR, et al. Trauma and conditional risk of posttraumatic stress disorder in two American Indian reservation communities. Soc Psychiatry Psychiatr Epidemiol. 2013 Jun. 48 (6):895-905. [QxMD MEDLINE Link].
  15. Kisely S, Alichniewicz KK, Black EB, Siskind D, Spurling G, Toombs M. The prevalence of depression and anxiety disorders in indigenous people of the Americas: A systematic review and meta-analysis. J Psychiatr Res. 2017 Jan. 84:137-152. [QxMD MEDLINE Link].
  16. Roth, S.; Newman, E.; Pelcovitz, D.; Van Der Kolk, B.; Mandel, F. S. Complex PTSD in victims exposed to sexual and physical abuse: Results from the DSM-IV Field Trial for Posttraumatic Stress Disorder". Journal of traumatic stress. Journal of traumatic stress. 1997. 10 (4):539–55.
  17. Freyd J & P Birrell. Blind to Betrayal. Hoboken: Wiley.; 2013.
  18. Freyd JJ, Klest B, Allard CB. Betrayal trauma: relationship to physical health, psychological distress, and a written disclosure intervention. J Trauma Dissociation. 2005. 6(3):.:83-104.
  19. Carr CP1, Martins CM, Stingel AM, Lemgruber VB, Juruena MF. The role of early life stress in adult psychiatric disorders: a systematic review according to childhood trauma subtypes. J Nerv Ment Dis. 2013. 201(12):1007-20.
  20. Olsson KA, Kenardy JA, De Young AC, Spence SH. Predicting children's post-traumatic stress symptoms following hospitalization for accidental injury: combining the Child Trauma Screening Questionnaire and heart rate. J Anxiety Disord. 2008 Dec. 22(8):1447-53. [QxMD MEDLINE Link].
  21. Sonne SC, Back SE, Diaz Zuniga C, Randall CL, Brady KT. Gender differences in individuals with comorbid alcohol dependence and post-traumatic stress disorder. Am J Addict. 2003 Oct-Dec. 12(5):412-23. [QxMD MEDLINE Link].
  22. Schwartz AC, Bradley R, Penza KM, Sexton M, Jay D, Haggard PJ, et al. Pain medication use among patients with posttraumatic stress disorder. Psychosomatics. 2006 Mar-Apr. 47(2):136-42. [QxMD MEDLINE Link]. [Full Text].
  23. Brooks M. Heavy drinking, PTSD in college students linked. Medscape Medical News. January 23, 2014. [Full Text].
  24. Read JP, Wardell JD, Colder CR. Reciprocal associations between PTSD symptoms and alcohol involvement in college: a three-year trait-state-error analysis. J Abnorm Psychol. 2013 Nov. 122(4):984-97. [QxMD MEDLINE Link].
  25. Yaffe K, Vittinghoff E, Lindquist K, Barnes D, Covinsky KE, Neylan T, et al. Posttraumatic stress disorder and risk of dementia among US veterans. Arch Gen Psychiatry. 2010 Jun. 67(6):608-13. [QxMD MEDLINE Link]. [Full Text].
  26. Rodriguez BF, Weisberg RB, Pagano ME, Machan JT, Culpepper L, Keller MB. Mental health treatment received by primary care patients with posttraumatic stress disorder. J Clin Psychiatry. 2003 Oct. 64(10):1230-6. [QxMD MEDLINE Link].
  27. Connor KM, Davidson JR. Further psychometric assessment of the TOP-8: a brief interview-based measure of PTSD. Depress Anxiety. 1999. 9(3):135-7. [QxMD MEDLINE Link].
  28. Hamilton A. Diagnosis and rating of anxiety. Special Publication: Br J Psychiatry; 1969. 3:76-79.
  29. Hamilton M. Development of a rating scale for primary depressive illness. Br J Soc Clin Psychol. 1967 Dec. 6(4):278-96. [QxMD MEDLINE Link].
  30. Brunet A, Saumier D, Liu A, Streiner DL, Tremblay J, Pitman RK. Reduction of PTSD Symptoms With Pre-Reactivation Propranolol Therapy: A Randomized Controlled Trial. Am J Psychiatry. 2018 Jan 12. appiajp201717050481. [QxMD MEDLINE Link].
  31. Hogberg G, Pagani M, Sundin O, Soares J, Aberg-Wistedt A, Tarnell B, et al. Treatment of post-traumatic stress disorder with eye movement desensitization and reprocessing: outcome is stable in 35-month follow-up. Psychiatry Res. 2008 May 30. 159(1-2):101-8. [QxMD MEDLINE Link].
  32. Ponniah K, Hollon SD. Empirically supported psychological treatments for adult acute stress disorder and posttraumatic stress disorder: a review. Depress Anxiety. 2009. 26(12):1086-109. [QxMD MEDLINE Link].
  33. Bronson D, Franco K, Budur K. Posttraumatic stress disorder in primary care patients. Compr Ther. 2007 Winter. 33(4):208-15. [QxMD MEDLINE Link].
  34. Nijdam MJ, Gersons BP, Reitsma JB, de Jongh A, Olff M. Brief eclectic psychotherapy v. eye movement desensitisation and reprocessing therapy for post-traumatic stress disorder: randomised controlled trial. Br J Psychiatry. 2012 Mar. 200(3):224-31. [QxMD MEDLINE Link].
  35. Harrison P. Evidence Supports Psychological Therapies for PTSD Kids. Medscape Medical News. December 11, 2012. [Full Text].
  36. Gillies D, Taylor F, Gray C, O'Brien L, D'Abrew N. Psychological therapies for the treatment of post-traumatic stress disorder in children and adolescents. Cochrane Database Syst Rev. 2012 Dec 12. 12:CD006726. [QxMD MEDLINE Link].
  37. Davis LL, Frazier EC, Williford RB, Newell JM. Long-term pharmacotherapy for post-traumatic stress disorder. CNS Drugs. 2006. 20(6):465-76. [QxMD MEDLINE Link].
  38. Bisson JI, Ehlers A, Matthews R, Pilling S, Richards D, Turner S. Psychological treatments for chronic post-traumatic stress disorder. Systematic review and meta-analysis. Br J Psychiatry. 2007 Feb. 190:97-104. [QxMD MEDLINE Link].
  39. Germain A, Shear MK, Hall M, Buysse DJ. Effects of a brief behavioral treatment for PTSD-related sleep disturbances: a pilot study. Behav Res Ther. 2007 Mar. 45(3):627-32. [QxMD MEDLINE Link].
  40. Raskind MA, Peskind ER, Hoff DJ, Hart KL, Holmes HA, Warren D, et al. A parallel group placebo controlled study of prazosin for trauma nightmares and sleep disturbance in combat veterans with post-traumatic stress disorder. Biol Psychiatry. 2007 Apr 15. 61(8):928-34. [QxMD MEDLINE Link].
  41. Brooks M. New WHO Guideline on Mental Health Care After Trauma. Medscape Medical News. Available at https://www.medscape.com/viewarticle/809185. Accessed: August 14, 2013.
  42. Tol WA, Barbui C, van Ommeren M. Management of acute stress, PTSD, and bereavement: WHO recommendations. JAMA. 2013 Aug 7. 310(5):477-8. [QxMD MEDLINE Link].
  43. Litz BT, Engel CC, Bryant RA, Papa A. A randomized, controlled proof-of-concept trial of an Internet-based, therapist-assisted self-management treatment for posttraumatic stress disorder. Am J Psychiatry. 2007 Nov. 164(11):1676-83. [QxMD MEDLINE Link].
  44. Shalev AY, Ankri Y, Gilad M,. Long-Term Outcome of Early Interventions to Prevent Posttraumatic Stress Disorder. J Clin Psychiatry. 2016. 77(5):580-587.
  45. Ot'alora G M, Grigsby J, Poulter B, Van Derveer JW 3rd, Giron SG, Jerome L, et al. 3,4-Methylenedioxymethamphetamine-assisted psychotherapy for treatment of chronic posttraumatic stress disorder: A randomized phase 2 controlled trial. J Psychopharmacol. 2018 Oct 29. 269881118806297. [QxMD MEDLINE Link].
  46. Martin A, Naunton M, Kosari S, Peterson G, Thomas J, Christenson JK. Treatment Guidelines for PTSD: A Systematic Review. J Clin Med. 2021 Sep 15. 10 (18):[QxMD MEDLINE Link].
  47. [Guideline] American Psychological Association. Clinical Practice Guideline for the Treatment of Posttraumatic Stress Disorder (PTSD) in Adults. February 24, 2017. [Full Text].
  48. [Guideline] ISTSS Guidelines Committee. ISTSS PTSD Prevention and Treatment Guidelines Methodology and Recommendations. 2019. [Full Text].
  49. Bisson, J. Post Traumatic Stress Disorder. Occupational Medicine. 2007. 57 Issue 6:399-403.
  50. Matthew J. Friedman MD PhD. Handbook of PTSD. 2. Guilford; 2014.
  51. Hoskins, M., Pearce, J., Bethell, A., et al. Pharmacotherapy for post-traumatic stress disorder: Systematic review and meta-analysis. The. British Journal of Psychiatry : The Journal of Mental Science,. 2015. 206 (2):93-100.
  52. Haagen, JF; Smid, GE; Knipscheer, JW; Kleber, RJ. "The efficacy of recommended treatments for veterans with PTSD: A metaregression analysis.". Clinical Psychology Review. 2015. 40:184–94.
  53. Krystal JH, Rosenheck RA, Cramer JA, Vessicchio JC, Johnes, KM, et al. Adjunctive risperidone treatment for antidepressant-resistant symptoms of chronic military service-related PTSD. JAMA. Aug 2011. 306(5):461-568.
  54. Davenport L. Add-on Antipsychotic Promising for PTSD, Anxiety. Medscape Medical News. Available at https://www.medscape.com/viewarticle/893386. March 5, 2018; Accessed: March 7, 2018.
  55. Brunet A, Orr SP, Tremblay J, Robertson K, Nader K, Pitman RK. Effect of post-retrieval propranolol on psychophysiologic responding during subsequent script-driven traumatic imagery in post-traumatic stress disorder. J Psychiatr Res. 2008 May. 42(6):503-6. [QxMD MEDLINE Link].
  56. Hoge CW, Auchterlonie JL, Milliken CS. Mental health problems, use of mental health services, and attrition from military service after returning from deployment to Iraq or Afghanistan. JAMA. 2006 Mar 1. 295(9):1023-32. [QxMD MEDLINE Link].
  57. Hoge CW, Castro CA, Messer SC, McGurk D, Cotting DI, Koffman RL. Combat duty in Iraq and Afghanistan, mental health problems, and barriers to care. N Engl J Med. 2004 Jul 1. 351(1):13-22. [QxMD MEDLINE Link].
  58. Turner JH, Neylan TC, Schiller NB, Li Y, Cohen BE. Objective evidence of myocardial ischemia in patients with posttraumatic stress disorder. Biol Psychiatry. 2013 Dec 1. 74(11):861-6. [QxMD MEDLINE Link].
  59. Vaccarino V, Bremner JD. Traumatic stress is heartbreaking. Biol Psychiatry. 2013 Dec 1. 74(11):790-2. [QxMD MEDLINE Link].
  60. Cassels C. PTSD Independently Linked to Ischemic Heart Disease. Medscape [serial online]. Available at https://www.medscape.com/viewarticle/814375. Accessed: December 2, 2013.

Author

T Allen Gore, MD, MBA, CMCM, DFAPA Volunteer Associate Professor, Department of Psychiatry, Howard University School of Medicine; Senior Psychiatrist and Director, Medical Education, Comprehensive Psychiatric Emergency Program, District of Columbia Department of Mental Health

T Allen Gore, MD, MBA, CMCM, DFAPA is a member of the following medical societies: American Psychiatric Association, National Association of Managed Care Physicians, National Medical Association

Disclosure: Nothing to disclose.

Coauthor(s)

Specialty Editor Board

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

Chief Editor

Acknowledgements

The authors would like to thank all colleagues and students who contributed to this article. We are especially grateful to the following individuals:

Georgianna M Richards-Reid, MD, Staff Physician, Department of Neurology, Howard University Hospital, Howard University College of Medicine

Zachary Osborne, MD; Ross University School of Medicine

Bobbi Adams, BS; University of Alabama