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BMJ 2007;334:789-793 (14 April), doi:10.1136/bmj.39162.538553.80
Jonathan I Bisson, clinical senior lecturer in psychiatry
Cardiff University, University Hospital of Wales, Cardiff CF14 4XW
Vivid descriptions of reactions to traumatic events span many centuries, although their nature has changed over time.1 Post-traumatic stress disorder was first recognised as a diagnosable psychiatric disorder in the third edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-III)w1 and ICD-10 (International Classification of Diseases, 10th edition).2 Its very existence continues to attract debate, with several authors arguing that culturally determined, understandable emotions to traumatic events are being pathologised.w2 However, even its most ardent critics are more concerned by overdiagnosis than by whether post-traumatic stress disorder should be used as a label for the severe mental health problems some people experience after traumatic events.3 This article provides an overview of our current understanding of the disorder, who it affects, and the best approaches to its prevention and management.
I consulted recent systematic searches used to prepare Cochrane reviews and BMJ Clinical Evidence on prevention and treatment of post-traumatic stress disorder, as well as those used to prepare the National Institute for Health and Clinical Excellence (NICE) guidelines for post-traumatic stress disorder. I searched PubMed using the terms "epidemiology", "neurobiology", and "neuroimaging" in conjunction with "post-traumatic stress disorder". I also used a personal archive of references.
Box 1 shows the characteristic features of the disorder. It occurs after a traumatic event that involved actual or threatened death or serious injury, or a threat to the physical integrity of self or others.4 For the DSM classification, the person must also have experienced intense fear, helplessness, or horror when the event occurred. The symptoms must have been present for at least one month (the one month criterion does not apply in the ICD-10 classification) and, crucially, they must also cause clinically significant distress or impairment in social, occupational, or other important areas of functioning. Acute post-traumatic stress disorder becomes chronic if it lasts for longer than three months. Symptoms usually begin shortly after the trauma, but they are said to have delayed onset if they start at least six months later. Most people diagnosed with delayed onset post-traumatic stress disorder actually had symptoms within six months of the trauma, but they presented late or their symptoms were not recognised initially. For a few patients the onset of symptoms truly is delayed.w3
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Traumatic experiences can usually be assimilated without the development of a pathological response.w4 If this is unsuccessful, post-traumatic stress disorder can develop, with pathological fear structures characterised by excessive response elements such as avoidance, physiological reactivity, and resistance to modification.w5 Central to cognitive theories of post-traumatic stress disorder are pre-existing beliefs and models of the world, and the difficulty of assimilating information provided by a traumatic experience into them.5 6 One prominent theory5 distinguishes between memories that are easily verbally recalled and give rise to emotions related to the trauma and memories that cannot be deliberately accessed and give rise to symptoms such as dreams and flashbacks. Another theory suggests that the disorder develops when the traumatic memory induces a sense of current threat promoted by excessively negative appraisals of what happened.6
Although still in its infancy, with many findings still needing confirmation, our knowledge of the neurobiology of post-traumatic stress disorder is improving. The amygdala receives information about external stimuli and determines their importance. This then triggers emotional responses including a "fight, flight, or freezing" response and alterations in stress hormones and catecholamines. The hippocampus and medial prefrontal cortex (fig 1
) influence the response of the amygdala in determining the final fear response. Hippocampal lesions have been associated with a stronger fear response and smaller hippocampal volume has been associated with post-traumatic stress disorder,7 although whether this is a cause or an effect of the disorder is unknown.w6 Neuroimaging studies have shown decreased activity in medial prefrontal and anterior cingulate areas to be correlated with increased activity in the amygdala.8 It has therefore been suggested that post-traumatic stress disorder represents a failure of medial prefrontal and anterior cingulate networks to regulate the activity of the amygdala, which results in hyper-reactivity to threat.9
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The recent replication of the US national comorbidity survey of 5692 adults found that the lifetime prevalence of post-traumatic stress disorder was 6.8%12 and the 12 month prevalence was 3.5%13; about a third of those affected had a severe form of the condition. However, similar epidemiological studies of adolescents and young adults in Germanyw7 and adults in Australiaw8 produced far more conservative estimatesprevalence at 12 months was 0.7% and 1.2%, respectively. Comorbidity rates are often more than 80%.14 The most common comorbid conditions are depressive disorders, panic disorder, other anxiety disorders, and substance misuse or dependence. Anyone can develop the disorder after a traumatic event, but the incidence increases with the severity of the trauma. Studies have reported an incidence of more than 50% for rape,14w9 30-40%w10 for disasters, and around 19% for veterans of the Vietnam war.w11 Rates for other traumas including accidents and non-physical assaults tend to be lower.14w9 Factors associated most closely with the development of post-traumatic stress disorder are perceived lack of social support and peritraumatic dissociation, but neither increase the risk by more than 50%.15 16 Box 2 lists the factors associated with the disorder across several studies.
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Many people experience traumatic stress symptoms shortly after traumatic events. More than 90% of female victims of sexual assault satisfy the symptom criteria for post-traumatic stress disorder within a week of the event,w12 and 31% of 1010 Londoners described substantial stress 11-13 days after the bombings in London on 7 July 2005.17 Prospective research suggests that rates reduce rapidly over time. After the 11 September terrorist attacks in New York, probable post-traumatic stress disorder in people living south of 110th Street reduced from 7.5% at one month to 1.6% at four months and 0.6% at six months.18 This recovery trajectory is important when deciding how best to provide for individuals after traumatic events.
Despite the associated factors it is difficult to predict exactly who will develop post-traumatic stress disorder after a traumatic event. Various screening instruments have been developed,19 and one of the simplestthe 10 item trauma screening questionnairew13 (box 3)is one of the best validated.19 This questionnaire is probably more helpful in detecting people with the chronic disorder than as a predictive screening instrument shortly after a traumatic event. This is because it produces a high number of false positives unless a high incidence of the chronic disorder is expected.w14 A full assessment that equates to a standard mental health assessment is needed to diagnose the disorder. This should look at presentation, background, mental state examination result, risk assessment result, social factors including support network, and information from other sources including relatives.
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Formal psychological interventions targeted at everyone involved in traumatic events have been ineffective.20w15 w16 Meta-analyses have indicated no differences between people who received an intervention and those who did not in the first six months.20w15 w16 Some studies have reported more negative outcomes in people who receive one-off individual interventions based on critical incident stress debriefing, particularly those with higher levels of symptoms.w17-w19 This has led to concerns about this form of input and recommendations that it should not be used.20 More attention is now being focused on developing stepped or stratified models of response in which immediate practical, social, and emotional support is offered by non-mental health professionals. People with severe ongoing symptoms are offered a formal assessment and a more complex intervention if post-traumatic stress disorder that is not improving is detected.20 21
The most researched complex early interventions have used trauma focused cognitive behaviour therapy over four to 12 sessions, starting from one to three months after the traumatic event.w20-22 These contain components similar to those used to treat the chronic disorder (box 4). No research has suggested a formal role for the early prescription of drugs. However, guidelines from the United Kingdom's National Institute for Health and Clinical Excellence suggest that acute phase symptoms, such as severe insomnia, could be managed with hypnotics or antidepressants.20 Concern about prescribing of benzodiazepines has resulted in many prescribers preferring to recommend a sedative antidepressant or an
agonist, such as prazosin.w23
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A wide range of psychological and pharmacological approaches have been used to treat the chronic disorder. Unfortunately, no good direct comparisons of the two approaches have been carried out, making it difficult to determine their relative efficacies.
Psychological treatment
The psychological treatments with the best evidence are trauma focused cognitive behaviour therapy, which comprises varying combinations of exposure therapy and trauma focused cognitive therapy, and eye movement desensitisation and reprocessing.20 22 23 Both are individual treatments usually provided over the course of up to 12 sessions (box 4; fig 2
). Exposure therapy commonly involves the patient describing the traumatic event in great detail, taping this account, and listening to it repeatedly. In trauma focused cognitive therapy, distorted beliefs and misinterpretations about the traumatic event and its consequences are considered and challenged. In eye movement desensitisation and reprocessing, the recipient focuses on the traumatic experience, associated thoughts, emotions, and sensations while receiving bilateral physical stimulation, most commonly by following the therapist's finger as it is moved from side to side.
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The efficacy of various drugs has provoked considerable debate and conflicting recommendations. A Cochrane review24 and the American Psychiatric Association25 reported benefits for selective serotonin reuptake inhibitorssertraline and paroxetine. NICE do not recommend sertraline, mainly because data from unpublished studies were included in their meta-analysis, and no drug satisfied their predetermined threshold for significant clinical improvement.20 Paroxetine, mirtazapine, amitryptyline, and phenelzine were all significantly better than placebo, although studies of all but paroxetine had small sample sizes. Adding olanzapine to an antidepressant also seemed to be better than adding placebo to augment treatment in people with chronic post-traumatic stress disorder who did not respond fully to antidepressant drugs alone.
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The NICE management guidelines for the chronic disorder recommend that all patients should be offered a course of trauma focused cognitive behaviour therapy or eye movement desensitisation and reprocessing, normally on an individual outpatient basis.20 Trauma focused psychological treatment should usually be given for eight to 12 sessions, with some sessions lasting for 90 minutes if the trauma is considered during the session. The number of sessions may need to be increased, especially after multiple traumatic events and when accompanied by comorbidity or traumatic bereavement. An alternative trauma focused treatment or augmentation with drug treatment should be considered if no improvement is seen. Paroxetine and mirtazapine are recommended for general use, and amitriptyline and phenelzine under specialist supervision. Other factors may precipitate prescription of drugs including patient choice, serious ongoing threat, and lack of immediate availability of psychological treatment. Caution is needed when prescribing because of the well documented problems associated with some antidepressants in recent years.w26
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Few longitudinal follow-up studies of post-traumatic stress disorder have been carried out. In one of the largest cross sectional studies, more than a third of people reported having the disorder six years after they first developed it, with a 50% chance of remission at two years.14 However, these results are of limited value in determining prognosis accurately. Whatever the true figure, for many people with the chronic disorder their condition is severe and enduring.w27 Treatment can help some people many years after they developed the disorder, so that the duration of symptoms should not influence the decision about whether or not to offer treatment.
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This article has focused on adults, but children and adolescents often experience similar symptoms after traumatic events. Younger children often present with other phenomena directly related to the trauma (such as repetitive play and drawing) or more general emotional and behavioural difficulties such as regression, new fears, and aggression.20 Research on post-traumatic stress disorder in children and adolescents lags behind research in adults, but it is increasing. Some evidence suggests that trauma focused cognitive behaviour therapy adapted for age, circumstances, and level of development should be offered to children and adolescents with the disorder, irrespective of the traumatic event.20 The NICE guidelines recommend family involvement where appropriate, and they conclude that there is currently no good evidence for widely used treatments such as play therapy, art therapy, or family therapy for post-traumatic stress disorder.20
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