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Post traumatic stress disorder PTSD

Post-traumatic stress disorder (PTSD) is a severe condition with a lifetime prevalence of about 12.5% in women and 6.2% in men (Pigott, 1999). About one in four individuals exposed to trauma develop the syndrome. Drug treatments are still being developed, mostly using antidepressants. Few systematic data are available on the pharmacoeconomics of the condition. [Pg.65]

McCrone P, Knapp M, Cawkill P (2001). Post-traumatic stress disorder (PTSD) in the UK Armed Forces health economic consideration. In press. [Pg.67]

A prospective, randomized, placebo-controlled trial of paroxetine in adults with chronic post-traumatic stress disorder (PTSD) was recently conducted (Marshall etal., 2007). The subjects were New Yorkers, predominantly female (67%) and Hispanic (65.4%). Seventy subjects entered the study and after a one week placebo lead-in, 52 subjects were randomized to placebo or paroxetine for ten weeks. The subjects were treated with a flexible dosage design (mean dosage, 40.4 mg/day). Dropout rates were 32% for paroxetine and 51.9% for placebo. There were no differences in rates of adverse effects between treatment arms. Paroxetine was superior to placebo in ameliorating the primary symptoms of PTSD (56% vs. 22.2%). [Pg.99]

Panic disorder Agoraphobia with panic disorder Agoraphobia without panic disorder Specific phobia Social phobia Generalised anxiety disorder Mild anxiety and depression disorder Obsessive compulsive disorder Acute stress disorder Post-traumatic stress disorder (PTSD) Adjustment disorder Panic disorder without agoraphobia Panic disorder with agoraphobia Agoraphobia Specific phobia Social phobia (also called social anxiety disorder) Generalised anxiety disorder Obsessive compulsive disorder Acute stress disorder Post-traumatic stress disorder (PTSD)... [Pg.129]

The development of mild forms of anxiety and neuroveg-etative and/or cognitive responses to stress may represent an adaptive evolutionary step against environmentally (external) or self-triggered (internal) threats, but maladaptive reactions have also emerged in human evolution. Thus, anxiety disorders are maladaptive conditions in which disproportionate responses to stress, or even self-evoked responses, are displayed. Anxiety disorders are one of the most frequent psychiatric illnesses, and have a lifetime prevalence of 15- 20% [1, 89]. The most common presentations are generalized anxiety disorder, with a lifetime prevalence rate of close to 5% [1, 89] social anxiety disorder, with very variable lifetime prevalence rates ranging from 2 to 14% [90] panic disorder, with rates from 2 to 4% [1,89] and post-traumatic stress disorder (PTSD), with a prevalence rate close to 8%. Specific phobias, acute stress and obsessive-compulsive behavior are other clinical presentations of anxiety disorders. [Pg.899]

Panic disorder is characterized by the occurrence of panic attacks that occur spontaneously and lead to persistent worry about subsequent attacks and/or behavioral changes intended to minimize the likelihood of further attacks. Sporadic panic attacks are not limited, however, to those with syndromal panic disorder as they do occur occasionally in normal individuals and in those with other syndromal psychiatric disorders. The hallmark of panic disorder is that the panic attacks occur without warning in an unpredictable variety of settings, whereas panic attacks associated with other disorders typically occur in response to a predictable stimulus. For example, a person with acrophobia might experience a panic attack when on a glass elevator. A patient with obsessive-compulsive disorder (OCD) with contamination fears may have a panic attack when confronted with the sight of refuse, and a combat veteran with post-traumatic stress disorder (PTSD) may experience a panic attack when a helicopter flies overhead or an automobile backfires. [Pg.129]

Post-traumatic Stress Disorder (PTSD). The same distinction holds true for PTSD. Reminders of the tranma (e.g., sexual intimacy for a rape survivor loud noises for a combat veteran) can trigger panic attacks. Furthermore, PTSD is associated with a variety of avoidant behaviors that can resemble agoraphobia. In the case of PTSD, the avoidance is specifically targeted at reminders of the trauma. For example, places or people who in some way cue memories of the traumatic event are avoided. As for agoraphobia, the avoidance tends to be less specific. It is any sitnation from which it would be difficult to escape should a panic attack occur that is avoided. [Pg.140]

Post-traumatic Stress Disorder (PTSD). Persistent anxiety is an invariable feature of both GAD and PTSD. In the case of GAD, the worry relates to a wide array of situations. As for PTSD, the worry relates to a perceived threat that is often directly, or at least indirectly, reminiscent of the previous trauma. [Pg.147]

Although we are focusing on the primary sleep disorders, sleep disturbance quite often occurs as a symptom of another illness. Depression, anxiety, and substance abuse can impair the quality of sleep, though in the setting of chronic insomnia, other psychiatric disorders account for less than 50% of cases. Nightmares are a frequent complication of post-traumatic stress disorder (PTSD), and pain, endocrine conditions, and a host of medical illnesses can produce sleep problems. Thus, when discussing insomnia or hypersomnia, we are well advised to remember that these can be either a symptom of a psychiatric syndrome, a medical illness, or a sleep disorder. [Pg.260]

Most of such studies have excluded women. In one study of 1272 female pretrial detainees, over 80% met criteria for at least one psychiatric disorder, with substance abuse and post-traumatic stress disorder (PTSD) being the most common (Teplin et al., 1996). Similar results were found in 805 women felons, with high rates of substance abuse, borderline personality disorders, and ASP, compared to respective rates in the community (Jordan et al., 1996). [Pg.210]

The selective serotonin reuptake inhibitors (SSRI) have been used in adults for a wide variety of disorders, including major depression, social anxiety (social phobia), generalized anxiety disorder (GAD), eating disorders, premenstrual dysphoric disorder (PMDD), post-traumatic stress disorder (PTSD), panic, obsessive-compulsive disorder (OCD), trichotillomania, and migraine headaches. Some of the specific SSRI agents have an approved indication in adults for some of these disorders, as reviewed later in this chapter. The SSRIs have also been tried in children and in adults for symptomatic treatment of pain syndromes, aggressive or irritable ( short fuse ) behavior, and for self-injurious and repetitive behaviors. This chapter will review general aspects of the SSRIs and discuss their approved indications in children and adolescents. [Pg.274]

Pediatric patients who develop psychiatric syndromes following acute medical illness or injury or invasive procedures (e.g., a child who develops post-traumatic stress disorder [PTSD] following a motor vehicle accident and trauma a child who develops PTSD following stem cell transplantation)... [Pg.631]

In four instances, the agency has invoked this rule at the time of approval of supplements for new indications for psychotropic drugs already approved for other psychiatric indications. It was noted in the approval letters for these supplements that, since the drugs in question would likely be used in children and/ or adolescents with the newly approved indications, the FDA required the sponsors of these products to conduct studies that would be pertinent to such use in the pediatric population. Since the products were ready for approval in adults, the FDA deferred the required pediatric studies to a future date. Alternatively, sponsors could make an argument for waiver of the requirement. The drug products and indications for which the FDA has required studies under the Pediatric Rule are as follows paroxetine for social anxiety disorder sertraline for post-traumatic stress disorder (PTSD) olanzapine for acute mania in bipolar disorder and fluoxetine in premenstrual dysphoric disorder (PMDD). [Pg.731]

Post-traumatic stress disorder (PTSD)—Occurs following the experience of a severe threat to life or physical well-being. [Pg.113]

Another important factor that may favor placebo responses in clinical studies is probably the patient recruitment strategy, as suggested by the following observation two almost identically designed studies with fluoxetine vs. placebo in the treatment of post-traumatic stress disorder (PTSD) were performed, but only one of them resulted in a significant difference between... [Pg.167]

Post-traumatic Stress Disorder (PTSD) Scales... [Pg.201]

Some of the growth in antidepressant use may be related to the broad application of these agents for conditions other than major depression. For example, antidepressants have received FDA approvals for the treatment of panic disorder, generalized anxiety disorder (GAD), post-traumatic stress disorder (PTSD), and obsessive-compulsive disorder (OCD). In addition, antidepressants are commonly used to treat pain disorders such as neuropathic pain and the pain associated with fibromyalgia. Some antidepressants are used for treating premenstrual dysphoric disorder (PMDD), mitigating the vasomotor symptoms of menopause, and treating stress urinary incontinence. Thus, antidepressants have a broad... [Pg.647]

Food and Drug Administration (FDA) approved the first clinical trial of MDMA (ecstasy) as a treatment for post-traumatic stress disorder (PTSD) in the United States. As of 2002 the proposed research waited for additional approvals. [Pg.24]

Post traumatic stress disorder (PTSD) is the only psychiatric condition whose definition demands a particular stressor to precede its appearance. Unlike the other anxiety disorders, it is only in the past decade that the biology of PTSD has come under scrutiny. Furthermore, although PTSD can occur following various traumatic events (for example, sexual abuse, accidents and torture), most emphasis has been placed on combat-related disorders. [Pg.227]

Pathological inability to forget aversive events may be therefore explained by reduced NE transmission in the PFC (Mueller et al., 2008b). Therefore, the NE system might playan important role in the pathology of generalized anxiety disorder (GAD), panic disorder (PD) and post-traumatic stress disorder (PTSD). However, different NE pathways may be involved. [Pg.372]

September 2004 during a nightmare that unfolded in Washington State and Arizona. Local conditions — mold, pollen, daily controlled forest fire burnings, pesticides — brought on severe MCS, and along with it, post-traumatic stress disorder (PTSD). [Pg.85]


See other pages where Post traumatic stress disorder PTSD is mentioned: [Pg.396]    [Pg.274]    [Pg.120]    [Pg.895]    [Pg.72]    [Pg.574]    [Pg.42]    [Pg.107]    [Pg.111]    [Pg.126]    [Pg.264]    [Pg.397]    [Pg.497]    [Pg.580]    [Pg.618]    [Pg.660]    [Pg.188]    [Pg.242]    [Pg.292]    [Pg.184]    [Pg.81]   
See also in sourсe #XX -- [ Pg.477 , Pg.484 , Pg.485 , Pg.487 , Pg.491 , Pg.492 ]




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