|
|
||||||||
CLINICAL PRACTICE |
From the G.V. (Sonny) Montgomery VA Medical Center in Jackson, Miss, and the University of Mississippi School of Medicine in Jackson.
Address correspondence to Roy R. Reeves, DO, PhD, Chief of Mental Health, G.V. (Sonny) Montgomery VA Medical Center (11M), 1500 E Woodrow Wilson Dr, Jackson, MS 39216-5116. E-mail: roy.reeves{at}med.va.gov
As the conflict in Iraq continues, public health authorities in the United States anticipate that many returning soldiers will suffer from posttraumatic stress disorder (PTSD). Initially, most of these veterans are likely to consult their primary care physicians about health problems. However, the diagnosis of PTSD is often missed in primary care settings. The author encourages physicians to become better prepared to recognize this disorder in their patients and initiate proper treatment or appropriate referral. Current diagnostic approaches and treatment modalities for combat-related PTSD are reviewedwith an emphasis on clinical procedures for the primary care physician.
In a study involving 746 veterans, Magruder et al1 found that physicians in primary care clinics recognized PTSD in only 40 (46.5%) of 86 patients who were identified with this diagnosis by the Clinician Administered PTSD Scale for DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, 4th Edition).
The present article reviews mental health problems that are commonly seen by primary care physicians as a result of patients' participation in combat, focusing on approaches to the diagnosis and management of PTSD, which is the most prominent of these disorders.
| Stressors Faced By Soldiers in Modern Warfare |
|---|
|
|
|---|
In addition to these stressors, soldiers also face concerns regarding terrorist tactics. As widely noted in the public media, soldiers in these settings often have difficulty determining whether the civilians they encounter are would-be suicide bombers.3 Because of the changing nature of warfare in the 21st century,4 the "frontline" has subsumed individuals in many active-duty support roles that, when compared to combat-ready troops, had previously been considered "safe" (eg, truck drivers, medical personnel).2 Finally, soldiers currently serving in the Middle East combat theater also confront the potential of abuse or execution if captured as well as the possible mutilation and desecration of their bodies by the hands of enemy combatants.
| Psychiatric Disorders Resulting From Exposure to Military Conflict |
|---|
|
|
|---|
The psychiatric differential diagnosis for military patients is broad and varies depending on several factors, including the type and severity of traumatic exposure and the time that has passed since the precipitating event.7 Following exposure to severe trauma, mental disorders tend to occur in three sequential phases.7 In the immediate phaseduring or immediately after traumatic eventsindividuals may experience feelings of anxiety, confusion, disbelief, fear, and numbness. Such problems as acute stress disorder, adjustment disorders, brief psychotic disorder, substance abuse, and exacerbation of preexisting mental illness are considerations.7 In the delayed phase (generally up to 2 weeks after trauma), individuals may experience apathy, autonomic arousal, grief, intrusive thoughts, social withdrawal, or somatic symptoms. Differential diagnoses at this point include anxiety disorders, depressive disorders, psychotic disorders, somatoform disorders, and substance abuse, as well as early PTSD.7 Later, in the chronic phase (months to years after precipitating events), patients may report feelings of disappointment, resentment, sadness, and persistent intrusive symptoms. Diagnoses to consider in this phase include PTSD; depression, dysthymia, and other mood disorders; schizophrenia and other psychotic disorders; and substance abuse or dependence.7
Veterans seeking treatment in the civilian sector will usually be in the chronic phase of illness.7 Thus, the present article focuses on PTSD and related disorders, which are the most common mental health problems expected to occur in this cohort.7 Although this article focuses on treatment of veterans of modern warfare, the same principles of diagnosis and treatment may apply to any patient with PTSD, regardless of the type of stressor that induced the disorder.
Response to traumatic stress varies from person to person. Yet, under sufficient stress, anyone can succumb to mental disturbance. It is normal to have time-limited posttraumatic stress responses that do not persist or impair functioning.7 Such responses are often necessary for survival. However, when catastrophic stress overwhelms adaptive coping responses, posttraumatic psychiatric disorders result.7
Acute Stress Disorder
In the acute phase of abnormal response to trauma (<4 weeks after
trauma), the cluster of symptoms is referred to as acute stress
disorder.8 This
disorder is rarely seen by primary care physicians. Based on the criteria
established in the Text Revision of the
DSM-IV,8 a
patient diagnosed with acute stress disorder must, following a traumatic
event, have at least three dissociative symptoms (eg, depersonalization or
derealization, dissociative amnesia), one or more symptoms of reexperiencing
the trauma (eg, flashback episodes), symptoms of anxiety or increased arousal
(eg, exaggerated startle response), and marked avoidance of stimuli-arousing
recollections of the trauma. These symptoms must cause clinically significant
difficulties in functioning and persist from 2 days to 4
weeks.8 Acute stress
disorder is considered a precursor to
PTSD.8
Posttraumatic Stress Disorder
When the pathologic response to trauma lasts more than 4 weeks, it is
referred to as
PTSD.8 Patients with
PTSD develop symptoms in three categories: reexperiencing the trauma, avoiding
stimuli associated with the trauma, and increased autonomic
arousal.8 Trauma may
be reexperienced as distressing recollections and dreams, flashbacks (in which
the patient may feel and act as if the trauma were recurring), and psychologic
or physiologic stress reactions upon exposure to stimuli associated with the
trauma. Symptoms of avoidance include efforts to refrain from thoughts or
activities related to the trauma, reduced capacity to remember events related
to the trauma, anhedonia, blunted affect, feelings of detachment or
derealization, and a sense of a foreshortened future. Symptoms of increased
arousal include exaggerated startle response, hypervigilance, insomnia,
irritability, and outbursts of
anger.8 To be
diagnosed with PTSD, a patient must exhibit at least one symptom of
reexperiencing, three symptoms of avoidance, and two symptoms of increased
arousaland these symptoms must persist for more than 1
month.8 In addition,
the diagnosis of PTSD requires that the patient's disturbance cause
"clinically significant distress of impairment in social, occupational,
or other important areas of
functioning."8
The DSM-IV-TR criteria for a diagnosis of PTSD are shown in
Figure 1.
|
| Assessment of PTSD in Primary Care Settings |
|---|
|
|
|---|
|
Patients with PTSD may seek consultation in a variety of ways. Although some patients will want to talk about their experiences, most patients will have difficulty discussing their thoughts and feelings about what happened to them.2 It is important not to press traumatized patients too soon or too intensely to talk about their experiences. Rather, patients should be allowed to discuss their traumatic experiences when they are ready to do so. The National Center for PTSD2 recommends that physicians begin the assessment process by concentrating on the immediate needs of the patient and by being prepared to explore the traumatic exposure later in the assessment process. Thus, assessment should start with stabilization and proceed in the following sequence2:
| Treatment Modalities and Psychosocial Interventions |
|---|
|
|
|---|
Education for the Whole Patient: Psychoeducational Interventions
Unfortunately, patients may have misconceptions about mental illness and
PTSD that can interfere with their ability to accept and adhere to effective
treatment regimens. Patient education can help to remove many misconceptions
and improve patients' levels of self-understanding and symptom recognition, as
well as reduce the level of fear and shame they may feel about their
symptoms.10,11
Education empowers patients, providing them with knowledge about the causes of
his or her symptoms, of what will happen in treatment, and of how recovery is
expected to proceed. Patient education should stress the concept that many
symptoms of PTSD are the result of reactions to stress. Patients should be
encouraged to interpret their reactions as a response to overwhelming stress
rather than as a personal weakness. This approach will often lessen the
patient's fears about entering or maintaining
treatment.10,11
Coaching in alternative coping mechanisms may provide patients with practical techniques to deal with the intense emotional problems that they might be having. Coping skills that are commonly taught to patients with PTSD include anger management, anxiety management, communication improvement, and relaxation techniques.10,11 Such training helps patients regain a sense of control over their emotions and related physical symptoms.
Families are intricately involved in the lives of traumatized patients. Both families and patients may benefit from family counseling, as well as couples counseling, parenting classes, and training in conflict resolution.10,11 Family members may also be able to provide relevant patient history (eg, emotionality, drug abuse, sleep habits, socialization) that the patients themselves are unable or unwilling to report.
Cognitive restructuring is designed to help patients review and correct erroneous trauma-related beliefs by providing education about the relationships between thoughts and emotions, by exploring common negative thoughts held by traumatized patients, by identifying personal negative beliefs, by developing alternative interpretations, and by practicing new ways of thinking.10,11 This treatment modality also involves individual self-monitoring of thoughts and the practice of learned techniques in real-life settings.10,11 Finally, cognitive restructuring may help veterans deal with changed perceptions of personal identity caused by participation in combat.
Exposure therapy may be considered after patients are prepared to confront their trauma-related emotions and painful memories. This form of therapy is based on repeated verbalization of traumatic memories by patients.11 Patients are repeatedly exposed to their own individualized fear stimuli until their fear responses are consistently diminished.11 It is important that physicians providing this form of treatment have proper training and experience, however, because it has been found that a patient's condition may deteriorate if this type of therapy is used improperly.11
Psychopharmacologic Intervention
The observation of physiologic alterations (eg, adrenergic hyperactivity),
as well as psychologic alterations, associated with PTSD has led to the use of
pharmacologic agents to treat patients with this
disorder.12
Pharmacotherapy should not be considered the primary modality for managing
PTSD; it is one option among other potential treatment courses previously
discussed. The most effective intervention for PTSD may involve a combination
of pharmacotherapy and psychotherapeutic
modalities.10
Several medications have been used to treat patients with PTSD, some of them
based on well-designed clinical trials and others apparently based solely on
anecdotal
evidence.12
Although, to date, only the antidepressants sertraline hydrochloride and
paroxetine have been approved by the US Food and Drug Administration (FDA) for
the treatment of patients with PTSD, clinical observation of psychophysiologic
alterations associated with the disorder has led to the study of other
antidepressants, mood-stabilizing agents, adrenergic-inhibiting agents, and
antipsychotic
agents.12
AntidepressantsThe most frequently prescribed and most
carefully studied pharmacologic agents used to treat patients with
PTSD.12 A growing
body of literature provides evidence to consider antidepressants the
pharmacologic treatment of first choice for managing the
disorder.12
Virtually every antidepressant available has been used in some context to
attempt to manage the clinical symptoms of
PTSD.12
Selective Serotonin Reuptake Inhibitors: The medications in this class of antidepressants inhibit the reuptake of serotonin by neurons, resulting in increased amounts of serotonin in synapses and improved functioning of serotonin in the central nervous system.12,13 Serotonin has a regulatory effect on norepinephrine activity through the locus ceruleus, helping to modulate excessive external stimuli and reduce feelings of fear. Research and clinical practice have shown that selective serotonin reuptake inhibitors (SSRIs) are effective for managing anxiety, depression, and panic attacks.12
There are several reasons that SSRIs are the current medications of choice for managing PTSD.13 They ameliorate all three PTSD symptom categories. They are effective in managing the psychiatric disorders that often occur comorbidly with PTSD (eg, depression, panic disorder, social phobia). They may reduce such clinical symptoms as aggressive, impulsive, and suicidal behaviors that often complicate management of PTSD, and they cause relatively few adverse effects.13
Open-label and double-blind trials have demonstrated that the SSRIs citalopram hydrobromide, fluoxetine, fluvoxamine maleate, paroxetine, and sertraline are all effective in the treatment of patients with PTSD.13 In addition, paroxetine and sertraline have been assessed in large multisite double-blind controlled trials, and, as previously mentioned, the FDA has approved each of these medications for treatment of patients with major symptom clusters of PTSD.14
The adverse effects of paroxetine, sertraline, and other SSRIs are generally more tolerable for patients than those of other categories of antidepressants.12 Escitalopram oxalate, a relatively new SSRI, may also eventually prove beneficial for patients with PTSD, but clinical experience using this drug to manage PTSD is limited at this time.15
Tricyclic Antidepressants: In addition to antidepressant effects, tricyclic antidepressants (TCAs) have antipanic effects.16-18 Because of the resemblance between panic attacks and severe PTSD arousal symptoms, TCAs may be helpful for managing PTSD. Small controlled clinical trials have been conducted using the TCAs amitriptyline hydrochloride, imipramine, and desipramine.16-18 Amitriptyline, compared with placebo, in 46 veterans with PTSD resulted in better outcomes on the Hamilton Depression, Hamilton Anxiety, Clinical Global Impression, and Impact of Event scales after 8 weeks of treatment.16 A study of 34 veterans with PTSD who were treated with imipramine, the monoamine oxidase inhibitor (MAOI) phenelzine, or placebo showed global assessment improvement in 75% of patients taking imipramine, 64% of patients taking phenelzine, and 27% of patients taking placebo.17 An investigation of 18 veterans with PTSD who were treated with desipramine showed improvement in symptoms of depression but of no other symptoms related to PTSD.18
Tricyclic antidepressants carry the risk of cardiac conduction disturbances, sedation, and overdose.16-18 Because SSRIs and other antidepressants that cause much fewer adverse effects than TCAs are now available, TCAs are no longer commonly prescribed for depression or related mental disturbances.12,13
Monoamine Oxidase Inhibitors: Like TCAs, MAOIs produce antipanic effects. They have been used to treat patients with mixed conditions of anxiety and depression.19 A quantitative analysis by Southwick et al,19 which included 15 mostly open-label clinical trials of TCAs and MAOIs, found that 82% of patients with PTSD who were treated with the MAOI phenelzine reported a reduction in intrusive symptoms, compared with 45% of patients treated with a TCA. Unfortunately, MAOIs must be used with caution because of the risk of hypertensive crisis.19 Thus, they currently are rarely prescribed.
Moclobemide, a reversible inhibitor of monoamine oxidase type-A, is associated with less risk of hypertensive crisis and has been shown in clinical studies to reduce symptoms in all three PTSD symptom categories.20 However, moclobemide is not yet available in the United States.
Other Antidepressants: Several other antidepressants have been investigated for the treatment of patients with PTSD. For example, nefazodone and trazodone hydrochloride are potentially useful because they increase serotonin activity, though not selectively. In six open-label trials reported by Hidalgo et al,21 nefazodone was found to reduce anxiety, nightmares, and global ratings in patients with PTSD. In addition, it was found to possibly help reduce PTSD-related sleep disturbance.21 As of 2001, however, the FDA has required manufacturers and pharmacists to use a black box warning label on nefazodone because of potential risk for hepatotoxicity and liver failure.22 Trazodone has not been proven significantly effective in management of the core symptoms of PTSD.14 Furthermore, because it has a somewhat sedative effect, some clinicians prescribe it in low dosages to treat patients with insomnia.14
Bupropion, duloxetine hydrochloride, mirtazapine, and venlafaxine hydrochloride are other antidepressants that are potentially useful for treating patients with PTSD.23 However, none of these medications have been tested in clinical trials for PTSD. Neither are they approved by the FDA for treatment of patients with PTSD.
Mood-Stabilizing AgentsThe sensitization and kindling
of the limbic system has been hypothetically proposed as a cause of
physiologic changes in
PTSD.24 In this
model, repeated traumatic stress leads to sensitization and kindling, with a
spontaneous limbic discharge resulting from
sensitization.24
Mood-stabilizing agents (ie, medications commonly used as anticonvulsants)
have the potential to prevent this sensitization and kindling or to modulate
these phenomena after they occur. Therefore, they may ameliorate PTSD
symptoms.
Investigations involving mood-stabilizing medications for PTSD management have been limited primarily to open-label studies.14,25,26 Carbamazepine has strong antikindling properties and has been effective in PTSD management in several small open-label clinical trials.23 Gabapentin, lamotrigine, lithium carbonate, topiramate, and valproate sodium have also shown effectiveness in PTSD management in at least one open-label study each.14,26 Thus, despite a strong theoretical basis, there has been only a small amount of systematic investigation to demonstrate the value of mood stabilizers for the treatment of patients with PTSD.
Adrenergic InhibitorsAutonomic dysregulation is
thought to explain many of the physiologic changes seen in patients with
PTSD.27 Patients
with the disorder have elevated levels of plasma norepinephrine at rest,
substantial norepinephrine increases when exposed to trauma-related stimuli,
and down regulation (ie, decrease in sensitivity) of norepinephrine receptors
in platelets due to increased circulation of
norepinephrine.27
Sustained periods of increased norepinephrine levels are thought to increase
the risk of PTSD by contributing to overconsolidation of memories of the
traumatic
event.28
Medications that decrease adrenergic (ie, norepinephrine-mediated) activity
may reduce anxious arousal in patients with PTSD. Propranolol hydrochloride
and other ß-adrenergic blockers reduce the peripheral effects of
norepinephrine.29,30
Propranolol has been shown to improve PTSD symptoms in one small clinical
trial,29 but it was
not helpful in another small
trial.30 Because
2-adrenergic receptor agonists (eg, clonidine, guanfacine
hydrochloride) act at noradrenergic autoreceptors to inhibit the firing of
cells in the locus ceruleus, they may also be responsible for reducing the
release of norepinephrine in the
brain.31 In small
open-label clinical trials, clonidine showed promise in reducing symptoms
among patients with
PTSD.31 The use of
prazosin hydrochloride, an
1-adrenergic receptor antagonist, resulted
in robust improvement of several PTSD symptoms, particularly sleep quality and
reduction of nightmares, in a double-blind crossover protocol by Raskind et
al.32
Antianxiety AgentsBenzodiapines and buspirone
hydrochloride are among the medications that are not currently recommended for
treating patients with PTSD.
Benzodiazepines: Frequently prescribed to reduce anxiety and promote sleep in patients.33 However, their efficacy in managing the specific symptoms of PTSD has not been established. In fact, they may worsen the disorder by virtue of their dissociative and disinhibitory properties.33 In addition, their potential for abuse through addiction remains a major area of concern.33 Therefore, benzodiazepines cannot be recommended for patients with PTSD.
Buspirone: A nonaddictive medication widely used to treat patients with anxiety.34 However, like benzodiazepines, the effectiveness of buspirone for managing the core symptoms of PTSD remains to be established.
Antipsychotic MedicationsAlthough psychotic symptoms
are not included in the diagnostic criteria for PTSD, some patients with PTSD
may experience brief psychotic episodes and also have psychotic symptoms as
part of a comorbid
disorder.4 Use of
older, "conventional" antipsychotic medications (eg, haloperidol)
is not recommended because of the risk of adverse effects and the availability
of more suitable
alternatives.35
Preliminary results suggest that the newer, atypical antipsychotic drugs (eg,
olanzapine, quetiapine fumarate, risperidone) may be useful for patients with
PTSD and psychotic symptoms to augment treatments with first- or second-line
medications.35 Such
patients include those experiencing agitation, dissociation, hypervigilance,
intense paranoia, or brief psychotic reactions associated with PTSD. Atypical
antipsychotic medications may cause serious adverse effects, including tardive
dyskinesia and neuroleptic malignant syndrome, though these effects are less
likely than with conventional antipsychotic
medications.35 Most
atypical antipsychotic drugs may also cause weight
gain.35
The goal of the pharmaceutical management of PTSD is symptom reduction and stabilization. Even if all symptoms do not completely resolve, patients may still benefit from medications by getting a good night's sleep and being less anxious and irritable. Figure 3 summarizes some of the medications that have proven effective or that are potentially effective for the clinical management of PTSD. Acute PTSD responds better to pharmaceutical management than does chronic PTSD, and, generally, the earlier treatment begins, the better.10,12,33
|
In all cases, physicians need to be aware of potential adverse effects associated with the medications prescribed. Appropriate patient monitoring is also essential. Pharmacotherapy should be used in combination with psychosocial treatment modalities as well as other treatment options to ensure a comprehensive approach to patient care.
Osteopathic Manipulative Treatment and PTSD
To date, there have been no studies investigating the effectiveness of
osteopathic manipulative treatment (OMT) in patients with PTSD. Nevertheless,
it seems logical that OMT could benefit these patients. One might hypothesize
that patients with posttraumatic stress are likely to have increased
sympathetic nervous system activity and associated somatic dysfunction,
particularly in the thoracolumbar region. Uncomfortable paravertebral muscle
spasm may accompany these dysfunctions. Thus, in my view, addressing these
dysfunctions with appropriate osteopathic manipulative techniques could aid in
the healing processas well as help improve patient-physician rapport
and patient compliance with supplemental therapeutic modalities.
| Other War-Related Mental Disorders |
|---|
|
|
|---|
A number of mental disorders, including depression, mania, panic disorder, and schizophrenia, commonly have an age of onset between the late teens and early 30sthe same age range of many individuals engaged in the nation's current military conflicts.2,5-8 In a person who is susceptible to a particular disorder, that disorder could be precipitated by the stresses of combat situations. In addition, mental disorders already present, but in latent or controlled states, could worsen as a result of the impact of such trauma.2,5-8 Thus, it is important for primary care physicians to consider the full range of possible psychiatric disorders before making a diagnosis.
|
| Ongoing Support for Patients With PTSD |
|---|
|
|
|---|
A number of helpful online resources on PTSD are available for both physicians and veterans. A list of these resources is presented in Figure 4.
| Conclusions |
|---|
|
|
|---|
The principles discussed in the current article are presented primarily in the context of combat-related PTSD. However, the same principles can apply to the treatment of all patients with PTSDregardless of the nature of the trauma. Some examples of noncombat-related causes of PTSD include physical assault, exposure to natural disasters, and terrorist attacks. Patients who have experienced such trauma may benefit from the same types of interventions provided to military veterans with PTSD.
Submitted January 3, 2006; accepted May 4, 2006.
| References |
|---|
|
|
|---|
2. Litz B, Orsillo SM. The returning veteran of the Iraq War: background issues and assessment guidelines. In: Iraq War Clinician Guide. 2nd ed. White River Station, Vt: National Center for Post-Traumatic Stress Disorder, Department of Veterans Affairs; 2004:21-32. Available at: http://www.ncptsd.va.gov/ncmain/ncdocs/manuals/iraq_clinician_guide_ch_3.pdf. Accessed April 13, 2007.
3. Montagne R, Hammes T. Italian's death and rules of engagement in Iraq [interview]. Morning Edition. Washington DC: National Public Radio. March 9, 2005. Available at: http://www.npr.org/templates/story/story.php?storyId=4527852. Accessed May 30, 2007.
4. Echevarria AJ II. Globalization and the Nature of War. Carlisle, Pa: Strategic War Studies Institute, US Army War College; 2003. Available at: http://www.strategicstudiesinstitute.army.mil/pdffiles/PUB215.pdf. Accessed May 30, 2007.
5. Kang HK, Natelson BH, Mahan CM, Lee KY, Murphy FM. Post-traumatic stress disorder and chronic fatigue syndrome-like illness among Gulf War veterans: a population-based survey of 30,000 veterans. Am J Epidemiol. 2003;157:141-148. Available at: http://aje.oxfordjournals.org/cgi/content/full/157/2/141. Accessed April 13, 2007.
6. Hoge CW, Castro CA, Messer SC, McGurk DM, Cotting, DI, Koffman RL.
Combat duty in Iraq and Afghanistan, mental health problems, and barriers to
care. N Eng J Med.2004; 351:13
-22.
7. Cozza SJ, Benedek DM, Bradley JC, Grieger TA, Nam TS, Waldrep DA. Topics specific to the psychiatric treatment of military personnel. In: Iraq War Clinician Guide. 2nd ed. White River Station, Vt: National Center for Post-Traumatic Stress Disorder, Department of Veterans Affairs; 2004:4-20. Available at: http://www.ncptsd.va.gov/ncmain/ncdocs/manuals/iraq_clinician_guide_ch_2.pdf. Accessed April 13, 2007.
8. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision. Washington, DC: American Psychiatric Press:2000 : 463-468.
9. Prins A, Kimerling R, Leskin G. PTSD in Iraq War veterans: implications for primary care. In: Iraq War Clinician Guide. 2nd ed. White River Station, Vt: National Center for Post-Traumatic Stress Disorder, Department of Veterans Affairs; 2004:58-61. Available at: http://www.ncptsd.va.gov/ncmain/ncdocs/manuals/iraq_clinician_guide_ch_7.pdf. Accessed April 13, 2007.
10. Ruzek JI, Curran E, Friedman MJ, Gusman FD, Southwick SM, Swales P, et al. Treatment of the returning Iraq War veteran. In: Iraq War Clinician Guide. 2nd ed. White River Station, Vt: National Center for Post-Traumatic Stress Disorder, Department of Veterans Affairs; 2004:33-45. Available at: http://www.ncptsd.va.gov/ncmain/ncdocs/manuals/iraq_clinician_guide_ch_4.pd. Accessed April 13, 2007.
11. Foa EB, Keane TM, Friedman MJ. Effective Treatments for PTSD: Practice Guidelines from the International Society for Traumatic Stress Studies. New York, NY: Guilford Press;2000 .
12. Schoenfeld FB, Marmar CR, Neylan TC. Current concepts in pharmacotherapy for posttraumatic stress disorder. Psychiatr Serv. 2004;55:519-531. Available at: http://ps.psychiatryonline.org/cgi/content/full/55/5/519. Accessed April 13, 2007.
13. Ursano RJ, Bell C, Eth S, Freidman M, Norwood A, Pfefferbaum B, et al. Practice guidelines for the treatment of patients with acute stress disorder and posttraumatic stress disorder. Am J Psychiatry. 2004;161(suppl 11):3-31. Available at: http://www.psych.org/psych_pract/treatg/pg/PTSD-PG-PartsA-B-C-New.pdf. Accessed April 13, 2007.
14. Asnis GM, Kohn SR, Henderson M, Brown NL. SSRIs versus non-SSRIs in post-traumatic stress disorder: an update with recommendations. Drugs. 2004;64:383 -404.[Medline]
15. Robert S, Hamner MB, Ulmer HG, Lorberbaum JP, Durkalski VL. Open-label trial of escitalopram in the treatment of posttraumatic stress disorder. J Clin Psychiatry.2006; 67:1522 -1526.[Medline]
16. Davidson J, Kudler H, Smith R, Mahorney SL, Lipper S, Hammett E, et
al. Treatment of posttraumatic stress disorder with amitriptyline and placebo.
Arch Gen Psychiatry.1990; 47:259
-266.
17. Frank JB, Kosten T, Giller EL Jr, Dan E. A randomized clinical
trial of phenelzine and imipramine for posttraumatic stress disorder.
Am J Psychiatry.1988; 145:1289
-1291.
18. Reist C, Kauffmann CD, Haier RJ, Sangdahl C, DeMet EM, Chicz-DeMet
A, et al. A controlled trial of desipramine in 18 men with posttraumatic
stress disorder. Am J Psychiatry.1989; 146:513
-516.
19. Southwick SM, Yehuda R, Giller E, Charney ES. Use of tricyclics and monoamine oxidase inhibitors in the treatment of PTSD: a quantitative review. In: Marburg MM, ed. Catecholamine Function in Posttraumatic Stress Disorder: Emerging Concepts. Washington, DC: American Psychiatric Press; 1994.
20. Neal LA, Shapland W, Fox C. An open trial of moclobemide in the treatment of post-traumatic stress disorder. Int Clin Psychopharmacol. 1997;12:231 -237.[Medline]
21. Hidalgo R, Hertzberg MA, Mellman T, Petty F, Tucker P, Weisler R, et al. Nefazodone in post-traumatic stress disorder: results from six open-label trials. Int Clin Psychopharmacol.1999; 14:61 -68.[Medline]
22. Jody DM. Important drug warning including black box information: Serzone [US Food and Drug Administration Web site]. 2001. Available at: http://www.fda.gov/medwatch/SAFETY/2002/serzone_deardoc.PDF. Accessed April 13, 2007.
23. Davidson J, Baldwin D, Stein DJ, Kuper E, Benattia I, Ahmed S, et
al. Treatment of posttraumatic stress disorder with venlafaxine extended
release: a 6-month randomized controlled trial. Arch Gen
Psychiatry. 2006;63:1158
-1165.
24. Grillon C, Morgan CA, Southwick SM, Davis M, Charney DS. Baseline startle amplitude and prepulse inhibition in Vietnam veterans with posttraumatic stress disorder. Psychiatry Res.1996; 64:169 -178.[Medline]
25. Keck PE Jr, McElroy SL, Friedman LM. Valproate and carbamazepine in the treatment of panic and posttraumatic stress disorders, withdrawal states, and behavioral dyscontrol syndromes [review]. J Clin Psychopharmacol.1992; 12(1 suppl):36S -41S.[Medline]
26. Hamner MB, Brodrick PS, Labbate LA. Gabapentin in PTSD: a retrospective, clinical series of adjunctive therapy. Ann Clin Psychiatry. 2001;13:141 -146.[Medline]
27. Yehuda R, Siever LJ, Teicher MH, Levengood RA, Gerber DK, Schmeidler J, et al. Plasma norepinephrine and 3-methoxy-4-hydroxyphenylglycol concentrations and severity of depression in posttraumatic stress disorder and major depressive disorder. Biol Psychiatry.1998; 44:56 -63.[Medline]
28. Pitman RK. Post-traumatic stress disorder, hormones, and memory [review]. Biol Psychiatry.1989; 26:221 -223.[Medline]
29. Kolb LC, Burris BC, Griffiths S. Propranolol and clonidine in the treatment of post-traumatic stress disorders of war. In: Van der Kolb BA, ed. Post-Traumatic Stress Disorder: Psychological and Biological Sequelae. Washington, DC: American Psychiatric Press;1984 : 98-105.
30. Kinzie JD. Therapeutic approaches to traumatized Cambodian refugees. J Traumatic Stress.1989; 2:75 -91.
31. Boehnlein JK, Kinzie JD. Pharmacologic reduction of CNS noradrenergic activity in PTSD: the case for clonidine and prazosin. J Psychiatr Pract.2007; 13:72 -78.[Medline]
32. Raskind MA, Peskind ER, Kanter ED, Petrie EC, Radant A, Thompson CE, et al. Reduction of nightmares and other PTSD symptoms in combat veterans by prazosin: a placebo controlled study. Am J Psychiatry. 2003;160:371-373. Available at: http://ajp.psychiatryonline.org/cgi/content/full/160/2/371. Accessed April 13, 2007.
33. Ramaswamy S, Madaan V, Qadri F, Heaney CJ, North TC, Padala PR, et al. A primary care perspective of posttraumatic stress disorder for the Department of Veterans Affairs. Prim Care Companion J Clin Psychiatry. 2005;7:180-187. Available at: http://www.psychiatrist.com/pcc/pccpdf/v07n04/v07n0407.pdf. Accessed April 13, 2007.
34. Hamner M, Ulmer H, Horne D. Buspirone potentiation of antidepressants in the treatment of PTSD. Depress Anxiety. 1997;5:137 -139.[Medline]
35. Newcomer JW. Metabolic considerations in the use of antipsychotic medications: a review of recent evidence [review]. J Clin Psychiatry.2007; 68(suppl 1):20 -27.
36. Lande RG, Marin BA, Chang AS, Lande GR. Gender differences and alcohol use in the US Army. J Am Osteopath Assoc. In press.
37. Weisberg RB, Bruce SE, Machan JT, Kessler RC, Culpepper L, Keller MB. Nonpsychiatric illness among primary care patients with trauma histories and posttraumatic stress disorder. Psychiatr Serv. 2002;53:848-854. Available at: http://ps.psychiatryonline.org/cgi/content/full/53/7/848. Accessed April 13, 2007.
38. Lande RG, Marin BA, Ruzek JI. Substance abuse in the deployment environment. In: Iraq War Clinician Guide. 2nd ed. White River Station, Vt: National Center for Post-Traumatic Stress Disorder, Department of Veterans Affairs; 2004:79-82. Available at: http://www.ncptsd.va.gov/ncmain/ncdocs/manuals/iraq_clinician_guide_ch_12.pdf. Accessed April 13, 2007.
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |