Psychotherapy for Military-Related PTSD A Review of ...Psychotherapy for Military-Related PTSD A...

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See discussions, stats, and author profiles for this publication at: http://www.researchgate.net/publication/280666600 Psychotherapy for Military-Related PTSD A Review of Randomized Clinical Trials ARTICLE in JAMA THE JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION · AUGUST 2015 Impact Factor: 30.39 · DOI: 10.1001/jama.2015.8370 DOWNLOADS 8 VIEWS 35 4 AUTHORS, INCLUDING: Maria Steenkamp NYU Langone Medical Center 25 PUBLICATIONS 186 CITATIONS SEE PROFILE Charles Marmar NYU Langone Medical Center 224 PUBLICATIONS 9,573 CITATIONS SEE PROFILE Available from: Maria Steenkamp Retrieved on: 18 August 2015

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PsychotherapyforMilitary-RelatedPTSDAReviewofRandomizedClinicalTrials

ARTICLEinJAMATHEJOURNALOFTHEAMERICANMEDICALASSOCIATION·AUGUST2015

ImpactFactor:30.39·DOI:10.1001/jama.2015.8370

DOWNLOADS

8

VIEWS

35

4AUTHORS,INCLUDING:

MariaSteenkamp

NYULangoneMedicalCenter

25PUBLICATIONS186CITATIONS

SEEPROFILE

CharlesMarmar

NYULangoneMedicalCenter

224PUBLICATIONS9,573CITATIONS

SEEPROFILE

Availablefrom:MariaSteenkamp

Retrievedon:18August2015

Page 2: Psychotherapy for Military-Related PTSD A Review of ...Psychotherapy for Military-Related PTSD A Review of Randomized Clinical Trials ARTICLE in JAMA THE JOURNAL OF THE AMERICAN MEDICAL

Copyright 2015 American Medical Association. All rights reserved.

Psychotherapy for Military-Related PTSDA Review of Randomized Clinical TrialsMaria M. Steenkamp, PhD; Brett T. Litz, PhD; Charles W. Hoge, MD; Charles R. Marmar, MD

IMPORTANCE Posttraumatic stress disorder (PTSD) is a disabling psychiatric disordercommon among military personnel and veterans. First-line psychotherapies most oftenrecommended for PTSD consist mainly of “trauma-focused” psychotherapies that involvefocusing on details of the trauma or associated cognitive and emotional effects.

OBJECTIVE To examine the effectiveness of psychotherapies for PTSD in military and veteranpopulations.

EVIDENCE REVIEW PubMed, PsycINFO, and PILOTS were searched for randomized clinicaltrials (RCTs) of individual and group psychotherapies for PTSD in military personnel andveterans, published from January 1980 to March 1, 2015. We also searched reference lists ofarticles, selected reviews, and meta-analyses. Of 891 publications initially identified, 36 wereincluded.

FINDINGS Two trauma-focused therapies, cognitive processing therapy (CPT) and prolongedexposure, have been the most frequently studied psychotherapies for military-related PTSD.Five RCTs of CPT (that included 481 patients) and 4 RCTs of prolonged exposure (thatincluded 402 patients) met inclusion criteria. Focusing on intent-to-treat outcomes,within-group posttreatment effect sizes for CPT and prolonged exposure were large (Cohen drange, 0.78-1.10). CPT and prolonged exposure also outperformed waitlist andtreatment-as-usual control conditions. Forty-nine percent to 70% of participants receivingCPT and prolonged exposure attained clinically meaningful symptom improvement (definedas a 10- to 12-point decrease in interviewer-assessed or self-reported symptoms). However,mean posttreatment scores for CPT and prolonged exposure remained at or above clinicalcriteria for PTSD, and approximately two-thirds of patients receiving CPT or prolongedexposure retained their PTSD diagnosis after treatment (range, 60%-72%). CPT andprolonged exposure were marginally superior compared with non–trauma-focusedpsychotherapy comparison conditions.

CONCLUSIONS AND RELEVANCE In military and veteran populations, trials of the first-linetrauma-focused interventions CPT and prolonged exposure have shown clinically meaningfulimprovements for many patients with PTSD. However, nonresponse rates have been high,many patients continue to have symptoms, and trauma-focused interventions showmarginally superior results compared with active control conditions. There is a need forimprovement in existing PTSD treatments and for development and testing of novelevidence-based treatments, both trauma-focused and non–trauma-focused.

JAMA. 2015;314(5):489-500. doi:10.1001/jama.2015.8370

Editorial page 453

Author Audio Interview atjama.com

Related article page 501

Supplemental content atjama.com

Author Affiliations: Steven andAlexandra Cohen Veterans Center forPosttraumatic Stress and TraumaticBrain Injury, New York UniversityLangone School of Medicine,New York, New York (Steenkamp,Marmar); VA Boston HealthcareSystem, Massachusetts VeteransEpidemiological Research andInformation Center (MAVERIC),Boston University School ofMedicine, Boston (Litz); Walter ReedArmy Institute of Research,Silver Spring, Maryland (Hoge).

Corresponding Author: Maria M.Steenkamp, PhD, Steven andAlexandra Cohen VeteransCenter for Posttraumatic Stressand Traumatic Brain Injury,New York University LangoneSchool of Medicine,One Park Ave, Room 8-107,New York, NY 10016([email protected]).

Section Editor: Mary McGraeMcDermott, MD, Senior Editor.

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P osttraumatic stress disorder (PTSD) is a disabling psychiat-ric condition common among military personnel and vet-erans, and consequently, a significant public health chal-

lenge. Approximately 13% of Iraq or Afghanistan veterans1 and10% of Gulf War veterans who experienced combat have PTSD,2

and 11% of Vietnam veterans continue to report PTSD symptomsthat impair functioning 40 years after the war.3 Military-relatedPTSD is often accompanied by a variety of mental and physicalhealth conditions, particularly depression, anxiety, and substancemisuse.4,5 War veterans with PTSD also have extensive functionalimpairments such as unemployment and income disparities,6 fam-ily and relationship difficulties,7 aggressive behavior,8 and poorquality of life.9 Twenty-three percent of Vietnam veterans withPTSD (compared with 4% among those without PTSD) reportedbeing unemployed when assessed 15 or more years after service,33% (compared with 16%) reported perpetrating serious interper-sonal violence in the past year, and 40% (compared with 10%)reported low well-being.10 Risk factors for PTSD in military popula-tions include war zone exposure, being wounded, younger agewhen deployed, less education, greater exposure to childhoodtrauma, and less social support during and after deployment.11 Ifleft untreated, military-related PTSD often follows a chroniccourse, resulting in lifelong dysfunction.12

Over the past 10 years, an increasing number of randomizedclinical trials (RCTs) of PTSD treatments in military personnel and vet-erans have emerged, coinciding with a major policy shift in the De-partments of Defense (DoD) and Veterans Affairs (VA) toward thera-pies considered evidence-based.13 Psychotherapy is moreconsistently recommended as first-line treatment for PTSD thanmedications across clinical practice guidelines and in DoD and VApractice settings. In this review, we focus on RCTs of individual andgroup psychotherapies for PTSD in military and veteran popula-tions to examine the degree of symptom improvement and effi-cacy relative to control conditions.

MethodsWe searched PubMed, PsycINFO, and PILOTS for RCTs of psycho-therapy for PTSD among military personnel or veterans, pub-lished from January 1980 (the year the PTSD diagnosis was firstintroduced) to March 1, 2015. PTSD was defined according to thediagnostic criteria accepted at the time of the RCTs, which mostoften followed the Diagnostic and Statistical Manual for MentalDisorders (Fourth Edition, Text Revision).14 This definitionincluded 3 clusters of symptoms following trauma, present for atleast 1 month, including reexperiencing the trauma (eg, intrusivethoughts or nightmares), avoiding reminders of the trauma, andhyperarousal (eg, hypervigilance, irritability, difficulty concentrat-ing). We also manually searched reference lists of articles,selected reviews, and meta-analyses.

We selected only English-language RCTs that (1) were con-ducted with service members, veterans, or both; (2) reported PTSDas an inclusion criterion; (3) reported at least pretreatment and post-treatment total scores on standardized PTSD clinical measures;(4) used either individual or group psychotherapy; and (5) did notsolely involve pharmacotherapies, pharmacologically augmentedpsychotherapy, or other biological treatments. We did not include

trials of collaborative care models, dosing studies, trials targeting spe-cific symptoms (eg, insomnia, anger) rather than the full syn-drome, or trials targeting substance use disorders comorbid withPTSD. We focused on intent-to-treat outcomes, when available.

ResultsOf 891 publications initially identif ied, 36 were included(Table 115-27,29,58 and Table 230-50; eFigure in the Supplement). Wegrouped trials of the most commonly studied first-line trauma-focused therapies (ie, therapies given the highest evidence recom-mendations in clinical guidelines) (Table 1), followed by second-lineinterventions (ie, therapies for which there is less evidence sup-porting effectiveness) (Table 2). The principal efficacy criteria,reported variably in published trials, included degree of clinicallysignificant PTSD symptom improvement (typically defined as a 10-or 12-point decline in self-reported or interviewer-assessed PTSDsymptoms),23 mean PTSD symptom level at posttreatment andfollow-up, loss of PTSD diagnosis, degree of symptom remission,and effect sizes (most commonly Cohen d, calculated as the differ-ence between 2 mean PTSD severity scores divided by the pooledSD [a d of 0.20 indicates a small effect size; a d of 0.50, a mediumeffect size; and a d of 0.80, a large effect size]).

First-Line PsychotherapiesThe diverse range of PTSD psychotherapies are broadly groupedinto “trauma-focused” and non–trauma-focused. Trauma-focusedtherapies are cognitive-behavioral treatments that involve a rangeof techniques that attend to the details of the trauma or associatedemotions or cognitive processes (beliefs, assumptions). The 3 mostwidely studied trauma-focused therapies, which are consideredleading evidence-based psychotherapies by all major clinicalguidelines,51 are cognitive processing therapy (CPT), prolongedexposure therapy, and eye movement desensitization and repro-cessing (EMDR) therapy (Box). All are manualized (ie, protocolizedin a session-by-session manner), delivered principally in specialtycare settings, use different techniques and theoretical rationales,require sustained engagement (typically 12 sessions), and can beemotionally demanding for patients. Prolonged exposure includesasking patients to repeatedly recount the trauma to extinguish fearresponses associated with the memory (a technique known as ima-ginal exposure) and to practice facing trauma reminders and trig-gers in the real world (known as in vivo exposure). CPT involveschanging maladaptive beliefs related to the trauma (known as cog-nitive restructuring), with the option of writing an account of thetrauma. EMDR also comprises exposure and cognitive restructuringelements but asks patients to maintain dual focus on an externalstimulus (eg, eye-movement tracking of therapist hand move-ments) while thinking about the trauma.

Meta-analyses of mostly civilian studies show large pre-posttreatment effects (within-group) and between-group effects com-pared with control conditions for these treatments, with generallycomparable outcomes for CPT, prolonged exposure, EMDR, andother trauma-focused modalities.52 In contrast, non–trauma-focused therapies attend principally to current life stressors, reac-tions, goals, or relationships. The only non–trauma-focused therapythat has received high-level evidence statements in PTSD clinical

Clinical Review & Education Review Psychotherapy for Military-Related PTSD

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Tabl

e1.

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com

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Psychotherapy for Military-Related PTSD Review Clinical Review & Education

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Tabl

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practice guidelines is stress inoculation training, which involves stressmanagement skills (eg, breathing, muscle relaxation) and applyingthese skills to day-to-day stressors and reminders of the trauma.

In 2008, CPT and prolonged exposure were selected by the VAfor nationwide dissemination in an attempt to better standardize carefor veterans, and 98% of VA centers now offer both.53,54 Initially,neither intervention was validated sufficiently in active duty mili-tary or veteran populations; they were originally tested largely in ci-vilian female survivors of sexual assault. EMDR has not been dis-seminated within the VA and DoD, and EMDR research has receivedcomparatively little VA or DoD funding but has strong evidence incivilian studies and high-level endorsement from many guidelinesinternationally. RCTs of stress inoculation training are lacking in vet-erans, and it is infrequently used in the VA and DoD.

Efficacy of CPTFive trials of CPT (that included 481 patients) met inclusion crite-ria; 4 enrolled veterans15-18 and 1 enrolled active-duty soldiers.19

The first included a waitlist comparison,15 and subsequent studiesused either a treatment-as-usual comparison or an active com-parison condition known as present-centered therapy, a non–trauma-focused treatment protocol focused largely on current lifeproblems. One noninferiority trial compared group CPT deliveredin person vs via telemedicine.18 Treatment dropout rates rangedfrom 16% to 35%.

Within-group intent-to-treat effect sizes for CPT werereported in 3 trials and were large (d = 0.78,18 d = 1.10,19 andd = 1.0217). All trials reported the percentage of patients attainingmeaningful symptom change (49%-67%), and the mean posttreat-ment PTSD scores, which remained at or above clinical cutoffs (eg,50 on the Clinician Administered PTSD Scale [CAPS] and 20 on thePTSD Scale-Interview [PSSI]), with a range of 48.03 to 64.97 forCAPS and 23.00 for PSSI. Four trials reported posttreatment PTSDdiagnosis,15-18 with approximately two-thirds of patients retainingtheir diagnosis (60%-72%). Only 1 trial reported symptom remis-sion (CAPS score <20) of 27%.16

Concerning comparisons to control conditions, CPT outper-formed waitlist approaches for mean PTSD symptom reduction(g = 1.12), loss of diagnosis, and meaningful symptom change, al-though the latter was no longer statistically significant by 1 monthposttreatment.15 CPT produced significantly greater symptom re-mission and clinically meaningful symptom improvement than treat-ment as usual in a study of Australian veterans (d = 0.97). Group dif-ferences in loss of diagnosis and meaningful symptom improvementwere nonsignificant at 3-month follow-up but remained significantfor symptom remission.16 In a trial comparing CPT and present-centered therapy for military sexual trauma, CPT resulted in signifi-cantly greater reduction in self-reported PTSD symptoms at post-treatment (d = 0.85), although group differences were no longersignificant by 2-, 4-, or 6-month follow-up.17 There were no signifi-cant group differences in interviewer-assessed PTSD symptoms. Atrial comparing group CPT with group present-centered therapy inactive-duty soldiers also found that self-reported PTSD symptomsimproved in both groups but statistically significantly more so in theCPT group (d = 0.40).19 Between-group differences were small andnot significant for interviewer-assessed PTSD symptoms at post-treatment (d = 0.21), 6-month (d = 0.22), and 12-month (d = 0.21)follow-up. There were no significant differences between groups in

the percentage of patients attaining clinically significant change inself-reported symptoms at posttreatment, 6-month, or 12-monthfollow-up.

In sum, trials of CPT for military-related PTSD have included bothveterans and active-duty personnel with combat or military sexualtrauma, have shown high methodological rigor (although fidelityproblems were present in 1 trial),17 and have had large effect sizeswhen compared with no treatment (waitlist) or treatment as usual.However, CPT was marginally superior to active, non–trauma-focused control comparisons.

Efficacy of Prolonged ExposureFour RCTs of prolonged exposure (that included 402 patients) metinclusion criteria.24-27 Earlier trials examined similar exposure-based mechanisms but not the full prolonged exposure protocol20-22

and included a large trial of an exposure-based group therapy thatdid not lead to meaningful PTSD symptom reduction or outper-form a present-centered control.23 The most robust trial of pro-longed exposure compared prolonged exposure with present-centered therapy in female veterans with sexual trauma,24 while 3small studies of combat veterans used minimal attention,26 treat-ment as usual,25 or present-centered therapy27 control conditions.Two of these trials26,27 focused primarily on glucocorticoid-relatedbiomarker responses associated with clinical improvement. Treat-ment dropout rates ranged from 13% to 39%.

Within-group intent-to-treat effect size for prolonged expo-sure was reported in 1 trial and was large (d = 0.80).24 One trialreported on clinically meaningful PTSD symptom reduction in theintent-to-treat sample, which occurred in 70% of patients.24

Mean posttreatment intent-to-treat symptom scores werereported in 2 trials and remained at or above clinical cutoffs forPTSD (52.9 [CAPS]24 and 18.9 [PSSI]25). One trial reported loss ofdiagnosis in the intent-to-treat sample and found that 61%retained their diagnosis after treatment.24 The only trial to reportremission (�20 CAPS) found remission in 17% of the intent-to-treat sample.24

When compared with control conditions, both prolonged ex-posure and present-centered therapy improved symptoms in fe-male veterans with predominantly sexual assault trauma, with a smallintent-to-treat effect size favoring prolonged exposure (d = 0.27);there were no significant group differences for clinically meaning-ful improvement at any point and no significant group differencesfor loss of diagnosis or symptom remission at either the 3- or 6-monthfollow-up.24 In a small sample of Israeli veterans, prolonged expo-sure resulted in greater symptom reduction than psychodynamictherapy (d = 1.80), and outcomes were maintained through 12-month follow-up.25 Prolonged exposure failed to outperform a mini-mal-attention control that consisted of 30-minute weekly symp-tom monitoring phone calls; both groups significantly improved, withno significant group differences.26 Last, a small RCT examining cor-tisol response following prolonged exposure found no significant dif-ferences between prolonged exposure and present-centeredtherapy on interviewer-assessed PTSD outcomes in the intent-to-treat sample, although significant differences favoring prolonged ex-posure were found in completers (d = 3.16 for prolonged exposurevs d = 1.08 for present-centered therapy).27

In sum, fewer methodologically robust trials for military-related PTSD are available for prolonged exposure than for CPT. With

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Tabl

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Clinical Review & Education Review Psychotherapy for Military-Related PTSD

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Copyright 2015 American Medical Association. All rights reserved.

Tabl

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Psychotherapy for Military-Related PTSD Review Clinical Review & Education

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Copyright 2015 American Medical Association. All rights reserved.

1 notable exception,24 sample sizes have tended to besmaller, and no large methodologically robust trials of pro-longed exposure have been published in US male veter-ans with combat trauma. The only available data on pro-longed exposure in US combat-exposed male veteranscome from 2 small trials that studied biomarkers associ-ated with clinical outcomes.26,27

Efficacy of EMDRRCTs of EMDR for military-related PTSD (all conducted priorto the wars in Iraq and Afghanistan) involved small samples,tested only brief interventions (1-3 sessions),28,55,56 or in-volved dismantling comparisons (eliminating eyemovements).57 They also generally did not use methodol-ogy consistent with modern trials. In the 2 trials testing ad-equate doses of EMDR there were large symptomreductions,58 and 78% of completers no longer met crite-ria for PTSD.29 EMDR performed comparably to variants inwhich the eye tracking was removed or when comparedwith an active non–trauma-focused therapy.58 EMDR out-performed waitlisting (ie, no treatment) and biofeedback-assisted relaxation, with results maintained at 9-monthfollow-up.29 In sum, the efficacy of EMDR remains largelybased on civilian studies59; additional studies in militarypopulations are needed.

Second-Line InterventionsGiven high dropout and nonresponse rates from first-linetherapies, an increasing number of trials have examined anarray of alternatives, including variations of cognitive-behavioral therapy38,44 or novel delivery modalities, suchas virtual reality36,39 or web-based content.33 A variant ofEMDR, accelerated resolution therapy, demonstrated largeeffects (d = 1.25) compared with an educational control con-dition similar to waitlisting in a preliminary RCT of veter-ans with PTSD.47

Other trials have tested complementary and alterna-tive therapies that are theoretically and mechanisticallydistinct. Acupuncture combined with usual care outper-formed usual care alone (d = 1.7)48; small trials haveshown some evidence of efficacy for mindfulness-basedinterventions,43 mantram repetition (ie, silent repetitionof a word or phrase with spiritual significance),34,45 atten-tion bias modif ication,49 and memory specif icitytraining.50 Healing touch therapy, involving tapping bodypoints while engaging in non–exposure-based guidedimagery, also demonstrated efficacy over treatment asusual (d = 0.85).41 These findings suggest that a variety ofdisparate treatment mechanisms are associated withreduced PTSD symptoms.

In contrast, treatments that have failed to demon-strate efficacy among veterans include relaxation, deepbreathing, biofeedback, and mindfulness-based stressreduction.30,35,42 A brief 3-session intervention consist-ing of writing about combat traumas produced little mean-ingful PTSD improvement and did not outperform writingabout one’s use of time.40 Cognitive-behavioral grouptherapy aimed at comorbid PTSD and depression,31 andTa

ble

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Clinical Review & Education Review Psychotherapy for Military-Related PTSD

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comorbid PTSD and substance dependence, did not substantiallyimprove symptoms and was equivalent to controls.

DiscussionThe past 10 years has seen unprecedented interest in identifying ef-fective PTSD treatments for service members and veterans. Find-ings from RCTs indicate a significant need for further treatment de-velopment and improvement. CPT and prolonged exposure, the 2most widely used first-line (ie, recommended) therapies, show largewithin-group (pretreatment to posttreatment) effect sizes. How-ever, effect sizes, which are more commonly used in psychology lit-erature than in medical literature, reflect mean outcomes and do notadequately capture heterogeneity in patient outcomes; betweenone-third and one-half of patients receiving CPT or prolonged ex-posure did not demonstrate clinically meaningful symptom change(when this outcome was reported). Approximately two-thirds of pa-tients receiving CPT or prolonged exposure retained their diagno-sis posttreatment. Mean PTSD scores have tended to remain at orabove diagnostic thresholds after treatment, and the 2 studies re-porting remission rates suggest that symptom remission is rela-tively uncommon. Most importantly, many trials of CPT and pro-longed exposure have compared patients receiving the interventionwith patients not receiving any standardized intervention (waitlist)or with patients receiving treatment as usual. When CPT and pro-longed exposure were compared with non–trauma-focused psy-chotherapies, such as present-centered therapy, similar levels ofsymptom improvement were often observed, particularly atfollow-up intervals.

Approximately one-fourth of patients enrolled in clinical trialsand receiving CPT and prolonged exposure dropped out during treat-ment. These proportions are broadly comparable to the propor-tions of dropouts in studies of trauma-focused therapies in civilians60

and trials of depression in veterans.61 Treatment nonretention hasbeen a significant problem in military-related PTSD care more gen-erally; several large observational studies in both the VA and DoDfound that only a small proportion of individuals receive a mini-mally adequate number of mental health encounters after PTSDdiagnosis.62 Reasons for not seeking treatment and dropout are com-plex and include stigma, confidentiality concerns, time demands, per-ceived treatment inefficacy, and discomfort with the therapist.62

Current VA policies emphasize CPT and prolonged exposure astreatments of choice. Clinical practice guidelines (including the VA/DoD guideline52), based largely on studies in civilians, also includeCPT and prolonged exposure as first-line recommendations for adultswith PTSD, although EMDR and other trauma-focused therapies aregiven at least equal standing (separate recommendations for ser-vice members and veterans are not made). Some evidence sug-gests that outcomes for PTSD treatment tend to be better amongcivilians than among veterans,63,64 although this has not been con-sistent and remains an empirical question. Potential reasons whytreatment outcomes may be worse among military and veteranpopulations include the extended, repeated, and intense nature ofdeployment trauma65 and the fact that service members are ex-posed not only to life threats but to traumatic losses and morally com-promising experiences that may require different treatmentapproaches.66-68 A recent meta-analysis comparing trauma-

focused and non–trauma-focused therapies (both civilian and mili-tary trauma) found that, in populations with more complex trauma,such as veterans and refugees, there was little difference in effi-cacy; moderate differences favoring trauma-focused therapies wereonly present for less complex traumas.69 Additional likely reasonsfor worse outcomes in veterans include comorbidities (eg, 87% ofveterans with PTSD presenting to VA primary care clinics have at least1 psychiatric comorbidity, with the mode being 3-4 disorders70) anddisability compensation incentives. To contextualize these find-ings, a recent narrative review of cognitive-behavioral therapy fordepression in veterans similarly showed that relatively few trials areavailable, cognitive-behavioral therapy often does not outperformcontrols, and results compare unfavorably with civilian outcomes.61

One unresolved issue is whether focusing on the trauma, eitherthrough exposure or cognitive reframing, is necessary for recovery.The findings that interventions such as present-centered therapyand, in civilians, interpersonal psychotherapy71 are associated withefficacy similar to that of trauma-focused therapy needs to be rec-onciled with the common assumption in the field that fidelity to atrauma-focused approach is essential for symptom improvement.VA/DoD treatment guidelines, and other guidelines, specify that pa-tient preference should be a guiding factor in treatment selection.Yet little research has been conducted on patient preferences or onother behavioral and biological predictors of dropping out of care,clearly the strongest influence on treatment effectiveness.62

Several large-scale military-related PTSD trials are currently on-going, including trials with active-duty service members, a popula-tion rarely studied but an important target for early interventions.

Box. Descriptions of First-Line Interventions

Cognitive therapy. Focuses on modifying dysfunctional thoughts,beliefs, and expectations by identifying, challenging, and replacingmaladaptive cognitions. Cognitive processing therapy (CPT) is themost widely used example of cognitive therapy in theDepartments of Defense and Veterans Affairs.

Exposure therapy. Comprises psychoeducation, imaginal ornarrative exposure (targeting trauma memories), in vivo exposure(targeting external stimuli or situations that the patient avoidsbecause of the trauma), and processing of thoughts and emotions,with the aim of confronting, rather than avoiding, fearedmemories and stimuli. Prolonged exposure therapy (PE) is themost widely used example of exposure therapy in theDepartments of Defense and Veterans Affairs.

Eye movement desensitization and reprocessing (EMDR). Askspatients to attend to emotionally disturbing material in briefsequential doses while focusing on an external stimulus, typicallytherapist-directed lateral eye movements. Additionally, treatmentinvolves identifying bodily sensations associated with the image,identifying an aversive cognition associated with the trauma, andidentifying an alternative positive cognition to replace the aversivecognition.

Stress inoculation training (SIT). Teaches anxiety-managementskills including relaxation training, breathing retraining, positivethinking and self-talk, assertiveness training, and thoughtstopping. It may also include cognitive restructuring and exposure,although these are optional elements.

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A large (N = 900) multisite trial is directly comparing CPT and pro-longed exposure in veterans,72 although it remains to be seen to whatextent continued focus on efficacy comparisons will improve care,particularly since equivalency between leading interventions has con-sistently been demonstrated in civilians.59,73 Ongoing trials focus al-most exclusively on 2 trauma-focused interventions, despite thesetherapies being rarely used in actual VA and DoD clinical practice (lessthan 10% of the time, in one estimate of New England region VAcenters74). The effectiveness of psychotherapies for PTSD as actu-ally delivered in the VA and DoD has received little empiricalattention.75

Limitations of this descriptive review (which did not use for-mal meta-analytic techniques or access all international data-bases) include the relatively small number of studies and samplesizes, limiting generalizability. Studies often did not report keyoutcomes, such as symptom remission, loss of diagnosis, or clini-cally important subthreshold PTSD76,77 (which would includeindividuals who met previous diagnostic criteria but no longermeet the latest criteria).78 It is also noteworthy that the metricsof meaningful symptom improvement (typically a 10- or 12-pointdecrease in PTSD scores) are researcher-defined, not patient-defined; patient perspectives and preferences have not been aprimary focus of research. Likewise, most trials have reportedonly total PTSD symptom scores, and the potential for differentialtreatment effects across symptom clusters remains unexamined.Trials also have not reported the need for continued care follow-ing CPT or prolonged exposure; for many patients, 12 sessions ofmanualized trauma- or non–trauma-focused treatment is insuffi-cient. Definitions of treatment dropout also differ between stud-ies, and studies often fail to delineate why patients dropped out.Moreover, military personnel and veterans participating in PTSDtrials are often taking psychotropic medications concurrently (ap-proximately three-fourths of participants in CPT and prolongedexposure trials), creating potential confounding. Data are lackingon the relative efficacy of psychotherapy compared with medica-tion or the synergistic effects of combined treatments.79 Last,although we considered group and individual therapy together,these 2 modalities are practically and mechanistically distinct. Arecent meta-analysis of civilian and veteran group therapies

found smaller effect sizes in combat samples; although grouptherapy outperformed waitlist controls, it did not outperformactive-comparison conditions.80

ConclusionsPTSD in military and veteran populations is a complex and difficult-to-treat disorder for which first-line trauma-focused psycho-therapy approaches are not optimal. Although efficacious for somepatients, first-line treatments have high nonresponse and dropoutrates, and patients often remain symptomatic. Two principal clini-cal conclusions can be drawn from this review. First, the availableevidence supports the use of either trauma-focused or structurednon–trauma-focused therapies, depending on patient preferencesor other factors that might promote treatment retention. Second,there is a need for improvement in existing PTSD treatments as wellas the development and testing of novel evidence-based treat-ment strategies, whether trauma-focused or non–trauma-focused.An increasing number of novel therapeutic approaches have beenshown efficacious to varying degrees, but progress in the field is un-likely without better understanding of treatment mechanisms, pa-tient preferences, factors influencing treatment engagement and re-tention, and behavioral and biomarker prediction of differentialtreatment responses.

ARTICLE INFORMATION

Author Contributions: Dr Steenkamp had fullaccess to all of the data in the study and takesresponsibility for the integrity of the data and theaccuracy of the data analysis.Study concept and design: Steenkamp, Litz.Acquisition, analysis, or interpretation of data:Steenkamp, Litz, Hoge, Marmar.Drafting of the manuscript: Steenkamp, Litz,Marmar.Critical revision of the manuscript for importantintellectual content: Hoge, Marmar.Administrative, technical, or material support: Litz.Study supervision: Litz, Marmar.

Conflict of Interest Disclosures: All authors havecompleted and submitted the ICMJE Form forDisclosure of Potential Conflicts of Interest andnone were reported.

Disclaimer: The views of this article are those ofthe authors and do not represent an official

position of the US Army, Department of Defense, orlisted institutions.

Additional Contributions: We thank CarolHundert, BS (VA Boston Healthcare System), andAmelia Tankersley, BA (VA Boston HealthcareSystem), for assistance with manuscriptpreparation. They received no compensation fortheir contributions.

Submissions: We encourage authors to submitpapers for consideration as a Review. Pleasecontact Mary McGrae McDermott, MD, [email protected].

REFERENCES

1. Kok BC, Herrell RK, Thomas JL, Hoge CW.Posttraumatic stress disorder associated withcombat service in Iraq or Afghanistan: reconcilingprevalence differences between studies. J NervMent Dis. 2012;200(5):444-450.

2. Kang HK, Natelson BH, Mahan CM, Lee KY,Murphy FM. Post-traumatic stress disorder andchronic fatigue syndrome-like illness among GulfWar veterans: a population-based survey of30,000 veterans. Am J Epidemiol. 2003;157(2):141-148.

3. Marmar CR, Schlenger W, Henn-Haase C, et al.Course of posttraumatic stress disorder 40 yearsafter the Vietnam War: findings from the NationalVietnam Veterans Longitudinal Study [publishedonline July 22, 2015]. JAMA Psychiatry. doi:10.1001/jamapsychiatry.2015.0803.

4. Kulka RA, Schlenger WE, Fairbank JA, et al.Trauma and the Vietnam War Generation: Report ofFindings From the National Vietnam VeteransReadjustment Study. New York, NY: Brunner/Mazel;1990.

5. Hoge CW, Terhakopian A, Castro CA, Messer SC,Engel CC. Association of posttraumatic stressdisorder with somatic symptoms, health care visits,

Clinical Bottom Line

• Posttraumatic stress disorder (PTSD) is a disabling psychiatriccondition common among military personnel and veterans

• A range of psychotherapies are available, but military-PTSD iscomplex and difficult to treat

• The available evidence supports the use of structuredtrauma-focused or non–trauma-focused approaches

• Although trauma-focused and non–trauma-focused interven-tions often improve symptoms, many patients continue to meetcriteria for PTSD after treatment

• There is an urgent need for innovative treatment strategies,whether trauma-focused or non–trauma-focused

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Copyright 2015 American Medical Association. All rights reserved.

and absenteeism among Iraq war veterans. Am JPsychiatry. 2007;164(1):150-153.

6. Savoca E, Rosenheck R. The civilian labor marketexperiences of Vietnam-era veterans: the influenceof psychiatric disorders. J Ment Health Policy Econ.2000;3(4):199-207.

7. Riggs DS, Byrne CA, Weathers FW, Litz BT. Thequality of the intimate relationships of maleVietnam veterans: problems associated withposttraumatic stress disorder. J Trauma Stress.1998;11(1):87-101.

8. McFall M, Fontana A, Raskind M, Rosenheck R.Analysis of violent behavior in Vietnam combatveteran psychiatric inpatients with posttraumaticstress disorder. J Trauma Stress. 1999;12(3):501-517.

9. Buckley TC, Mozley SL, Bedard MA, Dewulf AC,Greif J. Preventive health behaviors, health-riskbehaviors, physical morbidity, and health-relatedrole functioning impairment in veterans withpost-traumatic stress disorder. Mil Med. 2004;169(7):536-540.

10. Zatzick DF, Marmar CR, Weiss DS, et al.Posttraumatic stress disorder and functioning andquality of life outcomes in a nationallyrepresentative sample of male Vietnam veterans.Am J Psychiatry. 1997;154(12):1690-1695.

11. Xue C, Ge Y, Tang B, et al. A meta-analysis of riskfactors for combat-related PTSD among militarypersonnel and veterans. PLoS One. 2015;10(3):e0120270.

12. Tennant C, Goulston K, Dent O. Clinicalpsychiatric illness in prisoners of war of theJapanese: forty years after release. Psychol Med.1986;16(4):833-839.

13. Karlin BE, Ruzek JI, Chard KM, et al.Dissemination of evidence-based psychologicaltreatments for posttraumatic stress disorder in theVeterans Health Administration. J Trauma Stress.2010;23(6):663-673.

14. American Psychiatric Association. Diagnosticand Statistical Manual of Mental Disorders. 4th ed,text revision. Washington, DC: American PsychiatricAssociation; 2000.

15. Monson CM, Schnurr PP, Resick PA, FriedmanMJ, Young-Xu Y, Stevens SP. Cognitive processingtherapy for veterans with military-relatedposttraumatic stress disorder. J Consult Clin Psychol.2006;74(5):898-907.

16. Forbes D, Lloyd D, Nixon RDV, et al. A multisiterandomized controlled effectiveness trial ofcognitive processing therapy for military-relatedposttraumatic stress disorder. J Anxiety Disord.2012;26(3):442-452.

17. Surís A, Link-Malcolm J, Chard K, Ahn C, NorthC. A randomized clinical trial of cognitive processingtherapy for veterans with PTSD related to militarysexual trauma. J Trauma Stress. 2013;26(1):28-37.

18. Morland LA, Mackintosh MA, Greene CJ, et al.Cognitive processing therapy for posttraumaticstress disorder delivered to rural veterans viatelemental health: a randomized noninferiorityclinical trial. J Clin Psychiatry. 2014;75(5):470-476.

19. Resick PA, Wachen JS, Mintz J, et al. Arandomized clinical trial of group cognitiveprocessing therapy compared with grouppresent-centered therapy for PTSD among activeduty military personnel [published online May 4,2015]. J Consult Clin Psychol. doi:10.1037/ccp0000016.

20. Cooper NA, Clum GA. Imaginal flooding as asupplementary treatment for PTSD in combatveterans: a controlled study. Behav Ther. 1989;20(3):381-391. doi:10.1016/S0005-7894(89)80057-7.

21. Keane TM, Fairbank JA, Caddell JM, ZimeringRT. Implosive (flooding) therapy reduces symptomsof PTSD in Vietnam combat veterans. Behav Ther.1989;20(2):245-260. doi:10.1016/S0005-7894(89)80072-3.

22. Boudewyns PA, Hyer LA. Physiologicalresponse to combat memories and preliminarytreatment outcome in Vietnam veteran PTSDpatients treated with direct therapeutic exposure.Behav Ther. 1990;21(1):63-87. doi:10.1016/S0005-7894(05)80189-3.

23. Schnurr PP, Friedman MJ, Foy DW, et al.Randomized trial of trauma-focused group therapyfor posttraumatic stress disorder: results from adepartment of veterans affairs cooperative study.Arch Gen Psychiatry. 2003;60(5):481-489.

24. Schnurr PP, Friedman MJ, Engel CC, et al.Cognitive behavioral therapy for posttraumaticstress disorder in women: a randomized controlledtrial. JAMA. 2007;297(8):820-830.

25. Nacasch N, Foa EB, Huppert JD, et al.Prolonged exposure therapy for combat- andterror-related posttraumatic stress disorder:a randomized control comparison with treatmentas usual. J Clin Psychiatry. 2011;72(9):1174-1180.

26. Yehuda R, Pratchett LC, Elmes MW, et al.Glucocorticoid-related predictors and correlates ofpost-traumatic stress disorder treatment responsein combat veterans. Interface Focus. 2014;4(5):20140048.

27. Rauch SA, King AP, Abelson J, et al. Biologicaland symptom changes in posttraumatic stressdisorder treatment: a randomized clinical trial.Depress Anxiety. 2015;32(3):204-212.

28. Rogers S, Silver SM, Goss J, Obenchain J, WillisA, Whitney RL. A single session, group study ofexposure and Eye Movement Desensitization andReprocessing in treating Posttraumatic StressDisorder among Vietnam War veterans: preliminarydata. J Anxiety Disord. 1999;13(1-2):119-130.

29. Carlson JG, Chemtob CM, Rusnak K, HedlundNL, Muraoka MY. Eye movement desensitizationand reprocessing (EDMR) treatment forcombat-related posttraumatic stress disorder.J Trauma Stress. 1998;11(1):3-24.

30. Watson CG, Tuorila JR, Vickers KS, Gearhart LP,Mendez CM. The efficacies of three relaxationregimens in the treatment of PTSD in Vietnam Warveterans. J Clin Psychol. 1997;53(8):917-923.

31. Dunn NJ, Rehm LP, Schillaci J, et al. Arandomized trial of self-management andpsychoeducational group therapies for comorbidchronic posttraumatic stress disorder anddepressive disorder. J Trauma Stress. 2007;20(3):221-237.

32. Frueh BC, Monnier J, Yim E, Grubaugh AL,Hamner MB, Knapp RG. A randomized trial oftelepsychiatry for post-traumatic stress disorder.J Telemed Telecare. 2007;13(3):142-147.

33. Litz BT, Engel CC, Bryant RA, Papa A. Arandomized, controlled proof-of-concept trial of anInternet-based, therapist-assistedself-management treatment for posttraumaticstress disorder. Am J Psychiatry. 2007;164(11):1676-1683.

34. Bormann JE, Thorp S, Wetherell JL, Golshan S.A spiritually based group intervention for combatveterans with posttraumatic stress disorder:feasibility study. J Holist Nurs. 2008;26(2):109-116.

35. Lande RG, Williams LB, Francis JL, Gragnani C,Morin ML. Efficacy of biofeedback forpost-traumatic stress disorder. Complement TherMed. 2010;18(6):256-259.

36. Ready DJ, Gerardi RJ, Backscheider AG,Mascaro N, Rothbaum BO. Comparing virtual realityexposure therapy to present-centered therapy with11 U.S. Vietnam veterans with PTSD. CyberpsycholBehav Soc Netw. 2010;13(1):49-54.

37. Beidel DC, Frueh BC, Uhde TW, Wong N,Mentrikoski JM. Multicomponent behavioraltreatment for chronic combat-relatedposttraumatic stress disorder: a randomizedcontrolled trial. J Anxiety Disord. 2011;25(2):224-231.

38. Kent M, Davis MC, Stark SL, Stewart LA. Aresilience-oriented treatment for posttraumaticstress disorder: results of a preliminary randomizedclinical trial. J Trauma Stress. 2011;24(5):591-595.

39. McLay RN, Wood DP, Webb-Murphy JA, et al. Arandomized, controlled trial of virtual reality-gradedexposure therapy for post-traumatic stress disorderin active duty service members withcombat-related post-traumatic stress disorder.Cyberpsychol Behav Soc Netw. 2011;14(4):223-229.

40. Possemato K, Ouimette P, Knowlton P. A briefself-guided telehealth intervention forpost-traumatic stress disorder in combat veterans:a pilot study. J Telemed Telecare. 2011;17(5):245-250.

41. Jain S, McMahon GF, Hasen P, et al. HealingTouch with Guided Imagery for PTSD in returningactive duty military: a randomized controlled trial.Mil Med. 2012;177(9):1015-1021.

42. Kearney DJ, McDermott K, Malte C, MartinezM, Simpson TL. Effects of participation in amindfulness program for veterans withposttraumatic stress disorder: a randomizedcontrolled pilot study. J Clin Psychol. 2013;69(1):14-27.

43. Niles BL, Klunk-Gillis J, Ryngala DJ, SilberbogenAK, Paysnick A, Wolf EJ. Comparing mindfulnessand psychoeducation treatments forcombat-related PTSD using a telehealth approach.Psychol Trauma. 2012;4(5):538-547. doi:10.1037/a0026161.

44. Strachan M, Gros DF, Ruggiero KJ, Lejuez CW,Acierno R. An integrated approach to deliveringexposure-based treatment for symptoms of PTSDand depression in OIF/OEF veterans: preliminaryfindings. Behav Ther. 2012;43(3):560-569.

45. Bormann JE, Thorp SR, Wetherell JL, GolshanS, Lang AJ. Meditation-based mantram interventionfor veterans with posttraumatic stress disorder:a randomized trial. Psychol Trauma. 2013;5(3):259-267. doi:10.1037/a0027522.

46. Church D, Hawk C, Brooks AJ, et al.Psychological trauma symptom improvement inveterans using emotional freedom techniques:a randomized controlled trial. J Nerv Ment Dis. 2013;201(2):153-160.

47. Kip KE, Rosenzweig L, Hernandez DF, et al.Randomized controlled trial of acceleratedresolution therapy (ART) for symptoms ofcombat-related post-traumatic stress disorder(PTSD). Mil Med. 2013;178(12):1298-1309.

Psychotherapy for Military-Related PTSD Review Clinical Review & Education

jama.com (Reprinted) JAMA August 4, 2015 Volume 314, Number 5 499

Copyright 2015 American Medical Association. All rights reserved.

Downloaded From: http://jama.jamanetwork.com/ by a New York University User on 08/04/2015

Page 13: Psychotherapy for Military-Related PTSD A Review of ...Psychotherapy for Military-Related PTSD A Review of Randomized Clinical Trials ARTICLE in JAMA THE JOURNAL OF THE AMERICAN MEDICAL

Copyright 2015 American Medical Association. All rights reserved.

48. Engel CC, Cordova EH, Benedek DM, et al.Randomized effectiveness trial of a brief course ofacupuncture for posttraumatic stress disorder. MedCare. 2014;52(12)(suppl 5):S57-S64.

49. Kuckertz JM, Amir N, Boffa JW, et al. Theeffectiveness of an attention bias modificationprogram as an adjunctive treatment forpost-traumatic stress disorder. Behav Res Ther.2014;63:25-35.

50. Moradi AR, Moshirpanahi S, Parhon H, MirzaeiJ, Dalgleish T, Jobson L. A pilot randomizedcontrolled trial investigating the efficacy of MEmorySpecificity Training in improving symptoms ofposttraumatic stress disorder. Behav Res Ther.2014;56:68-74.

51. Forbes D, Creamer M, Bisson JI, et al. A guide toguidelines for the treatment of PTSD and relatedconditions. J Trauma Stress. 2010;23(5):537-552.

52. US Department of Veterans Affairs (VA) andDepartment of Defense. VA/DoD Clinical PracticeGuideline for Management of Post-TraumaticStress. VA website. http://www.healthquality.va.gov/guidelines/MH/ptsd/cpgPTSDFULL201011612c.pdf. 2010. Accessed July 6, 2015.

53. Karlin BE, Cross G. From the laboratory to thetherapy room: national dissemination andimplementation of evidence-basedpsychotherapies in the U.S. Department ofVeterans Affairs Health Care System. Am Psychol.2014;69(1):19-33.

54. Ruzek JI, Karlin BE, Zeiss A. Implementation ofevidence-based psychological treatments in theVeterans Health Administration. In: McHugh RK,Barlow DH, eds. Dissemination and Implementationof Evidence-Based Psychological Interventions. NewYork, NY: Oxford University Press; 2012:78-96.

55. Devilly GJ, Spence SH, Rapee RM. Statisticaland reliable change with eye movementdesensitization and reprocessing: treating traumawithin a veteran population. Behav Ther. 1998;29(3):435-455. doi:10.1016/S0005-7894(98)80042-7.

56. Jensen JA. An investigation of eye movementdesensitization and reprocessing (EMD/R) as atreatment for posttraumatic stress disorder (PTSD)symptoms of Vietnam combat veterans. Behav Ther.1994;25(2):311-325. doi:10.1016/S0005-7894(05)80290-4.

57. Pitman RK, Orr SP, Altman B, Longpre RE, PoiréRE, Macklin ML. Emotional processing during eyemovement desensitization and reprocessingtherapy of Vietnam veterans with chronicposttraumatic stress disorder. Compr Psychiatry.1996;37(6):419-429.

58. Boudewyns PA, Hyer LA. Eye movementdesensitization and reprocessing (EMDR) astreatment for post-traumatic stress disorder(PTSD). Clin Psychol Psychother. 1996;3(3):185-195.

59. Powers MB, Halpern JM, Ferenschak MP,Gillihan SJ, Foa EB. A meta-analytic review ofprolonged exposure for posttraumatic stressdisorder. Clin Psychol Rev. 2010;30(6):635-641.

60. Schottenbauer MA, Glass CR, Arnkoff DB,Tendick V, Gray SH. Nonresponse and dropout ratesin outcome studies on PTSD: review andmethodological considerations. Psychiatry. 2008;71(2):134-168.

61. Hundt NE, Barrera TL, Robinson A, Cully JA. Asystematic review of cognitive behavioral therapyfor depression in Veterans. Mil Med. 2014;179(9):942-949.

62. Hoge CW, Grossman SH, Auchterlonie JL,Riviere LA, Milliken CS, Wilk JE. PTSD treatment forsoldiers after combat deployment: low utilization ofmental health care and reasons for dropout.Psychiatr Serv. 2014;65(8):997-1004.

63. Bradley R, Greene J, Russ E, Dutra L, Westen D.A multidimensional meta-analysis of psychotherapyfor PTSD. Am J Psychiatry. 2005;162(2):214-227.

64. Watts BV, Schnurr PP, Mayo L, Young-Xu Y,Weeks WB, Friedman MJ. Meta-analysis of theefficacy of treatments for posttraumatic stressdisorder. J Clin Psychiatry. 2013;74(6):e541-e550.

65. Price M, Gros DF, Strachan M, Ruggiero KJ,Acierno R. Combat experiences, pre-deploymenttraining, and outcome of exposure therapy forpost-traumatic stress disorder in OperationEnduring Freedom/Operation Iraqi Freedomveterans. Clin Psychol Psychother. 2013;20(4):277-285.

66. Stein NR, Mills MA, Arditte K, et al; STRONGSTAR Consortium. A scheme for categorizingtraumatic military events. Behav Modif. 2012;36(6):787-807.

67. Litz BT, Stein N, Delaney E, et al. Moral injuryand moral repair in war veterans: a preliminarymodel and intervention strategy. Clin Psychol Rev.2009;29(8):695-706.

68. Steenkamp MM, Litz BT, Gray MJ, et al. A briefexposure-based intervention for service memberswith PTSD. Cognit Behav Pract. 2011;18(1):98-107.doi:10.1016/j.cbpra.2009.08.006.

69. Gerger H, Munder T, Barth J. Specific andnonspecific psychological interventions for PTSDsymptoms: a meta-analysis with problemcomplexity as a moderator. J Clin Psychol. 2014;70(7):601-615.

70. Magruder KM, Frueh BC, Knapp RG, et al.Prevalence of posttraumatic stress disorder inVeterans Affairs primary care clinics. Gen HospPsychiatry. 2005;27(3):169-179.

71. Markowitz JC, Petkova E, Neria Y, et al. Isexposure necessary? a randomized clinical trial ofinterpersonal psychotherapy for PTSD. Am JPsychiatry. 2015;172(5):430-440.

72. Schnurr PP, Chard KM, Ruzek JI, et al. Design ofVA Cooperative Study #591: CERV-PTSD,comparative effectiveness research in veteranswith PTSD. Contemp Clin Trials. 2015;41:75-84.

73. Benish SG, Imel ZE, Wampold BE. The relativeefficacy of bona fide psychotherapies for treatingpost-traumatic stress disorder: a meta-analysis ofdirect comparisons. Clin Psychol Rev. 2008;28(5):746-758.

74. Shiner B, D’Avolio LW, Nguyen TM, et al.Measuring use of evidence based psychotherapyfor posttraumatic stress disorder. Adm Policy MentHealth. 2013;40(4):311-318.

75. Institute of Medicine (IOM). Treatment forPosttraumatic Stress Disorder in Military andVeteran Populations: Final Assessment. IOM website.http://iom.nationalacademies.org/~/media/Files/Report Files/2014/PTSD-II/PTSD-II-RB.pdf. 2014.Accessed July 6, 2015.

76. Marshall RD, Olfson M, Hellman F, Blanco C,Guardino M, Struening EL. Comorbidity,impairment, and suicidality in subthreshold PTSD.Am J Psychiatry. 2001;158(9):1467-1473.

77. Stein MB, Walker JR, Hazen AL, Forde DR. Fulland partial posttraumatic stress disorder: findingsfrom a community survey. Am J Psychiatry. 1997;154(8):1114-1119.

78. Hoge CW, Riviere LA, Wilk JE, Herrell RK,Weathers FW. The prevalence of post-traumaticstress disorder (PTSD) in US combat soldiers:a head-to-head comparison of DSM-5 vs DSM-IV-TRsymptom criteria with the PTSD checklist. LancetPsychiatry. 2014;1(4):269-277. doi:10.1016/S2215-0366(14)70235-4.

79. Rothbaum BO, Price M, Jovanovic T, et al. Arandomized, double-blind evaluation ofD-cycloserine or alprazolam combined with virtualreality exposure therapy for posttraumatic stressdisorder in Iraq and Afghanistan War veterans. Am JPsychiatry. 2014;171(6):640-648.

80. Sloan DM, Feinstein BA, Gallagher MW, BeckJG, Keane TM. Efficacy of group treatment forposttraumatic stress disorder symptoms:a meta-analysis. Psychol Trauma. 2013;5(2):176-183.doi:10.1037/a0026291.

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