Abstract
Purpose of the review:
Sleep disturbances, insomnia and recurrent nightmares in particular, are among the most frequently endorsed symptoms of posttraumatic stress disorder (PTSD). The present review provides a summary of the prevalence estimates and methodological challenges presented by sleep disturbances in PTSD, highlights the recent evidence for empirically supported psychotherapeutic and pharmacological interventions for comorbid sleep disturbances implicated in PTSD, and provides a summary of recent findings on integrated and sequential treatment approaches to ameliorate comorbid sleep disturbances in PTSD.
Recent Findings:
Insomnia, recurrent nightmares, and other sleep disorders are commonly endorsed among individuals with PTSD; however, several methodological challenges contribute to the varying prevalence estimates. Targeted sleep-focused therapeutic interventions can improve sleep symptoms and mitigate daytime PTSD symptoms. Recently, attention has focused on the role of integrated and sequential approaches, suggesting that comprehensively treating sleep disturbances in PTSD is likely to require novel treatment modalities.
Summary:
Evidence is growing on the development, course, and treatment of comorbid sleep disturbances in PTSD. Further, interventions targeting sleep disturbances in PTSD show promise in reducing symptoms. However, longitudinal investigations and additional rigorous controlled trials with diverse populations are needed to identify key features associated with treatment response in order to alleviate symptoms.
Keywords: Post-Traumatic Stress Disorder, Sleep Disorders, Sleep Disturbances, Psychotherapy, Pharmacotherapy, Comorbidity
Introduction
Approximately 87% of posttraumatic stress disorder (PTSD) patients endorse subjective sleep disturbances [1]. There has been extensive growth of the literature on treatment modalities and recommendations for sleep comorbidities in PTSD within the last decade. Sleep disturbances are core features of PTSD and have been considered hallmark symptoms of the disorder [2]. These core sleep disturbances are identified within the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) diagnostic criteria with nightmares or distressing dreams among the intrusion symptoms and difficulty falling or staying asleep or restless sleep among the alterations in arousal and reactivity symptoms [3]. Insomnia and recurrent nightmares are two of the most distressing symptoms of PTSD [4-6], and generally exacerbate waking symptoms of the disorder [7,8]. A depiction of the cyclic relationship between the waking and nighttime symptoms that contribute to the development and maintenance of PTSD is provided in Figure 1.
Figure 1.
This model is a depiction of the cyclic pattern of daytime symptoms and sleep disturbances and disorders in the development and maintenance of PTSD. These cycles are potentially independent in that even if the PTSD cycle is reduced/eliminated within trauma-focused treatment, the sleep disorder cycle may remain. PTSD=Posttraumatic Stress Disorder.
Although chronic insomnia and recurrent nightmares are the most commonly endorsed sleep disturbances in PTSD, other clinical sleep disorders have been implicated, including obstructive sleep apnea (OSA) [9], periodic limb movement disorder (PLMD) [10], and rapid eye-movement sleep behavior disorder (RBD) [11]. Additionally, other comorbid psychiatric conditions such as mood, anxiety-related, and substance use disorders [12] can influence the clinical course of the sleep disturbances associated with PTSD, often creating an exacerbating feedback cycle. However, a majority of sleep-focused treatment approaches and outcomes have primarily focused on chronic insomnia, recurrent nightmares, and OSA.
In the past, PTSD-related sleep disturbances were viewed as secondary to PTSD but are now recognized as primary symptoms, as they contribute to the development and maintenance of PTSD [13,14], see Figure 1. Therefore, these symptoms may require tailored interventions [13]. Despite the high prevalence of sleep disturbances in PTSD, studies of the first-line treatments of PTSD, both psychotherapy and pharmacotherapy, seldom examine the efficacy of these therapeutic modalities for PTSD-related sleep symptoms. Clinically, this is problematic given the evidence for significant residual sleep problems during and following successful completion of evidenced-based PTSD-focused interventions [15-18]. Further, persistent sleep symptoms have the potential to compromise treatment responses to empirically supported PTSD-focused interventions. Finally, given recent evidence directly relating sleep disturbances to suicidal ideation and behaviors [19], there is a crucial need for effective sleep-focused interventions for this population.
The primary aim of this review is to highlight the recent evidence for empirically supported treatment interventions for comorbid sleep disturbances commonly implicated in PTSD (i.e. chronic insomnia, recurrent nightmares, OSA). We first provide a brief background on the prevalence and methodological challenges posed by sleep disturbances of PTSD. Finally, we review sleep-focused psychotherapy and pharmacotherapy interventions that have shown utility in treating these conditions, as well as discuss the importance of incorporating integrated and sequential treatment approaches.
Prevalence and Methodological Challenges of Sleep Disturbances in PTSD
Chronic Insomnia and PTSD
Insomnia, defined as difficulty initiating and/or maintaining sleep is the most persistent symptom endorsed among individuals with PTSD, ranging between 70%-91%. [4,20,21]. Data demonstrate that insomnia symptoms may be an antecedent rather than a consequence of PTSD [22-24]. For instance, two studies of military personnel [22,23] found soldiers with daytime sleep complaints [24] and pre-deployment insomnia [23] had significantly greater odds of developing PTSD, depression, and anxiety disorders following deployment. Similarly, insomnia symptoms at 4 months post-deployment significantly predicted PTSD symptoms as well as depression 12 months post-deployment among combat veterans [24]. These findings are consistent across populations, for example, in a civilian sample of motor vehicle survivors, subjective reports of insomnia symptoms one month after the accident predicted PTSD diagnosis a year later [25].
Although civilian and military populations with PTSD exhibit similar prevalence rates for insomnia, there are several methodological challenges to consider that may impact the rates of insomnia in PTSD-diagnosed populations. For instance, how insomnia is operationalized within a study (e.g., as a disorder with a specified frequency and duration of symptoms or as symptoms captured within PTSD), the sample characteristics or setting of a study (e.g., treatment-seeking vs population-based sample), the type of index trauma endorsed that may increase odds of insomnia (e.g. sexual/physical assault, combat-related), the type of measurement used to quantify symptoms (e.g., subjective vs objective reports), time elapsed from the index trauma (e.g. childhood vs. adult), as well as comorbid disorders known to exacerbate sleep symptoms (e.g. depression, OSA, traumatic brain injury [TBI]) [4,20,21,26].
Recurrent Nightmares and PTSD
Although insomnia symptoms often co-occur in several psychiatric disorders (e.g. depression, anxiety-related, substance abuse), recurrent trauma-related nightmares are highly specific to PTSD [27,28]. These nightmares seem to replicate part or all of the traumatic event(s) and their content is more logical and lacks the distortions characteristic of normal dreaming [27,28]. Subjective reports indicate that 52%-96% of individuals with PTSD endorse experiencing recurrent nightmares [6,20]. Recurrent nightmares also increase the risk for the development of PTSD. For instance, recurrent nightmares within one month of experiencing a traumatic event increased the risk for PTSD severity 6 weeks and one year following the trauma exposure [27,28]. Additionally, recurrent nightmares have been related to poor sleep quality, depression, and heightened risk for suicide attempts and deaths by suicide [19,31-35].
There is considerable variability in prevalence rates of recurrent nightmares. This variability is attributed to the differences in methodology, in particular, the criteria used to define and evaluate nightmares across studies [36], the PTSD status of the study sample, as well as the population being studied [37]. Another challenge in characterizing this phenomenon includes the reliance on self-report and the inability to capture nightmares during sleep laboratory monitoring, due to their infrequent occurrence in this type of setting [38].
Prevalence of Sleep Disorders in PTSD
Obstructive Sleep Apnea and PTSD
OSA is characterized by sleep-related decreases (hypopneas) or pauses (apneas) in respiration [9] leading to arousals and sleep fragmentations. The apnea-hypopnea index (AHI) is the number of apneas or hypopneas recorded per hour of sleep, and the most frequently used diagnostic tool for the identification of OSA symptom severity [39]. The prevalence estimates of OSA in PTSD and other trauma-exposed populations are high, ranging from 40%-90% [40-43]. Further, evidence suggest that increased PTSD severity increases the likelihood of screening positive for OSA [44]. While the exact pathophysiological relationship between OSA and PTSD is not currently known, it has been proposed that these disorders interact and the sleep fragmentation associated with each disorder may exacerbate the vulnerability for or the consequences of the other [45]. There are several factors that may contribute to the variability of OSA presence in PTSD, particularly, related to difference in the diagnostic criteria and sample characteristics [e.g. sex, age, body mass index (BMI)]. Another important factor to consider is the methods used to generate prevalence rates. For example, some studies specifically recruit for OSA with elevated risk features (e.g. sleep disturbances), which is likely to exaggerate prevalence estimates [46]. Given these concerns, further investigation is warranted regarding the causes, consequences, and possible mechanisms related to the link between OSA and PTSD.
Periodic Limb Movement Disorder and PTSD
PLMD is a sleep-related movement disorder characterized by periodic, stereotyped limb movements during sleep. These movements, which occur predominantly in non-REM sleep, are often associated with partial arousals or awakening [10]. The prevalence rates for PLMD in the general adult population range from 4%-11%; however, data suggest that rates are much higher in individuals with PTSD compared to healthy controls [47]. For instance, two studies have assessed PLMD in combat-exposed veterans. One study found that 33% of individuals with PTSD had periodic limb movements (PLM) that ranged between 2 to 33 per hour of sleep compared to 0% in the healthy controls [48]. The second study reported that 76% of Vietnam veterans with PTSD had clinically significant PLMs that ranged from 5.6 to 190.5 per hour of sleep [49]. Other studies have also found an elevated PLM index in PTSD patients compared to controls [50].
Factors that contribute to the prevalence estimates of PLMs in individuals with PTSD are related to methodological concerns. For instance, the aforementioned studies had small samples and were limited to combat-related PTSD. Other factors are related to medication use. Specifically, central nervous systems-acting medications such as antidepressants are commonly used to treat the PTSD symptom complex which can increase PLMs during sleep, and potentially exacerbate insomnia and other sleep disorders [51,52].
Rapid Eye-Movement Sleep Behavior Disorder and PTSD
RBD is a parasomnia characterized by REM sleep without atonia on polysomnography (PSG) and dream enactment behavior [11]. Approximately 60% of RBD cases are considered idiopathic. Individuals with PTSD frequently endorse prominent movements during sleep [4], and there is substantial evidence to support REM sleep abnormalities among PTSD patients [53,54]; however, limited data exist on the relationship between RBD and PTSD. One study found that 56% of RBD patients had comorbid PTSD [55]. A more recent study found that RBD prevalence estimates increased from 9% overall to 15% in PTSD patients [56], suggesting that PTSD may be a significant predictor of RBD. A key feature of RBD, REM sleep without atonia has been observed in PTSD patients in laboratory settings; albeit in small samples. Researchers [57] have proposed a novel diagnosis, trauma-associated sleep disorder (TSD), which incorporates trauma-related nightmare enactment related to specific clinical features, and extreme nocturnal manifestations of traumatic experiences, including disruptive nocturnal behaviors (e.g., vocalizations, choking bed partner). TSD is distinct from nightmare disorder by the excessive motor activation and the nightmares that are infrequently recalled upon awakening that may be observed in both REM and non-REM sleep.
There are some factors that may influence prevalence rates and the relationship between RBD and PTSD. Specifically, the medications used to treat the PTSD symptom complex can increase the incidence of RBD, and could potentially exacerbate core sleep features (i.e., insomnia, recurrent nightmares) implicated in PTSD [58].
In summary, a range of sleep disturbances are more prevalent in individuals with PTSD compared to the general population, beyond those that are part of the diagnostic criteria. However, methodologic factors complicate drawing conclusions about the true prevalence of each sleep disorder.
Psychotherapeutic Treatments for Sleep Disturbances in PTSD
There is substantial evidence to suggest that the therapeutic treatments for PTSD are generally less effective in ameliorating the sleep disturbances than the waking symptoms of the disorder [16-18, 59]. Thus, findings highlight the need for sleep-focused interventions. Few studies have examined the efficacy and mechanisms of psychotherapeutic and pharmacological treatments for disturbed sleep in PTSD. However, some recommendations have been made regarding the few studies that have investigated the effectiveness of sleep-focused interventions in patients with PTSD. Specifically, the American Psychological Association (APA) [60] and the Department of Veterans Affairs/Department of Defense VA/DoD [61] clinical practice guidelines for treating sleep disturbances in PTSD recommend cognitive behavioral therapy for insomnia (CBT-I) as the first line treatment for patients with insomnia disorder and PTSD. There has been inconsistency and low-grade evidence for effective treatment of trauma-related nightmares, as such, the APA and the VA/DoD makes no recommendations for the treatment of recurrent nightmares in PTSD. In contrast, there have been recommendations provided by the American Academy of Sleep Medicine (AASM) for the application of imagery rehearsal therapy (IRT) for treating recurrent nightmares in PTSD as well as nightmare disorder [62].
Cognitive-Behavioral Treatment for Insomnia in PTSD
CBT-I is an evidence-based first line treatment intervention aimed at enhancing overall sleep quality [63]. CBT-I comprises instruction in stimulus control and sleep restriction, cognitive restructuring of disruptive thoughts and worries that interfere with sleep, in addition to sleep hygiene education and relaxation training [64]. Recently, a meta-analysis reported clinically relevant changes for individually delivered CBT-I in reducing sleep onset latency and wake after sleep onset, while increasing sleep quantity and sleep efficacy [65]. Another meta-analysis reported medium to large effects (.77-1.13) from pre-treatment to post-treatment for improving sleep onset latency, wake after sleep onset, and sleep efficiency [66].
More recent studies have shown CBT-I to be efficacious within PTSD samples in the community [67] and the military [68]. For example, the first randomized clinical trial (RCT) in a community sample seeking treatment for PTSD, found that compared to waitlist controls, those in the CBT-I group had superior responses on all sleep diary measures, sleep quality, and PSG derived total sleep time [67]. They also reported that subjective insomnia severity ratings fell below the clinically significant cut-off in 41% of the CBT-I group. Similarly, the military sample found that the CBT-I group had significant improvements on sleep efficiency, sleep duration, sleep quality, and insomnia severity compared to controls [68]. In addition to the targeted interventions, CBT-I has also been effective in improving other PTSD symptoms, and subsequently reducing fear of sleep, a commonly reported element of PTSD [69].
Imagery Rehearsal Therapy for Nightmares in PTSD
IRT is the best studied psychotherapeutic intervention for recurrent nightmares in PTSD, and the only recommended treatment for nightmares associated with PTSD by the AASM [62]. There is evidence that IRT leads to increased mastery of nightmare content and experiences [70]. There are several treatment protocols that share the following basic components of IRT: choosing a repetitive nightmare, rescripting, i.e., rewriting, the nightmare during waking, and imaginally rehearsing the new dream script at bedtime [71]. Two meta-analyses summarized the effectiveness of IRT for treating recurrent nightmares in PTSD [72,73]. They reported large effect sizes for nightmare frequency, sleep quality, and overall PTSD severity. However, these meta-analyses were limited due to the combination of several treatment protocols with diverse post-traumatic populations (specifically, those not diagnosed with PTSD). Another limitation included the lack of potentially active control groups.
Among veteran populations with recurrent nightmares associated with PTSD, the effectiveness of IRT treatments have been mixed. For example, in the largest study comparing IRT to an active control group [74], the IRT group did not significantly differ from those in the control group on reducing nightmare frequency and PTSD severity and increasing sleep quality. Further, neither group showed significant changes on nightmare frequency post-treatment. The authors concluded that the content of veterans’ nightmares in addition to particular changes that were made in the nightmare script during imagery rehearsal may serve as important modifiers of treatment outcomes to be addressed in future large-scale research investigations.
Exposure, Relaxation, and Rescripting Therapy for Trauma-Related Nightmares
Another psychotherapeutic intervention for trauma-related nightmares is exposure, relaxation, and rescripting therapy (ERRT). ERRT is a variant of IRT, with a specific focus on written and oral exposure to the most distressing nightmare and traumatic-related thematic rescripting [75]. Currently, ERRT is not considered a recommended treatment for PTSD-related nightmares, however, RCT’s comparing ERRT to waitlist controls have shown promise in reducing subjective reports of nightmares frequency and severity, fear of sleep, insomnia, symptoms of PTSD and depression, while increasing sleep quality and quantity among civilians with PTSD symptoms [76,77]. Among veterans, one study showed reductions in nightmare frequency and PTSD severity, while showing increased sleep time [78]. Another study in military veterans with trauma exposure found significant improvements in sleep quality, nightmare frequency and severity, insomnia, and depression [79]. Most recently, a study of ERRT specifically for active duty military personnel with trauma-related nightmares found medium effect size reductions in nightmares and other symptoms, including insomnia, PTSD, and depression compared to a minimal contact control group [80]. The most recent RCT, in a civilian population, compared ERRT to a dismantled protocol excluding the nightmare exposure and rescripting processes, and found that both groups, regardless of the inclusion of exposure and rescripting, exhibited significant improvements on nightmare frequency and distress [81]. The authors noted that the dose of exposure (i.e. single session) in the full protocol of ERRT may have been too brief to show an incremental benefit. Future works are needed to identify what treatment components work best, and for whom these treatments are most beneficial.
Overall, there are several factors to consider when examining the efficacy of cognitive-behavioral interventions for nightmares. In general, several factors may contribute to the inconsistencies across studies, particularly related to the study design (i.e. waitlist vs. active control), inclusion of individuals with and without trauma-related nightmares (thus potentially impacting the severity of baseline symptoms), and the lack of a standard treatment protocol (e.g., inclusion of different treatment components, varying number of treatment sessions). Of particular importance are the varying inclusion/exclusion of different components (e.g., specific exposure, thematic rescripting, relaxation, etc.), see Table 1 for an example of the components and protocol variations.
Table 1.
Cognitive-Behavioral Treatment-Nightmares (CBT-N) Components and Protocol Variations
| Example Protocol Variations | |||||
|---|---|---|---|---|---|
| Treatment Components | IR (Krakow et al., 1995) [70] |
IR (Forbes et al., 2001) [104] |
IR (Germain et al., 2003) [105] |
IR (Nappi et al., 2010) [106] |
ERRT (Davis, 2009) [107] |
| Nightmare Selection | |||||
| Most Distressing | X | ||||
| Lesser Intensity | X | X | |||
| Repetitive | X | X | |||
| Exposure to Nightmare Content | |||||
| Direct exposure (Written or Oral) | X | X | |||
| No exposure | X | X | X | ||
| Sleep Behavior Modification | |||||
| Include sleep hygiene & stimulus control guidelines | X | ||||
| Relaxation Training | |||||
| Include relaxation training | X | ||||
| Psychoeducation on PTSD and Sleep | |||||
| Includes Psychoeducation | X | X | X | ||
| Rescripting Process | |||||
| Thematic Rescripting | X | ||||
| Change in “any” way | X | X | X | X | |
| Imagery Rehearsal | |||||
| Repeated imagining of new dream | X | X | X | X | X |
Note. CBT-N is a multicomponent treatment approach that typically involves psychoeducation, identifying a target nightmare, rescripting (i.e., rewriting) the nightmare, and repeatedly imagining the new dream before sleep. Some protocols include exposure, stimulus control therapy, and relaxation training. IR = Imagery Rehearsal. ERRT = Exposure, Relaxation, and Rescripting Therapy (ERRT).
Integrated and Sequential Psychotherapeutic Interventions
Given the evidence of residual insomnia and recurrent nightmares during and following PTSD-focused treatments [15,59], and that successful sleep-focused interventions may improve daytime PTSD symptoms, it is also essential to understand the potential benefit of integrated and sequential sleep-focused and PTSD-focused interventions. Recently there have been integrated protocols to examine the effectiveness of combined treatments for sleep disturbances in PTSD. Studies in both civilians [82] and veterans [83,84] using combined components of CBT-I and IRT found significant improvements in sleep quality, nightmare frequency, insomnia severity, PTSD symptoms and depression. Most recently, an RCT of CBT-I +IRT or IRT alone found significant reductions in nightmare frequency and distress, and sleep disturbances in a veteran population [85]; however, adding IRT did not contribute to significantly greater treatment benefits than those achieved with CBT-I alone. Additional studies are needed to substantiate these findings. Few investigations have included sequential approaches. Recently, a trial examining the effectiveness of IRT before CBT for PTSD compared to CBT alone found no benefit of the sequential treatment protocol on PTSD symptoms [86]. Although, the group receiving IRT did show greater improvements in nightmare frequency, nightmare distress, and sleep quality than the CBT group. Finally, there are ongoing clinical trials investigating integrated CBT-I and PE (NCT02774642), Cognitive Processing Therapy (PT) and ERRT (NCT02236390), and CPT and cognitive behavioral therapy for insomnia and nightmares (CBT-in; NCT02773693) on sleep and PTSD outcomes in civilians and military personnel.
Other Therapeutic Treatments for Sleep Disturbances in PTSD
Treatment of Obstructive Sleep Apnea in PTSD
Continuous positive airway pressure (CPAP) is the gold standard recommended therapy for OSA. CPAP acts as a splint to prevent the upper airway soft tissue from collapsing [87]; using air under pressure to maintain airway patency during sleep. Few investigations have provided preliminary evidence that adherence to CPAP for OSA reduces nightmare frequency in both idiopathic and trauma-related nightmare suffers. Two studies [88,89] found that a reduction in nightmare frequency was related to CPAP adherence. More recent, two additional studies [90,91] found that CPAP treatment for OSA significantly improved subjective PTSD symptoms among veterans with PTSD. They also found that the percentage of CPAP adherence predicted the observed improvements.
Pharmacological Treatments for Sleep Disturbances in PTSD
Several classes of medications have been evaluated for reducing insomnia and recurrent nightmares in PTSD patients, to include the selective serotonin reuptake inhibitors (SSRIs), typical/atypical antipsychotics, tricyclic antidepressants, alpha-1 and alpha-2 adrenergic receptor antagonists [92,93]. Despite, the effectiveness of psychotherapeutic interventions (e.g. CBT-I) demonstrating beneficial long-term outcomes over medications, benzodiazepines and non-benzodiazepines receptor agonist, as well as off-label medications for sleep disturbances continue to be a primary treatment recommendation in individuals with PTSD [94].
Pharmacological Treatments for Insomnia in PTSD
There have been limited studies examining the benefits of pharmacological treatments for insomnia in individuals with PTSD. The novel non-benzodiazepine benzodiazepine receptor agonist (NBRA) zolpidem was reported to be beneficial for insomnia associated with PTSD [95]. Another study found that NBRA eszopiclone led to greater improvements in PTSD symptoms and associated insomnia relative to placebo [96]. Trazodone, a 5HT2 antagonist/SSRI, with sedative effects is frequently used in low doses to treat insomnia related to PTSD [97]. Given the limited evidence for the efficacy of pharmacological treatments for insomnia in PTSD, the VA/DoD treatment guidelines recommend medications as second-line treatments [61]. Finally, given the risk of excessive daytime sleepiness, pharmacological treatments with sedative properties should be used with caution. Recently, a clinical trial has been approved to investigate the efficacy of trazadone, eszopiclone, or gabapentin in reducing insomnia symptoms in patient with PTSD (NCT03668041).
Pharmacological Treatments for Recurrent Nightmares in PTSD
Trazodone and SSRIs, including Fluvoxamine and Nefazodone, may have some utility in treating nightmare disturbances in PTSD populations [98]. However, none of these pharmacological agents have been tested in RCTs. Additional pharmacotherapies, including topiramate, lose-dose cortisol, and gabapentin have been identified as having low level evidence for the effectiveness in managing recurrent nightmares in PTSD [98]. The greatest advancement in the pharmacological treatment of trauma-related nightmares is prazosin, an alpha-1 adrenoceptor antagonist. Studies in civilian [99] and military [100] populations have reported on the effectiveness of prazosin in the treatment of nightmares. Collectively, these studies found decreases in trauma-related nightmares and distressed awakenings not related to nightmares. They also reported improvements in sleep quality and other sleep disturbances.
A systematic review and meta-analysis on the efficacy of prazosin reported significant improvements in nightmare frequency, sleep quality, and PTSD severity [101]. However, a large multi-site study examining the efficacy of prazosin for combat-related PTSD, found no benefit of prazosin over placebo in reducing nightmare frequency or PTSD severity [102]. Given the mixed findings and limited evidence, the VA/DoD clinical practice guidelines make no recommendation for or against prazosin for the treatment of recurrent nightmares [62]. A recent meta-analysis investigating the efficacy of IRT and prazosin suggests that this downgrade of prazosin may be premature, as the treatment effects of prazosin were found to be comparable to those of IRT [103]. More work is needed to identify characteristics of response to these different treatment options.
Conclusions
Sleep disturbances, such as chronic insomnia and recurrent nightmares, are among the most distressing symptoms of PTSD and significantly contribute to the development, maintenance, and clinical course of the disorder. Other prominent sleep disorders, including OSA, RBD, PLMD, as well as other psychiatric disorders may be comorbid with PTSD and have implications for successful treatment. The prevalence rates of comorbid sleep disturbances in PTSD are high, but estimates may be indicative of several methodological challenges, including how sleep symptoms are operationalized within a study, sample characteristics or setting of a study, type of index trauma endorsed, type of measurement used to quantify symptoms, inability to capture specific sleep disturbances during sleep laboratory monitoring, and varying comorbid disorders known to exacerbate symptoms.
Psychotherapeutic treatments designed to specifically target chronic insomnia and recurrent nightmares have shown promise in alleviating symptoms. Clinical practice guidelines by APA and VA/DoD recommend CBT-I for insomnia, and AASM recommends IRT as a first line treatment for nightmares. The expansion of psychotherapeutic treatment modalities is encouraging; however, a lack of standardized delivery and high dropout rates continue to impose significant challenges in attaining successful outcomes. Additional RCTs are needed to understand features associated with treatment responsiveness. Pharmacological treatments for the overall PTSD symptom complex have rarely investigated the effectiveness of treatments for chronic insomnia and recurrent nightmares. Some pharmacological treatments, including antidepressants and atypical antipsychotics have provided evidence for the efficacy of sleep disturbances in PTSD, however, findings are limited due to methodological challenges and the absence of larger RCTs. Presently, the alpha-1 adrenoceptor antagonist prazosin is the only recommended pharmacological treatment for trauma-related nightmares by the AASM’s clinical practice guidelines.
Relatively few studies have directly investigated the efficacy of integrated and sequential interventions on sleep disturbances in PTSD. There is opportunity for future investigations to determine the effectiveness of integrated and sequential approaches, to examine the suitability of these treatment modalities to specific patient populations, and to identify when these approaches are warranted with other interventions.
Acknowledgments
Disclosure Statement: All Authors declare no conflicts of interest. The views expressed here are the authors’ and do not necessarily represent the views of the Department of Veterans Affairs or the United States government. J.A.B.'s time was supported by a Center Grant from the National Institute of General Medical Sciences, Grant Number 5P20GM103653-08. K.E.M.’s time was supported by Career Development Award Number IK2 CX001874 from the United States Department of Veterans Affairs Clinical Sciences R&D (CSRD) Service.
Footnotes
Human and Animal Rights Statement: This article does not contain any studies with human or animal subjects performed by any of the authors.
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