Sleep Disturbances in Patients with Nonepileptic Seizures.

OBJECTIVE: Up to 20% of patients treated for epileptic seizures experience psychogenic nonepileptic paroxysms (PNES). These patients present a significant burden for the health care systems because of poor treatment outcomes. The presented review aims to summarize the current state of knowledge on sleep disturbances in patients with nonepileptic seizures.
METHODS: Articles were acquired via PubMed and Web of Science, and papers between January 1990 and March 2020 were extracted. Inclusion criteria were (1) published in a peer-reviewed journal: (2) studies in humans only; or (3) reviews on a related topic; (4) English language. The exclusion criteria were: (1) abstracts from conferences; (2) commentaries; (3) subjects younger than 18 years. From primary assessment, 122 articles were extracted; after obtaining full texts and secondary articles from reference lists, 45 papers were used in this review.
RESULTS: Limited data are available regarding sleep disorders in PNES patients, over the last 30 years only nine original research papers addressed sleep problems in patients with PNES with only six studies assessing objectively measured changes in sleep. Current literature supports the subjective perception of the sleep disturbances with mixed results in objective pathophysiological findings. Conflicting results regarding the REM phase can be found, and studies reported both shortening and prolonging of the REM phase with methodological limitations. Poor sleep quality and shortened duration have been consistently described in most of the studies.
CONCLUSION: Further research on a broader spectrum of patients with PNES is needed, primarily focusing on objective neurophysiological findings. Quality of life in patients suffering from PNES can be increased by good sleep habits and treatment of comorbid sleep disorders.

Introduction

As many as one-fifth of patients, who show up at specialized neurological departments with seizures do not meet the diagnostic criteria for epilepsy. Most of these patients suffer from dissociative seizures, otherwise known as “nonepileptic seizures”. These dissociative seizures (otherwise psychogenic nonepileptic seizures, PNES) are, according to DSM-5, a type of the conversion disorder belonging to the functional neurological symptom disorders (FNSD).1 They manifest with paroxysmal, sudden changes in motor activity, behaviour, cognitive processing with changes in consciousness, or autonomic functions associated with dysfunction in the processing of anxiety.2–4 PNES episodes may include motor behaviour, intrinsic sensory or cognitive deviations. PNES can be confused with partial or generalized epileptic seizures, and the patient may continue to communicate with the environment or stop responding.5 PNES is a complex neuropsychiatric disorder at the border of neurological and psychiatric disciplines that has been largely overlooked and avoided by mental health providers.6–8 The diagnosis of PNES is also made in 20 to 50% of inpatients in departments specialized in epilepsy9,10 and can be present in up to 25% of patients treated for refractory epilepsy.11–14 The prevalence estimates are further complicated by common comorbidity between PNES and epilepsy that occurs in 20% to 60% of the individuals with epilepsy.15 PNES are more prevalent in women, most of whom are aged between 15 and 35 years.8,16,17

Patients with PNES have high health care consumption, and they are reaching a level of disability in everyday life similar to that of patients with epilepsy.18,19 Their prospective treatment outcomes are not favourable. In a 10-year follow-up study, the treatment outcome was rated as poor in 44% of patients (seizures persisted or patients remained dependent on care).20

Despite advances in diagnostic and evidence-based treatment, current knowledge about PNES has not been sufficiently translated into clinical practice.8,21 In some studies, the diagnosis of PNES is delayed up to nine years after the onset of symptoms.21,22 The delayed diagnosis is then associated with poor prognosis.22–24 Although the diagnosis should be made by video electroencephalograph (vEEG), most health care providers do not use this test.24 Unfortunately, this can lead to an unnecessary overlook of PNES diagnosis as vEEG usually detects seizures that do not have EEG correlates of the epileptic activity. However, there are also situations where even long-term follow-up does not lead to the recording of typical seizures.25

Also, the pathophysiology of PNES is not well understood.26,27 Physical or sexual abuse in anamnesis is frequent. It occurs in up to 84% of these patients.27–29 Patients with PNES are characterized by difficulty verbalizing their emotions, especially when anxious and manifest them via somatic symptoms instead.30 Recent advances in the search for possible neurophysiological biomarkers in functional MRI studies indicate abnormalities in emotional, cognitive, executive, and sensorimotor neuronal circuits.24,31,32 Psychobiological studies have shown that patients with PNES may be less tolerant of emotional arousal33 and show high alexithymia (difficulty identifying and describing internal emotional experiences),3,34,35 dissociation,6,36 somatization rates,3 and tendencies to avoid emotions altogether.36,37 Some researchers describe patients with PNES is a heterogeneous group.26,31,38,39 However, Kalogjera-Sackellares (1996) described two leading “causes” of PNES: post-traumatic PNES, acute or distant trauma, and developmental PNES emotional deprivation or psychological trauma during developmental periods.40 As noted above, PTSD and history of traumatic events are highly prevalent among patients with PNES.27,41,42 Some authors have conceptualized PNES as manifestations of PTSD;43 however, only half of the patients with PNES have PTSD.28 Several comorbidities are usually present, especially mood, anxiety and sleep disorders, personality disorders, chronic pain other disorders with somatic symptoms.44

Patients with PNES are prone to more somatic symptoms than the healthy control group or patients with epilepsy. Examples of such symptoms are the higher incidence of somatic syndromes (fibromyalgia, chronic pain, chronic fatigue syndrome, migraine headaches),45 mood and anxiety disorders (including PTSD) and personality disorders.41,42,46 These comorbid conditions can and should be addressed together with dissociative seizures in complex neuropsychiatric treatment. Regarding treatment, various psychotherapies and pharmacological therapies for PNES have been investigated.7,24,26 The treatment of choice is cognitive behavioural therapy.42,47,48

According to literature maintaining proper sleep hygiene and the daily regime is essential in managing patients with PNES and it is discussed whether sleep disorders can have an effect and if so to what extent they can disrupt treatment of patients with PNES.44 Our first focus was to objectify whether PNES can occur in sleep according to contemporary literature and researches and whether there are specific changes in sleep patterns that can be quantified. Since insomnia and changes in the sleep duration, in general, are associated with various psychiatric disorders, we tried to establish whether there is a link between sleep duration and dissociative seizures. Clinical praxis needs to understand specific sleep problems in patients with PNES to improve the quality of life and address these issues in the management and treatment plan. Following research questions were formulated:

(1) Do dissociative episodes occur during the sleep or only while awake?

(2) Does the total length of sleep differ from the norm in patients with dissociative seizures? Are there any objectively assessed changes in sleep duration?

(3) Is the sleep architecture altered in patients with dissociative episodes?

(4) Do patients with dissociative seizures experience sleep disorders other than insomnia?

Method

These narrative review articles were obtained via PubMed and Web of Science, and papers between January 1990 and March 2020 were extracted. We made a sequence of literature searches using the keywords: dissociative seizures, sleep disorders, insomnia, PNES and psychogenic nonepileptic paroxysms. Keywords were used in all possible permutations. Selected papers met inclusion criteria: (1) published in peer-reviewed journals; (2) human studies; or (3) reviews on the related topic; (4) English language. We included original articles that diagnosed patients via vEEG according to DSM-5 or ICD-10 criteria. Articles included both patients with exclusive PNES a patient with comorbid epilepsy. The exclusion criteria were: (1) abstracts from conferences; (2) commentaries; (3) subjects younger than 18 years. We excluded studies in children, reasoning the neurodevelopmental nature of sleep in them. More articles were found from the references of the primary articles. The primary process selected a total of 122 items. Adjusting for the inclusion and exclusion criteria, 34 pieces were selected. After a full-text assessment by the research team, 21 papers were included, all articles and their inclusion were subjected to open discussion and decision by the research team. Secondary papers from the primary articles’ references were also searched, and eligible papers were added to the first list (n = 24). In summary, 45 papers were included in the review (Figure 1).49

Figure 1

Summary of the selection process.

Results

Contemporary literature included in this review found predominantly subjective changes in sleep in patients with PNES. There is a lack of objective evidence to support these subjective complaints.50 According to one study, patients with PNES, are more prone to sleep disturbances than patients with epilepsy.51 We further divide our findings according to the research questions and summarise the table of original research papers included in this review (Table 1).

Table 1

Summary of Original Research Studies

Study	Sample Size	Study Design	Methodology	Results
Bazil et al25	8 females with PNES; 10 females with ES	Comparative prospective study	Objective sleep measures: polysomnography over one night, PNES and ES verified by vEEG	Percentage of REM sleep was significantly higher for women with PNES (23±1%) than those with ES (18±1%).
Latreille et al51 *	17 with PNES; 10 with ES	Comparative pilot prospective study	Objective sleep measures: vEEG monitoring and actigraphy; Questionnaires: PSQI, ISI, ESS, MEQ, daily sleep diary	Patients with PNES more frequently reported moderate-severe changes in sleep patterns, notably sleeping less than usual, waking up 1–2 h earlier, and having trouble returning to sleep.
Latreille et al50 *	17 with PNES; 10 with ES	Comparative pilot prospective study	Objective sleep measures: vEEG monitoring and actigraphy; Questionnaires: PSQI, ISI, ESS, MEQ, daily sleep diary	PNES subjects showed greater sleep onset latency (48.7 ± 47.5 min vs 14.0 ± 13.4 min; p = 0.02). PNES subjects reported worse sleep quality (10.8 ± 5.1 vs 5.8 ± 2.9; p = 0.01) and were more likely to meet clinical criteria for insomnia relative to epilepsy subjects (50% vs 10%, p = 0.05)
Thacker et al52	12 with PNES	Case series study	Objective sleep measures: continuous vEEG monitoring in sleeping patients with PNES	All patients had a well‐organized posterior α rhythm immediately before the onset of clinical changes despite the appearance of sleep.
Bazil & Walczak.55	1116 seizures (280 PNES) in 188 patients	Retrospectively examined vEEG monitoring	Retrospectively examined video-EEG monitoring	PNES were rare between midnight and 6 a. m. and never occurred during sleep.
Duncan et al56	142 with PNES; 100 with ES	Comparative prospective study	Semi-structured interview verified by vEEG	84/142 patients with PNES (59%) and 47/100 with epilepsy (47%) gave a history of events during sleep (p = 0.062). In patients with PNES, significant associations were found between a history of sleep events and: convulsive clinical semiology, antiepileptic drug treatment, fatigue, suicide attempts, mood disorder, and physical abuse. A particularly strong association with social security benefit was also found (odds ratio 4.0, p<0.001).
Orbach et al59	27 subjects	Retrospective study	Objective sleep measures: vEEG; Two epileptologists blindly reviewed cases with suspect PNES together with control cases	In a minority of patients (<1%), PNES began either while the patient was sleeping, or within several awakening seconds.
Graham & Kyle62	225 patients with PNES; sample recruited online via patient charities (N=205) and a consecutive clinical sample (N=20)	Preliminary cross-sectional analysis;	Questionnaires: SCI, PSQI, Sleep item from the CORE-10, WSAS, GADS, PHQ	Poor sleep was common in both samples (89% in the clinical range) and was characterised by low sleep efficiency (M=65.40%) and low total sleep time (M=6.05h). In regression analysis, sleep quality was negatively associated with FND-related functional impairment, accounting for 16% of the variance and remaining significant after introducing mood variables.
Popkirov et al67	22 with PNES; 44 with ES	Comparative prospective study	Objective sleep measures: 5-day video EEG recording, polysomnography performed on the third night of monitoring.	9% of patients with ES and 9% of patients with PNES had mild sleep-disordered breathing. 7% of patients with ES and 14% of patients with PNES had mild or moderate OSAS. Time awake after sleep onset was high in both groups. There were no significant differences in sleep architecture between the groups except for a difference in average N3 sleep stage proportion. PLMs were common in both groups, and 27% of patients with PNES had high PLM rates and high arousal indices.

Notes: *The team of Latreille et al published their data in two separate studies (2018, 2019) focused on different outcomes. In the first part, they assessed subjective aspects of the sleep via questionnaires, in the second part objective assessment of sleep architecture was conducted via vEEG.

Abbreviations: vEEG, video electroencephalography; REM, rapid eye movement; PNES, psychogenic nonepileptic paroxysms; ES, epileptic seizures; OSAS, obstructive sleep apneas; PSQI, Pittsburgh Sleep Quality Index; ISI, Insomnia Severity Index, ESS, Epworth Sleepiness Scale, MEQ, Morningness-Eveningness Questionnaire; SCI, Sleep Condition Indicator, WSAS, Work and Social Adjustment Scale; GADS, Generalised Anxiety Disorder Scale, PHQ, Patient Health Questionnaire; PLMs, periodic limb movements.

Do Dissociative Seizures Occur During Sleep or Only While Awake?

Patients with PNES frequently describe dissociative seizures occurring in sleep, when monitored by telemetry they are usually preceded by awakening,52,53 which can be recorded on EEG. It is an open question of whether dissociative seizures may occur in sleep or not.

One of the first studies by Thacker et al reported dissociative seizures in 12 patients, who seemed to be asleep, but according to video-EEG, were awake.52 Later works reported up to 13% of PNES episodes happens during seeming sleep.5 However, dissociative convulsions have rarely been observed in proper sleep confirmed by electroencephalography (EEG).54

PNES are not evenly dispersed throughout 24 hours. Psychogenic symptoms are believed to be only present when the person is awake. If PNES happens during sleep, studies imply that they are awake with their closed eyes (experiences “a pseudo-sleep”). In contrast, epileptic seizures often occur during normal sleep.52,55,57,58 Still, Orbach et al found that a small proportion of patients (<1%) can develop PNES during the sleep (most commonly in N2 or N3 of NREM (non-rapid eye movement sleep) or within seconds of waking up. The EEG finding of the seizure itself was at the waking stage.59 Similarly, Seneviratne et al found that the chances of developing PNES in wakefulness are approximately four times higher compared with the sleeping state (ODDs-ratio: 4.27, 95% CI: 2.44–7.48). Moreover, he found that the majority of dissociative seizures occurred in the night interval while being awake.60

There is also another quite common research problem - in patients who experience dissociative seizures, it is unlikely that the episode will occur when monitored. Patients with different types of paroxysms also require a different approach. Both dissociative seizures and epileptic seizures may be present in the same patient. Besides, a dissociative attack in a patient with epilepsy can appear on the telemetry unit, perhaps from the stress caused by the pressure to “perform” and have the attack recorded.61

In summary, PNES onsets are much more frequent in an awake state, most commonly in the night interval. Even though patients with PNES states that they are asleep at the onset of the dissociative seizure, objective methods suggest that PNES event is preceded by awakening and true nature of dissociative seizures in sleep is still unclear.

Does the Subjective Sleep Length Differ from the Norm in Patients with Dissociative Seizures? Are There Objectively Assess Changes in Sleep Duration?

Phillips et al showed that patients with PNES reported worse subjective sleep quality than epilepsy patients and a control patient group. The frequency of clinically diagnosed sleep disorders in PNES patients (29%) did not diverge from patients with epilepsy (21%) and the control group (22%). Those differences were not explainable by different medication, BMI of the patients or comorbid sleep-disordered breathing.13 In a study with a larger group of patients with probable neurological disorders, counting PNES as well, up to 89% of the sample were at high risk group for the insomnia diagnosis.62 Patients in the study also presented subjectively worse quality of sleep, reduced sleep time compared to the healthy sample, and those were negatively connected with functional impairment in everyday functioning.62

Latreille et al recently pointed out that PNES patients are more prone to poor sleep hygiene than patients with epilepsy. The paper further compared sleep problems in patients with PNES and patients with epilepsy. Video electroencephalography (vEEG) was performed and validated subsequently by a neurologist—the subjects of the study filled in the Beck Depression Inventory-II (BDI-II). One item of the said inventory is focused on the changes in the sleep patterns. All subjects also filled in the Epilepsy Quality of Life Inventory-10 (QOLIE-10), which assesses health-related aspects of life quality in epilepsy patients.50,63 This tool was initially validated for use in epilepsy, nowadays it is used in PNES patients.64

Compared to the epilepsy group, patients with PNES were more likely to have mild to severe sleep changes, mostly shorter sleep length by up to 1–2 hours, and difficulty falling asleep again. These changes in sleep patterns were linked with lower quality of life. These results propose that sleep disturbance is a more pronounced problem in PNES than in epilepsy. It is not identified whether it can be attributed to paradoxical insomnia (or “poor perception of sleep”, a tendency to underestimate total sleep time) or whether PNES patients are more prone to sleep problems than a healthy population. They may also be at risk due to overlapping somatic and psychiatric diagnoses.64 The cited paper says that sleep disorders can be more prevalent among PNES patients, up to one-third of the studied group had been diagnosed with the sleep disorder. If we manage to improve sleep, we can observe a decrease in various symptoms of PNES, and that can lead to improvement of the patient’s quality of life and further alleviate other symptoms of PNES. A recent study reported that comorbid sleep disorders in patients with mental illnesses could harm treatment results and serve as barriers to treatment.65

In summary, only limited data regarding objective changes in sleep duration are available in the current literature. Over 30 years included in our review, we found only three research papers that worked explicitly with sleep duration in patients with PNES and proposed that sleep disturbance can significantly affect life quality. However, the research papers did not confirm subjective complaints via polysomnography. It is advisable to look for sleep disorders in PNES patients and treat them if possible, for future research, we propose an objective assessment of sleep via polysomnography on a larger sample of patients with PNES.

Is the Sleep Architecture Altered in Patients with Dissociative Seizures?

One study examined sleep architecture in eight PNES subjects and ten epilepsy patients via EEG in specialized epilepsy department.25 The authors examined the structure of sleep by polysomnography, comparing PNES and epilepsy patients. Video-EEG monitoring validated by neurologists verified the epileptic seizures and PNES, and clinical neurophysiologists and psychiatrist evaluated patients with PNES. During the study, the patients did not have any anticonvulsants or antidepressants. Caffeine consumption was prohibited, and all patients with diagnosed sleep disorders were excluded, although this exclusion was made solely on anamnestic data. During polysomnography and 24 hours, long observation after no seizures were captured that would disrupt the sleep structure.66 Study found that the proportion of REM sleep was more notable in females PNES patients (23%) than in epileptic female patients (18%). REM latency was slightly lower in patients with PNES, although this difference was not statistically significant. No significant differences were found in the sleep duration, slow-wave sleep or sleep efficiency. Besides, there were no differences in N1 and N2 stages. This paper proposes that PNES patients have similar architecture disturbances to patients with major depression with increased REM sleep.66

Two limited studies (n <20) reported worse sleep quality reported by patients13 and prolonged REM phases during polysomnography in patients with PNES than epilepsy patients.25

Regarding the objective sleep architecture, the authors of the study Latreille et al found a nonsignificant trend towards a reduced duration of the REM phase in PNES patients compared to individuals with epilepsy.50 This contradicts the Bazil et al results, which found the opposite relationship. This difference may be caused by the discontinuation of antidepressants in Bazil et al study.66 One possible exploration of the REM phase increase in PNES patients is a rebound phenomenon.

Two recent studies by Popkirov et al and Latreille et al found that sleep architecture was generally comparable in patients with PNES and epilepsy.51,67 Popkirov et al examined the occurrence of sleep disorders in a group of 22 PNES patients and 44 epilepsy patients.67 In contrast to Bazil et al findings, no differentiation in the REM phase was observed; instead, patients with PNES had shorter slow-wave sleep duration than patients with epilepsy.66

Latreille et al compared sleep-wake patterns in a prospective observational study in PNES and epilepsy patients. Twenty-seven subjects were included in the study, of which 17 had PNES, and 10 were diagnosed epilepsy. Compared to epilepsy controls, the PNES patients showed increased latency of sleep onset (on average about 30 minutes longer than controls). Otherwise, both groups had a similar sleep architecture. However, the PNES patients subjectively had poorer sleep quality measured by Pittsburgh Sleep Quality Index (10.8 ± 5.1 versus 5.8 ± 2.9; p = 0.01; higher score indicates the worse quality of sleep) and met the clinical criteria for insomnia more often than patients with epilepsy (50% vs 10%, p = 0.05). In addition, a higher number of patients with PNES admits taking sleep medications (44% vs 0%, p = 0.01).51 In general, the authors found more evidence about subjective foundation rather than an objective basis of sleep disturbances in patients with PNES. Patients with PNES are more likely to report generally worse sleep quality and almost 70% report usage medication for sleep. The majority of patients with PNES met the diagnostic criteria for moderate to severe insomnia. However, actigraphy did not show this trend; both groups had similar sleep latency and showed comparable motor activity during the night and day. It can be theorised that based on the fact that the sensor measures motor activity, sleep latency may be underestimated when patients are at rest or even when they are awake. Otherwise, the sleep architecture between PNES and epilepsy was very similar.51

In summary, these studies imply that sleep disorders are common in PNES patients. Still, there is no consistent objective confirmation of sleep structure changes in this group than patients with epilepsy. Besides, it appears that in patients with PNES, sleep disorders may be associated with an increased tendency to somatisation, another form of conversion symptom associated with PNES and other functional disorders.7

Do Patients with Dissociative Attacks Have Sleep Disorders Other Than Insomnia?

Sleep can be useful in distinguishing PNES from other neurological disorders. Pseudo-cataplexy (“psychogenic” narcolepsy), “pseudo-parasomnia” and PNES may have a similar appearance.58 Cataplexy and parasomnia are the most common sleep disorders that can be confused with epilepsy.68,69 Cataplexy is a sudden loss of muscle tone or falls caused by strong positive or negative emotions; it is usually a symptom of narcolepsy.70 Parasomnias are complex or bizarre behaviours that result from sleep.68 Somnambulism, sleep terror, and rapid eye movement sleep behaviour disorder (RBD) are common parasomnias that could be mistaken for nocturnal epilepsy.71 There are no literature data on the presence of these parasomnias in PNES, and studies that monitored overnight EEG video did not describe them.13,57

Popkirov et al found a comparable percentage of sleep-disordered breathing in epileptic patients and PNES patients (9%), while periodic limb disturbance was more frequent in patients with PNES than patients with epilepsy (27% vs 9%). However, the study was conducted on a limited sample (22 patients with PNES and 44 with epilepsy).67

PNES and post-traumatic stress disorder (PTSD) are often linked via experienced psychological trauma, thus sleep abnormalities, especially nightmares that occur in PTSD, might be similar in PNES.58

One theory states that the body mass index could be higher in PNES patients compared to epilepsy patients.72 As a result, sleep-related respiratory distress could be more pronounced in PNES patients than in healthy subjects. The Royal Melbourne Hospital Epilepsy Monitoring Unit is routinely using polysomnography in all patients monitored by video-EEG, and published their findings in 87 patients: 43 with epilepsy, 17 with PNES, and 4 with both.13 Data were assessed using the Pittsburgh Sleep Quality Index (PSQI), a scale evaluating sleep quality, where an interval from 0 to 5 indicates high sleep quality and above 5 low quality (PSQI).73 Patients with PNES had from the beginning higher PSQI scores (11.0) compared to patients with epilepsy (7.8). Clinically significant sleep disordered breathing (measured by Apnoea/hypopnoea index over 15) was diagnosed in 19 of 87 (22%) patients. OSA (obstructive sleep apnea) was diagnosed in 15 of them, one patient was diagnosed with CSA (central sleep apnea), and three patients were diagnosed with mixed sleep apnea. Sleep-disordered breathing was diagnosed in 5 of 17 patients with PNES compared to 9 of 43 patients with epilepsy and 5 of 23 patients in the control group. Although the frequency of sleep-disordered breathing in patients with PNES was higher, it did not reach significance due to the limited number of subjects. The authors found significantly higher PSQI scores in PNES patients compared to epilepsy patients and control group, which is in agreement with previous findings.13 Contrary to the previously theorized relationship of BMI and PNES, quality of sleep in patients with PNES compared with epilepsy group does not seem to be associated with differences in BMI in this study.

In summary, the current literature does not describe significantly higher proportions of sleep disorders other than insomnia. However, there exists some scarce evidence of higher incidence of periodic limb movement syndrome in those patients. Therefore, further research with a higher number of patients is needed to confirm these findings further.

Conclusion

Dissociative seizures (PNES) present a relatively common and disabling disorder. There is a lack of research in its aetiology and treatment. This is probably due to the relatively low effectiveness of treatment of these patients in the past. In the last decade, however, neuropsychiatric approaches have improved diagnostics with video EEG monitoring, and randomized controlled trials have demonstrated the effectiveness of cognitive behavioural therapy.

Studies included in this review put forward that sleep problems are common in PNES patients. Besides the nature of sleep disorders, the patient may be more prone to somatization, which could be interpreted as other forms of conversion, and many PNES patients have other comorbid functional disorders.7

Understanding the specific sleep problem of PNES, especially when sleep is essential for good health, can offer insight into improving the quality of life. Future research should utilize video EEG monitoring on a broader selection of patients with PNES to evaluate the physiology of sleep in patients with PNES, as insight into sleep disturbances may allow further understanding of the aetiology and symptoms of PNES.

In summary, contemporary literature and original research papers found more evidence of subjective sleep quality than objective, measurable changes and disorders in PNES patients. Education of patients with PNES about sleep hygiene and the significance of proper sleep habits should be included in the basic management of PNES patient. Physicians should also assess sleep in PNES patients and treat sleep disorders according to guidelines to improve overall health and quality of life.