Sleepwalking, sleep terrors, sleeptalking and sleep paralysis are some of the behavioural manifestations associated with the partial arousals from sleep known as parasomnias — a group of sleep disorders defined as undesirable physical events or experiences that occur during the initiation of sleep, during sleep or during arousal from sleep.1 Although more common in children, parasomnias can occur at any age.
During sleep, the brain cycles regularly between wakefulness, nonrapid eye movement (NREM) sleep and rapid eye movement (REM) sleep. Nonrapid eye movement sleep is subdivided into four stages: stage I, a transitional stage between wake and sleep; stage II, which makes up most of the sleep period; and stages III and IV, which typically occur in the first half of the night and during which more profound stimulus is required to wake the sleeper. Parasomnias occur when transitions between these stages are blurred (commonly between stages III/IV and the awake state), causing behaviours that lack the complete awareness and mentation associated with wakefulness.1
There are two criterion-based classifications of sleep disorders: the Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-V) classification2 and the International Classification of Sleep Disorders (ICSD) classification.1 The DSM-V uses a “lumping versus splitting” approach and is less comprehensive than the ICSD classification. In this review, we use the ICSD classification (Box 1). The ICSD classification divides parasomnias into six groups of disorders that can emerge from either NREM or REM sleep, be related to drug or substance use or be a symptom of another medical disorder. Of parasomnias, REM sleep behaviour disorder is most commonly associated with an underlying neurologic condition.1
International Classification of Sleep Disorders for parasomnia1
Disorders of arousal from nonrapid eye movement sleep
Confusional arousals
Sleepwalking
Sleep terrors
Parasomnias usually associated with rapid eye movement sleep
Rapid eye movement sleep behaviour disorder
Recurrent isolated sleep paralysis
Nightmare disorder
Other parasomnias
Sleep-related dissociative disorders
Sleep enuresis
Sleep-related groaning
Exploding head syndrome
Sleep-related hallucinations
Sleep-related eating disorder
Parasomnia, unspecified
Parasomnia due to drug or substance use
Parasomnia due to medical condition
In this review, we address parasomnias in adults;3 sleep disorders in children have recently been reviewed elsewhere.4 Nonrapid eye movement parasomnias are relatively rare, episodic, often self-limiting events that may not be captured during a polysomnogram. Consequently, their systematic study is often limited to case reports and small case series. Because there have been no large randomized controlled trials of interventions and there are no guidelines available (with the exception of nightmares), the level of evidence for management options is low and is largely limited to the opinion of experts. The sources of evidence used in this review are shown in Box 2.
Evidence used in this review
We searched Web of Science and MEDLINE for reviews and guidelines on the assessment and treatment of parasomnias, as well as for specific parasomnias (from 2008 to 2012). We also reviewed the citations for parasomnias in the International Classification of Sleep Disorders1 and the Diagnostic and Statistical Manual of Mental Disorders, fifth edition.2
Rapid eye movement sleep behaviour disorder, an REM parasomnia, is a more prevalent condition associated with both iatrogenic causes and medical conditions. It can be reliably confirmed by polysomnography, which has resulted in a higher level of evidence and a best practice guideline.5
How do parasomnias commonly present?
All parasomnias occur from sleep, and NREM parasomnias usually occur among individuals aged 5–25 years with a family history of similar parasomnias (e.g., sleepwalking or sleep terrors) and involve physical and verbal activity of varying complexity. Typically, the sleeper returns to sleep and is amnestic in the morning, with the behaviour being reported by others or discovered because items have been moved or used during the night or the events have resulted in injury.1
External (e.g., noise, temperature change) or internal (e.g., apnea, periodic limb movement) events may cause an arousal or partial awakening, usually from stage III and IV sleep, which occurs in the first 90 minutes of the sleep period. Arousal or partial awakening can also occur during stage II sleep later in the night.2 Sleep deprivation or disruption from any cause (e.g., restless legs syndrome, obstructive sleep apnea) can precipitate these events in susceptible individuals.
In contrast, REM sleep behaviour disorder is characterized by verbalizations and actions consistent with dream enactment (e.g., fight or flight behaviours) that usually awaken the sleeper who, unlike those with NREM parasomnias, can often recall the event, including the dream and its associated actions.1
The characteristics of NREM and REM parasomnias are summarized in Table 1. Distinguishing between NREM and REM parasomnias is important because the treatment and prognosis are different. Nonrapid eye movement parasomnias are more common in younger people and are usually “outgrown” by young adulthood, whereas REM parasomnias present in late adult life and are associated with degenerative brain diseases.2
Characteristics of parasomnias
The major differential diagnoses for both NREM and REM parasomnia include nocturnal seizures, intoxicated states, medication-induced complex behaviours, nocturnal panic attacks and dissociative disorders.2
Are investigations required for diagnosis?
Parasomnias are typically diagnosed by obtaining a careful clinical history that assesses the timing, expression and form of the behaviour in the home environment (Box 3). A sleep diary (to exclude sleep deprivation as a precipitant) and a partner’s log of the events are useful tools. (See http://yoursleep.aasmnet.org/pdf/sleepdiary.pdf for an example of a sleep diary.)
Clinical questions to aid in the diagnosis of parasomnia
Rule out sleep deprivation
Time in and out of bed and total sleep time, ideally from a one-week sleep diary
Exclude external causes of sleep loss
Elective
Shift work
Caregiving: young children, ill family member, pets
Rule out effects of intoxication or withdrawal
Alcohol use
Current pattern of use
Any binge drinking?
Substance use
Current pattern of use
Intoxication with stimulants
Withdrawal from sedatives
Rule out sleep disorders causing sleep instability
Sleep apnea
Periodic limb movement disorder
Restless legs syndrome
Narcolepsy
Rule out medical disorders or treatments associated with sleep instability
Syndromes causing pain or discomfort at night
“Alerting” medications (e.g., second-generation antidepressants [selective serotonin reuptake inhibitor, serotonin–norepinephrine reuptake inhibitor], stimulants, dopamine agonists)
Confirm presence of NREM parasomnias in other family members and during the patient’s childhood
In the absence of such a history, expand the screen to include other pathologies, including nocturnal seizures
Timing of events
NREM parasomnias predominate in the first third of the night, REM parasomnias in the last third
Morphology of events
Stereotypical, brief events are more likely to be ictal
Marked autonomic arousal is characteristic of sleep terrors
Confusion on awakening is likely with NREM parasomnias but absent with REM parasomnias
Eyes tend to be open in NREM parasomnias but closed in REM parasomnias
Amnesia of the event is characteristic of NREM parasomnias, but REM parasomnias are characterized by recall of dreams or dream fragments
Note: NREM = nonrapid eye movement, REM = rapid eye movement.
Referral to a specialist in sleep disorders should be considered for patients whose activities are potentially harmful or very disturbing to others, or if polysomnography is required.
It is not cost-effective to obtain a polysomnogram for patients with NREM parasomnia, except to exclude other causes of additional sleep instability (e.g., obstructive sleep apnea, periodic limb movement disorder, narcolepsy). Because one of the ICSD diagnostic criteria for REM sleep behaviour disorder requires the demonstration of REM sleep without atonia,1 polysomnography is needed to confirm this diagnosis and to rule out comorbid sleep disorders, such as obstructive sleep apnea or periodic limb movement disorder, which are more prevalent in adults and may need to be a focus of management.
How are specific parasomnias managed?
Although incompletely understood, the pathophysiology of NREM and REM parasomnias differ; however, there are commonalities in their management.
There have been no large, randomized controlled treatment trials for all parasomnias, and guidelines are limited to the management of nightmares8 and REM sleep behaviour disorder.5
Parasomnias commonly associated with NREM sleep
There are three main types of NREM parasomnias: confusional arousals, sleepwalking and sleep terrors (Table 1). We have included sleep-related eating disorders and sleeptalking in this section because they emerge from NREM sleep. The DSM-V classifies sleep-related eating as a subtype of sleepwalking, and the ICSD notes that sleeptalking can occur during any stage of sleep.
Confusional arousals
Confusional arousals can occur any time sleep is interrupted9 and can accompany sleep-disruptive conditions, such as narcolepsy, obstructive sleep apnea, periodic limb movement disorder or by forced awakenings, especially in sleep-deprived individuals. Drugs and medications6 that disrupt sleep can also cause confused arousals.10
Typically, these events are brief and may include sleeptalking and simple motor behaviours that occur without responsiveness to the environment.3 Because of the sleeper’s amnesia, they may only be noted by his or her bed partner. The frequency of events decreases with age;11 persistence into the twenties is usually associated with comorbidities or medications.12
Two variants of confused arousals have been described: severe morning sleep inertia (sleep drunkenness, similar to the confusion, disorientation and slowed responses seen on awakening from slow wave sleep) and sleep-related sexual behaviours (commonly referred to as sexsomnia). Sexual behaviours (e.g., vocalizations, fondling, masturbation, intercourse and sexual assault) emerge as part of a confused arousal from sleep, although partial seizures and other pathologies should be considered.13
Isolated confusional arousals in adults rarely come to clinical attention. For patients who present with confusional arousals, important measures to maximize sleep stability include improving sleep hygiene, avoiding centrally acting medications or drugs, and preventing sleep deprivation. The use of benzodiazepines14 and specific serotonin reuptake inhibitors (SSRIs),15 in conjunction with education about sleep and stress management and taking appropriate precautions (Box 4), may be effective. Anecdotal evidence suggests that scheduled awakenings (setting the alarm for 1 hr after sleep onset) can be helpful.16
Safety precautions for patients with parasomnia
Identify, then reduce or eliminate known precipitating factors
Avoid sleep deprivation: maintain a regular sleep–wake schedule with a constant waking time
Limit, preferably eliminate, the use of alcohol and recreational drugs
Maximize safety of the sleeping environment
Sleep on the lowest floor in the house
Use a mattress on the floor
Sleep solo or use two queen-sized mattresses pushed together for co-sleeping
Minimize or pad bedside furniture
Secure bedside light above bed but out of reach
Use plastic cups or bottles, if bedside water is required
Consider child-proof door knobs, door wedges or alarms
Remove or lock any weapons or dangerous household items
Patients with confusional arousals (as well as those with other parasomnias) should be counselled to not co-sleep with children, because even a single event has the potential for very serious consequences. It is also useful for patients to let others know of the disorder if they are going on a group trip (e.g., business trip, camping).
Sleepwalking
Sleepwalking is the result of a series of complex behaviours that occur while the patient is in an altered state of consciousness. A spectrum of activity may be seen; the most simple events include sitting up in bed in a confused manner before walking. Usually the individual’s eyes are open (in contrast, the eyes remain closed in REM parasomnias).1
Agitated ambulation is more common in older sleepwalkers, is often associated with a perceived threat or dreams promoting “fight or flight” behaviour, and may result in injury to bystanders. Rarely, sleepwalking may lead to injury or death for the sleeper17 or others.14
The co-occurrence of predisposing factors is required to precipitate sleepwalking episodes, and sleepwalking is unlikely in the absence of one or more of these factors.18 Genetic susceptibility is the predominant predisposing factor, and sleep deprivation, touch, noise, stress, alcohol, medications and fever are potential triggers.
The cause of sleepwalking is unknown, although the pathophysiology clearly involves slow wave sleep. Although the macroarchitecture of sleep in people who sleepwalk is essentially normal, there may be more fragmentation of slow wave sleep.19 Single photon emission computed tomography during an episode of sleepwalking supports the co-occurrence of sleeping and waking states caused by selective activation and hypoactivation of neural circuits.20
In addition to the usual safety precautions (Box 4), the patient can be counselled to avoid sleep deprivation, and comorbid sleep disorders (e.g., obstructive sleep apnea21) can be treated via nonpharmacologic and pharmacologic interventions. Scheduled awakenings, psychotherapy, relaxation exercises and hypnosis may be helpful,22 but pharmacotherapy is often required for patients with frequent or hazardous episodes (arbitrarily defined as more than 50% of nights). Clonazepam is commonly used, with more limited evidence for other benzodiazepines, imipramine, paroxetine and melatonin.16
Sleep terrors
Sleep terrors — events typically lasting between 30 seconds and 5 minutes23 — commence with the sleeper sitting up in bed, emitting a loud scream and showing the typical autonomic manifestations of intense fear.1 Associated dream imagery may be reported and incoherent vocalizations can occur; the sleeper may bolt from the bed and run in an apparent attempt to avoid harm, thereby injuring themselves or others.24
The pathophysiology of sleep terrors is unknown, but it is assumed that slow wave sleep instability accounts for these disturbances. There is an association between sleep terrors and psychiatric disorders;10,25 sleepers with night terrors exhibit a high level of depression, anxiety, and obsessive–compulsive and phobic traits on the Minnesota Multiphasic Personality Inventory.25 Tricyclic antidepressants and benzodiazepines may be effective and should be considered if the sleep terrors are potentially harmful.4
Sleeptalking
Sleeptalking or somniloquy, classified in ICSD under “sleep disorders associated with conditions classified elsewhere,”1 is a common parasomnia that ranges from isolated speech to full conversations without recall. It occurs in all sleep states and can be associated with obstructive sleep apnea, other disorders of arousal and REM-related parasomnias.23 There are no specific treatments, and the clinical approach is to eliminate or reduce the conditions with which it is associated.
Sleep-related eating disorder
This parasomnia is classified in DSM-V under sleepwalking,2 whereas ICSD classifies it as “other parasomnias.”1 Sleep-related eating disorder is best conceptualized as the combination of the binge eating of bulimia nervosa with the disordered arousal, confused behaviour and amnesia (partial or full) of a parasomnia arising from NREM sleep.10 Food and beverages are consumed in a hurried and out-of-control manner, with high-calorie foods being preferred. Sometimes unusual (e.g., slabs of butter) or toxic foodstuffs (e.g., uncooked chicken) may be ingested. Variable, diminished awareness and recall distinguishes sleep-related eating disorder from nocturnal eating syndrome,26 in which excessive amounts of food are eaten before or during the sleep period in full consciousness.
The pathophysiology of sleep-related eating disorder is unclear, but it is associated with other sleep disorders27 including sleepwalking, restless legs syndrome, periodic limb movement disorder, obstructive sleep apnea and narcolepsy28 and medications, including zolpidem.29 Successful treatment of the associated sleep disorder can substantially improve this parasomnia.
Management of sleep-related eating disorder usually requires specialist care with attention to safety (because of the potential ingestion of toxic foods). First steps include normalizing the patient’s eating schedule, preventing sleep deprivation and minimizing alcohol and substance use. If medication is required, the current preferred choice by experts is topiramate, with SSRI agents and dopamine agonists being second-line options.30
Parasomnias usually associated with REM sleep
There are 3 parasomnias associated with REM sleep: REM sleep behaviour disorder, recurrent isolated sleep paralysis and nightmare disorder.
REM sleep behaviour disorder
Two clinical forms of REM sleep behaviour disorder are seen: acute and chronic.31 The acute form is associated with specific medications and substance abuse or withdrawal, and the chronic form is subdivided into either idiopathic or secondary to a neurologic disease.5
Rapid eye movement sleep behaviour disorder is characterized by activity in REM sleep causing injury or sleep disruption. Polysomnography is required to confirm the associated electromyographic abnormalities. In REM sleep behaviour disorder, there is a loss of REM atonia with excessive muscle tone, twitches on electromyography, and movements that often appear to be dream enactment, potentially causing injury to the sleeper or bed partner. Episodes usually occur about once a week, but may be as often as four times nightly over consecutive nights. In contrast to all NREM parasomnias, the sleeper awakens rapidly without confusion and often with good recall of a dream that corresponds with the enacted behaviours that can include talking, laughing, swearing, shouting, reaching, grabbing, flailing, punching, hitting or running.5
Because REM sleep behaviour disorder emerges from REM sleep, which is maximal in the last half of the night, this is the time when events are most likely to occur. Patients with narcolepsy, a condition characterized by REM periods at sleep onset, are at risk of REM sleep behaviour disorder, and their events can occur earlier in the night.5
Rapid eye movement sleep behaviour disorder is considered to be a long-standing and progressive disorder, although an acute form can emerge during REM sleep rebound states (e.g., the first night on continuous positive airway pressure for obstructive sleep apnea), withdrawal from alcohol, sedative hypnotic agents or REM suppressant medications.5
The major predisposing factors are male sex, age greater than 50 years, and an underlying neurologic disease, particularly Parkinson disease, Lewy body dementia and stroke.5 Rapid eye movement sleep behaviour disorder is a well-established risk factor for neurodegenerative disease, with studies indicating that 40%–65% of patients with this disorder develop a defined neurodegenerative phenotype within the subsequent 10 years.32 Narcolepsy and post-traumatic stress disorder are associated with REM sleep behaviour disorder,1 as are the use of SSRI and serotonin norepinephrine reuptake inhibitors.33
The exact pathophysiology of REM sleep behaviour disorder is unclear, but it may be caused by reduced dopamine transporters in the striatum34 and diminished striatal dopaminergic innervation.35 The onset may be gradual or rapid and the course is progressive; spontaneous remissions are very rare, although dream enactment may subside during the late stages of a neurodegenerative disorder.
Rapid eye movement sleep behaviour disorder can be diagnosed based on clinical history, which should include the bed partner’s account. This is the only parasomnia that can be readily confirmed by polysomnography, which shows an excessive amount of sustained electromyographic activity in REM sleep. Of patients with REM sleep behaviour disorder, 70% will have periodic limb movements during NREM sleep.36
As with other parasomnias, there have been no large trials of treatment for this condition, but case series have shown that clonazepam is most commonly used for this condition.5 Screening for obstructive sleep apnea should be undertaken before starting treatment with clonazepam. The most troublesome adverse effect associated with clonazepam therapy is morning confusion and memory impairment.5 Melatonin in high doses is an alternative to clonazepam, and there is some anecdotal support for the use of dopamine agonists such as pramipexole.5 A novel alarm system for patients unresponsive to medications has been described recently.37
Sleep paralysis
Sleep paralysis is the inability to perform voluntary movements at sleep onset or on awakening.1 Although consciousness is preserved and recall is present, the patient is unable to speak or move at first. Respiration is unaffected, although patients may feel as if they are unable to breathe because the accessory respiratory muscles are atonic, but diaphragmatic breathing is maintained. Episodes last seconds to minutes and resolve spontaneously, but they can be aborted if the patient is touched or spoken to. The frequency can vary from once-in-a-lifetime to several times in a year. During the first few episodes, intense anxiety accompanies the paralysis. Auditory, visual or tactile hallucinations can occur and may accompany a perception of an ominous presence in the room.1
Sleep deprivation, irregular sleep–wake schedules (e.g., from jet lag or shift work) and stress are predisposing factors, and the condition is more likely to occur when the sleeper is in the supine position. These factors may facilitate a state dissociation in which elements of REM sleep persist into wakefulness causing the phenomenon.1
Causes of secondary sleep paralysis (narcolepsy and other neuropsychiatric illnesses) should be excluded through a detailed physical examination, medical, psychiatric and sleep history, and appropriate investigations. Patient education and ensuring adequate, regular sleep periods are important. If the episodes are frequent, the patient should practise moving his or her little finger during drowsy sleep, because this action, if performed during an episode, may abort it.1 There have been no trials of psychologic or pharmacologic interventions, but SSRIs may be helpful because they suppress REM sleep and are well tolerated.38,39
Nightmare disorder
Nightmare disorder is characterized by recurrent nightmares with intense disturbing dreams involving anxiety, anger or disgust that cause prolonged awakenings.1 Multiple nightmares within a single sleep period may occur and follow similar themes.
Nightmares are strongly associated with psychopathology and are inversely correlated with measures of well-being.3 Many medications, including antidepressants, antihypertensives and dopamine receptor agonists, can cause nightmares.1
Nightmares are distinguished from other parasomnias because of the detailed recall of the dream, whereas in sleep terrors, dream activity, if present, is patchy. Nightmares can be a component of ictal events1 that will require video electroencephalography to make the diagnosis.
Nightmares are a common feature of both acute stress disorder and post-traumatic stress disorder and occur in both NREM and REM sleep. The label nightmare disorder is only applied to these disorders when the severity of the nightmares is such that it requires clinical attention. Frequently, other symptoms of post-traumatic stress disorder may have resolved even though nightmares persist.
A guideline8 indicates that both psychologic and pharmacologic approaches may be helpful in treating nightmares.13,40 A common psychologic approach is imagery rehearsal,41 where the patient chooses a repetitive nightmare, changes its story line to make it less distressing or bring its story to a safe conclusion and then mentally rehearses the changed dream imagery. A recent meta-analysis confirmed that this and other psychologic approaches are effective.42 The use of prazosin has reduced post-traumatic nightmares in two small clinical trials involving military veterans.43
Other parasomnias
This remaining group of “other” parasomnias (Box 1) cannot be easily categorized as NREM- or REM-related behaviours. With the exception of sleep enuresis, which is predominantly a disorder of childhood (reviewed elsewhere44,45), these parasomnias are relatively rare. Sleep-related dissociative disorders can mimic parasomnia, but the dissociative episode always arises from wakefulness,46 is accompanied by daytime dissociative symptoms and usually resolves with treatment of the dissociative disorder.
Exploding head syndrome47 is characterized by the perception of a sudden loud noise in the head as the patient is falling asleep or awakening from sleep. At first, the patient may believe that he or she is having a stroke. The frequency is highly variable: single episodes are usual but clusters of episodes can occur. When the events effect daytime functioning, a trial of clonazepam, clomipramine, nifedipine, flunarizine or topiramate48 may be helpful.
Sleep-related hallucinations are called hypnogogic hallucinations if they occur when the patient is falling asleep or hypnopompic hallucinations if they occur when the patient is awakening. The hallucinations are predominantly visual but can be auditory, tactile or kinetic, and they may frighten the sleeper.1 Because hypnopompic hallucinations are one of the symptoms of narcolepsy, this diagnosis needs to be excluded by polysomnography.
Conclusion
Parasomnias, like in the fictional case described in Box 5, are relatively rare, yet are fascinating and important clinical syndromes. Sleep instability characterized by arousals in various stages of consciousness with variable later recall are characteristic of NREM parasomnias and that instability can be improved by addressing sleep hygiene, avoiding substance use, preventing sleep deprivation and, when required, using medications that promote sleep depth and continuity.
Applying the results of this review in clinical practice (fictional case)
Martin, a 35-year-old executive, was brought to the emergency department by his wife after he had fallen down the stairs at 1:30 am. On questioning, he reported that at a conference last year, he was discovered, confused and naked, outside his hotel room with no memory of how he got there.
Martin had been a bed-wetter until age 10 and had been known to sleepwalk as a child. On his twelfth birthday, he had gotten up in the middle of the night and urinated in his brother’s shoes. He continued to experience “minor events” with decreased frequency in his teens but after a “night on the town” at age 19, he left the family home and was found asleep the next morning in his friend’s house two blocks away. Because all doors were locked, it was assumed that he climbed in through an open window.
Martin’s wife comments that he is a restless sleeper who frequently talks and groans in his sleep, but that he is otherwise a healthy, well-adjusted individual who has never abused drugs or alcohol. In the past year, he has complained to her that his sleep is lighter and that he wakes up easily throughout the night. Last month, Martin started to make sexual advances to his wife during the night, which have not been unwelcomed, yet sometimes it seems as though “he’s not quite there.” He does not remember these episodes the next morning.
Based on his history, Martin has confused arousals, sleepwalking and sexsomnia. The history of childhood onset with a strong family history (his father and two paternal uncles were sleepwalkers) and exacerbation by alcohol are common features of nonrapid eye movement parasomnia. A review of Martin’s two-week sleep diary and his wife’s charting of events showed that as his workweek progressed, he electively decreased his amount of sleep, resulting in a substantial sleep debt (1.5 h/night) by the end of the week, where his parasomnia behaviours were also clustered. He did not consent to a medication trial (clonazepam) but he agreed to safety-proof their bedroom (Box 4), ensure a 7.5-hour sleep period each night, and arise at the same time each day, including weekends. After making these changes, he reported less restless and more restorative sleep, and the frequency of parasomnia decreased to “once or twice a week.” The prophylactic use of clonazepam for his frequent transatlantic trips was discussed, but he declined this option for now, stating “I am growing out of this.”
In contrast, REM parasomnias occur within the context of greater conscious awareness, resulting in better recall and reflect the admixture of REM sleep with its associated dream imagery, voluntary muscle atonia and wakefulness. In this group of parasomnias, clinical experience has shown that the same advice about sleep hygiene, avoiding substance use and preventing sleep deprivation used in NREM is helpful. Clonazepam, pramipexole and melatonin are the medications commonly used to manage REM sleep behaviour disorder.
Parasomnias are not benign conditions and potentially place the sleeper and bed partner at risk of injury and may be associated with other disorders that require careful consideration. Parasomnias can be successfully managed by appropriate investigation, education and the strategic use of psychologic and pharmacologic therapies.
Key pointsParasomnias are very common and are not related to underlying psychiatric disease.
Parasomnias may be complex and prolonged.
Evaluation and treatment of parasomnias is suggested for patients whose activities are potentially harmful or very disturbing to others.
Medication effects or central nervous disease should be considered for REM sleep behaviour disorder in younger patients.
Footnotes
Competing interests: None declared.
This article has been peer reviewed.
Contributors: Jonathan Fleming performed the literature review. Both authors drafted the article, revised it critically for important intellectual content and approved the version submitted for publication.
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