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Sleep Disorders

Last Updated: April 3, 2006
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Synonyms and related keywords: sleep disorders, primary sleep disorders, disorders of initiating and maintaining sleep, DIMS, dyssomnias, insomnia, parasomnias, sleep-wake cycle disturbances, sleep apnea, obstructive sleep apnea, OSA, REM sleep, non-REM sleep, polysomnography, sleep maintenance, sleep onset, circadian rhythm, circadian cycle, nightmare, sleepwalk, sleepwalking, hypersomnia, narcolepsy, somnambulism

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Author: Curley L Bonds, MD, Associate Clinical Professor of Psychiatry, Director Consultation and Evaluation Services, Psychiatry, University of California at Los Angeles, Neuropsychiatric Institute and Hospital

Coauthor(s): Michael A Lucia, MD, FAASM, Owner/CEO, Pulmonary, Allergy and Sleep Medicine, Sierra Pulmonary and Sleep Consultants, LLC

Curley L Bonds, MD, is a member of the following medical societies: Academy of Psychosomatic Medicine

Editor(s): Denis F Darko, MD, FACP, DFAPA, Executive Director, Clinical Research and Development, Neuroscience Global Licensing Medical Director, Clinical Neuroscience Therapy Area, CNS and Pain Control Research Area, AstraZeneca Pharmaceuticals LP; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine; Iqbal Ahmed, MD, Program Director, General and Geriatric Psychiatry Residency Programs, Vice Chair for Education, Professor, Department of Psychiatry, John A Burns School of Medicine, University of Hawaii; Harold H Harsch, MD, Program Director of Geropsychiatry, Department of Geriatrics/Gerontology, Associate Professor, Department of Psychiatry, Assistant Professor, Department of Medicine, Froedtert Hospital, Medical College of Wisconsin; and Stephen Soreff, MD, President of Education Initiatives, Nottingham, NH; Faculty, Metropolitan College of Boston University, Boston, MA

Disclosure


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Background: Sleep disorders are among the most common clinical problems encountered in medicine, including in psychiatry. The Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) divides all sleep disorders into 3 general groups: primary, secondary to a mental disorder, and others, namely those related to a general medical condition or substance abuse.

Primary sleep disorders are presumed to result from an endogenous disturbance in sleep-wake generating or timing mechanisms, often complicated by behavioral conditioning. Primary sleep disorders are further subdivided into parasomnias and dyssomnias. Parasomnias are characterized by abnormal behavioral or physiological events in association with sleep, sleep stages, or sleep-wake transitions, rather than increased or decreased sleep. Parasomnias include nightmare disorder, sleep terror disorder, and sleepwalking disorder. Dyssomnias are characterized by abnormalities in the amount, quality, or timing of sleep. These include primary insomnia and hypersomnia, narcolepsy, breathing-related sleep disorder (ie, sleep apnea), and circadian rhythm sleep disorder. This article focuses primarily on insomnia, rather than the numerous other sleep disorders.

Primary insomnia is the general term for difficulty in initiating or maintaining sleep. Because sleep requirements vary from individual to individual, insomnia is considered clinically significant when a patient perceives the loss of sleep as a problem. Insomnia may be characterized further as acute (transient) or chronic.

Pathophysiology:

Rapid eye movement and nonrapid eye movement

Sleep is divided into 2 categories, rapid eye movement (REM) and nonrapid eye movement (NREM). Each of these sleep states is associated with distinct central nervous system activity.

NREM sleep is further divided into 4 progressive categories, termed stages 1-4 sleep. The arousal threshold rises with each stage of sleep, with stage 4 (delta) being the sleep state from which a person is least able to be aroused, characterized by high-amplitude slow waves.

REM sleep is characterized by muscle atonia, episodic REMs, and low-amplitude fast waves on electroencephalogram (EEG) readings. Dreaming occurs mainly during REM sleep.

Disturbances in the pattern and periodicity of REM and NREM sleep are often found when people aver to experiencing sleep disorders.

Sleep-wake cycles

Sleep-wake cycles are governed by a complex group of biological processes that serve as internal clocks.

The suprachiasmatic nucleus, located in the hypothalamus, is thought to be the body's anatomic timekeeper, responsible for the release of melatonin on a 25-hour cycle.

The pineal gland secretes less melatonin when exposed to bright light; therefore, the level of this chemical is lowest during the daytime hours of wakefulness.

Multiple neurotransmitters are thought to play a role in sleep. These include serotonin from the dorsal raphe nucleus, norepinephrine contained in neurons with cell bodies in the locus ceruleus, and acetylcholine from the pontine reticular formation. Dopamine, on the other hand, is associated with wakefulness.

Abnormalities in the delicate balance of all of these chemical messenger systems may disrupt various physiologic, biologic, behavioral, and EEG parameters responsible for REM (ie, active) sleep and NREM (slow-wave) sleep.

Frequency:

  • In the US: Approximately one third of all Americans have sleep disorders at some point in their lives. Approximately 20-40% of adults report difficulty sleeping at some point each year. Approximately 17% of adults consider the problem to be serious. Sleep disorders are a common reason for patient visits throughout medicine. Approximately one third of adults have insufficient sleep syndrome. Twenty percent of adults report chronic insomnia.

Mortality/Morbidity:

  • Chronic insomnia is associated with an increased risk of depression and accompanying danger of suicide, anxiety, excess disability, reduced quality of life, and increased use of health care resources.
  • Insufficient sleep can result in industrial and motor vehicle crashes, somatic symptoms, cognitive dysfunction, depression, and decrements in daytime work performance owing to fatigue or sleepiness.

Sex:

  • Primary insomnia is more common in women, with a female-to-male ratio of 3:2. Hormonal variations during the menstrual cycle or during menopause may cause disruptions in sleep.
  • Obstructive sleep apnea is more common in men (4%) than in women (2.5%).

Age:

  • Increasing age predisposes to sleep disorders (5% in persons aged 30-50 y and 30% in those aged 50 y or older).
  • People who are elderly experience a decrease in total sleep time, with more frequent awakenings during the night.
  • People who are elderly have a higher incidence of general medical conditions and are more likely to be taking medications that cause sleep disruption.


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History: Insomnia may present as decreased sleep efficiency or decreased total hours of sleep, with some associated decrease in productivity or well-being. Sleep quality is more important than the total number of hours slept because sleep requirements vary from person to person. Compare the total number of hours slept with each individual's lifelong normal night sleep time.

  • Initial insomnia is characterized by difficulty falling asleep, with increased sleep latency (time between going to bed and falling asleep). Initial insomnia is frequently related to anxiety disorders.
  • Middle insomnia refers to difficulty maintaining sleep. Decreased sleep efficiency is present, with fragmented unrestful sleep and frequent waking during the night. Middle insomnia may be associated with medical illness, pain syndromes, or depression.
  • In terminal insomnia, also referred to as early morning wakening, patients consistently wake up earlier than needed. This symptom is frequently associated with major depression.
  • Alterations of the sleep-wake cycle may be a sign of circadian rhythm disturbances, such as those caused by jet lag and shift work.
  • Hypersomnia, or excessive daytime sleepiness, is often attributable to ongoing sleep deprivation or poor quality sleep for reasons ranging from sleep apnea to substance abuse or medical problems.
  • In delayed sleep phase syndrome, the patient is unable to fall asleep until very early morning. As time progresses, the onset of sleep becomes progressively delayed.
  • Sleepwalking, also called somnambulism, refers to episodes of complex behaviors during NREM sleep (stages 3 and 4) of which the patient is amnestic afterward.
  • Nightmares are repeated awakenings from sleep caused by vivid and distressing recall of dreams. Nightmares usually occur during the second half of the sleep period. Upon wakening from the dream, the person rapidly reorients to time and place.
  • Night terrors are recurrent episodes of abrupt awakening from sleep characterized by a panicky scream, with intense fear and autonomic arousal. The individual usually has no recall of the details of the event and is unresponsive during the episode. Night terrors occur during the first third of the night, during stages 3 and 4 of NREM sleep.
  • The bed partner of patients who snore may provide a history of snoring. Such a history may help identify whether a patient experiences obstructive sleep apnea.

Causes: The major causes of insomnia may be divided into medical conditions, psychological conditions, and environmental problems.

  • Medical conditions
    • Cardiac conditions include ischemia and congestive heart failure.
    • Neurologic conditions include stroke, degenerative conditions, dementia, peripheral nerve damage, myoclonic jerks, restless leg syndrome, hypnic jerk, and central sleep apnea.
    • Endocrine conditions affecting sleep are related to hyperthyroidism, menopause, the menstrual cycle, pregnancy, and hypogonadism in elderly men.
    • Pulmonary conditions include chronic obstructive pulmonary disease, asthma, central alveolar hypoventilation (the Ondine curse), and obstructive sleep apnea syndrome (associated with snoring).
    • Gastrointestinal conditions include gastroesophageal reflux disease.
    • Hematological conditions include paroxysmal nocturnal hemoglobinuria, which is a rare, acquired, hemolytic anemia associated with brownish-red morning urine.
    • Substances that may result in insomnia include stimulants, opioids, caffeine, and alcohol, or, withdrawal from any of these also may cause insomnia.
    • Medications implicated in insomnia include decongestants, corticosteroids, and bronchodilators.
    • Other conditions include fever, pain, and infection.
  • Psychiatric conditions: Bear in mind that the major psychiatric conditions now are known to have a biological basis and constitute a subset of medical conditions.
    • Depression may cause alterations in REM sleep. As many as 40% of people with depression have insomnia.

    • Posttraumatic stress disorder (PTSD) can produce vivid and terrifying nightmares.
    • Anxiety disorders predispose to insomnia. The most common of these are generalized anxiety disorder, panic disorder, and anxiety disorders not otherwise specified.
    • Thought disorders and misperception of sleep state are other potential states that cause insomnia.
    • Psychotropic medications, such as antidepressants, may interfere with normal REM sleep patterns.
    • Rebound insomnia from benzodiazepines or other hypnotic agents is common.
  • Environmental problems
    • Stressful or life-threatening events (eg, bereavement, PTSD) may cause insomnia.
    • Shift work may disturb the sleep cycle, as might jet lag or changes in altitude.
    • Sleep deprivation may occur as a result of an overly warm sleeping environment, environmental noise, or frequent intrusions (such as in an intensive care unit setting).
  DIFFERENTIALS Section 4 of 10   Click here to go to the previous section in this topic Click here to go to the top of this page Click here to go to the next section in this topic
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Alcoholism
Anxiety Disorders
Bipolar Affective Disorder
Breathing-Related Sleep Disorder
Chronic Obstructive Pulmonary Disease
Depression
Emphysema
Hyperthyroidism
Hypoparathyroidism
Obstructive Sleep Apnea-Hypopnea Syndrome
Opioid Abuse
Posttraumatic Stress Disorder


Other Problems to be Considered:

Stimulant abuse (eg, amphetamine abuse)


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Alcoholism

Anxiety Disorders

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Patient Education



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Lab Studies:

  • Hemoglobin and hematocrit
  • Arterial blood gases
  • Thyroid function tests
  • Drug and alcohol toxicology screening

Imaging Studies:

  • Although no imaging studies are indicated directly for the workup of insomnia, underlying medical conditions require appropriate investigation using suitable studies.

Other Tests:

  • Oximetry may be performed during sleep to examine blood oxygen levels for clinically important desaturations suggestive of sleep apnea or other sleep-disordered breathing.
  • A Beck Depression Index or similar clinical screening tool may be used to detect an underlying depressive illness as a contributing factor in insomnia.
  • An Epworth Sleepiness Score or other objective measure of daytime sleepiness may lead to clues of another underlying sleep disorder. For example, approximately 20% of patients with sleep apnea present with a history of nighttime insomnia; however, patients are excessively sleepy by day and have an abnormal score on the Epworth Sleepiness Scale.

Procedures:

  • Subjective measures of sleep are obtained by means of a sleep journal.
    • A sleep journal kept for approximately 2 weeks may help determine the extent of the sleep disturbance.
    • Patients should record the total hours slept per night, frequency of nighttime awakenings, and level of restfulness provided after sleep.
    • Further objective history might be available if patients have a sleep partner who keeps a 2-week journal or provides history.
  • Objective measures of sleep may be obtained using EEG monitoring or polysomnography.
    • Monitored polysomnography is the criterion standard for evaluating measures of sleep. This study includes measures of multiple channels of electroencephalogram (EEG), electrooculogram (EOG), chin and leg electromyogram, nasal and oral airflow, oximetry, abdominal and chest movements, and ECG. Monitored polysomnography can help the physician discriminate between REM and NREM sleep, as well as causes of sleep arousal.
    • Polysomnogram may be useful in determining the etiology of the sleep disturbance.
    • These studies may be helpful in determining sleep and wakefulness in the intensive care unit or in the sleep laboratory.
    • Patients with chronic medical conditions, such as fibromyalgia or anxiety disorders, often have characteristic alpha brain-wave activity that intrudes into the deeper stages of sleep. This activity can readily be seen on the EEG during the polysomnogram (PSG).
    • Patients with insomnia often have some degree of sleep-state misperception, wherein they perceive and believe that they achieve significantly less sleep than they actually do. This can be documented by correlating the EEG findings from the PSG with patient subjective reports of sleep duration and onset.
  TREATMENT Section 6 of 10   Click here to go to the previous section in this topic Click here to go to the top of this page Click here to go to the next section in this topic
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Medical Care: Evaluate patients for other primary sleep disorders (eg, sleep apnea) and for underlying medical, psychiatric, and substance abuse disorders, and institute appropriate treatment. Sleep hygiene and behavioral strategies are used in combination with medication to treat insomnia, particularly primary insomnia.

Surgical Care: Surgical referral may be indicated to correct some underlying medical conditions that cause insomnia, such as for palate surgery in some cases of sleep apnea.

Consultations: Consultation can help evaluate patients for medical (including psychiatric) causes of insomnia. The evaluation team optimally should include a psychiatrist, neurologist, pulmonologist, sleep medicine specialist, and dietitian.

Diet:

  • No special diet is needed to treat insomnia, but large meals and spicy foods should be avoided in the 3 hours before bedtime.
  • Patients should avoid sleep-disturbing substances such as alcohol, nicotine, and caffeine. Alcohol creates the illusion of good sleep, but sleep architecture is affected adversely. Nicotine and caffeine are stimulating and should be avoided in the second half of the day, from late afternoon on.
  • Consumption of tryptophan-containing foods may help induce sleep. The classic example is warm milk.

Activity:

  • Strenuous exercise during the day may promote better sleep, but this same exercise during the 3 hours before bedtime can cause initial insomnia.
  • Stimulating activities should be avoided 3 hours before bedtime. Examples include tense movies, exciting novels, thrilling television shows, arguments, and vigorous physical exercise other than coitus.

  MEDICATION Section 7 of 10   Click here to go to the previous section in this topic Click here to go to the top of this page Click here to go to the next section in this topic
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Many agents are useful in treating insomnia. Short-term drug therapy is preferred to restore a normal sleep pattern. Generally, hypnotic drugs are approved for 2 weeks or less of continuous use. In chronic insomnia, longer courses may be indicated, which require long-term monitoring to ensure ongoing appropriate use of the medication.

Barbiturates and chloral hydrate are seldom used now because of safety concerns related to their undesirably low therapeutic indexes.

Drugs that block the histamine type 1 receptor are used primarily in over-the-counter preparations, are inexpensive, and are helpful to some patients. However, in view of the anticholinergic properties of these agents, caution should be exercised in their use with older patients and with those who have disorders such as prostatic hypertrophy, cognitive disorders, and constipation. In addition, most of these drugs have a long duration of action, and their sedative effects may persist well into the following day.

Zolpidem (Ambien) and zaleplon (Sonata) are the newest and, arguably, the safest agents that are US Food and Drug Administration (FDA) approved for short-term hypnotic use. Zolpidem (Ambien CR) has recently released an extended-release version that lasts slightly longer than the original preparation. In addition, the FDA recently approved the new agent eszopiclone (Lunesta) as the first agent for long-term use in the management of chronic insomnia.

Drug Category: Benzodiazepines -- Benzodiazepine receptor agonists are the mainstay in treatment of insomnia. Flurazepam, temazepam, quazepam, estazolam, and triazolam are the benzodiazepines that are approved by the US Food and Drug Administration as hypnotics.

These drugs bind to a special benzodiazepine site on the GABA receptor complex, enhancing activity of this neurotransmitter. All have variable half-lives and different metabolites that affect their onset and duration of action. This class of drugs suppresses REM sleep and reduces stages 3 and 4 sleep while increasing stage 2 sleep. The drug described here, temazepam, is only one example of this class of medications. A more detailed discussion of the other agents in this class can be found elsewhere in the text.
Drug Name
Temazepam (Restoril) -- Intermediate rate of absorption and duration of action make this drug useful for treating initial and middle insomnia. Has no active metabolite, which reduces cognitive impairment and grogginess the following day.
Adult Dose15-30 mg PO qhs
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; narrow-angle glaucoma; untreated obstructive sleep apnea; history of substance abuse; severe uncontrolled pain
InteractionsCimetidine, disulfiram, isoniazid, and estrogen increase plasma levels of benzodiazepines; benzodiazepines may increase levels of digoxin and phenytoin; alcohol and other sedating drugs have additive effects with benzodiazepines
Pregnancy X - Contraindicated in pregnancy
PrecautionsCaution in chronic respiratory or hepatic disease and in elderly patients; avoid in individuals with history of substance abuse; effect of respiratory compromise more pronounced when ingested with alcohol; may have associated tolerance, dependence, daytime sedation/hangover effect, and withdrawal syndromes; long-term use may result in cognitive dysfunction and rebound insomnia when discontinued
Drug Category: Imidazopyridine -- Zolpidem is the sole member of this class of medications. It binds at a benzodiazepine receptor subtype (omega I). Found more in CNS more than in peripheral nervous system, which helps to account for hypnotic effect with no significant muscle-relaxant properties. Unlike benzodiazepines, normal sleep architecture not suppressed.
Drug Name
Zolpidem (Ambien) -- Rapidly absorbed, with fast onset (20-30 min) of action, which makes this a good drug for sleep induction. Decreases sleep latency and increases duration of sleep.
Adult Dose5-20 mg PO qhs
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity
InteractionsIncreases toxicity of alcohol and other CNS depressants
Pregnancy B - Usually safe but benefits must outweigh the risks.
PrecautionsDecrease dose to 5 mg in patients who are elderly or debilitated because of greater possibility of impaired motor and/or cognitive difficulties; not recommended in breastfeeding mothers (drug excreted in milk)
Caution with pulmonary dysfunction
Drug Category: Pyrazolopyrimidine -- Zaleplon is the sole agent in this class of nonbenzodiazepine hypnotics.
Drug Name
Zaleplon (Sonata) -- Not structurally related to benzodiazepines, barbiturates, or other drugs with known hypnotic properties. Interacts with GABA-benzodiazepine receptor complex, causing effects in sedation. Should be taken immediately before bedtime.
Decreases time to sleep onset. Shorter onset of action means peak serum concentrations achieved within 1 h of administration. This may account for lower incidence of daytime grogginess and less withdrawal rebound insomnia.
Adult Dose10 mg PO qhs; dose may be halved or doubled depending on patient weight and/or response to drug
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity
InteractionsMay interact with drugs metabolized by aldehyde oxidase and CYP3A4, including diphenhydramine and cimetidine; cimetidine significantly increases levels of zaleplon; may enhance response to alcohol, barbiturates, and other CNS depressants
Pregnancy C - Safety for use during pregnancy has not been established.
PrecautionsTaking drug while still awake and active may cause hallucination, short-term memory impairment, impaired coordination, light-headedness, and dizziness; failure of insomnia to remit after 7-10 d of treatment may indicate need for evaluation for primary psychiatric or medical illness; limit treatment to 7-10 d and reevaluate patient if drug to be taken for >2-3 wk (do not prescribe zaleplon in quantities exceeding 1-mo supply); in hepatic function impairment, reduce dose to 5 mg PO hs; caution in patients exhibiting signs or symptoms of depression
Drug Category: Pyrrolopyrazine -- This is another nonbenzodiazepine sedative/hypnotic drug class indicated to improve sleep onset and maintenance.
Drug Name
Eszopiclone (Lunesta) -- Nonbenzodiazepine hypnotic pyrrolopyrazine derivative of the cyclopyrrolone class. The precise mechanism of action is unknown but is believed to interact with GABA-receptor at binding domains close to or allosterically coupled to benzodiazepine receptors. Indicated for insomnia to decrease sleep latency and improve sleep maintenance. Short half-life of 6 h. Higher doses (ie, 2 mg for elderly adults and 3 mg for nonelderly adults) are more effective for sleep maintenance, whereas lower doses (ie, 1 mg for elderly adults and 2 mg for nonelderly adults) are suitable for difficulty in falling asleep.
Decreases sleep latency and improves sleep maintenance.
Adult DoseNonelderly adults: 2 mg PO hs; may increase to 3 mg PO hs prn
Elderly adults: 1 mg PO hs initially; not to exceed 2 mg PO hs
Severe hepatic impairment: Do not exceed 2 mg PO hs
Pediatric Dose<18 years: Not established
>18 years: Administer as in adults
ContraindicationsDocumented hypersensitivity
InteractionsCYP3A4 and CYP2E1 substrate; potent CYP3A4 inhibitors (eg, ketoconazole, itraconazole, clarithromycin, nefazodone, ritonavir, nelfinavir) increase AUC, Cmax, and t1/2 and therefore potential toxicity (decrease dose); potent CYP3A4 inducers (eg, rifampicin) increase clearance; coadministration with alcohol or other CNS depressants may increase effect and toxicity (decrease dose); coadministration with olanzapine may decrease DSST scores; sleep onset may be delayed if taken with or immediately after a high-fat or heavy meal
Pregnancy C - Safety for use during pregnancy has not been established.
PrecautionsMay cause dysgeusia, headache, or coldlike symptoms; rare adverse effects associated with hypnotics include short-term amnesia, confusion, agitation, hallucinations, worsened depression, or suicidal thoughts; high doses (ie, 6-12 mg) produce euphoric effects similar to those of diazepam 20 mg; anxiety, abnormal dreams, nausea, and upset stomach may occur within 48 h after discontinuing; alertness may be affected the following day, use caution while operating machinery or driving a car
Drug Category: Melatonin receptor agonist -- Ramelteon is the first and only nonscheduled insomnia medication with a novel mechanism of action.
Drug Name
Ramelteon (Rozerem) -- Melatonin receptor agonist with high selectivity for human melatonin MT1 and MT2 receptors. MT1 and MT2 are thought to promote sleep and be involved in maintenance of circadian rhythm and normal sleep-wake cycle. Indicated for insomnia characterized by difficulty with sleep onset.
Adult Dose8 mg PO 30 min before bedtime on empty stomach
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity; strong cytochrome P450 CYP1A2 inhibitors (eg, fluvoxamine); severe hepatic impairment
InteractionsMajor substrate of cytochrome P450 CYP1A2 and minor substrate of CYP2C and CYP3A4; strong CYP1A2 inhibitors (eg, fluvoxamine) increase AUC up to 190-fold and Cmax 70-fold; strong CYP inducers (eg, rifampin) decrease total exposure by mean of 80%; strong CYP3A4 inhibitors (eg, ketoconazole) and strong CYP2C9 inhibitors (eg, fluconazole) may increase serum levels
Pregnancy C - Safety for use during pregnancy has not been established.
PrecautionsCaution in mild hepatic impairment; adverse effects that led to discontinuation in clinical trials included dizziness, nausea, fatigue, headache, and worsening insomnia; has been associated with decreased testosterone levels and increased prolactin levels (changes related to these hormones should be carefully monitored)
Drug Category: Antidepressants -- Although no antidepressants are approved specifically for use in the treatment of sleep disorders, a cyclic antidepressant, trazodone (Desyrel), is used routinely for this purpose.
Drug Name
Trazodone (Desyrel) -- Mechanism of action not fully understood. Thought to selectively inhibit serotonin uptake by brain synaptosomes and potentiate behavioral changes induced by serotonin precursor, 5-HT. Major adverse effect is sedation.
Adult DoseStarting dose: 50 mg PO qhs
Usual dose range for insomnia: 50-100 mg, PO but up to 300 mg may be needed; not to exceed 400 mg
Pediatric DoseNot established
ContraindicationsDocumented hypersensitivity
InteractionsMay enhance response to alcohol, barbiturates, and other CNS depressants; may decrease hypoprothrombinemic effects of warfarin; digoxin and phenytoin serum levels may increase with concomitant trazodone
Pregnancy C - Safety for use during pregnancy has not been established.
PrecautionsHypotension has occurred, including orthostatic hypotension and syncope; may produce drowsiness, dizziness, or blurred vision; observe caution while driving or performing other tasks requiring alertness, coordination, or dexterity; priapism reported in patients taking trazodone; patients with prolonged or inappropriate penile erection should immediately seek emergency medical treatment and discontinue drug
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Further Inpatient Care:

Further Outpatient Care:

In/Out Patient Meds:

Deterrence/Prevention:

Complications:

  • Mood and anxiety disorders may develop from untreated sleep disturbances, and current medical literature supports the theory that these brain-based mental status changes are risk factors for morbidity and mortality from a host of medical conditions (eg, cardiovascular disease).

Prognosis:

  • The prognosis varies widely depending on the etiology of the insomnia or other sleep disorder. For example, insomnia due to obstructive sleep apnea resolves with successful treatment of the apnea, while insomnia due to refractory major depression is itself refractory until a successful treatment can be found for the depression.

Patient Education:

  • All individuals should be taught and encouraged to practice good sleep hygiene, as outlined in Medical Care.

  • Educating the patient's family about proper sleep hygiene is imperative, especially because the patient's spouse can be adversely affected by sleep disorders such as sleep apnea.
  • Use the bed for sleep and sex only (no television watching or reading in bed).
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Medical/Legal Pitfalls:

  • Patients should be warned to not drive or operate machinery while taking sedative-hypnotic medications. Document these admonitions clearly in the medical record.
  • Caution is advised in the treatment of patients who are elderly and others who may be at increased risk for falls.
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