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Audio-Digest FoundationFamily Practice


Volume 57, Issue 28
July 28, 2009

The following is an abstracted summary, not a verbatim transcript, of the lectures/discussions on this audio program. If, after reviewing the summary, you would like to hear the contents and earn CME/CE credit, simply use your browser's back button to return to the order page and add this program to your cart.

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Sleep Disorders: Diagnosis and Management

From the University of California, Los Angeles’s 3rd Annual Advances in Sleep Medicine

Educational Objectives

The goal of this program is to improve management of insomnia and obstructive sleep apnea (OSA). After hearing and assimilating this program, the clinician will be better able to:

1.   Describe predisposing, precipitating, and perpetuating factors leading to insomnia.

2.   Discuss medical, psychiatric, and circadian rhythm problems associated with insomnia.

3.   Choose appropriate drugs and sleep hygiene methods for treating individuals with insomnia.

4.   Distinguish patients with OSA from those with central sleep apnea.

5.   Identify patients who might benefit from surgical vs nonsurgical treatment of OSA.

Faculty Disclosure

In adherence to ACCME Standards for Commercial Support, Audio-Digest requires all faculty and planning committee members to disclose relevant financial relationships within the past 12 months that might create any personal conflicts of in­terest. For this program, the following has been disclosed: Dr. Ancoli-Israel serves as a consultant and/or scientific board member for Arena, Cephalon, Ferring Pharmaceuticals, Orphagen Pharmaceuticals, Pfizer, Philips Respironics, sanofi-aventis, Sepracor, Schering-Plough, Somaxon Pharmaceuticals, and Takeda Pharmaceuticals. Dr. Avidan is on the Speaker’s Bureaus for Cephalon, Pfizer, Sepracor, and Takeda. In thier lectures, both speakers present information related to off-label use of a therapy, product, or device.  The planning committee reported nothing to disclose.

Acknowledgments

Drs. Ancoli-Israel and Avidan were recorded at 3rd Annual Advances in Sleep Medicine, sponsored by the David Gef­fen School of Medicine at the University of California, Los Angeles, and held February 21, 2009, in Marina del Rey, CA. The Audio-Digest Foundation thanks the speakers and the sponsors for their cooperation in the production of this program.

Update on Management of Insomnia

Sonia Ancoli-Israel, PhD, Professor of Psychiatry, University of California, San Diego, School of Medicine, and Director, Gillin Sleep and Chronomedicine Research Center, University of California, San Diego, La Jolla, CA

Definition of insomnia: difficulty initiating or sustaining sleep, or nonrestorative sleep; insufficient sleep must result in daytime consequence, eg, irritability or difficulty concentrating; many patients unaware of deficits in function; ask others who know patient well about effects of sleep loss

Predisposing, precipitating, and perpetuating factors (3Ps): predisposing factors    innate; eg, depressive or anx­ious personality; does not necessarily lead to insomnia; precipitating factors   include medications, sudden stress; may lead to acute insomnia; once removed, sleep returns to normal; perpetuating factors  habits nonconducive to sleep; serve as treatment targets

Prevalence: according to surveys, 10% to 20% of patients meet diagnostic criteria; 30% to 50% complain of diffi­culty sleeping (at some point); primary care practices    1 in 2 patients have insomnia; ask patients about sleep;  »5% of chronic insomniacs  make appointment for sleep problems; »25% might mention it, if seeing physician for different chief complaint (»66% never mention insomnia)

Impact of insufficient sleep: impaired cognitive function (memory and concentration); poor general health (eg, in­creased risk for viral illnesses, falls, and mortality), particularly in older adults; psychiatric disorders; poor job per­formance; reduced quality of life;  decreased safety (from vehicular accidents); effects on family and coworkers; increased health care costs    due to secondary effects of insufficient sleep; generalized malaise leads to repeated physician visits

Comorbidities

Overview: formerly, distinction made between primary and secondary insomnia; National Institutes of Health (NIH)’s 2005 State-of-the-Science Conference statement    insomnia comorbid with other conditions (not second­ary); difficult to know which condition arose first (eg, depression vs insomnia)

Psychiatric disorders: untreated insomnia increases risk (particularly for depression); patient survey and 1-yr fol­low-up  in those whose insomnia resolved, fewer had psychiatric disorders, including depression, anxiety disor­ders, and alcohol abuse; 7 to 8 studies show untreated insomnia increases risk for depression; study    fluoxetine plus placebo vs fluoxetine plus eszopiclone for insomnia and depression; fluoxetine plus eszopiclone treatment im­proved depression more than fluoxetine alone; similar studies in other psychiatric disorders  

Medical conditions and treatments: wide range of conditions disturb sleep    eg, dementias, Parkinson’s disease, headaches, cardiovascular (CV) disease, pulmonary disorders, gastrointestinal disorders; medications    anticholinergics, activating antidepressants, antihypertensives, and bronchodilators, central nervous system stimu­lants, statins, corticosteroids, decongestants,  b-agonists, diuretics, histamine2 blockers, and smoking cessation aids; to improve sleep, adjust dose or time of day medication taken; over-the-counter drugs; caffeine, alcohol, and nicotine  disrupt sleep; ask patients about timing and quantity; alcohol consumption in evening helps in falling asleep but leads to wakefulness later in night; any drug that affects neurotransmitter systems likely associated with insomnia

Circadian rhythm disorders: common in patients with insomnia; circadian rhythms    24 hr; standard phase    sleepiness begins at 10 to 11 pm  (core body temperature drops); sleep duration, 7 to 8 hr (adults); adolescents    sleepiness delay (1-2 AM) and delay in normal awakening (11 am to  noon); drop in core body temperature occurs later; need 9 to 10 hr of sleep; adults  most outgrow delayed sleep pattern, but some become “night owls”; take detailed sleep history to distinguish between sleep deprivation and phase delay; standard question    “What time would you take a test?”; answer of afternoon or early evening    likely phase delayed; older adults    advanced sleep phase (ie, sleepiness occurs at 6-7 pm, wakefulness 3-5 am); commonly complain of awakening during night; first scenario    forced wakefulness until 10:30 pm; person still waking up at 3 to 5 am; daytime napping becomes part of pattern to stay awake at night; second scenario  evening naps (30 min to 1 hr) result in sleep-onset prob­lems; not insomnia; advanced sleep phase plus bad habits (napping in evening); conclusion   treatment available for shifting sleep phase; no morbidity or mortality associated with advanced sleep phase

Treatment of Insomnia

Behavioral therapy: most effective (according to NIH conference); more effective than pharmacologic therapy; sleep hygiene    promotes good habits; by itself not as effective as when combined with stimulus-control therapy or sleep restriction; relaxation training    effective

Cognitive behavioral therapy (CBT)

Overview: cognitive    aimed at maladaptive thoughts one has about sleep; behavioral (sleep hygiene)    exercise; increase exposure to bright light (melatonin secreted in darkness); darkness in bedroom; avoid naps (to increase sleep drive); sleep environment    dark and quiet; comfortable temperature; “worry time”    10 to 15 min/day each day at same time; effective for those patients who worry at night; other tips    avoid heavy meals and drink­ing within 3 hr of bedtime; when awakened during night, avoid looking at clock;  for better chance of returning to sleep, do not open eyes; use night light if going to bathroom

Efficacy: treatment study    CBT plus temazepam, CBT alone, temazepam alone, or placebo; end point    amount of time patient awake at night; CBT    immediate improvement after treatment (maintained for 2 yr); temazepam    initial improvement, then worse over time; combination  improvement, then slightly worse (not as effective as either treatment alone); conclusions    CBT effective; consider integrating into practice or refer­ring patients

Pharmacologic Therapy

Self-treatments: include alcohol and herbal remedies; melatonin    no data to show efficacy; useful for circadian rhythm changes but not effective for sleep-onset problems

Antihistamines: diphenhydramine used more often than any other drug for sleep; advantages    inexpensive and easy to obtain; disadvantages    efficacy not consistent; tolerance develops; residual effects; no well-defined ef­fective dose; poorly defined half-life; adverse effects    dry mouth, blurred vision, urinary retention, constipation, and diminished cognitive function; study    diphenhydramine (25-50 mg) causes symptoms of delirium (eg, con­fusion, agitated behavior, poor sleep) in older cognitively intact patients; take-home message    drugs not benign, particularly in older adults; consistent use increases risk for side effects; similar conclusion reached by NIH panel

Sedating antidepressants: include trazodone, doxepin, and amitriptyline; used at low doses; little evidence to sup­port efficacy or safety in nondepressed individuals; some potential adverse events (not seen often); no well-defined dose; NIH  short-term trazodone use improves most sleep, but effect may not last >2 wk; doxepin    effective for »4 wk; no data on other antidepressants; all antidepressants have potentially significant adverse effects; monitor pa­tients and choose treatment carefully

Drugs approved by Food and Drug Administration (FDA): older benzodiazepines    long half-lives; many (eg, flurazepam, triazolam) have severe side effects; temazepam effective and commonly used; newer drugs    shorter half-lives (eg, zolpidem 2 hr, zaleplon 1 hr, eszopiclone 6 hr); zolpidem extended-release    longer half-life than regular zolpidem; ramelteon    shorter half-life; long-term use    only 3 approved; eszopiclone (eg, Lunesta); ra­melteon (eg, Rozerem), and Zolpidem extended-release (eg, Ambien CR); others  approved for short-term use; use clinical judgment on continuing use; efficacy and safety    all newer drugs safe and effective for short-term management; longer studies (>1 yr; available for some) show continued efficacy and safety without rebound; NIH statement    frequency and severity of adverse effects for newer drugs much lower than in older benzodiazepines; ramelteon    works on melatonin receptors (not g-aminobutyric acid [GABA] receptors); alters circadian rhythms more than sleep; not sedating, but helps with sleep onset; nonaddictive

Determining drug choices: 1) chief complaint    falling asleep or staying asleep; newer drugs for difficulty falling asleep; eszopiclone and zolpidem extended-release maintain sleep; can take zaleplon during night (as long as ³4 hr before awakening time); use complaint to decide on drug; 2) amount of time available for being in bed    8 hr ideal; read label for required inactivity (7-8  hr for most drugs, except zaleplon [4 hr] and ramelteon [none]); ad­vise patients to stay in bed for sufficient time (ie, avoid getting up while still sedated; 3) sleep history    diaries and questionnaires; bottom line    talk to patient about sleep hygiene (eg, alcohol and caffeine ingestion), medi­cal and psychiatric problems, and stress

Sample questions: difficulty falling or staying asleep; ability to function; falling asleep at inappropriate times (in­somniacs have difficulty sleeping during the day, but feel fatigued); ideal choice of sleep/wake times; time in bed vs time asleep (many insomnia patients spend too much time in bed); other symptoms (eg, restless legs syn­drome, sleep apnea [SA]);

Last resort: consider referral to sleep clinic

Obstructive Sleep Apnea

Alon Y. Avidan, MD, MPH, Associate Professor, Department of Neurology, David Geffen School of Medicine at University of California, Los Angeles, Director, Neurology Clinic, Director, Neurology Residency Program, and Associate Director, UCLA Sleep Disorders Center,

Background and epidemiology:  obstructive sleep apnea (OSA) likely in »30% of patients who snore; likelihood in­creases with    male sex, overweight (body mass index [BMI] >35), age ³40 yr, and family history; other factors    large neck size in males >17 yr of age; high blood pressure (BP)

Clinical signs and symptoms: lesion — at level of velopharynx, where posterior pharynx contacts soft palate; velo­pharyngeal space    critical area where breathing stops; parapharyngeal fat pads also occlude velopharyngeal air space; sleep-disordered breathing spectrum    normal breathing and snoring on one end; apnea on opposite end; middle of spectrum   respiratory effort-related arousals (snoring in crescendo pattern), daytime sleepiness, and hy­popneas (incomplete apneas; do not always result in complete airway occlusions but pathophysiology and treat­ment similar to that of OSA); polysomnography (PSG)    absence of air flow ³10 sec; usually increased respiratory effort, some paradoxic breathing (chest and abdomen working in opposition), oxygen desaturation <4%, compared to oxygen level before event, electroencephalographic (EEG) evidence for arousal; in OSA, 50 to 60 events per hour of sleep

Distinction between obstructive and central apnea

Obstructive: cessation of nasal and oral airflow; patient trying to overcome resistance to airflow and generating breathing effort; paradoxic breathing; EEG shows arousal and delayed oxygen desaturation (response to obstruc­tion); daytime sleepiness; effects on CV system   most patients develop physiologic response (eg, bradycardia) during event; some develop sinus arrest; ventricular fibrillation most pathologic  

Central: no airflow or breathing effort; pathophysiology  due to CV disease, brainstem lesions, stroke, or conges­tive heart failure; treatment    similar to that for OSA (but better addressed with bilevel positive pressure [biPAP] ventilation)

Upper airway resistance syndrome: crescendo snoring; laborious breathing; EEG arousal; explains fatigue and sleepiness in patients with narrow air space but without obesity

Snoring: independent risk factor for hypertension or stroke; associated with high BP and daytime sleepiness; treated with weight loss and positional therapy

Effects of OSA: unrefreshing sleep, poor memory, irritability, and impotence; physical examination (PE)    height-to-weight ratio, BMI, neck circumference, oral air space, and size of uvula and soft palate

Mallampati system: classification system (I-IV) to document ease of intubation; ask patient to extend tongue; higher score means increased risk for OSA; positive correlation with apnea/hypopnea index (AHI; indication of severity of OSA)

Neck circumference and intranasal examination: neck    in men, >17 in; in women, >16 in; intranasal examination  check for nasal polyps or other obstructions that would preclude nasal CPAP; document tonsil size (tonsillectomy curative in children) and size of soft palate and uvula (resection option)

Facial morphology: certain syndromes (eg, Pierre Robin sequence) can push soft palate closer to velopharyngeal air space; physical features (children)    tonsillar hypertrophy, adenoidal hypertrophy, obesity, and impaired growth and development; often present with hyperactivity

Diagnosing OSA: PSG (common)    EEG, eye electrodes (to track rapid eye movement [REM] sleep), snoring, air­flow, respiratory effort, and oxygen saturation; add leads if parasomnia suspected; recommend 2 electromyographic (EMG) electrodes on chin and leg; hypnogram    illustration of sleep stages, oxygen saturation, and other physio­logic parameters over time; pronounced  hypoxemia during REM sleep

Nonsurgical Treatment

Self-treatments: weight loss; positional therapy; avoiding substances that worsen apnea (eg, alcohol, long-acting sedative hypnotics); positional therapy    tennis balls to make sleeping on back uncomfortable (causes low back pain); wedge pillow

CPAP therapy:  pneumonic splint (as pressure increased from 0 to 15 cm H2O, dimensions of upper airway im­prove);  adherence    challenging (patients complain about claustrophobia and appearance of equipment); involve family or bed partner; improvement takes months (need motivated patient)

Oral appliances: used for snoring or mild OSA; tongue-retaining (ineffective and uncomfortable); Home | Latest Releases | Search | Subscribe Now! | Past Issues | Series Specials | About ADF
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