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Table 2 Common sleep disorders in children

From: Pediatric sleep disturbances and treatment with melatonin

Sleep disorder

Epidemiology

Clinical features

Diagnostic criteria

Treatment options

Obstructive sleep apnea

Prevalence: 1–5%

Onset: 2–8 years of age

M:F = 1:1

More frequent in blacks and people with craniofacial abnormalities, Down syndrome, neuromuscular diseases, or choanal atresia

Snoring

Unusual sleep positions

Sleep-related paradoxical breathing

Bedtime enuresis or diaphoresis

Morning headaches

Cognitive/behavioural problems

Excessive daytime sleepiness

Enlarged adenoids and tonsils

Pectus excavatum

PSG apnea–hypopnea index > 1.5 per hour

Adeno-tonsillecto-my

CPAP, nasal steroids, rapid maxillary expansion

Confusional arousals

Prevalence: 17.3% in 3–13-year-olds, 2.9–4.2% in children older than 15 years

M:F = 1:1

Positive family history

Sleep drunkenness

Unusual behaviour

Slowed responsiveness

Slurred speech

Confused after awakening

Occurs during the first half of the sleep period, no memory of the event

History

Re-assurance

Increase total sleep time

Scheduled awakenings

Bedroom/home safety counselling

Sleep terrors

Prevalence: 1–.5%

Onset: early childhood

M:F = 1:1

Intense fear

Difficulty in awakening from episode

Dangerous activities

Occurs during the first half of the sleep period, no memory of the event

Overlap with other parasomnias

History

Re-assurance

Increase total sleep time

Scheduled awakenings

Bedroom/home safety counselling

-Benzo-diazepines

Nightmares

Prevalence: 10–50% in 3–5-year-olds

Onset: 3–6 years of age; peaks: 6–10 years of age

M:F = 1:1

Unpleasant dreams

Increased sympathetic activity

Occurs during the second half of the sleep period, memory of the event

Reluctance to sleep increases

Association with mood disorders or post-traumatic stress disorder

History

Re-assurance

Increase total sleep time

Scheduled awakenings

Bedroom/home safety counselling

Cognitive behavioural therapy, SSRI (off-label use)

Behavioural insomnia of childhood

Prevalence: 10–30%

M:F = 1:1

Sleep-onset association type

Limit-setting type

History

Prevention, parental education, and extinction techniques

Delayed sleep phase disorder

Prevalence: 7–16% in adolescents

Onset: adolescence

Positive familiar history in 40% of cases

Difficulty in falling asleep and waking up at socially acceptable times

Night owl

History

Sleep diary and/or actigraphy for at least 1 week

Sleep hygiene education

Regular sleep–wake schedule

Avoid bright lights before bedtime

Melatonin

Bright light therapy

Use of sleep logs to monitor progress

Restless legs syndrome

Prevalence: 2%

More common in F

Positive familiar history

Urge to move legs with discomfort

Begins in the evening, worsens with rest, eases with movement

Association with iron deficiency

Association with negative behaviour and mood, and decreased cognition and attention

Increased prevalence in children with ADHD

History

PSG

Presence of two of the following: disturbed sleep; a first-degree relative with the condition; five or more periodic limb movements per hour of sleep during PSG

Avoid nicotine and caffeine

Dis-continue offending medications

Iron replacement in the case of deficiency

Severe cases: levodopa, dopamine agonists, gabapentin

  1. PSG polysomnography, CPAP continuous positive airway pressure, M males, F females, SSRI selective serotonin re-uptake inhibitors, ADHD attention deficit/hyperactivity disorder