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Medical and Neurological Causes 111<br />

cations may produce insomnia (5), particularly at higher doses, especially during<br />

the initial period of use.<br />

Amelioration of a skin condition may require a relatively short duration of treatment,<br />

and therefore may cause only short-term sleep disruption. The use of hypnotic<br />

medication, especially shorter acting medications that are unlikely to produce<br />

daytime sedation, may be ideally suited to a skin condition that has brief course<br />

(such as poison ivy dermatitis) or intermittent exacerbation (such as eczema). Many<br />

of the antihistamine medications used to reduce allergic response and itching are<br />

sedating, improving sleep initiation and maintenance somewhat, but may cause<br />

residual daytime effects on alertness and cognitive performance (6). The use of<br />

medications such as amitriptyline or trazadone, which may improve the component<br />

of insomnia caused by depression and pain, should be considered if duration and<br />

severity of insomnia warrants their use, and if other medical conditions do not preclude<br />

their use.<br />

Problems in the nasopharynx, oropharynx, and larynx are a common cause of<br />

sleep disruption. The most widely recognized condition that can be caused by the<br />

pharyngeal tree is obstructive sleep apnea (OSA), which can be seen in association<br />

with conditions such as nasal polyps, excessive submucosal oropharyngeal adipose<br />

tissue, oropharyngeal or nasopharyngeal mass lesions, macroglossia, uvular hypertrophy,<br />

retrognathia, and pharyngeal muscle weakness. The neck may permit OSA<br />

to occur if it is short, broad, restricted in motion, or has anterior adipose deposition.<br />

Mass lesions, hyoid pathology, and cervical spine degenerative changes can also<br />

cause OSA. Sleep apnea can produce secondary insomnia through chronic disruption<br />

of sleep continuity, and secondary insomnia in turn makes patients less tolerant<br />

of treatment with continuous positive airway pressure (CPAP) ventilation. The<br />

diagnostic PSG will show worsened sleep efficiency, less deep sleep, more frequent<br />

arousal from sleep, and longer arousal when OSA is complicated by insomnia.<br />

Upper airway resistance syndrome (UARS) may typify such a condition, where<br />

less severely disordered breathing causes a disproportionately profound degree of<br />

sleep disruption.<br />

When insomnia complicates UARS and OSA, treatment with CPAP is poorly<br />

tolerated and may require the adjunctive use of sedating medications, which will<br />

worsen obstructive breathing to some extent. The availability of auto-titrating CPAP<br />

and biphasic ventilation units may allow for more comfortable treatment, adjusting<br />

the level of positive pressure required to overcome airway obstruction at any given<br />

time. However, even the automatic changes in pressure settings may cause arousal<br />

in a patient who suffers from insomnia. Because CPAP therapy is the most universally<br />

effective method of treating obstructive breathing during sleep, the addition<br />

of a medication to improve sleep initiation and continuity is a reasonable option.<br />

Shorter acting hypnotic medications (estazolam, zaleplon, zolpidem) will least<br />

affect the overall architecture of sleep, but will only provide benefit for the initial<br />

hours of sleep. Re-dosing of these medications may be considered, with the caveat<br />

that patients are more likely to awaken with a “hangover” effect that mitigates some

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