Insomnia Insomnia
Insomnia Insomnia
Insomnia Insomnia
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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