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Sleep Disorders and Sleep Deprivation: An Unmet Public

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<strong>Sleep</strong> <strong>Disorders</strong> <strong>and</strong> <strong>Sleep</strong> <strong>Deprivation</strong>: <strong>An</strong> <strong>Unmet</strong> <strong>Public</strong> Health Problem<br />

http://www.nap.edu/catalog/11617.html<br />

ENSURING ADEQUATE DIAGNOSIS AND TREATMENT 225<br />

for release in 2006, should provide important advances for the diagnosis of<br />

chronic sleep loss <strong>and</strong> sleep disorders.<br />

Summary of Formal Evaluation Reviews<br />

Three recent in-depth reviews have been performed to examine the<br />

effectiveness of portable monitoring devices (Ross et al., 2000; ATS, 2004;<br />

Tice, 2005). As described above, these reports were largely aimed at evaluating<br />

the literature regarding the accuracy of clinical diagnosis relative to<br />

reference in lab polysomnography, with some attempt at also evaluating<br />

the literature relative to cost-effectiveness <strong>and</strong> clinical prediction. In 1998,<br />

the Agency for Healthcare Research <strong>and</strong> Quality performed a literature<br />

review <strong>and</strong> meta-analysis on studies of portable monitoring for OSA.<br />

The review concluded that at the time there was insufficient evidence to<br />

make firm recommendations for use of portable monitoring for the diagnosis<br />

of sleep apnea (Ross et al., 2000).<br />

<strong>An</strong> executive summary on the systematic review <strong>and</strong> practice parameters<br />

for portable monitoring in the investigation of suspected sleep apnea<br />

in adults was published in 2004 by an evidence review committee consisting<br />

of members from the American Thoracic Society, the American College of<br />

Chest Physicians, <strong>and</strong> the American Academy of <strong>Sleep</strong> Medicine (ATS, 2004;<br />

Flemons <strong>and</strong> Littner, 2003). In that summary, the following recommendations<br />

were made:<br />

• Given the available data, the use of portable device was not recommended<br />

for general screening.<br />

• The use of portable devices was not recommended in patients with<br />

comorbid conditions or secondary sleep complaints.<br />

• The use of portable devices should require review of raw data by<br />

trained sleep specialists.<br />

The review committee also recognized the need for further development<br />

of portable devices <strong>and</strong> suggested several goals for future research. It<br />

was found that most studies on portable monitoring were performed primarily<br />

on white males with OSA who had few comorbidities. The evidence<br />

review committee recommended that future studies should include more<br />

diverse populations, other than patients with sleep apnea, that are not subject<br />

to selection bias. Additional recommendations were that future studies<br />

should address clinical predictive algorithms in combination with portable<br />

monitoring in the diagnosis of sleep apnea, <strong>and</strong> study design should assess<br />

the cost-effectiveness <strong>and</strong> outcomes associated with different diagnostic <strong>and</strong><br />

management strategies.<br />

Copyright © National Academy of Sciences. All rights reserved.

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