State of home sleep studies

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Classification of portable monitors

The technology for data acquisition and analysis for home monitors has evolved rapidly, and several devices have been modified repeatedly over the years. The American Academy of Sleep Medicine, formerly the American Sleep Disorders Association, developed a classification system for portable monitors based on the number and type of parameters recorded (Table 1) [7].

Defining breathing-disordered events

Although polysomnography is widely recognized as the reference standard for evaluating patients who are suspected of sleep apnea, the methods and criteria for defining events are not standardized across sleep laboratories or research studies [5]. In general, breathing disturbances are identified during polysomnography by a clear reduction in a measurement of breathing, with or without an accompanying decrease in oxygen saturation or arousal [5]. The most common method for detecting reductions

Existing guidelines and reviews

In 1994, the American Sleep Disorders Association practice parameters recommended that polysomnography remain the standard for the diagnosis, determination of severity, and treatment of sleep apnea [22]. Unattended portable recording was viewed as an acceptable alternative only under the following circumstances: (1) when initiation of treatment was urgent and polysomnography unavailable, (2) when patients could not undergo polysomnography because of mobility issues, or (3) as a follow-up to

Rating the evidence

To avoid bias in assessing a diagnostic test such as a portable monitor, several key factors must be considered. Selection bias may be introduced if consecutively referred patients are not used. Verification bias may be introduced if the decision to perform a reference standard (in this case, polysomnography) is influenced by the results of the test being evaluated (a portable monitor). Table 2 depicts how the system by Sackett et al [26] for rating evidence would apply to studies evaluating a

Further research directions

Additional research on portable monitors is required to address several issues. Most monitors have been studied by only a single group of investigators. All studies have taken place on patients referred to a sleep center. It is yet to be proven what the effect of changing the studied clinical population would have on the diagnostic performance of these monitors. Primary care populations, women, non-whites, and patients with comorbid illness have not been studied adequately; therefore, the

Portable monitors in a clinical decision algorithm

Like any diagnostic test, the results of testing with portable monitors are most useful when applied to the appropriate clinical context. The results of a negative portable monitoring study would have different implications for a mildly symptomatic patient with a low pretest probability compared with a symptomatic patient with a high pretest probability. The probability that a patient has sleep apnea based on clinical factors alone can be estimated using one of several clinical prediction rules

Summary

Many different portable monitors have been used to assess patients with suspected sleep apnea. There is limited evidence for the use of type 2 monitors, especially in the unattended setting in which there may be high rates of data loss. Type 3 monitors have low likelihood ratios for negative tests and can be used to “rule out” sleep apnea. The ability of type 3 monitors to “rule in” sleep apnea is less convincing, but this may improve with the use of improved technology, such as nasal pressure

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