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A clinician’s guide to recurrent isolated sleep paralysis

B. Sharpless

Neuropsychiatric Disease and Treatment July 19, 2016 DOI: 10.2147/ndt.s100307 (opens in new tab) via Semantic Scholar

Summary

AI-generated from the abstract

Sleep paralysis is a frightening event in which a person awakens conscious but temporarily unable to move, due to lingering REM-sleep muscle atonia, often accompanied by vivid hallucinations. When it occurs without narcolepsy or other medical conditions, it is called isolated sleep paralysis. The condition is underrecognized by nonsleep specialists, partly because patients are reluctant to disclose episodes and because medical training lacks coverage. A growing body of research documents its prevalence, risk factors, and clinical impact. Available treatments include pharmacological and psychotherapeutic interventions, but these require more empirical support from larger, well-controlled trials.

Study at a glance

Characteristics Review Peer reviewed
Keywords Medicine
Key finding Sleep paralysis is an underrecognized sleep–wake disorder that requires more empirical support for available pharmacological and psychotherapeutic treatments.

Abstract

This review summarizes the empirical and clinical literature on sleep paralysis most relevant to practitioners. During episodes of sleep paralysis, the sufferer awakens to rapid eye movement sleep-based atonia combined with conscious awareness. This is usually a frightening event often accompanied by vivid, waking dreams (ie, hallucinations). When sleep paralysis occurs independently of narcolepsy and other medical conditions, it is termed “isolated” sleep paralysis. Although the more specific diagnostic syndrome of “recurrent isolated sleep paralysis” is a recognized sleep–wake disorder, it is not widely known to nonsleep specialists. This is likely due to the unusual nature of the condition, patient reluctance to disclose episodes for fear of embarrassment, and a lack of training during medical residencies and graduate education. In fact, a growing literature base has accrued on the prevalence, risk factors, and clinical impact of this condition, and a number of assessment instruments are currently available in both self-report and interview formats. After discussing these and providing suggestions for accurate diagnosis, differential diagnosis, and patient selection, the available treatment options are discussed. These consist of both pharmacological and psychotherapeutic interventions which, although promising, require more empirical support and larger, well-controlled trials.

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