Sleep Tests in the Non-Contact Era of the COVID-19 Pandemic: Home Sleep Tests Versus In-Laboratory Polysomnography

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Clin Exp Otorhinolaryngol. 2020;13(4):318-319
Publication date (electronic) : 2020 November 1
doi : https://doi.org/10.21053/ceo.2020.01599
1Department of Biomedical Laboratory Science, Jungwon University, Goesan, Korea
2Obstructive Upper Airway Research (OUaR) Laboratory, Department of Pharmacology, Seoul National University College of Medicine, Seoul, Korea
3Ischemic/Hypoxic Disease Institute, Seoul National University College of Medicine, Seoul, Korea
4Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea
5Department of Otorhinolaryngology-Head and Neck Surgery, Seoul National University Hospital, Seoul, Korea
Received 2020 July 21; Accepted 2020 August 10.

Coronavirus disease 2019 (COVID-19) is affecting millions of people around the world, both socially and economically, and has fundamentally changed people’s lifestyles. Masks and disinfectants have become essential items and social distancing became inevitable in light of the finding that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes COVID-19, could be detected in aerosols for several hours. Even in the absence of direct enforcement by the government, the tendency to avoid direct face-to-face contact seems to be widespread throughout our society. Many people are reluctant to come to the hospital because of concerns about contracting COVID-19 in the hospital. This leads to an important question: how should sleep tests be conducted in this non-contact era? Ultimately, the paradigm of sleep testing needs to be changed in response to this trend.

In-laboratory polysomnography (PSG) is the gold standard for diagnosing obstructive sleep apnea (OSA) because of its high diagnostic accuracy and low failure rate. These advantages of in-laboratory PSG may be due to the presence of a supervisor. Nonetheless, the disadvantages of in-laboratory PSG, including high costs, long waiting times, and hospital stays, could offset its merits. The first classification of portable monitors (PMs) divided them into four types according to the type and number of parameters and personnel attendance (type 1 to type 4) [1]. However, this classification of PMs did not reflect new technologies, and therefore an alternative categorization scheme including sleep, cardiovascular, oximetry, position, effort, and respiratory parameters (SCOPER) was developed in 2011 [2]. The American Academy of Sleep Medicine Task Force developed guidelines for the use of PMs without observation for the diagnosis of OSA in 2007 [3] and updated the information in 2017 [4]. The guidelines recommend using PMs in patients with a high pretest probability of moderate to severe OSA without significant comorbid medical conditions. The use of a PM can also be considered if in-laboratory PSG is impossible due to immobility or serious illness.

Comparative studies have reported good diagnostic performance of PMs for suspected OSA patients, as demonstrated by strong agreement between the apnea-hypopnea index acquired from PMs and in-laboratory PSG. However, home sleep tests seem to have a higher failure rate than in-laboratory PSG [5,6]. Nonetheless, a recent randomized crossover study showed no significant differences in sensor quality and the number of non-interpretable tests between home sleep testing using type 2 PMs and in-laboratory monitoring using the same type 2 PMs [7].

As mentioned above, the clinical guidelines for the use of PMs limit the possible subjects to patients with a high pretest probability of moderate to severe OSA because of concerns that PM may have a higher false negative rate in the diagnosis of mild to mderate OSA. Indeed, the sensitivity and specificity of PMs for OSA vary depending on the severity of OSA and the type of monitor [8]. The recently developed type 3 PMs seem to have overcome the problem of low sensitivity, which is a disadvantage of existing PMs, even in mild OSA [9,10]. Whether OSA patients prefer a home sleep test or in-laboratory PSG depends on the hook-up location. When patients were hooked-up in the hospital and asked to return home for the sleep recording, the preference rate for home sleep monitoring was lower than that for in-laboratory testing [6,7]. When the hook-up was performed at patients’ home, in contrast, the trend was reversed [11,12]. These results indicate that transportation is a critical factor determining patients’ preference for a test location, and if transportation is inconvenient, patients will be willing to accept spending the night under observation in unfamiliar circumstances.

To address transportation-related concerns regarding home sleep tests, it is necessary to develop innovative PMs that can be easily worn and operated by patients at home. To minimize the failure rate, it is necessary to establish a self-monitoring system of sensor signals and to develop remotely controllable devices. Thanks to innovations in data transmission technology, this is no longer an impossible dream.

According to an evaluation of a hypothetical cohort of 1,000 Medicaid patients with suspected OSA [13], diagnostic testing using a type 3 PM and the therapeutic strategy of home sleep monitoring with an auto-titrating continuous positive airway pressure (CPAP) device could save more than $400,000 compared to in-laboratory PSG and in-laboratory PSG with a fixed-titration CPAP device. Considering the high cost of in-laboratory sleep tests, the deterioration of economic conditions due to the increase in unemployment resulting from COVID-19, and the increasing adoption of non-face-to-face-meetings in daily life, the transition to home sleep testing is an essential requirement in the current non-contact era.

Notes

No potential conflict of interest relevant to this article was reported.

AUTHOR CONTRIBUTIONS

Conceptualization, Writing–original draft, review & editing: all authors.

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