Home-based Diagnosis of Obstructive Sleep Apnea in an Urban Population
Open accessAbstract
Study objectives Home-based diagnosis of obstructive sleep apnea (OSA) with portable monitoring (PM) is increasingly utilized, but remains understudied in underserved and minority populations. We tested the feasibility of home PM in an urban population at risk for OSA compared to in-laboratory polysomnography (PSG) and examined patient preference with respect to home PM versus PSG. Methods Randomized crossover study of home PM (WatchPAT200) and in-laboratory simultaneous PSG and PM in 75 urban African Americans with high pre-test probability of OSA, identified with the Berlin questionnaire. Results Fifty-seven of 75 participants were women, average age 45 ± 11 years (mean ± SD), 35% with ≤ high school education, and 76% with annual household income < $50,000. Technical failure rates were 5.3% for home vs. 3.1% for in-laboratory PM. There was good agreement between apnea hypopnea index on PSG; AHIPSG and AHI on home PM (mean ± 2 SD of the differences = 0.64 ± 46.5 and intraclass correlation coefficient; ICC = 0.73). The areas under the curve for the receiver-operator characteristic curves for home PM were 0.90 for AHIPSG ≥ 5, 0.95 for AHIPSG ≥ 10, and 0.92 for AHIPSG ≥ 15. 62/75 (82%) participants preferred home over in-laboratory testing. Conclusions Home PM for diagnosis of OSA in a high risk urban population is feasible, accurate, and preferred by patients. As home PM may improve access to care, the cost-effectiveness of this diagnostic strategy for OSA should be examined in underserved urban and rural populations. Clinical trials registration ClinicalTrials.gov, identifier: NCT01997723.
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Two cross-over studies randomized patients to home-based PAT, and in-laboratory simultaneous PSG and PAT.
“Two cross-over studies randomized patients to home-based PAT, and in-laboratory simultaneous PSG and PAT.”
From Clinical Practice Guideline for Diagnostic Testing for Adult Obstructive Sleep Apnea: An American Academy of Sleep Medicine Clinical Practice Guideline (2017) · cites this paper as [106]
The Methods (Protocol) say participants were randomized to a home WatchPAT200 session or an in-laboratory session with simultaneous PSG and WatchPAT200. The Abstract identifies this as one randomized crossover study, so this source supports the study design but not the claim that there were two studies. (LLM, conf=0.88)
Experimental — accuracy not yet measuredA single study that evaluated the performance of the PAT device in the home against in-laboratory PSG using a cutoff of AHI ≥ 5 reported a specificity of 0.43 (95% CI: 0.22 to 0.66).
“A single study that evaluated the performance of the PAT device in the home against in-laboratory PSG using a cutoff of AHI ≥ 5,106 reported a specificity of 0.43 (95% CI: 0.22 to 0.66).”
From Clinical Practice Guideline for Diagnostic Testing for Adult Obstructive Sleep Apnea: An American Academy of Sleep Medicine Clinical Practice Guideline (2017) · cites this paper as [106]
The Methods and Results report a comparison of home WatchPAT200 testing with in-laboratory PSG and a specificity of 0.43 at an AHI threshold of ≥5. The stated 95% confidence interval (0.22 to 0.66) is not available in our copy: Table 3 appears only as an image reference, and the accompanying Results text does not give that interval. (LLM, conf=0.88)
Experimental — accuracy not yet measuredWhen two studies evaluated the home-based PAT device against in-laboratory PSG at an AHI cutoff of ≥ 15, specificity ranged from 0.77 to 1.00 and sensitivity ranged from 0.92 to 0.96.
“When two studies evaluated the home-based PAT device against in-laboratory PSG at an AHI cutoff of ≥ 15, specificity ranged from 0.77 to 1.00 and sensitivity ranged from 0.92 to 0.96.”
From Clinical Practice Guideline for Diagnostic Testing for Adult Obstructive Sleep Apnea: An American Academy of Sleep Medicine Clinical Practice Guideline (2017) · cites this paper as [106]
The Results report that home WatchPAT200 was compared with in-laboratory PSG at an AHI cutoff of ≥15 and had specificity of 0.77, with sensitivity of at least 0.90. Our copy does not give the claimed sensitivity range of 0.92–0.96 or report a second study with specificity of 1.00, so it supports only part of the two-study range. (LLM, conf=0.85)
Experimental — accuracy not yet measured
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- Authors
- Garg, N., Rolle, A. J., Lee, T. A., & Prasad, B.
- Affiliations
- University of Illinois Chicago (US)
- Corresponding author
- Prasad, Bharati
- Venue
- Journal of Clinical Sleep Medicine
- Published
- 2014-08-15
- Volume
- 10
- Issue
- 8
- Pages
- 879-885
- ISSN
- 1550-9389 (ISSN-L)
- 1550-9397
- PMC
- PMC4106942
- OpenAlex
- W2332543859
- Cited by
- 85
- References
- 3
- Citations by year
- 2026: 6 · 2025: 8 · 2024: 7 · 2023: 11 · 2022: 7 · 2021: 15 · 2020: 7 · 2019: 4 · 2018: 6 · 2017: 8 · 2016: 2 · 2015: 4
- FWCI
- 2.91
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Clinical Sleep Medicine (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (KM1CA156717)
- Topics
- Health Sciences › Medicine › Physiology › Obstructive Sleep Apnea Research
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
- Keywords
- obstructive sleep apnea, home-based diagnosis, portable monitoring, polysomnography, African Americans, urban population, underserved populations, patient preferences, apnea-hypopnea index, diagnostic accuracy, Berlin questionnaire
- MeSH terms
- Female, Humans, Male, Middle Aged, Monitoring, Physiologic, Self Care, Urban Population, Polysomnography, Cross-Over Studies, Sleep Apnea, Obstructive
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