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P074 Night-to-night variability in obstructive sleep apnoea severity is associated with hypertension and high misdiagnosis rates

INTRODUCTION: The impact of night-to-night variability in obstructive sleep apnoea (OSA) severity on important health outcomes such as blood pressure is unknown. This study aimed to determine the effects of night-to-night variability in the apnoea/hypopnoea index (AHI) on hypertension risk and OSA m...

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Detalles Bibliográficos
Autores principales: Lechat, B, Naik, G, Reynolds, A, Aishah, A, Scott, H, Loffler, K, Vakulin, A, McEvoy, R, Adams, R, Catcheside, P, Eckert, D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10109422/
http://dx.doi.org/10.1093/sleepadvances/zpab014.118
Descripción
Sumario:INTRODUCTION: The impact of night-to-night variability in obstructive sleep apnoea (OSA) severity on important health outcomes such as blood pressure is unknown. This study aimed to determine the effects of night-to-night variability in the apnoea/hypopnoea index (AHI) on hypertension risk and OSA misdiagnoses. METHODS: In-home nightly monitoring of 67,278 participants from 151 countries, over ~170 nights per participant between July 2020 to March 2021 using a validated under mattress sleep analyser. Blood pressure measurements were available in 12,295 participants. OSA was defined as a mean nightly AHI >15events/h. Night-to-night variability was assessed as the standard deviation of AHI across nights. RESULTS: 22.6% (95% CI: 20.9–24.3) of the cohort (13% of women, 25% of men) had an average AHI> 15 events/h sleep. The average nightly AHI variability ranged from 3±1 in people without OSA to 14±6 in people with severe OSA. Higher mean AHI (OR [95% CI], 1.44 [1.29, 1.61]) and greater nightly variability in AHI (1.57 [1.39, 1.76]) were associated with hypertension. In people with a mean AHI of ≥5 events/h, high night-to-night AHI variability was associated with a ~30% increased risk in hypertension, independent of OSA severity category. Likelihood of misdiagnosis of OSA based on a single night compared to the mean across all nights was ~20%; this decreased with more monitoring nights. CONCLUSIONS: These findings highlight the novel, important information that simple multi-night monitoring of OSA can yield. This includes the potential importance of night-to-night variation and its contribution to hypertension and increased confidence of OSA diagnoses.