An assessment of a simple clinical technique to estimate pharyngeal collapsibility in people with obstructive sleep apnea.


Journal

Sleep
ISSN: 1550-9109
Titre abrégé: Sleep
Pays: United States
ID NLM: 7809084

Informations de publication

Date de publication:
13 10 2020
Historique:
received: 20 08 2019
revised: 31 01 2020
pubmed: 9 4 2020
medline: 15 4 2021
entrez: 9 4 2020
Statut: ppublish

Résumé

Quantification of upper airway collapsibility in obstructive sleep apnea (OSA) could help inform targeted therapy decisions. However, current techniques are clinically impractical. The primary aim of this study was to assess if a simple, novel technique could be implemented as part of a continuous positive airway pressure (CPAP) titration study to assess pharyngeal collapsibility. A total of 35 participants (15 female) with OSA (mean ± SD apnea-hypopnea index = 35 ± 19 events/h) were studied. Participants first completed a simple clinical intervention during a routine CPAP titration, where CPAP was transiently turned off from the therapeutic pressure for ≤5 breaths/efforts on ≥5 occasions during stable non-rapid eye movement (non-REM) sleep for quantitative assessment of airflow responses (%peak inspiratory flow [PIF] from preceding 5 breaths). Participants then underwent an overnight physiology study to determine the pharyngeal critical closing pressure (Pcrit) and repeat transient drops to zero CPAP to assess airflow response reproducibility. Mean PIF of breaths 3-5 during zero CPAP on the simple clinical intervention versus the physiology night were similar (34 ± 29% vs. 28 ± 30% on therapeutic CPAP, p = 0.2; range 0%-90% vs. 0%-95%). Pcrit was -1.0 ± 2.5 cmH2O (range -6 to 5 cmH2O). Mean PIF during zero CPAP on the simple clinical intervention and the physiology night correlated with Pcrit (r = -0.7 and -0.9, respectively, p < 0.0001). Receiver operating characteristic curve analysis indicated significant diagnostic utility for the simple intervention to predict Pcrit < -2 and < 0 cmH2O (AUC = 0.81 and 0.92), respectively. A simple CPAP intervention can successfully discriminate between patients with and without mild to moderately collapsible pharyngeal airways. This scalable approach may help select individuals most likely to respond to non-CPAP therapies.

Identifiants

pubmed: 32267509
pii: 5817777
doi: 10.1093/sleep/zsaa067
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Sleep Research Society 2020. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com.

Auteurs

Amal M Osman (AM)

Neuroscience Research Australia (NeuRA), School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.
Adelaide Institute for Sleep Health, A Flinders Centre of Research Excellence, College of Medicine and Public Health, Flinders University, Bedford Park, SA, Australia.
CRC for Alertness, Safety and Productivity, Melbourne, Australia.

Benjamin K Tong (BK)

Neuroscience Research Australia (NeuRA), School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.

Shane A Landry (SA)

CRC for Alertness, Safety and Productivity, Melbourne, Australia.
Sleep and Circadian Medicine Laboratory, Department of Physiology and School of Psychological Sciences, Monash University, Melbourne, Victoria, Australia.

Bradley A Edwards (BA)

CRC for Alertness, Safety and Productivity, Melbourne, Australia.
Sleep and Circadian Medicine Laboratory, Department of Physiology and School of Psychological Sciences, Monash University, Melbourne, Victoria, Australia.

Simon A Joosten (SA)

Monash Lung and Sleep, Monash Health Clayton, Victoria, Australia.
School of Clinical Sciences, Monash University, Melbourne, Victoria, Australia.

Garun S Hamilton (GS)

Monash Lung and Sleep, Monash Health Clayton, Victoria, Australia.
School of Clinical Sciences, Monash University, Melbourne, Victoria, Australia.

Jennifer M Cori (JM)

CRC for Alertness, Safety and Productivity, Melbourne, Australia.
Institute for Breathing and Sleep, Austin Health, Heidelberg, Victoria, Australia.

Amy S Jordan (AS)

CRC for Alertness, Safety and Productivity, Melbourne, Australia.
Institute for Breathing and Sleep, Austin Health, Heidelberg, Victoria, Australia.

David Stevens (D)

Adelaide Institute for Sleep Health, A Flinders Centre of Research Excellence, College of Medicine and Public Health, Flinders University, Bedford Park, SA, Australia.
CRC for Alertness, Safety and Productivity, Melbourne, Australia.

Ronald R Grunstein (RR)

CRC for Alertness, Safety and Productivity, Melbourne, Australia.
Woolcock Institute of Medical Research and the University of Sydney, Glebe, NSW, Australia.

R Doug McEvoy (RD)

Adelaide Institute for Sleep Health, A Flinders Centre of Research Excellence, College of Medicine and Public Health, Flinders University, Bedford Park, SA, Australia.
CRC for Alertness, Safety and Productivity, Melbourne, Australia.

Peter G Catcheside (PG)

Adelaide Institute for Sleep Health, A Flinders Centre of Research Excellence, College of Medicine and Public Health, Flinders University, Bedford Park, SA, Australia.
CRC for Alertness, Safety and Productivity, Melbourne, Australia.

Danny J Eckert (DJ)

Neuroscience Research Australia (NeuRA), School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.
Adelaide Institute for Sleep Health, A Flinders Centre of Research Excellence, College of Medicine and Public Health, Flinders University, Bedford Park, SA, Australia.
CRC for Alertness, Safety and Productivity, Melbourne, Australia.

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