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OSA and CV Outcomes in Patients With High Risk AF
Sponsor: National University of Singapore
Summary
The POACH study is part of the Cardiosleep research program. It is a prospective, observational, multicentre study conducted in Singapore. The recruitment target is 1365 patients. Eligible patients with AF and high cardiovascular risk will be recruited for a home-based sleep study using a FDA-approved portable device. The patients will be divided into 2 groups based on the presence or absence of OSA using apnoea-hypopnoea index ≥ 15 events/hour. The AF will be treated as per local standard practice. Participation in the POACH study will not affect the management of AF. Follow-up will be conducted every 6 months until the median follow-up duration has reached 2 years. The primary endpoint is a four-component composite of all-cause mortality, myocardial infarction, stroke and heart failure hospitalisation. Antecubital venous blood samples will be taken from the patients in the morning after the sleep study for targeted mass spectrometry which will measure 83 circulating metabolites. Sparse Principal Component Analysis will be used for data reduction. Identification of distinct associations between metabolic perturbations and OSA will be performed.
Official title: Prospective Study on Obstructive Sleep Apnea and Cardiovascular Outcomes in Patients With Atrial Fibrillation and High Cardiovascular Risk
Key Details
Gender
All
Age Range
22 Years - 99 Years
Study Type
OBSERVATIONAL
Enrollment
1365
Start Date
2019-07-01
Completion Date
2028-06-30
Last Updated
2024-06-12
Healthy Volunteers
No
Interventions
Overnight sleep study
The patients will undergo an overnight sleep study using Watch-PAT sleep study device
Locations (1)
Chi-Hang Lee
Singapore, Singapore