Cardiovascular Disease Clinical Trial
Official title:
Sleep Apnea cardioVascular Endpoints Study - Investigating the Effectiveness of Treatment With CPAP vs Standard Care in Reducing CV Morbidity and Mortality in Patients With Co-existing CV Disease and Moderate-severe Obstructive Sleep Apnea.
Obstructive Sleep Apnea (OSA) is a condition in which a person stops breathing for several seconds at a time due to relaxation of the throat muscles. This can occur many times during sleep. It is known to cause sleepiness and poor concentration during the day. Research indicates that OSA may be a modifiable risk factor for cardiovascular disease due to its association with hypertension, stroke, heart attack and sudden death. The standard therapy for symptomatic OSA is continuous positive airway pressure (CPAP). CPAP has been shown to effectively reduce snoring, obstructive episodes and daytime sleepiness and to modestly reduce blood pressure and other risk factors for cardiovascular disease. The overall aim of SAVE is to determine if CPAP can reduce the risk of heart attack, stroke or heart failure for people with OSA.
There is increasing evidence to indicate that OSA is an important modifiable risk factor for
CV disease including stroke, MI, and heart failure. Increased nocturnal arterial blood
pressure (BP), hypercoagulability, oxidative stress, inflammation, insulin resistance and
cardiac arrhythmias are all associated with OSA. These effects are presumed to accelerate
the progression of atheromatous disease, particularly within the coronary or cerebral
vasculature. Moreover, OSA also appears to increase the risk of sudden death during sleep,
which is different from the circadian pattern of sudden death in those without OSA,
suggesting that episodes of apnea may have a direct triggering effect for cardiac
arrhythmias or MI.
CPAP is now standard therapy for symptomatic OSA, with adherence to treatment comparable to
that of other therapies for common chronic diseases. CPAP can eliminate apneas and improve
daytime sleepiness, mood and quality of life. Furthermore, short term (1-3 months)
randomised controlled trials of CPAP have shown modest reductions in blood pressure (BP) and
other markers of CV disease, including C-reactive protein (CRP) and coagulation. However,
the epidemiological data is complicated by potential residual confounding factors and the
randomised evidence is limited. Thus, a direct causal link between OSA and CV disease
remains inconclusive. The management of OSA, therefore, remains principally directed towards
symptom control rather than CV risk modification.
The present trial aims to test whether long-term use of CPAP can reduce the incidence of CV
events. If the trial shows that CPAP treatment of OSA reduces the incidence of CV events it
will influence clinical practice toward the early detection and management of OSA, and add
CPAP to the range of strategies available for the prevention of CV disease.
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
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