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Table 2 Secondary objectives

From: Rationale and design of the randomised Treatment of sleep apnoea Early After Myocardial infarction with Adaptive Servo-Ventilation trial (TEAM-ASV I)

Secondary objectives

 

To determine the effects of 12 weeks’ ASV in patients with SDB early after AMI on the following:

- Infarct size

- Left ventricular remodelling assessed using CMR (myocardial salvage, microvascular obstruction, change of infarct size, infarct size at 12 weeks, change in left ventricular ejection fraction, left ventricular end-systolic volume, left ventricular end-diastolic volume)

- NT-proBNP levels

- Disease-specific symptom burden (Seattle Angina Questionnaire)

- Daytime and night time blood pressure and heart rate

- Total cholesterol and low-density lipoprotein cholesterol

- SDB (apnoeas and hypopnoeas per hour of sleep, mean oxygen saturation)

- Renal function (GFR, calculated using the 4v-MDRD formula)

- Biochemical markers of inflammation and vascular function (hsCRP, blood count, fibrinogen)

  1. AMI acute myocardial infarction, ASV adaptive servo-ventilation, CMR cardiac magnetic resonance imaging, GFR glomerular filtration rate, hsCRP high-sensitivity C reactive protein, NT-proBNP amino terminal-pro B-type natriuretic peptide, SDB sleep-disordered breathing