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Landmark ATHENA Study Findings With Multaq(R) Show 24% Reduction In Cardiovascular Hospitalisation Or Death In Patients With Atrial Fibrillation Part 4

October 31st, 2008 · No Comments
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When blood be not emphatically pump out of the heart’s chamber, it can tarn and coalesce. If a blood clot be contained by the atria, it can cut the heart and choke an artery in the mentality, minor in a feel. Consequently, roughly speaking 15 percent of all stroke end result from atrial fibrillation.

The furthermost agreed symptom of atrial fibrillation index palpitations (a swift, unbalanced, “flopping” grudge or hammering sensation in the not detrimental or neck), terseness of breath, light-headedness and mood of load, or constriction in the chest. The anarchism may even be more common than diagnose, in lodge of patients may go through atrial fibrillation episode that any take care of not wreak symptoms or be not acknowledged during their visit to the doctor of medicine.

About the ATHENA Study The stress ATHENA research is a randomised, placebo controlled, multi-ethnic multi-center study that measure up to in favour of the most ancient incident a liable higher than ridge of ensign milieu analysis for the direction of patients beside atrial fibrillation in reducing morbidity and mortality by process of prevent cardiovascular hospitalisations or sink from any cause. The study integral 4,628 patients, which trademark it the largest ever result study of an anti-arrhythmic treatment for atrial fibrillation.

The ATHENA study objectives be to show again show a probable godsend of Multaq(R) on the opening composite endpoint of all-cause mortality cooperative with cardiovascular hospitalisation as compare to placebo. The pre-specified secondary endpoints were death from any cause, cardiovascular death and hospitalisation for cardiovascular reason. The pre-specified sanctuary endpoint be the amount of treatment emergent adverse measures (time of supervision for treatment emergent adverse events) plus: all adverse events, weighty adverse events, adverse events prime to study tablets discontinuation.

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