LONDON, September 1, 2015 /PRNewswire/ --
-Theuniquebreadth and maturity ofGARFIELD-AF Registry data presentedatESC Congress 2015provides real-world insightson theevolution ofmanaging AF in everyday clinical practiceacross the globe-
The first-ever two-year outcomes from the Global Anticoagulant Registry in the Field - Atrial Fibrillation (GARFIELD-AF) showcased at ESC Congress 2015 expose that all-cause death was the most frequent major event in more than 17,000 newly diagnosed AF patients, far exceeding the rate of stroke or major bleeding. These two-year prospective outcomes from cohorts 1 and 2 show a mortality rate of 3.83% per person year compared to stroke rates of 1.25% per person year and major bleeding rates of 0.70% per person year. [1]
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Additional one-year outcomes from more than 28,000 AF patients in cohorts 1-3, demonstrate a likely impact of comorbidities on increasing mortality, stroke and major bleeding. Patients with moderate-to-severe chronic kidney disease and those with a history of myocardial infarction had a markedly higher mortality rate than the overall population (9.4% and 6.9% respectively, compared to 4.0%).[1] "These data from the GARFIELD-AF registry indicate the importance of comorbidities in predicting patient outcomes and can offer physicians guidance in managing AF," said Professor Sam Goldhaber of Harvard Medical School and the Brigham and Women's Hospital. "The results suggest physicians should consider increasing the prescription of anticoagulants in AF patients with these comorbidities."
Insights from nearly 40,000 patients with AF across the four sequential GARFIELD-AF cohorts from 2010 to 2015 show a shift in how AF is being managed across the globe. Overall, patients initiated on anticoagulant treatment for stroke prevention increased from 57.4% to 71.1%. Use of vitamin K antagonists (VKAs) and antiplatelets (combined or alone) fell from 83.4% to 50.6%, whilst use of non-vitamin K antagonist oral anticoagulants (NOACs) with or without an antiplatelet increased from 4.1% to 37.0%.[1] "This evolution in treatment patterns is consistent with the adoption of innovative therapies for stroke prevention," said Professor Ajay Kakkar, Professor of Surgery at University College London and Director of the Thrombosis Research Institute. "The remaining challenge, however, is to ensure that the correct patient receives the appropriate therapy."
Professor John Camm of St George's University, London expanded on the treatment patterns revealed in GARFIELD-AF: "While we are seeing an overall increase in the use of appropriate anticoagulation therapy, GARFIELD-AF reveals a substantial variation in NOAC uptake between countries. Analysis in over 20,000 newly diagnosed AF patients across Europe from cohorts 1-3 showed these variations ranged from 2.6% to 58.0%.[2] The ongoing insights being gathered across countries and different care settings will help clinicians better understand how to improve care and outcomes for AF patients."
GARFIELD-AF is the largest ongoing prospective registry of patients with newly diagnosed AF and at least one additional stroke risk factor. The ongoing real-world insights continuing to be gathered from the GARFIELD-AF Registry are being converted into real-world evidence that help inform and identify areas where the medical community can continue to improve patient outcomes.
AdditionallyGARFIELD-AF datain specific regions and patient populationswerepresented at ESC Congress 2015:
Vitamin K antagonist control in Eastern and Southeastern Asia[ 3 ]
GARFIELD-AF insights show fewer INR readings, longer intervals between readings and lower INR values in Eastern and Southeastern Asia (n=3,627) compared to countries in other regions of the world (n=13,546). For patients receiving VKAs for newly diagnosed AF in Eastern and Southeastern Asia, results showed:
Stroke, major bleeding and mortality in newly diagnosed atrial fibrillation with moderate-to-severe chronic kidney disease: results from GARFIELD-AF[ 4 ]
One-year outcomes in 17,159 patients with AF reveal differences between patients with moderate-to-severe chronic kidney disease (n=1,760) and those with no or mild chronic kidney disease (n=15,399):
About the GARFIELD-AF Registry
GARFIELD-AF is an independent academic research initiative, led by an international steering committee under the auspices of the Thrombosis Research Institute (TRI), London, United Kingdom.
It is an international observational, multicentre study of patients with newly diagnosed AF. It will follow 57,000 patients from at least 1,000 centres in 35 countries in the Americas, Eastern and Western Europe, Asia, Africa and Australia. Nearly 45,000 patients were recruited in four sequential cohorts between December 2009 and July 2015. The fifth and final cohort began recruiting at the beginning of August 2015.
Contemporary understanding of AF is based on data gathered in controlled clinical trials. Whilst essential for evaluating the efficacy and safety of new treatments, these trials may not be representative of everyday clinical practice and, hence, uncertainty persists about the real-life burden and management of this disease. GARFIELD-AF seeks to provide insights into the impact of anticoagulant therapy on thromboembolic and bleeding complications seen in this patient population. It will provide a better understanding of the potential opportunities for improving care and clinical outcomes amongst a representative and diverse group of patients and across distinctive populations. This should help physicians and healthcare systems to appropriately adopt innovation to ensure the best outcomes for patients and populations.
The registry started in December 2009. Four key design features of the GARFIELD-AF protocol ensure a comprehensive and representative description of AF. These are:
Included patients must have been diagnosed with non-valvular AF within the previous 6 weeks and have at least one additional risk factor for stroke; as such they are potential candidates for anticoagulant therapy to prevent blood clots leading to stroke. It is left to the investigator to identify a patient's stroke risk factor(s), which need not be restricted to those included in established risk scores. Patients are included whether or not they receive anticoagulant therapy, so current and future treatment strategies and failures can be properly understood in relation to patients' individual risk profiles.
The GARFIELD-AF Registry is funded by an unrestricted research grant from Bayer Pharma AG (Berlin, Germany).
The burden of AF
Up to 2% of the global population has AF.[ 5 ] Around 10 million people in Europe[ 6 ], 5.1 million people in the USA[ 7 ] and up to 8 million people in China have AF.[ 8 ], [ 9 ] It is estimated that its prevalence will increase by approximately 2.5-fold by 2050[1 0 ] as the global population ages[1 1 ] . AF confers a five-fold increase in the risk of stroke,[ 12 ] and one in five of all strokes is attributed to this arrhythmia.[ 13 ] Ischaemic strokes associated with AF are often fatal, and those patients who survive are left more frequently and more severely disabled and more likely to suffer a recurrence than patients with other causes of stroke. In consequence, the risk of death from AF-related stroke is doubled and the cost of care is increased by 50%.[ 1 4 ]
AF occurs when parts of the atria emit uncoordinated electrical signals. This causes the chambers to pump too quickly and irregularly, not allowing blood to be pumped out completely. [ 1 5 ] As a result, blood may pool, clot and lead to thrombosis, which is the number one cardiovascular killer in the world.[ 1 6 ] If a blood clot leaves the left atrium, it could potentially lodge in an artery in other parts of the body, including the brain. A blood clot in an artery in the brain leads to a stroke. Ninety-two per cent of fatal strokes are caused by thrombosis.[ 1 7 ] People with AF also are at high risk for heart failure, chronic fatigue and other heart rhythm problems.[1 8 ] Stroke is a major cause of death and long-term disability worldwide - each year 6.7 million people die[1 6 ] and 5 million are left permanently disabled.[1 9 ]
About the TRI
The TRI is a charitable foundation and multi-disciplinary research institute dedicated to the study of thrombosis and related disorders. TRI's mission is to provide excellence in thrombosis research and education, to develop new strategies to prevent and treat thrombosis and thereby improve quality of care, advance clinical outcomes and reduce healthcare costs. The TRI is a member of University College London Partners' Academic Health Science Network.
For more information, visit http://www.tri-london.ac.uk/garfield.
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