Anticoagulant benefits for atrial fibrillation decrease with age
The net clinical benefit of anticoagulants for atrial fibrillation (AF)—one of the most important causes of irregular heartbeats and a leading cause of stroke—decreases with age, as the risk of death from other factors diminishes their benefit in older patients, according to a study led by researchers at UC San Francisco.
The multi-institutional study of nearly 15,000 AF patients found that the anticoagulant warfarin was not beneficial after age 87 and another, apixaban, after age 92. As a result, physicians should consider all mortality risks, such as cancer and end-stage kidney disease, when recommending anticoagulants to older adults with AF, the researchers said.
The study is online Nov. 11, 2019, in Circulation: Cardiovascular Quality and Outcomes (CCQO), to coincide with a presentation at the annual American Heart Association Scientific Sessions 2019.
“Many prior studies looking at the benefit of blood thinners found older adults benefit more than younger adults, but they narrowly focus on atrial fibrillation and strokes and don’t account for all other health conditions affecting older adults,” said lead author Sachin Shah, MD, MPH, assistant professor of medicine at UCSF. “Our study is the first to find that when taking these factors into consideration, anticoagulant benefit actually decreases with age.”
Atrial fibrillation affects an estimated 2.2 million Americans, according to the National Stroke Association, and about 15 percent of people who have strokes have AF. The stroke association estimates that up to 80 percent of strokes among people with AF could have been prevented.
While patients age 75 and older are at higher risk for stroke and advised to use anticoagulants, there is little evidence of their net benefit in this population. Advancing age also increases the likelihood of death from non-AF causes, thereby limiting the benefit or harm from AF and anticoagulant treatment.
Indeed, anticoagulant use in older patients with atrial fibrillation is similar to prostate specific antigen (PSA) testing. PSA testing is common in elderly men, despite evidence that those without aggressive prostate cancer are unlikely to benefit from diagnosis and treatment and may face significant risks for quality of life if they undergo prostate surgery.
“Competing risk of death is an important consideration when estimating the net clinical benefit of anticoagulation therapy,” Shah said. “Failing to account for competing risks likely overestimates the net clinical benefit of anticoagulation, an effect that is more pronounced at older ages and with more effective anticoagulants.”
In the CCQO study, Shah and his colleagues, including collaborators from Kaiser Permanente Northern and Southern California, reviewed the records of 14,946 adults from January 2006 to June 2009 in the Anticoagulation and Risk Factors in Atrial Fibrillation-Cardiovascular Research Network. They selected patients age 75 and older, with an average age of 81.
The researchers used a computerized decision analytic model called the Atrial Fibrillation Decision Support Tool (AFDST), developed by the University of Cincinnati, to determine the potential benefit of anticoagulants. The model uses patient characteristics and guidelines on AF treatment from the American College of Cardiology, American Heart Association and Heart Rhythm Society to offer a recommendation.
The research team estimated the lifetime net clinical benefit of warfarin and apixaban relative to no treatment in quality-adjusted life years (QALY). QALY is a measure of disease burden that includes both the length of life and its quality, with one QALY equaling one year in perfect health.
Using 0.10 lifetime QALYs as the minimal net clinical benefit, warfarin started at 0.45 QALYs at age 75, then fell below 0.10 at age 87, while apixaban started at 0.74 QALYs at age 75, then fell below 0.10 at age 92.
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