Alle Storys
Folgen
Keine Story von REACH STEERING COMMITTEE mehr verpassen.

REACH STEERING COMMITTEE

Atrial Fibrillation Found to be Common in Patients With Atherothrombosis, Increases Risk of Cardiovascular Death, Heart Attack and Stroke

Tokyo, November 7 (ots/PRNewswire)

- Large, International REACH Registry Also Shows Many Patients
With  Atrial Fibrillation are Undertreated With Antiplatelet and
Anticoagulant  Therapies
A significant portion of patients with atherothrombosis also have
atrial fibrillation (AF), greatly increasing their risk for
cardiovascular death, heart attack and stroke, according to new
findings from the large, international REACH registry published today
in the American Heart Journal.(1) The findings also showed that
standard treatments including anticoagulant and antiplatelet
therapies are underused in AF patients.
The new findings from the REACH (REduction of Atherothrombosis
for Continued Health) registry showed that AF was present in
approximately 12% of patients who had atherothrombotic disease, which
includes coronary artery disease (CAD), peripheral artery disease
(PAD), and cerebrovascular disease (CVD). The findings also showed
that, among patients with or at risk for atherothrombotic disease,
the risk for death and non-fatal cardiovascular outcomes was greater
for AF vs. non-AF patients, including more than twice as high for CV
death (3.2% vs 1.4%; p<0.0001), 87% higher for death from all causes
(4.3% vs. 2.3%, p<0.0001), 50% higher for non-fatal stroke (2.4% vs
1.6%, p<0.0001), and nearly 50% higher for the combined endpoint of
CV death/heart attack/stroke and/or hospitalization for
atherothrombotic events (17.9% vs 12.1%, p<0.0001). Despite these
higher risks in AF patients, only a little more than half received
anticoagulant therapy, only 60 percent received antiplatelet therapy,
and less than one in five received both.
"We've known that AF is a major risk factor for ischemic stroke,
but its prevalence and impact in the broader population of patients
with atherothrombosis was previously unclear," said, lead author
Shinya Goto, MD, PhD, FACC, Department of Medicine, Tokai University
School of Medicine, Kanagawa, Japan. "Our findings help fill that
gap, and show across all atherothrombotic disease categories, AF
consistently increases the risk of death and non-fatal CV outcomes.
For example, the combined endpoint of CV death, heart attack and
stroke and/or hospitalization for atherothrombotic events was higher
in AF patients no matter what form of atherothrombotic disease they
initially had, and was highest in patients initially recruited with
PAD. Further, our analysis underscores the need to determine the
optimal management of AF patients with or at risk for
atherothrombosis."
About the New REACH Analysis
The REACH registry is a large, contemporary, representative and
geographically diverse cohort of stable outpatients with or at high
risk of atherothrombosis.2,(3),(4) A total of 68,236 patients with
either established atherothrombotic disease (CAD, PAD, or CVD,
n=55,814) or at least three risk factors for atherothrombosis
(n=12,422) were enrolled from 5,587 physician practices in 44
countries (in Europe, North and South America and Asia) in 2003-2004.
For this new analysis, the investigators identified REACH
registry patients with or without AF, then compared those two groups
in terms of risk factors, drug usage and one-year cardiovascular (CV)
outcomes (CV death, heart attack and stroke).
AF status and one-year follow-up data were available for 63,589
patients. The prevalence of AF was 12.5%, 13.7%, 11.5%, and 6.2%
among CAD, CVD, PAD, and risk factor-only patients, respectively; and
11.7% in patients with symptomatic atherothrombotic disease (CAD,
CVD, or PAD together as one group). These prevalence rates are
substantially higher than the estimated prevalence in the general
population aged 40 years or more (2.3%) or 65 years or more
(5.9%).(5)
Of the total 6,814 AF patients, 6.7% experienced CV death,
non-fatal MI or non-fatal stroke within a year. Among the findings,
the investigators showed that, after statistically adjusting for
differences including age, sex, smoking, hypertension, diabetes, and
hypercholesterolemia, the risks for death and non-fatal CV outcomes
were worse in AF vs. non-AF patients:
- CV death 129% greater (3.2% vs 1.4%; p<0.0001)
    - All-cause death 87% greater (4.3 vs 2.3, p<0.0001)
    - Non-fatal stroke 50% greater (2.4% vs 1.6%, p<0.0001)
    - The combined endpoint of CV death/heart attack/stroke and/or
      hospitalization for atherothrombotic event 48% greater (17.9% vs
      12.1%, respectively; p<0.0001), and highest in patients initially
      recruited
    with PAD (27.1%)
Only 58.4% of AF patients received antiplatelet agents, and only
53.1% received anticoagulant therapy. The rate of bleeding requiring
hospitalization was higher in AF vs non-AF patients, respectively:
1.5% vs 0.8% (p<0.0001); the investigators speculated that this may
have been due to the more frequent use of anticoagulants (53.1% vs
7.1%).
References
1. Goto S, Bhatt DL, Rother J, Alberts M, Hill MD, Ikeda Y, et
al. Prevalence, clinical profile, and cardiovascular outcomes of
atrial fibrillation patients with atherothrombosis. Am Heart J
2008;156:855-863.
2. Bhatt DL, Steg PG, Ohman EM, Hirsch AT, Ikeda Y, Mas JL, et
al. International prevalence, recognition, and treatment of
cardiovascular risk factors in outpatients with atherothrombosis.
JAMA 2006;295(2):180-189.
3. Ohman EM, Bhatt DL, Steg PG, Goto S, Hirsch AT, Liau CS, et
al. The REduction of Atherothrombosis for Continued Health (REACH)
Registry: an international, prospective, observational investigation
in subjects at risk for atherothrombotic events-study design. Am
Heart J 2006;151(4):786 e1-10.
4. Steg PG, Bhatt DL, Wilson PWF, D'Agostino R, Ohman EM, Rother
J, et al. One-year cardiovascular event rates in outpatients with
atherothrombosis. JAMA. 2007;297:1197-1206.
5. Feinberg WM, Blackshear JL, Laupacis A, Kronmal R, Hart RG.
Prevalence, age distribution, and gender of patients with atrial
fibrillation. Analysis and implications. Arch Intern Med
1995;155(5):469-73.

Contact:

For Further Information, please contact: Nick James, Chandler Chicco
Agency, +44(0)7776-258-990, n.james@cca-uk.com; Dr. Deepak Bhatt, On
Behalf of the REACH STEERING COMMITTEE, +1-857-203-6840/6841; Dr.
Shinya Goto, Tokai University, +81-463-58-1211