People more likely to take heart medicines in combo pill
American Heart Association Late-Breaking Clinical Trial Report - Embargoed until 9:57 a.m. PT / 12:57 p.m. ET
November 05, 2012
Study Highlights:
- People with heart disease are much more likely to take preventive medications if they’re combined in a single pill known as a “polypill.”
- When patients took medicines regularly, it translated into better blood pressure and lipid control.
- Benefits were seen despite above-average levels of treatment at the outset.
LOS ANGELES, Nov. 5, 2012 — People are much more likely to take heart medicines if they’re combined in one pill, according to a late-breaking clinical trial presented at the American Heart Association’s Scientific Sessions 2012.
“This is the first time the impact of a fixed-dose, combination strategy has been tested in people with cardiovascular disease,” said Simon Thom, M.D., F.R.C.P., lead author of the Use of a Multidrug Pill In Reducing cardiovascular Events (UMPIRE) trial and professor of cardiovascular medicine and pharmacology at Imperial College London, U.K.
“People who have suffered heart attacks or strokes or those at high risk of such problems need to take preventive medications, including antiplatelet drugs 
(such as aspirin), cholesterol-lowering and blood pressure-lowering drugs . But the reality is that many people in this high-risk category get out of the habit of taking the recommended medications,” Thom said. “This happens for a variety of reasons; some of which may be corrected by a single, simple, fixed dose combination pill – a combination known as a ‘polypill.’”
(such as aspirin), cholesterol-lowering and blood pressure-lowering drugs . But the reality is that many people in this high-risk category get out of the habit of taking the recommended medications,” Thom said. “This happens for a variety of reasons; some of which may be corrected by a single, simple, fixed dose combination pill – a combination known as a ‘polypill.’”There has been uncertainty about a fixed dose combination strategy for cardiovascular disease prevention. While many physicians have anticipated that adherence might be improved, the reduced number of drugs and doses could offset the benefits of simplicity, Thom said.
“This trial showed improvements in adherence being paralleled by improvements in blood pressure and cholesterol, despite the control group in the trial being treated much better than average.”
Typically, in high-income countries such as the United States only about 50 percent of people take all the needed cardiovascular medications, Thom said. In low- and middle-income countries, only 5 percent to 20 percent do.
Researchers studied whether changing the delivery of several medications into one fixed-dose, combination pill might improve adherence and, therefore, improve blood pressure and cholesterol control. The researchers followed more than 2,000 men and women (average age 62) with cardiovascular disease in Europe and India for an average 15 months. Half of the participants were given a combination pill of aspirin, a cholesterol-lowering agent (statin) and two blood pressure-lowering drugs. The other half took their medications as usual, with multiple pills and doses.
Researchers noted that the group taking a single pill improved adherence by a third and had improved blood pressure and cholesterol levels compared to those taking multiple pills.
The findings also likely apply to Americans, Thom said. “We deliberately chose two quite different settings – Western Europe and India, with half the patients from each region, although the trial did include well-treated populations in both locations. Seeing broadly similar findings in each region suggests generalizability.”
Similar trials are being conducted in Australia and New Zealand.
Co-authors are: Jane Field, B.Sc.; Neil Poulter, M.D., F.R.C.P.; Anushka Patel, M.D., Ph.D.; Dorairaj Prabhakaran, M.D., Ph.D.; Alice Stanton, M.D., Ph.D.; Rick Grobbee, M.D., Ph.D.; Michiel Bots, M.D., Ph.D.; Srinath Reddy, M.D., Ph.D.; Raghu Cidambi, L.L.B.; Severine Bompoint, B.Sc.; Laurent Billot, B.Sc.; and Anthony Rodgers, M.D., Ph.D.
The European Union’s 7th Framework Program funded the study. Dr. Reddy’s Laboratories in Hyderabad, India provided the fixed-dose, combination medication.
Disclosures are here http://newsroom.heart.org/pr/aha/document/DISCLOSURES.pdf 
To learn more about preventing heart disease, visit www.MyLifeCheck.org .
.Follow news from the American Heart Association’s Scientific Sessions 2012 via Twitter: @HeartNews.
Statements and conclusions of study authors that are presented at American Heart Association scientific meetings are solely those of the study authors and do not necessarily reflect association policy or position. The association makes no representation or warranty as to their accuracy or reliability. The association receives funding primarily from individuals; foundations and corporations (including pharmaceutical, device manufacturers and other companies) also make donations and fund specific association programs and events. The association has strict policies to prevent these relationships from influencing the science content. Revenues from pharmaceutical and device corporations are available at www.heart.org/corporatefunding .
.###
Note: The UMPIRE presentation is 9:57am PT, Monday, Nov. 5, in Petree Hall D.
For Media Inquiries:
AHA News Media in Dallas: (214) 706-1396
AHA News Media Office, Nov. 3-7,
at the Los Angeles Convention Center: (213) 743-6205
For Public Inquiries: (800)AHA-USA1 (242-8721)
.png)
No hay comentarios:
Publicar un comentario