Older patients are willing to take medications for cardiovascular disease prevention, but only if the drug has much more benefit than risk, according to a report published online first

Terri R. Fried, M.D., of Yale University School of Medicine, New Haven, Conn., and the VA Connecticut Healthcare System, and colleagues examined the willingness of older adults to take medications for primary cardiovascular disease prevention according to benefits and harms. For this study, 356 in-person interviews were performed with community-living older persons (average age, 76). The participants were asked about their willingness to take medication for primary prevention of heart attack (myocardial infarction). The medication was described as reducing the participant's risk of having a heart attack over the next five years, but with various types and severity of adverse effects, including fatigue, dizziness, nausea and fuzzy or slowed thinking.
Most participants (88 percent) indicated they would take the medication if it had no adverse effects, providing an absolute benefit of six fewer persons with heart attack out of 100, approximating the average risk reduction of currently available medications. "As the absolute benefit offered by the medication increased, so did the proportion willing to take the medication," the authors note. "In contrast, large proportions (48 percent to 69 percent) were unwilling or uncertain about taking medication with average benefit causing mild fatigue, nausea, or fuzzy thinking, and only 3 percent would take medication with adverse effects severe enough to affect functioning."
"The central finding of this study was the large influence exerted by the presence of adverse effects on older persons' decisions about whether to take a medication," the authors write. "These results suggest that clinical guidelines and decisions about prescribing these medications to older persons need to place emphasis on both benefits and harms," they conclude.
Source-Eurekalert
MEDINDIA









