Bone Density Improved with Zoledronic Acid
A single intravenous dose of the osteoporosis drug zoledronic acid improved bone mineral density in a group of frail elderly women living in nursing homes and long-term-care facilities, according to an article published online in April 2015 by JAMA Internal Medicine.
A release from the publisher notes that nearly two million frail elderly Americans live in long-term care facilities and many of them have osteoporosis and bone fracture rates higher than less impaired elderly individuals. A hip fracture can be dire, decreasing mobility, independence and often leading to death, according to background in the study.
Susan L. Greenspan, M.D., of the University of Pittsburgh, and coauthors conducted a clinical trial to determine the efficacy and safety of zoledronic acid to treat osteoporosis in frail elderly women living in long-term care facilities. Zoledronic acid was chosen because it can be given in a single intravenous dose and the effect can last for two years.
The two-year study included 181 women 65 or older with osteoporosis, including women with cognitive impairment, immobility and multiple coexisting illnesses, who were living in nursing homes and assisted-living facilities. Of the women, 89 were assigned to receive a single 5-mg dose of zoledronic acid and 92 were assigned to receive placebo, while all participants received daily vitamin D and calcium supplementation.
The authors measured hip and spine bone mineral density (BMD) at 12 and 24 months, as well as adverse events, which included falls.
The average total hip BMD increased more in the treatment group than in the placebo group both at 12 months (2.8 percent vs. -0.5 percent) and at 24 months (2.6 percent vs. -1.5 percent), according to the results. The average spine BMD also increased more in the treatment group than placebo group at 12 months (3 percent vs. 1.1 percent) and at 24 months (4.5 percent vs. 0.7 percent).
Overall, in the measure of adverse events, there were no significant differences in the number of deaths, fractures or cardiac disorders. The treatment and placebo groups’ fracture rates were 20 percent (18 women) and 16 percent (15 women), respectively, and mortality rates were 16 percent (14 women) and 13 percent (12 women), respectively. There were no significant differences between groups in the number of single fallers but more participants in the treatment group has multiple falls (49 percent vs. 35 percent), although this difference did not remain significant after adjusting for baseline frailty, the results indicate.