TY - JOUR
T1 - Population-based study of the effectiveness of bone-specific drugs in reducing the risk of osteoporotic fracture
AU - Perreault, Sylvie
AU - Dragomir, Alice
AU - Blais, Lucie
AU - Moride, Yola
AU - Rossignol, Michel
AU - Ste-Marie, Louis Georges
AU - Fernandès, Julio Cesar
PY - 2008/3
Y1 - 2008/3
N2 - Aim: Evidence supports bone-specific drugs (BSDs) efficacy in the fracture risk reduction. But treatment rates for osteoporosis among high-risk patients are far below the recommended guidelines. A major concern about BSDs is the lack of adherence with treatment. Objective: To determine if BSDs decrease fracture risk in high-risk elderly women in real clinical setting. Methods: A nested case-control design was used in a cohort of elderly women from the Quebec health databases. Women enter into the cohort if they are 70 years or older between 1995 and 2003. Nested case-controls were designed for women with a diagnosis of osteoporosis (OP) and for those with a prior fracture. All cases of fractures occurring during follow-up were matched with 10 randomly selected controls based on age, time period, bone mass density testing, and having a diagnosis of OP or a prior fracture. Use of BSDs before the index date was categorized as follows: short-term (≤1 year), intermediate-term (>1 and ≤3 years), and long-term (>3 years). We used an adjusted conditional logistic regression model to assess BSD effect on fracture. Results: Among 3170 women who had a fracture, of these women, 1824 had OP and 1346 had a prior fracture. Only long-term exposure to BSDs among women with OP reduced the fracture risk by 16% (odds ratio: 0.84; 0.73-0.97). Among women with OP, a high number of medical services or use of anticonvulsants or narcotics increased the fracture risk by 12-73%. Among women with a prior fracture, a high number of medical services or risk of fall or use of benzodiazepines, antidepressants, or narcotics increased the fracture risk by 23-77%. Conclusion: The incidence of fractures decreased by 16% among women with OP whenmore than 80% of BSDs was used for at least 3 years. Among women with a prior fracture, fracture risk reduction was not significant. Exposure to BSDs among women with a prior fracture is troubling, given that only approximately 12% of these individuals were being treated, and only 2% was using BSDs for the long term.
AB - Aim: Evidence supports bone-specific drugs (BSDs) efficacy in the fracture risk reduction. But treatment rates for osteoporosis among high-risk patients are far below the recommended guidelines. A major concern about BSDs is the lack of adherence with treatment. Objective: To determine if BSDs decrease fracture risk in high-risk elderly women in real clinical setting. Methods: A nested case-control design was used in a cohort of elderly women from the Quebec health databases. Women enter into the cohort if they are 70 years or older between 1995 and 2003. Nested case-controls were designed for women with a diagnosis of osteoporosis (OP) and for those with a prior fracture. All cases of fractures occurring during follow-up were matched with 10 randomly selected controls based on age, time period, bone mass density testing, and having a diagnosis of OP or a prior fracture. Use of BSDs before the index date was categorized as follows: short-term (≤1 year), intermediate-term (>1 and ≤3 years), and long-term (>3 years). We used an adjusted conditional logistic regression model to assess BSD effect on fracture. Results: Among 3170 women who had a fracture, of these women, 1824 had OP and 1346 had a prior fracture. Only long-term exposure to BSDs among women with OP reduced the fracture risk by 16% (odds ratio: 0.84; 0.73-0.97). Among women with OP, a high number of medical services or use of anticonvulsants or narcotics increased the fracture risk by 12-73%. Among women with a prior fracture, a high number of medical services or risk of fall or use of benzodiazepines, antidepressants, or narcotics increased the fracture risk by 23-77%. Conclusion: The incidence of fractures decreased by 16% among women with OP whenmore than 80% of BSDs was used for at least 3 years. Among women with a prior fracture, fracture risk reduction was not significant. Exposure to BSDs among women with a prior fracture is troubling, given that only approximately 12% of these individuals were being treated, and only 2% was using BSDs for the long term.
KW - Bone-specific drug
KW - Effectiveness
KW - Osteoporosis
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U2 - 10.1002/pds.1551
DO - 10.1002/pds.1551
M3 - Article
C2 - 18213734
AN - SCOPUS:40949104381
SN - 1053-8569
VL - 17
SP - 248
EP - 259
JO - Pharmacoepidemiology and drug safety
JF - Pharmacoepidemiology and drug safety
IS - 3
ER -