Comparative Fracture Risk During Osteoporosis Drug Holidays After Long-Term Risedronate Versus Alendronate Therapy A Propensity Score-Matched Cohort Study

被引:18
|
作者
Hayes, Kaleen N. [1 ,2 ]
Brown, Kevin A. [3 ,4 ]
Cheung, Angela M. [2 ,5 ,6 ]
Kim, Sandra A. [5 ,7 ]
Juurlink, David N. [3 ,8 ]
Cadarette, Suzanne M. [9 ,10 ,11 ]
机构
[1] Brown Univ, Sch Publ Hlth, 121 South Main St,Box G-5121-8, Providence, RI 02903 USA
[2] Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada
[3] Univ Toronto, Dalla Lana Sch Publ Hlth, ICES, Toronto, ON, Canada
[4] Publ Hlth Ontario, Toronto, ON, Canada
[5] Univ Toronto, Dept Med, Toronto, ON, Canada
[6] Univ Hlth Network, Toronto, ON, Canada
[7] Womens Coll Hosp, Ctr Osteoporosis & Bone Hlth, Toronto, ON, Canada
[8] Sunnybrook Res Inst, Toronto, ON, Canada
[9] Univ Toronto, Leslie & Fac Pharm, Toronto, ON, Canada
[10] ICES, Toronto, ON, Canada
[11] Univ N Carolina, Eshelman Sch Pharm, Chapel Hill, NC 27515 USA
基金
加拿大健康研究院;
关键词
IDENTIFYING PATIENTS; ADMINISTRATIVE DATA; BISPHOSPHONATES; VALIDATION; CARE; INTERVENTION; MANAGEMENT; BONE;
D O I
10.7326/M21-2512
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: An osteoporosis drug holiday is recommended for most patients after 3 to 5 years of therapy. Risedronate has a shorter half-life than alendronate, and thus the residual length of fracture protection may be shorter. Objective: To examine the comparative risks of drug holidays after long-term (>= 3 years) risedronate versus alendronate therapy. Design: Population-based, matched, cohort study. Setting: Province-wide health care administrative databases providing comprehensive coverage to Ontario residents aged 65 years or older between November 2000 and March 2020. Patients: Persons aged 66 years drug holiday were matched 1:1 on propensity score to those who had long-term alendronate therapy and a drug holiday. Measurements: The primary outcome was hip fracture within 3 years after a 120-day ascertainment period. Secondary analyses included shorter follow-up and sex-specific estimates. Cox proportional hazards models were used to estimate hazard ratios (HRs) for fracture risk between groups. Results: A total of 25077 propensity score-matched pairs were eligible (mean age, 81 years; 81% women). Hip fracture rates were higher among risedronate than alendronate drug holidays (12.4 and 10.6 events, respectively, per 1000 patient-years; HR, 1.18 [95% CI, 1.04 to 1.34]; 915 total hip fractures). The association was attenuated when any fracture was included as the outcome (HR, 1.07 [CI, 1.00 to 1.16]) and with shorter drug holidays (1 year: HR, 1.03 [CI, 0.85 to 1.24]; 2 years: HR, 1.14 [CI, 0.96 to 1.32]). Limitation: Analyses were limited to health care administrative data (potential unmeasured confounding), and some secondary analyses contained few events. Conclusion: Drug holidays after long-term therapy with risedronate were associated with a small increase in risk for hip fracture compared with alendronate drug holidays. Future research should examine how best to mitigate this risk.
引用
收藏
页码:335 / +
页数:12
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