Rabenda V, Mertens R, Fabri V, Vanoverloop J, Sumkay F, Vannecke C, Deswaef A, Verpooten G A, Reginster J Y
WHO Collaborating Center for Public Health Aspects of Osteoarticular Disorders, University of Liège, Liège, Belgium.
Osteoporos Int. 2008 Jun;19(6):811-8. doi: 10.1007/s00198-007-0506-x.
Adherence is now one of the major issues in the management of osteoporosis and several papers have suggested that vertebral fractures might be increased in patients who do not follow appropriately their prescriptions. This paper relates the strong relationship existing between adherence to anti-osteoporosis treatment and the risk of subsequent hip fracture.
A study was performed to investigate adherence to bisphosphonate (BP) therapy and the impact of adherence on the risk of hip fracture (Fx).
An exhaustive search of the Belgian national social security database was conducted. Patients enrolled in the study were postmenopausal women, naive to BP, who received a first prescription of alendronate. Compliance at 12 months was quantified using the medication possession ratio (MPR). Persistence was calculated as the number of days from the initial prescription to a gap of more than 5 weeks after completion of the previous refill. A logistic regression model was used to estimate the impact of compliance on the risk of hip fracture. The impact of persistence on hip fracture risk was analysed using the Cox proportional hazards model.
The mean MPR at 12 months was significantly higher among patients receiving weekly (n = 15.021) compared to daily alendronate (n = 14,136) (daily = 58.6%; weekly = 70.5%; p < 0.001). At 12 months, the rate of persistence was 39.45%. For each decrease of the MPR by 1%, the risk of hip Fx increased by 0.4% (OR: 0.996; CI 95%: 0.994-0.998; p < 0.001). The relative risk reduction for hip Fx was 60% (HR: 0.404; CI 95%: 0.357-0.457; p < 0.0001) for persistent compared to non-persistent patients.
These results confirm that adherence to current therapeutic regimens remains suboptimal.
依从性现已成为骨质疏松症管理中的主要问题之一,多篇论文表明,未正确遵医嘱的患者椎体骨折风险可能会增加。本文阐述了抗骨质疏松治疗的依从性与后续髋部骨折风险之间存在的紧密关系。
开展了一项研究,以调查双膦酸盐(BP)治疗的依从性以及依从性对髋部骨折(Fx)风险的影响。
对比利时国家社会保障数据库进行了详尽检索。纳入研究的患者为绝经后女性,初用BP,接受阿仑膦酸钠首次处方治疗。使用药物持有率(MPR)对12个月时的依从性进行量化。持续性计算为从初始处方到上次配药完成后间隔超过5周的天数。采用逻辑回归模型估计依从性对髋部骨折风险的影响。使用Cox比例风险模型分析持续性对髋部骨折风险的影响。
与每日服用阿仑膦酸钠的患者(n = 14,136)相比,每周服用阿仑膦酸钠的患者(n = 15,021)在12个月时的平均MPR显著更高(每日服用 = 58.6%;每周服用 = 70.5%;p < 0.001)。在12个月时,持续性率为39.45%。MPR每降低1%,髋部骨折风险增加0.4%(比值比:0.996;95%置信区间:0.994 - 0.998;p < 0.001)。与非持续性患者相比,持续性患者髋部骨折的相对风险降低60%(风险比:0.404;95%置信区间:0.357 - 0.457;p < 0.0001)。
这些结果证实,目前治疗方案的依从性仍然欠佳。