Penning-van Beest F J A, Erkens J A, Olson M, Herings R M C
PHARMO Institute, P.O.Box 85222, 3508, AE Utrecht, The Netherlands.
Osteoporos Int. 2008 Apr;19(4):511-7. doi: 10.1007/s00198-007-0466-1. Epub 2007 Sep 14.
Among 8,822 new female bisphosphonate users, non-compliant bisphosphonate use was associated with a 45% increased risk of osteoporotic fracture compared to compliant use (MPR >or=80%). Classifying compliance into five categories, fracture risk gradually increased with poorer compliance. These results emphasize the importance of treatment compliance in obtaining maximal treatment benefit.
Bisphosphonates are widely used to treat osteoporosis and reduce fracture risk. Low compliance is frequent and will limit treatment benefit.
New female users of alendronate or risedronate between 1999-2004, aged >or=45 years were identified from PHARMO-RLS, including drug-dispensing and hospitalization data of >or= 2 million residents of the Netherlands. Patients were followed until first hospitalisation for an osteoporotic fracture, death, or end of study period. Compliance with bisphosphonates during follow-up was measured over 90-day intervals using Medication Possession Ratio (MPR). The association between compliance and fracture risk was analyzed using time-dependent Cox-regression.
The study cohort included 8,822 new female bisphosphonate users, contributing in total 22,484 person-years of follow-up. During follow-up, 176 osteoporotic fractures occurred (excluding the first six months). Non-compliant bisphosphonate use was associated with a 45% increased fracture risk compared to compliant use (MPR >or= 80%). Classifying compliance into five categories, fracture risk gradually increased with poorer compliance (p-value <0.05 for trend). A MPR <20% was associated with an 80% increased fracture risk compared to a MPR >or= 90%.
These results show a statistically significant association between level of compliance with bisphosphonates and level of fracture risk, emphasizing the importance of treatment compliance in obtaining maximal treatment benefit.
在8822名新使用双膦酸盐的女性中,与依从性良好的使用情况(药物持有率[MPR]≥80%)相比,双膦酸盐使用不依从与骨质疏松性骨折风险增加45%相关。将依从性分为五类,骨折风险随着依从性变差而逐渐增加。这些结果强调了治疗依从性对于获得最大治疗益处的重要性。
双膦酸盐被广泛用于治疗骨质疏松症并降低骨折风险。依从性低很常见,这会限制治疗益处。
从荷兰PHARMO-RLS数据库中识别出1999年至2004年间年龄≥45岁的新使用阿仑膦酸钠或利塞膦酸钠的女性,该数据库包括荷兰200多万居民的药物配给和住院数据。对患者进行随访,直至首次因骨质疏松性骨折住院、死亡或研究期结束。使用药物持有率(MPR)以90天为间隔测量随访期间双膦酸盐的依从性。使用时间依赖性Cox回归分析依从性与骨折风险之间的关联。
研究队列包括8822名新使用双膦酸盐的女性,总共随访了22484人年。随访期间,发生了176例骨质疏松性骨折(不包括前六个月)。与依从性良好的使用情况(MPR≥80%)相比,双膦酸盐使用不依从与骨折风险增加45%相关。将依从性分为五类,骨折风险随着依从性变差而逐渐增加(趋势p值<0.05)。与MPR≥90%相比,MPR<20%与骨折风险增加80%相关。
这些结果表明双膦酸盐的依从水平与骨折风险水平之间存在统计学上的显著关联,强调了治疗依从性对于获得最大治疗益处的重要性。