Imaz I, Zegarra P, González-Enríquez J, Rubio B, Alcazar R, Amate J M
Agency for Health Technologies Assessment, Instituto de Salud Carlos III. Science and Innovation Ministry, 5 Monforte de Lemos, Madrid, 28029, Spain.
Osteoporos Int. 2010 Nov;21(11):1943-51. doi: 10.1007/s00198-009-1134-4. Epub 2009 Dec 5.
Systematic review of adherence to bisphosphonates for the treatment of osteoporosis finds suboptimal levels of persistence and compliance. Poor bisphosphonate compliance increases fracture risk.
The objectives of the study were to measure the persistence and compliance with bisphosphonates for the treatment of osteoporotic patients, and to estimate the influence of compliance on fracture risk.
A systematic review of bisphosphonate adherence in clinical practise provided new evidence to perform a meta-analysis of the means of bisphosphonate persistence and compliance, with a subsequent meta-analysis of fracture risk comparing poorly versus highly compliant patients.
Fifteen articles, totalling 704,134 patients, met our inclusion criteria. Most of the patients were postmenopausal women treated with bisphosphonates. The 3.95% of the patients received hormone replacement therapy, but the rest received bisphosphonates. The meta-analysis of five articles totalling 236,540 patients, who were followed for 1 year, provided a pooled persistence mean of 184.09 days. The meta-analysis of five articles, totalling 234,737 patients, who were also followed for 1 year, provided a pooled medication possession ratio mean of 66.93%. The meta-analysis of six articles, totalling 171,063 patients, who were followed for varying periods of time between 1 and 2.5 years, provided a pooled 46% increased fracture risk in non-compliant patients versus compliant patients. The increased fracture risk was lower for non-vertebral (16%) and hip (28%) than for clinical vertebral fractures (43%).
Persistence and compliance are suboptimal for postmenopausal women undergoing bisphosphonate therapy for osteoporosis. The clinical consequence of this low compliance is an increased risk of fracture, which is lower for non-vertebral than for clinical vertebral fractures.
对双膦酸盐治疗骨质疏松症依从性的系统评价发现,持续性和依从性水平未达最佳。双膦酸盐依从性差会增加骨折风险。
本研究的目的是衡量双膦酸盐治疗骨质疏松症患者的持续性和依从性,并评估依从性对骨折风险的影响。
对临床实践中双膦酸盐依从性的系统评价提供了新证据,以便对双膦酸盐持续性和依从性的均值进行荟萃分析,随后对依从性差与依从性高的患者的骨折风险进行荟萃分析。
15篇文章,共计704134名患者,符合我们的纳入标准。大多数患者是接受双膦酸盐治疗的绝经后妇女。3.95%的患者接受激素替代疗法,但其余患者接受双膦酸盐治疗。对5篇文章(共计236540名患者,随访1年)进行的荟萃分析得出合并持续性均值为184.09天。对5篇文章(共计234737名患者,同样随访1年)进行的荟萃分析得出合并药物持有率均值为66.93%。对6篇文章(共计171063名患者,随访时间在1至2.5年之间不等)进行的荟萃分析得出,依从性差的患者与依从性好的患者相比,骨折风险总体增加46%。非椎体骨折(16%)和髋部骨折(28%)的骨折风险增加幅度低于临床椎体骨折(43%)。
对于接受双膦酸盐治疗骨质疏松症的绝经后妇女,持续性和依从性未达最佳。这种低依从性的临床后果是骨折风险增加,非椎体骨折的风险增加幅度低于临床椎体骨折。