Wilk A, Sajjan S, Modi A, Fan C-P S, Mavros P
Department of Biostatistics, Virginia Commonwealth University, Richmond, VA, USA.
Osteoporos Int. 2014 Dec;25(12):2777-86. doi: 10.1007/s00198-014-2827-x. Epub 2014 Aug 12.
Pharmacologic therapy is recommended to reduce future fracture risk. We examined osteoporosis medications dispensed to older women after first fracture. Only 23 % received therapy during the first year post-fracture. Prior osteoporosis therapy, a prior osteoporosis diagnosis, and older age were good predictors of post-fracture osteoporosis therapy.
Pharmacologic therapy is recommended after osteoporotic fracture to reduce future fracture risk. The objective of this retrospective study was to examine osteoporosis therapy dispensed to women post-fracture.
We identified women ≥50 years old in a large administrative claims database from 2003 to mid-2012 who were continuously enrolled 2 years before (baseline) and 1 year after first osteoporotic fracture. Exclusions were Paget's disease or malignant neoplasm. Pre- and post-fracture osteoporosis therapies (oral and parenteral) were assessed overall and by fracture site.
A total of 47,171 women of mean (SD) age of 63 (10) years were eligible; fractures included 8 % hip, 17 % vertebral, 73 % non-hip/non-vertebral, and 3 % multiple fracture sites. Only 18 % received osteoporosis therapy within 90 days and 23 % within 1 year post-fracture. Overall, 19 % of women had a prior osteoporosis diagnosis; 20 % had received osteoporosis therapy during baseline. Of 37,649 (80 %) women without baseline therapy, only 9 % initiated pharmacologic therapy within 1 year. The adjusted odds ratio (OR) of therapy within 1 year post-fracture was significantly greater for women who had received baseline osteoporosis therapy (versus none) and who had vertebral (OR 12.7, 95 % confidence interval (CI) 11.2-14.5), hip (15.2, 12.5-18.7), or non-hip/non-vertebral fracture (34.4, 31.7-37.3). Other significant predictors included pre-fracture osteoporosis diagnosis (1.6, 1.4-1.7) and older age (OR range, 1.3-1.7). Treatment adherence was significantly better among women with baseline osteoporosis diagnosis.
The substantial post-fracture treatment gap represents an important unmet need for women with osteoporotic fractures. Fracture liaison or adherence programs could lead to improved post-fracture treatment rates.
推荐药物治疗以降低未来骨折风险。我们研究了首次骨折后给予老年女性的骨质疏松症药物。骨折后第一年仅有23%的患者接受了治疗。既往骨质疏松症治疗、既往骨质疏松症诊断以及高龄是骨折后骨质疏松症治疗的良好预测因素。
骨质疏松性骨折后推荐药物治疗以降低未来骨折风险。这项回顾性研究的目的是研究骨折后给予女性的骨质疏松症治疗情况。
我们在一个大型行政索赔数据库中确定了2003年至2012年年中年龄≥50岁的女性,她们在首次骨质疏松性骨折前2年(基线)和骨折后1年持续参保。排除佩吉特病或恶性肿瘤患者。对骨折前后的骨质疏松症治疗(口服和肠外)进行总体评估,并按骨折部位评估。
共有47171名平均(标准差)年龄为63(10)岁的女性符合条件;骨折类型包括8%为髋部骨折,17%为椎体骨折,73%为非髋部/非椎体骨折,3%为多部位骨折。骨折后90天内仅有18%的患者接受了骨质疏松症治疗,骨折后1年内为23%。总体而言,19%的女性有既往骨质疏松症诊断;20%的女性在基线时接受过骨质疏松症治疗。在37649名(80%)基线时未接受治疗的女性中,仅有9%在1年内开始药物治疗。骨折后1年内接受过基线骨质疏松症治疗(与未接受治疗相比)以及发生椎体骨折(比值比12.7,95%置信区间11.2 - 14.5)、髋部骨折(15.2,12.5 - 18.7)或非髋部/非椎体骨折(34.4,31.7 - 37.3)的女性接受治疗的校正比值比显著更高。其他显著的预测因素包括骨折前骨质疏松症诊断(1.6,1.4 - 1.7)和高龄(比值比范围1.3 - 1.7)。基线时有骨质疏松症诊断的女性治疗依从性明显更好。
骨折后治疗差距巨大,这代表了骨质疏松性骨折女性一项重要的未满足需求。骨折联络或依从性项目可能会提高骨折后治疗率。