Solomon Daniel H, Avorn Jerry, Katz Jeffrey N, Finkelstein Joel S, Arnold Marilyn, Polinski Jennifer M, Brookhart M Alan
Divisions of Pharmacoepidemiology, Brigham and Women's Hospital, Boston, MA 02120, USA.
Arch Intern Med. 2005 Nov 14;165(20):2414-9. doi: 10.1001/archinte.165.20.2414.
Long-term compliance with pharmacologic treatments for many asymptomatic conditions may be suboptimal, but little is known about compliance with medications used for osteoporosis. This study was undertaken to assess the level and determinants of compliance with drugs prescribed for osteoporosis.
This retrospective cohort study used pharmacy claims data from US Medicare and filled prescriptions from a state pharmaceutical benefits program. We included persons 65 years or older who initiated use of a medication for osteoporosis (alendronate sodium, calcitonin, hormone therapy, raloxifene hydrochloride, or risedronate) from January 1, 1996, through December 31, 2002. The outcome of interest was suboptimal medication compliance, defined as equal to or less than 66% of days with medication during a 60-day period.
One year after initiating treatment for osteoporosis, 45.2% of the 40,002 patients were not continuing to fill prescriptions. Five years after initiation, 52.1% of patients were not continuing to fill prescriptions for an osteoporosis medication. Several characteristics independently predicted compliance: female sex, younger age, fewer comorbid conditions, using fewer nonosteoporosis medications, bone mineral density testing before and after initiating a medication, a fracture before and after initiating a medication, and nursing home residence during the 12 months before initiating a medication. However, models adjusted for the significant patient variables explained only 6% of the variation in compliance.
Most patients who initiate a medication for osteoporosis do not continue to take it as prescribed. Although several patient characteristics significantly correlated with compliance, adjusted models explained little of the variation.
对于许多无症状疾病,长期坚持药物治疗的效果可能不太理想,但对于骨质疏松症用药的依从性却知之甚少。本研究旨在评估骨质疏松症处方药的依从水平及其决定因素。
这项回顾性队列研究使用了美国医疗保险的药房报销数据以及一个州药物福利计划的已填充处方。我们纳入了年龄在65岁及以上、于1996年1月1日至2002年12月31日期间开始使用骨质疏松症药物(阿仑膦酸钠、降钙素、激素疗法、盐酸雷洛昔芬或利塞膦酸盐)的患者。感兴趣的结局是用药依从性欠佳,定义为在60天期间内用药天数等于或少于66%。
在开始骨质疏松症治疗一年后,40002名患者中有45.2%未继续取药。开始治疗五年后,52.1%的患者未继续取骨质疏松症药物的处方。有几个特征可独立预测依从性:女性、年龄较小、合并症较少、使用的非骨质疏松症药物较少、开始用药前后进行骨密度检测、开始用药前后发生骨折以及在开始用药前12个月居住在养老院。然而,对显著的患者变量进行调整后的模型仅解释了依从性变异的6%。
大多数开始使用骨质疏松症药物的患者并未按规定持续服药。尽管有几个患者特征与依从性显著相关,但调整后的模型对变异的解释很少。