OSTEOPOROSIS IN THE COMMUNITY: FINDINGS FROM A NOVEL COMPUTERIZED REGISTRY IN A LARGE HEALTH ORGANIZATION IN ISRAEL

I. Goldshtein, A. Nguyen, G. Chodick, V. Shalev, S. Ish-Shalom, J. Chandler
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引用次数: 18

Abstract

Background: Osteoporosis is a growing public health concern due to its rising prevalence and excess morbidity and mortality. Automated patient registries have gained great importance in health and disease management of major chronic diseases, but are rarely used in osteoporosis. Objectives: To construct an automated, population-based registry of osteoporosis. Setting: The electronic medical records and pharmacy databases of a 2 million member health organization in Israel (Maccabi Healthcare Services). Methods: Included in the registry were adults who were diagnosed with osteoporosis diagnosis, had major osteoporotic fractures, or purchased relevant medications, between 2000 and 2013. In addition, we included patients with low bone density as extracted from over 140,000 measurements reports, using an automated optical character recognition (OCR) system. Two-thirds of the cases were validated by more than one inclusion criterion. Results: A total of 118,141 osteoporosis patients were identified. The point prevalence of osteoporosis among members aged 50 or above in 2013 was 19%. The mean age at registry entry was 62 (SD=12) and 66 (SD=14) years for females and males, respectively. The highest annual risk of developing osteoporosis (27 per 1000) was recorded among females aged 65-75. In 28% of the patients, there was no indication of treatment with osteoporosis therapy. Conclusions: To the best of our knowledge, this is one of the first real-world automated registries of osteoporosis. Similar registries may provide valuable data for real-time monitoring of trends, quality of care, and outcome research in osteoporosis and its complications.
社区骨质疏松症:来自以色列一家大型卫生组织的新型计算机登记的发现
背景:骨质疏松症是一个日益严重的公共卫生问题,由于其发病率和死亡率的上升。自动化患者登记在主要慢性疾病的健康和疾病管理中具有重要意义,但很少用于骨质疏松症。目的:建立一个以人群为基础的骨质疏松症自动登记系统。背景:以色列一个拥有200万会员的卫生组织(马卡比卫生保健服务)的电子医疗记录和药房数据库。方法:纳入2000年至2013年期间被诊断为骨质疏松症、发生骨质疏松性骨折或购买相关药物的成年人。此外,我们使用自动光学字符识别(OCR)系统,从超过140,000份测量报告中提取了低骨密度的患者。三分之二的病例通过一个以上的纳入标准得到验证。结果:共发现118141例骨质疏松症患者。2013年50岁及以上会员骨质疏松点患病率为19%。女性和男性登记时的平均年龄分别为62岁(SD=12)和66岁(SD=14)。在65-75岁的女性中,患骨质疏松症的年风险最高(27 / 1000)。28%的患者没有骨质疏松症治疗的适应症。结论:据我们所知,这是第一个真实世界的骨质疏松症自动登记。类似的登记可以为实时监测骨质疏松症及其并发症的趋势、护理质量和结局研究提供有价值的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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