Yu Jingbo, Tang Jackson, Li Zhiyi, Sajjan Shiva, O'Regan Christopher, Modi Ankita, Sazonov Vasilisa
Center for Observational and Real-World Evidence (CORE), Merck & Co., Inc., Kenilworth, NJ, USA.
Asclepius Analytics Ltd., Wanchai, Hong Kong.
Int J Womens Health. 2015 Nov 17;7:913-8. doi: 10.2147/IJWH.S88627. eCollection 2015.
To estimate the proportion of osteoporosis patients in whom initiating strontium ranelate treatment, under new EMA guidelines, should be contraindicated because of a history of cardiovascular events or risk for cardiovascular events.
This was a retrospective analysis of medical and pharmacy claims using the Clinical Practice Research Datalink database. Patients were included if they had ≥1 prescription of strontium from September 1, 2008 to August 31, 2013, were aged ≥50 as of the index date (the date of the first ever strontium ranelate prescription), and had ≥1 year of medical records pre-index. Cardiovascular events occurring any time pre-index were identified, which included ischemic heart disease, cerebrovascular disease, uncontrolled hypertension, and peripheral arterial disease. Cardiovascular risk factors assessed included 1) diabetes or hypertension any time pre-index; 2) hyperlipidemia in the 12 months pre-index; or 3) obesity in the 12 months pre-index.
A total of 7,474 patients were included: 90.4% were women, with an average age of 76.5 years, and 84.5% used osteoporosis therapy, either bisphosphonates or non-bisphosphonates, prior to strontium initiation. A total of 23.6% of patients experienced ≥1 cardiovascular event prior to strontium initiation; the rate was lower among female patients than in male patients (22.4% vs 35.3%, P<0.01). A total of 45.9% had risk factors for cardiovascular events (without cardiovascular event history).
More than one-fifth of osteoporosis patients in the UK who used strontium had a cardiovascular event history, and one-half had cardiovascular risk factors prior to strontium initiation.
评估在新的欧洲药品管理局(EMA)指南下,因有心血管事件病史或心血管事件风险而禁忌启动雷奈酸锶治疗的骨质疏松症患者比例。
这是一项使用临床实践研究数据链数据库对医疗和药房索赔进行的回顾性分析。纳入标准为:2008年9月1日至2013年8月31日期间有≥1次雷奈酸锶处方;截至索引日期(首次开具雷奈酸锶处方的日期)年龄≥50岁;索引前有≥1年的医疗记录。确定索引前任何时间发生的心血管事件,包括缺血性心脏病、脑血管疾病、未控制的高血压和外周动脉疾病。评估的心血管危险因素包括:1)索引前任何时间的糖尿病或高血压;2)索引前12个月内的高脂血症;或3)索引前12个月内的肥胖症。
共纳入7474例患者:90.4%为女性,平均年龄76.5岁,84.5%在开始使用雷奈酸锶之前使用过骨质疏松症治疗药物,包括双膦酸盐或非双膦酸盐。共有23.6%的患者在开始使用雷奈酸锶之前经历过≥1次心血管事件;女性患者的发生率低于男性患者(22.4%对35.3%,P<0.01)。共有45.9%的患者有心血管事件危险因素(无心血管事件病史)。
在英国,使用雷奈酸锶的骨质疏松症患者中,超过五分之一有心血管事件病史,二分之一在开始使用雷奈酸锶之前有心血管危险因素。