Brandt Jaden, Alessi-Severini Silvia, Singer Alexander, Leong Christine
College of Pharmacy, University of Manitoba.
J Popul Ther Clin Pharmacol. 2019 Jan 22;26(1):e22-e38. doi: 10.22374/1710-6222.26.1.3.
Administrative data covering all prescriptions from April 2001-March 2016 for BZD and Z-Drugs for patients ≥18 years was used. Consumption was calculated as DDD/1000-person days. Dose intensity (DI) was determined by conversion of individual daily doses to Diazepam Milligram Equivalents (DME). Pharmacologic exposure (PE) was calculated as DME-DDD/1000-person days. Prevalence was determined as the proportion of the adult population with receipt of ≥1 prescription in a given year. Changes were assessed using either Poisson or simple linear regression at an alpha of 0.05.
Z-Drug usage (~99% zopiclone) statistically increased on every measure over the course of the study period; consumption (8.2 to 28.6 DDD/1000-person days), PE (4.1 to 14.3 DME-DDD/1000-person days), DI (5.0 to 5.43 DME/day) and prevalence (2.0% to 4.8%). For BZD the only statistically significant changes were in DI (17.1 to 20.1 DME/day) and prevalence (9.3% to 8.1%). Consumption and PE gradually increased from 2001 to 2011 for BZD before declining thus producing a non-significant trend for BZD.
1)评估15年间加拿大普通成年人群中苯二氮䓬类药物(BZD)和Z类药物的使用趋势,评估指标包括:a)消耗量;b)药理暴露量;c)剂量强度;d)使用 prevalence。2)证明地西泮毫克当量(DME)测量方法与传统药物利用标准测量方法(如限定日剂量(DDD)系统)结合使用时的效用。
使用2001年4月至2016年3月期间≥18岁患者所有BZD和Z类药物处方的管理数据。消耗量计算为DDD/1000人日。剂量强度(DI)通过将个体每日剂量转换为地西泮毫克当量(DME)来确定。药理暴露量(PE)计算为DME-DDD/1000人日。prevalence确定为给定年份中接受≥1张处方的成年人口比例。使用泊松回归或简单线性回归评估变化,α=0.05。
在研究期间,Z类药物的使用(约99%为佐匹克隆)在各项指标上均有统计学显著增加;消耗量(从8.2增加到28.6 DDD/1000人日)、PE(从4.1增加到14.3 DME-DDD/1000人日)、DI(从5.0增加到5.43 DME/天)和prevalence(从2.0%增加到4.8%)。对于BZD,唯一有统计学显著变化的是DI(从17.1增加到20.1 DME/天)和prevalence(从9.3%下降到8.1%)。BZD的消耗量和PE在2001年至2011年逐渐增加,之后下降,因此BZD的趋势无统计学显著性。
1)从2001年到2016年,Z类药物的使用显著增加,而BZD的使用仅在DI方面有所增加。2)与仅依赖DDD相比,基于DME的测量能够进一步解读BZD的利用情况。