Fralick Michael, Martins Diana, Tadrous Mina, Gomes Tara
, MD, PhD, is with the Sinai Health System and the Department of Medicine, University of Toronto, Toronto, Ontario.
, MSc, was, during the period of the study, with Unity Health Toronto, Toronto, Ontario.
Can J Hosp Pharm. 2022 Spring;75(2):104-107. doi: 10.4212/cjhp.v75i2.3066. Epub 2022 Apr 4.
Three large cardiovascular outcome trials have investigated the safety of sodium glucose cotransporter 2 (SGLT2) inhibitors.
To analyze the nationwide dispensing of SGLT2 inhibitors before and after the publication of these trials.
A cross-sectional study was conducted of monthly prescription dispensing of SGLT2 inhibitors from May 23, 2014, to April 30, 2019, using nationwide data for Canada. An autoregressive integrated moving average (ARIMA) model was fitted to the monthly number of tablets dispensed for each SGLT2 inhibitor; the model included a ramp intervention function at the publication dates of interest to estimate the impact on SGLT2 inhibitor dispensing patterns.
The rate of canagliflozin and dapagliflozin dispensing declined after publication of results of the empagliflozin cardiovascular trial in September 2015. After publication of results of the canagliflozin trial in June 2017, which indicated a reduction in cardiovascular events and an increase in the risk of lower-limb amputation, canagliflozin remained the most commonly dispensed SGLT2 inhibitor, but its rate of dispensing declined further. In contrast, the rate of empagliflozin dispensing increased, while the rate of dapagliflozin dispensing was unchanged. After publication of the dapagliflozin trial in November 2018, which indicated no clear reduction in cardiovascular events, short-term trends in dispensing of canagliflozin, empagliflozin, and dapagliflozin were largely unaffected.
The cardiovascular outcome trials appeared to have an important impact on the dispensing of SGLT2 inhibitors in Canada.
三项大型心血管结局试验对钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂的安全性进行了研究。
分析这些试验发表前后SGLT2抑制剂在全国范围内的配药情况。
利用加拿大全国数据,对2014年5月23日至2019年4月30日期间SGLT2抑制剂的月度处方配药情况进行横断面研究。对每种SGLT2抑制剂每月配药片数拟合自回归积分滑动平均(ARIMA)模型;该模型在感兴趣的发表日期包含一个斜坡干预函数,以估计对SGLT2抑制剂配药模式的影响。
2015年9月恩格列净心血管试验结果发表后,卡格列净和达格列净的配药率下降。2017年6月卡格列净试验结果发表,表明心血管事件减少但下肢截肢风险增加后,卡格列净仍是最常配药的SGLT2抑制剂,但其配药率进一步下降。相比之下,恩格列净的配药率上升,而达格列净的配药率未变。2018年11月达格列净试验结果发表,表明心血管事件无明显减少后,卡格列净、恩格列净和达格列净配药的短期趋势基本未受影响。
心血管结局试验似乎对加拿大SGLT2抑制剂的配药有重要影响。