Emulating a Target Trial Using Primary-Care Electronic Health Records: Sodium-Glucose Cotransporter 2 Inhibitor Medications and Hemoglobin A1c

被引:3
作者
Kalia, Sumeet [1 ,2 ,5 ]
Saarela, Olli [1 ]
O'Neill, Braden [2 ]
Meaney, Christopher [2 ]
Moineddin, Rahim [2 ]
Sullivan, Frank [4 ]
Greiver, Michelle [2 ,3 ]
机构
[1] Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada
[2] Univ Toronto, Temerty Fac Med, Dept Family & Community Med, Toronto, ON, Canada
[3] North York Gen Hosp, Toronto, ON, Canada
[4] Univ St Andrews, Sch Med, Populat & Behav Sci Div, St Andrews, Scotland
[5] Univ Toronto, Temerty Fac Med, Dept Family & Community Med, 500 Univ Ave, Toronto, ON M5G 1V7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
diabetes; electronic health records; glucose-lowering medications; marginal structural models; primary care; randomized controlled trials; SGLT2; INHIBITORS; CLINICAL-TRIALS; TYPE-2; MORTALITY; OUTCOMES;
D O I
10.1093/aje/kwad011
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Substantial effort has been dedicated to conducting randomized controlled experiments to generate clinical evidence for diabetes treatment. Randomized controlled experiments are the gold standard for establishing cause and effect. However, due to their high cost and time commitment, large observational databases such as those comprised of electronic health record (EHR) data collected in routine primary care may provide an alternative source with which to address such causal objectives. We used a Canadian primary-care data repository housed at the University of Toronto (Toronto, Ontario, Canada) to emulate a randomized experiment. We estimated the effectiveness of sodium-glucose cotransporter 2 inhibitor (SGLT-2i) medications for patients with diabetes using hemoglobin A1c (HbA1c) as a primary outcome and marker for glycemic control from 2018 to 2021. We assumed an intention-to-treat analysis for prescribed treatment, with analyses based on the treatment assigned rather than the treatment eventually received. We defined the causal contrast of interest as the net change in HbA1c (percent) between the group receiving the standard of care versus the group receiving SGLT-2i medication. Using a counterfactual framework, marginal structural models demonstrated a reduction in mean HbA1c level with the initiation of SGLT-2i medications. These findings provided effect sizes similar to those from earlier clinical trials on assessing the effectiveness of SGLT-2i medications.
引用
收藏
页码:782 / 789
页数:8
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