Table 2. Use of SGLT2 Inhibitors by Time.
Empagliflozin | Placebo | |
---|---|---|
All participants | N=3304 | N=3305 |
Active trial period | ||
12 months | 2920/3164 (92%) | 21/3159 (1%) |
24 months | 1661/1884 (88%) | 41/1875 (2%) |
36 months | 270/326 (83%) | 12/323 (4%) |
Participants entering PTFU | N=2472 | N=2419 |
Active trial period | ||
12 months | 2264/2423 (93%) | 13/2363 (1%) |
24 months | 1319/1483 (89%) | 30/1417 (2%) |
36 months | 254/297 (86%) | 10/289 (3%) |
Post-trial period | ||
12 months | 885/2186 (40%) | 804/2147 (37%) |
24 months | 1078/2376 (45%) | 972/2312 (42%) |
Active trial periods defined using 12, 24, and 36 months follow-up visit windows. Use in the active trial defined as a participant reporting taking ≥80% of allocated study drug or open-label SGLT2 inhibitor (denominators are those known to be alive in each period). Post-trial periods defined using information nearest to 12 and 24 months since completion of active trial follow-up. Post-trial open-label SGLT2 inhibitor use was ascertained from review of participant’s medical records, or where necessary, direct contact with participants (denominators are those who joined post-trial follow-up, had a follow-up in the period and were known to be alive in the relevant period). Use of open-label SGLT2 inhibitor in the empagliflozin group versus placebo group in the post-trial period after excluding participants on kidney replacement therapy in the relevant periods was 880/2032 (43%) vs 797/1960 (41%) at 12 months and 1069/2129 (50%) vs 961/2015 (48%) at 24 months.