Table 2.
Follow‐up | Pt. at risk | Non‐persistent patients | Incidence of non‐persistencea (%) | Cumulative incidencea (%) | Pt. who switched initial DOAC | Percentage | |||
---|---|---|---|---|---|---|---|---|---|
Pt. at risk | To any anticoagulant | Percentage | To VKA | ||||||
Any DOAC | |||||||||
≤6 wk | 77 333 | 5781 | 8 | 8 | 5912 | 266 | 5 | 241 | 91 |
6 wk‐6 mo | 70 100 | 13 963 | 19 | 27 | 14 661 | 1139 | 8 | 726 | 64 |
6‐mo‐1 y | 44 569 | 3494 | 7 | 34 | 4439 | 1356 | 31 | 875 | 65 |
1‐2 y | 23 239 | 3150 | 9 | 43 | 5058 | 2543 | 50 | 1639 | 65 |
2‐3 y | 13 005 | 1372 | 8 | 51 | 2622 | 1657 | 63 | 1101 | 66 |
3‐4 y | 5301 | 593 | 13 | 64 | 1931 | 1572 | 81 | 1123 | 71 |
Total | 28 353 | 64 | 34 623 | 8533 | 25 | 5705 | 67 |
Abbreviations: DOAC, direct oral anticoagulant; Pt, patients, VKA, vitamin K antagonist.
Estimated by cumulative incidence as determined from survival tables in Kaplan Meier analyses.