Table 1.
Measures | |
---|---|
NOACs | 492* |
Dabigatran | 181/492 (36.8%) |
Reversal with idarucizumab | 44/181 (24.2%) |
Rivaroxaban | 215/492 (43.7%) |
Apixaban | 40/492 (8.1%) |
NOACs not specified | 56/492 (11.4%) |
Age, y† | Median, 77 (IQR, 68–83) |
Women | 233/492 (47.4%) |
NOAC last intake before stroke, h† | Median, 8 (IQR, 2.5–14.5) |
≤12 | 80/145 (55.2%) |
13–24 | 43/127 (33.9%) |
>24 | 10/130 (7.7%) |
Precise time/range not reported | 347/492 (70.5%) |
Laboratory† | |
Prolonged PT | 7/16 (43.8%) |
Prolonged aPTT | 34/124 (27.4%) |
Prolonged TT in dabigatran | 23/27 (85.2%) |
TT, dTT, or dabigatran concentration in dabigatran | 37/94 (39.4%) |
Anti-Xa assay in rivaroxaban or apixaban | 43/91 (47.3%) |
NIHSS on admission | Median, 10 (IQR, 6–16)† |
dTT indicates diluted thrombin time; IQR, interquartile range; NIHSS, National Institutes of Health Stroke Scale; NOAC, non–vitamin K antagonist oral anticoagulants; and TT, thrombin time.
Includes 30 patients receiving intra-arterial treatment.
Among patients with complete individual-level data.