Table 2.
Characteristic | No ATT | APT | p | AC | p | APT + AC | p | N |
---|---|---|---|---|---|---|---|---|
Stroke severity at admission | ref. | β (95% CI) | β (95% CI) | β (95% CI) | ||||
NIHSS at admission a | 1.00 | −0.31 (−0.47 to −0.15) | <0.001 | −0.81 (−1.05 to −0.58) | <0.001 | −1.10 (−1.61 to −0.59) | <0.001 | 34,483 |
n = 18,096 | n = 11,187 | n = 4574 | n = 626 | |||||
History of AIS/TIA | 1.00 | −0.74 (−1.11 to −0.37) | <0.001 | −1.12 (−1.59 to −0.66) | <0.001 | −1.20 (−1.99 to −0.41) | 0.003 | 7892 |
n = 1568 | n = 4334 | n = 1693 | n = 297 | |||||
3 month follow-up outcomes | ref. | aOR (95% CI) | aOR (95% CI) | aOR (95% CI) | ||||
Functional outcome (mRS > 3) b | 1.00 | 1.06 (0.98–1.14) | 0.135 | 1.28 (1.15–1.42) | <0.001 | 1.40 (1.11–1.75) | 0.003 | 28,464 |
n = 14,912 | n = 9226 | n = 3808 | n = 518 | |||||
History of AIS/TIA | 1.00 | 0.90 (0.75–1.07) | 0.239 | 1.01 (0.81–1.26) | 0.939 | 1.15 (0.81–1.63) | 0.447 | 6424 |
n = 1217 | n = 3562 | n = 1399 | n = 246 | |||||
Recurrent ischaemic stroke c | 1.00 | 1.26 (1.11–1.44) | <0.001 | 1.54 (1.29–1.83) | <0.001 | 1.09 (0.75–1.59) | 0.650 | 29,503 |
n = 15,616 | n = 9554 | n = 3790 | n = 543 | |||||
History of AIS/TIA | 1.00 | 1.01 (0.79–1.30) | 0.923 | 1.23 (0.91–1.66) | 0.186 | 0.89 (0.53–1.51) | 0.673 | 6671 |
n = 1250 | n = 3749 | n = 1404 | n = 268 | |||||
ICH d | 1.00 | 1.27 (1.05–1.53) | 0.013 | 0.98 (0.74–1.29) | 0.867 | 0.79 (0.40–1.58) | 0.512 | 29,640 |
n = 15,689 | n = 9629 | n = 3784 | n = 538 | |||||
History of AIS/TIA | 1.00 | 1.09 (0.67–1.77) | 0.718 | 1.14 (0.63–2.03) | 0.670 | 0.59 (0.17–2.03) | 0.402 | 6698 |
n = 1247 | n = 3777 | n = 1410 | n = 264 | |||||
Deathe | 1.00 | 1.10 (0.99–1.21) | 0.059 | 1.60 (1.41–1.80) | <0.001 | 1.69 (1.29–2.21) | <0.001 | 28,524 |
n = 14,939 | n = 9252 | n = 3814 | n = 519 | |||||
History of AIS/TIA | 1.00 | 0.71 (0.57–0.88) | 0.002 | 0.99 (0.77–1.27) | 0.940 | 0.89 (0.57–1.39) | 0.620 | 6442 |
n = 1218 | n = 3577 | n = 1401 | n = 246 |
AC: anticoagulation; AIS: acute ischaemic stroke; aOR: adjusted odds ratio; APT: antiplatelet therapy; ATT: antithrombotic therapy; ICH: intracerebral haemorrhage; mRS: modified Rankin scale; N: number of patients; NIHSS: National Institutes of Health Stroke Scale; ref.: reference; TIA: transient ischaemic attack; 95% CI: 95% confidence interval.
Adjusted beta-coefficients and odds ratios of outcome events in the respective antithrombotic therapy group as compared to no antithrombotic therapy (reference beta coefficient/odds ratio of 1.00). Comparisons of stroke severities were calculated using a quantile regression model, the comparisons of the 3-months follow-up outcomes using binomial logistic regression models. The analyses were adjusted for the following covariates.
Covariates included in all analyses: age (continuous), sex (categorical), serum glucose on admission (continuous), systolic blood pressure on admission (continuous), time between stroke onset and admission (continuous), history of ischaemic stroke, intracranial haemorrhage, hypertension, diabetes, atrial fibrillation (categorical variables).
Additional covariates for each analysis:
Premorbid mRS (ordinal).
Premorbid mRS (ordinal), intravenous thrombolysis (categorical), endovascular treatment (categorical), NIHSS on admission (continuous).
Intravenous thrombolysis (categorical), endovascular treatment (categorical), NIHSS on admission (continuous), modified TOAST aetiology (categorical).
Intravenous thrombolysis (categorical), endovascular treatment (categorical), NIHSS on admission (continuous).