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. 2020 Jul 7;11:581. doi: 10.3389/fneur.2020.00581

Table 2.

Study outcomes.

Outcomes Alteplase Group Control Group Binary Logistic Regression Analysis
Unmatched cohort (n = 51) (n = 84) Adjusted OR (95% CI) P-value
Primary outcomes
mRS ≤ 1 at 3 months, n (%) 28 (54.9) 40 (47.6) 0.30 (0.12, 0.74) 0.009
Early neurological deterioration, n (%) 8 (15.7) 27 (32.1) 2.55 (1.05, 6.16) 0.038
Secondary and safety outcomes
mRS ≤ 2 at 3 months, n (%) 40 (78.4) 62 (73.8) 0.43 (0.16, 1.12) 0.084
mRS ≥ 4 at 3 months, n (%) 5 (9.8) 13 (15.5) 3.14 (0.90, 10.91) 0.072
Intracranial hemorrhage, n (%) 2 (3.9)* 0
Death, n (%) 0 1 (2.0)
Matched cohort (n = 42) (n = 42) Unadjusted OR (95% CI) P-value
Primary outcomes
mRS ≤ 1 at 3 months, n (%) 28 (66.7) 14 (33.3) 0.25 (0.10, 0.62) 0.003
Early neurological deterioration, n (%) 5 (11.9) 13 (31.0) 3.32 (1.06, 10.37) 0.039
Secondary and safety outcomes
mRS ≤ 2 at 3 months, n (%) 35 (83.3) 26 (61.9) 0.33 (0.12, 0.90) 0.031
mRS ≥ 4 at 3 months, n (%) 3 (7.1) 10 (23.8) 4.06 (1.03, 16.02) 0.045
Intracranial hemorrhage, n (%) 2 (5.0)* 0
Death, n (%) 0 1 (2.5)

mRS, modified Rankin scale score; OR, odds ratio.

These models were adjusted for baseline NIHSS score and history of ischemic stroke.

Univariate logistic regression analysis was performed due to the failure of fitting a multivariate model adjusted for baseline NIHSS score and history of ischemic stroke.

*

There were two cases (3.9%) of parenchymal hemorrhage type 2 according to the criteria of ECASS II in the alteplase group, one of the two cases had symptomatic intracranial hemorrhage in the infarcted region and left severe disability.