Skip to main content

Table 3 Outcomes after intravenous thrombolysis in END group versus non-END group

From: Early neurological deterioration in acute ischemic stroke patients after intravenous thrombolysis with alteplase predicts poor 3-month functional prognosis - data from the Thrombolysis Implementation and Monitor of Acute Ischemic Stroke in China (TIMS-China)

Outcomes

No. (%) of patients

Unadjusted OR

(95% CI)

P value

Adjusted OR

(95% CI)a

P value

END group

(n = 81)

non-END group

(n = 1026)

Primary outcome

 mRS 3–6 at 3 months

66(83.54)

376(37.41)

8.49(4.62–15.60)

< 0.0001

8.25(3.77–18.03)

< 0.0001

Safety outcomes

 SICH (SITS-MOST)

15(18.52)

1(0.10)

232.83(−)

< 0.0001

109.77(−)

0.001

 SICH (ECASS II)

30(37.04)

5(0.49)

120.12(44.74–322.50)

< 0.0001

90.46(19.84–412.44)

< 0.0001

 SICH (NINDS)

30(37.04)

22(2.14)

26.84(14.47–49.79)

< 0.0001

12.53(5.15–30.49)

< 0.0001

 Mortality at 7

26(32.50)

16(1.56)

30.39(15.39–60.01)

< 0.0001

20.92(7.45–58.72)

< 0.0001

 Mortality at 3 months

36(45.00)

59(5.86)

13.13(7.86–21.94)

< 0.0001

8.06(3.91–16.62)

< 0.0001

  1. aAdjusted baseline variables: prior stroke/TIA, Systolic BP before thrombolysis, Diastolic BP before thrombolysis, glucose before thrombolysis, FBG before thrombolysis, Systolic BP at 2 hours after thrombolysis, Diastolic BP at 2 hours after thrombolysis, LDL after thrombolysis, TC after thrombolysis, Aspirin use within 7 days after thrombolysis, clopidogrel use within 7 days after thrombolysis, OCSP subtypes
  2. Abbreviations: mRS modified Rankin Scale, SICH symptomatic intracranial hemorrhage, SITS-MOST safe implementation of treatments in stroke-monitoring, ECASS II second European–Australasian acute stroke study, NINDS National Institute of Neurological Disorders and Stroke