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. 2022 Feb 10;327(8):1–12. doi: 10.1001/jama.2022.0948

Table 4. Outcomes of Patients Taking a NOAC Who Had an Acute Ischemic Stroke and Received Intravenous Alteplase in the ARAMIS Registry.

No. (%) of patients who had an acute ischemic stroke by timing of last NOAC dose prior to strokea
Overall (n = 47) 0-24 h ago (n = 8) 0-48 h ago (n = 25) >48 h ago (n = 22)
Primary outcome
Symptomatic intracranial hemorrhage within 36 h 2 (4.3) 0 2 (8.0) 0
Secondary outcomes
Life-threatening or serious systemic hemorrhage within 36 h 0 0 0 0
Any alteplase complicationb 3 (6.4) 0 3 (12.0) 0
Inpatient mortality 2 (4.3) 0 1 (4.0) 1 (4.6)
In-hospital mortality or discharged to hospice 4 (8.5) 0 2 (8.0) 2 (9.1)
Able to ambulate independently at hospital dischargec 28/45 (62.2) 5/8 (62.5) 12/24 (50.0) 16/21 (76.2)
Free of disabilities (modified Rankin Scale score of 0-1 at hospital discharge)d 14/40 (35.0) 1/7 (14.3) 4/21 (19.0) 10/19 (52.6)
Functionally independent (modified Rankin Scale score of 0-2 at hospital discharge)d 17/40 (42.5) 2/7 (28.6) 6/21 (28.6) 11/19 (57.9)
Discharge location
Home 26 (55.3) 5 (62.5) 10 (40.0) 16 (72.7)
Hospice 2 (4.3) 0 1 (4.0) 1 (4.5)
Inpatient rehabilitation facility 11 (23.4) 2 (25.0) 7 (28.0) 4 (18.2)
Skilled nursing facility 6 (12.8) 1 (12.5) 6 (24.0) 0
Hospital length of stay >4 d 19 (40.4) 3 (37.5) 14 (56.0) 5 (22.7)

Abbreviations: ARAMIS, Addressing Real-world Anticoagulant Management Issues in Stroke; NOAC, non–vitamin K antagonist oral anticoagulant.

a

These data are from a subset of patients participating in the ARAMIS registry. The reported date and time that the patient last took their anticoagulant medication was used to generate the time epochs; however, if the exact date and time was not available, the response to the question “Did patient stop anticoagulant medication >2 days prior to stroke onset?” was alternatively used to define the time epochs of less than 48 hours and greater than 48 hours.

b

Includes symptomatic intracranial hemorrhage within 36 hours, life-threatening or serious systemic hemorrhage within 36 hours, or other serious complications (those that required additional medical interventions or prolonged length of stay).

c

Data are expressed as No./total (%).

d

Data are expressed as No./total (%). The modified Rankin Scale has a score range of 0 to 6 with 0 being no symptoms; 1, no significant disability; 2, slight disability; 3, moderate disability; 4, moderately severe disability; 5, severe disability; and 6, death.