1. General & ASPECTS Definition for "Large Core"
A **large core ischemic infarct** is typically defined in clinical practice and trials by:
* An **ASPECTS (Alberta Stroke Program Early Computed Tomography Score) of ≤5**.
* A **cerebral infarct volume of >50 to 70 mL**.
2. Core Characteristics (Infarct Core)
On Computed Tomography Perfusion (CTP) imaging, the established **infarct core** (non-viable tissue) is precisely defined by:
* A reduction in **regional cerebral blood flow (rCBF) to <30%** compared to normal brain tissue (often represented as `rCBF <30%` or `CBF <30%` on perfusion maps).
3. Perfusion Characteristics (Penumbra & Mismatch)
The hypoperfused but salvageable brain tissue surrounding the core (the **ischemic penumbra**) is defined by:
* A delay on the **time-to-maximum of the tissue residue function (Tmax) map of >6.0 seconds** (Tmax >6.0s).
* The **perfusion mismatch** represents the volume difference (or ratio) between this total hypoperfused area (Tmax >6.0s) and the established infarct core (rCBF <30%).
Based on the 2026 guidelines and the clinical trials evaluating large core (referred to as "large corridors") strokes, the benefit of Endovascular Therapy (EVT) versus best medical management varies depending on the ASPECTS score, the treatment time window, and the patient's baseline functional status:
1. No Significant Difference in the TESLA Trial (ASPECTS 2 to 5)
While most large core trials (such as SELECT2, ANGEL-ASPECT, TENSION, and LASTE) demonstrated a clear benefit for EVT over medical management
, the TESLA trial stood out as an exception.
ASPECTS 2 to 5: The TESLA trial evaluated patients with an ASPECTS of 2 to 5 within a 24-hour window and found no significant difference in clinical outcomes between patients who underwent EVT and those who received best medical management alone
2. Time Window Constraints for ASPECTS 0–2 (Very Large Core)
The guidelines differentiate recommendations based on how early the patient presents:
Late Window (6 to 24 hours): There is no established recommendation or benefit shown for EVT in patients presenting in the late window with an ASPECTS of 0 to 2. The Class 1 recommendation for EVT in the 6–24 hour window is strictly reserved for patients with an ASPECTS of 3 to 5
Early Window (0 to 6 hours): For patients with ASPECTS 0 to 2, EVT is still supported in the early window as a Class 2a (moderate) recommendation rather than Class 1
. (Note: The LASTE trial, which showed benefit for EVT, included a majority of patients with ASPECTS ≤2).
3. Prestroke Disability (mRS ≥ 2)
The baseline functional level of the patient is a major determinant of whether EVT offers a proven benefit over medical management:
mRS ≥ 2: Across all time windows (0–6 hours and 6–24 hours) and all large core ASPECTS levels (0–2 and 3–5), patients with a prestroke modified Rankin Scale (mRS) score of ≥2 (indicating pre-existing disability) have insufficient data to determine (IDD) any benefit of EVT over medical management
"General Considerations for EVT" Flow Chart:
Overall, for all vessel occlusions amenable for EVT, a discussion with INR is recommended. "General Considerations for EVT" follows a colour coding:
Green boxes are "signposts" of criteria to consider for EVT: baseline function, clinical, radiographic, and timing (last seen well) characteristics of the patient.
Purple boxes are consideration elements that warrant further discussion with INR as these patients do not automatically get considered for EVT.
Blue boxes represent patients that require an individualized approach.
The Yellow box represent patients that have met all previous criteria (Pre-stroke status, Signs and Severity of Deficit, Imaging criteria) and are candidates for EVT.
Please note detailed imaging criteria, listed below ("CSBPR 2018 Guidelines - Imaging Criteria for EVT") for patients within 6hrs and beyond 6hrs after stroke onset.
RAPID Training (www.irapid.com/training-rapid)
DEFUSE3 criteria
ICA or MCA-M1 occlusion (carotid occlusions can be cervical or intracranial; with or without tandem MCA lesions) by MRA or CTA AND
Target Mismatch Profile on CT perfusion or MRI (ischemic core volume is < 70 ml (CBF<30), mismatch ratio is >/= 1.8 and mismatch volume* is >/= 15 ml) Alternative neuroimaging inclusion criteria (if perfusion imaging or CTA/MRA is technically inadequate): If CTA (or MRA) is technically inadequate:
Tmax>6s perfusion deficit consistent with an ICA or MCA-M1 occlusion AND Target Mismatch Profile (ischemic core volume is < 70 ml, mismatch ratio is >1.8 and mismatch volume is >15 ml as determined by RAPID software)
DAWN criteria (core measured CBF<30)
0-<21 cc core infarct and NIHSS ≥ 10 (and age ≥ 80 years old)
0-<31 cc core infarct and NIHSS ≥ 10 (and age < 80 years old)
31 cc to <51 cc core infarct and NIHSS ≥ 20 (and age < 80 years old)
Lastly a word of caution. ALWAYS ensure you look at NCCT to assess hypo-density and correlate this with CBF core recalling that you may have a sub-acute infarct with luxury perfusion (therefore CBF>30 i.e. not showing as core on threshold to CBF map).
High observation for specific post-TPA patients meeting below criteria
After a code stroke resuscitation, the patient needs a monitored bed for neurologic monitoring.
On the B4 Stroke Unit, there will ultimately be several types of beds.
Post-TPA ONLY - Level 1 (total 9 beds, currently 6, MRP = Orange Team) -these beds can provide every to every 2 hourly neuro vital signs, there is cardiac monitoring as well, there are no arterial lines, there are no infusions of vasoactive agents including pressors or infusions of labetalol, however certain medications requiring cardiac monitoring such as phenytoin, amiodarone can be provided. Other medications can be given IV, but and intermittent dosing.
Post-TPA and/or Post-EVT Level 2 (total 6 beds, currently 2, MRP = ICU) - these are equivalent to B5ICU beds, these patients can have vasoactive agents, have cardiac monitoring, and can have arterial lines, therefore if the patient requires infusion of vasoactive agents, which typically does require arterial line monitoring, these patients can go to this bed.
Definitions of ICU "levels":
Level I = observation, no vasoactive infusions, no BiPAP
Level II = observation, vasoactive infusions, invasive arterial/BP measurement, non-invasive ventilation - i.e. BiPAP
Level III = all advanced ICU measures, including above, and mechanical ventilation
Active Research Studies - Inclusion/Exclusion Criteria - Point of Care Reference Material:
When patients are repatriated, at times we may want to fax completed notes, beyond the written consultation note. For this purpose, the following ED Fax numbers can be utilized to fax the report:
Hospital ED / FAX #
North York General / 416-756-6793
Mackenzie Health / 905-883-2138
Toronto Western / 414-603-5288
Scarborough and Rouge- General Site / 416-431-8164
Scarborough and Rouge-Centenary Site / 416-281-7455
ICU Fellow #s - direct
ICU CONSULT RESIDENT - 88111
Emerg/Float/Rapid 88121
CRCU blue 88197
CRCU green 88118
CVICU 88114
B5ICU 88112 (AM) Overnight 88114 (4PM-7AM M-F, and W/E) - During COVID-19, 88112 for B5ICU and B4ICU Level 2
Rapid Response 7887 - Rapid RN direct access Line
ICU Extensions
B5 4189
D4 7811
C3 4182
C5 4187
CRCU 4196
M2 extended ICU 7811
PACU 4240
Neuroradiology fellow 1404