Canadian Stroke Best Practice Recommendations Acute Stroke Management 7th Edition
Canadian Stroke Best Practice Recommendations Acute Stroke Management 7th Edition
doi:10.1017/cjn.2022.344
Review Article
ABSTRACT: The 2022 update of the Canadian Stroke Best Practice Recommendations (CSBPR) for Acute Stroke Management, 7th edition, is a
comprehensive summary of current evidence-based recommendations, appropriate for use by an interdisciplinary team of healthcare pro-
viders and system planners caring for persons with an acute stroke or transient ischemic attack. These recommendations are a timely oppor-
tunity to reassess current processes to ensure efficient access to acute stroke diagnostics, treatments, and management strategies, proven to
reduce mortality and morbidity. The topics covered include prehospital care, emergency department care, intravenous thrombolysis and
endovascular thrombectomy (EVT), prevention and management of inhospital complications, vascular risk factor reduction, early rehabili-
tation, and end-of-life care. These recommendations pertain primarily to an acute ischemic vascular event. Notable changes in the 7th edition
include recommendations pertaining the use of tenecteplase, thrombolysis as a bridging therapy prior to mechanical thrombectomy, dual
antiplatelet therapy for stroke prevention,1 the management of symptomatic intracerebral hemorrhage following thrombolysis, acute stroke
imaging, care of patients undergoing EVT, medical assistance in dying, and virtual stroke care. An explicit effort was made to address sex and
gender differences wherever possible. The theme of the 7th edition of the CSBPR is building connections to optimize individual outcomes,
recognizing that many people who present with acute stroke often also have multiple comorbid conditions, are medically more complex, and
require a coordinated interdisciplinary approach for optimal recovery. Additional materials to support timely implementation and quality
monitoring of these recommendations are available at www.strokebestpractices.ca.
RÉSUMÉ : Recommandations canadiennes pour les pratiques optimales de soins de l’AVC : prise en charge de l’AVC en phase aiguë, 7e
édition, mise à jour des lignes directrices de pratique 2022. La version mise à jour de 2022 de la section des Recommandations canadiennes
Corresponding author: M. Patrice Lindsay, Senior Editor, Canadian Stroke Best Practice Recommendations, Director, Health Systems, Heart and Stroke Foundation of Canada,
Toronto, Canada. Email: [email protected]
Cite this article: Heran M, Lindsay P, Gubitz G, Yu A, Ganesh A, Lund R, Arsenault S, Bickford D, Derbyshire D, Doucette S, Ghrooda E, Harris D, Kanya-Forstner N, Kaplovitch E,
Liederman Z, Martiniuk S, McClelland M, Milot G, Minuk J, Otto E, Perry J, Schlamp R, Tampieri D, van Adel B, Volders D, Whelan R, Yip S, Foley N, Smith EE, Dowlatshahi D,
Mountain A, Hill MD, Martin C, and Shamy M. (2024) Canadian Stroke Best Practice Recommendations: Acute Stroke Management, 7th Edition Practice Guidelines Update, 2022.
The Canadian Journal of Neurological Sciences 51: 1–31, https://doi.org/10.1017/cjn.2022.344
© Heart and Stroke Foundation of Canada, 2022. Published by Cambridge University Press on behalf of Canadian Neurological Sciences Federation. This is an Open Access article,
distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits
non-commercial re-use, distribution, and reproduction in any medium, provided that no alterations are made and the original article is properly cited. The written permission of
Cambridge University Press must be obtained prior to any commercial use and/or adaptation of the article.
pour les pratiques optimales de soins de l’AVC portant sur la prise en charge de l’AVC en phase aiguë (septième édition) est un résumé complet
des recommandations actuelles fondées sur des données probantes. Son utilisation est pertinente pour une équipe interdisciplinaire de dis-
pensateurs de soins de santé et de planificateurs du système de santé qui s’occupent de patients ayant subi un AVC en phase aiguë ou un
accident ischémique transitoire (AIT). Ces recommandations sont l’occasion idéale de réévaluer les processus actuels afin de garantir un accès
rapide aux diagnostics, aux traitements et aux stratégies de prise en charge de l’AVC en phase aiguë, qui s’avèrent efficaces pour réduire la
mortalité et la morbidité. Les sujets abordés comprennent les soins préhospitaliers; les soins au service des urgences; la thrombolyse intra-
veineuse et la thrombectomie endovasculaire; la prévention et la prise en charge des complications en milieu hospitalier; la réduction des
facteurs de risque vasculaire; la réadaptation précoce; et les soins de fin de vie. Ces recommandations se rapportent principalement à un
accident vasculaire ischémique aigu. Les changements notables apportés à cette septième édition comprennent des recommandations con-
cernant l’utilisation de la ténectéplase; la thrombolyse comme traitement de transition avant une thrombectomie mécanique; la bithérapie
antiplaquettaire pour la prévention de l’AVC1; la prise en charge de l’hémorragie intracérébrale (HI) symptomatique après une thrombolyse;
l’imagerie de l’AVC en phase aiguë; les soins aux patients à qui l’on administre une thrombectomie endovasculaire; l’aide médicale à mourir
(AMM); et les soins virtuels de l’AVC. Des efforts importants ont été déployés pour aborder les différences liées au sexe et au genre dans la
mesure du possible. Le thème de la septième édition des Recommandations est « établir des liens pour optimiser les résultats individuels »,
mettant l’accent sur le fait suivant : de nombreuses personnes ayant subi un AVC en phase aiguë présentent souvent plusieurs troubles con-
comitants; leur cas est plus complexe sur le plan médical, et elles nécessitent une approche interdisciplinaire coordonnée pour obtenir un
rétablissement optimal. Des documents supplémentaires pour soutenir la mise en oeuvre en temps opportun et le suivi de la qualité de
ces recommandations sont accessibles à www.pratiquesoptimalesavc.ca.
Keywords: Stroke; Transient ischemic attack; Practice guideline; Thrombolytic therapy; Thrombectomy; Stroke units; Vascular imaging;
Emergency medical services
(Received 8 November 2022; final revisions submitted 12 December 2022; date of acceptance 12 December 2022; First Published online 19
December 2022)
in the current module. Systematic reviews, meta-analyses, random- An explicit effort was made to address sex and gender differences
ized controlled trials, and observational studies were included, as wherever possible. The first four sections of this guideline pertain
available. The literature for this module was current to September to all people presenting with signs of acute stroke or TIA.
2022. Following a standardized abstraction format, evidence tables The remaining sections pertain largely to the management of acute
were constructed including content from selected studies and pro- ischemic stroke and TIA. Guidelines for the management of patients
vided to the writing group for review. The writing group discussed with ICH were released in 2020,18 while those for subarachnoid
and debated the strength, importance, clinical relevance, and appli- hemorrhage and cerebral venous thrombosis are in development.
cability of the evidence and, through consensus, developed a draft
set of proposed recommendations. During this process, additional
literature may have been identified and used to develop a final set Acute Stroke Management Recommendations, 7th Edition,
of proposed recommendations. Evidence levels were assigned Update 2022
based on the quality of available evidence, using the Grading of
Note, please refer to online Supplemental Material accompanying
Recommendations, Assessment, Development and Evaluations
these recommendations for additional definitions, information,
(GRADE) system.15–17 Expert opinion was used to formulate rec-
inclusion criteria, and other implementation content. This manu-
ommendations in the absence of evidence. These guidelines have
script has been translated into French and is also available as an
undergone extensive internal and external review, and consensus
online supplement.
was achieved for all content. For additional details of the method-
ology and additional materials to support these recommendations,
including rationales, system implications, performance measures,
knowledge translation and implementation tools, evidence tables, Section 1: Stroke Awareness, Recognition, and Response
and an extended summary of the evidence, please visit: www. Many members of the general public are unable to recognize the
strokebestpractices.ca. Supplemental online materials are available signs and symptoms of a stroke, or they attribute them to a less
with this publication to support many of the recommendations serious health issue.19–21 While 61% of the population in Canada
included. knows at least one sign of stroke, only 33% know at least two
and only 10% know all three, based on the FAST (Face, Arms,
Speech, Time) mnemonic.22 The failure to recognize the signs of
Summary of Changes and Updates in the Acute Stroke an acute stroke, either by the persons witnessing one or the person
Management Stroke, 7th Edition, 2022 experiencing one, can delay contact with emergency services,
Significant updates and new additions to the CSBPR for Acute which may in turn decrease a patient’s opportunity to receive
Stroke Management, 7th edition 2022 are based, in part, on the time-sensitive treatments. The number of public health campaigns
results from several new, important clinical trials. Notable changes designed to increase recognition of the signs and symptoms of
in the 7th edition include recommendations pertaining the use of stroke has increased over the past decade. One of the best recog-
tenecteplase, thrombolysis as a bridging therapy prior to mechani- nized programs in the healthcare community is FAST. The results
cal thrombectomy, dual antiplatelet therapy (DAPT) for stroke of a systematic review23 suggest that stroke education using mass
prevention,1 the management of symptomatic intracerebral hem- media campaigns can increase the likelihood of symptom recogni-
orrhage (ICH) following thrombolysis, acute stroke imaging tion by 20% and increase the likelihood that persons would call
(Section 4), pre- and post-op care of patients undergoing EVT emergency services by 19%. Mass media campaigns have also been
(Section 5), medical assistance in dying (MAiD) (Section 11), and shown to be associated with increases in the use of thrombolytic
virtual stroke care in the ED and inpatient care (Sections 4 and 8). agents following acute stroke.24
ii. All members of the public and all healthcare providers should be educated that stroke is a medical emergency [Strong recommendation; Low quality of
evidence].
a. Education for the public and healthcare providers should include information that stroke can affect persons of any age including newborns,
children, and adults. [Strong recommendation; Low quality of evidence].
b. Education for the public and healthcare providers should emphasize the benefits of early emergency treatment [Strong recommendation; Moderate
quality of evidence].
iii. Awareness campaigns and education for the public and healthcare providers should emphasize recognition of the signs and symptoms of stroke,
including the use of an acronym such as FAST (Face, Arms, Speech, Time) to facilitate awareness of and easy recall of these signs [Strong
recommendation; Moderate quality of evidence].
a. The public and healthcare providers should respond immediately when witnessing someone experiencing signs or symptoms of stroke by calling
9-1-1 or their local emergency number [Strong recommendation; Moderate quality of evidence], even if the signs or symptoms resolve. Refer to online
Supplemental Materials, Box 1B for additional information on discussions with emergency medical services (EMS) dispatch.
b. The public should be aware of the importance of following instructions from the EMS dispatch centre [Strong recommendation; Low quality of
evidence]. Refer to Section 3 Emergency Medical Services Management of Acute Stroke for additional information.
Section 2: Triage and Initial Diagnostic Evaluation of neuroimaging to identify minor events as well as the increased
Transient Ischemic Attack (TIA) and Non-Disabling Stroke use of antiplatelet agents, anticoagulants, antihypertensive agents,
People experiencing signs of stroke require rapid assessment, diag- lipid-lowering agents, and carotid revascularization has been
nosis, and determination of risk for a recurrent stroke. Patients shown to significantly reduce the risk of major stroke after an ini-
diagnosed to have TIA, or subacute, non-disabling ischemic tial minor event in recent years. In the TIARegistry.Org group
strokes who are not candidates for hyperacute treatment with study, 78.4% of patients were seen by a stroke specialist within
intravenous thrombolysis and/or EVT still require timely 24 h of the event.25 Most patients received key urgent investigations
assessment and management, which can often be provided in an before discharge, and appropriate treatments were initiated. For
outpatient setting. The goal of outpatient management is to rapidly example, 5.0% of patients received a new diagnosis of atrial fibril-
identify neurovascular risk factors, which may have precipitated lation, of which 66.8% received anticoagulant therapy before
the index event, and to initiate treatments to reduce the risk of discharge. Carotid stenosis of ≥50% was found in 15.5% of
recurrent events. The increased use and availability of sensitive patients, of which 26.9% underwent carotid revascularization
2. Triage and Initial Diagnostic Evaluation of Transient Ischemic Attack and Non-Disabling Stroke Recommendations 2022
Notes
• Section 2 recommendations pertain to the initial management of patients with a suspected acute transient ischemic attack (TIA) or acute ischemic stroke who
are not candidates for acute thrombolysis or endovascular intervention. For patients with suspected acute stroke that warrant hyperacute assessment to
determine eligibility for intravenous thrombolysis and endovascular thrombectomy (EVT), refer to the current CSBPR Acute Stroke Management treatment
recommendations, Sections 4 and 5.
• Refer to online Supplemental Materials for additional notes about this section.
2.0
i. Patients with acute stroke or TIA who present to an outpatient setting (such as primary care) or to a hospital should undergo clinical evaluation by a
healthcare professional with stroke expertise to determine the patient’s risk for recurrent stroke and initiate appropriate and timely investigations
and management strategies [Strong recommendation; Moderate quality of evidence].
ii. Shared decision-making should take into account patient values, preferences, health goals, medical complexity, social determinants of health, health
literacy, and health needs [Strong recommendation; Low quality of evidence].
2.1 HIGH Risk for Recurrent Stroke (Symptom Onset Within Last 48 hours)
i. Individuals presenting within 48 hours of symptoms consistent with a new acute stroke or TIA (especially transient focal motor or speech symptoms, or
persistent stroke symptoms) are at the highest risk for recurrent stroke and should be immediately sent to an emergency department (refer to Clinical
Consideration 2.1[3]) with a capacity for stroke care, which includes on-site brain imaging and ideally access to acute stroke treatments [Strong
recommendation; Moderate quality of evidence].
ii. Urgent brain imaging (computerized tomography [CT] or magnetic resonance imaging [MRI]) with concurrent neurovascular imaging (e.g., CT angiography
[CTA] or MR angiography [MRA]) should be completed as soon as possible and before discharge from the emergency department [Strong recommendation;
Moderate quality of evidence].
iii. Patients presenting after 48 hours from the onset of an acute stroke or TIA should receive a comprehensive clinical evaluation and investigations as soon as
possible by a healthcare professional with stroke expertise [Strong recommendation; Low quality of evidence]. Refer to Section 2.2 for more information on
investigations.
a. CTA of the head and neck from aortic arch to vertex, performed at the time of initial brain CT is recommended as an ideal way to assess both
extracranial and intracranial circulation [Strong recommendation; Moderate quality of evidence]. Note: Some facilities may not have CTA readily
available and so the timing and type of vascular imaging will need to be based on available resources and local practice protocols.
b. Neurovascular imaging is recommended to identify patients with significant symptomatic extracranial carotid artery stenosis (i.e., 50%–99%
stenosis), which should trigger an urgent referral for potential carotid revascularization [Strong recommendation; High quality of evidence].
c. CTA is the first-line vascular imaging test for stroke or TIA patients. If CTA is not possible, MRA and carotid ultrasound for extracranial vascular imaging
are reasonable alternatives as first-line tests for assessment of carotid vessels, and selection should be based on availability and patient
characteristics [Conditional recommendation; Low quality of evidence].
(Continued)
(Continued )
2. Triage and Initial Diagnostic Evaluation of Transient Ischemic Attack and Non-Disabling Stroke Recommendations 2022
a. Normal CT head despite symptoms persisting >24 hours. If diffusion-weighted imaging MRI is negative, cerebral ischemia is unlikely.
b. Normal CT head where there is suspected brainstem or cerebellar ischemia (CT head is relatively insensitive for detecting strokes in the posterior
fossa due to bone artifact).
a. Initial blood work: Hematology (complete blood count), electrolytes, coagulation (aPTT, INR), renal function (creatinine, estimated glomerular
filtration rate), random glucose, ALT [Strong recommendation; Low quality of evidence]. Refer to online Supplemental Materials, Table 2A for full
list of recommended laboratory tests.
b. Additional laboratory tests may be completed during the patient encounter or as an outpatient, including a lipid profile (fasting or non-fasting); and
screening for diabetes with either a glycated hemoglobin (HbA1c), fasting glucose or 75g oral glucose tolerance test [Strong recommendation; Low
quality of evidence]. Refer to Diabetes Canada Guidelines for additional information related to glucose testing.
c. (NEW FOR 2022) Giant Cell Arteritis: If giant cell arteritis is suspected (e.g., retinal ischemia or headache), ESR or CRP should be measured [Strong
recommendation; Low quality of evidence].
ii. (NEW FOR 2022) Extensive thrombophilia testing for hereditary hypercoagulable disorders is not recommended for routine investigation of a patient with
arterial ischemic stroke and should be limited to selected situations [Strong recommendation; Low quality of evidence].
a. If a hypercoagulable state is suspected, consultation with a healthcare professional with hematology or thrombosis expertise should be considered
[Strong recommendation; Low quality of evidence].
ii. For patients being investigated for an acute embolic ischemic stroke or TIA, ECG monitoring for 24 hours or more is recommended as part of the initial
stroke work-up to detect paroxysmal atrial fibrillation in patients who would be potential candidates for anticoagulant therapy [Strong recommendation;
High quality of evidence].
iii. For patients being investigated for an embolic ischemic stroke or TIA of undetermined source whose initial short-term ECG monitoring does not reveal
atrial fibrillation but a cardioembolic mechanism is suspected, continuous ECG monitoring for at least 2 weeks is recommended to improve detection of
paroxysmal atrial fibrillation in selected patients aged ≥55 years who are not already receiving anticoagulant therapy but who would be potential
candidates for anticoagulant therapy [Strong recommendation; High quality of evidence]. Refer to CSBPR Secondary Prevention of Stroke module Section 7
for additional guidance in management of patients with stroke and atrial fibrillation.13 Refer to the current Canadian Cardiovascular Society recommendations
on atrial fibrillation.28
2.4B Echocardiography
iv. Routine echocardiography is not required for all patients with stroke [Strong recommendation; Low quality of evidence].
v. Echocardiography should be considered for patients with an embolic ischemic stroke or TIA of undetermined source or when a cardioembolic etiology or
paradoxical embolism is suspected [Strong recommendation; Moderate quality of evidence].
vi. For patients ≤60 years who are being investigated for an embolic ischemic stroke or TIA of undetermined source, echocardiography with saline bubble
study is recommended for detection of a patent foramen ovale (PFO) if it may change patient management (i.e., in patients who would be potential
candidates for PFO closure or anticoagulant therapy if a PFO were detected) [Strong recommendation; Moderate quality of evidence].
a. Contrast-enhanced (agitated saline) transesophageal echocardiography or transcranial Doppler has greater sensitivity than transthoracic
echocardiography for detection of right-to-left cardiac and extra-cardiac shunts and should be conducted when available, [Strong
recommendation; Moderate quality of evidence].
(Continued)
(Continued )
2. Triage and Initial Diagnostic Evaluation of Transient Ischemic Attack and Non-Disabling Stroke Recommendations 2022
2.5 Functional Assessment
i. Patients with stroke should be assessed for neurological impairments and functional limitations (e.g., cognitive evaluation, screening for depression,
screening for dysphagia, screening for aphasia, screening for fitness to drive, need for rehabilitation therapy, assistance with activities of daily living,
functional mobility) [Strong recommendation; Moderate quality of evidence]. Refer to Rehabilitation and Recovery Following Stroke module29 for additional
information.
ii. Patients with stroke found to have neurological impairments that could impact daily functioning should be referred to the appropriate rehabilitation
specialist for in-depth assessment and management [Strong recommendation; Moderate quality of evidence].
2.6 (NEW FOR 2022) Virtual Care for Secondary Stroke Prevention
i. Secondary stroke prevention services should establish information technology infrastructure and protocols to increase and ensure access to
virtual care delivery for patients who do not require in-person visits. Emphasis should be placed on considerations for those individuals who do not
require in person visits such as, for patients living in rural and remote settings who do not have local access to healthcare professionals with stroke
expertise [Strong recommendation; Low quality of evidence]. Refer to CSBPR Virtual Stroke Care Implementation Toolkit for additional information at
www.strokebestpractices.ca.
ii. Clinicians should follow established/validated criteria to determine the best form of visit for each patient at each encounter (i.e., virtual or in person) based
on the purpose, goals, digital literacy, and availability for each visit [Strong recommendation; Low quality of evidence]. Refer to Heart & Stroke Virtual Care
Decision Framework for additional information and criteria at www.strokebestpractices.ca
2. The use of virtual care for stroke prevention should include decision tools to identify patients who require in-person visits and those who can reasonably be
managed through virtual care, and a scheduling mechanism for virtual visits that support a collaborative team approach to care where appropriate and
feasible. Refer to Heart & Stroke Virtual Care Decision Framework for additional guidance and criteria at www.strokebestpractices.ca.
3. A contingency plan should be established to quickly see patients in person should the need arise following a virtual care encounter. Refer to CSBPR Virtual
Stroke Care Implementation Toolkit for additional information at www.strokebestpractices.ca.
4. Virtual care-enabled evaluations of patients for secondary stroke prevention should be modeled on the topics defined in the post-stroke checklist and core
elements of stroke prevention care. Refer to CSBPR Post Stroke Checklist for additional information at www.strokebestpractices.ca.
5. Validated approaches to virtual neurological exams should be followed.
6. Processes should be in place to book follow-up tests, referrals, and other consultations after a virtual care visit.
7. Processes to ensure appropriate documentation and communication to other team members who may be involved in remote care should be in place.
8. Patients and their families should be encouraged to acquire home blood pressure monitors where appropriate and education or reliable resources on
proper use should be provided. Mechanisms should be in place for follow-up and management of blood pressure for patients using home blood pressure
devices, by either primary care providers or a stroke prevention service.
9. For timely investigations, the use of prolonged cardiac monitors, if available, that can be sent to patient’s homes, self-applied, and returned by mail, should
be considered.
before discharge. The 1-year estimate of risk of the primary experience fewer delays in receiving appropriate diagnostic tests,
outcome, a composite of death from cardiovascular causes, and are more likely to receive revascularization treatments, if eli-
nonfatal stroke, and nonfatal acute coronary syndrome, was gible. In 2020, 69.0% of patients with stroke admitted to hospital in
6.2% (95% confidence interval [CI] 5.5–7.0%). Estimates of stroke Canada were transported by EMS.30 The odds of a patient receiving
at days 2, 7, 30, 90, and 365 were 1.5%, 2.1%, 2.8%, 3.7%, and 5.1%, treatment with intravenous thrombolysis were increased by 52% if
respectively. These estimates were almost half of those compared the patient was transported by EMS and increased by 75% if a
with historical cohorts, possibly reflecting faster access to preven- system of hospital prenotification was employed.31 Given the
tive care in the contemporary cohort. The availability of TIA out- time-sensitive nature of acute stroke treatment, it is imperative
patient clinics appears to be increasing. Based on the results of a that patients who may be candidates for these therapies be trans-
geospatial analysis, there were 123 secondary prevention clinics ported directly to comprehensive stroke centers as quickly as
in Canada, as of 2016.26 While over 87% of the population had possible and whenever possible. The 90-day outcomes of patients
access to such a clinic within a 1-h drive, only 69.2% has access who received EVT following direct transport have been shown
to a service that operates 5–7 days a week. to be better than those who were first transported to a primary
stroke center.32,33 However, in a recent cluster-randomized trial34
in which paramedics transporting patients with ischemic stroke
Section 3: Emergency Medical Services
were randomized to the PASTA pathway (including structured
Emergency medical services (EMS) play a critical role in prehospi- prehospital information collection, prompted prenotification, and
tal assessment and management of patients with suspected stroke. structured handover of information) or standard care, there was
Patients arriving to hospital using EMS following a stroke no significant difference between groups in the proportion of patients
ii. EMS communications centre: All regions in Canada should implement a dispatch process through their EMS communications centres to rapidly recognize
signs or symptoms of stroke (e.g., FAST: Face, Arms, Speech, Time), prioritize response to the scene, and transport the patient to a hospital capable of
providing acute services for rapid diagnosis and time-sensitive treatment of stroke (such as neuroimaging, and acute thrombolysis) [Strong
recommendation; Low quality of evidence].
iii. After dispatching the ambulance, it is recommended that EMS communications centre personnel provide pre-arrival instructions to the person reporting
the stroke (e.g., unlock door, move pets, determine stroke symptom onset time, determine current medications), in order to expedite, optimize, and
improve safety for prehospital care [Conditional recommendation; Low quality of evidence]. Note: If the person experiencing the signs of stroke is the one to
contact EMS, they may not be able to comply with these requests.
Note: The on-scene goal is to recognize and mobilize. It is of the utmost importance to rapidly and safely transport suspected patients with stroke, as on-
scene management for patients with stroke is limited.
i. To minimize time to acute treatment for thrombolysis or EVT, EMS personnel should use a validated acute stroke out-of-hospital diagnostic screening tool
that includes the components of FAST [Strong recommendation; Moderate quality of evidence].
a. To optimize access to EVT, patients who demonstrate FAST signs of stroke should then undergo a valid secondary screen to assess stroke severity,
which may be used to identify candidates for direct transport to an EVT capable centre where possible [Strong recommendation; Moderate quality
of evidence]. Note: The purpose of the second screen is to look for possible EVT candidates, such as people exhibiting signs of cortical dysfunction
(e.g., aphasia, visual changes, neglect).
b. Screening for potential stroke and likelihood of large vessel occlusion (LVO) should be done early in the on-scene assessment. If the stroke screen is
positive, all on-scene actions from that point should be focused on moving to the ambulance and beginning transport [Strong recommendation;
Moderate quality of evidence].
ii. Treatments that are not immediately required could be undertaken while the patient is enroute to the hospital or after hospital arrival [Strong
recommendation; Low quality of evidence].
iii. EMS personnel should obtain information from the patient, family members or other witnesses about the suspected stroke event, including presenting
symptoms, time of onset or time of symptom recognition and time last known well, sequence of events, co-morbid conditions, current medications
(especially anticoagulants), and any formal or informal advance directives that may influence care by EMS and in the emergency department [Strong
recommendation; Moderate quality of evidence]. Refer to online Supplemental Materials Box 3A for additional information.
iv. On-scene time with any patient with suspected stroke should be as short as possible; ideally a median time of <20 minutes [Strong recommendation; Low
quality of evidence].
v. Initial assessment provided by paramedics should include capillary blood glucose measurement [Strong recommendation; Moderate quality of evidence].
a. Ideally capillary blood glucose measurement should be done on-scene to inform transport decisions [Conditional recommendation; Low quality of
evidence].
vi. Prior to transport, on-scene EMS personnel should provide instructions to the patients’ family, including recommending that the family member or other
decision-maker accompany the patient to hospital or be accessible by phone for decision-making; confirming time last known well; and providing
information about existing health conditions, current medications, and other information as needed [Strong recommendation; Low quality of evidence].
iii. Patients with suspected stroke should be triaged by EMS as Canadian Triage Acuity Scale (CTAS) Level 2 in most cases and as a CTAS Level 1 for patients
with compromised airway, breathing, or cardiovascular function [Strong recommendation; Moderate quality of evidence].
iv. Pre-notification: While enroute to the receiving hospital that provides acute stroke services, EMS should notify the emergency department of the incoming
suspected acute stroke patient and provide sufficient details such that a “Code Stroke” can be activated at that time [Strong recommendation; Moderate
quality of evidence]. Refer to online Supplemental Materials Box 3A for additional information.
v. Patients with suspected stroke who are considered ineligible for intravenous thrombolytic therapy or EVT (e.g., they are outside the time window) should
still be transported immediately to the closest hospital capable of providing acute stroke diagnosis and management services, where assessment and
determination can be made for transport to a higher level of care as appropriate [Strong recommendation; High quality of evidence].
(Continued)
(Continued )
i. Transfer of care from paramedics to receiving hospital personnel should occur with minimal delay and patients with suspected acute stroke who are
potentially eligible for thrombolytic therapy or EVT should receive highest priority in the emergency department triage queue [Strong
recommendation; Moderate quality of evidence]. Refer to Section 4.1 for more information.
ii. At hospital arrival, paramedics should provide the receiving hospital with verbal and written information related to the patient’s stroke onset time, last
known well time, presenting symptoms, and medications, to facilitate rapid assessment and decision-making [Strong recommendation; Low quality of
evidence]. Refer to online Supplemental Materials Box 3A for more information.
1. The standard window for intravenous thrombolysis is 4.5 hours and the standard time window for EVT is 6 hours. However, patients may be considered
eligible beyond these windows based on clinical factors and neuroimaging findings.
2. Direct transport in many regions may take one of two potential pathways based on local or regional considerations:
a. Patients who may be eligible for intravenous thrombolysis may be directed to the closest centre, which may be a primary/advanced stroke centre or
comprehensive stroke centre.
b. Patients who are likely candidates for EVT may be directed to (1) an EVT-enabled comprehensive stroke centre OR (2) a primary centre to rapidly
receive intravenous thrombolysis and then be considered for transport to an EVT-enabled comprehensive stroke centre.
3. On-scene time is an important variable that EMS professionals can control and needs to be monitored closely. Time lost due to inefficient on-scene care
cannot be made up during subsequent transport to hospital, regardless of the use of lights and sirens.
4. Patients should be transported by the method that allows the shortest transport time. In the event that a ground EMS response may cause significant delay
in the patient transport, air transport should be considered where available.
5. Pre-notification contact with the receiving emergency department should be initiated as soon as possible; where possible, the paramedics and receiving
emergency department physician or stroke team member should communicate while enroute.
6. For EVT-eligible patients, processes and or algorithms should be put in place that will easily enable a discussion to arrange for the patient to
be transferred to the EVT-enabled comprehensive stroke centre in a timely manner. A three-way conference call among the referring clinician
(paramedic or emergency department physician at a primary/advanced stroke centre), the receiving physician at the EVT-enabled centre, and the
ambulance service involved in patient transport should support decision-making regarding direct to EVT centre or closer centre for initial
imaging and assessment.
7. Mobile Stroke Units: The Canadian Stroke Best Practices writing group is currently unable to make a recommendation about mobile
stroke units as published data on their use in the context of Canadian geography and health system organization are lacking. The group encourages
further research into mobile stroke units in Canada as high-quality studies from other jurisdictions suggest that the use of these specialized
units is associated with a reduced time to thrombolysis, an increased proportion of patients receiving thrombolysis, and better functional outcomes
at 90 days.
who received thrombolysis (49.7% [PASTA] vs. 52.6% [standard assessment. Given that some acute stroke symptoms including
care], adjusted odds ratio [OR]=0.84, 95% CI 0.60–1.17). fatigue, anxiety, and dizziness may overlap with other cardio-
Paramedics in the PASTA group took an average of 13.4 min longer vascular and general medical conditions,38 it is important to iden-
to clear a care episode. tify patients who are experiencing stroke “mimics” and to avoid
After completing a brief screen tool to confirm signs and unnecessary and expensive investigations and inappropriate
symptoms of a stroke, using an instrument such as FAST35 or long-term prevention treatments. Patients presenting with stroke
the Cincinnati Prehospital Stroke Scale,36 EMS personnel should symptoms may ultimately be diagnosed with other conditions such
then conduct a subsequent screen to identify potential patients as migraine headache, vertigo, metabolic disturbances, brain
with large vessel occlusions (LVOs) in the anterior circulation tumors, or presyncope/syncope.39 The NIHSS can be used to
who may be potential candidates for EVT. While several vali- quickly screen for stroke-specific symptoms. For all patients
dated scales are currently available, most of which are derived arriving to hospital with suspected stroke or TIA, immediate
from 3–6 components of the National Institutes of Health brain and vascular imaging is the highest priority investigation
Stroke Scale (NIHSS), the sensitivities and specificities of these once any life-threatening issues with respiration and circulation
scales are not ideal37 and most have not been externally validated have been ruled out or addressed. A non-contrast CT scan is con-
in the field. sidered to be the imaging standard and the most cost-effective
method to be used initially to identify acute ischemic stroke
and to rule out intracranial hemorrhage.40 While MRI with
Section 4: Emergency Department Evaluation
DWIs may be more sensitive in detecting early changes associated
Standard assessments for patients with suspected acute stroke pre- with ischemia, especially in patients with small infarcts, this tech-
senting to the ED include a rapid neurological examination and nology may be not immediately available in many centers.41 In
urgent brain and vascular imaging, followed by monitoring of vital the year 2019/20, there were 288 MRI machines in 378 facilities
signs, blood work, cardiovascular investigations, blood pressure across Canada, equating to an availability of 10 units per million
management, glucose control, dysphagia screening, and seizure population.42 Combined multimodal vascular imaging is
4. Emergency Department Evaluation and Management of Patients with Transient Ischemic Attack and Acute Stroke Recommendations 2022
4.1 Initial Emergency Department Evaluation
i. All patients presenting to an emergency department with suspected acute stroke should be immediately assessed and undergo investigations without
delay to establish a diagnosis and determine eligibility for thrombolysis and/or endovascular thrombectomy (EVT) [Strong recommendation; High quality
of evidence].
a. Patients with suspected acute stroke should have a rapid initial evaluation for airway, breathing, and circulation [Strong recommendation; High quality of
evidence].
b. Patients with suspected stroke should be triaged as Canadian Triage Acuity Scale (CTAS) Level 2 in most cases and as CTAS Level 1 for patients with
compromised airway, breathing, or cardiovascular function [Strong recommendation; Low quality of evidence].
ii. Patients with suspected acute stroke should have a rapid neurological examination to determine focal neurological deficits using a validated scale such as
FAST (Face, Arm, Speech, Time) [Strong recommendation; Moderate quality of evidence]; and to assess for stroke severity using a validated screen [Strong
recommendation; High quality of evidence].
a. A standardized stroke scale such as the National Institutes of Health Stroke Scale (NIHSS) should be included in the initial assessment [Strong
recommendation; High quality of evidence].
b. Initial assessment should include consideration of time of stroke symptom onset, stroke mimics, development of a plan for further management, and
establishment of goals for care [Strong recommendation; Low quality of evidence] Refer to Section 2 Triage and Initial Diagnostic Evaluation of
Transient Ischemic Attack and Non-Disabling Stroke for additional information.
iii. Patients with suspected acute stroke should undergo an assessment of heart rate and rhythm, blood pressure, temperature, oxygen saturation, point-of-
care glucose, and presence of seizure activity [Strong recommendation; High quality of evidence].
a. (NEW FOR 2022) Use or non-use of anticoagulants, including the timing of the last dose taken, should be sought and recorded [Strong
recommendation; Moderate quality of evidence].
iv. Acute blood work should be conducted as part of the initial evaluation [Strong recommendation; Moderate quality of evidence].
a. Initial blood work should include electrolytes, random glucose, complete blood count (CBC), coagulation status (INR, aPTT), and creatinine [Strong
recommendation; High quality of evidence]. Refer to online Supplemental Materials Table 2A for additional information on recommended laboratory
investigations for acute stroke and TIA.
Note: Initial blood work tests should not delay imaging or treatment decisions and treatment initiation for intravenous thrombolysis and EVT.
v. Seizure assessment: Seizure in the presence of suspected acute stroke is not a contraindication for reperfusion and could be treated using appropriate
short-acting medications (e.g., lorazepam IV) if the seizures are not self-limited [Strong recommendation; High quality of evidence]. Refer to Section 9
Inpatient Prevention and Management of Complications Following Stroke for additional information.
Note: If initial brain imaging reveals a hemorrhagic stroke, refer to CSBPR Management of Intracerebral Hemorrhage18 module for additional information.
i. All patients with suspected acute stroke should undergo brain and vascular imaging computerized tomography (CT) or magnetic resonance imaging (MRI)
[Strong recommendation; High quality of evidence].
a. Vascular imaging should be performed from arch-to-vertex and include the extra- and intra-cranial circulation to determine eligibility for acute
treatment [Strong recommendation; High quality of evidence].
Note: Primary stroke centres should make all efforts to perform combined CT and CTA on patient arrival. The CT and CTA should be done at same time
and not in separate visits to the imaging suite. Stroke centres that cannot do CTA should have pre-planned arrangements for rapid transfer of appropriate
patients. They should complete non-contrast CT (NCCT) and offer intravenous thrombolysis as appropriate and then rapidly transfer the patient to a
comprehensive stroke centre for more advanced imaging and consideration for EVT. (Refer to IV thrombolysis Section 5 for additional information).
ii. All patients with suspected acute ischemic stroke who arrive at hospital within 6 hours who are potentially eligible for intravenous thrombolysis and/or EVT
should undergo immediate non-contrast CT (NCCT) combined with CT angiography (CTA) of the head and neck, performed and interpreted without delay
[Strong recommendation; High quality of evidence]. Refer to online Supplemental Materials for eligibility criteria in Boxes 4A, 4B, 5A, 5B, and 5C.
iii. All patients with suspected ischemic stroke due to large vessel occlusion (LVO) arriving 6 to 24 hours after stroke symptom onset (including stroke on
awakening or with unknown onset time) and who are potentially eligible for late window EVT should undergo immediate brain imaging with NCCT with CTA
and CT perfusion (CTP); or magnetic resonance imaging (MRI) with MR angiography (MRA) and MR perfusion (MRP) [Strong recommendation; High quality of
evidence]; or CT with multiphase CTA [Strong recommendation; Moderate quality of evidence]. Refer to Section 4.1 for criteria regarding screening with use of
validated screening tools. Refer to online Supplemental Materials Box 4C for additional information.
iv. A validated triage tool, such as ASPECTS, should be used to rapidly identify patients who may be eligible for EVT and who may require transfer to a different
facility for EVT [Strong recommendation; Moderate quality of evidence].
v. Advanced CT imaging such as CT perfusion (CTP) or multiphase CTA to assess pial collateral vessels is strongly encouraged as part of initial imaging to aid
patient selection for EVT [Strong recommendation; Moderate quality of evidence]. However, advanced imaging must not substantially delay decision-
making and treatment with intravenous thrombolysis or EVT. Refer to online Supplemental Materials Boxes 4A, 4B, 4C, 5A, 5B, and 5C for additional
information.
Note: If there are signs of hemorrhage on initial CT images there is no need to proceed to CTP imaging as part of initial imaging and CTA should be
completed based on the clinical judgement of the treating physician.
Note: In most Canadian centres a CT approach may be more practical and more readily available than an MR approach. Choice of imaging modality
should be based on most immediate availability and local resources.
Refer to Section 5 Acute Ischemic Stroke Treatment for information on administration of intravenous thrombolysis and EVT.
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4. Emergency Department Evaluation and Management of Patients with Transient Ischemic Attack and Acute Stroke Recommendations 2022
2. Patients with a known allergy to contrast dye or with existing renal failure should not be excluded from consideration for EVT.
4.3 Acute Blood Pressure Management
i. Patients with ischemic stroke eligible for thrombolytic therapy: Blood pressure should be lowered and sustained below 185/110 while initiating and during IV
thrombolysis therapy, and for the next 24 hours for ischemic stroke patients who are eligible for thrombolytic therapy [Strong recommendation; Low quality of
evidence].
ii. Patients with ischemic stroke not eligible for thrombolytic therapy: Patients with moderate blood pressure elevation (up to 220 mmHg systolic) should
not be routinely treated if they are not eligible for thrombolytic therapy [Conditional recommendation; Low quality of evidence].
a. Patients with extreme blood pressure elevation (e.g., systolic BP >220 or diastolic BP >120 mmHg) should be considered for blood pressure lowering
therapy if they are not eligible for thrombolytic therapy [Conditional recommendation; Low quality of evidence].
iii. Rapid or excessive lowering of blood pressure should be avoided as this might exacerbate existing ischemia or might induce ischemia, particularly in the
setting of intracranial or extracranial arterial occlusion [Conditional recommendation; Low quality of evidence].
a. Reducing the blood pressure by approximately 15% and not >25% over the first 24 hours, with further gradual reduction thereafter to targets for
long-term secondary stroke prevention, may be considered [Conditional recommendation; Low quality of evidence].
Note: Refer to CSBPR Management of Intracerebral Hemorrhage module18 for information on blood pressure management of hemorrhagic stroke.
1. The choice of agents to manage blood pressure should be based on current Hypertension Canada blood pressure treatment guidelines. Refer to www.
hypertension.ca.
i. Patients with acute ischemic stroke or TIA should have a 12-lead ECG to assess cardiac rhythm and identify atrial fibrillation or flutter or evidence of
structural heart disease (e.g., myocardial infarction and left ventricular hypertrophy) [Strong recommendation; Moderate quality of evidence].
ii. Unless a patient is hemodynamically unstable, ECG should not delay assessment for intravenous thrombolysis and EVT and can be deferred until after a
decision regarding acute treatment is made [Strong recommendation; Moderate quality of evidence].
Note: For patients being investigated for an acute embolic ischemic stroke or TIA of undetermined source whose initial short-term ECG monitoring does not
reveal atrial fibrillation but a cardioembolic mechanism is suspected, refer to CSBPR Secondary Prevention of Stroke module, Section 7 for additional
information.
Refer to CSBPR Secondary Prevention of Stroke module13 for additional information on echocardiography and rhythm monitoring.
i. All patients with suspected acute stroke should have their blood glucose concentration checked on arrival to the emergency department (or review glucose
provided by EMS for any immediate management required) [Strong recommendation; Moderate quality of evidence].
Refer to online Supplemental Materials Table 2A Recommended Laboratory Investigations for Patients with Acute Stroke or Transient Ischemic Attack for
additional information. Refer to Section 3 Emergency Medical Services Management of Acute Stroke for additional information on EMS management.
ii. Hypoglycemia should be corrected immediately using local protocols [Strong recommendation; High quality of evidence].
iii. Although no optimal glucose target has been identified in the acute stage, it may be reasonable to treat hyperglycemia (glucose >20 um/l) as per local
protocols as this has been associated with increased risk of hemorrhagic transformation when treating with intravenous thrombolysis [Conditional
recommendation; Low quality of evidence].
ii. Swallowing assessment: All patients with acute stroke or TIA should have a swallowing screen completed as soon as possible as part of initial assessment
by a practitioner trained to use a validated swallowing screening tool; however, screening should not delay decision-making regarding eligibility for
reperfusion treatments [Strong recommendation; High quality of evidence].
a. Ideally swallowing screens should be done within 24 hours of hospital arrival, including for patients that receive acute stroke treatments such as
intravenous thrombolysis and EVT [Strong recommendation; Moderate quality of evidence].
b. Patients should remain NPO (nil per os [no oral intake]) until a swallowing screen is completed, for patient safety [Strong recommendation; High
quality of evidence].
c. Oral medications should not be administered until a swallowing screen using a validated tool has been completed and found to be normal [Strong
recommendation; Moderate quality of evidence]; alternate routes such as intravenous and rectal administration should be considered while a patient
is NPO.
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4. Emergency Department Evaluation and Management of Patients with Transient Ischemic Attack and Acute Stroke Recommendations 2022
d. A patient’s clinical status can change in the first hours following a stroke or TIA; therefore, patients should be closely monitored for changes in
swallowing ability following initial screening [Strong recommendation; Low quality of evidence].
e. Patients found to have abnormal swallowing ability on screening should remain NPO and be referred to a healthcare professional with expertise in
this area for further swallowing assessment [Strong recommendation; Moderate quality of evidence].
Note: Swallow assessments are particularly important for patients discharged to the community directly from the emergency department or repatriated
to a lower level of care.
Refer to Section 9 Inpatient Prevention and Management of Complications Following Stroke, and CSBPR Rehabilitation and Recovery following Stroke
module,29 Section 7 for additional information on screening for swallowing ability and dysphagia management.
iii. Urethral catheters: The use of indwelling urethral catheters should generally be avoided due to the risk of urinary tract infections [Strong
recommendation; Moderate quality of evidence]. Refer to Section 9 Inpatient Prevention and Management of Complications Following Stroke for
additional information.
a. Insertion of an indwelling urethral catheter should be considered for patients undergoing EVT when necessary, but this should not delay beginning
the procedure. The need to retain the catheter should be reconsidered after the end of the EVT procedure, and the use of the catheter should be
discontinued as soon as the patient is able to resume voiding on their own [Conditional recommendation; Low quality of evidence].
b. Insertion of an indwelling urethral catheter is not routinely needed prior to intravenous thrombolysis unless the patient is acutely retaining urine and
is unable to void. If inserted for patient-specific reasons, it should not delay acute treatment [Strong recommendation; Moderate quality of evidence].
c. If used, indwelling catheters should be reassessed daily and removed as soon as possible [Strong recommendation; High quality of evidence].
d. Fluid status and urinary retention should be included as part of routine monitoring of vital sign assessments [Strong recommendation; Moderate
quality of evidence].
iv. Temperature: Temperature should be routinely monitored and treated per local protocols [Strong recommendation; Moderate quality of evidence]. Refer
to Section 9 Inpatient Prevention and Management of Complications Following Stroke for additional information.
v. Oxygen: Supplemental oxygen is not required for patients with normal oxygen saturation levels [Strong recommendation; Moderate quality of evidence].
i. Virtual acute stroke care networks should be in place and readily available when stroke expertise is not available on-site, to allow access to consultations
with stroke experts for acute stroke assessment, diagnosis, and treatment, including acute thrombolytic therapy and decision-making for EVT [Strong
recommendation; Moderate quality of evidence].
ii. Consulting and referring sites should have standardized protocols and processes in place to ensure access to stroke experts through virtual healthcare
modalities, available 24 hours a day, seven days a week to provide equitable access to time-driven advanced stroke care across Canada [Strong
recommendation; Moderate quality of evidence].
iii. The consultant should be a physician with specialized training in acute stroke management and must have timely access to diagnostic-quality
neurovascular (e.g., brain CT, CTA) images during the virtual acute stroke consultation [Strong recommendation; High quality of evidence]. Refer to
CSBPR Virtual Stroke Care Implementation Toolkit for additional information at www.strokebestpractices.ca.
Note: The decision to use acute stroke therapies in emergency management requires imaging to rule out hemorrhage. Refer to Sections 4, 5, and 6 in this
document for additional information on imaging and revascularization.
iv. Real-time two-way audiovisual communication should be in place to enable remote clinical assessment of the patient by the consulting stroke expert
[Strong recommendation; Moderate quality of evidence].
a. Virtual acute stroke modalities including video-conferencing and teleradiology systems may be considered to support screening and decision-
making regarding candidacy for thrombolysis and/or EVT in appropriate cases and to facilitate transfer to endovascular-enabled stroke
centres [Strong recommendation; Moderate quality of evidence].
b. The benefits of telephone consultation without video are not well-established and every attempt should be made to connect via a video link
[Conditional recommendation; Low quality of evidence].
v. All laboratory and diagnostic results required by the consultant should be made readily available during the virtual acute stroke care consultation [Strong
recommendation; Moderate quality of evidence].
vi. Referring physicians should follow an established protocol or algorithm that describes the critical steps and inclusion/exclusion criteria for thrombolysis
and/or recanalization therapies, which are agreed to by both the referring and consulting sites [Strong recommendation; High quality of evidence].
Refer to Section 3 Emergency Medical Services Management of Acute Stroke for additional information.
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4. Emergency Department Evaluation and Management of Patients with Transient Ischemic Attack and Acute Stroke Recommendations 2022
vii. Referring physicians and nursing staff who may be involved in virtual acute stroke consultations should ideally be trained in administration of the NIHSS,
so they can assist the telestroke consultant efficiently and competently during the remote video neurological examination [Strong recommendation;
Moderate quality of evidence].
viii. The most responsible physician remains the attending physician at the referring site. Decision-making is a consensus process that is achieved in
consultation with the attending medical staff at the referring site, the patient and family, and the consulting physician with stroke expertise [Strong
recommendation; Low quality of evidence].
ix. A consulting physician with stroke expertise should remain accessible as they may be required to provide ongoing guidance to the referring site following
initial consultation [Strong recommendation; Low quality of evidence].
x. Protocols should be in place that define patient transfer criteria to a more advanced stroke care facility when clinically indicated (e.g., for endovascular [if
available], neurosurgical intervention) [Strong recommendation; Low quality of evidence].
a. The virtual acute stroke care system should identify the stroke centres that are able to provide endovascular and neurosurgical care [Strong
recommendation; Low quality of evidence].
b. For patients who are deemed eligible for endovascular treatment or neurosurgical interventions, protocols should be in place to define the process
for patient transfer [Strong recommendation; Moderate quality of evidence]. Refer to Section 6 Acute Antithrombotic Therapy for additional
information.
xi. The use of standardized documentation should be considered for both the referring site and the consulting site, in accordance with hospital processes,
jurisdictional legislation, and regulatory bodies [Strong recommendation; Low quality of evidence]. This may include:
a. A consultation note provided by the consulting physician to the referring site at the end of the consultation, to be included in the patient medical
record [Strong recommendation; Low quality of evidence].
b. A discharge summary sent by the referring site to the consulting virtual acute stroke physician to provide feedback about the patient’s outcome
[Strong recommendation; Low quality of evidence].
c. For patients who are transferred to another hospital (e.g., “drip and ship”), a discharge summary from the receiving hospital to the referring
physician and the virtual acute stroke physician [Strong recommendation; Low quality of evidence].
xii. Processes should be in place to ensure timely and effective transfer of up-to-date, relevant information in the patient medical record (e.g., patient
progress, treatment plans, plans for ongoing follow-up, discharge recommendations) from the consulting healthcare provider to the referring site, in
accordance with clinical care processes, organizational requirements, jurisdictional legislation, and regulatory requirements [Strong recommendation;
Low quality of evidence]. Refer to CSBPR Transitions and Community Participation Following Stroke Section 3.3 for additional information.43
xiii. Data related to the virtual acute stroke consultation and outcome should ideally be collected by the virtual acute stroke program for continuing quality
improvement [Strong recommendation; Low quality of evidence].
i. Consulting physicians and other healthcare professionals involved in virtual acute stroke consults should have expertise and experience in managing
patients with stroke [Strong recommendation; Low quality of evidence].
ii. It is recommended that virtual acute stroke care providers attain and maintain the necessary competencies required to provide safe, competent virtual care
and to create a satisfactory telehealth encounter for both the patient and the healthcare provider [Strong recommendation; Low quality of evidence].
iii. Referring and consulting service providers should be trained to use the virtual acute stroke system and should understand their roles and responsibilities
for the technical and clinical aspects of an acute virtual stroke care consultation [Strong recommendation; Low quality of evidence].
iv. Virtual stroke care training should include physicians, nurses, therapists, and any support staff (e,g., members of technology department) who may be
involved in any virtual acute stroke consultation or therapy appointment [Strong recommendation; Low quality of evidence].
v. Ongoing virtual acute stroke training and education with a regular update cycle is useful to ensure competency of providers [Strong recommendation; Low
quality of evidence]. Refer to CSBPR Virtual Stroke Care Implementation Toolkit for additional information and resources for staff training, at www.
strokebestpractices.ca.
vi. Continuing education in online and face-to-face formats is useful to ensure remote-based practitioners have access to ongoing education [Strong
recommendation; Low quality of evidence].
1. Mock acute stroke patient scenarios and practice cases may be helpful, especially for acute/emergent virtual stroke care at new sites, and where the
ongoing volume of cases is low.
2. Routine checks of acute virtual stroke care equipment (both video-conferencing and imaging systems such as PACS) should be done to ensure the
equipment will function properly in an emergency. This may be done as part of routine checks on other emergency equipment such as crash carts.
Some systems may have a back-up system or alarms for malfunctioning equipment.
3. Where electronic health records are available, health information sharing regulations that comply with provincial and federal privacy legislation should be
developed, to allow an individual patient’s record to be shared with referring and consulting facilities.
4. Efforts should be made to design telestroke technology, so it is easy to use and operate, to facilitate adoption of the technology and decrease the time
needed to meet educational requirements.
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4. Emergency Department Evaluation and Management of Patients with Transient Ischemic Attack and Acute Stroke Recommendations 2022
Box 4B Imaging Criteria for Consideration of Endovascular Thrombectomy in Patients Arriving Within 6 Hours of Stroke Onset
4B.1. For anterior circulation: Imaging Criteria for Endovascular Thrombectomy in Patients Arriving Within 6 Hours of Stroke Onset
1. Presence of an intracranial artery occlusion in the anterior circulation on CTA or MRA, including occlusion of the terminal internal carotid artery or
proximal MCA
AND
2. Presence of a small to moderate ischemic core on non-contrast CT or MRI, usually consistent with an ASPECTS score of ≥6 for the anterior circulation.
a. Patients presenting with an intracranial artery occlusion and large core, such as those with an ASPECT score <6, may be considered for EVT based on
expected risks and benefits, after consultation with a physician with stroke expertise and with the treating neurointerventionalist, along with the
patient and/or family and/or substitute decision-makers.
4B.2 For posterior circulation: Imaging Criteria for Consideration of Endovascular Thrombectomy for Patients Arriving Within 6 Hours of Stroke
Onset
1. Patients presenting with an intracranial occlusion of the posterior circulation (e.g., the basilar artery) may be considered for EVT based on expected risks
and benefits, after consultation with a physician with stroke expertise and with the treating neurointerventionalist, along with the patient and family or
substitute decision-maker.
Note: Randomized trials are ongoing, and this recommendation will be reviewed once the results become available.
extremely important, and in highly selected cases, perfusion scans contrast to these findings, the NOR-TEST 249 trial of alteplase
with CT or MRI has the potential to identify patients with an versus tenecteplase 0.4 mg/kg was halted early due to safety
ischemic penumbra and potentially viable brain tissue who concerns, which included an increased risk of intracranial hem-
may be appropriate for acute reperfusion therapies. Perfusion orrhage and mortality; however, the dose in the tenecteplase
scans can be especially useful in selecting patient eligible for group was higher (0.4 mg/kg) than is currently recommended
endovascular therapy in the 6-to-24-h window whereas in the (0.25 mg/kg). In the EXTEND-IA TNK,50 where patients with
0-to-6-h time frame, and most cases can be selected with the LVO received treatment with both thrombolysis and EVT, a sig-
use of CT and CTA alone. nificantly higher number of patients receiving tenecteplase 0.25
mg/kg achieved substantial reperfusion (22% vs. 10%, p = 0.02
Section 5: Acute Ischemic Stroke Treatment for superiority), although the percentage of patients who were
functionally independent at 90 days or who had achieved an
While the weight of evidence clearly indicates that treatment with
excellent outcome did not differ between groups. Several clinical
intravenous alteplase, administered within 4.5 h of symptom trials comparing tenecteplase with alteplase (ATTEST2
onset, improves functional outcomes and reduces the risks of NCT0281440) and tenecteplase with placebo, or best medical
death or disability,44,45 there are limited data on the benefit of management (TIMELESS NCT03785678, TWIST NCT0318
treatment beyond this window. The most recent trials of throm- 1360, and TEMPO-2 NCT02398656) are ongoing.
bolytic therapy in the extended time window include EXTEND46 A 2021 Cochrane review51 that included the results of 19 trials
and WAKE-UP,47 in which patients presenting with symptoms adds to the growing body of evidence indicating that EVT per-
beyond 4.5 h or with unknown time of onset were selected for formed within 6 h of symptom onset is an extremely effective
treatment on the basis of advanced imaging. In both trials, treatment for patients with LVO in the anterior circulation.
patients receiving alteplase were more likely to achieve an excel- Treatment with EVT was associated with a significantly higher
lent outcome (mRS 0–1) at 90 days, relative increase 44%46% and likelihood of favorable outcome (RR = 1.61, 95% CI 1.42 to
61%,47 symptomatic ICH and death were higher in the interven- 1.82) with a high certainty of evidence, without a significantly
tion group. increased risk of symptomatic intracranial hemorrhage
The results from several recent trials indicate that tenecte- (RR = 1.46, 95% CI 0.91 to 2.36) compared with usual care, which
plase, a newer thrombolytic agent that has pharmacokinetic in many cases included the use of alteplase. For selected patients,
advantages over alteplase, is non-inferior to alteplase. Among the treatment window for EVT may be even longer. A pooled
the completed trials to date, the AcT trial48 was the first to report analysis of six randomized controlled trials52 including patients
that tenecteplase at a dose of 0.25 mg/kg (maximum 25 mg) is who received treatment between 6 and 24 h after the onset of
non-inferior to standard dose alteplase. At 90 days, 36.9% of symptoms also found significantly better outcomes in patients
patients in the tenecteplase group achieved the primary outcome in the intervention group. There was a significant shift in the
(mRS score of 0–1) versus 34.8% in the alteplase group (unad- ordinal analysis of mRS scores favoring less disability in the
justed difference = 2.1%, 95% CI -2.6% to 6.9%; adjusted relative thrombectomy group (adjusted OR =2·54, 95% CI 1·83–3·54).
risk [RR] = 1·1, 95% CI 1·0 to 1·2), meeting the non-inferiority The odds of achieving an mRS score of 0–1 or 0–2 at 90 days were
threshold (the lower bound 95% CI of which was set at greater both significantly higher in the EVT group (adjusted OR = 2·41,
than -5%). There was no significant difference between groups 95% CI 1·07–5·43 and adjusted OR = 3·88, 95% CI 1·94–7·78,
in terms of mortality at 90 days (15.3% vs. 15.4%), or in the pro- respectively). The number needed to treat for one more patient
portion with symptomatic ICH at 24 h (3.4% vs. 3.2%). In to be independent with EVT was 2.6.
b. If there is uncertainty about interpretation of CT imaging, urgent consultation with a radiologist either on-site or through virtual telestroke services is
recommended [Strong recommendation; Low quality of evidence].
ii. Beyond 6 hours of stroke symptom onset or last known well: All patients with disabling acute ischemic stroke who are between 6 and 24 hours of stroke
symptom onset or last known well should be rapidly screened to determine eligibility for urgent advanced neurovascular imaging and acute stroke
treatments [Strong recommendation; Moderate quality of evidence]. Refer to online Supplemental Materials Box 5A for a summary of treatment time
windows.
2. If a large vessel occlusion (LVO) is present, consideration for thrombolysis beyond 4.5 hours from the time the patient was last known well should not delay
decisions regarding EVT.
i. All eligible patients with disabling ischemic stroke, who can receive intravenous thrombolysis with either alteplase or tenecteplase within 4.5 hours of stroke
symptom onset time or last known well time should be offered intravenous thrombolysis [Strong recommendation; High quality of evidence]
Refer to online Supplemental Materials Box 4A for detailed recommendations on neuroimaging. Refer to online Supplemental Materials Box 5A for time
windows, Box 5B for inclusion and exclusion criteria for intravenous thrombolysis eligibility. Refer to Section 5.1 Clinical Considerations for information
about patients who arrive beyond the 4.5-hour time window.
ii. All eligible patients should receive intravenous thrombolysis as soon as possible after hospital arrival [Strong recommendation; High quality of evidence],
with a target median door-to-needle time of <= 30 minutes and a door-to-needle time of <= 60 minutes in at least 90% of treated patients [Strong
recommendation; Moderate quality of evidence]
a. Treatment should be initiated as soon as possible after patient arrival and CT scan completion [Strong recommendation; High quality of evidence].
b. Every effort should be made to ensure door-to-needle times are routinely monitored and improved [Strong recommendation; Moderate quality of
evidence].
iii. Alteplase dose: If using alteplase, the dose of 0.9 mg/kg to a maximum of 90 mg total dose should be administered, with 10% (0.09 mg/kg) given as an
intravenous bolus over one minute and the remaining 90% (0.81 mg/kg) given as an intravenous infusion over 60 minutes [Strong recommendation; High
quality of evidence].
iv. (NEW FOR 2022) Tenecteplase may be considered as an alternative to alteplase within 4.5 hours of acute stroke symptom onset [Strong recommendation;
Moderate quality of evidence].
a. Tenecteplase dose: If administering Tenecteplase, the dose of 0.25 mg/kg up to a maximum of 25 mg should be administered, given as a single bolus
over 5 seconds [Strong recommendation; Moderate quality of evidence].
Caution: The dosing of alteplase and tenecteplase for stroke is NOT the same as the dose protocols for administration of these medications for
myocardial infarction or massive pulmonary embolism.
v. Individuals receiving IV thrombolysis should be closely monitored for the first 24 hours for complications from IV thrombolysis administration:
a. For patients with sudden deterioration during or following administration of IV thrombolysis, an emergent CT scan should be done [Strong
recommendation; Moderate quality of evidence].
b. For patients with orolingual angio-edema:
1. IV thrombolysis should be discontinued if still infusing at the first signs of angioedema [Strong recommendation; Moderate quality of
evidence].
2. The following medications are recommended: antihistamines (H1 blocker [e.g., diphenhydramine], H2 blocker [e.g., famotidine]). Consider
glucocorticoids inhaled racemic epinephrine as part of standard airway management [Strong recommendation; Low quality of evidence].
For patients with symptomatic ICH following IV thrombolysis refer to section 5.6.
c. Systemic hemorrhage: For patients with spontaneous systemic hemorrhage at a non-compressible site (e.g., gastrointestinal hemorrhage, oral
hemorrhage), IV thrombolysis should be discontinued, consideration should be given to lowering blood pressure, and hemostatic management
should be considered [Strong recommendation; Low quality of evidence].
1. Consultation with appropriate specialists should be undertaken to aid in achieving hemostasis [Strong recommendation; Low quality of
evidence].
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1. Consent: Intravenous thrombolysis and EVT are considered the standard of care for acute stroke treatment. Routine procedures for emergency consent
apply.
2. Intravenous thrombolytic administration for patients on Direct oral anticoagulants (DOACs): Intravenous thrombolytics should not routinely be
administered to patients on DOACs who present with acute ischemic stroke. In comprehensive stroke centres with access to specialized tests of
DOAC levels and reversal agents, thrombolysis could be considered, and decisions should be based on individual patient characteristics, in consultation
with thrombosis specialists, patients, and their families.
a. The benefits and risks of providing intravenous thrombolysis to a patient who is being treated with the combination of antiplatelet and low-dose
DOAC (i.e., COMPASS trial protocol) are unclear. Treatment may be considered in consultation with a stroke expert.
b. Anticoagulation is not a contraindication for EVT, and the decision to treat should be based on individual patient factors and assessment of benefit
and risk.
c. Patients who present with stroke who are taking a DOAC may be considered for rapid reversal if otherwise eligible for IV thrombolysis and if a reversal
agent is readily available. Consultation with an expert in stroke care in strongly advised for these cases.
3. The use of epinephrine in angioedema or refractory hypotension should be reserved for life-threatening emergencies due to increased risk of hypertension
post-medication administration.
4. There are some situations where clinical trial data to support the use of intravenous thrombolytic therapy is more limited. In these situations, urgent
consultation with a stroke expert is recommended along with the clinical judgment of the treating physician and discussion with the patient or
substitute decision-makers.
a. For example, this may apply to pediatric patients with stroke (newborn to age 18 years); and pregnant women who experience an acute ischemic
stroke. Refer to Canadian Stroke Best Practices Management of Acute Stroke During Pregnancy Consensus Statement for additional information.53
5. (NEW FOR 2022) Evidence for the use of intravenous thrombolysis and EVT is derived from randomized trials that enrolled patients who were functionally
independent at baseline. The use of intravenous thrombolysis and/or EVT in patients who are not functionally independent may be considered, based on
careful review of risks and benefits for the patient. The patient’s goals of care should be discussed in consultation with a physician with stroke expertise,
and/or a neurointerventionalist, and the patient and/or family and/or substitute decision-makers.
6. (NEW FOR 2022) Hypertension with symptomatic ICH: In patients with symptomatic ICH who are hypertensive (>185/110 mm HG), blood pressure should
be lowered, however, the specific target and duration of therapy are unknown at this time.
i. Patients already admitted to hospital* who present with a sudden onset of new stroke symptoms should be rapidly evaluated without delay for eligibility
for acute stroke treatment and provided with access to appropriate acute stroke treatments (including IV thrombolysis and EVT) [Strong recommendation;
Moderate quality of evidence].
Note: When an inpatient has a stroke while in hospital, all other sections of the CSBP modules apply to these patients for assessment, diagnosis,
management, and recovery.
* “Admitted to hospital” is defined as any person admitted to an emergency department, inpatient unit, or outpatient clinic or rehabilitation service in a
hospital setting.
Refer to Section 4.2 and to online Supplemental Materials Boxes 4A, 4B, and 4C for detailed recommendations on neuroimaging-based selection criteria.
i. Endovascular Thrombectomy (EVT) should be offered within a coordinated system of care including coordination among emergency medical services,
access to rapid neurovascular (brain and vascular) imaging, the emergency department, the stroke team and radiology, local experts in neuro
intervention, anesthesia, and access to a stroke unit for ongoing management [Strong recommendation; High quality of evidence].
ii. EVT is indicated in patients based on imaging selection, most commonly performed with non-contrast CT head and CT angiography (including extracranial
and intracranial arteries) [Strong recommendation; High quality of evidence]. Refer to online Supplemental Materials Box 5C for inclusion criteria for EVT.
iii. EVT may be indicated in patients with proximal anterior circulation occlusions who have received intravenous thrombolysis, as well as those who are not
eligible for intravenous thrombolysis [Strong recommendation; High quality of evidence].
iv. Intravenous thrombolysis should be provided to all eligible patients, including those patients who are also eligible for EVT [Strong recommendation; High
quality of evidence].
a. For patients who are also eligible for intravenous thrombolysis, this should be initiated while simultaneously preparing the angiography suite for EVT
[Strong recommendation; High quality of evidence]. Treatment with either intravenous thrombolysis or EVT should not be delayed for any reason.
v. For large artery occlusions in the anterior circulation, EVT should be considered based on patient pre-morbid function, clinical deficit, and imaging findings.
Patients who can be treated within 6 hours of symptom onset (i.e., arterial access within 6 hours of last known well time) should receive EVT [Strong
recommendation; High quality of evidence]. Refer to online Supplemental Materials Box 4B for Imaging Inclusion Criteria for endovascular thrombectomy.
vi. Selected patients with LVO and who are eligible based on premorbid status and advanced neuroimaging, should be treated with EVT within 24 hours of last
known well time (i.e., arterial access within 24 hours of last known well time) [Strong recommendation; High quality of evidence]. Refer to online
Supplemental Materials Box 4C for imaging inclusion criteria for EVT beyond 6 hours from stroke symptom onset.
(Continued)
(Continued )
viii. For endovascular interventions, procedural sedation is generally preferred over intubation and general anesthesia in most patients [Strong
recommendation; Moderate quality of evidence]
ix. General anesthesia is appropriate if medically indicated (e.g., for airway compromise, respiratory distress, depressed level of consciousness, severe
agitation, or other indication potentially impairing the technical ability to perform the procedure, as determined by the treating physician). General
anesthesia may also be considered if technical complexity is expected during the stroke intervention. In such cases, excessive and prolonged hypotension
and time delays should be avoided [Strong recommendation; Moderate quality of evidence].
1. For patients transferred to an EVT-enabled hospital, repeat neuroimaging immediately on arrival, to confirm eligibility, may be considered. The decision to
repeat may be based on multiple factors: initial imaging features (including quality), clinical presentation, adjuvant medical therapies, changes in health
status, and delay in arrival to the EVT-enabled site. Repeat imaging may include part or all of the neuroimaging recommended in Section 4.2.
2. Device selection should be at the discretion of the interventionalists based on clinical and technical factors during the procedure.
3. There should be a process at EVT centres to activate anesthesia without delay when deemed necessary.
4. Patients with stroke discovered on awakening or with unknown last known well time should be considered for EVT if eligible based on imaging findings and
clinical presentation. Refer to online Supplemental Materials Box 5C for more information.
5. For patients undergoing EVT following administration of thrombolysis, there should not be a delay in proceeding to EVT to determine clinical effectiveness
of thrombolysis.
6. (NEW FOR 2022) When a patient who is eligible for both intravenous thrombolysis and EVT presents DIRECTLY TO AN EVT-CAPABLE HOSPITAL, a decision
not to administer intravenous thrombolysis and proceed straight to EVT must balance both the patient-related and operational factors in play at that
moment, for that patient. The overarching focus is to improve patient outcomes while safely reducing door-to-needle and door-to-puncture times. The
main driver for an excellent outcome remains “time is brain”.
Note: Clinical consideration 6 is controversial. It will be updated as additional evidence becomes available. In the meantime, clinicians involved in acute
stroke care should focus on improving patient outcomes while safely reducing door-to-needle and door-to-puncture times. The main driver for excellent
outcomes remains “time is brain”.
i. Seizure in the presence of suspected acute stroke is not a contraindication for revascularization and could be treated using appropriate short-acting
medications (e.g., lorazepam IV) if the seizures are not self-limited [Conditional recommendation; Low quality of evidence].
Note: Section 5.6 applies to patients experiencing a cerebral or systemic hemorrhage following administration of intravenous thrombolysis. Refer to CSBPR
guidelines on Management of Intracerebral Hemorrhage for additional information.18
i. Intracranial hemorrhage should be considered if there is a change in neurological symptoms or signs, especially a reduction in level of consciousness, or a
spike in blood pressure with persisting blood pressure elevation, or new or worsened headache [Strong recommendation; Moderate quality of evidence].
ii. An immediate non-contrast CT head should be done to assess for intracranial hemorrhage [Strong recommendation; Moderate quality of evidence].
iii. The patient should be accompanied to the CT by a member of the stroke team and the results reviewed immediately. If there is no intracranial
hemorrhage, CTA should be urgently considered to identify intracranial occlusion and the need for urgent EVT should be considered [Strong
recommendation; Moderate quality of evidence].
iv. If intracranial hemorrhage is identified, the intravenous thrombolysis infusion should be discontinued immediately if it is still running [Strong
recommendation; Moderate quality of evidence].
v. If intracranial hemorrhage is identified, blood work, including a complete blood count (CBC) and INR (PT), as well as type and cross, should be drawn
[Strong recommendation; Moderate quality of evidence], with STAT results requested [Strong recommendation; Low quality of evidence].
vi. The following agents may be considered, as they have shown potential benefit and limited harm: cryoprecipitate, human fibrinogen concentrate fresh
frozen plasma, tranexamic acid. Use of these medications should be considered on an individual, case-by-case basis [Conditional recommendation; Low
quality of evidence].
vii. The following treatment options should probably be avoided as they have not shown benefit and have shown potential for harm: prothrombin complex
concentrates, platelet transfusions, factor VIIa [Conditional recommendation; Low quality of evidence].
(Continued)
(Continued )
Note: For systemic hemorrhage, follow local protocol for management guidance.
i. A diagnosis of systemic bleeding should be considered when the following are present or suspected [Strong recommendation; Moderate quality of evidence]:
a. Visible bleeding at a compressible site
b. Reduction in blood pressure, localized pain, diaphoresis, or other signs of hypovolemic shock.
ii. If systemic bleeding is identified, blood work including a CBC, INR (PT), and fibrinogen, should be drawn [Strong recommendation; Moderate quality of
evidence], with STAT results requested [Strong recommendation; Low quality of evidence].
iii. If systemic bleeding is identified, the intravenous thrombolysis infusion should be discontinued immediately if it is still running [Strong recommendation;
Moderate quality of evidence].
iv. If there is visible bleeding (e.g., at the IV site, abrasion, epistaxis), compression should be applied, and the application of ice considered [Strong
recommendation; Moderate quality of evidence].
v. Patient should be transfused as required and according to local protocols [Strong recommendation; Low quality of evidence].
Refer to Section 4.2 and Box 4A for detailed recommendations on neuroimaging-based selection criteria, and online Supplemental Materials for additional
information.
While these criteria are designed to guide clinical decision-making, the decision to use thrombolysis should be based on the clinical judgment of the
treating physician. The relative benefits of thrombolysis versus potential risks or contraindications should be weighed on an individual basis.
Inclusion Criteria
Patients should be considered eligible for intravenous thrombolysis and/or EVT if they fulfill the following clinical criteria:
• Diagnosed with an acute ischemic stroke.
• The stroke is disabling (i.e., significantly impacting function), usually defined as National Institutes of Health Stroke Scale (NIHSS)>4.
• The risks and benefits of thrombolysis are within the patient’s goals of care and take into consideration their functional status prior to stroke.
Relative Exclusion Criteria (requiring clinical judgement based upon the specific situation. Consult Stroke Specialist at Comprehensive Stroke Centre if
there are any questions or concerns about these criteria)
Historical
• History of intracranial hemorrhage.
Clinical
• Stroke symptoms due to another non-ischemic acute neurological condition such as seizure with post-ictal Todd’s paralysis or focal neurological signs due
to severe hypo- or hyperglycemia.
• Hypertension refractory to aggressive hyperacute antihypertensive treatment such that target blood pressure <180/105 cannot be both achieved and
maintained.
(Continued)
(Continued )
• Currently prescribed and taking a direct non-vitamin K oral anticoagulant. Refer to Section 5.2 Clinical Considerations for additional information.
CT or MRI Findings
• CT showing early signs of extensive infarction (e.g., >1/3 of middle cerebral artery [MCA] territory, or ASPECTS score <6).
Laboratory
• Blood glucose concentration <2.7 mmol/L or >22.2 mmol/L.
Refer to Section 4.2 and Boxes 4B and 4C for detailed recommendations on neuroimaging-based selection criteria.
Patients should be considered eligible for endovascular thrombectomy if they fulfill the following clinical criteria:
1. Diagnosed with an acute ischemic stroke.
2. The stroke is disabling (i.e., significantly impacting function), usually defined as National Institutes of Health Stroke Scale (NIHSS)>4.
3. There is a proven, clinically relevant (symptomatic), intra- or extracranial acute arterial occlusion that is amenable to endovascular intervention.
4. The risks and benefits of endovascular thrombectomy are within the patient’s goals of care and take into consideration their functional status prior to
stroke.
5. Age ≥18 years. (Refer to pediatric guidelines for treatment <18 years of age).
a. Currently, there is no evidence for EVT in pediatric populations and the decision to treat should be based on the potential benefits and risks of the
therapy, made by a physician with pediatric stroke expertise in consultation with the EVT provider and the patient and/or family or substitute
decision-makers.
6. Intravenous thrombolysis: If intravenous thrombolysis is given in conjunction with endovascular thrombectomy, refer to Box 5B for additional inclusion
criteria.
7. Premorbid condition criteria: In general, individuals considered eligible for EVT are those who were deemed functionally independent before their index
stroke (i.e., mRS <3) and have a life expectancy >3 months. Note: These criteria are based on major clinical trial inclusion criteria. Decisions should be based
on these factors, clinical judgement, and the patient’s goals of care.
8. Imaging: Patients must qualify for imaging criteria in early and late windows as described in Boxes 4B and 4C.
9. Time to treatment: The decision to proceed with EVT should be shared by the physician with clinical stroke expertise and the neuro-interventionalist, who
will use the available imaging information as is indicated.
a. Specifically:
i. Patients should have immediate neurovascular imaging (see above) to determine eligibility. Patients can be considered for imaging within a
24-hour window from stroke symptom onset or last known well.
ii. For patients presenting <6 hours from stroke symptom onset or last known well to initiation of treatment (i.e., arterial puncture), all patients
who meet eligibility criteria should be treated.
iii. For patients presenting between 6 and 24 hours from last known well, selected patients may be treated if they meet clinical and imaging
criteria and based on local protocols and available expertise in EVT.
Section 6: Acute Antiplatelet Therapy no significant difference between groups in the frequency of symp-
tomatic ICH.
Early antiplatelet therapy, provided soon after ischemic stroke, is
Short-term DAPT, for up to 21 days following ischemic stroke,
known to improve outcomes. Acetylsalicylic acid (ASA) is the most with either clopidogrel or ticagrelor is more effective than ASA
commonly used agent. Results from two of the largest trials of ASA alone in reducing the risk of recurrent ischemic stroke in selected
from several decades ago, the Chinese Acute Stroke Trial (CAST)54 patients. In the POINT trial, Johnston et al.56 estimated that for
and the International Stroke Trial (IST)55 represent the majority every 1,000 patients treated with 75 mg clopidogrel plus 81 mg
of the evidence base. In CAST, there were 5.4 fewer deaths aspirin for 90 days, 15 ischemic strokes would be prevented but
and 4.7 fewer recurrent strokes per 1000 patients treated with 5 major hemorrhages would result. The greatest protection from
daily aspirin of 160 mg after 4 weeks. In the aspirin arm of the fac- treatment was seen in the first 21 days during which the risk of
torial IST, patients with a suspected acute ischemic stroke received a major ischemic event was lowered by 35%. Although the antipla-
300 mg/day of aspirin and a similar number avoided aspirin for telet regimen in the CHANCE trial57 was slightly different than in
14 days. The risk of recurrent ischemic stroke was significantly the POINT trial, the results were similar, in that the risk of recur-
lower in the aspirin arm, with a number needed to treat of 91, with rent ischemic stroke was reduced by 33% in the DAPT group.
a. For patients with delayed swallow screen or potential dysphagia, ASA (81 mg daily) or clopidogrel (75 mg daily) may be administered by enteral tube
or ASA (325 mg daily) by rectal suppository [Strong recommendation; Moderate quality of evidence]. Note: ASA and clopidogrel should only be
administered orally once dysphagia screening has been performed and indicates an absence of potential dysphagia.
ii. For endovascular thrombectomy (EVT) patients who did not receive intravenous thrombolysis and with no other contraindications, administration of an
antiplatelet agent should not be delayed [Strong recommendation; Moderate quality of evidence].
iii. For patients with stroke who are discharged directly from the emergency department to the community, antiplatelet therapy should be started prior to
discharge [Strong recommendation; Moderate quality of evidence].
i. For patients receiving intravenous thrombolysis therapy, antiplatelet therapy should be avoided within the first 24 hours; antiplatelet therapy could then be
initiated after brain imaging has excluded secondary hemorrhage [Strong recommendation; Moderate quality of evidence].
Refer to Secondary Prevention of Stroke module Sections 6 and 7 for additional information on antithrombotic therapy and anticoagulation for people with atrial
fibrillation beyond the acute period.
a. ASA 162 mg loading dose followed by ASA 81 mg daily plus clopidogrel 300-600 mg loading dose followed by clopidogrel 75 mg daily, for 21 days
[Strong recommendation; High quality of evidence].
OR
b. ASA 162 mg load dose followed by ASA 81 mg daily plus ticagrelor 180 mg loading dose followed by ticagrelor 90 mg BID for 30 days [Strong
recommendation; Moderate quality of evidence].
Note: The choice of the antiplatelet agent to add to ASA (i.e., clopidogrel or ticagrelor) should be based on individual patient and clinical factors,
including the risk of moderate to severe hemorrhage described in the clinical trials.
iii. Use of dual antiplatelet therapy for longer than prescribed, as per 6.2ii/a and 6.2ii/b, following a TIA or minor stroke is not recommended unless there is a
specific indication (e.g., arterial stent; symptomatic intracranial artery stenosis), due to an increased risk of bleeding [Strong recommendation; Moderate
quality of evidence].
a. Patients should be counselled that their dual antiplatelet regimen should be followed by single antiplatelet therapy with either ASA or clopidogrel
indefinitely [Strong recommendation; High quality of evidence].
iv. Patients not meeting criteria for dual antiplatelet therapy should be initiated on a single antiplatelet agent within 24 hours of symptom onset. Suggested
regimens include either:
a. ASA 162 mg loading dose followed by 81 mg daily [Strong recommendation; High quality of evidence].
OR
b. Clopidogrel 300 to 600 mg loading dose followed by 75 mg daily [Strong recommendation; High quality of evidence].
ii. Patients with stroke who are found to have atrial fibrillation should receive oral anticoagulation instead of antiplatelet therapy [Strong recommendation;
High quality of evidence], with timing of initiation at the discretion of the physician based on patient-specific factors including size of infarct [Strong
recommendation; Moderate quality of evidence].
1. Patients who are at a very high risk for TIA or minor ischemic stroke caused by high-grade carotid stenosis who are candidates for urgent carotid
endarterectomy or carotid stenting should be reviewed with the surgeon or interventionalist to determine the appropriate timing and selection of
antiplatelet agent(s).
2. For patients on dual antiplatelet therapy, gastrointestinal protection may be considered for those at higher risk of gastrointestinal bleeding.
3. For patients with acute stroke or TIA and non-valvular atrial fibrillation, anticoagulation should be initiated; however, there is a lack of randomized evidence to
guide specific timing. According to expert consensus, a general approach to the target timing of initiation of DOAC therapy post-stroke is as follows:
a. For patients with a brief TIA and no visible infarct or hemorrhage on imaging, anticoagulation may be started within the first 24 hours post-TIA.
b. For patients with a minor clinical stroke/small non-hemorrhagic infarct on imaging, anticoagulation may be started 3 days post-stroke.
(Continued)
(Continued )
c. For patients with a moderate clinical stroke/moderate-sized infarct on imaging (without hemorrhage on CT), anticoagulation may be started 6 to
7 days post-stroke.
d. For patients with a severe clinical stroke/large-sized infarct on imaging (without hemorrhage on CT), anticoagulation may be started 12 to 14 days
post-stroke.
e. Antiplatelet therapy may be used prior to initiating anticoagulation.
Refer to CSBPR Secondary Prevention of Stroke module Sections 6 and 7 for additional information on management of atrial fibrillation and choice of
therapeutic agents.13
4. For patients who experience a stroke while receiving one antiplatelet agent, stroke etiology should be reassessed and addressed, and all other vascular risk
factors aggressively managed. Continuing the current antiplatelet agent or switching to a different agent are reasonable options. At the time of writing,
evidence is lacking to make more specific recommendations.
5. (NEW FOR 2022) Platelet function assays and pharmacogenetic testing may indicate antiplatelet activity and patients with potential clopidogrel resistance;
however, the clinical implications for stroke prevention treatment are unclear at the time of writing and publication.
In the THALES trial,1 patients with minor acute ischemic stroke of 0–3) at 1 year.58–60 The data are limited for patients over the age
treated with 90 mg ticagrelor twice a day þ 75–100 aspirin mg/ of 60 years. In the DESTINY 2 trial,61 82 patients with a median age
day also experienced fewer recurrent strokes and death within of 70 years were randomized to hemicraniectomy or standard care:
30 days (5.5% vs. 6.6%, HR = 0.83, 95% CI 0.71–0.96, number a significantly higher proportion of patients in the surgical group
needed to treat =92), compared with patients treated with aspirin were alive and living without severe disability (mRS score of 0–4) at
alone.1 However, these benefits were accompanied by a 3.5 to 4 6 months (38% vs.18%, OR = 2.91, 95% CI 1.06–7.49) compared
times increased risk of severe or fatal bleeding and intracranial with patients in the medical management group. However, no
hemorrhage. patients in either the surgical or medical care groups had overall
good outcomes (mRS score of 0–2) at 6 or 12 months and most
of the survivors required assistance with most bodily needs. In a
Section 7: Hemicraniectomy recent systematic review, which included the results from seven
Due to higher risks of cerebral edema, increased intracranial pres- trials, including DESTINY 2, as well as six trials of patients
sure, and subsequent cerebral herniation, mortality is higher for aged <60 years (DESTINY,59 DESTINY II,61 DECIMAL,60 and
patients with malignant MCA stroke. For these patients, decom- HAMLET),62 the odds of a favorable outcome (mRS 0–3) at 1 year
pressive hemicraniectomy may be a surgical option. In persons were significantly higher in the surgical group (adjusted OR = 2.95,
under the age of 60 years, early decompressive hemicraniectomy 95% CI 1.55–5.60) and the odds of death at 1 year were signifi-
increases the odds of a reasonable functional outcome (mRS score cantly lower (adjusted OR = 0.16; 95% CI 0.10–0.24).
i. For patients aged 18 – 60 years old, hemicraniectomy should be considered as a life-saving measure for patients in the early stages of extensive (malignant)
middle cerebral artery (MCA) territory ischemic stroke (defined as infarction size >50% MCA territory on visual inspection, or an ischemic lesion volume
>150 cm3 and concomitant clinical features) if patients or their substitute decision-makers are willing to accept a significant risk of living with a degree of
disability that may leave them dependent on others for their activities of daily living. [Strong recommendation; High quality of evidence].
a. Hemicraniectomy could also be considered for patients aged 60 – 80 years [Conditional recommendation; Moderate quality of evidence].
ii. Posterior fossa decompression should be considered early in patients with significant cerebellar stroke with evidence of mass effect and/or hydrocephalus
[Strong recommendation; Low quality of evidence].
iii. Patients at risk for malignant edema should have a consultation with a stroke specialist and neurosurgeon [Strong recommendation; Low quality of
evidence].
a. If these services are not available on-site, patients should be considered for expedited transfer to a centre where advanced stroke care and
neurosurgical services are available [Strong recommendation; Low quality of evidence].
i. Urgent decisions regarding decompressive craniectomy should be undertaken based on discussions with patient, family members, and substitute decision-
maker regarding a potential decompressive craniectomy [Strong recommendation; Low quality of evidence].
a. Patients with severe stroke due to large vessel occlusions may be at higher risk of developing malignant edema. In these patients, early discussions
should be considered [Conditional recommendation; Low quality of evidence].
b. Key issues to be discussed with the patient, family members, and substitute decision-makers include stroke diagnosis and prognosis if untreated, the
risks of surgery, the possible and likely outcomes following surgery including the odds of living with severe disability, and the patient’s previously
expressed wishes concerning treatment in the event of catastrophic illness [Strong recommendation; Low quality of evidence].
(Continued)
(Continued )
i. Patients at risk of malignant edema should be monitored in an intensive care unit or neuro step-down unit [Strong recommendation; Low quality of
evidence].
a. Monitoring should include assessments of level of consciousness (e.g., Glasgow Coma Scale, Canadian Neurological Scale Score (CNS)), worsening
symptom severity, and blood pressure at least hourly or more frequently if the patient’s condition requires it [Strong recommendation; Low quality
of evidence].
b. If changes in status occur, the stroke team and neurosurgeon should be notified immediately for re-evaluation of the patient [Strong
recommendation; Low quality of evidence]. Changes in status include level of drowsiness/consciousness, change in CNS score by ≥1 point, or
change in National Institutes of Health Stroke Scale (NIHSS) score by ≥4 points [Strong recommendation; Low quality of evidence].
ii. In patients selected for decompressive craniectomy, surgery should be performed within 48 hours from stroke onset, and ideally before clinical
deterioration occurs [Strong recommendation; Moderate quality of evidence].
iii. Patients with suspected elevation in intracranial pressure may be managed according to institutional protocols (e.g., administration of hyperosmolar
therapy, head of bed elevation) [Conditional recommendation; Low quality of evidence].
1. Global disability and quality of life outcomes are similar regardless of whether the hemicraniectomy was for right or left sided MCA infarction.
2. Whereas age alone is not a reason to forego hemicraniectomy, the DESTINY II trail reported that for 0% of patients over 60 years had mild or no disability
(mRS of 0 – 2), and only 7% could function independently (mRS 0-3) after hemicraniectomy surgery.
Section 8: Acute Stroke Unit Care outcome (OR = 0.77, 95% CI 0.69 to 0.87), and death or depend-
ency (OR = 0.75, 95% CI 0.66 to 0.85) at a median follow-up of
Patients who are admitted to stroke units are more likely to survive,
1 year. These results were based on moderate quality evidence.
return home, and regain their independence compared to patients Stroke unit care was superior regardless of age, sex, initial stroke
who are admitted to non-specialized units. The most recent update severity, stroke type, trial quality, and duration of follow-up.
of the Stroke Unit Trialists’ Collaboration63 identified 29 random- In Canada, access to stroke unit care varies by region. A survey
ized and quasi-randomized trials, including 5,902 participants, conducted in 2013/14 identified 32 stroke units within the province
comparing stroke unit care with alternative, less organized care of Ontario, of which 21 were acute stroke units, 10 were integrated
(e.g., an acute medical ward). Compared to less organized forms stroke units, and 1 which was classified as a rehabilitation stroke
of care, stroke unit care was associated with a significant reduction unit.64 The estimated average number of stroke patients served
in the odds of death (OR = 0.76, 95% CI 0.66 to 0.88), a poor per stroke unit was 604 with large variation across centers.
a. Facilities without a dedicated stroke unit must strive to focus care on the priority elements for comprehensive stroke care delivery, including
clustering patients, having an interdisciplinary team, providing access to early rehabilitation, using stroke care protocols, conducting case
rounds, and providing patient education [Strong recommendation; Moderate quality of evidence].
Note: Stroke unit care is the gold standard for care following acute stroke. Alternate models may be discussed with system planners and should
only be considered if it is not possible to create or access a stroke unit. Refer to online Supplemental Materials Box 8A Optimal Acute Inpatient
Stroke Care for additional information.
ii. The core interdisciplinary stroke team should consist of healthcare professionals with stroke expertise including physicians, nurses, occupational
therapists, physiotherapists, speech-language pathologists, social workers, dietitians, patients, and family members [Strong recommendation; High
quality of evidence], who are ideally available seven days a week [Strong recommendation; Low quality of evidence].
a. All interdisciplinary stroke teams should include hospital pharmacists to promote patient safety; conduct medication reconciliation; provide
education to the team and patients and families about medications and their side effects, adverse effects, and interactions; promote
adherence; and participate in discharge planning which could include addressing special needs for patients, such as individual dosing packages
[Strong recommendation; Moderate quality of evidence].
b. Additional members of the interdisciplinary team may include discharge planners or case managers, (neuro)psychologists, palliative care
specialists, recreation and vocational therapists, spiritual care providers, peer supporters, and stroke recovery group liaisons [Strong
recommendation; Moderate quality of evidence].
(Continued)
(Continued )
d. All professional members of the interdisciplinary stroke team should have specialized training in stroke care and recovery [Strong recommendation;
Moderate quality of evidence].
iii. The interdisciplinary stroke team should assess all patients as soon as possible after admission to hospital, and ideally within 48 hours, and formulate a
management plan [Strong recommendation; High quality of evidence].
iv. Assessments of impairment, functional activity limitations, role participation restrictions, and environmental factors should be conducted using
standardized, valid assessment tools [Strong recommendation; Moderate quality of evidence].
a. Patients should be assessed for areas such as dysphagia, mood and cognition, mobility, functional assessment, temperature, nutrition, bowel and
bladder function, skin breakdown, vision, apraxia, neglect, and perception [Strong recommendation; Moderate quality of evidence]. Refer to Section
9 Inpatient Prevention and Management of Complications Following Stroke for additional information.
b. Patients should have a formal and individualized assessment to determine the type of ongoing post-acute rehabilitation services they require as
soon as their status has stabilized, and within the first 72 hours post-stroke, using a standardized protocol [Strong recommendation; Moderate
quality of evidence]. Refer to CSBPR Rehabilitation and Recovery Following Stroke module29 Section 3 for additional information.
c. Tools should be adapted for use with patients who have communication differences or limitations as required [Strong recommendation; Moderate
quality of evidence].
v. Discharge planning discussions, prevention therapies, and venous thromboembolism prophylaxis should be initiated soon after arrival on the acute stroke
unit [Strong recommendation; Moderate quality of evidence]. Refer to Section 9 Inpatient Prevention and Management of Complications Following Stroke for
additional information.
Section 9: Inpatient Prevention and Management of include pharmacological venous thromboembolism prophylaxis,68
Complications Following Stroke 2022 and the use of thigh-high intermittent pneumatic compression
Medical complications are relatively common following stroke and (IPC) devices,69 to prevent thromboembolism, dysphagia screen-
may negatively impact the recovery process, with the potential to ing to reduce the risk of pneumonia,70 and the avoidance of the
result in poorer outcomes.65 Estimates of the percentage of patients use of indwelling catheters to prevent urinary tract infections.71
who experience at least one medical complication during hospitali- Early mobilization post-stroke can reduce the length of hospitali-
zation vary widely from 25%66 to 85%.67 Some of the most com- zation and is associated with greater ability to perform activities of
monly cited complications include urinary tract infections, fever, daily living at 3 months.72 Cardiac investigations should also be
pneumonia, and deep vein thrombosis (DVT). Examples of mea- conducted to identify previously undetected or paroxysmal atrial
sures that can be taken to reduce the risks of these complications fibrillation, or other cardiac abnormalities.73,74
ii. Patients should be evaluated and treatment plans initiated for secondary prevention of vascular risk factors, including hypertension, diabetes,
dyslipidemia and smoking cessation [Strong recommendation; Moderate quality of evidence]. Refer to CSBPR Secondary Prevention of Stroke module
for additional information.13
(Continued)
(Continued )
iv. Transition planning should begin as a component of the initial admission assessment and continue throughout hospitalization as part of ongoing care of
patients with acute stroke [Strong recommendation; Moderate quality of evidence]. Refer to CSBPR Transitions and Community Participation Following
Stroke module43 Section 3 for additional information.
v. All patients, family members, and informal caregivers should receive timely and comprehensive information, education, and skills training about stroke
from interdisciplinary team members [Strong recommendation; Moderate quality of evidence]. Refer to CSBPR Transitions and Community Participation
Following Stroke module43 Sections 1 and 2 for additional information.
vi. Patients should undergo an initial screening for depression, including screening for a history of depression [Strong recommendation; Moderate quality of
evidence]. Refer CSBPR Mood, Cognition and Fatigue75 Section 1 for additional information.
vii. Stroke assessments should include evaluation of risk factors for depression, particularly a history of depression [Strong recommendation; Low quality of
evidence].
viii. Patients should undergo an initial screening for vascular cognitive impairment when indicated [Strong recommendation; Moderate quality of evidence].
Refer to CSBPR Mood, Cognition and Fatigue75 Section 2 for additional information.
i. Patients with suspected ischemic stroke or TIA should have a 12-lead electrocardiogram (ECG) to assess for atrial fibrillation, concurrent myocardial
infarction, or structural heart disease (e.g., left ventricular hypertrophy) as potential causes of or risk factors for stroke [Strong recommendation;
Moderate quality of evidence].
ii. For patients being investigated for an acute embolic ischemic stroke or TIA, ECG monitoring for 24 hours or more is recommended as part of the initial
stroke work-up to detect paroxysmal atrial fibrillation in patients who would be potential candidates for anticoagulant therapy [Strong recommendation;
High quality of evidence].
iii. For patients being investigated for an acute embolic ischemic stroke or TIA of undetermined source whose initial short-term ECG monitoring does not
reveal atrial fibrillation but a cardioembolic mechanism is suspected, prolonged ECG monitoring for at least 2 weeks is recommended, as soon as
practically possible, to improve detection of paroxysmal atrial fibrillation in selected patients ≥55 years who are not already receiving anticoagulant
therapy but would be potential anticoagulant candidates [Strong recommendation; High quality of evidence]. Refer to CSBPR Secondary Prevention of
Stroke module13 for additional information.
iv. Routine echocardiography is not recommended for all patients with stroke. Echocardiography should be considered for patients with an embolic ischemic
stroke or TIA of undetermined source, or when a cardioembolic etiology or paradoxical embolism is suspected [Strong recommendation; Moderate quality
of evidence].
v. For patients ≤60 years who are being investigated for an embolic ischemic stroke or TIA of undetermined source, echocardiography with saline bubble
study is recommended for detection of a patent foramen ovale (PFO) if it may change patient management (i.e., in patients who would be potential
candidates for PFO closure or anticoagulant therapy if a PFO were detected) [Strong recommendation; Moderate quality of evidence].
a. Contrast-enhanced (agitated saline) transesophageal echocardiography or transcranial Doppler has greater sensitivity than transthoracic
echocardiography for detection of right-to-left cardiac and extra-cardiac shunts and should be conducted when available [Strong
recommendation; Moderate quality of evidence].
iv. For patients with stroke admitted to hospital and who are immobile for >30 days, the use of ongoing venous thromboembolism prophylaxis (e.g., with
pharmacological venous thromboembolism prophylaxis) is recommended [Strong recommendation; Low quality of evidence].
v. If intermittent pneumatic compression is considered after the first 24 hours of admission, venous leg Doppler studies should be considered [Strong
recommendation; Low quality of evidence].
(Continued)
(Continued )
1. Use of LMWH or UFH should be weighed against the potential risk for intracerebral hemorrhage for each individual patient.
ii. For temperature >37.5 Celsius, frequency of monitoring should be increased, temperature-reducing measures should be initiated, causes of possible
infection such as pneumonia or UTI should be investigated, and antipyretic and antimicrobial therapy should be initiated as required [Strong
recommendation; Moderate quality of evidence].
9.4 Mobilization
Definition: Mobilization is the process of getting a patient to move in the bed, sit up, stand, and eventually walk.
i. All patients admitted to hospital with acute stroke should have an initial assessment, conducted by rehabilitation professionals, as soon as possible after
admission and using a standardized tool [Strong recommendation; Moderate quality of evidence].
ii. Initial screening and assessment should be commenced as early as possible, and ideally within 48 hours of admission by rehabilitation professionals who
are in direct contact with the patient [Strong recommendation; Moderate quality of evidence]. Refer to the CSBPR Rehabilitation and Recovery Following
Stroke module29 for additional recommendations on mobilization following an acute stroke.
iii. Rehabilitation therapy should begin as early as possible once the patient is determined to be medically able to participate in active rehabilitation [Strong
recommendation; High quality of evidence].
iv. Early prolonged mobilization of patients within the first 24 hours after a stroke, especially a severe stroke, is not recommended [Strong recommendation;
High quality of evidence].
v. Earlier mobilization may be reasonable for some patients with acute stroke (e.g., people with milder strokes or TIA) but caution is advised and clinical
judgement should be used [Conditional recommendation; Low quality of evidence].
Note: Contraindications to early mobilization include, but are not restricted to, patients who have had an arterial puncture for an interventional procedure;
or patients who have unstable medical conditions, low oxygen saturation, and/or lower limb fracture or injury.
Refer to CSBPR Rehabilitation and Recovery Following Stroke module for additional recommendations on mobilization following an acute stroke.29
a. Patients who have an immediate post-stroke seizure should be monitored for recurrent seizure activity [Strong recommendation; Low quality of
evidence].
b. Recurrent seizures in patients with ischemic stroke should be treated as per local treatment recommendations for seizures in other neurological
conditions [Strong recommendation; Moderate quality of evidence].
ii. A single, self-limiting seizure occurring at the onset or within 24 hours after an ischemic stroke is considered an “immediate” post-stroke seizure and does
not require long-term anticonvulsant medications [Conditional recommendation; Low quality of evidence].
iii. Prophylactic use of anticonvulsant medications in patients with ischemic stroke is not recommended [Strong recommendation; Moderate quality of
evidence]
iv. Continuous or repeat electroencephalogram monitoring in patients with a stroke and unexplained reduced level of consciousness should be considered
[Conditional recommendation; Moderate quality of evidence].
ii. The swallowing, nutritional and hydration status of patients with stroke should be screened as early as possible, ideally within 24 hours of admission, using
validated screening tools [Strong recommendation; Moderate quality of evidence].
iii. Abnormal results from the initial or ongoing swallowing screens should trigger a prompt referral to a speech-language pathologist, occupational therapist,
dietitian, and/or other trained dysphagia clinicians for more detailed assessment and management of swallowing, feeding, nutritional, and hydration
status [Strong recommendation; Moderate quality of evidence].
a. An individualized management plan should be developed to address therapy for dysphagia, dietary needs, and specialized nutrition plans [Strong
recommendation; Moderate quality of evidence].
(Continued)
(Continued )
iv. For patients who cannot safely swallow or meet their nutrient and fluid needs orally, enteral nutrition (e.g., nasogastric tube feeding) should be considered
in consultation with the patient, family, or substitute decision-maker, and the interdisciplinary team as early as possible after admission, usually within the
first three days of admission [Strong recommendation; Moderate quality of evidence]. Refer to CSBPR Rehabilitation and Recovery Following Stroke module
Section 7 for additional information on dysphagia screening, assessment, and management.29
a. Nasogastric feeding tubes should be replaced by gastric-jejunum tube (GJ-tube) if the patient requires a prolonged period of enteral feeding [Strong
recommendation; Moderate quality of evidence]
9.7 Continence
i. Indwelling catheters should be used cautiously due to the risk of UTIs [Strong recommendation; High quality of evidence].
a. If used, indwelling catheters should be assessed daily and removed as soon as possible [Strong recommendation; High quality of evidence].
b. Peri care and infection prevention strategies should be implemented to minimize risk of infection [Strong recommendation; Moderate quality of
evidence]. Refer to Section 4.6(iii) for additional information.
ii. Patients with stroke should be screened for urinary incontinence and retention, with or without overflow; fecal incontinence; and constipation [Strong
recommendation; Moderate quality of evidence].
iii. The use of a portable ultrasound machine is recommended as the preferred non-invasive method to assess post-void residual [Conditional
recommendation; Low quality of evidence].
iv. Patients with stroke with urinary incontinence should be assessed by trained personnel using a structured functional assessment to determine cause and
develop an individualized management plan [Strong recommendation; Moderate quality of evidence].
v. Patients with stroke with urinary incontinence should have a bladder-training program implemented [Conditional recommendation; Low quality of
evidence].
a. The bladder training program should include timed and prompted toileting on a consistent schedule [Conditional recommendation; Moderate
quality of evidence].
b. Appropriate intermittent catheterization schedules should be established based on amount of post-void residual [Conditional recommendation;
Moderate quality of evidence].
vi. Patients with stroke with persistent constipation or bowel incontinence should have a bowel management program implemented [Strong
recommendation; Moderate quality of evidence].
ii. For patients with stroke wearing a full or partial denture it should be determined if they have the neuromotor skills to safely wear and use the appliance(s)
[Strong recommendation; Low quality of evidence].
iii. For patients where there are concerns about oral hygiene and/or appliances, a referral to a dentist for consultation and management should be made as
soon as possible [Strong recommendation; Moderate quality of evidence].
iv. Patients with stroke should receive oral care consistent with the Canadian Dental Association recommendations, and the oral care should address areas
such as frequency of oral care (ideally after meals and before bedtime); types of oral care products (toothpaste, floss, mouthwash); and management for
patients with dysphagia [Strong recommendation; Moderate quality of evidence].
Section 10: Advance Care Planning there was a perceived lack of urgency by participants, many of whom
felt the physician and/or family members would make decisions in
Advance care planning (ACP) is a process of reflection and com-
accordance with their wishes; second, there was a lack of initiation by
munication in which individuals reflect on their wishes and values
HCPs to discuss issues around ACP; third, HCPs expressed hesita-
to make decisions regarding their healthcare in consultation with tion about initiating discussions related to ACP, and uncertainty as
healthcare providers, should they become incapable of participat- the best timing for such discussions. Fourth, there was also a lack of
ing in decision-making at a later date.76 While there is evidence understanding of ACP, especially as compared to advance directives,
supporting ACP in the primary care setting, there are limited data designation of care, and living wills.
on ACP in acute care in general, and even less following stroke. Although no stroke-specific studies have been published that
Green et al.77 used participant observation and semi-structured inter- examine the effectiveness of ACP, several studies included patients
views to gather information related to the communication process with stroke. Results from a small number of studies suggest that
regarding ACP from 14 patients, recruited from an acute stroke unit interventions aimed at increasing ACP have been successful in sig-
and 2 rehabilitation units, and 4 HCPs. Four key themes emerged as nificantly increasing the likelihood that end-of-life wishes are
to why or why not participants engaged in the ACP process. First, known and respected.78,79
ii. Respectful advance care planning should be integrated as part of a comprehensive care plan, taking into consideration values and preferences
with information regarding the patient’s illness, understanding, prognosis, medically appropriate treatments and future medical care [Strong
recommendation; Low quality of evidence].
iii. Advance care planning may include identifying a substitute decision-maker (proxy, agent, or power of attorney), and discussing the patient’s personal
values and preferences to be applied in future if the need arises to make healthcare decisions or provide consent on behalf of the patient [Strong
recommendation; Moderate quality of evidence].
a. Advance care planning discussions should be documented and reassessed regularly with the active care team and substitute decision-maker,
especially when there is a change in the patient’s health status [Strong recommendation; Low quality of evidence].
1. The interdisciplinary stroke care team should have the appropriate communication skills and knowledge to respectfully address the physical, spiritual,
cultural, psychological, ethical, and social needs of the person with stroke and their family and informal caregivers.
2. Ensure advance care planning discussions are individualized and culturally sensitive.
3. Processes should be established to support, patients, family and healthcare staff who are experiencing conflicts over advanced care decisions being made
by the patient or substitute decision maker. Referrals can be made to social work, palliative care, spiritual care, and ethics.
Section 11: Palliative and End-of-Life Care provider(s) should raise the topic; however, there is agreement that
the approach should be interdisciplinary and patient- and family-
Palliative care is an approach that aims to reduce suffering and
centered. The palliative care needs of patients following stroke are
improve the quality of life for people who are living with life-limit- typically related to the management of common symptoms such as
ing illness through the provision of pain and symptom manage- dyspnea, pain, and xerostomia.83 While palliative care pathways
ment, psychological, social, emotional, spiritual, and practical have been developed to ensure that patients receive the most
support, and support for caregivers during the illness and after appropriate care possible in the last days of life, there is an absence
the death of the person they are caring for.80 Palliative care of high-quality evidence to suggest that current pathways are effec-
provides comprehensive care throughout a person’s illness trajec- tive, highlighting the need for additional research in this area.84 In
tory and is not solely limited to end-of-life care. The role of terms of specific interventions designed to address many common
palliative care may be complicated as prognosis in the earliest palliative care issues, a systematic review by Cowey et al.85 con-
phase of stroke can be unclear.81 There is currently no integrated cluded that there was insufficient evidence to recommend the best
model of palliative care in stroke care addressing the appropriate and most effective approaches to this important and essential com-
moment to initiate palliative care discussions82 or which healthcare ponent of care.
i. A palliative approach should be used when there has been a catastrophic stroke or a stroke in the setting of significant pre-existing comorbidity, to
optimize care for the patients, and their family members and informal caregivers [Strong recommendation; Low quality of evidence].
ii. The interdisciplinary stroke team should have discussions with the patient and decision-makers regarding the patient’s goals of care that includes
consideration of the patient’s diagnosis, prognosis, values, wishes, and whether care should focus on comfort or on prolonging life [Strong
recommendation; Low quality of evidence].
a. There should be regular communication with the patient, family, and informal caregivers to ensure their goals and needs are being met [Strong
recommendation; Low quality of evidence].
b. Palliative and end-of-life discussions should be ongoing and take into account reflect any changes in diagnosis or prognosis [Strong
recommendation; Low quality of evidence].
c. Topics to be discussed with patients, families, and informal caregivers may include the appropriateness of life-sustaining measures, including
mechanical ventilation, enteral/intravenous feeding, and intravenous fluids, and the purpose of all medications, including those for symptom
management [Strong recommendation; Low quality of evidence].
iii. Palliative care discussions should be documented and reassessed regularly with the healthcare team and substitute decision-maker [Strong
recommendation; Low quality of evidence].
iv. Patients, families, informal caregivers, and the healthcare team should have access to palliative care specialists, particularly for consultation about
patients with difficult-to-control symptoms, complex or conflicted end-of-life decision-making, or complex psycho-social family issues [Strong
recommendation; Low quality of evidence].
v. Decisions to initiate, withdraw, or forgo life-prolonging treatments after stroke, including artificial nutrition and hydration, should be made in discussion
with the patient, family, and informal caregivers as appropriate, taking into account the best interests of the person, and including whenever possible
their prior expressed wishes, either in an advanced care plan or through discussions [Strong recommendation; Low quality of evidence].
(Continued)
(Continued )
vii. Organ and tissue donation should be discussed with families and informal caregivers as appropriate [Strong recommendation; Low quality of evidence].
viii. Supportive counselling, funeral support, and bereavement resources should be provided to families and informal caregivers after the patient’s death
[Strong recommendation; Low quality of evidence].
1. The interdisciplinary stroke team should have the appropriate communication skills and knowledge to respectfully address the physical, spiritual, cultural,
psychological, ethical and social needs of the person with stroke, their family and informal caregivers who are involved in the patient’s end-of-life care.
2. For patients with stroke at the end of life, the following areas may be considered where appropriate (note, other areas may be relevant as well for each
individual):
c. Oral care
d. Eye care
e. Pain
f. Delirium
g. Respiratory distress and upper airway secretions
j. Seizures
k. Anxiety and depression. Refer to CSBPR Mood, Cognition and Fatigue module Section 1 for additional information.75
l. Interdisciplinary support for patients, families, and caregivers during dying process
m. Preferred location of palliative care (e.g., home, hospice, another supportive living environment)
n. Preferred person to be notified of patient’s death
Challenges and Future Directions further refinement in the understanding of the risks and benefits
of combination therapy could alter these recommendations.
The 7th update of the Canadian Stroke Best Practice
Specifically, it is anticipated that further experience with tenecte-
Recommendations for Acute Stroke Management provides a
plase may impact this calculus in important ways.
detailed series of recommendations applicable to the care of all
We are also excited about the prospect of further develop-
adults in Canada who have sustained an ischemic stroke or TIA.
ments in the evidence to support EVT for patients with acute
These guidelines have been developed through a rigorous process;
ischemic stroke of the posterior circulation. These patients were
efforts must now turn to their rapid implementation, especially of
excluded from the landmark thrombectomy trials published
the new recommendations, based on emerging high-quality
between 2014 and 2018, and upon which current recommenda-
evidence, so as to increase equitable access to timely acute stroke tions are based. With the advent of data from high-quality ran-
care for all people in Canada. domized trials, we expect to be able to provide more specific
This edition of the guidelines has incorporated Tenecteplase recommendations about thrombectomy for patients suffering
0.25 mg/kg as an alternate thrombolytic for acute ischemic stroke strokes of the posterior circulation in the next edition of these
based on the landmark Canadian AcT trial. It is expected that the guidelines.
knowledge of the clinical applications of tenecteplase will continue The field of neuroprotection is also likely to advance in the com-
to advance, particularly as it pertains to its use in the setting of ing years. The ESCAPE NA-1 trial suggested that nerinetide could
patients with intracranial arterial occlusions who may or may be an effective neuroprotectant in patients with acute ischemic
not be candidates for thrombectomy. stroke not receiving thrombolysis, and that hypothesis is currently
Thrombectomy with or without thrombolysis is the topic of being tested in the Canadian-led ESCAPE NEXT trial. If that trial
several recent randomized trials; this issue will likely be settled should be successful, it will be the first instance in the history of
by the time the next edition of these guidelines is ready for publi- clinical neuroscience that a neuroprotectant agent has been found
cation. At present, trials that most closely reflect Canadian practice to be clinically effective in humans. Such a discovery could
suggest that thrombolysis should NOT be withheld for patients have significant ramifications for the management of acute ische-
who are also candidates for thrombectomy; all eligible patients mic stroke and may also influence the care of patients with ICH,
should receive thrombolysis, regardless of whether they also subarachnoid hemorrhage, traumatic brain injury, and cardiac
may receive thrombectomy. We acknowledge the possibility that arrest.
The advent of mobile stroke units suggests radical change in the easier. CCRP members included Ashley Voth, Sarah Blanchard-Eng, Allan
way acute stroke care could be delivered, at least for some people in Morrison, Patricia Pollock, Heather Purvis, Donna Sharman, Andy Sharman,
Canada. While high-quality randomized trials in the USA, and Louise Nichol.
Germany, and Australia have suggested that mobile stroke units
reduce time to treatment, increase treatment eligibility, and lead Funding. The development of the CSBPR is funded by Heart & Stroke. No
to better outcomes, we do not feel able to provide specific recom- funds for the development of these recommendations come from commercial
interests, including pharmaceutical and device companies. Writing group mem-
mendations for Canadian practice until real-world research
bers and external reviewers are volunteers who do not receive any remuneration
addresses our political, economic, and geographic realities.
for their participation. All participants complete a conflict of interest declara-
We hope that further research will help to address the question tion prior to participating.
of how mobile stroke units may contribute to the further optimi-
zation of stroke care in Canada. Conflicts of Interest. The following authors have identified actual or potential
Lastly, at this time, our knowledge of sex and gender differences conflicts of interest which have been mitigated through the design of a multi-
in acute stroke is evolving. In addition to pregnancy and hormone disciplinary writing group model and additional measures by the advisory com-
therapy, the prevalence of risk factors such as hypertension and mittee as required. Michel Shamy holds a CIHR SPOR Grant, New Frontiers in
atrial fibrillation are higher in women. Stroke symptom severity, Research Fund Grant, participation on a Data Safety Monitoring Board or
presentation, and treatment effectiveness are areas that require fur- Advisory Board for the FRONTIER Trial. Patrice Lindsay is a voluntary
ther research. member of the March of Dimes After Stroke Advisory Board. Gord Gubitz
The focus throughout these guidelines and stroke systems is Site Investigator for AcT, ESCAPE-NEXT, and ECSC-2. Amy Yu holds a
National New Investigator Award from the Heart & Stroke Foundation of
development in Canada and globally has been on an integrated sys-
Canada. Aravind Ganesh received funding from Canadian Institutes of
tem to provide seamless care to the patient with vascular risk fac-
Health Research and Alberta Innovates (paid directly to the Institution),
tors and multimorbidity. Such an approach requires coordinated received research funding from the Canadian Institutes of Health Research,
systems to be in place in all regions of Canada; a challenge given Canadian Cardiovascular Society, Alberta Innovates, Campus Alberta
its vast geographical area with many smaller isolated communities. Neuroscience, Sunnybrook Research Institute INOVAIT, Government of
Quality monitoring and efforts to improve care are ongoing, and Canada – New Frontiers in Research Fund, Microvention, Alzheimer Society
these recommendations will be updated within the next several of Canada, received consulting fees from MD Analytics, My Medical Panel,
years as new evidence emerges. Figure 1, CTC Communications Corp, Atheneum, Deep Bench, Research on
Mind, Creative Research Designs, received payment or honoraria for lectures,
Supplementary material. To view supplementary material for this article, presentations, speakers bureaus, manuscript writing or educational events from
please visit https://doi.org/10.1017/cjn.2022.344. Figure 1, Alexion, Biogen, has a patent filed for a system for patient monitoring
and delivery of remote ischemic conditioning or other cuff-based therapies, is
Acknowledgments. Heart & Stroke gratefully acknowledges the Acute Stroke Member of editorial board of Neurology: Clinical Practice, Neurology, Stroke,
Management writing group leaders and members, all of whom have volunteered Frontiers in Neurology, and holds stock options for SnapDx, Advanced Health
their time and expertise to the update of these recommendations. Members of Analytics (AHA Health Ltd), TheRounds.com, Collavidence. Sacha Arsenault
the Canadian Stroke Consortium were involved in all aspects of the develop- is a voluntary member of the March of Dimes After Stroke Advisory Board.
ment of these recommendations. The recommendations underwent external Devin Harris received research funding from the Canadian Institutes of
review by: Philip A Barber, Treena Bilous, Renee Denise Cashin, Luciana Health Research and Brain Canada (paid directly to institution), participated
Catanese, Seemant Chaturvedi, Michael Chow, Adam A. Dmytriw, Ian on a Data Safety Monitoring Board or Advisory Board for PulsePoint
Drennan, Claire Dyason, Barb Field, Romayne Gallagher, Peter A. Randomized Controlled Trial (DSMB), and is Council Chair, B.C. Patient
Gooderham, M. Shazam Hussain, Ebru Kaya, Katie Lin, Gordon McDonald, Safety and Quality Council. Eric Kaplovitch is an External consultant for the
Stefan Pagliuso, Trudy Robertson, Julie Savoie, Joanna Schaafsma, Brenda Canadian government through RCGT re: vaccine safety and holds Leadership
Semenko, Ravinder Jeet Singh, Sean William Taylor, Aleksander Tkatch, or fiduciary roles in the Canadian Society of Vascular Medicine (unpaid).
Jenny P. Tsai, Gregory Brett Walker, and Hope Weisenberg. Zachary Liederman received an honoraria for presentation at annual
We thank the Canadian Stroke Best Practices and Quality Advisory Thrombosis Canada conference (warfarin in 2022) as well as creation of patient
Committee members: Eric E. Smith (Co-Chair), Anita Mountain (Co-Chair), education pamphlet (cancer associated thrombosis), participated on Advisory
Aline Bourgoin, Gord Gubitz, Dar Dowlatshahi, Dylan Blacquiere, Margie board work with SOBI regarding ITP treatment (Avatrombopag), and partici-
Burns, Louise Clement, Thalia Field, Farrell Leibovitch, Christine Papoushek, pated on CanVECTOR Training, Mentoring, & Early Career Development
Jeffrey Habert, Joyce Fung, Michael D Hill, Eddy Lang, Pascale Lavoie, Beth Platform (unpaid). Shauna Martiniuk is a member of the MSH Emergency
Linkewich, Colleen O’Connell, Jai Shankar, Debbie Timpson, Theodore Associates and received hourly funding for time spent in meetings. Genevieve
Wein, and Katie White. The performance measures were reviewed and updated Milot participated on a Data Safety Monitoring Board or Advisory Board, is a
by the Heart & Stroke health systems quality council including Amy Yu (Chair), Royal College of Canada council member, and holds a role on the Fellowship
Michael Hill, Aravind Ganesh, Sacha Arsenault, Christine Hawkes, Jessalyn affair board. Jeffrey Minuk provides medical expertise for CMPA cases for
Holodinsky, Raed Joundi, Laura Gioia, Noreen Kamal, Shannon MacDonald, McCarthy-Tetreault and received payment for expert testimony – McCarthy-
Katharine Mckeen, Kathryn Yearwood, Leigh Botly, and Laura Holder. Tetreault – written expertise only. Erica Otto is a member of Canadian Society
We acknowledge and thank Norine Foley and the evidence analysis team at of Hospital Pharmacists (CSHP) and Canadian Pharmacists Association
workHORSE; Shelley Sharp and Trish Helm-Neima for the review of Acute (CPhA), received speaker honoraria from CSHP, received review honoraria from
Stroke Management Performance Measures; Adrian Salonga for writing group CPhA for reviewing neurology topic chapters, received peer-reviewed salary sup-
participation and contributions, Laurie Charest of Heart & Stroke for her port grant from the Ontario Heart and Stroke Foundation, and received peer-
coordination of the CSBPR teams and processes; and Francine Forget Marin reviewed grant funding from the Canadian Institutes of Health Research.
and the Heart & Stroke internal teams who contributed to the development Jeffrey Perry holds a Heart and Stroke Foundation Mid-Career award (paid to
and publication of these recommendations (Translation, Communications, institution). David Volders received a donation from Medtronic Inc for organiz-
Knowledge Translation, Engagement, Health Policy, and Digital Solutions). ing an EVT training day for radiologists from Newfoundland. Eric E. Smith holds
Heart & Stroke is especially grateful to the members of the Community research funding from the Canadian Institutes of Health Research, Brain Canada,
Consultation and Review Panel who reviewed this module and shared their per- Weston Brain Institute. Weston Family Foundation (Payments made to
sonal experiences and insights on what made or could have made their journey University of Calgary) holds a Grant from UpToDate; Royalties/Licenses for
Alnylam, Bayer, Biogen, Cyclerion, Javelin, Eli Lilly (topics not related to manu- 9. Boulanger JM, Lindsay MP, Gubitz G, et al. Canadian Stroke Best Practice
script), received consulting fees from the US National Institutes of Health, and is Recommendations for Acute Stroke Management: prehospital, Emergency
an Associate Editor of American Heart Association. Dar Dowlatshahi holds a Department, and Acute Inpatient Stroke Care, 6th Edition, Update 2018. Int
CIHR grant as co-PI, received consulting fee for advisory board on anticoagula- J Stroke. 2018;13:949–84.
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