Linking To And Excerpting From “2021 Guideline for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack: A Guideline From the American Heart Association/American Stroke Association” With A An Outstanding Resource From The American Family Physician

In addition to today’s resource, please see and review the outstanding summary article from the American Family Physician, Secondary Prevention of Ischemic Stroke: Updated Guidelines From AHA/ASA [PubMed Abstract] [Full-Text HTML] [Full-Text PDF]. Am Fam Physician. 2022;105(1):99-102

Today, I review, link to, and excerpt from  2021 Guideline for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack: A Guideline From the American Heart Association/American Stroke Association [PubMed Abstract] [Full-Text HTML] [Full-Text PDF]. Stroke. 2021 Jul;52(7):e364-e467. doi: 10.1161/STR.0000000000000375. Epub 2021 May 24.

There are 113 similar articles in PubMed.

The above article has been cited by 1,003 articles in PubMed.

All that follows is from the above resource.

TOP 10 Take-Home Messages for the Secondary Stroke Prevention Guideline

1. Specific recommendations for prevention strategies often depend on the ischemic stroke/transient ischemic attack subtype. Therefore, new in this guideline is a section describing recommendations for the diagnostic workup after ischemic stroke, to define ischemic stroke etiology (when possible), and to identify targets for treatment in order to reduce the risk of recurrent ischemic stroke. Recommendations are now grouped by etiologic subtype.
2. Management of vascular risk factors remains extremely important in secondary stroke prevention, including (but not limited to) diabetes, smoking cessation, lipids, and especially hypertension. Intensive medical management, often performed by multidisciplinary teams, is usually best, with goals of therapy tailored to the individual patient.
3. Lifestyle factors, including healthy diet and physical activity, are important for preventing a second stroke. Low-salt and Mediterranean diets are recommended for stroke risk reduction. Patients with stroke are especially at risk for sedentary and prolonged sitting behaviors, and they should be encouraged to perform physical activity in a supervised and safe manner.
4. Changing patient behaviors such as diet, exercise, and medication compliance requires more than just simple advice or a brochure from their physician. Programs that use theoretical models of behavior change, proven techniques, and multidisciplinary support are needed.
5. Antithrombotic therapy, including antiplatelet or anticoagulant agents, is recommended for nearly all patients without contraindications. With very few exceptions, the combination of antiplatelets and anticoagulation is typically not indicated for secondary stroke prevention. Dual antiplatelet therapy is not recommended long term, and short term, dual antiplatelet therapy is recommended only in very specific patients, including those with early arriving minor stroke and high-risk transient ischemic attack or severe symptomatic intracranial stenosis.
6. Atrial fibrillation remains a common and high-risk condition for second ischemic stroke. Anticoagulation is usually recommended if the patient has no contraindications. Heart rhythm monitoring for occult atrial fibrillation is usually recommended if no other cause of stroke is discovered.
7. Extracranial carotid artery disease is an important and treatable cause of stroke. Patients with severe stenosis ipsilateral to a nondisabling stroke or transient ischemic attack who are candidates for intervention should have the stenosis fixed, likely relatively early after their ischemic stroke. The choice between carotid endarterectomy and carotid artery stenting should be driven by specific patient comorbidities and features of their vascular anatomy.
8. Patients with severe intracranial stenosis in the vascular territory of ischemic stroke or transient ischemic attack should not receive angioplasty and stenting as a first-line therapy for preventing recurrence. Aggressive medical management of risk factors and short-term dual antiplatelet therapy are preferred.
9. There have been several studies evaluating secondary stroke prevention of patent foramen ovale closure since the previous guideline in 2014. It is now considered reasonable to percutaneously close patent foramen ovale in patients who meet each of the following criteria: age 18–60 years, nonlacunar stroke, no other identified cause, and high risk patent foramen ovale features.
10. Patients with embolic stroke of uncertain source should not be treated empirically with anticoagulants or ticagrelor because it was found to be of no benefit.

1. INTRODUCTION

Each year, ≈795 000 individuals in the United States experience a stroke, of which 87% (690 000) are ischemic and 185 000 are recurrent.1 Approximately 240 000 individuals experience a transient ischemic attack (TIA) each year.2 The risk of recurrent stroke or TIA is high but can be mitigated with appropriate secondary stroke prevention. In fact, cohort studies have shown a reduction in recurrent stroke and TIA rates in recent years as secondary stroke prevention strategies have improved.3,4 A meta-analysis of randomized controlled trials (RCTs) of secondary stroke prevention therapies published from 1960 to 2009 showed a reduction in annual stroke recurrence from 8.7% in the 1960s to 5.0% in the 2000s, with the reduction driven largely by improved blood pressure (BP) control and use of antiplatelet therapy.5 The changes may have been influenced by changes in diagnostic criteria and differing sensitivities of diagnostic tests over the years.
The overwhelming majority of strokes can be prevented through BP control, a healthy diet, regular physical activity, and smoking cessation. In fact, 5 factors—BP, diet, physical inactivity, smoking, and abdominal obesity—accounted for 82% and 90% of the population-attributable risk (PAR) for ischemic and hemorrhagic stroke in the INTERSTROKE study (Global and regional effects of potentially modifiable risk factors associated with acute stroke in 32 countries).5a Similarly, the Global Burden of Disease Study showed that 90.5% (95% uncertainty interval, 88.5–92.2) of the global burden of stroke was attributable to modifiable risk factors.6 A modeling study showed that targeting multiple risk factors has additive benefits for secondary prevention; specifically, aspirin, statin, and antihypertensive medications, combined with diet modification and exercise, can result in an 80% cumulative risk reduction in recurrent vascular events.7 Although the benefits of a healthy lifestyle and vascular risk factor control are well documented,8,9 risk factors remain poorly controlled among stroke survivors.10–14

1.4. Scope of the Guideline

The aim of the present guideline is to provide clinicians with evidence-based recommendations for the prevention of future stroke among survivors of ischemic stroke or TIA. It should be noted that this guideline does not cover the following topics, which have been addressed elsewhere:
• Acute management decisions (covered in the “2019 Update to the 2018 Guidelines for the Early Management of Patients With Acute Ischemic Stroke”16),
• Intracerebral hemorrhage (ICH; covered in the “Guidelines for the Management of Spontaneous Intracerebral Hemorrhage”17),
• Primary prevention (covered in the “Guidelines for the Primary Prevention of Stroke”18 and “2019 American College of Cardiology/American Heart Association Guideline on the Primary Prevention of Cardiovascular Disease”19),
• Special considerations for stroke prevention in women (covered in the “Guidelines for the Prevention of Stroke in Women”20), and
• Cerebral venous sinus thrombosis (covered in “Diagnosis and Management of Cerebral Venous Thrombosis”22).
In general, with very few exceptions, the literature supports the concept that patients with TIA and those with ischemic stroke should be treated the same in terms of secondary prevention.
This guideline is divided into 4 sections:
1. Diagnostic Evaluation for Secondary Stroke Prevention
2. Vascular Risk Factor Management
3. Management by Etiology
4. Systems of Care for Secondary Ischemic Stroke Prevention.
The structure and scope of this guideline differ from those of the 2014 Guidelines for the prevention of stroke in patients with stroke and TIA9 in several ways.
First, the current guideline reflects numerous innovations and modifications that were incorporated into the AHA clinical practice guideline format. Introduced in 2017, modifications to AHA guidelines included making the text shorter and more user friendly; focusing guidelines on recommendations and patient management flow diagrams and less on extensive text and background information; formatting guidelines so that they can be easily updated with guideline focused updates; and including “chunks” of information after each recommendation.23
Second, the Diagnostic Evaluation and Systems of Care for Secondary Prevention sections are new. The Diagnostic Evaluation for Secondary Stroke Prevention section focuses on the evidence base for laboratory and imaging studies for guiding secondary stroke prevention decisions. Often these tests are completed in the inpatient setting. The Systems of Care for Secondary Prevention section contains 3 subsections: (1) Health Systems–Based Interventions for Secondary Stroke Prevention, (2) Interventions Aimed at Changing Patient Behavior, and (3) Health Equity. The Health Equity subsection is a refocus of the 2014 guideline’s section guiding management of high-risk populations.
Third, this guideline does not include a separate section on metabolic syndrome because there are no unique recommendations for metabolic syndrome aside from managing each of the individual components of the syndrome. Fourth, the section on alcohol use was expanded to include the use of other substances.
Finally, several additional conditions were included in the Management by Etiology section: congenital heart disease, cardiac tumors, moyamoya disease, migraine, malignancy, vasculitis, other genetic disorders, carotid web, fibromuscular dysplasia, dolichoectasia, and embolic stroke of undetermined source (ESUS).

Table 2. Associated AHA/ASA Guidelines and Statements
Title Organization Publication year
AHA/ASA guidelines
 Guidelines for Carotid Endarterectomy24 AHA/ASA 1998
 Guideline on the Management of Patients With Extracranial Carotid and Vertebral Artery Disease25 ASA/ACCF/AHA/AANN/AANS/ACR/ASNR/CNS/SAIP/SCAI/SIR/SNIS/SVM/SVS 2011
 Guideline on Lifestyle Management to Reduce Cardiovascular Risk26 AHA/ACC 2013
 Guideline for the Management of Overweight and Obesity in Adults27 AHA/ACC/TOS 2013
 Guideline for the Management of Patients With Atrial Fibrillation28 AHA/ACC/HRS 2014
 Guidelines for the Management of Spontaneous Intracerebral Hemorrhage17 AHA/ASA 2014
 Guidelines for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack9 AHA/ASA 2014
 Guidelines for the Prevention of Stroke in Women20 AHA/ASA 2014
 Guidelines for the Primary Prevention of Stroke18 AHA/ASA 2014
 Guideline for the Prevention, Detection, Evaluation and Management of High Blood Pressure in Adults29 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA 2017
 Guideline for the Management of Adults With Congenital Heart Disease30 AHA/ACC 2018
 Guideline on the Management of Blood Cholesterol31 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA 2018
 Guidelines for the Early Management of Patients With Acute Ischemic Stroke: 2019 Update to the 2018 Guidelines for the Early Management of Acute Ischemic Stroke16 AHA/ASA 2019
 Guideline on the Primary Prevention of Cardiovascular Disease19 ACC/AHA 2019
 Focused Update of the 2014 AHA/ACC/HRS Guideline for the Management of Patients with Atrial Fibrillation32 AHA/ACC/HRS 2019
 Guideline for the Management of Patients With Valvular Heart Disease33 ACC/AHA 2020
AHA/ASA statements
 Diagnosis and Management of Cerebral Venous Thrombosis22 AHA/ASA 2011
 Cervical Arterial Dissections and Association With Cervical Manipulative Therapy21 AHA/ASA 2014
 Physical Activity and Exercise Recommendations for Stroke Survivors34 AHA/ASA 2014
 Spontaneous Coronary Artery Dissection: Current State of the Science34a AHA/ASA 2018
AHA/ASA presidential advisory
 Defining Optimal Brain Health in Adults35 AH
AACVPR indicates American Association of Cardiovascular and Pulmonary Rehabilitation; AANN, American Association of Neuroscience Nurses; AANS, American Association of Neurological Surgeons; AAPA, American Academy of Physician Assistants; ABC, Association of Black Cardiologists; ACC, American College of Cardiology; ACCF, American College of Cardiology Foundation; ACPM, American College of Preventive Medicine; ACR, American College of Radiology; ADA, American Diabetes Association; AGS, American Geriatrics Society; AHA, American Heart Association; ASA, American Stroke Association; APhA, American Pharmacists Association; ASH, American Society of Hypertension; ASNR, American Society of Neuroradiology; ASPC, American Society for Preventive Cardiology; CNS, Congress of Neurological Surgeons; HRS, Heart Rhythm Society; NLA, National Lipid Association; NMA, National Medical Association; PCNA, Preventive Cardiovascular Nurses Association; SAIP, Society of Atherosclerosis Imaging and Prevention; SCAI, Society for Cardiovascular Angiography and Interventions; SIR, Society of Interventional Radiology; SNIS, Society of NeuroInterventional Surgery; SVM, Society for Vascular Medicine; SVS, Society for Vascular Surgery; and TOS, The Obesity Society.

1.5. Class of Recommendation and Level of Evidence

Recommendations are designated both a Class of Recommendation (COR) and a Level of Evidence (LOE). The COR indicates the strength of recommendation, encompassing the estimated magnitude and certainty of benefit in proportion to risk. The LOE rates the quality of scientific evidence supporting the intervention on the basis of the type, quantity, and consistency of data from clinical trials and other sources (Table 3).
Table 3. Applying Class of Recommendation and Level of Evidence to Clinical Strategies, Interventions, Treatments, or Diagnostic Testing in Patient Care (Updated May 2019)*

1.6. Abbreviations

Abbreviation Meaning/Phrase
ACC American College of Cardiology
ACS acute coronary syndrome
ACTIVE W Atrial Fibrillation Clopidogrel Trial With Irbesartan for Prevention of Vascular Events
AF atrial fibrillation
AHA American Heart Association
AHI apnea-hypopnea index
ARCH Aortic Arch Related Cerebral Hazard Trial
ARISTOTLE Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation
ASA American Stroke Association
ASAP Addressing Sleep Apnea Post Stroke/TIA
ASTRO-APS Apixaban for Secondary Prevention of Thromboembolism Among Patients With Antiphospholipid Syndrome
ASCVD atherosclerotic cardiovascular disease
BMI body mass index
BP blood pressure
BUST-Stroke Breaking Up Sitting Time After Stroke
CADISS Cervical Artery Dissection in Stroke Study
CARDIA Coronary Artery Risk Development in Young Adults
CAP Continued Access Registry
CAPRIE Clopidogrel Versus Aspirin in Patients at Risk of Ischaemic Events
CAS carotid artery stenting
CATHARSIS Cilostazol-Aspirin Therapy Against Recurrent Stroke With Intracranial Artery Stenosis
CEA carotid endarterectomy
CHANCE Clopidogrel in High-Risk Patients With Acute Non-Disabling Cerebrovascular Events
CICAS Chinese Intracranial Atherosclerosis
CLAIR Clopidogrel Plus Aspirin for Infarction Reduction
CLOSE Patent Foramen Ovale Closure or Anticoagulants Versus Antiplatelet Therapy to Prevent Stroke Recurrence
CNS central nervous system
COMMANDER HF A Study to Assess the Effectiveness and Safety of Rivaroxaban in Reducing the Risk of Death, Myocardial Infarction or Stroke in Participants With Heart Failure and Coronary Artery Disease Following an Episode of Decompensated Heart Failure
COMPASS Cardiovascular Outcomes for People Using Anticoagulation Strategies
COR Class of Recommendation
COSS Carotid Occlusion Surgery Study
CPAP continuous positive airway pressure
CREST Carotid Revascularization Endarterectomy versus Stenting Trial
CSPS Cilostazol for Prevention of Secondary Stroke
CT computed tomography
CTA computed tomographic angiography
CVD cardiovascular disease
DAPT dual antiplatelet therapy
DASH Dietary Approaches to Stop Hypertension
DCCT Diabetes Control and Complication Trial
DESERVE Discharge Educational Strategies for Reduction of Vascular Events
DHA docosahexaenoic acid
DiRECT Diabetes Remission Clinical Trial
DOAC direct-acting oral anticoagulant
ECST European Carotid Surgery Trial
EF ejection fraction
ENGAGE AF-TIMI 48 Global Study to Assess the Safety and Effectiveness of Edoxaban (DU-176b) vs Standard Practice of Dosing With Warfarin in Patients With Atrial Fibrillation
EPA eicosapentaenoic acid
EPIC-CVD European Prospective Investigation into Cancer and Nutrition-CVD case-cohort study
ESH-CHL-SHOT European Society of Hypertension and Chinese Hypertension League Stroke in Hypertension Optimal Treatment Trial
ESPRIT European/Australasian Stroke Prevention in Reversible Ischaemia Trial
ESPS2 Second European Stroke Prevention Study
ESUS embolic stroke of undetermined source
ExStroke Physical Exercise After Acute Ischaemic Stroke
FASTEST Efficacy and Safety of a TIA/Stroke Electronic Support Tool
FMD fibromuscular dysplasia
FOURIER Further Cardiovascular Outcomes Research With PCSK9 Inhibition in Subjects With Elevated Risk
GELIA German Experience With Low Intensity Anticoagulation
GLP-1 glucagon-like protein 1
HbA1c hemoglobin A1c
HR hazard ratio
ICA internal carotid artery
ICARUSS Integrated Care for the Reduction of Secondary Stroke
ICAS intracranial atherosclerotic stenosis
ICH intracerebral hemorrhage
IE infective endocarditis
IMPROVE-IT Improved Reduction of Outcomes: Vytorin Efficacy International Trial
INR international normalized ratio
INSPiRE-TMS Intensified Secondary Prevention Intending a Reduction of Recurrent Events in TIA and Minor Stroke Patients
IPE icosapent ethyl
IRIS Insulin Resistance Intervention After Stroke
JAM Japan Adult Moyamoya
JELIS Japan EPA Lipid Intervention Study
LDL low-density lipoprotein
LDL-C low-density lipoprotein cholesterol
LOE Level of Evidence
LV left ventricular
LVAD left ventricular assist devices
MACE major adverse cardiovascular event
MD mean difference
MI myocardial infarction
MIST Motivational Interviewing in Stroke
MRA magnetic resonance angiography
MRI magnetic resonance imaging
NAILED Stroke Nurse Based Age Independent Intervention to Limit Evolution of Disease After Stroke
NASCET North American Symptomatic Carotid Endarterectomy Trial
NAVIGATE ESUS Rivaroxaban Versus Aspirin in Secondary Prevention of Stroke and Prevention of Systemic Embolism in Patients With Recent Embolic Stroke of Undetermined Source
NIHSS National Institutes of Health Stroke Scale
ODYSSEY OUTCOMES Evaluation of Cardiovascular Outcomes After an Acute Coronary Syndrome During Treatment With Alirocumab
OMEMI Omega-3 Fatty Acids in Elderly Patients With Acute Myocardial Infarction
OR odds ratio
OSA obstructive sleep apnea
OXVASC Oxford Vascular Study
PAR population-attributable risk
PAST-BP Prevention After Stroke–Blood Pressure
PCSK9 proprotein convertase subtilisin/kexin type 9
PFO patent foramen ovale
PODCAST Prevention of Decline in Cognition after Stroke Trial
POINT Platelet-Oriented Inhibition in New TIA and Minor Ischemic Stroke
PRAISE Prevent Recurrence of All Inner-City Strokes Through Education
PREDIMED Prevención con Dieta Mediterránea
PREVAIL Prospective Randomised Evaluation of the Watchman LAA Closure Device in Patients With Atrial Fibrillation Versus Long Term Warfarin Therapy
PREVENTION Preventing Recurrent Vascular Events in Patients With Stroke or Transient Ischemic Attack
PRoFESS Prevention Regimen for Effectively Avoiding Second Strokes
PROTECT AF Watchman Left Atrial Appendage System for Embolic Protection in Patients With Atrial Fibrillation
PTAS percutaneous transluminal angioplasty and stenting
RCT randomized controlled trial
RE-ALIGN Randomized, Phase II Study to Evaluate the Safety and Pharmacokinetics of Oral Dabigatran Etexilate in Patients After Heart Valve Replacement
RE-LY Randomized Evaluation of Long-Term Anticoagulant Therapy
REDUCE-IT Reduction of Cardiovascular Events With Icosapent Ethyl–Intervention Trial
REGARDS Reasons for Geographic and Racial Differences in Stroke Study
RESPECT Randomized Evaluation of Recurrent Stroke Comparing PFO Closure to Established Current Standard of Care Treatment
RESPECT ESUS Dabigatran Etexilate for Secondary Stroke Prevention in Patients With Embolic Stroke of Undetermined Source
RISE-UP Recovery in Stroke Using PAP
ROCKET AF Rivaroxaban Once Daily Oral Direct Factor Xa Inhibition Compared With Vitamin K Antagonism for Prevention of Stroke and Embolism Trial in Atrial Fibrillation
RR relative risk
SAMMPRIS Stenting and Aggressive Medical Management for Preventing Recurrent Stroke in Intracranial Stenosis
SAPPHIRE Stenting and Angioplasty With Protection in Patients at High Risk for Endarterectomy
SAPT single antiplatelet therapy
SAVE Sleep Apnea Cardiovascular Endpoints
SBP systolic blood pressure
SCD sickle cell disease
SIT Silent Cerebral Infarct Transfusion multi-center clinical trial
Sleep SMART Sleep for Stroke Management and Recovery Trial
SMART Second Manifestations of Arterial Disease
SOCRATES Soluble Guanylate Cyclase Stimulator in Heart Failure Studies
SPAF Stroke Prevention in Atrial Fibrillation Study
SPARCL Stroke Prevention by Aggressive Reduction in Cholesterol Levels
SPS3 Secondary Prevention of Small Subcortical Strokes
STANDFIRM Shared Team Approach Between Nurses and Doctors for Improved Risk Factor Management for Stroke Patients
STOP Stroke Prevention Trial in Sickle Cell Anemia
SUCCEED Secondary Stroke Prevention by Uniting Community and Chronic Care Model Teams Early to End Disparities
SUSTAIN Systemic Use of Stroke Averting Interventions
STRENGTH Outcomes Study to Assess Statin Residual Risk Reduction With Epanova in High CV Risk Patients With Hypertriglyceridemia
SWiTCH Stroke With Transfusions Changing to Hydroxyurea
TARDIS Triple Antiplatelets for Reducing Dependency after Ischaemic Stroke
T2D type 2 diabetes
TCAR transcarotid artery revascularization
TCD transcranial Doppler
TEE transesophageal echocardiography
THALES Acute Stroke or Transient Ischaemic Attack Treated With Ticagrelor and ASA for Prevention of Stroke and Death
TIA transient ischemic attack
TOSS Trial of Cilostazol in Symptomatic Intracranial Arterial Stenosis
TST Treat Stroke to Target
TWiTCH TCD With Transfusions Changing to Hydroxyurea
UKPDS United Kingdom Prospective Diabetes Study
VAST Vertebral Artery Stenting Trial
VHD valvular heart disease
VISP Vitamin Intervention for Stroke Prevention
VISSIT Vitesse Intracranial Stent Study for Ischemic Stroke Therapy
VIST Vertebral Artery Ischemic Stenting Trial
VISTA Virtual International Stroke Trials Archive
VITATOPS Vitamins to Prevent Stroke
VKA vitamin K antagonist
VLDL very-low-density lipoprotein
VZV varicella zoster virus
WARCEF Warfarin vs. Aspirin in Reduced Cardiac Ejection Fraction
WARSS Warfarin-Aspirin Recurrent Stroke Study
WASID Warfarin-Aspirin Symptomatic Intracranial Disease
WEAVE Wingspan Stent System Post Market Surveillance

2. General Concepts

2.1. Definitions

Figure 1 illustrates the writing group’s conceptual representation of ischemic stroke subtypes.
Figure 1Conceptual representation of ischemic stroke subtypes. Percentages are approximate and are informed by Kolominsky-Rabas et al36 and Gardener et al.37 Precise percentages will depend on extent of testing and patient populations. Ischemic stroke subtype definitions are informed by the TOAST (Trial of Org 10172 in Acute Stroke Treatment) classification scheme38 unless otherwise indicated. ESUS indicates embolic stroke of undetermined source.
Lacunar stroke: Lacunar syndrome, with normal computed tomography (CT)/magnetic resonance imaging (MRI) or subcortical stroke measuring <1.5 cm in diameter on CT or MRI. Most, although not all, of lacunar strokes are due to small vessel disease.
Stroke attributable to small vessel disease: Subcortical stroke measuring <1.5 cm in diameter on CT or MRI without evidence of a concomitant cortical infarct.
Cardioembolic stroke: Stroke attributable to arterial occlusion from an embolus that presumably arose in the heart. Clinical and brain imaging findings are similar to those described in large artery atherosclerosis. Evidence of a previous TIA or stroke in >1 vascular territory supports a clinical diagnosis of cardioembolic stroke.
Cryptogenic stroke: An imaging-confirmed stroke with unknown source despite thorough diagnostic assessment (including, at a minimum, arterial imaging, echocardiography, extended rhythm monitoring, and key laboratory studies such as a lipid profile and hemoglobin A1c [HbA1c]).
Stroke caused by large artery atherosclerosis: Ischemic stroke in the vascular distribution of a major intracranial or extracranial artery with >50% stenosis or occlusion on vascular imaging. Clinical findings include those of cerebral cortical involvement or brainstem or cerebellar dysfunction. Cortical and cerebellar lesions and brainstem or subcortical lesions >1.5 cm are considered potentially caused by large artery atherosclerosis. Diagnostic studies should exclude potential sources of cardioembolic embolism.
ESUS: A stroke that appears nonlacunar on neuroimaging without an obvious source after a minimum standard evaluation (including arterial imaging, echocardiography, extended rhythm monitoring, and key laboratory studies such as a lipid profile and HbA1c) to rule out known stroke etiologies such as cardioembolic sources and atherosclerosis proximal to the stroke.39
A diagnosis of ESUS implies that the stroke is embolic in origin, given the nonlacunar location; however, the source of the embolus is unknown, despite a minimal standard evaluation. Although cryptogenic stroke similarly implies that the cause of the origin is unknown, the stroke is not necessarily embolic. Individuals with ESUS have cryptogenic stroke, but the converse is not always the case.

2.2. Shared Decision-Making

Shared decision-making is a key component of patient-centered care.

2.3. Contraindications

Treatment should always be tailored to patients’ individual situations. Therefore, as a rule, we did not include the statement “unless contraindicated” in the recommendations. It is implicit that if a recommendation is contraindicated in a patient’s circumstance, it should not be implemented.

2.4. Adherence

A key component of secondary stroke prevention is assessing and addressing barriers to adherence to medications and a healthy lifestyle. If a patient has a recurrent stroke while on secondary stroke prevention medications, it is vital to assess whether they were taking the medications that they were prescribed and, if possible, to explore and address factors that contributed to nonadherence before assuming that the medications were ineffective.

2.5. Antithrombotic Dosing

Unless stated otherwise in the recommendations herein, the international normalized ratio (INR) goal for warfarin is 2.0 to 3.0 and the dose of aspirin is 81 to 325 mg.

2.6. Application Across Populations

Unless otherwise indicated, the recommendations in this guideline apply across race/ethnicity, sex, and age groups. Special considerations to address health equity are delineated in section 6.3, Health Equity.

3. Diagnostic Evaluation for Secondary Stroke Prevention

Synopsis

Patients presenting with signs and symptoms of acute stroke will undergo an evaluation tailored to ensure that, when appropriate, they receive reperfusion therapy (Figure 2). Imaging recommendations based on acute treatment considerations overlap with, but are not identical to, imaging recommendations based on secondary stroke prevention considerations. Recommendations presented in this guideline focus
Figure 2Algorithm for evaluating patients with a clinical diagnosis of stroke for the purposes of optimizing prevention of recurrent ischemic stroke. Colors correspond to Class of Recommendation in Table 3. CT indicates computed tomography; CTA, computed tomography angiogram; ECG, electrocardiogram; MRA, magnetic resonance angiography; MRI, magnetic resonance imaging; PFO, patent foramen ovale; SOE, source of embolism; TCD, transcranial Doppler; TEE, transesophageal echocardiography; TTE, transthoracic echocardiography; and US, ultrasound. *Basic laboratory tests include complete blood count, troponin, prothrombin time, partial thromboplastin time, glucose, hemoglobin A1c, creatinine, and fasting or nonfasting lipid profile. †When a patient has a transient neurological deficit clinically characteristic of transient ischemic attack, the patient should be evaluated in the same manner as a patient who has an ischemic stroke with a corresponding cerebral infarct on imaging. ‡TTE, TEE, TCD, cardiac MRI, or cardiac CT.
on evaluations done for the purposes of confirming the diagnosis of stroke and characterizing its pathomechanism by identifying potential sources of cardioembolism, thromboembolism from large artery atherosclerosis, dissection, or other disease processes such as hypercoagulability. Confirmation of stroke diagnosis may require follow-up head imaging because of poor sensitivity of noncontrast CT for small or hyperacute infarcts. Some conditions associated with stroke and with specific therapies are common (eg, AF), whereas others are relatively rare (eg, endocarditis). The variable yield of testing means that treating physicians need to exercise judgment on the likelihood that a test will alter management in a given clinical situation.
This entry was posted in American Heart Association, American Stroke Association, Secondary Prevention Of Stroke And TIA, Stroke, Stroke Prevention Guidelines, TIA (Transient Ischemic Attack), Transient Ischemic Attack. Bookmark the permalink.