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a 52 y/o man comes to the ED with 5 hours of left arm weakness. An MD says he cannot receive alteplase since he is outside the window. Do you agree?
NO! (the optimal window is 4.5hrs i guess, but guidelines changed and now it can be given anytime 24 hours post onset)
Secondary Stoke Prevention: Aspirin dose ranges _____-325mg with lower doses having less _______________
81, side effects
Secondary Stoke Prevention: Aspirin dose ranges 81-325mg with lower doses having less SEs (like ________ irritation or ______________)
Gi, bleeding
Secondary Stoke Prevention: Aspirin dose ranges 81-325mg with lower doses having less SEs
Dosage forms: tablets (EC or chewable) and _____________
suppositories
Secondary Stoke Prevention: Clopidogrel is rapidly absorbed and extensively metabolized to ________ drug
active
Secondary Stoke Prevention: ______________ is a rapidly absorbed prodrug that is extensively metabolized to active drug in the liver
Clopidogrel
Secondary Stoke Prevention: Clopidogrel is a rapidly absorbed prodrug that is extensively metabolized to active drug in the __________
liver
Secondary Stoke Prevention: Clopidogrel is a rapidly absorbed prodrug that is extensively metabolized to active drug in the liver
the onset of action with the LD is about _________, while the maintenance dose is about 3 days
2 hours
according to the CAPRIE trial, which is better for MI, stroke, and vascular death outcomes: Aspirin vs. Clopidogrel
neither! (both will work)
Secondary Stoke Prevention: ERD/ASA stands for Extended-Release ___________ + Aspirin
Dipyridamole
Secondary Stoke Prevention: ERD/ASA stands for Extended-Release Dipyridamole + Aspirin
it is metabolized in the ________
liver
Secondary Stoke Prevention: ERD/ASA stands for Extended-Release Dipyridamole + Aspirin
it is metabolized in the liver
this drug dosage form cannot be _________ or _________
crushed or chewed
Secondary Stoke Prevention: ERD/ASA stands for Extended-Release Dipyridamole + Aspirin, which is metabolized in the liver
this drug dosage form cannot be crushed or chewed
this drug (of the 3 for secondary prevention) has the highest incidence of ____________
side effects (abdominal pain, diarrhea, and headache)
Secondary Stoke Prevention: ERD/ASA stands for Extended-Release Dipyridamole + Aspirin, which is metabolized in the liver
this drug dosage form cannot be crushed or chewed
this drug (of the 3 for secondary prevention) has the highest incidence of SEs (like ___________ (18%), ___________(13%), and __________ (40%))
abdominal pain, diarrhea, headache
according to the PRoFESS trial, ERD/ASA and Clopidogrel had similar outcomes when it came to stroke recurrence and stroke/MI/vascular death, but ___________ had more bleeding and had more discontinuations d/t SEs
ERD/ASA
according to the PRoFESS trial, ERD/ASA and Clopidogrel had similar outcomes when it came to stroke recurrence and stroke/MI/vascular death, but ERD/ASA had more __________ and had more discontinuations d/t ____________
bleeding, side effects
CHANCE trial included pts with NIHSS score <3 and/or ABCD2 score >4
it randomized ASA vs. ASA + Clopidogrel for 21 days → then d/c Clopidogrel and just do ASA
it found stroke and stroke/MI/CV death was reduced with _________ after 90 days
combination (ASA + Clopidogrel)
CHANCE trial included pts with NIHSS score <3 and/or ABCD2 score >4
it randomized ASA vs. ASA + Clopidogrel for 21 days → then d/c Clopidogrel and just do ASA
it found stroke & stroke/MI/CV death was reduced with combination (ASA + Clopidogrel) after 90 days
it found similar mortality and _________ with combo or with just ASA
bleeding
POINT trial included pts with ischemic stroke or high-risk TIA s/sx within 12 hours
it randomized ASA vs. ASA + Clopidogrel for 90 days
it found stroke & stroke/MI/CV death was reduced with _________ after 90 days
combination (ASA + Clopidogrel)
POINT trial included pts with ischemic stroke or high-risk TIA s/sx within 12 hours
it randomized ASA vs. ASA + Clopidogrel for 90 days
it found stroke & stroke/MI/CV death was reduced with combination (ASA + Clopidogrel) after 90 days
it found similar mortality between the two, however major __________ was worse in the combination group
hemorrhage
POINT trial included pts with ischemic stroke or high-risk TIA s/sx within 12 hours
it randomized ASA vs. ASA + Clopidogrel for 90 days
it found stroke & stroke/MI/CV death was reduced with combination (ASA + Clopidogrel) after 90 days
it found similar mortality between the two, however major hemorrhage was worse in the __________ group
combination
the ASA/AHA 2021 guidelines recommend ___________, OR __________, OR ____________ as initial antithrombic therapy for non-cardioembolic stroke
ASA, ERD/ASA, Clopidogrel (all are class I, level A recommendations)
the ASA/AHA 2021 guidelines recommend Aspirin, OR ERD/ASA, OR Clopidogrel as initial antithrombic therapy for non-cardioembolic stroke
_______________ may be beneficial in patients with minor stroke (NIHSS <3) or high-risk TIA (ABCD score >4) when started within 24 hours of onset and continued for 21-90 days → followed by ___________ treatment indefinitely
ASA + Clopidogrel, ASA alone (class I, level A recommendation)
the ASA/AHA 2021 guidelines recommend Aspirin, OR ERD/ASA, OR Clopidogrel as initial antithrombic therapy for non-cardioembolic stroke
ASA + Clopidogrel may be beneficial in patients with minor stroke (__________ score <3) or high-risk TIA (________ score >4) when started within 24 hours of onset and continued for 21-90 days → followed by ASA treatment indefinitely
NIHSS, ABCD2
the ASA/AHA 2021 guidelines recommend Aspirin, OR ERD/ASA, OR Clopidogrel as initial antithrombic therapy for non-cardioembolic stroke
ASA + Clopidogrel may be beneficial in patients with minor stroke (NIHSS score <3) or high-risk TIA (ABCD2 score >4) when started within _________ of onset and continued for __________ → followed by ASA treatment indefinitely
24 hours, 21-90 days
the ASA/AHA 2021 guidelines recommend Aspirin, OR ERD/ASA, OR Clopidogrel as initial antithrombic therapy for non-cardioembolic stroke
ASA + Clopidogrel may be beneficial in patients with minor stroke (NIHSS score _____) or high-risk TIA (ABCD2 score ______) when started within 24 hours of onset and continued for 21-90 days → followed by ASA treatment indefinitely
<3, >4
the ASA/AHA 2021 guidelines recommend Aspirin, OR ERD/ASA, OR Clopidogrel as initial antithrombic therapy for non-cardioembolic stroke
ASA + Clopidogrel may be beneficial in patients with minor stroke (NIHSS score <3) or high-risk TIA (ABCD2 score >4) when started within 24 hours of onset and continued for 21-90 days → followed by ASA treatment indefinitely
Antiplatelets are recommended over anticoagulants in patients with _____________ stroke
non-cardioembolic
risk factor modification is key to successful stroke prevention
Primary: control risk factors like ________, ________, and ________; diet/exercise; smoking cessation; treat A-fib
HTN, DM, HLD
risk factor modification is key to successful stroke prevention
Primary: control risk factors like HTN, DM, and HLD; diet/exercise; stopping __________; treating _____________
smoking, A-fib
risk factor modification is key to successful stroke prevention
Primary: control risk factors like HTN, DM, and HLD; diet/exercise; smoking cessation; treat A-fib
Secondary: alllll the primary things + anticoagulation for thromboembolic or hypercoagulable disease + __________ therapy
antiplatelet
True or False: A 21 y/o male non-smoker with NO HTN, HLD, or DM has zero risk of stroke
False (no one has a stroke risk of zero technically)
Non-modifiable stroke risk factors: age >______, family history, race (______ > Hispanics/Asians > Caucasians), gender (higher risk in ______), and prior stroke, TIA, or MI
55, AA, males
Modifiable stroke risk factors: HLD, smoking, physical inactivity, obesity, alcohol consumption, but _________ and _________ have the highest relative risk
HTN, A-fib
HTN is present in up to 70% of stroke patients
lowering BP can reduce stroke risk by 30-40% if patient is compliant
treatment recommendations: target BP <130/80mmHg, may initiate anti-hypertensives >_______ after acute stroke, and ________________ (drug class) are preferred for primary stroke prevention
48-72, CCBs
DM is present in 25-45% of all stroke patients & increases recurrent stroke risk by 60% if uncontrolled
all stroke patients are screened for DM with an HgbA1c goal of <_____%
7
DM is present in 25-45% of all stroke patients & increases recurrent stroke risk by 60% if uncontrolled
all stroke patients are screened for DM with an HgbA1c goal of <7%
inpatient glucose goals ________mg/dL (we should optimize their current regimen, or can initiate therapy based on their comorbidities)
140-180
HLD has NO clear evidence linking elevated cholesterol level and overall stroke risk
however, data supports recommendation of a ______-________ _________ for ALL patients
high-intensity statin
smoking doubles the risk of stroke, and risk starts to decrease after quitting and can disappear completely 5-years post-quitting
this risk includes _________ smoke
second-hand
Cardioembolic Stroke is a stroke that starts in the heart
most common etiology is from ____-________ ____________, then valvular heart disease/mechanical heart valve, then left ventricular mural thrombus
non-valvular atrial fibrillation
Cardioembolic Stroke is a stroke that starts in the heart
most common etiology is from non-valvular atrial fibrillation, then valvular heart disease/mechanical heart valve, then left ventricular mural thrombus
Stroke/TIA patients diagnosed with A-fib should automatically be considered for ______________
anticoagulation
Cardioembolic Stroke is a stroke that starts in the heart
Assessing stroke risk in Afib is done using the ______________ score
CHA2DS2-VASc
Cardioembolic Stroke is a stroke that starts in the heart
Assessing stroke risk in Afib is done using the CHA2DS2-VASc score
Stroke/TIA/thromboembolism is _______ points
2
Cardioembolic Stroke is a stroke that starts in the heart
Assessing stroke risk in Afib is done using the CHA2DS2-VASc score
Stroke/TIA/thromboembolism is 2 points; this automatically places patients into the ______-risk category (even if they have zero other risk factors!) for which _______ ___________ is recommended
high, oral anticoagulation
Cardioembolic Stroke is a stroke that starts in the heart
Assessing stroke risk in Afib is done using the CHA2DS2-VASc score
Stroke/TIA/thromboembolism is 2 points; this automatically places patients into the high-risk category for which oral anticoagulation is recommended
AHA/ASA 2021 guidelines for stroke prevention in non-valvular A-fib: what are the recommendations for prevention of first and recurrent stroke?
Warfarin or DOACs
Cardioembolic Stroke is a stroke that starts in the heart
AHA/ASA 2021 guidelines for stroke prevention in non-valvular A-fib: anticoagulation with Warfarin or DOACs can start within ___-___ _______ after a stroke, unless high risk for hemorrhage
2-14 days
Cardioembolic Stroke is a stroke that starts in the heart
AHA/ASA 2021 guidelines for stroke prevention in non-valvular A-fib: anticoagulation with Warfarin or DOACs can start within 2-14 days after a stroke, unless high risk for ___________
hemorrhage
Cardioembolic Stroke is a stroke that starts in the heart
AHA/ASA 2021 guidelines for stroke prevention in non-valvular A-fib: anticoagulation with Warfarin or DOACs can start within 2-14 days after a stroke, unless high risk for hemorrhage
for TIA, we can initiate __________ after the index event
immediately
Cardioembolic Stroke is a stroke that starts in the heart
AHA/ASA 2021 guidelines for stroke prevention in non-valvular A-fib: anticoagulation with Warfarin or DOACs (alone) can start within 2-14 days after a stroke, unless high risk for hemorrhage
Anticoagulation + Antiplatelet therapy is reasonable only for patients with clinically apparent ________
CAD (like ACS or a cardiac stent)