Acute Ischemic Stroke Management: Dr. Aldrin C Leman, Sps
Acute Ischemic Stroke Management: Dr. Aldrin C Leman, Sps
Acute Ischemic Stroke Management: Dr. Aldrin C Leman, Sps
MANAGEMENT
Ischemic stroke
• Caused by a blocked blood vessel in the brain.
Hemorrhagic Stroke
• Caused by a ruptured blood vessel in the brain.
Ischemic Hemorrhagic
80% 20%
Etiology of Ischemic Strokes
• Smoking • Ethnicity/Race
• 14 billion synapses
Suspected Stroke
History and Physical
Blood tests
Consult ECG and Chest X-ray
Neurologist CT or MRI brain
Acute
Hemorrhagic Non Acute Stroke
Acute Ischemic
Stroke Tumor
Stroke Migraine
SAH Seizures
ICH onset < 3 hours
Demyelination
Guidelines for
Guidelines for
Management of See Thrombolysis
Management of
Intracerebral Ischemic Stroke Checklist
Hemorrhage
AHA/ASA GUIDELINE
Guidelines for the Prevention of Stroke
in Patients With Stroke or Transient Ischemic Attack
The choice of specific drugs and targets should be individualized on the basis
of pharmacological properties, mechanism of action, and consideration of
pecific patient characteristics for which specific agents are probably
indicated (eg, extracranial cerebrovascular occlusive disease, renal
mpairment, cardiac disease, and diabetes) (Class IIa; Level of Evidence B).
(New recommendation)
AHA/ASA Guideline
Recommendations on Diabetes
For patients with atherosclerotic ischemic stroke or TIA and without known
CHD, it is reasonable to target a reduction of at least 50% in LDL-C or a
target LDL-C level of < 70 mg/dL to obtain maximum benefit (Class IIa; Level
of Evidence B). (New recommendation)
AHA/ASA Guideline
Recommendations on Lipids
For patients with atherosclerotic ischemic stroke or TIA and without known
CHD, it is reasonable to target a reduction of at least 50% in LDL-C or a
target LDL-C level of 70 mg/dL to obtain maximum benefit (Class Iia; Level of
Evidence B). (New recommendation)
Patients with ischemic stroke or TIA with low HDL-C may be considered for
treatment with niacin or gemfibrozil (Class IIb; Level of Evidence B)
AHA/ASA GUIDELINE
Guidelines for the Prevention of Stroke
in Patients With Stroke or Transient Ischemic Attack
Patients with ischemic stroke or TIA who are heavy drinkers should eliminate
or reduce their consumption of alcohol (Class I; Level of Evidence C).
Light to moderate levels of alcohol consumption (no more than 2 drinks per
day for men and 1 drink per day for nonpregnant women) may be
reasonable; nondrinkers should not be counseled to start drinking (Class IIb;
Level of Evidence B).
AHA/ASA Guideline
Recommendations on Cigarette Smoking
Healthcare providers should strongly advise every patient with stroke or TIA
who has smoked in the past year to quit (Class I; Level of Evidence C).
For patients with ischemic stroke or TIA who are capable of engaging in
physical activity, at least 30 minutes of moderate-intensity physical exercise,
typically defined as vigorous activity sufficient to break a sweat or
noticeably raise heart rate, 1 to 3 times a week (eg, walking briskly, using an
exercise bicycle) may be considered to reduce risk factors and comorbid
conditions that increase the likelihood of recurrent stroke (Class IIb; Level of
Evidence C).
At this time, the utility of screening patients for the metabolic syndrome
after stroke has not been established (Class IIb; Level of Evidence C). (New
recommendation)
For patients who are screened and classified as having the metabolic
syndrome, management should include counseling for lifestyle modification
(diet, exercise, and weight loss) for vascular risk reduction (Class I; Level of
Evidence C). (New recommendation)
Preventive care for patients with the metabolic syndrome should include
appropriate treatment for individual components of the syndrome that are
also stroke risk factors, particularly dyslipidemia and hypertension (Class I;
Level of Evidence A). (New recommendation)
AHA/ASA GUIDELINE
Guidelines for the Prevention of Stroke
in Patients With Stroke or Transient Ischemic Attack
Aspirin (50 mg/d to 325 mg/d) monotherapy (Class I; Level of Evidence A),
the combination of aspirin 25 mg and extended-release dipyridamole 200
mg twice daily (Class I; Level of Evidence B), and clopidogrel 75 mg
monotherapy (Class IIa; Level of Evidence B) are all acceptable options for
initial therapy. The selection of an antiplatelet agent should be
individualized on the basis of patient risk factor profiles, cost, tolerance, and
other clinical characteristics.
AHA/ASA Guideline
The addition of aspirin to clopidogrel increases risk of hemorrhage and is not
recommended for routine secondary prevention after ischemic stroke or TIA
(Class III; Level of Evidence A).
For patients who have an ischemic stroke while taking aspirin, there is no
evidence that increasing the dose of aspirin provides additional benefit.
Although alternative antiplatelet agents are often considered, no single
agent or combination has been studied in patients who have had an event
while receiving aspirin (Class IIb; Level of Evidence C).
NIHSS