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    NON-HEMORRHAGICSTROKE

    GUIDELINES FOR TREATMENT

    (Stroke Society of the Philippines Handbook, 6thed)

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    OBJECTIVE

    To present the guidelines for treatment of Acute Stroke and TransienIschemic Attack (TIA)

    To discuss briefly the guidelines for Antiplatelet Therapy inNoncardioembolic Stroke or Transient Ischemic Attack (TIA)

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    Outline

    Stroke Scales (Glasgow Coma Scale, NIHSS)

    Classification of Acute Stroke Based on Clinical Severity

    Guidelines for Management of TIA, Mild -, Moderate -, and Severe

    Early Specific Treatment of Ischemic Stroke

    Management of Increased Intracranial Pressure

    Guidelines for Antiplatelet Therapy in Noncardioembolic Stroke orTransient Ischemic Attack (TIA)

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    GLASGOW COMA SCALE

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    National Institute of HealthStroke Scale

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    CLASSIFICATION OFACUTE STROKE

    BASED ONCLINICAL SEVERITY

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    TRANSIENT ISCHEMIC ATTACK (T

    a transientepisode of neurological dysfunction caused by focal brain

    or retinal ischemia, withoutevidence of acute infarction in which clinical symtypically last less than an hour

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    MILD STROKE

    Alert patients with any (or combination) of the ff:

    Mild pure motor weakness of one side of the body

    Pure sensory deficit

    Slurred but intelligible speech

    Vertigo with incoordination

    Visual field defects alone

    or NIHSS score: 0-5

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    MODERATE STROKE

    Awake patient with significant motor and/or sensory and/or languagand/or visual deficit

    or

    Disoriented, drowsy or light stupor with purposeful response to painstimuli

    or

    NIHSS score: 6-21

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    SEVERE STROKE

    Deep stupor or comatose patient with non-purposeful response, decor decerebrate posturing to painful stimuli

    or

    Comatose patient with no response to painful stimulior

    NIHSS score: >22

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    Recommended Place of Treatment

    (TIA)OPD

    Occurred >2 wks prior (work-upshould be done within 24-48hrs)

    ASU w/in 48hrs

    Crescendo TIAs (multiple & incsymptoms)

    With known high-risk cardiac soembolism

    Known hypercoagulable state orsymptomatic ICA stenosis

    ABCD2score >3

    High Risk

    AF (valvular or non-valvular) Rheumatic MS Prosthetic heart valves Recent MI LV/LA thrombus Atrial myxoma Infective endocarditis Dilated cardiomyopathy Marantic endocarditis

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    a risk assessment tool designed toimprove the prediction of short-termstroke risk after a transient ischemicattack (TIA)

    to predict the risk of stroke within 2

    days after a TIA, but also predictsstroke risk within 90 days

    Higher ABCD2 scores are associatedwith greater risk of stroke during the2, 7, 30, and 90 days after a TIA

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    Mild Stroke

    ASU/ regular room

    Moderate Stroke

    ASU/ ICU

    Severe Stroke

    ICU

    Recommended Place of Treatmen

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    GUIDELINES

    Management Priorities

    Emergent Diagnostics

    Early Specific Treatment

    Delayed Management and Secondary Prevention

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    GUIDELINES FOR THEMANAGEMENT OF

    TRANSIENT ISCHEMIC ATTAC(TIA)

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    Transient Ischemic Attack

    Management Priorities Ascertain clinical dx of TIA

    Exclude common TIA mimics

    ID comorbidities

    ABCs of resuscitation

    Monitor the ff:

    NVS, pupil size, BP, MAP, RR, temp, SO2

    Perform stroke scales (NIHSS, GCS) and riskstratification using ABCD2scale

    Treat BP if MAP >130

    Avoid precipitous drop (not >15% of baselin

    24 hrs

    Do not use rapid-acting SL agents; when need

    titratable IV or short-acting oral antihyperten

    Ensure appropriate hydration

    0.9% NaCl

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    Emergent Diagnostics CBC

    CBG or RBS

    PT, aPTT ECG

    Cranial MRI-DWI is preferred; may doNCCT scan if MRI is not available/possible

    Transient Ischemic Attack

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    Transient Ischemic Attack

    Early Specific Treatment

    Cardioembolism NOT suspected

    ASA 160-325 mg/day as early aspossible & continue for 14 days

    ASA 80mg + Clopidogrel 75mgmay be considered for short-termtreatment

    Ensure neuroprotection*

    Cardioembolism Suspected

    IV heparin or SQ LMWH forindividuals at high risk of earlrecurrence (AF with thrombuor MI) or ASA 160-325mg/d

    anticoagulation is not possiblecontraindicated)

    If IE is suspected, give antibiDO NOT anticoagulate

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    Transient Ischemic Attack

    Delayed Management and Secondary Prevention

    Cardioembolism NOT suspected

    Give antiplatelets (ASA,clopidogrel, cilostazol, triflusal,dipyridamole + ASA)

    Control/treat risk factors Carotid UTZ (extracranialstenosis)

    TCD studies or CTA/MRA(intracranialstenosis)

    Cardioembolism Suspected

    Echocardiography and/or rcardiologist

    NOACs > dose-adjusted w

    ASA 160-325mg/day ifanticoagulation is contraind

    ASA + Clopidogrel is reaso

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    Transient Ischemic Attack

    Delayed Management and Secondary Prevention

    Screening for hypercoagulable states and drug/toxicology tests may beconsidered for young patients with TIA/stroke especially when no vrisk factors exist and no underlying cause is identified.

    If vasculitis is suspected, may do ESR, ANA and lupus anticoagulan

    TEE to rule out PFO in cryptogenic strokes

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    GUIDELINES FOR THEMANAGEMENT OF

    MILD STROKE

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    Mild Stroke

    Management Priorities Ascertain clinical dx of stroke

    Exclude common stroke mimics

    ID comorbidities

    ABCs of resuscitation Monitor the ff:

    NVS, pupil size, BP, MAP, RR, temp, SO2

    Perform and monitor stroke scales(NIHSS, GCS)

    Provide O2support to maintain SO

    Treat BP if MAP >130

    Avoid precipitous drop (not >15% of baselin

    24 hrs

    Do not use rapid-acting SL agents; when need

    titratable IV or short-acting oral antihyperten

    Ensure appropriate hydration

    0.9% NaCl

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    Emergent Diagnostics CBC

    CBG or RBS

    PT, aPTT

    ECG

    Cranial NCCT scan or MRI-DWI as soon aspossible

    If ICH is evident, compute for the hematomavolume

    Mild Stroke

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    Mild Stroke

    Early Specific Treatment(requires neuroimaging confirmation)

    ISCHEMIC

    ASA 160-325mg/day as early as possibleand continue for 14 days

    ASA 80mg + Clopidogrel 75mg mayconsidered for short-term treatment

    Ensure neuroprotection*

    Consider IV heparin or SQ LMWindividuals at high risk of early r(AF with thrombus, VHD, or M160-325mg/day (if anticoagulati

    possible or is contraindicated)

    Ensure neuroprotection*

    If IE is suspected, give antibiotiNOT anticoagulate

    Cardioembolism SuspectedCardioembolism NOT suspected

    (Thrombotic, Lacunar)

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    Mild Stroke

    Early Specific Treatment(requires neuroimaging confirmation)

    HEMORRHAGIC Early neurology and/or neurosurgery consult for all ICH cases

    Monitor and maintain target SBP 140mmHg during the first week

    Ensure neuroprotection*

    Early rehabilitation once stable within 72hrs

    Give AEDs for clinical seizures and proven subclinical or electrographic seizures Prophylactic AEDs and steroids are generallynot recommended.

    Monitor/ correct for metabolic parameters and coagulation/ bleeding abnormalities

    Follow recommendations for neurosurgical intervention

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    Mild Stroke

    Delayed Management and Secondary PreventionISCHEMIC

    Cardioembolism NOT suspected

    (Thrombotic, Lacunar)

    Give antiplatelets (ASA, clopidogrel,cilostazol, triflusal, dipyridamole, ER-dipyridamole + ASA)

    Control/treat risk factors

    Carotid UTZ (extracranialstenosis)

    TCD studies or CTA/MRA (intracranialstenosis)

    Cardioembolism Suspected

    Echocardiography and/or refer cardiologist

    NOACs > dose-adjusted warfari

    ASA 160-325mg/day if anticoagcontraindicated

    ASA + Clopidogrel is reasonabl

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    Mild Stroke

    Delayed Management and Secondary PreventionHEMORRHAGIC

    Long-term strict BP control and monitoring

    Contrast CT scan, 4-vessel cerebral angiogram, MRA or CTA if the is:

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    GUIDELINES FOR THEMANAGEMENT OF

    MODERATE STROKE

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    Moderate Stroke

    Management Priorities Ascertain clinical dx of stroke

    Exclude common stroke mimics

    ID comorbidities

    ABCs of resuscitation Monitor the ff:

    NVS, pupil size, BP, MAP, RR, temp, SO2

    Perform and monitor stroke scales (NIHSS,GCS)

    Provide O2support to maintain SO

    Treat BP if MAP >130

    Avoid precipitous drop (not >15% of baselin

    24 hrs

    Do not use rapid-acting SL agents; when need

    titratable IV or short-acting oral antihyperten

    Recognize and treat for early S/Sincreased ICP

    Ensure appropriate hydration

    0.9% NaCl

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    Emergent Diagnostics CBC

    CBG or RBS

    PT, aPTT

    Serum Na+ and K+

    ECG

    Cranial NCCT scan or MRI-DWI as soon aspossible

    If ICH is evident, compute for the hematoma volume

    Moderate Stroke

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    Moderate StrokeEarly Specific Treatment

    (requires neuroimaging confirmation)

    ISCHEMIC

    Cardioembolism NOT suspected

    Refer to neurologist for evaluation anddecision

    w/in 3-4.5hrs of stroke onset:

    IV thrombolysis (rt-PA)

    w/in 6hrs:

    Intra-arterial thrombolysis (in specialized

    centers)

    ASA 160-325mg/day 24 hrs aftetreatment and continue for 14 da

    Ensure neuroprotection*

    Early rehabilitation once stable whrs

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    Moderate StrokeEarly Specific Treatment

    (requires neuroimaging confirmation)

    ISCHEMIC

    Cardioembolism Suspected

    Refer to neurologist for evaluation anddecision

    w/in 3-4.5hrs of stroke onset:

    IV thrombolysis (rt-PA)

    w/in 6hrs:

    Intra-arterial thrombolysis (in specialized

    centers)

    If px is ineligible for thrombolyticor 24hrs post-rt-PA treatment:

    IV heparin or SQ LMWH for indhigh risk of early recurrence; or

    ASA 160-325mg/day if anticoagnot possible or is contraindicated

    Ensure neuroprotection*

    if IE is suspected, give antibioticsNOT anticoagulate

    Early rehabilitation once stable wi

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    Moderate StrokeEarly Specific Treatment

    (requires neuroimaging confirmation)

    HEMORRHAGIC Early neurology and/or neurosurgery consult for all ICH cases

    Monitor and maintain target SBP 140mmHg during the first week

    Ensure neuroprotection*

    Early rehabilitation once stable within 72hrs

    Give AEDs for clinical seizures and proven subclinical or electrographic seizures

    Prophylactic AEDs and steroids are generallynot recommended.

    Monitor/ correct for metabolic parameters and coagulation/ bleeding abnormalities

    Follow recommendations for neurosurgical intervention

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    Moderate Stroke

    Delayed Management and Secondary PreventionISCHEMIC

    Cardioembolism NOT suspected

    (Thrombotic, Lacunar)

    Give antiplatelets (ASA, clopidogrel,cilostazol, triflusal, dipyridamole, ER-dipyridamole + ASA)

    Control/treat risk factors

    Carotid UTZ (extracranialstenosis)

    Cardioembolism Suspected

    Echocardiography and/or refer cardiologist

    NOACs > dose-adjusted warfari ASA 160-325mg/day if anticoag

    contraindicated

    ASA + Clopidogrel is reasonabl

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    Moderate Stroke

    Delayed Management and Secondary PreventionHEMORRHAGIC

    Long-term strict BP control and monitoring

    Contrast CT scan, 4-vessel cerebral angiogram, MRA or CTA if the is:

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    GUIDELINES FOR THEMANAGEMENT OF

    SEVERE STROKE

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    Severe Stroke

    Management Priorities Ascertain clinical dx of stroke

    Exclude common stroke mimics

    ID comorbidities

    ABCs of resuscitation

    Monitor the ff:

    NVS, pupil size, BP, MAP, RR, temp, SO2

    Perform and monitor stroke scales (NIHSS,GCS)

    Provide O2support to maintain SO

    Treat BP if MAP >130

    Avoid precipitous drop (not >15% of baselin

    24 hrs

    Do not use rapid-acting SL agents; when need

    titratable IV or short-acting oral antihyperten

    Recognize and treat for early S/Sincreased ICP

    Ensure appropriate hydration

    0.9% NaCl

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    Emergent Diagnostics CBC

    CBG or RBS

    PT, aPTT

    Serum Na+ and K+ ECG

    Cranial NCCT scan or MRI-DWI as soon aspossible

    If ICH is evident, compute for the hematoma volume

    Severe Stroke

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    Severe StrokeEarly Specific Treatment

    (requires neuroimaging confirmation)

    ISCHEMIC

    Cardioembolism NOT suspected

    Refer to neurologist for evaluation anddecision

    w/in 3-4.5hrs of stroke onset:

    IV thrombolysis (rt-PA)

    w/in 6hrs:

    Intra-arterial thrombolysis (in specialized

    centers)

    ASA 160-325mg/day 24 hrs aftetreatment and continue for 14 da

    Ensure neuroprotection*

    Early rehabilitation once stable whrs

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    Severe StrokeEarly Specific Treatment

    (requires neuroimaging confirmation)

    ISCHEMIC

    Cardioembolism Suspected

    May give ASA 160-325mg/day

    Ensure neuroprotection*

    Refer to a neurologist for cases ofposterior circulation strokes within 12 hrsof onset for evaluation and decisionregarding thrombolytic therapy

    For cases of cerebellar infarct, reneurosurgeon as soon as possibl

    Early supportive rehabilitation

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    Severe StrokeEarly Specific Treatment

    (requires neuroimaging confirmation)

    HEMORRHAGIC

    Supportive treatment: Mannitol 20% 0.5-1g/kg BW q 4-6h for 3-7days

    Ensure neuroprotection*

    Give AEDs for clinical seizures and proven subclinical or electrographic seizures

    Prophylactic AEDs and steroids are generallynot recommended.

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    Severe StrokeEarly Specific Treatment

    (requires neuroimaging confirmation)

    HEMORRHAGIC Neurosurgical consult if:

    Px is not herniated

    Location of bleed is lobar, putamen, pallidum, or cerebellum

    Pxsfamily is willing to accept consequences of irreversible coma or persistent vegetative state

    ICP monitoring is contemplated and salvage surgery is considered

    Early supportive rehabilitation

    GOAL IS REDUCTION OF MORTALITY

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    Severe StrokeDelayed Management and Secondary Prevention

    ISCHEMIC

    Cardioembolism NOT suspected

    (Thrombotic, Lacunar)

    Give antiplatelets (ASA, clopidogrel,cilostazol, triflusal, dipyridamole, ER-dipyridamole + ASA)

    Control/treat risk factors

    Cardioembolism Suspected

    Echocardiography and/or refer cardiologist

    NOACs > dose-adjusted warfari ASA 160-325mg/day if anticoag

    contraindicated

    ASA + Clopidogrel is reasonabl

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    Severe StrokeDelayed Management and Secondary Prevention

    HEMORRHAGIC

    Long-term strict BP control and monitoring

    Contrast CT scan, 4-vessel cerebral angiogram, MRA or CTA if the is:

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    EARLY SPECIFIC TREATMENT OISCHEMIC STROKE

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    ANTITHROMBOTIC THERAPYIN ACUTE STROKE

    Aspirin (ASA)

    [Clopidogrel + ASA] vs ASA alone

    ClopidogrelASA vs ASA alone

    Cilostazol vs ASA

    LMWH

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    NEUROPROTECTION

    The Five H Principle:

    AVOID

    Hypotension, Hypoxemia, Hyperglycemia, Hypoglycemia andHypertherm

    during acute stroke in an effort to salvage the ischemic penum

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    Neuroprotective Interventions

    1. Avoid HYPOTENSION and allow permissive hypertension dthe first (7) days.

    Mean Arterial Pressure (MAP) = 2 (DBP) + SBP3

    Cerebral Perfusion Pressure (CPP) = MAP - ICP

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    Check if Px has any condition that may increase BP and address acc

    Treat if SBP >220 mmHg or DBP >120 mmHg, or MAP >130.

    Defer E BP therapy if MAP is within 110-130, or SBP = 185-220mor DBP = 105-120mmHg, UNLESS:

    Px is a candidate for thrombolytic therapy

    Presence of AMI, CHF, aortic dissection, acute pulmonary edema, ARF, andhypertensive encephalopathy

    Neuroprotective InterventionsBP Management in Acute Ischemic Stro

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    The use of IV Nicardepine is reasonable, readily available, easy to adand titrate, has short duration of action, and does not significantly af

    Although rare in acute ischemic stroke, arterial hypotension (a baselineSBP

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    In acute ischemic stroke, autoregulation is paralyzedin the affected tissues with

    passively following MAP. Rapid BP lowering further decrease in perfus

    penumbra.

    Hypertension is typically present in acute stroke, with spontaneous decline in the 7days with attainment of neurological stability. SBP dropped by 28% du

    first day whether or not medications were given.

    SBP and DBP drops of >20mmHg were associated with early neurological

    worsening, high rates of poor outcome or death, and larger volumes of inf

    Rationale for Permissive Hypertension

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    Treat if SBP > 180 mmHg

    Acute lowering of SBP to 140mmHg within 7 days is safe and imp

    outcome in patients with small-moderate size ICH not requiring surgintervention

    If ICP monitor is available, keep CPP >70mmHg

    Neuroprotective InterventionsBP Management in Acute Hypertensive I

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    Treat hypertension with modest reductions in BP to minimize vasospand delayed cerebral ischemia

    Preoperatively, for unsecured aneurysms, the use of IV Nicardepine target SBP

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    1. Avoid HYPOTENSION and allow permissive hypertension during the first (7) days.

    2. Avoid HYPOXEMIA

    Routine O2is not warranted for all stroke patients unless theres evidence of h

    or desaturation (target SO2>94%)

    Monitor oxygenation via pulse oximeter and/or determine ABG Provide ventilator support if the upper airway is threatened, sensorium is imp

    ICP is increased.

    Neuroprotective Interventions

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    1. Avoid HYPOTENSION and allow permissive hypertension during the first (7) days.

    2. Avoid HYPOXEMIA

    3. Avoid HYPERGLYCEMIA or HYPOGLYCEMIA

    Hyperglycemia causes lactic acidosis, increases free radical production, worsens cerebral weakens blood vessels

    Hypoglycemia can mimic a stroke

    Achieve glucose targets of 140-180mg/dl if the FBS is >140mg/dl or RBS isconsistently >180mg/dl

    Neuroprotective Interventions

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    1. Avoid HYPOTENSION and allow permissive hypertension during the first (7) days.

    2. Avoid HYPOXEMIA

    3. Avoid HYPERGLYCEMIA or HYPOGLYCEMIA

    Use an established and standardized IV insulin protocol for pxs who present extreme or persistent hyperglycemia, are critically ill, or who have received thr

    therapy for at least the first 24-48hrs of hospitalization SQ basal long-actin+ rapid-acting insulin

    For pxs who are feeding, add rapid-acting prandial (meal) insulin

    Avoid D5 IV fluids

    Neuroprotective Interventions

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    1. Avoid HYPOTENSION and allow permissive hypertension during the first (7) days.

    2. Avoid HYPOXEMIA

    3. Avoid HYPERGLYCEMIA or HYPOGLYCEMIA

    4. Avoid HYPERTHERMIA

    Associated withpoor outcome metabolic demand, free radical production, enh

    neurotransmitter release RR of 1-year mortality by 3.4 times

    Treat fever with antipyretics and cooling blankets. Investigate for source of feverinfection)

    Neuroprotective Interventions

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    Neuroprotective and Neurorestorative Dru

    Cerebrolysin

    Citicoline

    NeuroAID

    The use of drugs with neurorestorative andneuroprotective properties in acute stroke remains as a

    matter of preference of the attending physician.

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    ANTICOAGULATION INACUTE CARDIOEMBOLIC STRO

    Sources of Cardioembolic Stroke

    Low or Uncertain Risk High Risk

    MVP Mitral annular calcification Patent Foramen Ovale (PFO) Atrial Septal Aneurysm

    Calcific aortic stenosis Mitral valve strands

    AF (valvular or non-valvular) Rheumatic MS Prosthetic heart valves Recent MI

    LV/LA thrombus Atrial myxoma IE Dilated cardiomyopathy Marantic endocarditis

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    ANTICOAGULATION INACUTE CARDIOEMBOLIC STRO

    Features Suggestive of Cardioembolic Stroke

    Sudden onset of maximal deficit (

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    ANTICOAGULATION INACUTE CARDIOEMBOLIC STRO

    Features Suggestive of Cardioembolic Stroke

    Onset of symptoms after a Valsalva-provoking activity (e.g., coughing, bending)

    Infratentorial ischemic stroke (cerebellar, PCA, and multi-level infarcts, top-of-thsyndrome)

    Hemorrhagic transformation and early recanalization of occluded intracranial ves

    Neuroimaging finding of acute infarcts involving multiple vascular territories in t(predominantly carotid and MCA territories), or multiple levels of the posterior c

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    ANTICOAGULATION INACUTE CARDIOEMBOLIC STRO

    Indications and Contraindications for Anticoagulation in Patients with

    Cardioembolic Stroke

    Probably Indicated Contraindicated

    Intracardiac thrombus Mechanical prosthetic valve

    Recent MI CHF Bridging measure for long-term

    coagulation

    Bleeding diathesis Non-petechial intracranial

    hemorrhage Recent major surgery or trauma Infective endocarditis

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    ANTICOAGULATION INACUTE CARDIOEMBOLIC STRO

    How to anticoagulate

    Heparin 600-800 units per hour TIV via infusion pump. Heparin bolus IS NOT rec

    Perform aPTT as often as necessary, every 4-6hrs after dose adjustments, to keeplevels at 1.5-2.5x the control

    Infusion may be discontinued once oral anticoagulation with warfarin has reached

    therapeutic levels or once antiplatelet medication is initiated for secondary preven

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    ANTICOAGULATION INACUTE CARDIOEMBOLIC STRO

    The benefits of reducing early stroke recurrence should be weighed against the rihemorrhagic transformation

    higher in patients with large infarction, severe strokes or neurologic deficits, uncontrolled hypertension

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    MANAGEMENT OF

    INCREASED INTRACRANIALPRESSURE

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    MANAGEMENT OF INCREASED

    Signs and Symptoms of Increased ICP

    Deteriorating level of sensorium

    Cushings triad: hypertension, bradycardia, irregular respiration

    Anisocoria

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    MANAGEMENT OF INCREASED

    General

    Control agitation and pain with short-acting medications, such as NSAIDs an

    Treat fever aggressively. Avoid hyperthermia.

    Control seizures if present.

    Phenytoin 18-20mg/kg LD slow IV, then maintained at 3-5 mg/kg; or

    Levetiracetam 500mg IV q12

    Strict blood glucose control between 140-180mg/dl

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    MANAGEMENT OF INCREASED

    General

    Maintain normal fluid and electrolyte balance

    Avoid excessive free water or any hypotonic fluids such as D5W

    Maintain normal volume status

    Encourage hyperosmolar state with hypertonic saline and/or induce free water clwith mannitol or diuretics

    Use stool softeners to prevent straining

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    MANAGEMENT OF INCREASED

    Specific

    Elevate the head at 30-45 degrees to assist venous drainage.

    Do CSF drainage in the setting of hydrocephalus.

    Administer osmotic therapy:

    Give Mannitol 20% IV infusion: 0.5-1.5g/kg q 3-6h Hypertonic saline is an option

    Always maintain serum osmolality at 300-320mosmol/kg

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    MANAGEMENT OF INCREASED

    Specific

    Hyperventilate only in impending herniation by adjusting tidal volume (targetlevels of 30-35mmHg)

    Carefully intubate patients with respiratory failure defined as:

    SO2< 90% by pulse oximeter

    By ABG: PaO2 < 60 mmHg, and/ or PaCO2> 55mmHg

    Consider surgical evacuation or decompressive hemicraniectomy if indicated

    ICP catheter insertion

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    GUIDELINES FORANTIPLATELET THERAPY INNONCARDIOEMBOLIC

    STROKE OR TRANSIENTISCHEMIC ATTACK

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    GUIDELINES FOR ANTIPLATELET THERAPY IN

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    GUIDELINES FOR ANTIPLATELET THERAPY INNONCARDIOEMBOLIC STROKE OR TRANSIENT ISCHE

    ATTACK

    Although often considered for patients who have an ischemic strokewhile already on ASA, there is insufficient evidence to show that swian alternative antiplatelet agents or the use of antiplatelet combinatioreduces the risk for subsequent events.

    It is recommended that patients who develop recurrent stroke while

    antithrombotic therapy be re-evaluated for pathophysiology and risk

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    A good history and physical examination of patients could not beoveremphasized.

    Identification of stroke mimickers should be facilitated to rule outpossible diagnoses.

    Comorbid conditions should be addressed adequately.

    In our setting, there should be a conscious effort in the judicious usediagnostic examinations to maximize our resources in the managemestroke patients.

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    Care of critically ill patients is a TEAM EFFORT.

    Guidelines are guidelines. Management of patients should be individdepending on the patients clinical profile.

    Talk to your patients and their relatives.

    We are not GOD but we can be ANGELS.

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