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Medical management
of
By
S.A.KEERTHI VASAN 3rd year B.Sc.Nursing
DEPARTMENT OF MEDICAL SURGICAL NURSING
SHNC.
TYPES OF STROKE
85% Ischemic 15 % hemorrhagic
Ischemic Stroke
Embolic - cardiogenic sources such as atrial fibrillation
Thrombotic - associated with atherosclerotic plaque
Thrombolytic therapy
• It is used to treat ischemic stroke by
dissolving the already formed blood clot
that is blocking blood flow to the brain.
1. Fibrinolytic therapy
Non – fibrin specific fibrin specific
•Streptokinase
•Anistreplase.
•urokinase
Tissue plasminogen
Activators (t-PA).
 Alteplase
 Reteolase
 Tenecteplase
DIFFERENCE BETWEEN FIBRIN SPECIFIC AND NON SPECIFIC
AGENTS
FIBRIN SPECIFIC AGENTS
• Binds equally to circulating
and non circulating
plasminogen .
• Produces breakdown of clot
(local fibrinolysis )and
circulating plasminogen and
other plasma proteins thus
cause an unwanted leading
to bleeding .
• Half life of fibrin specific
agents is 18 mins
FIBRIN NON SPECIFIC AGENTS
• Binds preferentially to
plasminogen at the fibrin
surface (non circulating )
rather than circulating
plasminogen in blood .
• Risk of bleeding is less than
non specific agents .
• Activity is enhanced upon
binding to fibrin .
• The half life of tPA in the
bloodstream is rather than
5-10 minutes in humans
Mechanism of action
• The fibrinolytic action of tPA occurs at
the plasminogen is converted into
plasmin, whose enzymatic action then
digests fibrin and fibrinolytic , thus
breaking down the clot.
• Tissue plasminogen activators(tPA) is
used to produce localized fibrinolysis by
binding to the fibrin in the thrombi.
CLOT DISSOLUTION
PLASMINOGEN
PLASMINOGEN ACTIVATOR
PLASMIN
FIBRIN DEGRADATION PRODUCTS
t-PA IV administeration
• To reestablish blood flow through a
blocked artery to prevent cell death in
patients with the acute onset of ischemic
stroke.
• It must be administered within 3 to 41/2
hours of the onset.
• Patients are screened (noncontrast CT
scan, MRI, Blood test) carefully before
tPA can be given.
Intraarterial infusion
• Patients with an ischemic stroke when the
mechaincal thrombectomy is not an
option.
• It must be administered within 6 hours of
sudden onset .
• The tPA is administered through the
catheter and immediately targets the
clots.
Dosage and administration
• The dosage for t-PA is 0.9 mg/kg , with a
maximum dose of 90mg.
• 10% of the calculated dose is given IV bolus
over 1 minute.
• The remaining dose (90%) is given IV over 1
hour via an infusion pump.
• No other antithrombotic treatment for 24 h.
• Avoid urethral catheterization.
rtPA Alteplase
• Must be given within 4.5 hours of stroke
• Do not mix rt-PA with any other medications
• Do not use IV tubing with infusion filters.
• Must be on a cardiac monitor
 Must be given with an INFUSION PUMP
• When infusion is complete, saline flush with Normal
saline
• rt-PA must be used within 8 hours of mixing when
stored at room temperature or within 24 hours if
refrigerated
THROMBOLYSIS
Alteplase rTPA 0.9mg /Kg
10 % of total dose –Bolus 2-3 mins
90 % of total dose –Infuse over 60 mins
• Intracranial hemorrhage
• Active internal bleeding
• Endocarditis or acute pericarditis
ABSOLUTE CONTRAINDICATIONS
Indication contraindication
• Clinical diagnosis of
stroke.
• Onset of symptoms to
time of drug
administration ≤4.5 Hb.
• CT scan showing no
hemorrhage or edema
of >1/3 of the MCA
territory
• Age 18 ≥years.
• Consent by patient or
surrogate.
• Sustained bp
>185/110mmHg despite
treatment.
• Platelets <100,000 ;
Hct<25%; glucose <50
or >400 mg/dl.
• Use of heparin within
48 hrs and prolonged
PTT or elevated INR.
• Rapidly improving
symptoms
• Prior stroke or head
injury within 3 mon;
prior intracranial
• Avoid
taking BP in arm with IV’s or venipunctures
invasive procedures
unnecessary handling of the patient
unnecessary venous or arterial punctures
• Blood is drawn from IV saline lock if possible
• Apply pressure dressing to potential sources of bleeding
• Assess all secretions and excretions for blood
• Bed rest for 12 – 24 hours
Assessment during and after t-PA
• NPO for 6 hours post t-PA
• Complete swallow screen prior to any oral
intake
• If fails, keep NPO then reassess
DIET
Eligibility criteria for Tissue plasminogen Activators
Administration
• Age ≥ 18 years
• Clinical diagnosis of ischemic stroke.
• Time of onset of stroke known and is less than 3 hours
before treatment.
• Systolic blood pressure ≤185mm Hg:diastolic ≤110mm
Hg .
• No seizure at onset of stroke.
• Prothrombin time ≤15seconds or international
normalized ratio ≤1.7(if taking an anticoagulants,the
same guidance is used )
• Platelet count ≥100,000/mm3.
• Not received heparin during the past 48 hours with
elevated partial thromboplastin time.
• Glucose >50mg/dl.
• No prior intracranial hemorrhage , neoplasm,
arteriovenous malformation or aneurysm.
• No major surgical procedures or serious trauma within
14 days .
• No stroke , serious head injury, or intracranial surgery
within 3 months.
• No gastrointestinal or urinary bleeding within 21 days.
• No pregnancy.
• { There are more stringent criteria if t-PA is considered
for those patients in the 3.0 to 4.5 hours time
window.}
Anticoagulants &
platelet inhibitors
• After the patients has stabilized and to prevent
further clot formation.
• Patients with stroke caused by thrombi and
emboli may be treated with anticoagulants
&platelet inhibitors.
• For patients who have atrial fibrillation , oral
anticoagulants includes – WARFARIN,.
• platelet inhibitors includes –
ASPIRIN,CLOPIDOGREL,TICLOPIDINE.
• To reduce ICP, such as administering osmotic
diuretic (eg, mannitol)
Review & Questioner
• Time limitations for Intraarterial
infushion is -------
• tPA & drug should be administered
within -------
• List out the fibrinolytic drugs .
• Compare & contrast half life period of
fibrin specific and non-fibrin specific?
HemorRhagic stroke
weakened regions of blood vessels rupture as a
result of increased pressure
Anticoagulants
&
platelets inhibitors
Anticoagulants &platelets inhibitors are
contraindicated in hemorrhagic stroke
• The main drug therapy is to
management of hypertension.
• It may be of oral/IV agents are used to
maintain normal BP.(systolic BP less
than 160mmHg).
• Seizure prophylaxis in the acute
period after intracerebral &
subarachoid hemorrhage .(diazepam,
lorazepam)
BP relationship
• BP increase due to an arterial
occlusion,( ie.,an effort to
perfuse penumbra).
• Failure to recanalize ( with or
without thrombolytic therapy)
result in high BP and poor neuro
outcomes.
• Lowering BP starves penumbra,
worsens outcomes.
Why questions ?
• why Anticoagulants &platelets inhibitors are
contraindicated in hemorrhagic stroke ?
• Why fibrin specific agent is superior to non
fibrin specific thrombolytic agent?
• What are the screening protocol to be checked
before tPA treatment?
• List down any few absolute contraindication
for tPA.
• What is the dosage of tPA.
S.A.KEERTHI VASAN B.SC,NURSING

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Medical management of cerebro vascular accident a quick review

  • 1. Medical management of By S.A.KEERTHI VASAN 3rd year B.Sc.Nursing DEPARTMENT OF MEDICAL SURGICAL NURSING SHNC.
  • 2. TYPES OF STROKE 85% Ischemic 15 % hemorrhagic
  • 3. Ischemic Stroke Embolic - cardiogenic sources such as atrial fibrillation Thrombotic - associated with atherosclerotic plaque
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  • 6. Thrombolytic therapy • It is used to treat ischemic stroke by dissolving the already formed blood clot that is blocking blood flow to the brain.
  • 7. 1. Fibrinolytic therapy Non – fibrin specific fibrin specific •Streptokinase •Anistreplase. •urokinase Tissue plasminogen Activators (t-PA).  Alteplase  Reteolase  Tenecteplase
  • 8. DIFFERENCE BETWEEN FIBRIN SPECIFIC AND NON SPECIFIC AGENTS FIBRIN SPECIFIC AGENTS • Binds equally to circulating and non circulating plasminogen . • Produces breakdown of clot (local fibrinolysis )and circulating plasminogen and other plasma proteins thus cause an unwanted leading to bleeding . • Half life of fibrin specific agents is 18 mins FIBRIN NON SPECIFIC AGENTS • Binds preferentially to plasminogen at the fibrin surface (non circulating ) rather than circulating plasminogen in blood . • Risk of bleeding is less than non specific agents . • Activity is enhanced upon binding to fibrin . • The half life of tPA in the bloodstream is rather than 5-10 minutes in humans
  • 9. Mechanism of action • The fibrinolytic action of tPA occurs at the plasminogen is converted into plasmin, whose enzymatic action then digests fibrin and fibrinolytic , thus breaking down the clot. • Tissue plasminogen activators(tPA) is used to produce localized fibrinolysis by binding to the fibrin in the thrombi.
  • 11. t-PA IV administeration • To reestablish blood flow through a blocked artery to prevent cell death in patients with the acute onset of ischemic stroke. • It must be administered within 3 to 41/2 hours of the onset. • Patients are screened (noncontrast CT scan, MRI, Blood test) carefully before tPA can be given.
  • 12. Intraarterial infusion • Patients with an ischemic stroke when the mechaincal thrombectomy is not an option. • It must be administered within 6 hours of sudden onset . • The tPA is administered through the catheter and immediately targets the clots.
  • 13. Dosage and administration • The dosage for t-PA is 0.9 mg/kg , with a maximum dose of 90mg. • 10% of the calculated dose is given IV bolus over 1 minute. • The remaining dose (90%) is given IV over 1 hour via an infusion pump. • No other antithrombotic treatment for 24 h. • Avoid urethral catheterization.
  • 14. rtPA Alteplase • Must be given within 4.5 hours of stroke • Do not mix rt-PA with any other medications • Do not use IV tubing with infusion filters. • Must be on a cardiac monitor  Must be given with an INFUSION PUMP • When infusion is complete, saline flush with Normal saline • rt-PA must be used within 8 hours of mixing when stored at room temperature or within 24 hours if refrigerated
  • 15. THROMBOLYSIS Alteplase rTPA 0.9mg /Kg 10 % of total dose –Bolus 2-3 mins 90 % of total dose –Infuse over 60 mins
  • 16. • Intracranial hemorrhage • Active internal bleeding • Endocarditis or acute pericarditis ABSOLUTE CONTRAINDICATIONS
  • 17. Indication contraindication • Clinical diagnosis of stroke. • Onset of symptoms to time of drug administration ≤4.5 Hb. • CT scan showing no hemorrhage or edema of >1/3 of the MCA territory • Age 18 ≥years. • Consent by patient or surrogate. • Sustained bp >185/110mmHg despite treatment. • Platelets <100,000 ; Hct<25%; glucose <50 or >400 mg/dl. • Use of heparin within 48 hrs and prolonged PTT or elevated INR. • Rapidly improving symptoms • Prior stroke or head injury within 3 mon; prior intracranial
  • 18. • Avoid taking BP in arm with IV’s or venipunctures invasive procedures unnecessary handling of the patient unnecessary venous or arterial punctures • Blood is drawn from IV saline lock if possible • Apply pressure dressing to potential sources of bleeding • Assess all secretions and excretions for blood • Bed rest for 12 – 24 hours Assessment during and after t-PA
  • 19. • NPO for 6 hours post t-PA • Complete swallow screen prior to any oral intake • If fails, keep NPO then reassess DIET
  • 20. Eligibility criteria for Tissue plasminogen Activators Administration • Age ≥ 18 years • Clinical diagnosis of ischemic stroke. • Time of onset of stroke known and is less than 3 hours before treatment. • Systolic blood pressure ≤185mm Hg:diastolic ≤110mm Hg . • No seizure at onset of stroke. • Prothrombin time ≤15seconds or international normalized ratio ≤1.7(if taking an anticoagulants,the same guidance is used ) • Platelet count ≥100,000/mm3.
  • 21. • Not received heparin during the past 48 hours with elevated partial thromboplastin time. • Glucose >50mg/dl. • No prior intracranial hemorrhage , neoplasm, arteriovenous malformation or aneurysm. • No major surgical procedures or serious trauma within 14 days . • No stroke , serious head injury, or intracranial surgery within 3 months. • No gastrointestinal or urinary bleeding within 21 days. • No pregnancy. • { There are more stringent criteria if t-PA is considered for those patients in the 3.0 to 4.5 hours time window.}
  • 22. Anticoagulants & platelet inhibitors • After the patients has stabilized and to prevent further clot formation. • Patients with stroke caused by thrombi and emboli may be treated with anticoagulants &platelet inhibitors. • For patients who have atrial fibrillation , oral anticoagulants includes – WARFARIN,. • platelet inhibitors includes – ASPIRIN,CLOPIDOGREL,TICLOPIDINE. • To reduce ICP, such as administering osmotic diuretic (eg, mannitol)
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  • 26. Review & Questioner • Time limitations for Intraarterial infushion is ------- • tPA & drug should be administered within ------- • List out the fibrinolytic drugs . • Compare & contrast half life period of fibrin specific and non-fibrin specific?
  • 27. HemorRhagic stroke weakened regions of blood vessels rupture as a result of increased pressure
  • 28. Anticoagulants & platelets inhibitors Anticoagulants &platelets inhibitors are contraindicated in hemorrhagic stroke
  • 29. • The main drug therapy is to management of hypertension. • It may be of oral/IV agents are used to maintain normal BP.(systolic BP less than 160mmHg). • Seizure prophylaxis in the acute period after intracerebral & subarachoid hemorrhage .(diazepam, lorazepam)
  • 30. BP relationship • BP increase due to an arterial occlusion,( ie.,an effort to perfuse penumbra). • Failure to recanalize ( with or without thrombolytic therapy) result in high BP and poor neuro outcomes. • Lowering BP starves penumbra, worsens outcomes.
  • 31. Why questions ? • why Anticoagulants &platelets inhibitors are contraindicated in hemorrhagic stroke ? • Why fibrin specific agent is superior to non fibrin specific thrombolytic agent? • What are the screening protocol to be checked before tPA treatment? • List down any few absolute contraindication for tPA. • What is the dosage of tPA.