if its useful.....comment please....
its helps us have a short quick review about the medical managements of CVA.....
its describe about the types and how as a nurse how to care the patients on the bases of nursing care
3. Ischemic Stroke
Embolic - cardiogenic sources such as atrial fibrillation
Thrombotic - associated with atherosclerotic plaque
4.
5.
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
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)
23.
24.
25.
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?
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.