Documenti di Didattica
Documenti di Professioni
Documenti di Cultura
Dr Abhinav Gupta
Stroke team
Neurologist
Casualty doctor on duty
ICU doctor on duty
Neurosurgeon/ Interventional surgeon
Anesthetist on call
Stroke nurse
Cath lab Technician and Nurse
Imp questions to initiate thrombolysis protocol
1.Exact time when 1st symptom was noticed. IF TIME OF ONSET UPTO 4.5 HRS
THEN TPA GROUP IF TIME >4.5 HRS THEN THROMBECTOMY GROUP
2. Any maj surgery in 2 weeks
3. Recent maj stroke
4.SEND BLD INVESTIGATIONS
CBC, bld sugar, KFT, PT INR, Bld group, ECG
It is a possible acute stroke due to lack of blood supply to brain and the deficit can
be reversed depending on the damage found
We have all facilities for its treatment 24X7
We need to rush to confirm the diagnosis and treat after your approval
We have informed the financial counsellor who will detail you soon and guide you
for admission
Family not willing for admission or expensive treatment or other financial issues
which prompt delay: Confirm with the counsellor and Continue for diagnosis
confirmation.
Intervention after CT
CT normal or Early CT signs of ischemia Large infarct core ICH
Dosing of rTPA
TO BE STARTED AFTER ONLY THROMBOLYSIS SPECIAL CONSENT FORM TO BE
MADE
0.9 mg/kg IV; not to exceed 90 mg total dose; administer 10% of the total dose as
an initial IV bolus over 1 minute and the remainder infused over 60 minutes
Monitor and control blood pressure during and following administration
In patients without recent use of oral anticoagulants or heparin, treatment can be
initiated prior to the availability of coagulation study results
Discontinue if the pretreatment INR is >1.7 or the aPTT is elevated
ECASS-III
Placebo controlled trial of alteplase (rt-PA) in acute ischemic hemispheric stroke
where thrombolysis is initiated between 3 and 4 hours after stroke onset
Randomized 1:1 to receive intravenous rt-PA (alteplase 0.9mg/kg bodyweight,
maximally 90mg; 10% bolus plus one hour infusion) or placebo started between 3
and 4 hours from the onset of stroke.
Results:
A recent metaanalysis (Lancet 2004; 363 (9411): 768–
774) showed that thrombolysis with rt-PA may be
beneficial up to 270 minutes.
ASPECT
ASPECTS: The Alberta Stroke Program Early CT score 2001.
10 point topographic imaging score
ASPECT score
The Alberta Stroke Program Early CT Score (ASPECTS) is a systematic approach to
detect early CT signs like the insular ribbon sign or obscuration of the lentiform
nucleus.
Although the ASPECTS score was previously shown to be a strong predictor of
functional outcome after IVT, it has now been shown prospectively and
successfully to predict also the outcome after EVT.
An independent meta-analysis showed that EVT improves outcomes both in
patients with CT-based ASPECTS of 8 to 10 (ie, minimal ischemic damage) as well
as of 5 to 7 (ie, moderate ischemic damage).
On the contrary, patients with a low ASPECTS of 0 to 4 showed no treatment
benefit by EVT, suggesting that EVT has little or no efficacy in patients with large
ischemic core.
Practical clinical utility of the alberta stroke programe early CT score
Less than-3 hour patient
ASPECT is used as prognostic tool for less than 3 hours from stroke onset . If
ASPECT values are low, there is lack of major clinical recovery or response from
thrombolysis , even with successful recanalization.
They do not exclude patient from intravenous rt-PA therapy based on the extent
of EIC, unless it involves the entire MCA territory (ASPECT<3).
A low ASPECT may protend subsequent clinical deterioration in the form of
malignant MCA infarction.
Patients with good ASPECT are typically excellent candidates to include combined
I.V and I.A approach
Not a contraindication
Current aspirin, NSAID or antiplatelet drugs (dipyridamole, ticlopidine,
clopidogrel)
History of PUD (not currently active [>3 months])
Intraarterial thrombolysis ( PROACT )
IA thrombolysis ( dose 0.1mg/kg) given over 2 hours was significantly associated
with substantial increases in recanalization rates and good and excellent outcomes
in AIS. Intra-arterial thrombolytic treatment is gaining traction at some
comprehensive stroke facilities at tertiary hospitals. It is often administered as an
off-label therapy within 6 h of onset of stroke in patients with anterior circulation
and up to 12–24 h after onset in the posterior circulation
Indications for Mechanical Thrombectomy
Although IVT is a treatment option ≤4.5 hours after stroke onset, additional or
primary EVT can be performed within a more extended time window of 6 hrs in
anterior circulation and upto 24 hrs in posterior circulation .
Patients with significant deficits manifesting National Institutes of Health Stroke
Scale scores between 8 and 20 are more likely to benefit from reperfusion with
EVT.
EVT in patients presenting with minor to mild stroke severity and proximal large
vessel occlusion seems to be favorable and safe.
The Stent-Assisted Recanalization in Acute Ischemic Stroke (SARIS)
A 50-year-old man who collapsed and hit his head. His NIHSSS was 14.
Preliminary CT demonstrated no ischemic changes. Because of a frontal
scalp contusion systemic rtPA was eschewed in favor of direct IA injection
Lateral left CCA angiogram demonstrated no flow in the cervical ICA, but
minimal reconstitution of the cavernous ICA by meningeal collaterals.
Microcatheter injection explained the appearance: a bifid origin of the M1
segment, with a stump of M1 resembling an aneurysm, while the
microcatheter has entered a minor branch
The microcatheter was placed beyond the clot
1 mg of rtPA was injected; as the microcatheter was retracted into the
proximal clot, an additional 1 mg rtPA was injected. Then the microcatheter
was placed into the proximal clot and infusion of rtPA at 10 mg/hr was
begun. The 0.010-inch microguidewire was advanced approximately 10
inches and the microcatheter 20 inches after control injection
The Merci procedure is performed after femoral artery acess is obtained with the
Merci balloon guide, which comes in both 8- and 9-F outer diameters.
Once the balloon guide is in the conduit vessel of interest, a medium-sized
catheter (4.2- and 5.3-F outer diameters), the distal access catheter (used for
triaxial support), and microcatheter of choice are advanced over the microwire to
the clot under direct fluoroscopic guidance.
The microwire is then exchanged for the Merci retriever system with placement
distal to the clot .
The balloon guide is then inflated. Using a slow, steady pulling motion, the
retriever engages the clot while the distal access catheter position is maintained.
Then, as the clot moves more proximally, the distal access catheter, microcatheter,
and retriever are moved toward the guide while aggressive aspiration is
performed from the guide.
The retriever can be resheathed and the steps repeated.
Stent Retriever Technique
Retrievable stents are self-expandable stent-like devices that are fully retrievable.
Therefore, these devices combine the advantages of prompt flow restoration and
mechanical thrombectomy. Excellent recanalization results can be achieved with
this technique with rates of Thrombolysis in Cerebral Infarction (TICI) grade 2a/b
or 3 flow as high as 90%. low rates of symptomatic ICH and low mortality rates.
Cont
At the stent retriever technique, the target vessel is entered with a 0.014-inch
guidewire and a suitable microcatheter between 0.018 and 0.027 inch.
The thrombus is crossed with the guidewire, and the microcatheter is placed distal
to the thrombus. The stent retriever is advanced to the distal end of the
microcatheter.
Then, the microcatheter is removed to deploy the device under fluoroscopy. A
control angiogram is performed after successful unfolding of the device.
The sizes of stent retriever devices range from 3.0×15 mm to 6.0×30 mm;
however, typically a 6.0-mm device is used. After a short period of time, the
device is pulled back with continuous aspiration.
The procedure is repeated until a TICI grade of 2b or 3 is reached
Th Thrombectomy
Penumbra
The Penumbra system has 3 main components:
A reperfusion catheter, separator, and a thrombus removal ring.
The Penumbra procedure is performed after arterial access is obtained and usually
after systemic heparinization. All components of the Penumbra system are
deliverable through a 6-F standard guide catheter, but an 070 Neuron catheter
(Penumbra, Inc.) is the guide designed for the system. The reperfusion catheter is
then advanced past the guide catheter over a guidewire and placed proximal to
the clot. The catheters and separators are available in different sizes for various
arterial diameters. The guidewire is then removed from the reperfusion catheter,
and the penumbra separator is advanced through the reperfusion catheter. The
aspiration pump is then started and a continuous aspiration, clot disruption-
debulking process is performed with the separator. In general, the Penumbra
device works better in straight arterial segments than around curves or at branch
points because the separator may cause arterial . In addition, the largest catheter
possible should be used to allow for the greatest amount of aspiration because
suction decreases dramatically with decreasing vessel diameter
Penumbra
Penumbra Thrombus Perturbation and Aspiration System
Aspiration Technique