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Chapter 5: Intra-arterial treatment of ischemic stroke
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Figure 5.8 Native imaging of the cervical region
demonstrates the ease with which the modern guide catheters, in this case the Neuron MAX 0.088", traverse tortuous anatomy (in this case a 360° loop) to allow distal purchase. Care must be taken, however, during multiple passes. It is easy for the guide catheter to move or lose position, and then subsequent (inadvertent) advancement may oppose the catheter tip against the vessel wall, resulting in dissection.
arch anatomy or proximal large vessel stenosis/tortuosity, or occluded femoral arteries. Typically a 6 French sheath may be placed, and the procedure can be performed with a 6 French guide such as a soft-tip Envoy or Neuron catheter (Penumbra, USA). If the 5 French system is considered, there are still various choices of guides such as the Navien™ 058, Envoy, Chaperon, DAC 057, Neuron™ 053, and 5 MAX catheter.
One additional word of caution in utilizing these newer-generation guide catheters in difficult vasculature: Although these catheters are excellent for improving distal purchase, and even can be advanced across 360° loops (Figure 5.8) the catheter tip will at times abut directly against the vessel wall in this type of configuration. Care should be taken to place the catheter in a straight segment either well proximal to, or well beyond such a loop, so that any guide catheter movement will not dissect the vessel at this point.
Unsuccessful thrombectomy
Even after difficult catheterization is accomplished, thrombectomy itself may be unsuccess­ful. Inadequate time of aspiration is one reason for aspiration thrombectomy failure. Aspiration of 5–15 minutes is reasonable for the Penumbra system, depending on catheter size. Upsizing the device where possible is a reasonable next step. The 5 MAX and ACE device, as stated, is intended for terminal ICA occlusions and large MCA (M1), and possibly even basilar artery occlusions, while the 4 MAX and 3 MAX are designed more for distal occlusions (e.g. M2 and beyond). The 3 MAX specifically is longer than the other catheters, with the specific intent to reach more distal occlusions. Guide catheter and reperfusion catheter compatibility should be checked. It may also be usef ul to abandon standard convention here, and commence aspiration thrombectomy from the mid-clot position (to ensure that the appropriate target area is covered).
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Chapter 5: Intra-arterial treatment of ischemic stroke
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ABCD
EF G
Figure 5.9 A 66-year-old gentleman with NIHSS of 19, no improvement noted with IV a lteplase. CT angiogram
showed occluded left ICA and MCA. Patient was intubated since could not cooperate during cerebral angiogram. This confirmed occlusion of left ICA (A) with minimal trickle of contrast in carotid bulb, best seen in lateral view (B). Microwire could be advanced, therefore 4 French vertebral artery catheter was placed near origin and exchange length microwire was advanced intracranially into left ICA for support. There is no intracranial filling noted in AP or lateral vi ew (C, D, E, F). A 4 mm Spider distal embolic protection device was advanced into distal left ICA (G) and after performing angioplasty with 5 mm × 30 mm monorail balloon, an Xact stent measuring 9– 7 mm × 40 mm was deployed successfully (H). Guide catheter run confirmed terminal left ICA occlusion involving whole supraclinoid segment (I). Microcatheter injection demonstrates thrombus in left MCA extending f rom M1 to M2 segments (J). Solitaire stent-retriever device was used with distal aspiration through 5 MAX c atheter, and complete recanalization was achieved with visualization of left ophthalmic artery, near fetal origin of left posterior cerebral artery, left A CA and TICI 2b filling of left MCA (K, L, M). Follow-up guide catheter injection demonstrates residual 35% stenosis in the stent (N, O). DWI sequence of MRI (P) on following day demon strated scattere d left MCA distribution acute i nfarct involving the left temporal, frontal, and parietal lobes and left basal ganglia. Patient was discharged to acute rehabilitation and had mild hemiparesis with dysarthria.
In the case of stent-retrievers, there may be variable strategies, for instance making another pass with the same retriever or using a new stent-retriever (same or different company); using direct aspiration with an intermediate catheter such as Neuron 4 MAX or 5 MAX; or using intra-arterial thrombolytics. There is no established dose regimen for IA recombinant tPA, although 22 mg is the maximum dose in the Interventional Manage­ment of Stroke 3 trial protocol. In clinical practice, typical IA tPA doses used are much less than this
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.
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Chapter 5: Intra-arterial treatment of ischemic stroke
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IJ K
H
LM NO
P
Figure 5.9 (cont.)
Tandem stenosis/occlusions
A tandem occlusion is a rare presentation of acute stroke that involves occlusion of the proximal cervical ICA at the bifurcation with an intracranial MCA occlusion, although the distal lesion may also involve the ACA territory. The underlying pathophysiology involves either atherosclerotic disease or a dissection of the proximal vasculature leading to complete occlusion and an embolus causing a distal tandem occlusion. Two approaches exist for the treatment of tandem occlusions, treating either the proximal occlusion or the distal occlusion first; th ere is no consensus o n which approach is more efficacious, but we prefer treating the proximal occlusion first followed by distal occlusion (Figure 5.9).
The concerns for angioplasty and stent placement in acute setting includes the proce­dure's technical feasibility (e.g. the success of stent insertion under severe stenosis or occlusion and the distal embolization caused by manipulation of highly vulnerable plaque),
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Chapter 5: Intra-arterial treatment of ischemic stroke
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safety (e.g. the potential risk of developing acute in-stent stenosis due to the lack of antiplatelet premedication), related complications (e.g. cerebral hyperperfusion syndrome (CHS)) and effectiveness for improving patients’ neurological deficits and long-term follow-up. It may be difficult to cross the lesion with a distal protection device, and thus a proximal method of protection (e.g. flow reversal or balloon occlusion) may have to be employed. However, with a downstream MCA occlusion, the added step of utilizing a protection device may not confer much additional benefit. In a study of 22 cases that had emergent carotid artery angioplasty and stenting, but had not received dual antiplatelet medications if they h ad already received IV alteplase, none of these patients developed in-stent thrombosis. In a nother study of 23 patients, it was concluded that primary stenting of the extracranial carotid artery combined with intracranial mechanical throm­bectomy can be an effective treatment for tandem occlusions, can be performed with a high rate of technical success, and can achieve good clinical outcomes in selected patients. However, the incidence of symptomatic intracranial hemorrhage (SICH) may be higher than in other patient populations and may be associated with the use of Abciximab and advanced patient age. Therefore, aggressive antiplatelet use should be avoided in such
23
. W e are careful about monitoring blood pressure closely and control it to keep it
cases less than 120 mmHg if we achieved good recanalization distally; otherwise, keep between 120 and 140 mmHg.
Conclusions
Interventional stroke therapy presents one of the most difficult procedures in the neuro­endovascular realm. The “need for speed”, unfavorable anatomy, recalcitrant clot, and critically ill patients all interact to create a complex treatment scenario. Adequate planning, from medication agents to specific materials, can all help to minimize procedural risks and technical failures.
References
1. Furlan A, Higashida R, Wechsler L, et al. Intra-arterial prourokinase for acute ischemic stroke. The PROACT II study: a randomized controlled trial. Prolyse in Acute Cerebral Thromboembolism. JAMA 1999;282:2003–11.
2. Smith WS, Sung G, Saver J, et al. Mechanical thrombectomy for acute ischemic stroke: final results of the Multi MERCI trial. Stroke 2008;39:1205–12.
3. PPST Investigators. The Penumbra pivotal stroke trial: safety and effectiveness of a new generation of mechanical devices for clot removal in intracranial large vessel occlusive disease. Stroke 2009;40:2761–8.
4. Berkhemer OA, Fransen PS, Beumer D, et al. A randomized trial of intraarterial treatment for acute ischemic stroke. N Engl J Med 2015;372:11–20.
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5. Campbell BC, Mitchell PJ, Kleinig TJ, et al. Endovascular therapy for ischemic stroke with perfusion-imaging selection. N Engl J Med 2015;372:1009–18.
6. Goyal M, Demchuk AM, Menon BK, et al. Randomized assessment of rapid endovascular treatment of ischemic stroke. N Engl J Med 2015;372:1019–30.
7. Saver JL, Goyal M, Bonafe A, et al. Solitaire with the Intention for Thrombectomy as Primary Endovascular Treatment for Acute Ischemic Stroke (SWIFT PRIME) trial: protocol for a randomized, controlled, multicenter study comparing the Solitaire revascularization device with IV tPA with IV tPA alone in acute ischemic stroke. Int J Stroke 2015;10:439–48.
8. del Zoppo GJ, Higashida RT, Furlan AJ, et al. PROACT: a phase II randomized trial of recombinant pro-urokinase by direct
Chapter 5: Intra-arterial treatment of ischemic stroke
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arterial delivery in acute middle cerebral artery stroke. PROACT Investigators. Prolyse in Acute Cerebral Thromboembolism. Stroke 1998;29:4–11.
9. Adams HP, Jr., Effron MB, Torner J, et al. Emergency administration of Abciximab for treatment of patients with acute ischemic stroke: results of an international phase III trial: Abciximab in Emergency Treatment of Stroke Trial (AbESTT-II). Stroke 2008;39:87–99.
10. Broderick JP, Palesch YY, Demchuk AM, et al. Endovascular therapy after intravenous t-PA versus t-PA alone for stroke. N Engl J Med 2013;368:893–903.
11. Hussein HM, Georgiadis AL, Vazquez G, et al. Occurrence and predictors of futile recanalization following endovascular treatment among patients with acute ischemic stroke: a multicenter study. AJNR Am J Neuroradiol 2010;31:454–8.
12. Natarajan SK, Karmon Y, Snyder KV, et al. Prospective acute ischemic stroke outcomes after endovascular therapy: a real-world experience. World Neurosurg 2010;74:455–64.
13. Janjua N, El-Gengaihy A, Pile-Spellman J, Qureshi AI. Late endovascular revascularization in acute ischemic stroke based on clinical-diffusion mismatch. AJNR Am J Neuroradiol 2009;30:1024–7.
14. Levi M, Eerenberg E, Kamphuisen PW. Bleeding risk and reversal strategies for old and new anticoagulants and antiplatelet agents. J Thromb Haemost 2011;9:1705–12.
15. Cooper ES, Bracey AW, Horvath AE, et al. Practice parameter for the use of fresh­frozen plasma, cryoprecipitate, and platelets. Fresh-Frozen Plasma, Cryoprecipitate, and Platelets Administration Practice Guidelines Development Task Force of the College of American Pathologists. JAMA 1994;271:777–81.
16. Yoon W, Seo JJ, Kim JK, et al. Contrast enhancement and contrast extravasation on computed tomography after intra-arterial thrombolysis in patients with acute ischemic stroke. Stroke 2004;35:876–81.
17. Qureshi AI, Hussein HM, Janjua N, Harris­Lane P, Ezzeddine MA. Postprocedure intravenous eptifibatide following intra­arterial reteplase in patients with acute ischemic stroke. J Neuroimaging 2008;18:50–5.
18. Qureshi AI, Harris-Lane P, Kirmani JF,
et al
. Intra-arterial reteplase and intravenous acute ischemic stroke: an open-label, dose-ranging, phase I study. Neurosurgery 2006;59:789–96; discussion 96–7.
19. Flint AC, Cullen SP, Faigeles BS, Rao VA. Predicting long-term outcome after endovascular stroke treatment: the totaled health risks in vascular events score. AJNR Am J Neuroradiol 2010;31:1192–6.
20. Kwon HJ, Chueh JY, Puri AS, Koh HS. Early detachment of the Solitaire stent during thrombectomy retrieval: an in vitro investigation. J Neurointerv Surg 2015;7:114–17.
21. Kurre W, Vorlaender K, Aguilar-Perez M, et al. Frequency and relevance of anterior cerebral artery embolism caused by mechanical thrombectomy of middle cerebral artery occlusion. AJNR Am J Neuroradiol 2013;34:1606–11.
22. Khatri P, Hill MD, Palesch YY, et al. Methodology of the Interventional Management of Stroke III Trial. Int J Stroke 2008;3:130–7.
23. Heck DV, Brown MD. Carotid stenting and intracranial thrombectomy for treatment of acute stroke due to tandem occlusions with aggressive antiplatelet therapy may be associated with a high incidence of intracranial hemorrhage. J Neurointerv Surg 2015;7:170–5.
Abciximab in patients with
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Chapter
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Carotid angioplasty and stenting: complication avoidance
6
and management
Ramachandra P. Tummala
Introduction
From the ongoing debate and trials addressing the indications for and relative efficacy of carotid angioplasty and stenting (CAS) versus carotid endarterectomy (CEA) in stroke prevention, a key message emerges: both CAS and CEA are durable treatments when carried out successfully, with the bulk of strokes occurring periprocedurally in head-to-head trials Meticulous attention to complication avoidance and management during CAS is fundamen­tal to its overall success in stroke prophylaxis. While CAS is generally straightforward, certain patients continue to pose technical challenges during various stages of the procedure.
Table 6.1 summarizes the major randomized clinical trials regarding CAS. The following
techniques are the result of experience with these technical difficulties and complications. The purpose of the present chapter is not to discuss the merits or disadvantages of carotid stenting, nor is it to compare carotid stenting with CEA. The risks of endovascular therapy must always be weighed against the risks of surgery or medical therapy in the individual patient. It is with the anticipation that an increased number of complex cases will be referred for endovascular therapy that the described techniques may be germane. Some of these technical “pearls” are already used at other centers; undoubtedly many more are unknown to our group but already used by other experienced interventionalists. The following techniques have allowed the expansion of the endovascular limits of treating carotid artery disease, and we believe they are useful for complication avoidance and management.
1
.
Standard technique for carotid angioplasty and stenting
The approach for routine CAS is fairly standardized with minor institutional variations (Figure 6.1). We perform almost all of these procedures through a transfemoral approach. Through a groin sheath, we advance a 5 French diagnostic catheter (often a Simmons 2 configuration catheter) into the mid common carotid artery (CCA) and obtain a diag­nostic angiogram, including baseline intracranial runs. Under normal conditions, we advance a stiff exchange length wire into the distal external carotid artery (ECA) and exchange the diagnostic catheter and groin sheath for a long introducer sheath (often a 90 cm long 6 French Cook Shuttle, Cook Incorporated, Bloomington, IN). Alternatively with tortuous anatomy, various other guide catheters can be used. After positioning the tip of the introducer or guide catheter (for simplicity we will refer to these devices as guide
Complications of Neuroendovascular Procedures and Bailout Techniques, ed. Rakesh Khatri, Gustavo J. Rodriguez, Jean Raymond and Adnan I. Qureshi. Published by Cambridge University Press. © Cambridge University Press 2016.
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Table 6.1 Summary of randomized clinical trials of carotid angioplasty and stenting (CAS) versus carotid endarterectomy (CAE)
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CAVATAS
8
Wallstent
9
SAPPHIRE
10
EVA-3S
11
SPACE
12
CREST
Year published 2001 2001 2004 2006 2006 2010
Period of enrollment
May 1992 to July 1997
January 1997 to June
August 2000 to July 2002
September 2000 to September 2005
March 2001 to March 2006
December 2000 through July 2008
1999
Country Europe,
Australia, and Canada
Inclusion criteria Presence of
clinically important stenosis determined by local criteria
United States United States France Germany,
Austria, and Switzerland
Symptomatic ICA stenosis 60%
Symptomatic ICA stenosis 50%, asymptomatic ICA stenosis 80%, and 1 high-risk surgical criteria
Symptomatic ICA stenosis 60%
Symptomatic ICA stenosis 50% according to NASCET criteria or 70% according to ECST criteria
United States and Canada
Symptomatic ICA stenosis 50% on angiography, 70% on US, on CTA or MRA if the stenosis on US was 50–69%. In 2005 extended to asymptomatic stenosis of 60% or angiography, 70% US, or 80% on CTA or MRA if the stenosis on US was 50–69%.
Determination of eligibility
Non­invasive techniques
Angiography Doppler ultrasound
or angiography
Conventional angiography or Doppler plus MRA
Duplex ultrasound or angiography
Angiography, CTA, MRA, US
or angiography
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Table 6.1 (cont.)
Requirements for interventionalists
CAVATAS
Not specified
8
Wallstent
Not specified Required to submit
9
SAPPHIRE
10
experience and results
11
EVA-3S
Performed at least 12 carotid stenting procedures or at least 35 stent placement procedures in the supra­aortic trunks, of which at least 5 were in the carotid artery
12
SPACE
Performed at least 25 successful consecutive percutaneous carotid angioplasties or stent procedures
Primary end point
30-day rate of disabling stroke or death
Ipsilateral stroke or procedure­related or vascular death at 1 year
A composite of death, stroke, or MI within 30 days after the intervention or death or ipsilateral stroke between 31 days and 1 year
Any stroke or death within 30 days after treatment
Ipsilateral ischemic stroke or death from randomization to 30 days after procedure
Intervention CEA CAS CEA CAS CEA CAS CEA CAS CEA CAS CEA CAS
Patients
246 240 112 107 151 159 259 261 565 567 1240 1262
treated, n
Mean age, y 67 67 70 67 72 72 70 69 68 68 69 69
Symptomatic 91% 88% 100% 100% 29% 30% 100% 100% 100% 100% 53% 53%
Men 70% 69% 62% 66% 68% 68% 78% 72% 72% 72% 66% 64%
CAD 37% 39% 74% 85% 24% 21%
Angina 29% 37%
13
CREST
More than 12 procedures per year, with complication and death rate <3% for asymptomatic and <5% among symptomatic patients
The primary end point was the composite of any stroke, myocardial infarction, or death during the periprocedural period or ipsilateral stroke within 4 years after randomization.
MI 17% 19% 28% 19% 13% 11%
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Previous CEA 24% 29%
CHF 4% 7% 18% 18%
History of stroke 39% 37% 37% 40% 24% 27% 20% 13% 43% 44%
History of TIA 26% 25% 62% 65% 32% 31% 23% 25% 31% 30%
Hypertension 58% 53% 82% 69% 85% 86% 72% 73% 76% 75% 86% 86%
Diabetes mellitus 13% 14% 28% 34% 27% 26% 26% 22% 28% 26% 30% 31%
Hyperlipidemia 32% 34% 58% 55% 79% 80% 56% 58% 86% 83%
Stenosis (mean) 77% 75% 75% 76%
Contralateral
8% 10% 1% 5% 3% 2%
occlusion
Technical success 89% 97% 89% 93%
Primary end
5.9% 6.4% 3.6%12.1% 20.1% 12% 3.9% 9.6% 6.3% 6.8% 6.8% 7.2%
point rates
30-day combined
9.9% 10% 4.5% 12.1% 5.4% 4.8% 3.9% 9.6% 6.5% 7.7% 4.5% 5.2% periprocedural complication rate
CAD: coronary artery disease; CHF, congestive heart failure; ECST, European Carotid Surgery Trial; CTA: computed tomography angiography; MI: myocardial infarction; MRA: magnetic resonance angiography, NASCET, North American Symptomatic Carotid Endarterectomy Trial; TIA, transient ischemic attack; US: ultrasound.
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Chapter 6: Carotid angioplasty and stenting
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Table 6.2 Common devices in a typical carotid stent placement procedure
Closed cell carotid stent Wallstent and NexStent (Boston Scientific Natick, MA)
Xact (Abbott Vascular, IL)
Open cell carotid stent Acculink (Abbott Vascular, IL)
Precise (Cordis, NJ) Exponent (Medtronic, MN) Protégé (Covidien, CA) Zilver 518® RX (Cook Medical, IN)
Distal embolic protection device Angioguard (Cordis, NJ)
Emboshield (Abbott Vascular, IL) Accunet (Abbott Vascular, IL) Spider (Covidien, CA) Gore Embolic Filter (Gore, DE) FilterWire EZ (Boston Scientific, MA) FiberNet (Medtronic, MN)
Proximal embolization protection devices
Gore Flow Reversal System (Gore, AZ) Mo.Ma (Medtronic, MN)
BCA
Figure 6.1 A 68-year-old
gentleman with symptomatic right ICA stenosis. A: AP view demonstrates right ICA stenosis measuring about 60%. A 6 French Cook shuttle guide is also visualized. B: A 7 mm to 10 mm × 40 mm Acculink stent deployed across stenosis. Distal embolic protection device is also visualized in distal cervical ICA.
C: Post angioplasty, improved
lumen with residual stenosis of about 25%.
devices) in the distal CCA, the patient is anticoagulated with intravenous heparin to achieve an activated clotting time of greater than 250 seconds. Using roadmap guidance, we cross the stenotic lesion with a distal embolic protection device that is deployed in a straight segment of the distal cervical internal carotid artery (ICA). We only perform pre-stenting angioplasty (predilatation) if the lesion is too stenotic to cross with the stent delivery system. After stent deployment, a post-stenting angioplasty (postdilatation) is performed. If the patient’s baseline heart rate is less than 80, we administer 0.2 mg of intravenous glycopyrrholate or 0.4 mg atropine, prior to angioplasty. Final angiographic images includ­ing intracranial runs are reviewed prior to retrieval of the distal embolic protection device. At the conclusion of the procedure, we use most of the various commercially available devices for percutaneous closure if the common femoral artery access is suitable. Routine carotid stenting can be performed relatively quickly with minimal blood loss. Usual devices in routine practice are provided in Table 6.2.
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