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Stenting vs medical management in intracranial stenosis
1. STENTING VS MEDICAL MANAGEMENT
IN INTRACRANIAL ARTERIAL STENOSIS
FOR- STENTING
Dr Prashant Makhija
2. EVIDENCE
ï± 8â10% of all ischemic strokes in America, 30% to 50% of
strokes in the Asian population1
ï± With medical therapy alone risk of recurrent stroke
unacceptably high, approximately 23% at 1 year1
ï± Several studies demonstrate success with intracranial stenting
ï§ SSYLVIA Trial- 61 pts(70.5% intracranial stenosis), 95% success
rate, 1 mth 6.6% strokes & 0% mortality, 7.3% strokes later
than 1 mth, FDA granted a humanitarian device exemption2
1.
J NeuroIntervent Surg 2012 4: 397-406
2.
AJNR: 26, October 2005
3. Study
n
Technical
success rate
(%)
30 day ipsilat
stroke /death
rate
Wingspan
study(2007)
45
100
4.5
Fiorella et
al(2007)
78
98.8
6.1
NIH
registry(2008)
129
96.7
9.6
ï± Anand Alurkar et al (2013)- 182 patients, 97.44% success
rate, 1mth stroke incidence 11 (5.64%), of which 2 (1.02%) were
major, 2 deaths(mortality=1.09%)
ï± Simon Chun Ho Yu et al (2013)- 65 pts, 93.8% success rate, 66
stenotic lesions, ISR 16.7%, periprocedural stroke or death rate
was 6.1%, no interval strokes 1-year follow-up
4. THE OPPOSITION- SAMMPRIS
ï± SAMMPRIS- RCT 451 pts, 30-day rate of stroke or death was
14.7% in the PTAS group and 5.8% in the medicalmanagement group
ï± Why so ?
ï§ Experience - higher rate in the current study does not reflect
inexperience of the operators (NIH registry data- 9% at high
enrolling sites versus 23% at low enrolling sites)
ï inherently high risk to the procedures with the device used in the
trial, which does not decline with user experience
ï§ Design - 2-step procedure with a long exchange wire
ï difficulty with wire control, can cause perforations and
subarachnoid hemorrhage or wire injury of small perforating
arteries
5. ï§ Vessel size & lesion- trial mandated that lesions had to be 14 mm
long and arteries had to have a normal diameter of 2.0 to 4.5 mm
ï treatment of small vessels(2.5 to 2.75 mm)is problematic, more
likely to have restenosis, acute thrombosis, more prone to injury
with PTAS
ï >10 mm (Mori C) lesions, higher rates of death, ipsilateral stroke,
in stent restenosis after angioplasty
ï§ Medical therapy- team (neurologist, study coordinator, lifestyle
coach), study coordinator counted ptsâ antiplatelet medications,
lifestyle coach developed personal action plans, contacted pts every
2 wks for the first 3 months & then monthly thereafter
ï Idealistic , difficult to achieve in âreal-worldâ situations
1.
2.
Michael P. Marks. Stroke. 2012;43:580-584
Alex Abou-Chebl and Helmuth Steinmetz. Stroke. 2012;43:616-620
6. CONCLUSION
ï± SAMMPRIS trial, set a higher bar for the investigation of
endovascular therapy for symptomatic intracranial stenosis
ï± Supports modification but not discontinuation of our approach to
intracranial angioplasty and/or stent placement for intracranial
stenosis
ï± PTAS remains a valuable tool for patients refractory to medical
therapy
ï± Do Not Throw the Baby Out with the BathwaterâŠ
(T. KRINGS )