Pham minh thong advances in diagnosis of Acute Ischemic Stroke jfim hanoi 2015

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Advances in Diagnosis of Acute Ischemic Stroke Prof. Pham Minh Thong Bach Mai University Hospital Hanoi-Viet Nam Journées Francophones dImagerie Médicale 14 th Annual Meeting, Hanoi, nov 2015

Transcript of Pham minh thong advances in diagnosis of Acute Ischemic Stroke jfim hanoi 2015

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Advances in Diagnosis of Acute Ischemic Stroke

Prof. Pham Minh Thong Bach Mai University Hospital

Hanoi-Viet Nam

Journées Francophones d’Imagerie Médicale 14th Annual Meeting, Hanoi, nov 2015

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Introduction

•  Ischemic: 80% of stroke

•  3rd leading cause of dead in United States

•  2025: prediction of 1.2 millions patients/year •  In Viet Nam, stroke is top cause of Death (account

for 18% - 2008)

•  Cardiovascular disease, diabetes… 2

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Diagnostic Tools

•  Multi choices in diagnosis

•  CT Scanner -> MRI •  Perfusion -> Multiphase

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CT SCANNER

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•  “Emergency imaging of the brain is recommended before any specific treatment for AIS. Non-enhanced CT will provide the necessary information for initial treatment of IV r-tPA (Class I; level of Evidence A - same as 2013)*”

*AHA/ASA-stroke guide line 2015 5

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CT Non-contrast 6

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•  Rule out the hemorrhage •  Identify ischemic lesion

•  Tips: • Change the window level

– C: 8 – W: 32

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ASPECTS

•  ≥ 6: favorable clinical outcome* *Stroke, 2008. 39(8): p. 2388-2391 9

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CT Angiography (MSCT)

•  “A non-invasive intracranial vascular study is strongly recommended. If not possible at the time of initial imaging, r-tPA should done first then try vascular imaging as quickly as possible (Class I, level A - New)”

*AHA/ASA-stroke guide line 2015 10

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CT Angiography

MIP (Single phase) VRT 11

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CT Perfusion •  “The benefit of CT perfusion, DWI/perfusion-weighted

imaging for selecting patients (ASPECTS<6…) for endovascular therapy are unknown (Class IIb; level C - New). Further randomized, controlled trials should be done*”

*AHA/ASA-stroke guide line 2015

Lesions = Core (irreversible )+ penumbra (reversible)

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CT Perfusion

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MRI

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MRI protocol

•  T2*: rule out hemorrhage + identify cerebral microbleeding

•  DWI: core of infarction •  FLAIR: parenchymal lesion/ absence of “flow voids” in

the occluded artery

•  TOF 3D: arterial occlusion site

•  PW: if possible

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- Rule out hemorrhage

- Identify cerebral microbleeding

-> risk factor of bleeding after treatment

T2*

Kidwell Stroke 2002; Nighoghossian Stroke 2002; Derex Cerebrovasc Dis 2004 16

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Identify occlusion site

T2*

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MRI TOF 3D

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•  ≥ 6: favorable clinical outcome*

L

ASPECTS

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•  ≥ 8: favorable clinical outcome*

Pc-ASPECTS

*Stroke, 2008. 39(9): p. 2485-90 21

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Acute stage < 6h 22

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Acute stage (6-24h) 23

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Early sub-acute stage: 48hrs - 3 weeks 24

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Late sub-acute stage 25

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Chronic stage 26

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MTT: mean transit time, CBF: Cerebral Blood Flow

TTP: Time to peak, CBV: Cerebral blood volume

MTT

CBV CBF

TTP

DWI PERFUSION - MECHANISM

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MRI Perfusion

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Match PW/DW -> no penumbra -> no indication of treatment

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Mismatch PW/DW

-> good indication for treatment

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Case Before

DWI DWI PWI PWI

After

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CT Scanner

–  Low sensitivity; PW only for anterior

circulation (64 slices)

–  2 times of contrast (Angio & PW)

–  Can not discover micro bleeding

–  Quick

–  Patient unstable -> fast scan

–  Widespread access

–  In case of contraindication with MRI

(Stent, pacemaker…)

MRI

•  Very high Sv & Sp; PW for

whole brain

•  Only 1 time of contrast (PW)

•  Identify micro bleeding

•  A little slower but acceptable

•  Patient need to be very stable

•  Mostly in big hospital

•  No radiation

Comparison

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Role of DWI&PW image

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AJNR, 2002

•  High sensitivity and specificity for detecting AIS •  DWI and CBV best predict final volume

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•  DWI = irreversible lesion = core of infarction •  Bigger core, worse outcome

•  In the MCA occlusion, core volume in DWI > 100cm3 -> no indication of treatment (>1/3 territory of MCA) •  >70cm3: poor prognosis even rapid recanalization*

•  <70cm3: good outcome (64%) after quick recanalization •  Other studies**:

–  V <16cm3: good outcome

–  V >36cm3: bad result

DWI

(*) Stroke,2009.40:p.2046-2054 (**)Stroke,2011.42(5):p.1251-4.

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•  Sn of PW ~[74-84%], Sp of PW ~[96-100%] •  Mismatch DW/PW = penumbra area

•  (PW – DW)/ DW x 100% > 20% -> significant difference*

DWI/PW

(*) EPITHETstudy-Stroke,2009.40:p.2046-2054

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•  N = 132 •  Volume of core in DWI: 43 ± 69,9cm3

p=0.00139 p=0.00028 (Fisher exact test)

In our research*

(*) NguyenDuyTrinh,PhamMinhThong2014

Time (min) <180

(n=76)

180-360

(n=29)

>360

(n=18)

V (cm3)

34,7 ± 54,1 55,2 ± 57,6 86,9 ± 114

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Volume

V<30cm3 V>30cm3 N

mRS ≤ 2 69 4 73

mRS > 2 21 37 58

Correlation between Volume of infarction and clinical recovery

•  V<30cm3: good prognosis

p < 0.05

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Volume Before treatment

(cm3) After treatment

(cm3)

P

Quick

recanalization(n=47) 42,3 ±54 47,4 ±54,9 0,912

Late/failed

recanalization (n=26) 39,1± 49,8 91,8±81,8 0,01559

Follow up after treatment

•  Good recanalization -> no change in infarction volume -> save penumbra tissue

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Case 1a •  Male patient, 53 years old •  Normal history •  Suddenly right hemiplegia •  Administered to hospital within 2nd hours •  NIHSS = 16 •  Left ICA occlusion, ASPECTS~8

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TICI = 3

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mRS = 1

Before

After

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Case 1b - Woman 75yo, 1st hour - M1 occlusion, large penumbra - Good recanalization - mRS~1pt after 3 months

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Problem

•  Some patients having less penumbra -> good outcome

•  In contrast, others who have good penumbra -> poor outcome

-> Other factors affect the clinical recovery (collateral?) -> Need a new method to evaluate salvageable brain quickly, reliably and widely available

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New update

•  CT Angiography Multiphase is a good choice •  Simple procedure

•  Just published in 2015

•  Data from PRoveIT (Menon et al) •  N = 147, comparison between CT Multiphase, single

phase and CT Perfusion

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Protocol •  Non contrast first then multiphase

•  Phase 1: •  Evaluate the carotid and brain circulation •  Double scan with contrast, then subtraction algorithm

•  Phase 2: •  Just only the brain •  Time for moving table+scan •  Total 8sec

•  Phase 3 •  Similar to phase 2

Menon et al., (2015). Neuroradiology, 000 (0). 47

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Evaluation

Menon et al., (2015). Neuroradiology, 000 (0). 48

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Evaluation

Menon et al., (2015). Neuroradiology, 000 (0). 49

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Evaluation scale Điểm Đánh gia (khi so sánh với bán cầu bên bệnh với bên lành)

0 Không quan sát thất bất ky nhánh mạch máu nào đi vào vùng nhồi máu tại bất ky phase nào

1 Có một vài nhánh mạch máu nho đi vào vùng nhồi máu tại bất ky phase nào

2 Chậm 2 phase hiện hình mạch máu vùng ngoại vi VÀ giảm đậm đô-tốc đô ngấm thuốc, HOẶC chậm 1 phase nhưng có vùng không có mạch máu

3 Chậm 2 phase hiện hình mạch máu vùng ngoại vi, HOẶC chậm 1 phase nhưng sô lượng mạch máu trong vùng nhồi máu giảm

4 Chậm 1 phase hiện hình mạch máu vùng ngoại vi, nhưng đậm đô va tốc đô ngấm thuốc thi tương tư

5 Không có chậm phase, quan sát thấy ngay các nhánh mạch máu bàng hê đi vào bình thường hoặc nhiều hơn trong vùng nhồi máu

•  0-3: nghèo bàng hệ (poor), 4: vừa (moderate), 5: tốt (good) 50

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Advantages

•  Quick and save the time, only 10-20 sec more after the MSCT Single phase

•  1 time inject contrast material >< twice in MSCT perfusion

•  Widely available and easy to perform (no complicated mathematical algorithm post process - only MIP reconstruction in 3 phases compared to perfusion reconstruction)

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Case 3 •  Male, 78 yo •  Diabetes •  Administered in 2nd hours •  Left hemiplegia •  NIHSS = 15 •  Perfusion: match

ischemic ~ CBV -> not favorable penumbra area -> no indication

•  BUT Multiphase score = 4 -> moderate collateral

•  Good recanalization after endovascular therapy -> good result after (mRS ~ 2)

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•  Menon et al., (2015). Neuroradiology, 000 (0).

Multi >< Single Phase

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Recommendation

•  CT Multiphase score ≥ 4 -> good collateral

•  CT Multiphase score ≤ 3 -> poor collateral

•  New method, useful in ESCAPE but need more trials to proved its value

•  Now applied in Bach Mai hospital protocol

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ESCAPE

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Design and results

•  Methods –  IV >< IV + MT in the first 4.5 hours –  238/316 received rt-PA with 118 control >< 120 intervention –  Treatment up to 12 hours with anterior circulation occlusion –  NO large infarct core (ASPECTs < 6), NO poor collateral (<50%

filling pial artery of the MCA in the CT Multiphase)

•  Results –  Stop early because of the efficacy –  Times from CT non contrast to groin puncture: 60mins/ to first

reperfusion: < 90 mins –  mRS 0-2: 29.3% >< 53% -> Thrombectomy is better –  Mortality: 19% >< 10.4% –  Symptomatic hemorrhage: 2.7% >< 3.6%

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Bach Mai hospital protocol

•  Noncontrast: 3.71 sec •  Phase 1:

•  Scantime 6.2s •  Delay (contrast injection) 14 sec •  Scantime 6.2 sec

•  Phase 2: •  Total time 5 + 3.71 sec

•  Phase 3: •  Total time 5 + 3.71 sec

-> Only 17 sec more 57

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•  Left M1 occlusion (19h00’ ASPECTS ~ 8 point)

Case 2a • Male, 75 years old, history of cardiac coronary disease • Stroke during hospitalizing time (17h30’) due to chest pain • Right hemiplegia, unconscious, G~13pt, NIHSS = 19

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PHASE 1 PHASE 2 PHASE 3

•  Multiphase score ~ 4 point (good collateral)

Multiphase

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TTP(Time to Peak)

CBF(Cerebral Blood Flow)

CBV(Cerebral Blood Volume)

•  Mismatch > 35%

Perfusion

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DSA (19h50’ – 20h10’)

•  Solitaire 6/20: 1 times •  TICI 3 62

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Follow up

•  G ~ 15pt •  NIHSS ~ 6pt •  mRS ~ 2 after 2 days

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Case 2b • Female, 57 years old; Atrial fibrillation, still using anticoagulant • Administered to BM hospital in 2nd hours (13h15’->14h30’) • Left hemiplegia, NIHSS = 18

•  Right ICA occlusion (14h45’ ASPECTS ~ 6 point) 64

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PHASE 1 PHASE 2 PHASE 3

Multiphase

•  Multiphase score ~ 2 point (poor collateral) 65

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DSA (15h15’ – 15h57’)

•  Solitaire 6/30: 4 times •  TICI 3

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MRI follow up

•  G 15pt •  NIHSS ~ 9pt •  mRS ~ 4 after 2 wks

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Conclusion •  CT Scanner noncontrast and MSCT is very important

and always/strongly recommended in AIS (in new guideline 2015) before any treatment – easy and accessible in all hospital

•  CT Multiphase: new choice, simple and beneficial than Perfusion and single phase

•  MRI only in big hospital, very useful especially in unknown time stroke patients

•  DWI/PW: good information but need more trial to prove its evidence and cut-off volume in prognosis

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THANK YOU FOR YOUR ATTENTION!