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Research ArticleNeurointervention

Reperfusion Rates Following Intra-Arterial Thrombolysis for Acute Ischemic Stroke: The Influence of the Method for Alteplase Delivery

G.A. Christoforidis, A. Slivka, Y. Mohammad, C. Karakasis, M. Kontzialis and M. Khadir
American Journal of Neuroradiology August 2012, 33 (7) 1292-1298; DOI: https://doi.org/10.3174/ajnr.A2973
G.A. Christoforidis
aFrom the Department of Radiology (G.A.C., M.Khadir.), University of Chicago Medical Center, Chicago, Illinois
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A. Slivka
bDepartments of Neurology (A.S., Y.M.)
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Y. Mohammad
bDepartments of Neurology (A.S., Y.M.)
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C. Karakasis
cRadiology (C.K., M.Kontzialis.), The Ohio State University Medical Center, Columbus, Ohio.
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M. Kontzialis
cRadiology (C.K., M.Kontzialis.), The Ohio State University Medical Center, Columbus, Ohio.
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M. Khadir
aFrom the Department of Radiology (G.A.C., M.Khadir.), University of Chicago Medical Center, Chicago, Illinois
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  • Fig 1.
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    Fig 1.

    Optimizing microcatheter position within a thrombus with gentle alteplase infusion can help ensure that alteplase (dots) surrounds the thrombus during treatment.

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    Fig 2.

    Arteriographic images were obtained before (A), early during alteplase infusion (B), late during alteplase infusion (C), and following alteplase infusion (D) in a patient with occlusion at the proximal M1 segment (arrow, A). The microcatheter tip is indicated by arrowheads. The microcatheter was initially positioned within the offending thrombus, and contrast injection suggests the expected distribution of the alteplase surrounding the thrombus (thrombus is outlined by dots, B). Contrast is identified in 1 major division branch distal to the thrombus (arrow, B) and proximal to the thrombus. Eventually thrombus begins to dissolve (C), and the microcatheter is repositioned to distribute alteplase throughout the thrombus in other divisions of the M1 segment (arrows, C). The final arteriogram demonstrates complete reperfusion and identification of 3 major branches originating from the M1 segment at the site of the thrombus.

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    Fig 3.

    Arteriograms obtained before (A), during microcathter positioning (B−D), and following alteplase infusion (E) in a patient with occlusion at the superior division of the middle cerebral artery at the M2 segment (arrow, A) demonstrate optimization of microcatheter placement. The microcatheter tip is indicated by arrows (B−D). Arrowheads (B−D) indicate contrast distribution during microcatheter contrast injection. B, The microcatheter tip (black arrow) is located along the distal aspect of the thrombus. Contrast administration in B indicates that given this position, thrombolytic agent would only be distributed within the distal aspect of the thrombus. Contrast injection in C indicates that the thrombolytic agent is delivered to the proximal and inferior aspect of the thrombus with significant amounts of alteplase escaping into vessels proximal to the occlusion site (white arrowheads). Contrast injection in D indicates that thrombolytics are delivered around the entire thrombus (outlined by dots) and serves as an optimal position for thrombolytic infusion. Note that contrast enters 2 involved branches in D, unlike in B or C. Involved branches will demonstrate stagnant contrast opacification, whereas uninvolved branches will demonstrate brisk flow of contrast. It is intuitive that stagnant contrast would also imply that alteplase would also tend to stagnate adjacent to the thrombus during its delivery. If the RMP method was used all 3 microcatheter positions depicted in B−D would be acceptable, whereas with the OAD method, only the position in D would be acceptable.

Tables

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    Table 1:

    Presenting clinical information and angiographic data dichotomized by the method of recanalization

    VariableRMP MethodOAD MethodTotalPValue
    No.404585
    Pretreatment NIHSS score16 (11–21)17 (12–21)16 (12–21).832a
    Time to treatment (min)298 (178–347)248 (204–304)270 (202–328).199a
    Median age (yr)68 (59–75)68 (54–76)68 (56–75).689a
    Female sex (%)12 (30.0%)23 (51.1%)35 (41.2%).0484b
    History of diabetes10 (25.0%)7 (15.6%)17 (20.0%).277b
    Systolic blood pressure148 (134–169)140 (129–169)147 (130–169).764a
    Admitting glucose value127 (111–173)113 (100–133)121 (103–146).0342a
    Admitting platelet level228 (194–256)216 (180–276)225 (186–264).986a
    Hematocrit level39.9 (36.3–42.9)39.1 (34.1–43.8)39.6 (35.1–43.1).506a
    Slow antegrade flow11 (27.5%)12 (26.7%)23 (27.1%).931b
    Good pial collaterals31 (77.5%)34 (75.6%)65 (76.5%).833b
    % proximal occlusion30 (72.5%)37 (82.2%)66 (77.6%).283b
    Location
        ICA4 (10.0%)8 (17.8%)12 (14.1%).531b
        MCA33 (82.5%)32 (71.1%)65 (76.5%)
        ACA0 (0%)1 (2.33%)1 (1.2%)
        BA3 (7.50%)4 (8.89%)7 (8.24%)
    • Note:—ACA indicates anterior cerebral artery; BA, basilar artery.

    • ↵a Wilcoxon rank sum Test.

    • ↵b Pearson correlation.

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    Table 2:

    Nominal logistic regression analysis for ≥50% reperfusion of the involved vascular territorya

    χ2Odds Ratio95% CIP> χ2
    Optimized alteplase delivery17.521.35.7–105<.0001
    Slow antegrade flow at onset9.2417.93.35–147.0024
    Time to treatment <270 minutes5.665.551.43–25.2.0174
    Presenting NIHSS score <164.285.621.19–33.1.0385
    Proximal occlusion5.329.431.59–77.3.0211
    Intercept3.20.0736
    • Note:—CI indicates confidence interval.

    • ↵a R2 = 0.459; N= 85; whole model fit P > χ2 <.0001.

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    Table 3:

    Stratification of methods of IA delivery of thrombolytics by reperfusion outcome indicates a significant (P < .0001, Pearson correlation) difference between reperfusion rates using the OAD method versus RMP methoda

    No.TICI Score
    0123
    RMP method4019 (47.5%)9 (22.5%)3 (7.5%)9 (22.5%)
    OAD method451 (2.22%)7 (15.6%)7 (15.6%)30 (66.7%)
    • ↵a TICI score of 0 = no reperfusion; TICI score of 1 = <50% reperfusion; TICI score of 2 = ≥50% reperfusion; TICI score of 3 = complete reperfusion.

    • View popup
    Table 4:

    Stratification of outcomes by methods of IA delivery of thrombolytics

    VariableNo.RMP MethodOAD MethodP Value
    No.4045
    ≥50% reperfusion8512 (30.0%)37 (82.2%)<.0001a
    24-hour change in NIHSS (median)851.0 (−81.75–7)6.0 (1–10).0110b
    NIHSS score change by hospital discharge853 (−8.25–8.0)9 (2–12).0064b
    mRS ≤2 at 1–3 months81c16 (41.0%)29 (69.1%).0112b
    Mortality at 3 months81c11 (28.2%)5 (11.9%).0656b
    Infarct volume8565.6 (19.4–156)30.3 (6.60–55.5).0116b
    Presence of hemorrhage8511 (27.5%)12 (26.7%).931a
    Hemorrhage ≥25 mL855 (12.5%)4 (8.89%).589a
    SHT854 (10.0%)2 (4.44%).318a
    • Note:—SHT indicates symptomatic hemorrhagic transformation.

    • ↵a Pearson correlation.

    • ↵b Wilcoxon rank sum test.

    • ↵c Excludes patients who were known to have an mRS score >2 prior to ictus.

    • View popup
    Table 5:

    Comparison of outcomes from clinical trials with the current study

    ParameterPROACT IIPROACT PlaceboIMSMulti MERCIPivotalaRMP MethodOAD Method
    Median NIHSS score1717181917.6b1617
    Minimum NIHSS score≥4≥4≥10≥8≥8≥4≥4
    Any recanalization66%18%56%68%81.6%52.5%97.5%
    Complete recanalization19%2%11%NA27.2%22.5%66.7%
    mRS <240%25%43%36%25%41%69.1%
    90-day mortality25%27%16%34%32.8%28.2%11.9%
    SHT10%2%6.3%9.8%11.2%10.0%4.44%
    • Note:—IMS indicates Interventional Management of Stroke; MERCI, Mechanical Embolus Removal in Cerebral Ischemia; PROACT, Prolyse in Acute Cerebral Thromboembolism; SHT, symptomatic hemorrhagic transformation.

    • ↵a Penumbra Pivotal Stroke Trial.

    • ↵b Mean.

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American Journal of Neuroradiology: 33 (7)
American Journal of Neuroradiology
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G.A. Christoforidis, A. Slivka, Y. Mohammad, C. Karakasis, M. Kontzialis, M. Khadir
Reperfusion Rates Following Intra-Arterial Thrombolysis for Acute Ischemic Stroke: The Influence of the Method for Alteplase Delivery
American Journal of Neuroradiology Aug 2012, 33 (7) 1292-1298; DOI: 10.3174/ajnr.A2973

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Reperfusion Rates Following Intra-Arterial Thrombolysis for Acute Ischemic Stroke: The Influence of the Method for Alteplase Delivery
G.A. Christoforidis, A. Slivka, Y. Mohammad, C. Karakasis, M. Kontzialis, M. Khadir
American Journal of Neuroradiology Aug 2012, 33 (7) 1292-1298; DOI: 10.3174/ajnr.A2973
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