Volume 81, Issue 6 pp. 849-856
Research Article

Computed tomographic perfusion to Predict Response to Recanalization in ischemic stroke

Maarten G. Lansberg MD, PhD

Corresponding Author

Maarten G. Lansberg MD, PhD

Department of Neurology, Stanford University, Stanford, CA

Address correspondence to Dr Lansberg, Stanford Stroke Center, 780 Welch Road, Suite 350, Palo Alto, CA 94304-5778. E-mail: [email protected]Search for more papers by this author
Soren Christensen PhD

Soren Christensen PhD

Department of Neurology, Stanford University, Stanford, CA

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Stephanie Kemp

Stephanie Kemp

Department of Neurology, Stanford University, Stanford, CA

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Michael Mlynash MD, MS

Michael Mlynash MD, MS

Department of Neurology, Stanford University, Stanford, CA

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Nishant Mishra MD, PhD

Nishant Mishra MD, PhD

Department of Neurology, Stanford University, Stanford, CA

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Christian Federau MD

Christian Federau MD

Department of Neurology, Stanford University, Stanford, CA

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Jenny P. Tsai MD

Jenny P. Tsai MD

Department of Neurology, Stanford University, Stanford, CA

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Sun Kim MD

Sun Kim MD

Department of Neurology, Stanford University, Stanford, CA

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Raul G. Nogueria MD

Raul G. Nogueria MD

Department of Neurology, Emory University, Atlanta, GA

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Tudor Jovin MD

Tudor Jovin MD

Department of Neurology, University of Pittsburgh, Pittsburgh, PA

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Thomas G. Devlin MD

Thomas G. Devlin MD

Chattanooga Center for Neurologic Research, Chattanooga, TN

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Naveed Akhtar MD

Naveed Akhtar MD

Department of Radiology, Saint Luke's Health System, Kansas City, MO

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Dileep R. Yavagal MD

Dileep R. Yavagal MD

Department of Neurology, University of Miami, Miami, FL

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Diogo Haussen MD

Diogo Haussen MD

Department of Neurology, Emory University, Atlanta, GA

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Seena Dehkharghani MD

Seena Dehkharghani MD

Department of Radiology, Emory University, Atlanta, GA

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Roland Bammer PhD

Roland Bammer PhD

Department of Radiology, Stanford University, Stanford, CA

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Matus Straka PhD

Matus Straka PhD

Stanford University, Stanford, CA

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Greg Zaharchuk MD

Greg Zaharchuk MD

Department of Radiology, Stanford University, Stanford, CA

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Michael P. Marks MD

Michael P. Marks MD

Department of Radiology, Stanford University, Stanford, CA

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Gregory W. Albers MD

Gregory W. Albers MD

Department of Neurology, Stanford University, Stanford, CA

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for the CT Perfusion to Predict Response to Recanalization in Ischemic Stroke Project (CRISP) Investigators

for the CT Perfusion to Predict Response to Recanalization in Ischemic Stroke Project (CRISP) Investigators

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First published: 09 May 2017
Citations: 115

Abstract

Objective

To assess the utility of computed tomographic (CT) perfusion for selection of patients for endovascular therapy up to 18 hours after symptom onset.

Methods

We conducted a multicenter cohort study of consecutive acute stroke patients scheduled to undergo endovascular therapy within 90 minutes after a baseline CT perfusion. Patients were classified as “target mismatch” if they had a small ischemic core and a large penumbra on their baseline CT perfusion. Reperfusion was defined as >50% reduction in critical hypoperfusion between the baseline CT perfusion and the 36-hour follow-up magnetic resonance imaging.

Results

Of the 201 patients enrolled, 190 patients with an adequate baseline CT perfusion study who underwent angiography were included (mean age = 66 years, median NIH Stroke Scale [NIHSS] = 16, median time from symptom onset to endovascular therapy = 5.2 hours). Rate of reperfusion was 89%. In patients with target mismatch (n = 131), reperfusion was associated with higher odds of favorable clinical response, defined as an improvement of ≥8 points on the NIHSS (83% vs 44%; p = 0.002, adjusted odds ratio [OR] = 6.6, 95% confidence interval [CI] = 2.1–20.9). This association did not differ between patients treated within 6 hours (OR = 6.4, 95% CI = 1.5–27.8) and those treated > 6 hours after symptom onset (OR = 13.7, 95% CI = 1.4–140).

Interpretation

The robust association between endovascular reperfusion and good outcome among patients with the CT perfusion target mismatch profile treated up to 18 hours after symptom onset supports a randomized trial of endovascular therapy in this patient population. Ann Neurol 2017;81:849–856

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