Author(s): Liebeskind DS, Kosinski AS, Saver JL, Feldmann E SONIA Inves
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Abstract BACKGROUND: The Stroke Outcomes and Neuroimaging of Intracranial Atherosclerosis (SONIA) study validated noninvasive imaging tests of intracranial atherosclerosis against catheter angiography in a prospective, blinded, multicenter setting. Critical evaluation of transcranial Doppler (TCD) and magnetic resonance angiography in the SONIA study standardized their performance and interpretation. We performed a similar analysis of computed tomography angiography (CTA) for the detection of intracranial stenosis. METHODS: Multicenter standardization of image acquisition and blinded, central interpretation of CTA performance were conducted in concert with the Warfarin-Aspirin Symptomatic Intracranial Disease (WASID) trial. Measurements of the intracranial arterial diameter were obtained to derive stenosis values. Correlation with catheter angiography was used to assess CTA performance characteristics. RESULTS: CTA measurements of intracranial stenosis were obtained in 120 vessel segments, with angiographic correlation in 52. CTA was performed as a noninvasive study prior to conventional angiography. CTA stenoses of 50-99\% or a flow gap were identified in 15 of 52 vessel segments, stenoses of <50\% in 5 of 52, and normal arterial diameters in 32 of 52 vessel segments. Based on the digital subtraction angiography (DSA) stenosis defined as 50-99\%, the positive predictive value (PPV) of CTA was only 46.7\% (95\% CI 21.3-73.4) and the negative predictive value (NPV) was 73.0\% (95\% CI 55.9-86.2). For DSA stenosis defined as 70-99\%, the PPV of CTA was 13.3\% (95\% CI 1.7-40.5) and the NPV was 83.8\% (95\% CI 68.0-93.8). CONCLUSIONS: CTA can accurately rule out the presence of severe stenosis due to intracranial atherosclerosis and may eliminate the need for angiography in many cases. Further prospective, blinded evaluation of CTA and optimization of cutpoints to predict angiographic disease will facilitate future trials of intracranial atherosclerosis.
This article was published in Interv Neurol
and referenced in Biochemistry & Analytical Biochemistry