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. 2022 Nov;53(11):3439-3445.
doi: 10.1161/STROKEAHA.121.038101. Epub 2022 Jul 22.

Estimating Perfusion Deficits in Acute Stroke Patients Without Perfusion Imaging

Affiliations

Estimating Perfusion Deficits in Acute Stroke Patients Without Perfusion Imaging

Dennys Reyes et al. Stroke. 2022 Nov.

Abstract

Background: Perfusion weighted imaging (PWI) is critical for determining whether stroke patients presenting in an extended time window are candidates for mechanical thrombectomy. However, PWI is not always available. Fluid-attenuated inversion recovery hyperintense vessels (FHVs) are seen in patients with a PWI lesion. We investigated whether a scale measuring the extent FHV could serve as a surrogate for PWI to determine eligibility for thrombectomy.

Methods: The National Institutes of Health (NIH) FHV score was developed to quantify the burden of FHV and applied to magnetic resonance imaging scans of stroke patients with fluid-attenuated inversion recovery and perfusion imaging. The NIH-FHV was combined with the diffusion weighted image volume to estimate the diffusion-perfusion mismatch ratio. Linear regression was used to compare PWI volumes and mismatch ratios with estimates from the NIH-FHV score. Receiver operating characteristic analysis was used to test the ability of the NIH-FHV score to identify a significant mismatch.

Results: There were 101 patients included in the analysis, of whom 78% had a perfusion deficit detected on PWI with a mean lesion volume of 47 (±59) mL. The NIH-FHV score was strongly associated with the PWI lesion volume (P<0.001; R2=0.32; β-coefficient, 0.57). When combined with diffusion weighted image lesion volume, receiver operating characteristic analysis testing the ability to detect a mismatch ratio ≥1.8 using the NIH-FHV score resulted in an area under the curve of 0.94.

Conclusions: The NIH-FHV score provides an estimate of the PWI lesion volume and, when combined with diffusion weighted imaging, may be helpful when trying to determine whether there is a clinically relevant diffusion-perfusion mismatch in situations where perfusion imaging is not available. Further studies are needed to validate this approach.

Keywords: ROC curve; humans; ischemic stroke; linear models; perfusion.

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Figures

Figure 1:
Figure 1:
NIH-FHV score for an MCA perfusion deficit: two slices of the FLAIR sequence of a patient and the corresponding perfusion deficit (dark blue arrows) on PWI are shown. There are not more than two FHV in the frontal region (red arrows) on a single slice thus it contributes 1 point. The insular (yellow) and temporal regions (green arrows) both have greater than two FHV on a single slice and contribute two points each. The parietal region (light blue arrows) contributes one point. The NIH-FHV score for this patient is 6.
Figure 2:
Figure 2:
Examples of calculating the NIH-FHV score in the ACA and PCA territories are shown. A NIH-FHV score of 1 (red arrow) is assigned to the ACA PWI deficit (blue arrow). A NIH-FHV score of 2 (red arrows) is assigned to the PCA PWI deficit (two blue arrows).
Figure 3:
Figure 3:
Examples from two different patients are show in which FHV are detected on the FLAIR scan (red arrows) in an area of ischemia on DWI despite the lack of a perfusion deficit reaching the 6 second threshold on the TTP map.
Figure 4:
Figure 4:
Panel A shows a scatter plot comparing the estimated mismatch (NIH-FHV / DWI volume) with the actual mismatch (PWI volume / DWI volume) for patients with PWI volume greater than 15 mL. Panel B shows the ROC curve for detecting a PWI volume > 15 mL with the NIH-FHV score. Panel C shows the ROC curve for detecting a mismatch ratio > 1.8 using the FHVmr (NIH-FHV score / DWI volume).
Figure 5:
Figure 5:
Two slices from both 2-dimentional (left) and 3-dimentional (right) FLAIR sequences acquired during the same scan for a single patient with a perfusion deficit are shown. The 2D FLAIR shows FHV (arrows) due to diminished inflow/outflow of arterial blood moving through the slices being acquired. The 3D FLAIR, for which all slices are acquired simultaneously, does not demonstrate FHV in the same regions (circles).

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