From clinical to tissue-based dual TIA: Validation and refinement of ABCD3-I score.

Neurology

From the Department of Neurology (Q.D., W.S., Y.X., L.X., W.Z., M.M., W.L., D.L., L.D., X.C., G.X., X.L.), Jinling Hospital, Medical School of Nanjing University, Nanjing, China; School of Medicine and Pharmacology (G.J.H.), The University of Western Australia, Perth, Australia; Department of Neurology (Q.C.), the Second Affiliated Hospital of Fujian Medical University, Fujian, China; and Department of Neurology (Y.H.), Jinling Hospital, Southern Medical University, Nanjing, China.

Published: April 2015

Objective: To investigate whether dual tissue-defined ischemic attacks, defined as multiple diffusion-weighted imaging lesions of different age and/or arterial territory (dual DWI), are an independent and stronger predictor of 90-day stroke than dual clinical TIAs (dual TIA).

Methods: Consecutive patients with clinically defined TIA were enrolled and assessed clinically and by MRI within 3 days. The predictive ability of the ABCD clinical factors, dual TIA, and dual DWI was evaluated by means of multivariate logistic regression.

Results: Among 658 patients who were included in the study and completed 90 days of follow-up, a total of 70 patients (10.6%) experienced subsequent stroke by 90 days. Multivariate logistic regression indicated that dual DWI was an independent predictor for subsequent stroke (odds ratio 4.64, 95% confidence interval 2.15-10.01), while dual TIA was not (odds ratio 1.18, 95% confidence interval 0.69-2.01). C statistics was higher when the item of dual TIA in ABCD3-I score was replaced by dual DWI (0.759 vs 0.729, p = 0.035). The net reclassification value for 90-day stroke risk was also improved (continuous net reclassification improvement 0.301, p = 0.017).

Conclusion: Dual DWI independently predicted future stroke in patients with TIA. A new ABCD3-I score with dual DWI instead of dual clinical TIA may improve risk stratification for early stroke risk after TIA.

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http://dx.doi.org/10.1212/WNL.0000000000001444DOI Listing

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