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Predictors of Early and Late Infarct Growth in DEFUSE 3.
Tate, William J; Polding, Laura C; Christensen, Søren; Mlynash, Michael; Kemp, Stephanie; Heit, Jeremy J; Marks, Michael P; Albers, Gregory W; Lansberg, Maarten G.
Afiliación
  • Tate WJ; Stanford University School of Medicine, Stanford, CA, United States.
  • Polding LC; Stanford University School of Medicine, Stanford, CA, United States.
  • Christensen S; Stanford Stroke Center, Palo Alto, CA, United States.
  • Mlynash M; Stanford Stroke Center, Palo Alto, CA, United States.
  • Kemp S; Stanford Stroke Center, Palo Alto, CA, United States.
  • Heit JJ; Department of Radiology, Stanford University School of Medicine, Stanford, CA, United States.
  • Marks MP; Department of Radiology, Stanford University School of Medicine, Stanford, CA, United States.
  • Albers GW; Stanford Stroke Center, Palo Alto, CA, United States.
  • Lansberg MG; Stanford Stroke Center, Palo Alto, CA, United States.
Front Neurol ; 12: 699153, 2021.
Article en En | MEDLINE | ID: mdl-34276547
Introduction: The goal of this study is to explore the impact of reperfusion and collateral status on infarct growth in the early and late time windows. Materials and Methods: Seventy patients from the DEFUSE 3 trial (Endovascular Therapy Following Imaging Evaluation for Ischemic Stroke) with baseline, 24-h, and late follow-up scans were evaluated. Scans were taken with DWI or CTP at time of enrollment (Baseline), with DWI or CT 24-h after enrollment (24-h), and with DWI or CT 5 days after enrollment (Late). Early infarct growth (between baseline and 24-h scans) and late infarct growth (between 24-h and late scans) was assessed for each patient. The impact of collateral and reperfusion status on infarct growth was assessed in univariate and multivariate regression. Results: The median early infarct growth was 30.3 ml (IQR 16.4-74.5) and the median late infarct growth was 6.7 ml (IQR -3.5-21.6) in the overall sample. Patients with poor collaterals showed greater early infarct growth (Median 58.5 ml; IQR 18.6-125.6) compared to patients with good collaterals (Median 28.4 ml; IQR 15.8-49.3, unadjusted p = 0.04, adjusted p = 0.06) but showed no difference in late infarct growth. In contrast, patients who reperfused showed no reduction in early infarct growth but showed reduced late infarct growth (Median 1.9 ml; IQR -6.1-8.5) compared to patients without reperfusion (Median 11.2 ml; IQR -1.1-27.2, unadjusted p < 0.01, adjusted p = 0.04). Discussion: In the DEFUSE 3 population, poor collaterals predict early infarct growth and absence of reperfusion predicts late infarct growth. These results highlight the need for timely reperfusion therapy, particularly in patients with poor collaterals and indicate that the 24-h timepoint is too early to assess the full impact of reperfusion therapy on infarct growth. Clinical Trial Registration: http://www.clinicaltrials.gov, Unique identifier [NCT02586415].
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Neurol Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Neurol Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
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