A novel method to assess pial collateralization from stroke perfusion MRI: subdividing Tmax into anatomical compartments.

Objectives: To develop and validate a quantitative and observer-independent method to evaluate pial collateral circulation by DSC-perfusion MRI and test whether this novel method delivers diagnostic information which is redundant to or independent from conventional penumbra imaging by the mismatch a...

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Publicado en:European Radiology Vol. 27; no. 2; pp. 618 - 627
Autores principales: Potreck, Arne, Seker, Fatih, Hoffmann, Angelika, Pfaff, Johannes, Nagel, Simon, Bendszus, Martin, Heiland, Sabine, Pham, Mirko
Formato: Journal Article
Publicado: Springer Nature Feb2017
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Feb2017
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s00330-016-4415-2
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        atl: A novel method to assess pial collateralization from stroke perfusion MRI: subdividing Tmax into anatomical compartments.
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        au:
          Potreck, Arne
          Seker, Fatih
          Hoffmann, Angelika
          Pfaff, Johannes
          Nagel, Simon
          Bendszus, Martin
          Heiland, Sabine
          Pham, Mirko
        affil: Department of Neuroradiology , Heidelberg University Hospital , INF 400 69120 Heidelberg Germany
      sug:
        subj:
          Stroke
          Magnetic Resonance Imaging Methods
          Collateral Circulation Physiology
          Brain Mapping Methods
          Stroke Physiopathology
          Cerebral Veins
          Reproducibility of Results
          Retrospective Design
          Male
          Observer Bias
          Female
          Aged
          Scales
          Aged: 65+ years
          Male
          Female
      ab: Objectives: To develop and validate a quantitative and observer-independent method to evaluate pial collateral circulation by DSC-perfusion MRI and test whether this novel method delivers diagnostic information which is redundant to or independent from conventional penumbra imaging by the mismatch approach.Methods: We retrospectively identified 47 patients with M1 occlusion who underwent MR diffusion/perfusion imaging and mechanical thrombectomy at our facility. By automated registration and segmentation, Tmax delays were attributed specifically to the pial, cortical and parenchymal compartments. The resulting pial volumes at delay were defined as the pial Tmax map-assessed collateral score (TMACS) and correlated with gold standard digital subtraction angiography (DSA). Mismatch ratio was assessed by conventional penumbra defining MRI criteria.Results: Strong correlation was found between TMACS and angiographically assessed collateral score (Pearson ρ = -0.74, p < 0.001). In multiple logistic regression, both good collaterals according to TMACS [OR 4.3 (1.1-19, p = 0.04)] and mismatch ratio ≥ 3.5 [OR 12.3 (1.88-249, p = 0.03)] were independent predictors of favourable clinical outcome.Conclusions: Perfusion delay in the pial compartment, as evaluated by TMACS, closely reflects the extent of pial collaterals in gold-standard DSA. TMACS and mismatch ratio were found to be complementary predictors of a favourable clinical outcome, each adding independent predictive information.Key Points: • MRI-DSC perfusion delay specific in the pial compartment reflects leptomeningeal collateralization. • A novel quantitative- and observer-independent marker of collateral status (TMACS) is introduced. • Quantification of collateral status leads to an independent predictor of neurological outcome.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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