4.6 Article

Clinical-radiomics Nomogram for Risk Estimation of Early Hematoma Expansion after Acute Intracerebral Hemorrhage

Journal

ACADEMIC RADIOLOGY
Volume 28, Issue 3, Pages 307-317

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.acra.2020.02.021

Keywords

Intracerebral hemorrhage expansion; Computed tomography; Radiomics analysis; Clinical risk factor; Nomogram

Funding

  1. Science and Technology Planning Projects of Wenzhou [Y20180112]
  2. Health Foundation for Creative Talents in Zhejiang Province, China [2016]
  3. Project Foundation for the College Young and Middle-aged Academic Leader of Zhejiang Province, China [2017]

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The study demonstrated that the noncontrast CT-based radiomics model outperformed the clinical-only model in predicting hematoma expansion in patients with spontaneous intracerebral hemorrhage, and the established clinical-radiomics nomogram showed good discrimination and calibration for detecting hematoma expansion.
Rationale and Objectives: Noncontrast CT-based radiomics signature has shown ability for detecting hematoma expansion (HE) in spontaneous intracerebral hemorrhage (ICH). We sought to compare its predictive performance with clinical risk factors and develop a clinical-radiomics nomogram to assess the risk of early HE. Materials and Methods: In total, 1153 patients with ICH who underwent baseline cranial CT within 6 hours and follow-up scans within 72 hours of stroke onset were enrolled, of whom 864 (75%) were assigned to the derivation cohort and 289 (25%) to the validation cohort. Based on LASSO algorithm or stepwise logistic regression analysis, three models (clinical model, radiomics model, and hybrid model) were constructed to predict HE. The Akaike information criterion (NC) and likelihood ratio test (LRT) were used for comparing the goodness of fit of the three models, and the AUC was used to evaluate their discrimination ability for HE. Results: The hybrid model (AIC = 681.426; chi(2) = 128.779) was the optimal model with the lowest AIC and highest chi-square values compared to the radiomics model (AIC = 767.979; chi(2) = 110.234) or the clinical model (AIC = 753.757; chi(2) = 56.448). The radiomics model was superior in the prediction of HE to the clinical model in both derivation (p = 0.009) and validation (p = 0.022) cohorts. In both datasets, the clinical-radiomics nomogram showed satisfactory discrimination and calibration for detecting HE (AUC = 0.771, Sensitivity = 87.0%; AUC = 0.820, Sensitivity = 88.1%; respectively). Conclusion: Among patients with acute ICH, noncontrast CT-based radiomics model outperformed the clinical-only model in the prediction of HE, and the established clinical-radiomics nomogram with favorable performance can offer a noninvasive tool for the risk stratification of HE.

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