4.6 Article

Development and Validation of Prediction Models for Severe Complications After Acute Ischemic Stroke: A Study Based on the Stroke Registry of Northwestern Germany

Journal

Publisher

WILEY
DOI: 10.1161/JAHA.121.023175

Keywords

ischemic stroke; machine learning; mortality; prediction; severe outcomes

Funding

  1. Massachusetts General Hospital Executive Committee on Research Fund for Medical Discovery Clinical Research Fellowship Award
  2. Deutsche Forschungsgemeinschaft (German Research Foundation) [431549029]
  3. National Institutes of Health-National Institute of Neurological Disorders and Stroke [R01NS082285, R01NS086905, U19NS115388]
  4. [SFB 1451]

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This study aims to build and validate prediction models for severe complications after acute ischemic stroke, and found that the performance of these models is superior to previously proposed approaches.
Background The treatment of stroke has been undergoing rapid changes. As treatment options progress, prediction of those under risk for complications becomes more important. Available models have, however, frequently been built based on data no longer representative of today's care, in particular with respect to acute stroke management. Our aim was to build and validate prediction models for 4 clinically important, severe outcomes after stroke. Methods and Results We used German registry data from 152 710 patients with acute ischemic stroke obtained in 2016 (development) and 2017 (validation). We took into account potential predictors that were available at admission and focused on in-hospital mortality, intracranial mass effect, secondary intracerebral hemorrhage, and deep vein thrombosis as outcomes. Validation cohort prediction and calibration performances were assessed using the following 4 statistical approaches: logistic regression with backward selection, l1-regularized logistic regression, k-nearest neighbor, and gradient boosting classifier. In-hospital mortality and intracranial mass effects could be predicted with high accuracy (both areas under the curve, 0.90 [95% CI, 0.90-0.90]), whereas the areas under the curve for intracerebral hemorrhage (0.80 [95% CI, 0.80-0.80]) and deep vein thrombosis (0.73 [95% CI, 0.73-0.73]) were considerably lower. Stroke severity was the overall most important predictor. Models based on gradient boosting achieved better performances than those based on logistic regression for all outcomes. However, area under the curve estimates differed by a maximum of 0.02. Conclusions We validated prediction models for 4 severe outcomes after acute ischemic stroke based on routinely collected, recent clinical data. Model performance was superior to previously proposed approaches. These predictions may help to identify patients at risk early after stroke and thus facilitate an individualized level of care.

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