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InferRead CT Stroke

InferRead CT Stroke is an advanced AI solution that quickly and accurately locates bleeding areas, measures bleeding volume, and detects midline shift in the brain. This enables clinicians to make quick, accurate decisions about the severity of the stroke and devise appropriate treatment plans. By reducing diagnosis time and providing accurate assessments, InferRead CT Stroke saves precious time for stroke patients and greatly improves their prognosis.

The comparison feature allows clinicians to track changes in bleeding area over time by comparing multiple CT scans of the same patient taken within a short period. This aids treatment evaluation and facilitates targeted interventions to improve patient outcomes.

‍

A black and white photo of a giraffe

Select a study to review AI outputs

View AI results in the deepcOS AI Evaluator
Hemorraghic Stroke

Key benefits

  • Rapid:
    - Calculate hemorrhage volume within 3 seconds.
    - Structured reports in a single click.
  • Precise:
    - Lesion location and classification.
    - Hemorrhage volume measurement with significantly higher accuracy than rough manual estimation.
  • Comprehensive:
    Intracerebral, epidural subdural, subarachnoid

Details

  • Regulatory:
FDA
CT
Brain
Neurology
Emergency
  • Clinical Applications:
FDA
CT
Brain
Neurology
Emergency
  • Modality:
FDA
CT
Brain
Neurology
Emergency
  • Body Part:
FDA
CT
Brain
Neurology
Emergency

Peer-reviewed publications

Discover the power of AI for your studies
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Increasing diagnostic quality through the collaboration of medical professionals and AI.

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Disclaimer: AI results are provided by external regulatory-approved AI solutions/partners. deepcOS communicates and displays clinical information to end-users. All medical devices available on deepcOS are regulatory cleared for use in the EU under the MDR/MDD. Only selected medical devices available on deepcOS are regulatory cleared for use in the US under the FDA. The worklist and DICOM viewer components are part of the product deepcOS AIDA (v2.0), which is classified as a software as medical device under the MDR, and is currently under revision by a notified body for obtention of CE certificate. Please contact our support team for further information (contact@deepc.ai).
FDA
CT
Brain
Neurology
Emergency
KSA
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KSA
FDA
FDA
FDA
FDA
CE
CE
CE
CE
UKCA
UKCA
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CT
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CT
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US
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DEXA
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Knee
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Breast
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Lungs
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Spine
Spine
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Prostate
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Whole Body
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