Affiliations 

  • 1 Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, UK; Radiological Sciences, Division of Clinical Neuroscience, University of Nottingham, UK. Electronic address: mszspp@nottingham.ac.uk
  • 2 Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, UK; Department of Medicine, National University of Malaysia, Malaysia. Electronic address: mszzl@nottingham.ac.uk
  • 3 Department of Neuroradiology, Nottingham University Hospitals, Queen's Medical Centre, Nottingham, UK; Department of Radiology, Royal Derby Hospital, Derby, UK. Electronic address: r.g.gallagher22@gmail.com
  • 4 Radiological Sciences, Division of Clinical Neuroscience, University of Nottingham, UK. Electronic address: mszdm3@nottingham.ac.uk
  • 5 Department of Neuroradiology, Nottingham University Hospitals, Queen's Medical Centre, Nottingham, UK; Imaging Department, Leicester Royal Infirmary, Leicester, UK. Electronic address: david.swienton@gmail.com
  • 6 Medical Physics and Clinical Engineering, Nottingham University Hospitals, Queen's Medical Centre, Nottingham, UK. Electronic address: msapm1@nottingham.ac.uk
  • 7 Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, UK. Electronic address: mszpb@nottingham.ac.uk
  • 8 Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, UK. Electronic address: mszns4@nottingham.ac.uk
  • 9 Radiological Sciences, Division of Clinical Neuroscience, University of Nottingham, UK; NIHR Nottingham BRC, UK. Electronic address: mszrad1@nottingham.ac.uk
Comput Biol Med, 2019 03;106:126-139.
PMID: 30711800 DOI: 10.1016/j.compbiomed.2019.01.022

Abstract

BACKGROUND: Spontaneous intracerebral haemorrhage (SICH) is a common condition with high morbidity and mortality. Segmentation of haematoma and perihaematoma oedema on medical images provides quantitative outcome measures for clinical trials and may provide important markers of prognosis in people with SICH.

METHODS: We take advantage of improved contrast seen on magnetic resonance (MR) images of patients with acute and early subacute SICH and introduce an automated algorithm for haematoma and oedema segmentation from these images. To our knowledge, there is no previously proposed segmentation technique for SICH that utilises MR images directly. The method is based on shape and intensity analysis for haematoma segmentation and voxel-wise dynamic thresholding of hyper-intensities for oedema segmentation.

RESULTS: Using Dice scores to measure segmentation overlaps between labellings yielded by the proposed algorithm and five different expert raters on 18 patients, we observe that our technique achieves overlap scores that are very similar to those obtained by pairwise expert rater comparison. A further comparison between the proposed method and a state-of-the-art Deep Learning segmentation on a separate set of 32 manually annotated subjects confirms the proposed method can achieve comparable results with very mild computational burden and in a completely training-free and unsupervised way.

CONCLUSION: Our technique can be a computationally light and effective way to automatically delineate haematoma and oedema extent directly from MR images. Thus, with increasing use of MR images clinically after intracerebral haemorrhage this technique has the potential to inform clinical practice in the future.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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