Skip to main content
Log in

The Pattern and Pace of Hyperacute Hemorrhage Expansion

  • Practical Pearl
  • Published:
Neurocritical Care Aims and scope Submit manuscript

Abstract

Background

Intracerebral hemorrhage (ICH) expansion is common during the first 24 h after onset, but the pattern and pace of hyperacute hemorrhage growth have not been described because serial imaging is typically performed over the course of hours and days, not minutes. The purpose of this study is to elucidate the spatial and temporal characteristics of hyperacute hemorrhage expansion within minutes of ICH onset.

Methods

An 86-year-old man with probable cerebral amyloid angiopathy developed an ICH while in the MRI scanner. Hyperacute hemorrhage growth was captured at three time points over a 14-min interval of MRI data acquisition and at fourth time point with CT 22 h later. MRI and CT datasets were spatially coregistered, and three-dimensional models of ICH expansion were generated.

Results

Longitudinal analysis revealed that the spatial pattern of ICH growth was asymmetric at each time point. Maximal expansion occurred along the anterior–posterior plane during the first 4 min but along the superior–inferior plane during the next 10 min. The temporal pace of ICH expansion was also non-uniform, as growth along the anterior–posterior plane outpaced medial–lateral growth during the first 4 min (2.8 vs. 2.5 cm), but medial–lateral growth outpaced anterior–posterior growth over the next 10 min (1.0 vs. 0.2 cm).

Conclusions

We provide evidence for asymmetric, non-uniform expansion of a hyperacute hemorrhage. These serial imaging observations suggest that hemorrhage expansion may be caused by local cascades of secondary vessel rupture as opposed to ongoing bleeding from a single ruptured vessel.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  1. Kazui S, Naritomi H, Yamamoto H, Sawada T, Yamaguchi T. Enlargement of spontaneous intracerebral hemorrhage: incidence and time course. Stroke. 1996;27:1783–7.

    Article  PubMed  CAS  Google Scholar 

  2. Brott T, Broderick J, Kothari R, et al. Early hemorrhage growth in patients with intracerebral hemorrhage. Stroke. 1997;28:1–5.

    Article  PubMed  CAS  Google Scholar 

  3. Fujii Y, Takeuchi S, Sasaki O, Minakawa T, Tanaka R. Multivariate analysis of predictors of hematoma enlargement in spontaneous intracerebral hemorrhage. Stroke. 1998;29:1160–6.

    Article  PubMed  CAS  Google Scholar 

  4. Fisher CM. Pathological observations in hypertensive cerebral hemorrhage. J Neuropathol Exp Neurol. 1971;30:536–50.

    Article  PubMed  CAS  Google Scholar 

  5. Jeong D, Jhaveri MD, Prabhakaran S. Magnetic resonance imaging characteristics at onset of spontaneous intracerebral hemorrhage. Arch Neurol. 2011;68:826–7.

    Article  PubMed  Google Scholar 

  6. Knudsen KA, Rosand J, Karluk D, Greenberg SM. Clinical diagnosis of cerebral amyloid angiopathy: validation of the Boston criteria. Neurology. 2001;56:537–9.

    Article  PubMed  CAS  Google Scholar 

  7. Kothari RU, Brott T, Broderick JP, et al. The ABCs of measuring intracerebral hemorrhage volumes. Stroke. 1996;27:1304–5.

    Article  PubMed  CAS  Google Scholar 

  8. Smith SM, Jenkinson M, Woolrich MW, et al. Advances in functional and structural MR image analysis and implementation as FSL. Neuroimage. 2004;23(Suppl 1):S208–19.

    Article  PubMed  Google Scholar 

  9. Wells WM 3rd, Viola P, Atsumi H, Nakajima S, Kikinis R. Multi-modal volume registration by maximization of mutual information. Med Image Anal. 1996;1:35–51.

    Article  PubMed  Google Scholar 

  10. Wang R and Wedeen VJ. TrackVis, Version 5.2, Athinoula A. Martinos Center for Biomedical Imaging Massachusetts General Hospital, Charlestown. http://www.trackvis.org, 2011.

  11. Fisher CM. Hypertensive cerebral hemorrhage. Demonstration of the source of bleeding. J Neuropathol Exp Neurol. 2003;62:104–7.

    PubMed  Google Scholar 

  12. Greenberg CH, Frosch MP, and Greenberg SM. Modeling the growth of microbleeds into macrobleeds (P485). Stroke: Abstracts from the 2010 International Stroke Conference. 2010;41:e376.

  13. Rosand J, Muzikansky A, Kumar A, et al. Spatial clustering of hemorrhages in probable cerebral amyloid angiopathy. Ann Neurol. 2005;58:459–62.

    Article  PubMed  Google Scholar 

  14. Brouwers HB, Biffi A, Ayres AM, et al. Apolipoprotein e genotype predicts hematoma expansion in lobar intracerebral hemorrhage. Stroke. 2012;43:1490–5.

    Article  PubMed  CAS  Google Scholar 

  15. Greenberg SM, Vonsattel JP, Segal AZ, et al. Association of apolipoprotein E epsilon2 and vasculopathy in cerebral amyloid angiopathy. Neurology. 1998;50:961–5.

    Article  PubMed  CAS  Google Scholar 

  16. Greenberg SM, Nandigam RN, Delgado P, et al. Microbleeds versus macrobleeds: evidence for distinct entities. Stroke. 2009;40:2382–6.

    Article  PubMed  Google Scholar 

  17. Mayer SA, Brun NC, Begtrup K, et al. Efficacy and safety of recombinant activated factor VII for acute intracerebral hemorrhage. N Engl J Med. 2008;358:2127–37.

    Article  PubMed  CAS  Google Scholar 

  18. Anderson CS, Huang Y, Wang JG, et al. Intensive blood pressure reduction in acute cerebral haemorrhage trial (INTERACT): a randomised pilot trial. Lancet Neurol. 2008;7:391–9.

    Article  PubMed  Google Scholar 

  19. ATACH Investigators. Antihypertensive treatment of acute cerebral hemorrhage. Crit Care Med. 2010;38:637–48.

    Google Scholar 

Download references

Acknowledgments

This study was supported by the NIH (R25NS065743).

Conflict of interest

The authors report no conflicts of interest or pertinent financial disclosures.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Scott B. Silverman.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Video Hyperacute hemorrhage expansion. Hemorrhage expansion is shown at each sequential time point of MRI and CT data acquisition, with time displayed in hour:minute format and with the corresponding hemorrhage volume displayed at each time point. The first part of the video displays hemorrhage expansion from a superior view, with 3-dimensional renderings of the hemorrhage (red) superimposed on an axial T1 pre-contrast image at the level of the cerebral microbleed seen on the gradient-recalled echo sequence. In the second part of the video, hemorrhage expansion is displayed from a posterior view, with 3-dimensional renderings of the hemorrhage superimposed on the same T1 pre-contrast axial image, as well as a T1 pre-contrast coronal image at the level of the thalamus. Of note, all images are displayed in non-radiological orientation, with the left side of the image (L) on the left side of the screen, and the right side of the image (R) on the right side of the screen. (MOV 2572 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Edlow, B.L., Bove, R.M., Viswanathan, A. et al. The Pattern and Pace of Hyperacute Hemorrhage Expansion. Neurocrit Care 17, 250–254 (2012). https://doi.org/10.1007/s12028-012-9738-5

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12028-012-9738-5

Keywords

Navigation