Volume 26, Issue 3 pp. 346-350
Original Research

CT Evolution of Hematoma and Surrounding Hypodensity in a Cadaveric Model of Intracerebral Hemorrhage

Shahram Majidi

Corresponding Author

Shahram Majidi

Zeenat Qureshi Stroke Institute, St Cloud, MN

Department of Neurology, George Washington University, Washington, D.C.

Correspondence: Address correspondence to Shahram Majidi, MD, Department of Neurology, George Washington University, 900 23rd Street NW, Washington, DC 20037, USA. Tel: 763-496-9283, E-mail: [email protected]Search for more papers by this author
Basit Rahim

Basit Rahim

Zeenat Qureshi Stroke Institute, St Cloud, MN

Search for more papers by this author
Sarwat I. Gilani

Sarwat I. Gilani

Zeenat Qureshi Stroke Institute, St Cloud, MN

Search for more papers by this author
Waqas I. Gilani

Waqas I. Gilani

Zeenat Qureshi Stroke Institute, St Cloud, MN

Search for more papers by this author
Malik M. Adil

Malik M. Adil

Zeenat Qureshi Stroke Institute, St Cloud, MN

Search for more papers by this author
Adnan I. Qureshi

Adnan I. Qureshi

Zeenat Qureshi Stroke Institute, St Cloud, MN

Search for more papers by this author
First published: 13 October 2015
Citations: 14

Dr. Majidi is supported by American Heart Association Clinical Research Program Award 13CRP17330020, Brain Edema at Cerebral Hemorrhage (BEACH) study.

Dr. Qureshi is supported by National Institute of Neurological Diseases and Stroke. Principal Investigator, Antihypertensive Treatment in Acute Cerebral Hemorrhage (ATACH)-II. U01NS061861 and American Heart Association Established Investigator Award 0840053N, Innovative Strategies for Treating Cerebral Hemorrhage.

ABSTRACT

BACKGROUND

The evolution of intracerebral hematoma and perihematoma edema in the ultra-early period on computed tomographic (CT) scans in patients with intracerebral hemorrhage (ICH) is not well understood. We aimed to investigate hematoma and perihematoma changes in “neutral brain” models of ICH.

METHODS

One human and five goat cadaveric heads were used as “neutral brains” to provide physical properties of brain without any biological activity or new bleeding. ICH was induced by slow injection of 4 ml of fresh human blood into the right basal ganglia of the goat brains. Similarly, 20 ml of fresh blood was injected deep into the white matter of the human cadaver head in each hemisphere. Serial CT scans of the heads were obtained immediately after hematoma induction and then 1, 3, and 5 hours afterward. Analyze software (AnalyzeDirect, Overland Park, KS, USA) was used to measure hematoma and perihematoma hypodensity volumes in the baseline and follow-up CT scans.

RESULTS

The initial hematoma volumes of 11.6 ml and 10.5 ml in the right and left hemispheres of the cadaver brains gradually decreased to 6.6 ml and 5.4 ml at 5 hours, showing 43% and 48% retraction of hematoma, respectively. The volume of the perihematoma hypodensity in the right and left hemisphere increased from 2.6 ml and 2.2 ml in the 1-hour follow-up CT scans to 4.9 ml and 4.4 ml in the 5-hour CT scan, respectively. Hematoma retraction was also observed in all five goat brains ICH models with the mean ICH volume decreasing from 1.49 ml at baseline scan to 1.01 ml at the 5-hour follow-up CT scan (29.6% hematoma retraction). Perihematoma hypodensity was visualized in 70% of ICH in goat brains, with an increasing mean hypodensity volume of 0.4 ml in the baseline CT scan to 0.8 ml in the 5-hour follow-up CT scan.

CONCLUSION

Our study demonstrated that substantial hematoma retraction and perihematoma hypodensity occurs in ICH in the absence of any new bleeding or biological activity of surrounding brain. Such observations suggest that active bleeding is underestimated in patients with no or small hematoma expansion and our understanding of perihematoma hypodensity needs to be reconsidered.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.