Evidence map›Paper›PMID 29867710›Full record

ArticleFrontiers in neurology2018

Cerebral Microcirculation and Histological Mapping After Severe Head Injury: A Contusion and Acceleration Experimental Model.

Judith Bellapart, Kylie Cuthbertson, Kimble Dunster, Sara Diab, David G Platts, Owen Christopher Raffel, Levon Gabrielian, Adrian Barnett, Jenifer Paratz, Rob Boots and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Judith BellapartDepartment of Intensive Care, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Kylie CuthbertsonDepartment of Histopathology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Kimble DunsterCritical Care Research Group, University of Queensland, Brisbane, QLD, Australia.
Sara DiabCritical Care Research Group, University of Queensland, Brisbane, QLD, Australia.
David G PlattsCritical Care Research Group, University of Queensland, Brisbane, QLD, Australia.
Owen Christopher RaffelCritical Care Research Group, University of Queensland, Brisbane, QLD, Australia.
Levon GabrielianMedical School, University of South Australia, Adelaide, SA, Australia.
Adrian BarnettCritical Care Research Group, University of Queensland, Brisbane, QLD, Australia.
Jenifer ParatzDepartment of Intensive Care, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Rob BootsDepartment of Intensive Care, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
John F FraserCritical Care Research Group, University of Queensland, Brisbane, QLD, Australia.
Royal Brisbane and Women's Hospital · AUPrince Charles Hospital · AUUniversity of Queensland · AUQueensland University of Technology · AUUniversity of South Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCerebral microcirculation after severe head injury is heterogeneous and temporally variable. Microcirculation is dependent upon the severity of injury, and it is unclear how histology relates to cerebral regional blood flow.

objectiveThis study assesses the changes of cerebral microcirculation blood flow over time after an experimental brain injury model in sheep and contrasts these findings with the histological analysis of the same regions with the aim of mapping cerebral flow and tissue changes after injury.

methodsMicrocirculation was quantified using flow cytometry of color microspheres injected under intracardiac ultrasound to ensure systemic and homogeneous distribution. Histological analysis used amyloid precursor protein staining as a marker of axonal injury. A mapping of microcirculation and axonal staining was performed using adjacent layers of tissue from the same anatomical area, allowing flow and tissue data to be available from the same anatomical region. A mixed effect regression model assessed microcirculation during 4 h after injury, and those results were then contrasted to the amyloid staining qualitative score.

resultsMicrocirculation values for each subject and tissue region over time, including baseline, ranged between 20 and 80 ml/100 g/min with means that did not differ statistically from baseline flows. However, microcirculation values for each subject and tissue region were reduced from baseline, although their confidence intervals crossing the horizontal ratio of 1 indicated that such reduction was not statistically significant. Histological analysis demonstrated the presence of moderate and severe score on the amyloid staining throughout both hemispheres.

conclusionMicrocirculation at the ipsilateral and contralateral site of a contusion and the ipsilateral thalamus and medulla showed a consistent decline over time. Our data suggest that after severe head injury, microcirculation in predefined areas of the brain is reduced from baseline with amyloid staining in those areas reflecting the early establishment of axonal injury.

Indexed as

amyloid precursor protein staininganemiahistologymicrocirculationmicrospheres

Identifiers

PMID29867710
PMCPMC5949334
OpenAlexW2800676118

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.