Usefulness of Addition of CT Perfusion to CT Angiography for Brain Death Diagnosis in a Child

2010 ◽  
Vol 41 (04) ◽  
pp. 189-192 ◽  
Author(s):  
R. Pellón ◽  
E. M. de Lucas ◽  
C. G. Fernández ◽  
A. F. Flórez ◽  
T. Piedra
2009 ◽  
Vol 11 (2) ◽  
pp. 261-271 ◽  
Author(s):  
Dolores Escudero ◽  
Jesús Otero ◽  
Lara Marqués ◽  
Diego Parra ◽  
José Antonio Gonzalo ◽  
...  

2009 ◽  
Vol 30 (8) ◽  
pp. 1566-1570 ◽  
Author(s):  
E. Frampas ◽  
M. Videcoq ◽  
E. de Kerviler ◽  
F. Ricolfi ◽  
V. Kuoch ◽  
...  

BMJ Open ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. e047305
Author(s):  
Susan Alcock ◽  
Divjeet Batoo ◽  
Sudharsana Rao Ande ◽  
Rob Grierson ◽  
Marco Essig ◽  
...  

IntroductionSevere traumatic brain injury (TBI) is a catastrophic neurological condition with significant economic burden. Early in-hospital mortality (<48 hours) with severe TBI is estimated at 50%. Several clinical examinations exist to determine brain death; however, most are difficult to elicit in the acute setting in patients with severe TBI. Having a definitive assessment tool would help predict early in-hospital mortality in this population. CT perfusion (CTP) has shown promise diagnosing early in-hospital mortality in patients with severe TBI and other populations. The purpose of this study is to validate admission CTP features of brain death relative to the clinical examination outcome for characterizing early in-hospital mortality in patients with severe TBI.Methods and analysisThe Early Diagnosis of Mortality using Admission CT Perfusion in Severe Traumatic Brain Injury Patients study, is a prospective cohort study in patients with severe TBI funded by a grant from the Canadian Institute of Health Research. Adults aged 18 or older, with evidence of a severe TBI (Glasgow Coma Scale score ≤8 before initial resuscitation) and, on mechanical ventilation at the time of imaging are eligible. Patients will undergo CTP at the time of first imaging on their hospital admission. Admission CTP compares with the reference standard of an accepted bedside clinical assessment for brainstem function. Deferred consent will be used. The primary outcome is a binary outcome of mortality (dead) or survival (not dead) in the first 48 hours of admission. The planned sample size for achieving a sensitivity of 75% and a specificity of 95% with a CI of ±5% is 200 patients.Ethics and disseminationThis study has been approved by the University of Manitoba Health Research Ethics Board. The findings from our study will be disseminated through peer-reviewed journals and presentations at local rounds, national and international conferences. The public will be informed through forums at the end of the study.Trial registration numberNCT04318665


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Vol 69 (4) ◽  
pp. 995
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GirijaP Rath ◽  
Siddharth Chavali ◽  
Deep Sengupta ◽  
SuryaK Dube

Neurology ◽  
2007 ◽  
Vol 68 (17) ◽  
pp. 1437-1437 ◽  
Author(s):  
S. Muehlschlegel ◽  
B. Voetsch ◽  
A. B. Singhal

2018 ◽  
Vol 39 (5) ◽  
pp. 515-529 ◽  
Author(s):  
Tanvir Rizvi ◽  
Prem Batchala ◽  
Sugoto Mukherjee

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