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Feasibility of individualised severe traumatic brain injury management using an automated assessment of optimal cerebral perfusion pressure: the COGiTATE phase II study protocol

医学 创伤性脑损伤 观察研究 神经重症监护 颅内压 脑灌注压 重症监护室 脑自动调节 第七节 颅内压监测 重症监护 急诊医学 随机对照试验 自动调节 物理疗法 血压 重症监护医学 脑血流 麻醉 内科学 精神科
作者
Erta Beqiri,Peter Smielewski,Chiara Robba,Marek Czosnyka,Manuel Cabeleira,Jeanette Tas,Joseph E. Donnelly,Joanne Outtrim,Peter J. Hutchinson,David Menon,Geert Meyfroidt,Bart Depreitere,Marcel Aries,Ari Ercole
出处
期刊:BMJ Open [BMJ]
卷期号:9 (9): e030727-e030727 被引量:88
标识
DOI:10.1136/bmjopen-2019-030727
摘要

Individualising therapy is an important challenge for intensive care of patients with severe traumatic brain injury (TBI). Targeting a cerebral perfusion pressure (CPP) tailored to optimise cerebrovascular autoregulation has been suggested as an attractive strategy on the basis of a large body of retrospective observational data. The objective of this study is to prospectively assess the feasibility and safety of such a strategy compared with fixed thresholds which is the current standard of care from international consensus guidelines.CPPOpt Guided Therapy: Assessment of Target Effectiveness (COGiTATE) is a prospective, multicentre, non-blinded randomised, controlled trial coordinated from Maastricht University Medical Center, Maastricht (The Netherlands). The other original participating centres are Cambridge University NHS Foundation Trust, Cambridge (UK), and University Hospitals Leuven, Leuven (Belgium). Adult severe TBI patients requiring intracranial pressure monitoring are randomised within the first 24 hours of admission in neurocritical care unit. For the control arm, the CPP target is the Brain Trauma Foundation guidelines target (60-70 mm Hg); for the intervention group an automated CPP target is provided as the CPP at which the patient's cerebrovascular reactivity is best preserved (CPPopt). For a maximum of 5 days, attending clinicians review the CPP target 4-hourly. The main hypothesis of COGiTATE are: (1) in the intervention group the percentage of the monitored time with measured CPP within a range of 5 mm Hg above or below CPPopt will reach 36%; (2) the difference in between groups in daily therapy intensity level score will be lower or equal to 3.Ethical approval has been obtained for each participating centre. The results will be presented at international scientific conferences and in peer-reviewed journals.NCT02982122.
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