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An Update on the COGiTATE Phase II Study: Feasibility and Safety of Targeting an Optimal Cerebral Perfusion Pressure as a Patient-Tailored Therapy in Severe Traumatic Brain Injury.
Tas, Jeanette; Beqiri, Erta; van Kaam, C R; Ercole, Ari; Bellen, Gert; Bruyninckx, D; Cabeleira, Manuel; Czosnyka, Marek; Depreitere, Bart; Donnelly, Joseph; Fedriga, Marta; Hutchinson, Peter J; Menon, D; Meyfroidt, Geert; Liberti, Annalisa; Outtrim, J G; Robba, C; Hoedemaekers, C W E; Smielewski, Peter; Aries, Marcel J.
Afiliación
  • Tas J; Department of Intensive Care Medicine, University of Maastricht, Maastricht University Medical Centre, Maastricht, The Netherlands. Jeanette.tas@mumc.nl.
  • Beqiri E; Brain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • van Kaam CR; Department of Physiology and Transplantation, University of Milan, Milan, Italy.
  • Ercole A; Department of Intensive Care Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Bellen G; University Division of Anaesthesia, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.
  • Bruyninckx D; Department of Neurosciences, Catholic University Leuven, University Hospital Leuven, Leuven, Belgium.
  • Cabeleira M; Department of Neurosciences, Catholic University Leuven, University Hospital Leuven, Leuven, Belgium.
  • Czosnyka M; Brain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Depreitere B; Brain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Donnelly J; Department of Neurosciences, Catholic University Leuven, University Hospital Leuven, Leuven, Belgium.
  • Fedriga M; Brain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Hutchinson PJ; Brain Physics Laboratory, Division of Neurosurgery, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.
  • Menon D; Department of Anaesthesia, Critical Care and Emergency, Spedali Civili University Hospital, Brescia, Italy.
  • Meyfroidt G; Department of Clinical Neurosciences, Cambridge University, Cambridge, UK.
  • Liberti A; University Division of Anaesthesia, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.
  • Outtrim JG; Department of Cellular and Molecular Medicine, Catholic University Leuven, University Hospital, Leuven, Belgium.
  • Robba C; Department of Intensive Care Medicine, University of Maastricht, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Hoedemaekers CWE; University Division of Anaesthesia, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK.
  • Smielewski P; Department of Anaesthesia and Intensive Care, Policlinico San Martino, IRCCS for Oncology and Neuroscience, Genoa, Italy.
  • Aries MJ; Department of Intensive Care Medicine, Radboud University Medical Centre, Nijmegen, The Netherlands.
Acta Neurochir Suppl ; 131: 143-147, 2021.
Article en En | MEDLINE | ID: mdl-33839835
INTRODUCTION: Monitoring of cerebral autoregulation (CA) in patients with a traumatic brain injury (TBI) can provide an individual 'optimal' cerebral perfusion pressure (CPP) target (CPPopt) at which CA is best preserved. This potentially offers an individualized precision medicine approach. Retrospective data suggest that deviation of CPP from CPPopt is associated with poor outcomes. We are prospectively assessing the feasibility and safety of this approach in the COGiTATE [CPPopt Guided Therapy: Assessment of Target Effectiveness] study. Its primary objective is to demonstrate the feasibility of individualizing CPP at CPPopt in TBI patients. The secondary objectives are to investigate the safety and physiological effects of this strategy. METHODS: The COGiTATE study has included patients in four European hospitals in Cambridge, Leuven, Nijmegen, and Maastricht (coordinating centre). Patients with severe TBI requiring intracranial pressure (ICP)-directed therapy are allocated into one of two groups. In the intervention group, CPPopt is calculated using a published (modified) algorithm. In the control group, the CPP target recommended in the Brain Trauma Foundation guidelines (CPP 60-70 mmHg) is used. RESULTS: Patient recruitment started in February 2018 and will continue until 60 patients have been studied. Fifty-one patients (85% of the intended total) have been recruited in October 2019. The first results are expected early 2021. CONCLUSION: This prospective evaluation of the feasibility, safety and physiological implications of autoregulation-guided CPP management is providing evidence that will be useful in the design of a future phase III study in severe TBI patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Presión Intracraneal / Lesiones Traumáticas del Encéfalo Tipo de estudio: Guideline / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Acta Neurochir Suppl Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Austria

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Presión Intracraneal / Lesiones Traumáticas del Encéfalo Tipo de estudio: Guideline / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Acta Neurochir Suppl Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Austria