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Brain Tissue Oxygenation-Guided Therapy and Outcome in Traumatic Brain Injury: A Single-Center Matched Cohort Study

Brain tissue oxygenation (PbtO(2))-guided therapy can improve the neurological outcome of traumatic brain injury (TBI) patients. With several Phase-III ongoing studies, most of the existing evidence is based on before-after cohort studies and a phase-II randomized trial. The aim of this study was to...

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Detalles Bibliográficos
Autores principales: Barrit, Sami, Al Barajraji, Mejdeddine, El Hadweh, Salim, Dewitte, Olivier, Torcida, Nathan, Andre, Joachim, Taccone, Fabio Silvio, Schuind, Sophie, Gouvêa Bogossian, Elisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315682/
https://www.ncbi.nlm.nih.gov/pubmed/35884694
http://dx.doi.org/10.3390/brainsci12070887
Descripción
Sumario:Brain tissue oxygenation (PbtO(2))-guided therapy can improve the neurological outcome of traumatic brain injury (TBI) patients. With several Phase-III ongoing studies, most of the existing evidence is based on before-after cohort studies and a phase-II randomized trial. The aim of this study was to assess the effectiveness of PbtO(2)-guided therapy in a single-center cohort. We performed a retrospective analysis of consecutive severe TBI patients admitted to our center who received either intracranial pressure (ICP) guided therapy (from January 2012 to February 2016) or ICP/PbtO(2)-guided therapy (February 2017 to December 2019). A genetic matching was performed based on covariates including demographics, comorbidities, and severity scores on admission. Intracranial hypertension (IH) was defined as ICP > 20 mmHg for at least 5 min. Brain hypoxia (BH) was defined as PbtO(2) < 20 mmHg for at least 10 min. IH and BH were targeted by specific interventions. Mann–Whitney U and Fisher’s exact tests were used to assess differences between groups. A total of 35 patients were matched in both groups: significant differences in the occurrence of IH (ICP 85.7% vs. ICP/PbtO(2) 45.7%, p < 0.01), ICU length of stay [6 (3–13) vs. 16 (9–25) days, p < 0.01] and Glasgow Coma Scale at ICU discharge [10 (5–14) vs. 13 (11–15), p = 0.036] were found. No significant differences in ICU mortality and Glasgow Outcome Scales at 3 months were observed. This study suggests that the role of ICP/PbtO(2)-guided therapy should await further confirmation in well-conducted large phase III studies.