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Dexamethasone for the treatment of traumatic brain injured patients with brain contusions and pericontusional edema Study protocol for a prospective, randomized and double blind trial

dc.contributor.authorPérez-Bárcena, Jon
dc.contributor.authorCastano-Leon, Ana Maria
dc.contributor.authorLagares Gomez-Abascal, Alfonso
dc.contributor.authorBarea-Mendoza, Jesus Abelardo
dc.contributor.authorNavarro Main, Blanca
dc.contributor.authorPomar Pons, Jaume
dc.contributor.authorPeriáñez Párraga, Leonor
dc.contributor.authorIbáñez Domínguez, Javier Angel
dc.contributor.authorChico-Fernandez, Mario
dc.contributor.authorLlompart-Pou, Juan Antonio
dc.contributor.authorFrontera-Juan, Guillem
dc.contributor.authorDEXCON TBI Trial Collaborators
dc.date.accessioned2024-09-18T06:42:45Z
dc.date.available2024-09-18T06:42:45Z
dc.date.issued2021-01-22
dc.description.abstractBackground: Traumatic brain injury (TBI) constitutes a leading cause of death and disability. Patients with TBI and cerebral contusions developing pericontusional edema are occasionally given dexamethasone on the belief that this edema is similar to that of tumors, in which the beneficial effect of dexamethasone has been demonstrated. Methods: The DEXCON TBI trial is a multicenter, pragmatic, randomized, triple-blind, placebo controlled trial to quantify the effects of dexamethasone on the prognosis of TBI patients with brain contusions and pericontusional edema. Adult patients who fulfill the elegibility criteria will be randomized to dexamethasone/placebo in a short and descending course: 4 mg/6 h (2 days); 4 mg/8 hours (2 days); 2 mg/6 hours (2 days); 2 mg/8 hours (2 days); 1 mg/8 hours (2 days); 1 mg/12 hours (2 days). The primary outcome is the Glasgow Scale Outcome Extended (GOSE) performed 1 month and 6 months after TBI. Secondary outcomes are: number of episodes of neurological deterioration; symptoms associated with TBI; adverse events; volume of pericontusional edema before and after 12 days of treatment; results of the neuropsychological tests one month and 6 months after TBI. The main analysis will be on an intention-to-treat basis. Logistic regression will estimate the effect of dexamethasone/placebo on GOSE at one month and at 6 months, dichotomized in unfavorable outcome (GOSE 1-6) and favorable outcome (GOSE 7-8). Efficacy will also be analyzed using the 'sliding dichotomy'. An interim and safety analysis will be performed including patients recruited during the first year to calculate the conditional power. A study with 600 patients would have 80% power (2 sided alpha = 5%) to detect a 12% absolute increase (from 50% to 62%) in good recovery. Discussion: This is a confirmative trial to elucidate the therapeutic efficacy of dexamethasone in a very specific group of TBI patients: patients with brain contusions and pericontusional edema. This trial could become an important milestone for TBI patients as nowadays there is no effective treatment in this type of patients.en
dc.description.sponsorshipThe Sociedad Española de Medicina Intensiva, Critica y Unidades Coronarias (SEMICYUC) through the Fundacion Espanola del Enfermo Critico (FEEC) is funding the run-in costs for this trial and up to 100 patients'recruitment. Full funding is being sought from public and private funding organizations for the main trial.es_ES
dc.format.number3es_ES
dc.format.pagee24206es_ES
dc.format.volume100es_ES
dc.identifier.citationPerez-Barcena J, Castano-Leon AM, Gomez-Abascal AL, Barea-Mendoza JA, Main BN, Pons JP, et al. Dexamethasone for the treatment of traumatic brain injured patients with brain contusions and pericontusional edema Study protocol for a prospective, randomized and double blind trial. Medicine (Baltimore). 2021 Jan 22;100(3):e24206.en
dc.identifier.doi10.1097/MD.0000000000024206
dc.identifier.e-issn1536-5964es_ES
dc.identifier.issn0025-7974
dc.identifier.journalMedicinees_ES
dc.identifier.otherhttps://hdl.handle.net/20.500.13003/19538
dc.identifier.pubmedID33546038es_ES
dc.identifier.puiL634212570
dc.identifier.scopus2-s2.0-85102089354
dc.identifier.urihttps://hdl.handle.net/20.500.12105/23226
dc.identifier.wos612835100118
dc.language.isoengen
dc.publisherLippincott Williams & Wilkins (LWW)
dc.relation.publisherversionhttps://dx.doi.org/10.1097/MD.0000000000024206en
dc.rights.accessRightsopen accessen
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectBrain contusions
dc.subjectDexamethasone
dc.subjectPericontusional edema
dc.subjectTraumatic brain injury
dc.subject.decsMétodo Doble Ciego*
dc.subject.decsDexametasona*
dc.subject.decsContusión Encefálica*
dc.subject.decsEdema Encefálico*
dc.subject.decsAntiinflamatorios*
dc.subject.decsHumanos*
dc.subject.decsEstudios Prospectivos*
dc.subject.decsEvaluación de Resultado en la Atención de Salud*
dc.subject.decsEnsayos Clínicos Controlados Aleatorios como Asunto*
dc.subject.meshRandomized Controlled Trials as Topic*
dc.subject.meshProspective Studies*
dc.subject.meshOutcome Assessment, Health Care*
dc.subject.meshBrain Edema*
dc.subject.meshHumans*
dc.subject.meshBrain Contusion*
dc.subject.meshAnti-Inflammatory Agents*
dc.subject.meshDexamethasone*
dc.subject.meshDouble-Blind Method*
dc.titleDexamethasone for the treatment of traumatic brain injured patients with brain contusions and pericontusional edema Study protocol for a prospective, randomized and double blind trialen
dc.typeresearch articleen
dspace.entity.typePublication
relation.isPublisherOfPublicationf94ef1f2-f26f-4ebc-84d7-bb83b401e22a
relation.isPublisherOfPublication.latestForDiscoveryf94ef1f2-f26f-4ebc-84d7-bb83b401e22a

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