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Dexamethasone for adult patients with a symptomatic chronic subdural haematoma (Dex-CSDH) trial: study protocol for a randomised controlled trial.
Kolias, Angelos G; Edlmann, Ellie; Thelin, Eric P; Bulters, Diederik; Holton, Patrick; Suttner, Nigel; Owusu-Agyemang, Kevin; Al-Tamimi, Yahia Z; Gatt, Daniel; Thomson, Simon; Anderson, Ian A; Richards, Oliver; Whitfield, Peter; Gherle, Monica; Caldwell, Karen; Davis-Wilkie, Carol; Tarantino, Silvia; Barton, Garry; Marcus, Hani J; Chari, Aswin; Brennan, Paul; Belli, Antonio; Bond, Simon; Turner, Carole; Whitehead, Lynne; Wilkinson, Ian; Hutchinson, Peter J.
Afiliación
  • Kolias AG; Department of Clinical Neurosciences, University of Cambridge, Cambridge Biomedical Campus, Cambridge, CB2 0QQ, UK. ak721@cam.ac.uk.
  • Edlmann E; Division of Neurosurgery, Addenbrooke's Hospital, Box 167, Cambridge, CB2 0QQ, UK. ak721@cam.ac.uk.
  • Thelin EP; Department of Clinical Neurosciences, University of Cambridge, Cambridge Biomedical Campus, Cambridge, CB2 0QQ, UK. ee291@cam.ac.uk.
  • Bulters D; Division of Neurosurgery, Addenbrooke's Hospital, Box 167, Cambridge, CB2 0QQ, UK. ee291@cam.ac.uk.
  • Holton P; Department of Clinical Neurosciences, University of Cambridge, Cambridge Biomedical Campus, Cambridge, CB2 0QQ, UK.
  • Suttner N; Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.
  • Owusu-Agyemang K; Wessex Neurological Centre, University Hospital Southampton NHS Foundation Trust, Tremona Rd, Southampton, Hampshire, SO16 6YD, UK.
  • Al-Tamimi YZ; Wessex Neurological Centre, University Hospital Southampton NHS Foundation Trust, Tremona Rd, Southampton, Hampshire, SO16 6YD, UK.
  • Gatt D; Institute of Neurosciences, Queen Elizabeth University Hospital, 1345 Govan Road, Glasgow, UK.
  • Thomson S; Institute of Neurosciences, Queen Elizabeth University Hospital, 1345 Govan Road, Glasgow, UK.
  • Anderson IA; Department of Neurosurgery, Sheffield Teaching Hospitals NHS Trust, Royal Hallamshire Hospital, Glossop Road, Sheffield, S10 2JF, UK.
  • Richards O; Department of Neurosurgery, Sheffield Teaching Hospitals NHS Trust, Royal Hallamshire Hospital, Glossop Road, Sheffield, S10 2JF, UK.
  • Whitfield P; Department of Neurosurgery, Leeds General Infirmary, Great George Street, Leeds, LS1 3EX, UK.
  • Gherle M; Department of Neurosurgery, Leeds General Infirmary, Great George Street, Leeds, LS1 3EX, UK.
  • Caldwell K; Department of Neurosurgery, Leeds General Infirmary, Great George Street, Leeds, LS1 3EX, UK.
  • Davis-Wilkie C; Southwest Neurosurgical Centre, Plymouth University Hospitals NHS trust, Plymouth, PL6 8DH, UK.
  • Tarantino S; Southwest Neurosurgical Centre, Plymouth University Hospitals NHS trust, Plymouth, PL6 8DH, UK.
  • Barton G; Division of Neurosurgery, Addenbrooke's Hospital, Box 167, Cambridge, CB2 0QQ, UK.
  • Marcus HJ; Cambridge Clinical Trials Unit (CCTU), Coton House, Level 6, Cambridge Biomedical Campus, Box 401, Cambridge, CB2 0QQ, UK.
  • Chari A; Division of Neurosurgery, Addenbrooke's Hospital, Box 167, Cambridge, CB2 0QQ, UK.
  • Brennan P; Norwich Medical School, University of East Anglia, Norwich, NR4 7TJ, UK.
  • Belli A; Imperial College Healthcare NHS Trust, South Kensington Campus, London, SW7 2AZ, UK.
  • Bond S; Royal London Hospital, Barts Health NHS trust, Whitechapel Road, London, E1 1BB, UK.
  • Turner C; Department of Clinical Neurosciences, University of Edinburgh, Western General Hospitals NHS Trust, Crewe Road, Edinburgh, EH4 2XU, UK.
  • Whitehead L; NIHR Surgical Reconstruction and Microbiology Research Centre & University Hospitals Birmingham NHS Foundation Trust, School of Clinical and Experimental Medicine, University of Birmingham, Institute of Biomedical Research (West), Room WX 2.61, Edgbaston, Birmingham, B15 2TT, UK.
  • Wilkinson I; Cambridge Clinical Trials Unit (CCTU), Coton House, Level 6, Cambridge Biomedical Campus, Box 401, Cambridge, CB2 0QQ, UK.
  • Hutchinson PJ; MRC Biostatistics Unit, Robinson Way, Cambridge Biomedical Campus, Cambridge, CB2 0SR, UK.
Trials ; 19(1): 670, 2018 12 04.
Article en En | MEDLINE | ID: mdl-30514400
ABSTRACT

BACKGROUND:

Chronic subdural haematoma (CSDH) is a common neurosurgical condition, typically treated with surgical drainage of the haematoma. However, surgery is associated with mortality and morbidity, including up to 20% recurrence of the CSDH. Steroids, such as dexamethasone, have been identified as a potential therapy for reducing recurrence risk in surgically treated CSDHs. They have also been used as a conservative treatment option, thereby avoiding surgery altogether. The hypothesis of the Dex-CSDH trial is that a two-week course of dexamethasone in symptomatic patients with CSDH will lead to better functional outcome at six months. This is anticipated to occur through reduced number of hospital admissions and surgical interventions.

METHODS:

Dex-CSDH is a UK multi-centre, double-blind randomised controlled trial of dexamethasone versus placebo for symptomatic adult patients diagnosed with CSDH. A sample size of 750 patients has been determined, including an initial internal pilot phase of 100 patients to confirm recruitment feasibility. Patients must be recruited within 72 h of admission to a neurosurgical unit and exclusions include patients already on steroids or with steroid contraindications, patients who have a cerebrospinal fluid shunt and those with a history of psychosis. The decision regarding surgical intervention will be made by the clinical team and patients can be included in the trial regardless of whether operative treatment is planned or has been performed. The primary outcome measure is the modified Rankin Scale (mRS) at six months. Secondary outcomes include the number of CSDH-related surgical interventions during follow-up, length of hospital stay, mRS at three months, EQ-5D at three and six months, adverse events, mortality and a health-economic analysis.

DISCUSSION:

This multi-centre trial will provide high-quality evidence as to the effectiveness of dexamethasone in the treatment of CSDH. This has implications for patient morbidity and mortality as well as a potential economic impact on the overall health service burden from this condition. TRIAL REGISTRATION ISRCTN, ISRCTN80782810 . Registered on 7 November 2014. EudraCT, 2014-004948-35 . Registered on 20 March 2015. Dex-CSDH trial protocol version 3, 27 Apr 2017. This protocol was developed in accordance with the SPIRIT checklist. Available as a separate document on request.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dexametasona / Hematoma Subdural Crónico / Glucocorticoides Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dexametasona / Hematoma Subdural Crónico / Glucocorticoides Tipo de estudio: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido