German Cranial Reconstruction Registry (GCRR)

• Verfasst von: Giese, Henrik [VerfasserIn]
• Verfasst von: Sauvigny, Thomas [VerfasserIn]
• Verfasst von: Sakowitz, Oliver [VerfasserIn]
• Titel: German Cranial Reconstruction Registry (GCRR)
• Titelzusatz: protocol for a prospective, multicentre, open registry
• Mitwirkende: Henker, Christian
• Verf.angabe: Henrik Giese, Thomas Sauvigny, Oliver W. Sakowitz, Michael Bierschneider, Erdem Güresir, Christian Henker, Julius Höhne, Dirk Lindner, Dorothee Mielke, Robert Pannewitz, Veit Rohde, Martin Scholz, Patrick Schuss, Jan Regelsberger
• E-Jahr: 2015
• Jahr: September 30, 2015
• Umfang: 5 S.
• Teil: volume:5
• Teil: year:2015
• Teil: number:9
• Teil: elocationid:e009273
• Teil: pages:1-5
• Teil: extent:5
• Fussnoten: Gesehen am 10.08.2021
• Titel Quelle: Enthalten in: BMJ open
• Ort Quelle: London : BMJ Publishing Group, 2011
• Jahr Quelle: 2015
• Band/Heft Quelle: 5(2015), 9, Artikel-ID e009273, Seite 1-5
• ISSN Quelle: 2044-6055
• DOI: doi:10.1136/bmjopen-2015-009273
• Datenträger: Online-Ressource
• Sprache: eng
• K10plus-PPN: 840662343

Abstract

Introduction Owing to increasing numbers of decompressive craniectomies in patients with malignant middle cerebral artery infarction, cranioplastic surgery becomes more relevant. However, the current literature mainly consists of retrospective single-centre (evidence class III) studies. This leads to a wide variability of technical approaches and clinical outcomes. To improve our knowledge about the key elements of cranioplasty, which may help optimising clinical treatment and long-term outcome, a prospective multicentre registry across Germany, Austria and Switzerland will be established. - Methods All patients undergoing cranioplastic surgery in participating centres will be invited to join the registry. Technical methods, materials, medical history, adverse events and clinical outcome measures, including modified Rankin scale and EQ-5D, will be assessed at several time points. Patients will be accessible to inclusion either at initial decompressive surgery or when cranioplasty is planned. Scheduled monitoring will be carried out at time of inclusion and subsequently at time of discharge, if any readmission is necessary, and at follow-up presentation. Cosmetic results and patient satisfaction will also be assessed. Collected data will be managed and statistically analysed by an independent biometric institute. The primary endpoint will be mortality, need for operative revision and neurological status at 3 months following cranioplasty. - Ethics and dissemination Ethics approval was obtained at all participating centres. The registry will provide reliable prospective evidence on surgical techniques, used materials, adverse events and functional outcome, to optimise patient treatment. We expect this study to give new insights in the treatment of skull defects and to provide a basis for future evidence-based therapy regarding cranioplastic surgery. - Trial registration number This trial is indexed in the German Clinical Trials Register (DRKS-ID: DRKS00007931). The Universal Trial Number (UTN) is U1111-1168-7425.