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dc.contributor.authorDel Río-Solá, Maria L.
dc.contributor.authorRial, Rodrigo
dc.contributor.authorLópez Espada, Cristina
dc.contributor.authorRodríguez-Morata, Alejandro
dc.contributor.authorVañó, Eliseo
dc.contributor.authorSpanish DRLs Vascular Collaborators Group
dc.date.accessioned2024-09-04T11:12:48Z
dc.date.available2024-09-04T11:12:48Z
dc.date.issued2024-08-05
dc.identifier.citationDel Río Solá, M.L. et. al. 68(2):210-217. [https://doi.org/10.1016/j.ejvs.2024.05.012]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/93937
dc.description.abstractObjective: The International Commission on Radiological Protection has highlighted the large number of medical specialties that use fluoroscopy outside diagnostic imaging departments without radiation protection programmes for patients and staff. Vascular surgery is one of these specialties. Thoracic endovascular aortic repair (TEVAR) is a complicated procedure requiring radiation protection guidance and optimisation. The recent EU Basic Safety Standards Directive requires the use and periodic updating of diagnostic reference levels (DRLs) for interventional procedures. The aim of this study was to determine doses for patients undergoing TEVAR with mobile Xray systems and hybrid rooms (fixed Xray systems) to obtain national DRLs and to suggest optimisation actions. Methods: This was a retrospective cross sectional study. The Spanish Chapter of Endovascular Surgery conducted a national survey in 11 autonomous communities representing around 77.6% of the Spanish population (47.33 million inhabitants). A total of 266 TEVAR procedures from 17 Spanish centres were analysed, of which 53.0% were performed in hybrid operating rooms. National DRLs were obtained and defined as the third quartile of the median values from the different participating centres. Results: The proposed national DRLs are: for kerma area product (KAP), 113.81 Gy$cm2 for mobile Xray systems and 282.59 Gy$cm2 for hybrid rooms; and for cumulative air kerma (CAK) at the patient entry reference point, 228.38 mGy for mobile systems and 910.64 mGy for hybrid rooms. Conclusion: Based on the requirement to know radiation doses for standard endovascular procedures, this study of TEVARs demonstrated that there is an increased factor of 2.48 in DRLs for KAP when the procedure is performed in a hybrid room compared with mobile C-arm systems, and an increased factor of 3.98 in DRLs for CAK when the procedure is performed with hybrid equipment. These results will help to optimise strategies to reduce radiation doses during TEVAR procedures.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectDiagnostic reference leveles_ES
dc.subjectDRLes_ES
dc.subjectEuropean Directivees_ES
dc.titleNational Diagnostic Reference Levels for Standard Descending Thoracic Endovascular Aortic Repair and Optimisation Strategieses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.ejvs.2024.05.012
dc.type.hasVersionVoRes_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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