Multicentre prospective observational study protocol for radiation exposure from gastrointestinal fluoroscopic procedures (REX-GI study).
Endoscopy, Gastrointestinal
/ statistics & numerical data
Fluoroscopy
/ statistics & numerical data
Gastrointestinal Diseases
/ diagnostic imaging
Gastrointestinal Tract
/ diagnostic imaging
Humans
Japan
Prospective Studies
Radiation Dosage
Radiation Exposure
/ statistics & numerical data
Radiography, Interventional
/ methods
Research Design
ERCP
diagnostic reference levels
endoscopy
gastrointestinal fluoroscopic procedure
radiation exposure
Journal
BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874
Informations de publication
Date de publication:
26 02 2020
26 02 2020
Historique:
entrez:
29
2
2020
pubmed:
29
2
2020
medline:
20
2
2021
Statut:
epublish
Résumé
Recently, the use of various endoscopic procedures under X-ray fluoroscopic guidance, such as endoscopic retrograde cholangiopancreatography (ERCP), interventional endoscopic ultrasonography (EUS), enteral endoscopy and stenting, has been rapidly increasing because of the minimally invasive nature of these procedures compared with that of surgical intervention. With the spread of CT and fluoroscopic interventions, including endoscopic procedures under X-ray guidance, high levels of radiation exposure (RE) from medical imaging have led to major concerns throughout society. However, information about RE related to these image-guided procedures in gastrointestinal endoscopy is scarce, and the RE reference levels have not been established. The aim of this study is to prospectively collect the actual RE dose and to help establish diagnostic reference levels (DRLs) in the field of gastroenterology in Japan. This is a multicentre, prospective observational study that is being conducted to collect the actual RE from treatments and diagnostic procedures, including ERCP, interventional EUS, balloon-assisted enteroscopy, enteral metallic stent placement and enteral tube placement. We will measure the total fluoroscopy time (min), the total dose-area product (Gycm Approval was obtained from the Institutional Review Board of Toyonaka Municipal Hospital (25 April 2019). The need for informed consent will be waived via the The UMIN Clinical Trials Registry, UMIN000036525.
Identifiants
pubmed: 32107268
pii: bmjopen-2019-033604
doi: 10.1136/bmjopen-2019-033604
pmc: PMC7202697
doi:
Banques de données
UMIN-CTR
['UMIN000036525']
Types de publication
Journal Article
Multicenter Study
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e033604Informations de copyright
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.
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