Requisitos básicos para los sistemas de registro y gestión de dosis en pacientes sometidos a exploraciones de diagnóstico por imagen

  1. Santiago Miquelez Alonso 1
  2. Miguel Ángel Peinado Montes 2
  3. José Miguel Fernandez Soto 3
  4. José Manuel Ordiales Solís 4
  5. Luis Alejo Luque 5
  6. Julio Fco. Almansa López 6
  7. Joan Font Gelabert 7
  1. 1 Complejo Hospitalario de Navarra, Pamplona
  2. 2 Hospital Universitario Central de Asturias

    Hospital Universitario Central de Asturias

    Oviedo, España


  3. 3 Hospital Clínico San Carlos, Madrid
  4. 4 Hospital de Mérida

    Hospital de Mérida

    Merida, España

  5. 5 Hospital Universitario de la Paz, Madrid
  6. 6 Hosp. Universitario Virgen de las Nieves, Granada
  7. 7 Hospital Universitari de Son Espasses, Palma de Mallorca
Revista de Física Médica

ISSN: 1576-6632

Year of publication: 2020

Volume: 21

Issue: 1

Pages: 41-53

Type: Article

DOI: 10.37004/SEFM/2020.21.1.004 DIALNET GOOGLE SCHOLAR lock_openOpen access editor

More publications in: Revista de Física Médica


Directive 2013/59/Euratom of 5 December 2013 laying down basic safety standards for protection against the dangers arising from exposure to ionising radiation, establishes in section 28 of its introduction that more strict requirements should be proposed in what information to patients, recording and notification of doses in medical procedures, use of reference levels for diagnosis (RLD) and availability of dose indicator devices concerns. Due to the development of said concepts in both the European and Spanish regulation (Real Decreto 601/2019 of 18 October 2019 about justification and optimization of the use of ionising radiation for radiological protection in medical exposures ) the Spanish Societies of Radiological Protection (SEPR) and Medical Physics (SEFM) have created a work group whose task is to make a report describing the requirements that a system for the recording and management of doses should fulfil.

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