Guía para el control de calidad y seguridad en aceleradores lineales de uso clínico

Autores/as

  • Françoise Lliso Valverde Unidad de Radiofísica, Servicio de Oncología Radioterápica. Hospital Universitari i Politécnic La Fe, Valencia.
  • Manuel Vilches Pacheco Servicio de Radiofísica y Protección Radiológica. Centro Médico de Asturias, Oviedo.
  • Miguel Martínez Albaladejo Servicio de Radiofísica. Hospital General Universitario Santa Lucía, Cartagena.
  • Pedro Almendral Manzano Servicio de Radiofísica. Hospital Universitario de Badajoz, Badajoz.
  • Eva Ambroa Rey Unidad de Radiofísica. Consorci Sanitari de Terrasa (CST), Terrassa, Barcelona.
  • Carlos Luis Ferrer Gracia Servicio de Radiofísica. Hospital Universitario La Paz, Madrid.
  • Jaime Pérez-Alija Fernández Servei de Radiofísica. Hospital de la Santa Creu i Sant Pau, Barcelona.
  • Ricardo Tortosa Oliver Servicio de Radiofísica. Hospital IMED, Elche. Servicio de Radiofísica. Hospital Francesc Borja, Gandía.

DOI:

https://doi.org/10.37004/sefm/2024.25.1.007

Palabras clave:

Radioterapia, acelerador lineal, control de calidad, análisis de riesgos, control estadístico de procesos

Resumen

El objetivo principal de este documento es constituir una guía para el diseño del programa de control de calidad en aceleradores lineales (CCAL) con montaje isocéntrico que incorpore los enfoques del control estadístico de procesos (CEP) y del análisis de riesgos. A  lo largo del texto se hace hincapié en que la guía no es prescriptiva y se anima a adaptarla a las necesidades específicas de cada centro.

Se presenta una breve descripción de las pruebas recomendadas. Se sugiere un conjunto de pruebas fundamentales y otras complementarias a las que se ha llegado teniendo en cuenta los resultados extraídos de una encuesta a los socios de la SEFM, así  como las propuestas de otras sociedades científicas, los comentarios de los fabricantes, y el consenso de este grupo de trabajo. Se  proporcionan recomendaciones de frecuencias y tolerancias para aceleradores representativos a título orientativo.

En los apéndices se abordan aspectos funcionales del acelerador lineal y su relación con las pruebas fundamentales del programa de  CCAL y se proporciona un ejemplo práctico de CEP aplicado a la variable dosis absorbida por unidad de monitor. Asimismo, se insta a los fabricantes, proveedores de material dosimétrico y gestores a utilizar la guía como referencia para colaborar en el mantenimiento de los equipos al nivel óptimo de calidad y seguridad requeridos.

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2024-05-05

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Guía para el control de calidad y seguridad en aceleradores lineales de uso clínico. (2024). Revista De Física Médica, 25(1), 77-122. https://doi.org/10.37004/sefm/2024.25.1.007

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