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null Clinical Audits in Radiation Oncology: Training for Auditors and Auditees

Clinical Audits in Radiation Oncology: Training for Auditors and Auditees

Enhancing Quality and Safety in Radiotherapy

Why Join the Course? 

Radiotherapy is a critical component of cancer treatment, requiring strict quality assurance to ensure patient safety and treatment efficacy. Clinical audits are not just a regulatory requirement under the Basic Safety Standards Directive (BSSD 2013/59/Euratom); they are a fundamental tool for fostering a strong quality culture in radiotherapy. By systematically assessing adherence to best practices, clinical audits help identify areas for improvement, promote collaboration among professionals, and harmonize quality standards across different centers. The course provides specialized training to equip professionals with the skills to conduct and participate in clinical audits effectively. It also equips professionals with the necessary skills to drive continuous improvement, ensuring high-quality, equitable, and safe radiotherapy treatments for all. 

Register at: http://docencia.recercasantpau.cat/ca/enllac-a-inscripcio/867 

Course Overview

  • Title: Clinical Audits in Radiation Oncology: Training for Auditors and Auditees.
  • Organized by: CAT-ClinART Project (EU4Health Programme) under Sant Pau Docent.
  • Location: Hospital Sant Pau, Barcelona, Spain (In-Person Only).
  • Dates: 10th to 13th June 2025.
  • Course Directors: Núria Jornet, Antonio Herreros and Gemma Sancho.
  • Target Audience: Radiation oncologists, medical physicists, RTTs, and quality managers.
  • Duration: 4 days.
  • Certification: Participants will receive a certification upon successful completion with Continuing Professional Development (CPD) points
  • Language: English. Course Objectives

Understand the principles and benefits of clinical audits in radiotherapy.

  • Learn the QUATRO methodology for comprehensive clinical audits in radiotherapy.
  • Develop skills to conduct both internal and external clinical audits.
  • Introduction to quality indicators, Quality standards and benchmarking.
  • Gain hands-on experience through case studies and real-life audit simulations.
  • Foster a culture of continuous quality improvement in radiotherapy departments.
  • Understand the legal framework, including compliance with the Basic Safety Standards Directive (BSSD 2013/59/Euratom). 

Benefits of Participation

  • Improve quality and safety in radiotherapy treatments.
  • Enhance collaboration between multidisciplinary teams.
  • Learn from leading experts in clinical audits.
  • Contribute to harmonizing radiotherapy practices in Catalonia and beyond. 

What does the course fee include? 

  • Course material. 
  • Certificate of completion with CPD points 
  • Opportunity to connect with leading experts in the field
  • 4 coffee breaks and 2 lunches.

Course Program

10th June 

TimeLectureFaculty 
8.30 - 9:00Registration  
9:00 - 9:15Welcome addressGemma Sancho
9:15 - 9:45Introduction to the course
Frame the course within a Quality Management System and also introduce the CAT-ClinART Project
Antonio Herreros
9:45-10:15Current situation of Clinical Audits in RT: Summary of QUADRANT results
Explain the results of the QUADRANT report on Clinical Audits in RT
Núria Jornet
10:15-10:45Audit vs Inspection
Herca position statement on the differences between a clinical audit and an inspection
Núria Jornet
10:45-11:15QUATRO and B-QUATRO audits: Commonalities and differences
Overview of QUATRO and B-QUATRO focusing on the commonalities and differences
Aude Vaandering
11:15 - 11:45Coffee Break 
11:45 - 12:15QUATRO terminology
Introduce the terminology used in QUATRO, including terminology used in the checklists
Primoz Strotjan
12:15 - 12:45Audit components
Go through the different components such as infrastructure, Patient Procedures, Equipment Procedures, Quality Management Structure
Aude Vaandering
12:45 - 13:15Audit QUATRO team
Introduction to the components of the QUATRO team, importance of team work and the roles of each component and the role of the team leader
Dirk Verellen
13:15-13:45Audit Structure
Introduction to the audit temporal structure; Preparation, Auditors vist and Final report
Primoz Strotjan

 

11th June 

TimeLectureFaculty
9:00 - 9:30Audit methodology: Checklists, standardized forms, observation and interviews
Introduction to the different tools for auditing
Primoz Strotjan
9:30 - 10:00Audit methodology B-QUATRO
B-QUATRO excel collection sheets and spider diagrams, the role of the Quality manager
Aude Vaandering
10:00 - 10:30Entrance and exit meetings
What should be covered in the entrance and exit meetings and to whom they are addressed
Dirk Verellen
10:30 - 11:00Coffee break 
11:00-11:30The role of the MPE
Explain the role of the MPE including the dosimetry audits
Dirk Verellen
11:30-12:00The role of the RO
Explain the role of the RO, including the attendance to MDT meetings, clinical record review, etc
Primoz Strotjan
12:00-12:30The Role of the RTT
Explain the role of the RTT, including the observation of practice at treatment units, education and training of RTTs, etc
Aude Vaandering
12:30 – 13:15Auditors code of conduct and required skills
Overview of the ethical principles, professional responsibilities, and key competencies required for auditors.
Primoz Strotjan
13:15 - 14:15Lunch 
14:15 - 15:00Dosimetry audit BQUATRO and QUATRO
Description of the dosimetry audits conducted during QUATRO audits and Dosimetry audits in BQUATRO through BeldART
Núria Jornet and Dirk Verellen
15:00 - 15:30Dosimetry audit CAT-ClinART
Introduction to the components of the QUATRO team, importance of team work and the roles of each component
WP4 Task group on dosimetry audits
15:30-16:30Clinical case audit
Demo on how the review of a clinical case would be performed
Primoz Strotjan, Dirk Verellen, Aude Vaandering
20:00-22:00Faculty Dinner 

 

12th June

TimeLectureFaculty
9:00 - 9:15Infrastructure checklists
Introduction to the practical exercice
Primoz Strotjan
9:15 - 10:15Practical in groups: Infrastructure checklists
45 min of team work filling in the checklist followed by a discussion
Primoz Strotjan, Dirk Verellen, Aude Vaandering, Núria Jornet
10:15 - 10:45Coffee Break 
10:45-11:00Patient related procedures checklists
Introduction to the practical exercice
Aude Vaandering
11:00-12:00Practical in groups: Patient related procedures checklists
45 min of team work filling in the checklist followed by a discussion
Primoz Strotjan, Dirk Verellen, Aude Vaandering, Núria Jornet
12:00-12:30What to do when we do not have standards?
Discussion on how to proceed when there are no standards
Dirk Verellen
12:30 - 14:30Lunch 
14:30 - 14:45Equipment and IT related checklists
Introduction to the practical exercice
Dirk Verellen
14:45 - 15:45Practical in groups: Equipment and IT related checklists
45 min of team work filling in the checklist followed by a discussion
Primoz Strotjan, Dirk Verellen, Aude Vaandering, Núria Jornet
15:45-16:00Quality management related checklists
Introduction to the practical exercice
Aude Vaandering
16:00- 17:00Practical in groups: Quality management related checklists
45 min of team work filling in the checklist followed by a discussion
Primoz Strotjan, Dirk Verellen, Aude Vaandering, Núria Jornet

 

13th June

TimeLectureFaculty
9:00– 9:30Writing the final report: dos and don’ts
How the final report should look like including practical examples
Primoz Strotjan
9:30 – 10:00Experience B-QUATRO
Explain lessons learnt from B-QUATRO audits and the feedback from auditors and auditees
Aude Vaandering
10:00-10:30How to maintain a permanent audit service
Experience from Belgium and B-QUATRO will be explained
Dirk Verellen
10:30 - 11:00Coffee break 
11:00 - 12:30Quality Indicators
Introduce the concept of quality indicator, types and how they are defined.
Aude Vaandering
12:30 - 13:00Presentation of CAT-ClinART QI
Describe the QI that will be collected within CATClinART clinical audit pilot
Xavier Maldonado
12:30 - 13:00Collection and benchmarking of QI in CAT-ClinART
Description and demonstration of the tools for QI reporting
Carles Muñoz
13:00-13:30Final conclusions
Wrap up and messages to take back home
Gemma Sancho

 

Faculty 

Dr. Antonio Herreros 

Medical Physics Expert. 

Servei d’Oncologia Radioteràpica. Hospital Clínic, Barcelona. Professor Associat Universitat de Barcelona, Spain 

Dra. Núria Jornet 

Medical Physics Expert. 

Servei de Radiofísica i Radioprotecció. Hospital de la Santa Creu i Sant Pau. Barcelona, Spain. 

Dra. Aude Vaandering 

RTT and Quality Manager 

Radiotherapy Department Cliniques Universitaires St Luc, Brussels, Belgium.

Professor Dirk Verellen 

Medical Physics Expert. 

Director Medical Physics Department and Professor Biomedical Physics. Iridium Netwerk, GZA Ziekenhuizen, Antwerp University, Antwerp, Belgium 

Professor Primoz Strotjan

Radiation Oncologist

Consultant Radiation Oncologist. Head of the Multidisciplinary Head and Neck Tumor Board. Head of the Working Group for Proton Therapy Implementation. Institute of Oncology Ljubljana, Slovenia

Dr. Xavier Maldonado 

Radiation Oncologist 

Director del Servei d’Oncologia Radioteràpica. Hospital de la Valle Hebron, Barcelona, Spain.

Dra. Gemma Sancho

Radiation Oncologists 

Directora del Servei d’Oncologia Radioteràpica. Hospital de la Santa Creu i Sant Pau, Barcelona, Spain. 

Dr. Carles Muñoz 

Medical Physics Expert

Director Servei de Radiofísica i Radioprotecció ICO. Institut Català d’Oncologia, Girona, Spain 

 

Registration

RegistrationRateDeadline
Early24015 th May 2025
Late3506 th June 2025

 

Registrations are limited to 35 participants. 

Registration link : 

http://docencia.recercasantpau.cat/ca/enllac-a-inscripcio/867