Podcasts + other contents Flashcards

1
Q

According to the MRPBA Domain 5: Radiation safety and risk
manager, RTs must:

A
  • Apply knowledge of equipment and instrumentation to confirm that it is in good order and operating within acceptable operating parameters.
  • Identify and take action to correct unacceptable condition or operation of equipment and instrumentation.
  • Follow protocols to record and report non-conformance of equipment.
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2
Q

it is the responsibility of the RTs to:

A
  • Equipment includes all main equipment and accessory equipment (instruments) used to image or treat a patient/client.
  • Good order may be achieved by following cleaning and hygiene protocols, calibration/testing regimes and acceptable operating standards.
  • Issues affecting the functioning of equipment must be fully resolved before imaging or treating patients/clients
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3
Q

Daily CT QA checks

A
  • lasers
  • scale grid
  • image quality (eg. CT# uniformity)
  • resolution checks
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4
Q

The Process of Care + 5 categories

A

The “process of care” in radiation oncology refers to a framework for facilitating the appropriateness, quality and safety of all treatments received by patients undergoing
radiation therapy

  • patient evaluation
  • treatment preparation
  • treatment delivery
  • treatment management
  • follow up evaluation and care
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5
Q

Routine daily QA on the LINAC

A
  • Lasers
  • Light field
  • Field sizes
  • Interlocks
  • kV, MV, CBCT Units
  • Beam – output and energy
  • Mechanical devices
  • Ancillary equipment
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6
Q

traditional role of an RT

A
  • Provide safe and effective
    delivery of radiation as
    prescribed
  • Perform daily equipment
    and new patient treatment
    QA
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7
Q

evolving role of an RT

A
  • Assessment of 2-D/3-D images to
    make decisions concerning patient
    alignment
  • Utilization of various motion
    management equipment
  • Adapting to changing modalities
    for IGRT and treatment (MRI
    linacs, surface imaging, particle
    therapy)
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8
Q

examples of tools and initiatives to facilitate safety and safety culture

A
  • staffing and schedules
  • standardisation
  • communication and facilities
  • lean methods
  • risk analysis
  • hierarchy of effectiveness
  • systems and human factors engineering
  • automated QA tools
  • peer reviews
  • daily morning huddles
  • safety rounds
  • routine public announcements and updates
  • incident learning
  • quality assurance committee
  • credentialing and training of staff
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9
Q

peer review

A

is an essential part of the safe delivery of radiation and an important aspect of a lifelong learning program for the clinical team

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10
Q

compare QA and peer review

A

QA is often taken to relate to objective/quantitative “right versus wrong” actions (e.g., Was the correct plan sent from the TPS to the treatment machine? Is the machine beam output correct?) that can readily lead to major clinical events that affect one or many patients.

Peer review is often used to refer to somewhat more subjective items such as target definition or dose selection.

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11
Q

rationale of QA in RT

A
  • reduces random and systematic errors across all steps in the process of care. This improves dosimetric and geometric accuracy and the precision.
  • Increases the probability that they will be recognized and rectified sooner if they do occur, thereby reducing their consequences for patient treatment.
  • Allows a reliable inter-comparison of results among different centres
  • High level of accuracy and consistency is achieved- this is the expectation with highly conformal treatments.
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12
Q

Rationale for stringent QA

A

Cumulative Errors
- There are many contributing factors to overall uncertainty
- Understand and Optimize each component
- Need to optimise each component to the extent practical i.e., address the errors that can be controlled so that the errors that can’t be controlled matter less.

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13
Q

define Quality System Management (QSM)

A

is the management of a QA program

QSM is the management of a QA program. It involves establishing policies, procedures, and responsibilities to ensure the effective implementation and continuous improvement of QA processes.

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14
Q

define acceptance testing

A

Acceptance of equipment is the process in which the supplier demonstrates the baseline performance of the equipment to the satisfaction of the customer

is to verify that the new equipment meets the baseline performance specifications agreed upon with the supplier. It involves a series of tests and measurements performed by the supplier to demonstrate the equipment’s functionality and performance capabilities to the customer.

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15
Q

define commissioning

A

Commissioning is the process of preparing the equipment for clinical service

is the process of preparing the equipment for clinical service following acceptance testing. This involves a more comprehensive set of tests, calibrations, and adjustments performed by qualified medical physicists to ensure that the equipment is operating accurately, safely, and according to the manufacturer’s specifications and clinical requirements.

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16
Q

define quality audits + rationale

A

is a systematic and independent examination to determine whether or not quality activities and results comply with planned arrangements and whether or not the arrangements are implemented effectively and are suitable to achieve the stated objectives

systematic, independent evaluations of a process, system, or organization to ensure that it meets established standards, requirements, and quality objectives

Evaluate the need for improvement or corrective action if those standards are not met.

17
Q

characteristics of quality audits

A

Should be regular and form part of a quality feedback loop to improve quality.
* Voluntary
* Regulatory
* Procedural or Practical

18
Q

What is level I Audit?

A
  • every two years
  • mail-out audit is an independent measurement of linac output under reference conditions.
  • Optically Stimulated Luminescent Dosimeters (OSLDs) are sent to a facility, irradiated, and returned to the ACDS for analysis.
  • All clinical photon and electron beams are included in the audit.
19
Q

level Ib audit

A
  • new linac
  • upon request
  • ACDS staff perform on-site measurements using ACDS dosimetry equipment
  • more accurate than level I
  • photon and electron outputs
  • FFF beams
  • small field beams
20
Q

What is level II Audit?

A
  • once every 4 years
  • a diagnostic test of the TPS performance
  • mail out audit
  • independent measurement of linac output under reference condition
  • Dose delivered to a rectilinear solid water phantom, with lung inhomogeneity in some cases, and measured using a 2D ion chamber array.
  • 3DCRT, IMRT, VMAT, IMRT/VMAT FFF
21
Q

level III audit

A
  • audit determines absorbed dose to water delivered to selected points within an anthropomorphic phantom
  • this is an end-to-end audit where the phantom undergoes all steps within radiotherapy treatment chain
22
Q

TPS QA - Checksum program + rationale

A

Monthly – e.g., performing checksums on beam data and executable files.

  • The program cannot be modified by the operators therefore it should be verified that it has not been corrupted by any virus or wrong operations.
  • The beam data can be modified (e.g., new measurement more precise)
23
Q

Forms of Peer review

A

Physician-led case oriented
- Radiation Oncologists-RTs, Physics (set-up differs)

Tumour Board
- Multiple physicians and members of the healthcare team from diverse disciplines.

Chart Rounds
- Members of the treatment team review each case (e.g., doses,
fields, treatment plans, patient setup)

Morbidity and Mortality(M&M) rounds/case conferences
- developed to provide a forum in which clinicians discuss adverse events in an attempt to improve patient safety and care

24
Q

Peer Review Audit Tool for Radiation Oncology (PRAT) steps

A
  1. Patient selection
  2. Preliminary scoring of each case
  3. Peer review meeting to discuss all cases and feed back to radiation oncologist
  4. Subsequent re-audit of all cases where a change in management was discussed
25
Q

patient specific QA involves

A
  • Delivery of plan dose in a phantom
  • Validation of photon fluence using a portal imaging system
  • Point dose measurement
  • Independent MU validations using MU check software
26
Q

PSQA tools

A

Phantoms
1. Point dose Check (IMRT QA phantom)
2. MapCheck 3
3. ArcCheck (and MapPHAN)
4. Octavius4D
5. Delta4

27
Q

mapcheck3

A
  • 2D patient plan QA
    • conventional IMRT and 3DCRT
  • 1527 SunPoint 2 diode detectors uniform throughout the array
    • smallest detector
    • high sensitivity
    • less drift
    • no dose volume average
  • field size 26x36
28
Q

difference between acceptance testing and commissioning

A

Acceptance testing focuses on verifying the equipment’s basic functionality as per the purchase agreement, while commissioning ensures that the equipment is properly calibrated and configured for clinical use within the specific radiation oncology department.

29
Q

PRAT + steps

A

peer review audit tool (PRAT)

  1. patient selection
  2. Preliminary scoring of each case
  3. Peer review meeting to discuss all cases and feed back to radiation oncologist
  4. Subsequent re-audit of all cases where a change in management was discussed.