Quality assurance Flashcards
What principle do we use to ensure patients receive minimal ionising radiation
ALARP Principle
What Does the ALARP principle stand for
As
Low
As
Reasonably
Possible
What is the ALARP principle
Principle of radiation protection to keep radiation doses to patients as low as reasonably possible
How is the ALARP principle upheld
- Dose optimisation by choice of technique
- Use of selection criteria to justify all exposures
- Production of optimal quality images W
What is quality assurance
The planned and systematic execution of procedures to ensure high quality images of high diagnostic yield at minimum radiation doseage
What does quality assurance entail
- Getting it right the first time every time
- Ensuring the consistent production of radiographs of adequate quality for diagnostic purposes
- Keeping doses to patients ALARP
Why is quality assurance important
- Reduces the necessity for retakes
- Minimises radiation exposure to patient
- Minimise costs
- Minimise inconvenience
- Saves time
What does IRMER 2017 say about quality assurance
The employer must implement and maintain a QA programme
AND
The operator must select equipment and methods to ensure that for each exposure the dose of ionising radiation to the individual undergoing the exposure is ALARP and in doing so must pay particular attention to quality assurance
List the overarching principles that define the operations within the quality assurance programme
Programme should be:
1. Comprehensive
2. Based one evidence based guidance
3. Convient to operate and maintain
4. Standards should require infrequent verification or modification
5. Formally recorded
When formulating a quality assurance programme which subject areas need to be covered
- QA of IRMER17 employers procedures
- QA of x ray equipment and patient dose
- QA of image processing and display equipment
- QA of image quality
Which documents are includes in the QA of IRMER17 Employers procedures
- Radiation protection file
- QA Procedures for training
What does the radiation protection file contain
All documentation, procedures and records that are essential to the safe use of x ray equipment
eg legal documents such as local rules, employers procedure, contingency plans
How often is the radiation protection file reviewed
Reviewed when practice circumstances change
or
at no greater than 3 year intervals
What should the QA programme for radiation protection files include
- A record of the existence of relent documents and procedures
- Record of review and modification of these documents
What does the QA of X ray equipment and patient dose ensure
that all equipment remains capable of adequate dose restriction
What should the QA of X ray equipment and patient dose documents include
- Inventory of all dental x-ray equipment and ancillary equipment which would influence patient dose
- Record of testing
- In-house checks
- Representative patient doses
- Remedial and suspension levels for action
List all the x ray equipment
- X ray set
- image receptor
- Phosphor paste readers
- Film cassettes
- Light boxes
- Computer screens used for viewing digital images
What are the 4 parts of testing dental x ray equipment
- Critical examintion
- Adequate testing
- Routine testing
- In house QA checks
What is the critical examination
Examination done on the rx ray equipment before it comes into clinical use
What does the critical examination include
- correct operation of safety features and Warning devices
- Sufficient protection for persons from exposure to ionising radiation
- Provide employer with adequate information about proper use testing and maintained of the equipment
Who is legally responsible to carry put the critical examination
Legal respossiblty of installer but the employer is advised to ensure that it has been performed
Who should the installer consult following their critical examination
The radiation protection advisor with regard to the nature, extent and rust soft the examination
What is adequate testing also referred to as
Acceptance testing
When does adequate testing need to happen
Prior to equipment being put into clinical use