Quality Assurance Flashcards
Define quality assurance
An organised effort by staff to ensure that the diagnostic images produced are of sufficiently high quality to consistently provide adequate diagnostic information at the lowest possible cost and the least possible exposure to the patient.
Why must we QA?
Due to:
- Human error
- Legislation
What are 3 ways of reducing human error?
Human error can be reduced by:
- Introducing simple systems, SOP
- Improving working environment
- Encouraging reporting without blame
What are SOPs?
Written guidelines on how to perform a task to make sure everyone does it the same way every time.
Why does legislation exist?
To ensure all establishments who expose people to radiation are taking responsibility for their actions. Radiation is dangerous.
What set of regulations protect the patient?
The Ionising Radiation (Medical Exposure) regulations (IR(ME)R 2017)
What set of regulations protect both staff and the public,
and also protect the patient in relation to equipment use?
The Ionising Radiation Regulations 2017 (IRR 2017)
There are specific roles in IRMER 17.
What is the Employer’s (boss) role in IRMER 17?
They must ensure their establishment is complying with IRMER7
- Compliance must be faultless as you can be inspected by the HSE.
What is the practitioner’s (person who justifies exposure) role in IRMER 17?
- Must be aware of and adhere to the correct referral criteria for dental exposures
- Assumes legal responsibility for the exposure when they put their name to it.
What is the referrer’s (one who refers the patient for radiographs) role in IRMER 17?
Responsible for viewing that radiograph and recording findings in the patients notes
What are the two specific regulations in IRMER?
- The employer shall establish QA programmes for standard operating procedures.
- The employer must ensure every practitioner and operator undertakes CPD:
- 5 hours of CPD specific to radiation safety every 5 yrs
What do SOPs involve in an X-ray department?
- How we justify the exposure
- To how we correctly identify the patient
- To how we collect equipment
- Expose the patient
- To how we clean the phosphor plates and develop them
How is QA carried out?
- Named person in charge of overseeing compliance
- Details of procedures involved
- Frequency procedures carried out
- Frequency records will be audited
- All the above must be put in writing
What do we look at in a Q.A programme?
- Image quality
- X-ray equipment
- Processing (film and digital)
- Working procedures
- Training
- Audit
How are high quality images ensured?
By auditing the images that are produced by using;
1) Image Quality Rating System on every image we take
(2) Film Reject Analysis
How should images be rated?
Either diagnostically acceptable (A) or diagnostically not acceptable (N)
Outline the steps of image quality rating system:
- Asses all images produced.
- Grade films by image quality
- Images are rated either 1, 2 or 3
- Collate Results - analyse monthly, quarterly or at least every six months.
- Feed-back results to staff.
What are the characteristics of an image quality rating 1?
Excellent – No errors of patient preparation, exposure, positioning, processing or film handling
What are the characteristics of an image quality rating 2?
Diagnostically acceptable – some errors in patient preparation, exposure, positioning, processing or handling which do not detract from the diagnostic utility of the radiograph
What are the characteristics of an image quality rating 3?
Unacceptable – Errors of patient preparation, exposure, positioning, image processing or reconstruction which render the radiograph diagnostically unacceptable. The image must be repeated.
As a health professional what % of A rated radiographs should you aim for?
> 95% for digital
90% for film
What is film reject analysis?
Film reject analysis is a component of QA.
It involves recording the reason you rejected the image
Why is film reject analysis important?
Because it is possible to spot trends.
Spotting trends will allow you to take appropriate action to try and minimise or eliminate errors.
It might indicate if an individual needs more training or support or if its something specific to equipment that hasn’t been picked up by QA test
What are the 5 steps of film reject analysis ?
- Collect all 3 rated films
- At end of each month assess these films
- Categorise faults e.g Exposure, Positioning, Processing etc
- ACT
- Repeat every month and compare results
Why should all N rated films be kept?
So they can be analysed.
If using a digital system, what should be recorded?
The date, time, nature of the deficiency and number of repeat radiographs must be recorded.
When is it recommended that reject analysis should be performed?
Aat the same time as image quality analysis.
How often should film reject analysis be carried out?
Preferably monthly, but at least every 6 months.
What is the IQRS audit cycle?
A continuous cycle
What are the 4 stages of the IQRS cycle?
- Asses - evaluate image
- Grade - 1, 2 or 3
- Results - analyse and look for ways to improve
- Feed-back to staff
REPEAT
How often should equipment be tested to check it is working satisfactorily?
Preferably annually but minimally every 3 years.
What should equipment checks involve?
- Representative patient doses
2. Annual routine maintenance
How are representative patient doses measured?
This is done by carrying out a series of exposures over a dosemeter which tells you the exact measurement of equivalent dose.
At DDH how often are equipment tests carried out?
Every 3 months
At DDH how often are medical physics tests carried out?
Every 3 years
What are important things to consider when processing film?
- Make sure newly stocked boxes aren’t used first
- Processor performance must be monitored and maintained
- Performance of digital system must be monitored.
Why should you be careful not to over order?
As films start to degrade as they age. You must not over order in case films aren’t used in time before the best before date
What are the best conditions for film storage?
Storage instructions are found inside box. Keep your stock;
- Out of sunlight
- Away from radiation
- At optimum humidity and temp.
What are the best conditions for digital - PSP storage?
- Cool and not too humid
- Avoid direct sunlight and UV
- Preferably in light protection/ cross infection barrier envelope.
- If not used for more than 24hrs after plate erased (exposure to bright light) it should be erased again.
What is the main method of testing performance?
Sensitometry