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Equipment Performance
 

 


The Quality Assurance (QA) Cycle of X-ray Equipment used in Diagnostic Radiology:
X-ray equipment undergoes a quality assurance cycle of specification, installation, critical examination, acceptance, commissioning, routine performance testing, maintenance and finally disposal that are the subject of regulations and guidance. The cycle is shown below.  RPC, acting as your RPA, is able to  assist you in most of the requirements of the equipment QA cycle.  Further explanation is provided below.


Specification of the X-ray Equipment:
The RPA should be consulted when drawing up a specification for new equipment.  In particular the restriction of patient exposure should be considered when purchasing radiological equipment.  RPC has the combined experience to assist in this decision. Additionally, during the specification process,  RPC will assess the suitability of the QA programme for new equipment, taking account of any special requirements recommended by the manufacturer.


Critical Examination, Acceptance and Commissioning:
The Radiology Manager must ensure that new equipment is not used clinically until a critical examination (by the installer) and commissioning tests have been completed.  This includes new installations, when equipment is re-installed in  another room and for replacement equipment such as X-ray tubes and image intensifiers. 

The purpose of the critical examination is to demonstrate to the purchaser that the designed safety features and warning devices operate correctly, that there is sufficient protection for persons from exposure to ionising radiation and that the equipment is safe to use in normal circumstances.  In all situations, it is the responsibility of the installer to ensure that the critical examination is performed to specification.  Any new installation must be subjected to a Critical Examination by the installer who should provide written evidence that this has been undertaken and with satisfactory results.  An RPA has to be consulted about the examination and the results.  The RPA may be the installerís or the purchaserís RPA; this should be agreed at the time of placing the order.

Newly installed X-ray equipment shall be commissioned to check that the equipment is ready for clinical use and when equipment is re-installed in another room. Commissioning ensures that the equipment is fit for clinical use and will enable baseline values, for future routine performance testing,  to be established.  Commissioning is undertaken by the purchaser's RPA in conjunction with the supplierís X-ray engineer.

Acceptance is undertaken by a representative of the purchaser, usually the RPA, in conjunction with the supplier. Its purpose is to verify that the engineer has supplied all the equipment specified and that the requirements of the contract have been met. The results of the commissioning tests and the purchase contract are needed to determine whether the equipment should be accepted.


Routine Performance Testing:
Regular radiation safety and performance surveys of diagnostic x-ray equipment are vital to ensure the optimum level of protection for both staff and patients while maintaining the highest image quality and so a suitable Quality Assurance programme is legally required (regulation 32 of the (IRR) Ionising Radiations Regulations).  This programme is usually regular in house tests, backed up by an annual radiation safety survey carried out by your RPA.  RPC has a lot of experience in carrying out such surveys. The safety surveys may however, be required more frequently, for more complex and higher dose imaging equipment.  The survey includes all parts of the imaging chain and ensures that the performance of your equipment is optimised.


Maintenance, Modification and Disposal:
Regular maintenance is also required by the IRR and this is usually arranged by having a contract with the equipment supplier, or other suitable body..  The RPA should be informed of any modifications, such as change of the imaging intensifier, as the further checks on the equipment's fitness of purpose may need to be checked.  The RPA may also be contacted for advice on the correct disposal route for X-ray generating equipment.


For further information call RPC on 020 8725 1050/1


 

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