Why is it essential to record autoclave sterilisation cycles?
We always advocate ongoing and correct recording of every sterilisation cycle made by an autoclave – this is for several reasons, all surrounding efficacy, safety, and compliance.
Verifying each cycle
Verifying the accuracy for each sterilisation cycle undertaken by the autoclave provides evidence that it was successful, and the autoclave reached and maintained the right temperature for the right length of time to sterilise the equipment and items within. In turn, this helps to reduce the risk of contamination.
This links in with quality control and assurance, consistent monitoring and identifying any deviations/failures that could be problematic.
Compliance with regulations
Compliance with UK industry standards and regulations often includes keeping documentation to produce if required. Maintaining accurate records for audits and inspections ensures you can demonstrate adherence to regulations and do not fail on this element.
Accountability
Keeping a historical record of sterilisation cycles provides an audit trail that can be traced back if any issues to arise in terms of contamination or autoclave failure. Legally, this helps to defend against any failure on the part of the autoclave or those using it.
Maintenance
Recording each cycle provides data on the performance of the autoclave over time, indicating when maintenance or calibration might be needed. This helps to extend the lifespan of the autoclave.
Each autoclave in question can also be monitored on an ongoing basis for performance, which is beneficial in spotting any issues early – this in turn leads to less disruption and potential downtime.
Ethical Considerations
Ethically, it is important to ensure that all sterilisation processes are performed accurately to protect patients against cross contamination. Keeping a record trail helps to ensure ethical practices are adhered to.
Overall, recording sterilisation cycles is an essential practice to maintain high standards of infection control, ensure the reliability of sterilized instruments, and comply with regulatory and safety requirements.
