Cervical Cytology

Quality assurance

Objective

     

    On completion of this section the cytotechnologist should know:

  • Understand the concepts of quality assurance, quality control and quality standards
  • Be aware of the main sources of error in cervical cytology and understand the reason for introducing IQA and EQA into the laboratory
  • Understand the significance of a false negative smear report and how the risk of false negative reporting can be minimised
  • Be aware of the main systems of IQA and EQA and how they are applied to laboratory procedures
  • Understand the routine laboratory work flow in the cytology laboratory and the process of tiered screening and reporting protocols

    In addition an advanced practitioner should:

  • Improve their knowledge of IQA and EQA procedures and how to set and achieve quality standards
  • Understand the role of managers and senior cytotechnologists in the cytology laboratory
  • Understand how to monitor the screening program at local, regional and national level
  • Understand some basic statistical methods of monitoring laboratory performance