Safety Tips for Laboratorians: How Laboratorians Can Safely Calculate Workload for FDA-Approved Semi-Automated Gynecologic Cytol
Posted Jul 26 2010 9:00pm
The purpose of this communication is to clarify for laboratories how workload should be calculated when using currently FDA-approved semi-automated gynecologic cytology screening devices. This communication is intended for cytotechnologists, technical supervisors, and laboratory managers using these systems and addresses how to count fields of view (FOV) and full manual slide reviews (FMR), as well as establishing maximum workload limits. Exceeding the designated maximum workload jeopardizes the ability of device users to detect precancerous and cancerous lesions of the cervix and is a public health risk.
What are the current issues with workload recording and maximum workload limits?
It has been brought to our attention that the current product labeling regarding workload recording for these devices has been difficult to interpret, resulting in variability and lack of standardization in counting methods.
In addition, individual maximum daily workload limits are not being established by the technical supervisor as mandated by CLIA’88. The maximum daily limit specified in each of the device product labeling is only an upper limit and should never be used as an expectation for daily productivity or as a performance target.
How can laboratorians safely calculate workload for FDA-approved semi-automated cytology screening device?
To ensure the safety and effectiveness of these devices, given their importance as women’s health screening tests, the FDA has determined that laboratorians should use the following method when calculating workload. The calculation method applies to both semi-automated cytology screening systems currently on the market (Hologic’s ThinPrep® Imaging System and Becton Dickinson’s Focal Point™ Guided Screening System):
All slides with full manual review (FMR) count as 1 slide (as mandated by CLIA’88 for manual screening)
All slides with field of view (FOV) only review count as 0.5 or ½ slide
Then, slides with both FOV and FMR count as 1.5 or 1½ slides
Use these values to count workload, not exceeding the CLIA maximum limit of 100 slides in no less than an 8-hour day.
FMR = 1 slide
FOV = 0.5 slide
FMR + FOV = 1.5 slides
Upper Limit = 100 slides
Note: ALL laboratories should have a clear standard operation procedure for documentation of their method of workload counting and for establishing workload limits.
The following are examples of different counting scenarios that a cytotechnologist may encounter:
Cytology slide count equivalents
One smear = 1 slide
One slide preparation which results in cell dispersion over one-half or less of the total available slide area = 0.5 slide
One conventional Pap smear slide = 1 slide
One manually screened (non-automated) liquid based cytology preparation = 1 slide
One FOV (Field of View) slide screened by the automated method = 0.5 slide
One FMR (Full manual review) slide screened by the automated method = 1 slide
Then, FOV + FMR screened by the automated method = 1.5 slides
Note: If an FMR slide is rescreened manually as part of 10% QC, it should be counted as 1 slide because it is assumed that this slide will not undergo an FOV review a second time.
Cytotechnologist screens non-gynecologic and automated gynecologic slide preparations in the same laboratory
15 smears = 15 slides
10 cytospin slides = 5 slides (10 x 0.5)
50 FOV only (automated screening) = 25 slides (50 x 0.5)