Attachment D: Image-Assisted Cytology Workload Assessment Survey - Cytotechnologist
Form Approved
OMB No. 0920-XXXX
Expiration Date (one year from date of approval)
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Image-Assisted Cytology Workload Assessment
Cytotechnologist Section
This section should be completed separately by each cytotechnologist listed in Workload Practices Survey, question 18.
See the Glossary at the end of this questionnaire for abbreviations.
Enter your cytotechnologist letter designation from Survey, question 18 ___________
What is your pay classification?
Salary
Hourly
On average, how many hours do you work in the laboratory per day?
Less than 4
4
5
6
7
8
9
10
More than 10
According to your laboratory practice, which of the activities (where you are free from work related activities) are included in your paid hours?
Breaks Number per day ____________ Length of time ____________________
Lunch Length of time ___________________________
Continuing education activities
Able to leave when maximum number of slides are screened (paid for a full day if less hours are worked)
How do you record your daily workload? Workload recording may include any combination of the following: Check all that are recorded separately in your laboratory.
Total of all slides screened (GYN + Non-GYN)
Gyn total slides only
Non-Gyn slides only
Total of slides screened by image assisted – FOV only
Total of slides screened by image assisted – FMR
For the most recent month of complete data, provide an estimate of the average number of slides you screen per day.
Slide type |
Number of Slides |
Total (GYN & non-GYN) |
|
GYN slides – Image-Assisted FOV |
|
GYN slides – FMR |
|
GYN slides – Standard Microscope |
|
For workload recording, how does your laboratory count a GYN slide? Select all that apply.
Each slide screened for FOV is counted as one half (0.5) slide
Each slide (FOV or FMR) is counted as 1 slide
Each slide that is screened for FOV and a FMR is performed, count as 1 slide
Each slide that is screened for FOV and a FMR is performed, count as1.5 slides
Other – Describe policy ___________________________________________________ _______________________________________________________________________ _______________________________________________________________________
For workload recording, how does your laboratory count a NON-GYN slide? Select all that apply.
Each case counts as 1 slide
Each slide counts as 1 slide
Each slide prepared by Cytospin® counts as 1 slide
Each slide prepared by Cytospin® counts as 0.5 slide
Each slide prepared by automated methods (other than Cytospin®) counts as 1 slide
Each slide prepared by automated methods (other than Cytospin®) counts as 0.5 slide
Each cell block slide counts as 1 slide
Each cell block slide counts as 0.5 slide
Each smear counts as 1 slide
Each smear counts as 0.5 slide
Other _________________________________________________________________ ______________________________________________________________________
What criteria are used for INCREASING a CT’s workload maximum? Select all that apply.
CT consistently screens their workload maximum in less than 8 hours
CT states they are able or want to screen more than their maximum
Technical Supervisor determines that the CT is qualified to screen more
Review of at least 10% rescreen
Comparison of CT interpretation with technical supervisor’s confirmation
Other – Describe your criteria ________________________________________
______________________________________________________________________________________________________________________________________________
What criteria are used for DECREASING a CT’s workload maximum? Select all that apply.
CT consistently is unable to screen their workload maximum
CT states they are unable to screen at their maximum
Technical Supervisor determines that the CT should screen less
Review of at least 10% rescreen
Comparison of CT interpretation with technical supervisor’s confirmation
Other – Describe your criteria: ______________________________________________
____________________________________________________________________________________________________________________________________________
Which method best describes your workflow process for Field of View (FOV) screening and Full Manual Review (FMR)?
I screen the FOVs on all of my slides using the semi-automated screening device. I flag cells where a FMR is indicated. A different CT performs the FMR.
I screen the FOVs on all of my slides using the semi-automated screening device. I flag cells where a FMR is indicated. A pathologist performs the FMR using a standard microscope.
I screen the FOVs and perform an immediate FMR when indicated. Both reviews are performed using the semi-automated screening device
I screen the FOVs on all of my slides using the semi-automated screening device. I flag cells where a FMR is indicated and I perform the FMR using a standard microscope.
I only perform the FMR on slides where a different CT has flagged cells indicating a FMR is required. I perform the FMR using the semi-automated screening device.
I only perform the FMR on slides where a different CT has flagged cells indicating a FMR is required. I perform the FMR using a standard microscope.
Other _____________________________________________________________ ______________________________________________________________________________________________________________________________________________
Please use your personal workload recording data from the most recent month of complete data to provide an average number of HOURS spent on both screening and non-screening tasks
Note: For the purposes of this survey, SCREENING includes any or all of the following tasks:
calibrating the microscope
matching a slide with a requisition and/or barcode scan
loading a slide onto a microscope stage and focusing
review a patient history and noting specific instructions
screening a slide
reviewing FOVs
performing FMR when required
marking cells, or “dotting” a slide
record results of the test
NON-SCREENING activities include everything else.
Slide Type |
Average Number of SCREENING HOURS per day |
Total GYN plus NON-GYN |
|
GYN slides – Image-Assisted FOV |
|
GYN slides –FMR |
|
GYN slides – Standard Microscope |
|
Activities |
Average number of NON-SCREENING HOURS per day |
Non-Screening |
|
Does your laboratory have a written policy that defines when a FMR is required?
No written policy
Yes, reasons listed in the policy include: (check all that apply)
Reactive cells seen in the FOVs
Abnormal cells seen in the FOVs
Patients with a history of being high risk
No endocervical component seen in the FOVs
Scant cellularity seen in the FOVs
Evidence of infection is seen in the FOVs
Discretion of CT, Explain___________________________________________
______________________________________________________________________________________________________________________________________
Are you comfortable with your current workload maximum? Which best describes how you feel about your workload maximum?
Guideline
Expected productivity target
Glossary
Abbreviation Definition________________________________________________
ASC-H Atypical squamous cells – cannot exclude HSIL
ASC-US Atypical squamous cells – of undetermined significance
CIN2 Cervical intraepithelial neoplasia
CT Cytotechnologist
Cytospin® Thermo Scientific - Shandon Cytospin® non-gyn thin layer centrifuge
FMR Full manual review
FN False negative interpretation
FNA Fine needle aspiration
FOV Field-of-view
FP False positive interpretation
GYN Gynecological cytology
HPV Human papilloma virus
HSIL High-grade squamous intraepithelial lesion
LSIL Low-grade squamous intraepithelial lesion
NILM Negative for Intraepithelial Lesion or Malignancy
Non-GYN Nongynecological cytology
TP True positive interpretation
File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
Author | CDC User |
File Modified | 0000-00-00 |
File Created | 2021-01-28 |