The CLIA '88 regulations require the laboratory to review at least ## 10% of the gynecologic cases interpreted as negative that are examined by each cytotechnologist. The review must include negative cases selected at random and from patients identiJed as a high risk group. To evaluate the validity
Evaluation of papnettrade; system for rescreening of negative cervical smears
β Scribed by R. Ashfaq; Y. Liang; M. H. Saboorian
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 577 KB
- Volume
- 13
- Category
- Article
- ISSN
- 8755-1039
No coin nor oath required. For personal study only.
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## Background: The autopap 300 qc system is an automated device for the analysis of conventionally prepared cervical cytology slides. the autopap system selects an enriched population of cases for human quality control (qc) review. the device assigns a score based on the likelihood that a slide is
## RESULTS. For the historic sensitivity study, the percentages of cases present within
The presence of endocervical component (ECs) on cervical smears is considered essential for determining the adequacy of the Pap smear. The absence of an endocervical component in a negative smear suggests that a repeat Pap smear should be taken. We evaluated 635 manually screened negative cervical s