Effects of transitioning from conventional methods to liquid-based methods on unsatisfactory Papanicolaou tests: Results from a multicenter US study
Authors
Owens, Christopher L.Peterson, Daniel J.
Kamineni, Aruna
Buist, Diana S. M.
Weinmann, Sheila
Ross, Tyler R.
Williams, Andrew E.
Stark, Azadeh
Adams, Kenneth F.
Field, Terry S.
Document Type
Journal ArticlePublication Date
2013-05-08Keywords
Vaginal SmearsPapanicolaou test
liquid based
unsatisfactory
conventional
SurePath
ThinPrep
Community Health and Preventive Medicine
Diagnosis
Health Services Research
Medical Pathology
Neoplasms
Oncology
Pathology
Women's Health
Metadata
Show full item recordAbstract
BACKGROUND: Papanicolaou (Pap) testing has transitioned from conventional preparations (CPs) to liquid-based preparations (LBPs) because of the perceived superiority of LBPs. Many studies conclude that LBPs reduce unsatisfactory Pap tests; However, some believe that the evidence substantiating this claim is weak. The authors studied the effect of the transition from CPs to LBPs on the proportion of unsatisfactory Pap tests in 4 health care systems in the United States participating in the National Institutes of Health-funded Screening Effectiveness and Research in Community-Based Healthcare (SEARCH) project. METHODS: The study cohort consisted of 548,174 women ages 21 to 65 years who had 1443,725 total Pap tests between 2000 and 2010. Segmented regression analysis was used to estimate the effect of adopting LBPs on the proportion of unsatisfactory Pap tests after adjusting for age. RESULTS: Three sites that implemented SurePath LBP experienced significant reductions in unsatisfactory Pap tests (estimated effect: site 1, -2.46%; 95% confidence interval [CI], -1.47%, -3.45%; site 2, -1.78%; 95% CI, -1.54%, -2.02%; site 3, -8.25%; 95% CI, -7.33%, -9.17%). The fourth site that implemented ThinPrep LBP did not experience a reduction in unsatisfactory Pap tests. The relative risk of an unsatisfactory Pap test in women aged >/=50 years increased after the transition to LBPs (SurePath: relative risk, 2.1; 95% CI, 1.9-2.2; ThinPrep: relative risk, 1.7; 95% CI, 1.5-2.0). CONCLUSIONS: The observed changes in the proportion of unsatisfactory Pap tests varied across the participating sites and depended on the type of LBP technology, the age of women, and the rates before the implementation of this technology. Cancer (Cancer Cytopathol) 2013. (c) 2013 American Cancer Society.Source
Cancer Cytopathol. 2013 May 8. doi: 10.1002/cncy.21309. Link to article on publisher's site
DOI
10.1002/cncy.21309Permanent Link to this Item
http://hdl.handle.net/20.500.14038/37228PubMed ID
23658145Related Resources
ae974a485f413a2113503eed53cd6c53
10.1002/cncy.21309