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Evidence for increasing usage of low-grade squamous intraepithelial lesion, cannot exclude high-grade squamous intraepithelial lesion (LSIL-H) Pap test interpretations
被引:6
|作者:
Walavalkar, Vighnesh
[1
]
Tommet, Douglas
[1
]
Fischer, Andrew H.
[1
]
Liu, Yuxin
[1
]
Papa, Debra M.
[2
]
Owens, Christopher L.
[1
]
机构:
[1] Univ Massachusetts, Sch Med, Dept Pathol, Div Cytopathol, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Obstet & Gynecol, Worcester, MA USA
关键词:
Pap test;
quality assurance;
low-grade squamous intraepithelial lesion cannot exclude high-grade squamous intraepithelial lesion;
LSIL-H;
QA;
CLINICAL-SIGNIFICANCE;
CATEGORY;
DIAGNOSIS;
SMEARS;
HSIL;
D O I:
10.1002/cncy.21346
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
BACKGROUND Pap test (PT) interpretations of low-grade squamous intraepithelial lesion (LSIL), cannot exclude high-grade squamous intraepithelial lesion (HSIL), or LSIL-H, are used in many laboratories; however monitoring its usage for quality assurance purposes is understudied. METHODS PTs from 2005 to 2010 were collected, and yearly frequencies of LSIL, HSIL, LSIL-H, and atypical squamous cells, cannot exclude HSIL (ASC-H) as a function of total PTs and total squamous intraepithelial lesions (SILs) were calculated. Two-year risk of cervical intraepithelial neoplasia 2 (CIN2) or worse (CIN2+) and CIN 3 or worse (CIN3+) was calculated. RESULTS A total of 352,220 PTs were identified including 17,301 abnormal PTs. LSIL-H usage increased from 2005 to 2010 (from 0.28% of total PTs in 2005 to 0.61% in 2010, P < .01; from 5.8% of total SILs in 2005 to 12% in 2010, P < .001). HSIL usage decreased significantly from 2005 to 2010 (from 0.7% of total PTs in 2005 to 0.48% in 2010, P = .048; from 14.5% of total SILs in 2005 to 9.5% in 2010, P < .01). Usage of LSIL and ASC-H did not change. Two-year risk of CIN2+ and CIN3+ for HSIL increased significantly from 2005 to 2010 (P < .01). Two-year risk of CIN2+ and CIN3+ for LSIL-H did not change significantly from 2005 to 2010. CONCLUSIONS The frequency of LSIL-H interpretations is significantly increasing at our institution, with a significant decrease in HSIL interpretations over the same period. Two-year risk of CIN2+ and CIN3+ for HSIL increased significantly as usage of LSIL-H increased and that of HSIL decreased. Laboratories using LSIL-H may benefit from monitoring its frequency to ensure its appropriate use. Cancer (Cancer Cytopathol) 2014;122:123-7. (c) 2013 American Cancer Society.
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页码:123 / 127
页数:5
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