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Value of high risk HPV combined liquid-based cytology testing in screening cervical disease in pregnancy women |
NI Qian ZHOU Yuehua NI Yunxiang▲ |
Department of Obstetrics and Gynecology, Shanghai Tongren Hospital, Shanghai 200336, China |
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Abstract Objective To investigate the necessity of routine screening of cervical diseases during pregnancy through the high-risk HPV detection combined with TCT examination. Methods From January 2013 to December 2015, in outpatinet of Obstetrics, Shanghai Tongren Hospital, 7316 pregnant women received the high-risk HPV detection and TCT examination in the first prenatal examination were selected. Pregnant women with high-risk HPV positive or abnormal TCT results received the colposcopy assessment, and those abnormal women further received the microscopic histological biopsy. Results In 7316 pregnant women, there were 584 high-risk HPV positive pregnant women, accounting for 7.98%, and 180 pregnant women with abnormal TCT examination, accounting for 2.46%. The sensitivity, specificity, positive predictive value and negative predictive value of high-risk HPV detection for cervical lesions was 91.40%, 93.09%, 14.55% and 99.88%, respectively, those of TCT examination was 86.02%, 98.62%, 44.44% and 99.82%, respectively, and those of high-risk HPV detection combined with TCT examination was 100.00%, 92.55%, 14.74% and 100.00%, respectively. There was no significant correlation between HPV load and severity of cervical lesions (P > 0.05). Conclusion In terms of cervical disease screening for pregnant women, the high-risk HPV detection combined with TCT examination has a higher sensitivity and negative predictive value than that of single application of HPV detection and TCT examination, which can find the cervical lesions timely, so that the disease can be detected and treated early.
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[1] Schiffman M,Wentzensen N. Human papillomavirus infection and the multistage carcinogenesis of cervical cancer [J]. Cancer Epidemiol Biomarkers Prev,2013,22(4):553-560.
[2] 谢锋,隋龙.HPV感染所致宫颈病变的诊断与治疗[J].国际生殖健康/计划生育杂志,2015,34(6):475-479.
[3] Sood AK,SoroskyJI,Mayr N,et al. Cervical cancer diagnosed shortly after pregnancy,prognostic variables and delivery routes [J].Obstet Gynecol,2000,95(6):832-838.
[4] 张翼海.妊娠合并宫颈病变误诊9例分析[J].中国误诊学杂志,2007,7(27):6577-6578.
[5] 贺桂芳,卞美璐,刘军,等.5296例妊娠和产后妇女宫颈细胞学筛查和随访[J].中日友好医院学报,2006,20(1):13-16.
[6] 闫立青,明含昕.妊娠期液基细胞学检测的评价[J].泰山医学院学报,2007,28(9):710-712.
[7] Matthews-Greer J,Rivette D,Reyes R,et al. Human papi-llomavi-rus detection:verification with cervical cytology [J]. Clin Lab Sci,2004,17(1):8-11.
[8] Zuo Z,Goel S,Carter JE,et al. Association of cervical cytologyand HPV DNA status during pregnancy with placental abnormal ities and preterm birth [J]. Am J Clin Pathol,2011, 136(2):260-265.
[9] Agorastos T,Chatzistamatiou K,Katsamagkas T,et al. Primary screening for cervical cancer based on high -risk human papillomavirus (HPV) detection and HPV 16 and HPV 18 genotyping,in comparison to cytology [J]. PLoS One,2015,10(3):e0119755.
[10] Stoler MH,Wright TC Jr,Sharma A,et al. High -risk human papillomavirus testing in women with ASC-US cytology:results from the ATHENA HPV study [J]. Am J Clin Pathol,2011,135(3):468-475.
[11] Saslow D,Solomon D,Lawson HW,et al. American Cancer Society, American Society for Colposcopy and Cervical Pathology,and American Society for Clinical Pathology screening guidelines for the prevention and early detection of cervical cancer [J]. J Low Genit Tract Dis,2012,16(3):175-204.
[12] Wright TC,Stoler MH,Behrens CM,et al. Primary cervical cancer screening with human papillomavirus:end of study results from the ATHENA study using HPV as the first-line screening test [J]. Gynecol Oncol,2015,136(2):189-197.
[13] Huh WK,Ault KA,Chelmow D,et al. Use of primary high-risk human papillomavirus testing for cervical cancer screening: interim clinical guidance [J]. Obstet Gynecol,2015,125(2):330-337.
[14] Jakobsson M,Gissler M,Sainio S,et al. Preterm delivery aftersurgical treatment for cervical intraepithelial neopl-asia [J]. Obstet Gynecol,2007,109(2 Pt 1):309-313.
[15] Noehr B,Jensen A,Frederiksen K,et al. Depth of cervical coneremoved by loop electrosurgical excision procedure and subsequentrisk of spontaneous preterm delivery [J]. Obstet Gynecol,2009,114(6):1232-1238.
[16] Kim JY,Lee DH,Kang JH,et al. The overtreatment risk of see-and-treat strategy in management of abnormal cervical cytology [J]. Gynecol Obstet Invest,2014,78(4):239-243.
[17] Bandieramonte G,Lomonico S,Quattrone P,et al. Laser conization assisted by crypt visualization for cervical intraepithelial neoplasia [J]. Obstet Gynecol,1998,91(2):263-269.
[18] Liu Y,Qiu HF,Tang Y,et al. Pregnancy outcome after the treatment of loop electrosurgical excision procedure or cold-knifeconization for cervical intraepithelial neoplasia [J]. Gynecol Obstet Invest,2014,77(4):240-244.
[19] Srisuwan S,Hamontri S,Kongsomboon K,et al. See -and -treatapproach to cervical intraepithelial lesions in HRH Princess MahaChakri Sirindhorn Medical Center [J]. Asian Pac J Cancer Prev ,2014,15(8):3483-3486.
[20] 林美丽,陈伟,马闪珊,等.基于尿液人乳头瘤状病毒检测对宫颈人乳头瘤状病毒感染诊断价值的Meta分析[J].中国医药导报,2015,12(6):64-70.
[21] Ebisch R,Rovers MM,Bosgraaf RP,et al. Evidence sup-porting see-and-treat management of cervical intrae-pithelial neoplasia:asystematic review and meta -analysis [J]. BJOG,2015. doi:10.1111/1471-0528.13530. [Epub ahead of print]. |
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