山东大学学报(医学版) ›› 2016, Vol. 54 ›› Issue (8): 69-71.doi: 10.6040/j.issn.1671-7554.0.2016.644
王雅芬,杨勇霞,刘娅,马德美,朱琳
WANG Yafen, YANG Yongxia, LIU Ya, MA Demei, ZHU Lin
摘要: 目的 分析宫颈细胞学阴性且高危型人乳头瘤病毒(HPV)阳性患者的宫颈活检病理结果,探讨Cervista HPV HR A9组病毒应用于此类人群分流的可行性。 方法 对1 376例于2011年1月至2016年1月健康查体的女性行新柏氏液基细胞学检测(TCT)和Cervista HPV HR检测,Cervista HPV HR检测结果分为A5/6、A7、A9组,将TCT阴性、HPV阳性患者转诊阴道镜检查,必要时行镜下宫颈活检术,分析A9组病毒感染与宫颈高级别上皮内瘤变CINII+(CINII及CINIII)的关系。 结果 A5/6组、A7组及A9组阳性者分别占28.41%、21.51%、50.07%。A5/A6组、A7组及A9组中CINII+的发生率分别为1.28%、3.38%、15.82%,A9组中CINII+的发生率明显高于另外两组,其差异具有统计学意义(P<0.001, P<0.001)。A9组病毒感染者发生CINII+的风险是A5/A6组感染者的12.37倍,是A7组感染者的4.68倍。 结论 Cervista HPV HR A9组病毒可用于TCT阴性、高危型HPV阳性者的分流。
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