[Clinical evaluation of the xMAP technology in detection of high-risk human papillomavirus].

Objective To evaluate the clinical application value of flexible multi-analyte profiling(xMAP)technology in detecting high-risk human papillomavirus(HR-HPV).Methods Totally 1 061 women,aged 21-65 years,were randomly enrolled into the study.Cervical exfoliated cells were used in xMAP technology and hybrid capture Ⅱ(hc2).Pathological diagnosis was used as golden standard.Consistency of these two methods was assessed.Results The sensitivity and specificity of xMAP technology were 80.31% and 85.83%,respectively.The positive and negative predictive values were 44.5% and 96.9%,respectively.The Kappa value for consistency between xMAP technology and hc2 was 0.58.Conclusions The specificity of xMAP technology is similar to hc2 test,but the sensitivity is inferior to hc2.However,these two methods show good consistency in the detection of HR-HPV.