Del Priore G, Maag T, Bhattacharya M, Garcia P M, Till M, Lurain J R
Department of Obstetrics and Gynecology, Northwestern University, Evanston, Illinois 60201.
Gynecol Oncol. 1995 Mar;56(3):395-8. doi: 10.1006/gyno.1995.1069.
The purpose of this study was to assess the ability of cytology to predict the results of colposcopically directed cervical biopsies in HIV-infected women. We performed a case-control study of 52 HIV(+), 31% of whom had AIDS, and 57 HIV(-) women referred to two tertiary care centers for colposcopy from July 1991 to November 1993. All 57 HIV(-) controls and 27 HIV (+) cases underwent colposcopy for evaluation of an abnormal Pap smear. The remaining HIV(+) cases (n = 25) had colposcopy as part of their routine assessment. In women with abnormal Pap smears, colposcopic biopsy agreed with the Pap smear results in 83% of 24 HIV(+) women and 65% of 37 controls (chi 2; P = 0.34). For patients with low-grade SIL on Pap smear, 14% of HIV(+) and 11% of HIV(-) women had moderate or severe dysplasia on biopsy (P = 0.52). The positive predictive value of an abnormal Pap smear was 96% in HIV(+) women vs 78% in noninfected patients (P = 0.05). In the overall series of 52 HIV(+) women, the Pap smear did not match the biopsy in 44% of patients and was less severe than the cervical biopsy results in 91% of these mismatches. The Pap smear had a sensitivity of 57%, a specificity of 92%, a positive predictive value of 96%, and a negative predictive value of 39%, when compared to biopsy results in HIV-seropositive patients. Pap smears missed 43% of biopsy-proven intraepithelial lesions in this series of HIV (+) women. However, when abnormal, the Pap smear was no worse in predicting the presence and degree of an intraepithelial lesion in HIV(+) women than in noninfected women. These characteristics may justify immediate treatment of HIV(+) women at the time of colposcopy after an abnormal Pap smear given its high positive predictive value.
本研究的目的是评估细胞学检查预测HIV感染女性阴道镜引导下宫颈活检结果的能力。我们对1991年7月至1993年11月转诊至两家三级医疗中心接受阴道镜检查的52例HIV阳性女性(其中31%患有艾滋病)和57例HIV阴性女性进行了病例对照研究。所有57例HIV阴性对照者和27例HIV阳性病例因巴氏涂片异常而接受阴道镜检查以进行评估。其余HIV阳性病例(n = 25)将阴道镜检查作为其常规评估的一部分。在巴氏涂片异常的女性中,阴道镜活检结果与巴氏涂片结果相符的情况在24例HIV阳性女性中占83%,在37例对照者中占65%(卡方检验;P = 0.34)。对于巴氏涂片显示低度鳞状上皮内病变的患者,14%的HIV阳性女性和11%的HIV阴性女性活检显示为中度或重度发育异常(P = 0.52)。HIV阳性女性巴氏涂片异常的阳性预测值为96%,而未感染患者为78%(P = 0.05)。在52例HIV阳性女性的整个系列中,44%的患者巴氏涂片结果与活检结果不匹配,在这些不匹配情况中,91%的巴氏涂片结果比宫颈活检结果轻。与HIV血清阳性患者的活检结果相比,巴氏涂片的敏感性为57%,特异性为92%,阳性预测值为96%,阴性预测值为39%。在这一系列HIV阳性女性中,巴氏涂片漏诊了43%经活检证实的上皮内病变。然而,当结果异常时,巴氏涂片在预测HIV阳性女性上皮内病变的存在和程度方面并不比未感染女性差。鉴于其高阳性预测值,这些特征可能说明在HIV阳性女性巴氏涂片异常时于阴道镜检查时立即进行治疗是合理的。