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. 2010 Nov 17;49(1):48–53. doi: 10.1128/JCM.01063-10

TABLE 1.

Amplicor HPV and HC-2 detection of HR HPV DNA in cervical specimens collected from women referred to colposcopy because of an ASC-US cytologya

Diagnosis group Total no. of specimens No. of specimens with indicated results [(%, 95% CI); P value] in indicated assay
HC-2 Amplicor with cutoff at:
0.2 1.0 1.5
All women 396 129 (32.6, 28.1-37.3) 164 (41.4, 36.7-46.3); 0.01 157 (39.7, 35.0-44.5); 0.05 156 (39.4, 34.7-44.3); 0.05
No CIN 316 81 (25.6, 21.1-30.7) 113 (35.8, 30.7-41.2); 0.01 107 (33.9, 28.9-39.3); 0.03 106 (33.5, 28.6-38.9); 0.04
CIN 1 47 20 (42.6, 29.5-56.7) 23 (48.9, 35.3-62.8); 0.68 22 (46.8, 33.3-60.8); 0.84 22 (46.8, 33.3-60.8); 0.84
CIN 2/3 29 27 (93.1, 72.0-99.2) 26 (89.7, 72.8-97.2); 1.0 26 (89.7, 72.8-97.2); 1.0 26 (89.7, 72.8-97.2); 1.0
CIN ? 4 1 (0.3, 0.0-1.6) 2 (0.5, 0.0-3.8); 1.0 2 (0.5, 0.0-3.8); 1.0 2 (0.5, 0.0-3.8); 1.0
a

Diagnoses were obtained at colposcopy with biopsy in the presence of cervical lesions. HPV DNA detection rates obtained with Amplicor using different cutoffs were compared with rates obtained with HC-2. HC-2, Hybrid Capture 2 assay; CIN, cervical intraepithelial neoplasia; CIN ?, CIN that could not be graded; CI, confidence interval.