TY - JOUR
T1 - Performance of Direct Visual Inspection of the Cervix with Acetic Acid and Magnification in a Previously Screened Population
AU - Rodríguez, Ana Cecilia
AU - Morera, Lidia Ana
AU - Bratti, Concepción
AU - Herrero, Rolando
AU - Cox, J. Thomas
AU - Morales, Jorge
AU - Alfaro, Mario
AU - Hutchinson, Martha
AU - Castle, Philip E.
AU - Hildesheim, Allan
AU - Schiffman, Mark
PY - 2004/4/1
Y1 - 2004/4/1
N2 - Objective. To assess the screening performance of direct visual inspection with acetic acid and ×2 magnification (VIAM) in a previously screened population, as performed by experienced gynecologic nurses with minimal training in VIAM. Patients and Methods. Performance of VIAM was evaluated in 2,080 women from a population-based cohort in Guanacaste, Costa Rica, 5 years after they had negative enrollment results of conventional and liquid-based cytologic analysis, cervigram, and human papillomavirus DNA by Hybrid Capture Tube Test (Digene Corporation, Gaithersburg, MD). The VIAM results were compared with repeat conventional Pap smears, liquid-based cytologic examinations, and cervicography, with adjudication of differences by reference to MY09/MY11L1 consensus primer polymerase chain reaction detection of oncogenic human papillomavirus DNA. Results. Less than 5% of women were classified as having positive results using VIAM. The VIAM positivity was also very low among women with high-grade squamous intraepithelial lesion conventional Pap smear results (8.3%), high-grade squamous intraepithelial lesion liquid-based cytologic results (6.3%), or cervigrams suggesting cervical intraepithelial neoplasia 2,3 or cancer (30%). The VIAM positivity was not associated with human papillomavirus DNA positivity. Conclusions. As we practiced it, VIAM was not sensitive for detection of possibly serious incident cervical lesions in this previously screened population where cytologic screening is in place.
AB - Objective. To assess the screening performance of direct visual inspection with acetic acid and ×2 magnification (VIAM) in a previously screened population, as performed by experienced gynecologic nurses with minimal training in VIAM. Patients and Methods. Performance of VIAM was evaluated in 2,080 women from a population-based cohort in Guanacaste, Costa Rica, 5 years after they had negative enrollment results of conventional and liquid-based cytologic analysis, cervigram, and human papillomavirus DNA by Hybrid Capture Tube Test (Digene Corporation, Gaithersburg, MD). The VIAM results were compared with repeat conventional Pap smears, liquid-based cytologic examinations, and cervicography, with adjudication of differences by reference to MY09/MY11L1 consensus primer polymerase chain reaction detection of oncogenic human papillomavirus DNA. Results. Less than 5% of women were classified as having positive results using VIAM. The VIAM positivity was also very low among women with high-grade squamous intraepithelial lesion conventional Pap smear results (8.3%), high-grade squamous intraepithelial lesion liquid-based cytologic results (6.3%), or cervigrams suggesting cervical intraepithelial neoplasia 2,3 or cancer (30%). The VIAM positivity was not associated with human papillomavirus DNA positivity. Conclusions. As we practiced it, VIAM was not sensitive for detection of possibly serious incident cervical lesions in this previously screened population where cytologic screening is in place.
KW - Cervical cancer
KW - Direct visual inspection
KW - Human papillomavirus
KW - Screening
KW - VIAM
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U2 - 10.1097/00128360-200404000-00009
DO - 10.1097/00128360-200404000-00009
M3 - Article
C2 - 15874851
AN - SCOPUS:16544393248
SN - 1089-2591
VL - 8
SP - 132
EP - 138
JO - Journal of Lower Genital Tract Disease
JF - Journal of Lower Genital Tract Disease
IS - 2
ER -