The objective of this review was to evaluate the current status of human pa
pillomavirus testing in predicting the presence of high-grade or invasive d
isease in the cervix in women with Papanicolaou smears reported as atypical
squamous cells of undetermined significance (ASCUS) or low-grade squamous
intraepithelial lesion. This is a review of many of the studies already pub
lished evaluating the utility of human papillomavirus testing as part of th
e triage for patients whose Papanicolaou smears were reported as ASCUS or l
ow-grade squamous intraepithelial lesion. Two triage approaches for follow-
up of such patients are presented, and recommendations are made as to which
is most cost-effective and safe. Data related to human papillomavirus test
ing were obtained with both currently available commercial kits for detecti
on of high-risk human papillomavirus and the polymerase chain reaction. The
re was variation in results reported, possibly related to populations studi
ed. The approach to management by cytologic screening and colposcopy, when
indicated, appeared over the long term to be equal to human papillomavirus
testing. In our opinion current human papillomavirus testing is of little c
linical use to the practitioner. Its use should be limited to appropriately
designed and implemented research studies.