Although cytology laboratories are mandated to rescreen at least 10% of cer
vicovaginal smears, there is no uniform national rescreening practice. Foll
ow-up data for 16,188 rescreened cervicovaginal smears were studied and dec
ision analysis was performed to determine an optimal rescreening strategy.
High-grade dysplasia was detected in 0.40% of women with a history of cervi
cal disease and in 0.04% without a history of cervical disease. Compared wi
th 0% rescreening of smears with 15% rescreening the cost to gain a year of
discounted life expectancy was $386,890 for women without a history of cer
vical disease, and $2,980 for women with a history of cervical disease. We
conclude that rescreening only smears from women with a history of cervical
disease could save US laboratories more than $11.2 million annually withou
t seriously compromising care.