Objective. The objective was to determine if repeating a Pap smear at
the time of an initial colposcopy has sufficient clinical benefit to j
ustify its clinical and financial costs. Methods. The records were rev
iewed of all patients who had an initial colposcopy at Queens Hospital
Center between 1984 and 1995. Data were gathered regarding the referr
al cytology, the cytology done at the time of colposcopy, and the resu
lts of any biopsies which were taken. The terminology for cytology and
histology done prior to 1989 was adjusted to the Bethesda classificat
ion system. A repeat Pap smear was defined as clinically valuable if i
t would have changed the patient's management, i.e., if it suggested m
ore advanced disease than the referral Pap and that the disease was no
t identified on the colposcopically directed biopsy. Results. Two thou
sand nine hundred sixty-nine records were reviewed. In 139 cases, no P
ap smear was repeated at the time of colposcopy. Of the remaining 2830
women, only 1347 (47.6%) showed exact correlation between their refer
ral Pap smear and the Pap done at the time of colposcopy. In another 1
016 (35.9%), the Pap at colposcopy was within one grade of the referra
l Pap. In 312 women, the Pap at the time of colposcopy was a higher gr
ade than the referral Pap. However, in 236, the higher grade of diseas
e was detected by the colposcopically directed biopsy. Of the remainin
g 76 women, 58 had a normal biopsy, but their Pap at the time of colpo
scopy showed low-grade squamous intraepithelial lesions (44) or high-g
rade squamous intraepithelial lesions (HGSIL) (14). Seventeen others h
ad a biopsy showing low-grade dysplasia while the Pap at the time of c
olposcopy showed HGSIL. In 1 patient, the repeat Pap showed malignant
cells while the biopsy showed a high-grade lesion. Based on the triage
protocols at our institution, this means that a repeat Pap at the tim
e of colposcopy would have indicated a cone biopsy in 31 patients (1.1
%) and more careful follow-up of another 44 patients (1.6%). Skipping
the repeat Pap smear would not have resulted in any missed cancers. In
our series of 2830 patients, the cost savings of skipping the repeat
smear would have been $68,580 or $24.23 per patient. On a national lev
el, skipping the repeat smear would save more than $24,000,000 annuall
y. Conclusion. Using current triage protocols at our institution, repe
ating the Pap smear at the time of an initial colposcopy would have ch
anged the management in 2.7% of patients and indicated a conization in
only 1.1% of patients. It is doubtful that this justifies its cost an
d the potential detrimental effects on the colposcopic examination. (C
) 1997 Academic Press.