R. Nahum et al., Antral follicle assessment as a tool for predicting outcome in IVF - Is ita better predictor than age and FSH?, J AS REPROD, 18(3), 2001, pp. 151-155
Purpose: The purpose of this study is to determine if baseline antral folli
cle assessment may serve as additional information in predicting in vitro f
ertilization outcome.
Methods: Prospective, descriptive preliminary study of in vitro fertilizati
on outcome. From July 1998 to July 1999 224 patients underwent antral folli
cle assessment (follicle 2-6 mm in diameter) on baseline of the planned, st
imulated in vitro fertilization cycle. The outcomes were analyzed with resp
ect to antral follicle assessment (less than or equal to6 or >6), basal cyc
le day 3 follicle stimulated harmone (less than or equal to 10 or > 10 IU/L
) and maternal age (less than or equal to 35 or > 35 years).
Results: The clinical pregnancy rate was significantly higher in the group
with baseline antral follicle >6 compared to that in the group with antral
follicle less than or equal to6 (51% vs. 19%, respectively). Controlling fo
r patient age, and basal follicle stimulated harmone, the pregnancy rate wa
s significantly higher in the group with antral follicle >6 compared to tha
t in the group with antral follicle less than or equal to6. The cancellatio
n rate was significantly increased with advancing maternal age, elevated ba
sal follicle stimulated harmone levels, and baseline antral follicle less t
han or equal to6. The cancellation rate was significantly higher in the gro
up with antral follicle >6 compared to that in the group with antral follic
le greater than or equal to6 (33% vs. 1%, respectively).
Conclusions: In vitro fertilization outcome is strongly correlated with bot
h maternal ages, basal cycle, day 3 follicle, stimulated harmone, and antra
l follicle assessment. Antral follicle assessment was a better predictor of
in vitro fertilization outcome than were age or follicle stimulated harmon
e. Antral follicle assessment may provide a marker for ovarian age that is
distinct from chronological age or hormonal markers.