Objective: To determine the magnitude of the risk and the predictive c
linical characteristics for development of preeclampsia when triploidy
is diagnosed in the second trimester. Methods: A retrospective analys
is of databases maintained by the cytogenetics laboratories at the Uni
versity of Iowa and University of North Carolina was performed to iden
tify all cases of triploidy. We examined the karyotype, maternal serum
screening (particularly the hCG level), ultrasound results, and evide
nce of maternal hypertensive disease. Results: Seventeen cases of trip
loidy were identified between 1987 and 1996. Preeclampsia or hypertens
ion complicated six of these cases with onset between 15 and 22.5 week
s' gestation. In these six cases, the serum hCG level was extremely hi
gh. Serum screening results were available in seven cases in which pre
eclampsia did not develop, and the hCG levels were under 0.09 multiple
s of the median in five of the seven cases. In all six cases in which
preeclampsia or hypertension developed, there was sonographic evidence
of placentomegaly. Sonographic findings in 16 of 17 cases revealed fe
tal growth restriction, oligohydramnios, fetal anomalies, placentomega
ly, or a combination of these. Conclusion: In our series of pregnancie
s complicated by triploidy, the risk of developing preeclampsia or hyp
ertension in the second trimester was 3570. It appears that elevated s
erum hCG levels and placentomegaly are associated with a higher risk o
f preeclampsia but low hCG levels are not. This information is importa
nt in counseling patients who are hesitant to terminate a pregnancy pu
rely for a fetal abnormality, even if the anomaly is lethal. (C) 1997
by The American College of Obstetricians and Gynecologists.