Objective
The objective of the study was to determine whether patients undergoing chorionic
villus sampling (CVS) prior to MPR are at increased risk for adverse outcome compared
to those who did not.
Study Design
We retrospectively identified multifetal pregnancy reduction (MPR) patients from an
established database. Maternal demographic data were collected. Outcomes including
complete pregnancy loss prior to 24 weeks' gestation, gestational age at delivery,
and birthweight were analyzed.
Results
There was no significant difference in pregnancy loss between the 2 groups (CVS [4%]
vs no CVS [7%], P = .098). When stratified by finishing number, there was a significantly lower loss
rate in the singleton CVS group (2% vs 9%, P = .025) and no significant difference in reduced twins. There was no significant
difference in the average gestational age of delivery or birthweight.
Conclusion
CVS prior to MPR does not increase the risk of pregnancy loss. Our data suggest that
CVS prior to singleton reduction may decrease the risk of adverse outcome.
Key words
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Article Info
Publication History
Published online: July 18, 2008
Accepted:
May 27,
2008
Received in revised form:
April 25,
2008
Received:
March 1,
2008
Footnotes
Cite this article as: Ferrara L, Gandhi M, Litton C, et al. Chorionic villus sampling and the risk of adverse outcome in patients undergoing multifetal pregnancy reduction. Am J Obstet Gynecol 2008;199:408.e1-408.e4.
Identification
Copyright
© 2008 Mosby, Inc. Published by Elsevier Inc. All rights reserved.