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A study to determine the incidence of structural congenital heart disease in monochorionic twins
Author(s) -
Manning Nicky,
Archer Nick
Publication year - 2006
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.1556
Subject(s) - monochorionic twins , medicine , incidence (geometry) , heart disease , cohort , zygosity , fetal echocardiography , obstetrics , twin to twin transfusion syndrome , twin pregnancy , fetus , conjoined twins , pregnancy , pediatrics , cardiology , prenatal diagnosis , genetics , physics , optics , biology
Objective To determine the incidence of structural heart disease in at least one of a monochorionic (MC) twin pair excluding any cardiac effects of twin‐twin transfusion syndrome (TTTS). Method A cohort study of 165 sets of MC twins undergoing detailed fetal echocardiography in a tertiary unit over a 4‐year period. Results The overall risk of at least one of a MC twin pair having a structural congenital cardiac anomaly was 9.1% (15/165); for monochorionic diamniotic (MC/DA) twins, this figure was 7.0% (11/158) but for monochorionic‐monoamniotic (MC/MA) twins the risk for at least one affected twin was 57.1% (4/7). If one of a pair of MC twins was affected, the risk to the other twin for a structural cardiac anomaly was 26.7% (4/15). Conclusions The incidence of structural heart disease in MC twins is increased, independent of TTTS. This justifies referral of these pregnancies for detailed fetal echocardiography as part of their assessment. If one twin is affected, the risk to the other twin is increased further. Copyright © 2006 John Wiley & Sons, Ltd.