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Prenatal pharmacotherapy for fetal anomalies: a 2011 update
Author(s) -
Hui Lisa,
Bianchi Diana W.
Publication year - 2011
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.2777
Subject(s) - polyhydramnios , medicine , fetus , congenital adrenal hyperplasia , pregnancy , prenatal diagnosis , pharmacotherapy , sacrococcygeal teratoma , pediatrics , congenital hypothyroidism , obstetrics , bioinformatics , thyroid , biology , genetics
Fetal therapy can be defined as any prenatal treatment administered to the mother with the primary indication to improve perinatal or long‐term outcomes for the fetus or newborn. This review provides an update of the pharmacological therapies that are solely directed at the fetus with anomalies and outlines a future transcriptomic approach. Fetal anomalies targeted with prenatal pharmacotherapy are a heterogeneous group of structural, endocrine, and metabolic conditions, including congenital cystic adenomatoid malformation (CCAM), congenital adrenal hyperplasia, congenital heart block, fetal tachyarrhythmias, inborn errors of metabolism, fetal thyroid disorders, and polyhydramnios. To date, the majority of pharmacotherapies for fetal anomalies have been evaluated only in retrospective, uncontrolled studies. The way forward will be with an evidence‐based approach to prenatal pharmacological interventions. Copyright © 2011 John Wiley & Sons, Ltd.