Management
The goal
of management of a growth-restricted fetus is to deliver the healthiest
possible infant at the optimal time. Continued management of pregnancy with
IUGR is based on the results of fetal testing.
Serial evaluations of fetal
biometry should be performed every 3 or 4 weeks to follow the extent of growth
restriction. Fetal monitoring is
important, and may include fetal move-ment counting, nonstress testing,
biophysical profiles, and Doppler studies. There are no specific therapies that
have proven beneficial for pregnancies complicated by IUGR.
The fetus
should be delivered if the risk of fetal death exceeds that of neonatal death,
although in many cases these risks are difficult to assess.
For example, a fetus with IUGR
with normal anatomic sur-vey, normal amniotic fluid volume, normal Doppler
studies, and normal fetal testing may not benefit from early delivery.
Conversely, the growth-restricted fetus with serial biometry measurements
documenting decreasing growth rate and/or mildly abnormal Doppler studies may
benefit from deliv-ery, with or without fetal maturity documentation.
Neonatal management of IUGR
infants may partially depend on gestational age, but includes preparation for
neonatal respiratory compromise, hypoglycemia, hypo-thermia, and hyperviscosity
syndrome. Growth-restricted fetuses have less fat deposition in late pregnancy,
so newborn euglycemia cannot be maintained by the normal mechanism of
mobilization of glucose by fat metabolism. Hyper-viscosity
syndrome results from the fetus’s attempt tocompensate for poor placental
oxygen transfer by increas-ing the hematocrit to more than 65%. After birth,
this marked polycythemia can cause multiorgan thrombosis, heart failure, and
hyperbilirubinemia. Overall, growth-restricted infants who survive the neonatal
period have a generally good prognosis.
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