- by Giancarlo Mari, M.D.
- Assistant Professor Department of
Obstetrics and Gynecology
- The Yale University School of
Medicine
-
- Editors Note: The subject of
Intrauterine Growth Retardation is a very important topic of concern, for if not
recognized, it can lead to a severely compromised fetus as well as fetal and/or neonatal
demise. Dr. Mari is a recognized, world authority on the diagnosis of IUGR by the
techniques described here.
-
Definition of IUGR
The term intrauterine growth
restriction (IUGR) is the most common generic term that is used to describe the fetus with
a birthweight at or below the 10th percentile for gestational age and sex. This term is
often erroneously used as synonymous of small for gestational age (SGA). The IUGR fetus is
a fetus that does not reach his potential of growth; whereas the SGA fetus is a fetus who
reaches his potential of growth. In other words, a fetus who has a potential of growth at
the 50th percentile but because of maternal, fetal, or placental disorders occurring alone
or in combination, becomes growth restricted (birthweight < 10th percentile) is a IUGR
fetus and he is at risk for adverse perinatal outcome. A fetus with a potential of growth
at the 7th percentile who reaches his potential of growth (7th percentile) is not a IUGR
fetus but a SGA fetus. He is a normal small fetus and he is not at risk for adverse
perinatal outcome.
The two components that
are necessary to define a IUGR fetus are:
- a) birthweight < 10th percentile;
- b) pathologic process that inhibits
expression of the normal intrinsic growth potential.
The two components that
are necessary to define a SGA fetus are:
- a) birthweight < 10th
percentile;
- b) absence of pathologic
process.
Incidence
The incidence of SGA fetuses
in the population is approximately 7%. Ten to fifteen percent of the SGA fetuses are IUGR
fetuses.
Etiology
Both maternal and paternal
race have a measurable effect on the fetal size, and, therefore an indirect effect on the
incidence of SGA. These racial influences can have an impact on clinical practice. The
application of a fetal growth curve derived from one population applied to a different
population can result in over- or underestimation of the true incidence of SGA.
Birthweight and fetal growth rates tend to be least among population of Asiatic extraction
and greatest in populations of Nordic extractions. These racial differences can be quite
dramatic, and at term the mean birthweight may vary as much as 1400 grams. The lowest mean
birthweight has been noted in Africa (New Guinea- Lumi's tribe: mean birthweight = 2400
grams); whereas the largest mean birthweight has been noted in the Caribbean (Aguilla;
mean birthweight = 3880 g).
IUGR may be considered the
consequence of a disease process within one or more of the three compartments that sustain
and regulate fetal growth - the maternal compartment, the placenta, or the fetus. In table
I the most common causes of IUGR are reported.
Diagnosis of the risk of
IUGR
Pregnancies at risk for IUGR
may be diagnosed on the basis of previous history (low fetal birth weight in earlier
pregnancies, etc.), associated disorders (autoimmune diseases, high blood pressure, etc.),
and toxic habits (smoker, etc). Previous history of IUGR is the most important risk
factor. In pregnancies with an increased risk, fetal growth should be closely
monitored.
Diagnosis of presumed or
suspected IUGR
This is perhaps the most
important and the most difficult diagnosis to make, when we consider that most of the
pregnancies are free of any associated conditions that would alert obstetricians to the
possibility of IUGR. The discrepancy between gestational age and the size of the uterus is
the most clearly indicative sign of IUGR. Therefore, basic screening for IUGR should be
done using serial symphysis fundal height (SFH), reserving ultrasound biometrical data for
those cases in which the SFH fell below the 5th percentile.
Diagnosis of probable IUGR
The diagnosis of IUGR is
based on biometrical parameters recorded during ultrasound scanning. In order to reduce
misreadings to a minimum, gestational age should be precisely determined. The most used
biometrical parameters are the biparietal diameter, head circumference, abdominal
circumference, head/abdominal circumference ratio, length of femur and humerus, estimated
fetal weight.
Fetal hemodynamics in
growth restriction
IUGR is in most of the cases
secondary to uteroplacental insufficiency. Much of the understanding of this phenomenon is
derived from animal research. However, the advent of pulsed and color Doppler
ultrasonography has allowed us to obtain non-invasive hemodynamic measurements from
several vascular beds of the uterine, placental and fetal circulation in humans.
Doppler ultrasound
Doppler ultrasound give us
information on the vascular resistance and, indirectly on the blood flow. Three indices
are considered related to the vascular resistance: S/D ratio (systolic/diastolic ratio),
resistance index (RI = systolic velocity - diastolic velocity/systolic velocity), and
pulsatility index (systolic velocity - diastolic velocity/mean velocity).
Uterine circulation
The main uterine artery is
the most commonly analyzed vessel. In normal pregnancy the S/D ratio or RI values
significantly decrease with advancing gestation until 24 to 26 weeks. In the absence of
this physiologic decrease, a higher incidence of hypertensive diseases and/or IUGR has
been widely documented.
Umbilical artery
In the normal fetus, the
pulsatility index decreases with advancing gestation. This reflects a decrease of the
placental vascular resistance. In fetuses with IUGR there is an increase of the
pulsatility index secondary to the decrease, absence or reversal of end- diastolic flow.
The changes of these waveforms are thought to be indicative of increased placental
resistance. The absent or reversed end-diastolic flows are strongly associated with an
abnormal course of pregnancy and a higher incidence of perinatal complications, when
compared to fetuses with IUGR but characterized by the presence of end-diastolic
flow.
Umbilical vein
The umbilical vein has a
continuous pattern following the first trimester. The presence of umbilical vein
pulsations is associated to an increased risk of adverse perinatal outcome.
Ductus venosus
The presence of reversed flow
in the ductus venosus is an ominous sign. Goncalves et al observed 5 fetuses with reverse
flow velocity waveforms at the ductus venosus and all the fetuses died in utero. In 18
other fetuses with abnormal umbilical and middle cerebral artery waveforms, but without
reverse flow in the ductus venosus, no deaths occurred.
Fetal cerebral circulation
The middle cerebral artery is
the vessel of choice to assess the fetal cerebral circulation because it is easy to
identify, has a high reproducibility, and it provides information on the brain sparing
effect. Additionally, it can be studied easily with an angle of zero degrees between the
ultrasound beam and the direction of blood flow and, therefore, information on the true
velocity of the blood flow may be obtained.
Brain sparing effect
Animal and human experiments
have shown that there is an increase in blood flow to the brain in the IUGR fetus. This
increase in blood flow can be evidenced by Doppler ultrasound of the middle cerebral
artery. This effect has been called "brain sparing effect" and is demonstrated
by a lower value of the pulsatility index. In IUGR fetuses with a pulsatility index below
the normal range there is a greater incidence of adverse perinatal outcome. The brain
sparing effect may be transient, as reported during prolonged hypoxemia in animal
experiments, and the overstressed human fetus can also lose the brain sparing effect. The
disappearance of the brain sparing effect is a very critical event for the fetus, and
appears to precede fetal death. Unfortunately, to demonstrate this concept, it is
necessary to perform a longitudinal study on severely IUGR fetuses up to the point of
fetal demise. This has been confirmed in a few fetuses in situations where obstetrical
intervention was refused by the parents. If these information's are confirmed on a larger
number of fetuses, the study of the middle cerebral artery may have tremendous implication
for determining the proper timing of delivery.
Based on our personal
experience, there are several phases of utero-placental insufficiency that may reflect
changes in fetal hemodynamics.
Severe utero-placental
insufficiency
A) The substrate for the
development of uteroplacental insufficiency may be laid down as early as the time of the
implantation. However, no effect is seen on growth or Doppler until 20-24 weeks gestation.
These fetuses do not have signs of growth restriction or abnormal Doppler ultrasound prior
to this period.
B) At 22-24 weeks gestation
if the fetus is measurably small by ultrasound, several Doppler patterns may occur. 1) The
umbilical artery may still have a normal pulsatility index (resistance index or S/D
ratio); the middle cerebral artery may have either a normal or abnormal pulsatility
index.
2) The umbilical artery has
an abnormal pulsatility index; the middle cerebral artery has either a normal or abnormal
value of pulsatility index.
3) The umbilical artery and
the middle cerebral artery have both an abnormal value of pulsatility index.
The fetus needs to be
monitored very closely. Bed rest and oxygen therapy may be useful; however, if both
vessels have an abnormal value at this early gestational age, it is very likely that the
process will deteriorate and the chance of a delivery at term is remote.
C) The pulsatility index of
the umbilical artery may increase and the pulsatility index of the middle cerebral artery
may decrease. The other fetal vessels may still appear normal and the only Doppler
abnormalities are the umbilical artery and middle cerebral artery. The fetus starts to
show signs of IUGR. The biophysical profile is normal.
At this time the lack of
fetal growth, and/or the development of preeclampsia/eclampsia, or a persistent abnormal
biophysical profile may interrupt the process with delivery of the fetus. These fetuses
are at lower risk for the development of respiratory distress syndrome and
intraventricular hemorrhage. We have reported that IUGR fetuses with brain sparing effect
are less likely to develop IVH. The reason is not completely understood. However,
production of steroids with stress may play an important role in this process.
If the fetus is not
delivered, the process continues.
D) At this time tricuspid
regurgitation may appear, ductus venosus reverse flow and umbilical vein pulsations may be
present intermittently. The biophysical profile may still appear normal.
E) Ductus venosus reverse
flow and umbilical vein pulsations are present continuously. The fetus starts to lose the
brain sparing effect. The biophysical profile becomes abnormal.
F) Fetal demise.
The time interval between E
and F is variable (from 6-12 hours to 2 weeks). Oligohydramnios may be present at any
stage of the above process.
This theory applies to a
specific, common IUGR and not to the fetuses who have other causes such as smoking,
abruption, and toxic drug exposure who may have a different pathology.
Mild utero-placental
insufficiency
Uteroplacental insufficiency
starts either at, or after the implantation. However, no effect is seen on Doppler and
growth until 26-32 weeks gestation. The umbilical artery and the middle cerebral artery
waveforms may be abnormal. However, the process is not severe enough to stop fetal growth
completely or to deteriorate as above. These cases may be followed with outpatient
monitoring and they often deliver at term.
Conclusion
Fetuses with IUGR show
evident modifications of Doppler parameters in the uteroplacental and fetal circulation.
At present, the condition of fetuses with IUGR can accurately be assessed by sequential
studies of Doppler waveforms from different vascular areas. There are, however, still many
uncertainties concerning the relationships between the Doppler changes and the metabolic
situation of the fetus and therefore, on the optimal timing of delivery to prevent an
intrauterine injury.