What may be causes of oligohydramnios?? Ans: in addition to
foetal urinary tract anomalies and in the absence of PROM, uteroplacental
insufficiency should be considered. Oligohydramnios may result from poor
placental transfusion with 1) maternal hypertension, 2) chronic placental
abruption and 3) autoimmune states such as systemic lupus and antiphospholipid
syndrome.
What about foetal AC in oligohydramnios ?? Ans. Foetal AC is
almost always low. In cases of oligohydramnios fetal abdominal circumference
growth typically lags that of the head. Also, the increased placental vascular
resist¬ance evident on umbilical artery Doppler studies may help corroborate
the diagnosis of oligohydramnios due to placental insufficiency.
The risk of fetal asphyxia and death is high when severe
oligohydramnios accompanies intrauterine growth restriction (FGR). Intensive
fetal testing and hospitalization should be considered in cases diagnosed after
the point of fetal viability . After 32 weeks, severe oligohydramnios and fetal
growth restriction should generally lead to evaluation for delivery.
How to assess likelihood of pulmonary hypoplasia??
Ans:- By measuring of chest circumference, use of thoracic-head
circumference ratio, calculating the lung area ratio [(chest area-cardiac
area)/chest area] It appears that the risk of pulmonary hypoplasia is greatest
when severe oligohydramnios is present from 16 to 24 weeks of gestation, the
period of alveolar proliferation.
Longstanding oligohydramnios predisposes to pulmonary
hypoplasia. Although the mechanism of this potentially lethal complication is
not clear, inhibition of fetal breathing, loss of lung liquid because of
reduction in amniotic pressure, and simple mechanical compression of the chest
have been proposed the end result is restricted lung growth leading to alveolar
volume inadequate to support postnatal respiration. Though several methods have
been proposed to predict pulmonary hypoplasia, no single criterion has adequate
sensitivity and specificity for clinical decision-making.(Measurement of chest
circumference, use of thoracic-head circumference ratio, calculating the lung
area ratio [(chest area-cardiac area)/chest area] and thin-slice three-dimensional
fetal lung volume/fetal body weight ratios have been proposed to assess the
presence of pulmonary hypoplasia.
Recently, magnetic resonance imaging and Doppler assessment of
fetal pulmonary tissues have also been utilized for prediction of pulmonary
hypoplasia. Use of MRI-based abnormal lung volume/fetal weight ratio , is assed
in research settings gave a sensitivity of 88% with a false positive diagnosis
of pulmonary hypoplasia of 12%. When chest development appears markedly
compromised in a pre-viable fetus with severe oligohydramnios, the option of
termination of pregnancy should be discussed within legal frame work of our
country.
Treatment options
Delivery
Although the outcome of severe, longstanding oligohydramnios is
at best guarded, lesser degrees of fluid restriction may be amenable to
intervention. Data suggests that most of the perinatal morbidity associated
with postdate pregnancy is confined to cases with an AFI of less than 5 cm and,
particularly, those that lack a MVP of at least 2 X 1 cm. In such cases,
continued expectant management and antepartum testing is
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