OBJECTIVE: We sought to develop a model quantifying the relative contr
ibutions of fetal swallowing and intramembranous flow to amniotic flui
d dynamics during human gestation. We then used the model to simulate
the impact of absent swallowing on amniotic fluid volume. STUDY DESIGN
: The model was developed with published data for normal human amnioti
c fluid volume and composition, human fetal urine flow rate and compos
ition (11 to 42 weeks), and extrapolated data from ovine lung fluid pr
oduction. Fetal swallowing and intramembranous flow were calculated wi
th assumptions that (1) swallowed fluid is isotonic to amniotic fluid,
(2) intramembranous flow is free water diffusion, and (3) 50% of lung
fluid is swallowed. The model was then applied to simulate absent fet
al swallowing and variable (0%, 50%) proportions of swallowed lung flu
id were used as a representation of esophageal atresia-tracheal fistul
a variations. RESULTS: Fetal swallowed volume and intramembranous flow
linearly increase until 28 to 30 weeks. Daily swallowed volume then e
xponentially increases to a maximum of 1006 ml/day at term, whereas in
tramembranous flow continues on a linear trend to reach 393 ml/day at
term. With absent swallowing and variable amounts of lung fluid swallo
wed (0%, 50%), predicted amniotic fluid volume is similar to normal va
lues through 20 weeks, exceeds the 95% confidence interval for normal
amniotic fluid volume at 29 to 30 weeks' gestation (similar to 2000 mi
), and then exponentially increases. Predicted amniotic fluid osmolali
ty (280 to 257 mOsm/kg) is slightly lower than actual values although
within the clinically normal range. CONCLUSIONS: This model indicates
that the normal reduction in amniotic fluid volume beginning at 34 wee
ks results from the marked increase in swallowed volume during the thi
rd trimester. Additionally, this model correlates well with the timing
of the initial clinical presentation of polyhydramnios observed in so
me fetuses with conditions that result in absent or reduced swallowing
or gastrointestinal atresia. Modeling of amniotic fluid dynamics can
predict normal changes in fetal fluid exchange and may aid in understa
nding of amniotic fluid imbalances.