Objective: To create a highly specific cascade testing scheme for fetal lun
g maturity using the lamellar body count, lecithin/sphingomyelin ratio (L/S
), and phosphatidylglycerol.
Methods: A nondedicated hematology analyzer (Sysmex NE 1500, Toa Medical El
ectronics, Los Angeles, CA) was used to determine the lamellar body counts
of 209 unspun amniotic fluid specimens. Maximally specific lamellar body co
unt cutoffs for biochemical maturity and immaturity were determined using r
eceiver operating characteristic curves. Biochemical lung maturity was defi
ned as either a mature WS ratio or phosphatidylglycerol. Biochemical lung i
mmaturity was defined as both an immature L/S ratio and an immature phospha
tidylglycerol.
Results: A lamellar body count of less than 8000 (n = 17) was 100% specific
for biochemical lung immaturity (positive predictive value = 100%, negativ
e predictive value = 86%). A lamellar body count of greater than 32,000 was
98% specific for biochemical lung maturity (positive predictive value = 99
%, negative predictive value = 63%).
Conclusion: Testing only specimens where the lamellar body count was greate
r than 8000 and less than or equal to 32,000 for the LIS ratio and phosphat
idylglycerol would preclude the need for 76% of all L/S and phosphatidylgly
cerol assays. Because the lamellar body count is quick, simple, and univers
ally available, it could serve as an extremely cost-effective screening tes
t for fetal lung maturity. (C) 1999 by The American College of Obstetrician
s and Gynecologists.