Previous analyses of prenatal screening for neural tube defects have g
enerally found benefits to exceed costs. The usual screening battery f
ollows an elevated maternal serum alphafetoprotein level with high res
olution ultrasound and/or amniocentesis. Current thinking focuses on w
eighing the risk of a false-negative (an abnormality missed) against t
he risk of an amniocentesis-induced fetal loss. This thinking neglects
the risk of a false positive (an unaffected fetus labeled abnormal) a
nd individual parents' preferences concerning a false-negative us a fe
tal loss. With these risks included, we find that high resolution ultr
asound is appropriate for all women with elevated serum alpha-fetoprot
ein. Women with moderately elevated serum alpha-fetoprotein who have n
egative ultrasound scans need no further testing, nor do women with hi
ghly elevated serum alpha-fetoprotein and positive ultrasound scans. F
urther testing using amniocentesis to confirm the ultrasound result is
appropriate for women with moderately elevated serum alpha fetoprotei
n and positive ultrasound scans, and for women with highly elevated se
rum alpha-fetoprotein and negative ultrasound scans. The actual cutoff
s defining normal, moderately elevated, and highly elevated serum alph
afetoprotein depend on several parameters, particularly the underlying
prevalence of neural tube defects and the parents' preferences.