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Anemia of Prematurity - Portal Neonatal

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AFP concentration in the maternal serum is usually lower than 500 ng/mL. Determining precise<br />

gestational age is essential because fetal AFP levels are age specific and can peak in a normal fetus<br />

at 12-15 weeks <strong>of</strong> gestation. For example, at 20 weeks' gestation, a maternal serum AFP<br />

concentration higher than 1,000 ng/mL would be indicative <strong>of</strong> an open NTD. The measurement <strong>of</strong><br />

maternal serum AFP levels is more than 75% accurate in detecting an open NTD at more than 15<br />

weeks <strong>of</strong> gestation. In patients in whom a question persists, amniotic AFP can be obtained. It is a<br />

significantly more accurate test, especially at 15-20 weeks' gestation, and detects approximately 98%<br />

<strong>of</strong> all open NTDs, although this method is not the preferred screening test. Amniotic fluid<br />

acetylcholinesterase levels add an increased degree <strong>of</strong> resolution.<br />

Detection <strong>of</strong> an NTD with fetal ultrasound in the hands <strong>of</strong> a skilled ultrasonographer usually is 98%<br />

specific. False-positive findings can result from multiple pregnancies or inaccurate fetal dating.<br />

However, closed NTDs also can sometimes remain undetected, especially in cases <strong>of</strong> skin-covered<br />

lipomyelomeningoceles and meningoceles, in which the AFP also may be normal. These closed<br />

NTDs comprise about 10% or more <strong>of</strong> total NTDs discovered. A skilled ultrasonographer can detect<br />

these lesions with almost 95% sensitivity.<br />

A partial list <strong>of</strong> the fetal anomalies that are associated with an elevated AFP is as follows:<br />

• Anencephaly<br />

• Spina bifida cystica<br />

• Encephalocele (leaking)<br />

• Conjoined twins<br />

• Omphalocele<br />

• Turner syndrome<br />

• Gastroschisis<br />

• Extrophy <strong>of</strong> the cloaca<br />

• Oligohydramniosis<br />

• Sacrococcygeal teratoma<br />

• Polycystic kidneys<br />

• Fetal death<br />

• Urinary tract obstruction<br />

If the parents decide not to terminate a pregnancy in which the fetus is affected with an NTD,<br />

extensive counseling takes place. Parents are educated on optimal prenatal care and expectations<br />

once a child is born. If diagnosed early enough, a discussion <strong>of</strong> fetal surgery is warranted. Currently,<br />

this option is available at only 2 major centers: Vanderbilt Medical Center and University <strong>of</strong><br />

Pennsylvania. Although this approach has not been proven scientifically advantageous, preliminary<br />

evidence suggests that this experimental approach has promise in decreasing resultant neurologic<br />

problems in the neonate. Long-term outcome data are currently lacking.<br />

If conventional delivery is chosen, the study by Shurtleff and his colleagues is important to note.<br />

Infants with NTD who were exposed to labor and vaginal delivery were more than 2 times more likely<br />

to have severe paralysis or motor deterioration than those delivered by cesarean section without<br />

labor. Although this remains a controversial point, most centers such as that <strong>of</strong> the author recommend<br />

a cesarean section prior to labor in mothers carrying a fetus with a myelomeningocele.<br />

EVALUATION AND TREATMENT: MEDICAL AND<br />

SURGICAL<br />

Neurologic lesions<br />

Section 8 <strong>of</strong> 11<br />

The myelomeningocele is a saccular protrusion containing a neural placode bathed in CSF (see<br />

Image 1). The surface <strong>of</strong> the sac is covered by arachnoid but no dura or skin. The sac appears<br />

velvety red or yellow with thin fragile vessels imbedded in the arachnoid. The nerve roots pass

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