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Anemia of Prematurity - Portal Neonatal

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Causes:<br />

umbilical artery, gastrointestinal atresias, and a narrow chest secondary to external<br />

compression. Infants are typically small for their stated gestational age (SGA). When an<br />

abdominal mass is found on examination <strong>of</strong> the infant in this clinical setting, it <strong>of</strong>ten<br />

represents multicystic-dysplastic kidney, enlarged urinary bladder, or prune-belly<br />

syndrome.<br />

• Polyhydramnios<br />

o Twin gestation with twin-to-twin transfusion (increased amniotic fluid in the recipient twin<br />

and decreased amniotic fluid in the donor) or multiple gestations, which can lead to twinto-twin<br />

transfusion syndrome<br />

o Fetal anomalies, including esophageal atresia (usually associated with a<br />

tracheoesophageal fistula), tracheal agenesis, duodenal atresia, and other intestinal<br />

atresias<br />

o CNS abnormalities and neuromuscular diseases that cause swallowing dysfunction<br />

o Congenital cardiac-rhythm anomalies associated with hydrops, fetal-to-maternal<br />

hemorrhage, and parvovirus infection<br />

o Maternal type 2 diabetes mellitus (more <strong>of</strong>ten than in oligohydramnios)<br />

o Chromosomal abnormalities, most commonly trisomy 21, followed by trisomy 18 and<br />

trisomy 13.<br />

o Fetal akinesia syndrome with absence <strong>of</strong> swallowing<br />

• Oligohydramnios<br />

o Fetal urinary tract anomalies, such as renal agenesis, polycystic kidneys, or any urinary<br />

obstructive lesion (eg, posterior urethral valves)<br />

o Maternal problems, including placental insufficiency, PROM, and chronic leakage <strong>of</strong> the<br />

amniotic fluid: The major maternal complication from oligohydramnios is<br />

chorioamnionitis, which has an incidence <strong>of</strong> 21-74%. The earlier chorioamnionitis occurs<br />

in pregnancy, the greater the fetal risk <strong>of</strong> bronchopulmonary dysplasia (BPD); neurologic<br />

complications; pulmonary hypoplasia; and, in severe cases, respiratory failure.<br />

o Maternal use <strong>of</strong> prostaglandin synthase inhibitors or angiotensin-converting enzyme<br />

(ACE) inhibitors<br />

o Postmaturity syndrome in infants when a pregnancy extends beyond 42 weeks'<br />

gestation (possibly caused by a decline in placental function)<br />

WORKUP Section 4 <strong>of</strong> 9<br />

Lab Studies:<br />

• Lecithin-sphingomyelin (L:S) ratio and phosphatidylglycerol (PG) levels in the amniotic fluid:<br />

If premature delivery is anticipated with either oligohydramnios or polyhydramnios, the<br />

amniotic fluid L:S ratio and PG concentration are helpful in determining the maturity <strong>of</strong> the<br />

fetal lungs and, therefore, in assessing the likelihood <strong>of</strong> respiratory distress syndrome.<br />

• Polyhydramnios<br />

o Glucose tolerance test for mothers with suspected type 2 diabetes mellitus<br />

o If associated fetal hydrops is present, screening for maternal antibodies to D, C, Kell,<br />

Duffy, and Kidd antigens to determine the mother's immunity<br />

o Kleihauer-Betke test to evaluate fetal-maternal hemorrhage<br />

o Venereal Disease Research Laboratories (VDRL) test to screen for syphilis<br />

o Immunoglobulin G (IgG) and immunoglobulin M (IgM) titers to evaluate for exposure to<br />

rubella, cytomegalovirus (CMV), and toxoplasmosis<br />

o Hemoglobin Bart in patients <strong>of</strong> Asian descent (heterozygous for alpha-thalassemia)

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