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9804<br />

FLEC<br />

9243<br />

growth factor-binding protein-4 (IGFBP-4), dramatically reducing IGFBP-4 affinity for IGF1 and IGF2,<br />

thereby regulating the availability of these growth factors at the tissue level. PAPP-A is highly expressed<br />

in first-trimester trophoblasts, participating in regulation of fetal growth. Levels in maternal serum<br />

increase throughout pregnancy. Low PAPP-A levels before the 14th week of gestation are associated with<br />

an increased risk for Down syndrome and trisomy 18. Nuchal translucency (NT): The NT measurement,<br />

an ultrasound marker, is obtained by measuring the fluid-filled space within the nuchal region (back of the<br />

neck) of the fetus. While fetal NT measurements obtained by ultrasonography increase in normal<br />

pregnancies with advancing gestational age, Down syndrome fetuses have larger NT measurements than<br />

gestational age-matched normal fetuses. Increased fetal NT measurements can therefore serve as an<br />

indicator of an increased risk for Down syndrome.<br />

Useful For: Prenatal screening for Down syndrome (nuchal translucency, pregnancy-associated plasma<br />

protein A, human chorionic gonadotropin) and trisomy 18 (pregnancy-associated plasma protein A,<br />

human chorionic gonadotropin)<br />

Interpretation: Screen-Negative: A screen-negative result indicates that the calculated screen risk is<br />

below the established cutoff of 1/230 for Down syndrome and 1/100 for trisomy 18. A negative screen<br />

does not guarantee the absence of trisomy 18 or Down syndrome. Screen-negative results typically do not<br />

warrant further evaluation. Screen-Positive: When a Down syndrome risk cutoff of 1/230 is used for<br />

follow-up, the combination of maternal age, pregnancy-associated plasma protein A, human chorionic<br />

gonadotropin, and nuchal translucency has an overall detection rate of approximately 85% with a<br />

false-positive rate of 5% to 10%. In practice, both the detection rate and false-positive rate increase with<br />

age, thus detection and positive rates will vary depending on the age distribution of the screening<br />

population.<br />

Reference Values:<br />

DOWN SYNDROME<br />

Calculated screen risks or =1/230 are reported as screen positive.<br />

TRISOMY 18<br />

Calculated screen risks or =1/100 are reported as screen positive. A numeric risk for trisomy 18 risk is provided with<br />

positive results on non-diabetic, non-twin pregnancies.<br />

An interpretive report will be provided.<br />

Clinical References: 1. Malone FD, Canick JA, Ball RH, et al: First-trimester or second-trimester<br />

screening, or both, for Down's syndrome. N Engl J Med 2005 Nov 10;353(19):2001-2011 2. Screening for<br />

fetal chromosomal abnormalities. ACOG Practice Bulletin No. 77. American College of Obstetricians and<br />

Gynecologists. Obstet Gynecol 2007;109:217–27 3. Wald NJ, Rodeck C, Hackshaw AK, Rudnicka A:<br />

SURUSS in Perspective. Semin Perinatol 2005;29:225-235<br />

Fite-Faraco Stain<br />

Useful For: Staining method for acid-fast organisms.<br />

Reference Values:<br />

The laboratory will provide a pathology consultation and stained slide.<br />

Flecainide, Serum<br />

Clinical Information: Flecainide (Tambocor) is a class I cardiac antiarrhythmic agent with<br />

electrophysiologic properties similar to lidocaine, quinidine, procainamide, and tocainide. Flecainide<br />

produces a dose-related decrease in intracardiac conduction in all parts of the heart, with the greatest<br />

effect on the His-Purkinje system. Atrial effects are limited. Flecainide causes a dose-related and plasma<br />

concentration-related decrease in single and multiple premature ventricular contractions and can suppress<br />

Current as of January 4, 2013 7:15 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong><strong>Laboratories</strong>.com Page 752

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