PreeclampsiaScreen™ T1 enables accurate detection of early onset preeclampsia risk, allowing for earlier intervention and management of the pregnancy.PreeclampsiaScreen™ T1 is the first screening test in the U.S. to measure three biochemical markers in the mother's serum associated with preeclampsia: PAPP-A (pregnancy-associated plasma protein-A); PlGF (placental growth factor) and AFP (alpha fetoprotein). Together, these three biochemical markers can contribute to accurate prediction of risk fo... Read more
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PreeclampsiaScreen T1
PreeclampsiaScreen™ T1 enables accurate detection of early onset preeclampsia risk, allowing for earlier intervention and management of the pregnancy.
PreeclampsiaScreen™ T1 is the first screening test in the U.S. to measure three biochemical markers in the mother's serum associated with preeclampsia: PAPP-A (pregnancy-associated plasma protein-A); PlGF (placental growth factor) and AFP (alpha fetoprotein). Together, these three biochemical markers can contribute to accurate prediction of risk for early onset preeclampsia.
PreeclampsiaScreen™ T1 is the first screening test in the U.S. to measure three biochemical markers in the mother's serum associated with preeclampsia: PAPP-A (pregnancy-associated plasma protein-A); PlGF (placental growth factor) and AFP (alpha fetoprotein). Together, these three biochemical markers can contribute to accurate prediction of risk for early onset preeclampsia.
PreeclampsiaScreen T1 Benefits:
- Highest sensitivity in a biochemical screen. Provides a detection rate of 60% at a 5% false positive rate for early onset preeclampsia when combined with patient history and demographics.
- 91% sensitivity when combined with 2 additional biophysical markers. Detection rate as high as 91% at a 5% false positive rate for early onset preeclampsia when combined with two additional biophysical markers: uterine artery Doppler pulsatility index (UtAD-PI) and mean arterial blood pressure (MAP).
- Practical. Helps you identify those patients who may require increased vigilance.
- Convenient. Can be ordered at the same gestational age/patient visit as first trimester aneuploidy screening.
- Timely. Results can be obtained as early as 10 weeks 2 days' gestation.
Product Overview
