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Erin Harkness

Created on March 11, 2024

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Transcript

WHAT?

BIOCHEMICAL ASSESSMENT

ASSESSMENT OF

  • A high-risk pregnancy is defined as a pregnancy in which the life or health of the mother or fetus is jeopardized by a disorder coincidental with or unique to pregnancy
  • Maternal high-risk status extends 30 days into the postpartum period​​ ​

High-Risk Pregnancy​

Quantitative Beta HCG testing

Progesterone Levels

NURSING CARE FOR ANTENATAL TESTING

Cell-free DNA

Sequential/Integrated screen

INDICATIONS FOR ANTENATAL TESTING

FETALINDICATIONS

Chorionic Villi Sampling

MATERNALINDICATIONS

Amniocentesis

HISTORY

WHAT NOW?

PREGNANCY IS HIGH RISK

ANTENATAL TESTING

1970

Testing began in 1970's​​ ​

EARLY TESTING

  • 1st and 2nd trimester

FETAL KICKS

FETAL MONITORING

BIOPHYSICAL PROFILE

LATER TESTING

  • 2nd and 3rd trimester ​​ ​

Quantitative Beta HCG Testing

  • Provides information on viability of pregnancy; level should double every 48 hours​

Free-cell DNA

  • Screening tool only
  • Offered to high-risk women (AMA, previous child with chromosome abnormality; first degree relative/sibling with chromosome abnormality)
  • Maternal blood draw as early as 10 weeks (can identify gender)​
  • Can identify > 99% of Down syndrome pregnancies; 97% of trisomy 18 pregnancies; and 87% of trisomy 13 pregnancies.​

Fetal Kicks

  • Frequently used to monitor pregnancies with conditions that could impact fetal oxygenation​
  • Varying protocols​
  • Follow Up needed:​
    • if <12 movements in 24 hours​
    • A change in fetal movement as reported by mom​
    • Any concern about fetal movement as reported by mom

Maternal Indications

  • Hypertensive disorders of pregnancy (Preeclampsia/HELLP, chronic, gestational)​​
  • Type 1 diabetes mellitus​​
  • Chronic disease in mother – renal, heart, autoimmune, clotting disorders, thyroid disease​​
  • AMA (over age 40)​
  • Psychosocial factors​
  • Sociodemographic factors​

Fetal Indications

  • Postdates​ (>41 weeks)​
  • Decreased fetal movement​​
  • IUGR, Abnormal dopplers​​
  • Previous fetal demise​​
  • Known fetal anomaly​​
  • Multiple gestation​​
  • Isoimmunization​​
  • Hydramnios (poly/oligo)​

Progesterone Levels

  • A tool for screening women at risk for spontaneous abortion; offer supplementation if low (debatable) ​

Chorionic Villi Sampling

  • Invasive; risk of 1 in 500 of miscarriage; performed between 10-13 weeks by specialist

Biophysical Profile

Biophysical profile: A noninvasive test to evaluate the health of the fetus. A provider performs the test with an ultrasound and uses a scoring system to rate the fetus in the following areas: body movement, muscle tone, breathing movements, amniotic fluid volume.

Fetal Indications

  • Postdates​ (>41 weeks)​
  • Decreased fetal movement​​
  • IUGR, Abnormal dopplers​​
  • Previous fetal demise​​
  • Known fetal anomaly​​
  • Multiple gestation​​
  • Isoimmunization​​
  • Hydramnios (poly/oligo)​

Amniocentesis

  • Invasive; risk of 1 in 500 of miscarriage; performed after 15 weeks by specialist or OB-GYN
Image Source
Terminology
Sequential/Integrated screen
  • PAPP-A (protein produced by the placenta in early pregnancy. Abnormal levels are associated with an increased risk for chromosomal abnormalities.
  • Total B-hCG (total beta-human chorionic gonadotropin)
  • MSAFP (Maternal serum alpha-fetoprotein)- Screens for “open neural tube” defects. Spina bifida and anencephaly are examples.
  • Chorionic villi sampling- chorionic villi are tiny projections of placental tissue that look like fingers and contain the same genetic material as the fetus. This test involves taking a sample of this tissue from the placenta to test of chromosomal abnormalities.
  • Amniocentesis- procedure used to take out a small sample of the amniotic fluid for testing. The fluid contains cells that have genetic information that can be used to diagnose genetic disorders.
  • Screening tool only
  • US between 11-13 weeks for measurement of Nuchal translucency
  • 1st maternal assay drawn (PAPP-A and HCG)
  • 2nd maternal assay drawn between 15-18 weeks (MSAFP) Screens for Trisomy 21 (Down's syndrome), Trisomy 18 (Edward's syndrome), Trisomy 13 (Patau syndrome) and neural tube defect (spina bifida)