What is the goal of prenatal testing?
Identify women at ↑ risk of medical complications, pregnancy complications, or fetal abnormalities
What is the most common chromosome abnormality?
2. Screening detects up to 95 % of pregnancies affected by Down syndrome
What are prenatal testing programs based on?
Prenatal screening programs based on maternal serum & USN testing
What routine labs are preformed during the first prenatal visit?
What routine labs are preformed during the 28 wk prenatal visit?
What other prenatal tests may be performed?
A. Down Syndrome, Trisomy 18
What other prenatal tests may be performed for at-risk women?
1. Thyroid function studies A. Abn. neurologic development risk in mom w/hypothyroidism 2. Genetic conditions A. CF B. Thalassemia
What is chorionic villus sampling? How is it performed?
When is chorionic villus sampling (CVS) performed?
What are the indications for CVS?
What are the advantages of CVS?
2. Preliminary results w/in 48 hrs
What are the disadvantages of CVS?
2. Spontaneous abortion risk slightly > amnio
What are the complications from CVS?
1. Fetal loss A. 0.7% w/in 14 days B. 1.3 % w/in 30 days C. 2% for loss anytime during pregnancy 2. Limb defects 3. Failure of obtaining sample 4. Vaginal bleeding 5. Chorioamnionitis 6. Fetomaternal hemorrhage
What is the Nuchal translucency screening test?
When is nuchal translucency screening test performed?
Performed @ 11-13 weeks
What is trisomy 13 and 18?
What is trisomy 21?
A. Most common chromosome abnormality in humans
What is trisomy 21 asst with?
What are the characteristics of turner’s syndrome?
1. Only affects females A. Short stature B. Webbed neck C. Edema of hands & feet D. Skeletal abnormalities E. Premature ovarian failure F. 1/3 w/coarctation of aorta
What are the indications for nuchal translucency screening test?
When is the quadruple screen performed?
2. 16th -18th weeks most accurate
What is included in the quadruple screen?
What is alpha fetoprotein? When is it increased?
What is hCG? When is it increased?
2. Inc levels in Trisomy 21