Normal Pregnancy & Antepartum Care Flashcards
Folic acid recommendations in pregnancy
Start folic acid supplementation at least 1 month before conception to reduce incidence of neural tube defects (NTD)
If no history of NTD — folic acid 0.4 mg
If hx of child with NTD — folic acid 4.0 mg
What are some important components of medical history to collect during the first prenatal visit?
Medical history — DM, HTN
Reproductive — PTD, preeclampsia, stillbith, previous C section
Family hx — DM
Nutritional — folic acid, weight gain
Social — EtOH, illicit drugs, smoking, employment
Psychosocial issues — depression, anxiety, domestic violence
Normal PE findings in pregnancy
Systolic murmurs, exaggerated splitting and S3
Palmar erythema
Spider angiomas
Linea nigra
Striae gravidarum
Chadwicks sign (blue coloration of vagina and cervix)
Prenatal labs usually done at 1st visit
CBC
Type and screen
Test for rubella, syphilis (RPR), Hep B surface Ag, HIV, gonorrhea, chlamydia
Cervical cytology
Screen for DM based on risk factors (everyone is screened at 28 weeks, but screen early if there is family hx, obesity, etc.)
Urine culture
Confirm pregnancy and viability, estimate gestational age and due date
Naegels rule for estimating due date
LMP minus 3 months + 7 days = expected date of delivery
[note: only useful in pts with regular 28 day cycles]
Due date can be estimated using date of LMP, PE of uterus size, or ultrasound exam. How does US help determine due date?
Crown Rump Length (CRL) between 6-11 weeks can determine due date within 7 days
At 12-20 weeks measuring femur length, biparietal diameter and abdominal circumference can determine due date w/i 10 days
In third trimester, due date can be off up to 3 weeks
What pt populations require genetic counseling in pregnancy?
Advanced maternal age (35+)
Previous child/family hx of birth defects or known genetic disorder
Previous child with undiagnosed mental retardation
Previous baby who died in neonatal period
Multiple fetal losses
Abnormal serum marker screening
Exposure to teratogens
Abnormal US findings
Most common autosomal recessive gene carried in North American whites, frequency of 1/25
Cystic fibrosis
[screening is offered to all pregnant women, people with family hx, partners of known CF carriers, US findings of echogenic bowel, sperm donors]
Duchenne muscular dystrophy and fragile X syndrome are examples of _______ inherited disorders
X-linked
Most common form of inherited mental retardation and second most common form of mental retardation after trisomy 21
Fragile X syndrome
Multiple tests are available for maternal screening for fetal aneuploidy. What screening tests may be done in the first trimester?
First trimester screening includes:
Maternal age
Fetal nuchal translucency (NT) thickness (echo free area at back of fetal neck between 10-14 wks)
Maternal serum b-hCG
Pregnancy associated plasma protein-A (PAPP-A)
An elevated beta-hCG and low PAPP-A is associated with ______
Downs syndrome
Multiple tests are available for maternal screening for fetal aneuploidy. What screening tests may be done in the second trimester?
Triple screen done between 16-20 wks: Beta-hCG, estriol, and maternal serum alpha fetoprotein (AFP) biomarkers
Or can do quadruple screen: beta-hCG, estriol, AFP, and inhibin A
Noninvasive prenatal test performed at 9-10 weeks with very high detection rates for trisomies and other sex chromosome abnormalities
Cell-free fetal DNA [if positive, proceed with invasive diagnostic testing like amniocentesis or CVS]
Second trimester testing may include amniocentesis and/or chorionic villi sampling — when are these tests usually performed (at how many weeks?)
Amniocentesis — 16-20 wks
CVS — 11 wks