Week 3 - Complex Antenatal Care Flashcards
Major expected outcome of fetal assessment
detection of fetal compromise
When is an anatomy scan typically conducted?
18 - 20 weeks
sometimes able to detect abnormalities - organs, MSK
When can the fetal HR first be detected by Doppler?
8 - 10 weeks
Fetal Assessment components (7)
1) Prenatal Screening
2) CVS/Amniocentesis
3) Ultrasounds
4) SFH for monitoring growth
5) Fetal health surveillance (electronic fetal monitoring, NST)
6) Fetal movement counting
7) Biophysical profile
Ultrasound major uses (7)
1) confirm pregnancy and viability
2) determine the gestational age
3) prenatal screening: NT, fetal anatomy, congenital anomalies
4) assess level of amniotic fluid
5) detect fetal growth
6) determine fetal position
7) detect placental previa or abruption
T or F: Prenatal screening is diagnostic.
FALSE
screen results are positive, additional testing will be offered
T or F: All pregnant people have a chance for trisomy 21, 18 and 13, not just those of advanced age
TRUE
also important to consider family history
Non-invasive Prenatal Screening (4)
1) Enhanced First Trimester Screening (eFTS)
2) Second Trimester Serum Screening
3) Integrated Prenatal Screening (IPS)
4) Non-invasive Prenatal Testing (NIPT)
1) Enhanced First Trimester Screening (eFTS)
nuchal translucency
-3+ mm: genetic disorders, abnormalities
-3.5+ mm: congenital heart defects
maternal serum bio markers: 11 - 14 weeks
screen for Trisomy 18, 21, maybe 13
2) Second Trimester Serum Screening
maternal serum - screening for neural tube defects
3) Integrated Prenatal Screening (IPS)
only for + screens, carrying twins or advanced maternal age greater than 40
screen for trisomy 13, 18, 21 as well as some sex-linked chromosomal disorders
4) Non-invasive Prenatal Testing (NIPT)
screening method for prenatal genetic material using cell-free DNA
take fetal DNA that is circulating in the maternal system
anytime after 9-10 weeks until the end of the pregnancy
high detection rates for Trisomy 13, 18, 21
screens for sex chromosome disorders
maternal venipuncture and results available in about 10 days
OHIP coverage limited
Chorionic villi
in placenta
allow for attachment to uterus, o2 and co2 exchange
CVS/Amniocentesis
DIAGNOSTIC tests
if a screening test is abnormal or if high risk
CVS
-10-13 weeks
-remove piece of placenta for the chorionic villi
Amniocentesis
->15 weeks
-amniotic fluid with fetal cells
-genetic info, lung maturity, fetal hemolytic disease
What safety mechanism is in place with CVS/Amniocentesis?
ultrasound guidance
Amniocentesis Maternal Risks (many)
Hemorrhage
Fetomaternal hemorrhage
Infection
Labour
Abruptio placentae
Damage to intestines or bladder
Amniotic fluid embolism
Amniocentesis Fetal Risks (many)
Death
Hemorrhage
Infection (amnionitis)
Injury from needle
Miscarriage or preterm labor
Leakage of amniotic fluid
Biophysical Profile (BPP)
more in-depth ultrasound offered for high-risk to assess fetal wellbeing
may be frequent, ongoing
BPP Scoring
higher score=better, more normal
out of 10
if just doing ultrasound component, out of 8
0 or 2 points, no 1
always even score
BPP Components
4 ultrasound assessments
Nonstress test (NST)
-evaluates FHR & response to movement
-20 minute observation where they’re placed on external fetal monitor
-non stress because there’s no uterine activity
5 discrete biophysical variables
1) fetal movement
2) fetal tone
-want flexed, not floppy
3) fetal breathing movements
-not breathing to gain oxygen, which is obtained from the mother through the placenta
-but do practice breathing - expansion of lungs
4) amniotic fluid volume
-measure pockets of fluid
5) FHR
High Risk Pregnancy
pregnancy in which the life or health of the client or infant is jeopardized by a disorder coincident with or unique to pregnancy
not a high prevalence
early intervention to improve health outcomes
When does a high risk pregnancy status extend to?
6 weeks postpartum
Common causes of bleeding in EARLY pregnancy (4)
1) miscarriage
2) premature dilation of cervix
3) ectopic pregnancy
4) molar pregnancy