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47 Cards in this Set

  • Front
  • Back
headaches + epigastric pn in pregnancy
preeclampsia
blue discoloration of cervix/vagina
chadwicks sign of pregnancy
softening of the cervix (multiplied cells) - goodell's sign
softening of the uterus (ladins sign and hegars sign) of pregnancy
darkening of the nipples
sign of pregnancy
naegele's rule (calculate due date)
LMP + 7 days - 3 months
complications of gestational diabetes
macrosomic babies
first prenatal visit
wt, ht, bmi, bp, assess uterine size and auscultation of fetal herat if >12 wks

also heart/lung/breast/pelvic exam are parts of initial prenatal visit

20 wks = level of umbilicus

pap smear if not performed in past year, test for clap/gonorrhae

urinarlysis and culture (proteinuria, glycosuria, hematuria)

cbc (detect/tx anemia)
screen for hemoglobinopathy if pt AA or mediterranean origin (sickle cell/thalassemia)

blood type, ab screen (rubella, syphillis, hepatitis, HIV)
education at initial visit regarding setabelts
pts need a 3 point seatbelt, should not put waistband over belly
old striae vs new striae
itching/pinkish vs silvery color (old)
breast changes in pregnancy
nipple darkens as pregnancy progresses
uterine size w pregnancy
full term; xyphoid
20 wks; umbilicus
16 wks; pubis symphiss
12 wks; mons pubis
when can you first detect fetal heart tones
6 wks gestation; (4 weeks post conception)

always calculate gestational age from LMP; while in embryo the gestational age will always be after conception (2 wk difference bc 2 weeks for ovulation)
nuchal translucency scan
should not perform after 14 wks

asessing fetus in midsaggital plane; if nuchal area is > 3 mm risk of chromosomal anomalies is estimated; if > 6 mm than 90% of fetuses will be detected with chromosomal anomalies (2nd to lymphedema ->
AFP
produced by fetal liver (baby albumin); always elevated in neural tube and frontal abdominal defects
bHCG
produced by palcenta
low afp, low estriol, high hcg
down syndrome
low afp, low estriol, low hcg
trisomy 18
high afp
neural tube defects
inhibin A
produced by placenta/ovary, ELEVATED in DS, normal in trisomies 13 and 18
how to diagnose chromosomal defect (prenatal diagnosis)
karyotyping based on amniocentesis, chorionic villus sampling, percutaneous sampling
2nd trimester visit (24-28 weeks)
perform glucose tolerance test;
3rd trimester labs
repeat hg/hct

Rh screening

syphillis if high rsik

STD

screen for group B beta-hemolytic streptococcus (prevent meningitis/pneumoniae of newborn)
fetal lie
transverse lie can be an indication for c section
fetal engagement
fetal head is engaged if 3/5 of fetal head are below the pelvic brim; happens late in 3rd trimester
fetal positioning; if fetal back lies on left side
on the right side
the babies occiput will be transverse

occiput will be right transverse
outlet diameter
> 8 cm; baby should have no problem
leopold maneuvers
sued to determine orientation of fetus;

1st; what are the fetal parts that line the fundus
2. hands parallel to fetus and see which side is fetal back
4. which fetal pole is headed toward the pelvis? palpate angle between fetal head and symphisis
mother vitals
bp > 140 = preeclampsia
inc temp = infection (chorioamnionitis)
pulse > 100 bpm - hypovolemia
nitrazine test
yellow = vaginal secretions
blue = amniotic fluid
nitrazine test
yellow = vaginal secretions
blue = amniotic fluid
fetal heart rate monitoring
when contracations start there is reduced flow into uterus and at maximum contraction there is no flow into uterus; so if the baby is compromised there will be manifestations in the heart rate

110-160 bpm = normal fetal hr; > 160 = tachy, <110 = brady - babies have severe problems and need to perform immediate delivery

short term variability; if you see no variability this is a bad sign (indicates nervous system is not responding or something)

early deceleration; fetal head compression within birth canal
late deceleration; sign of uteroplacental insufficiency (dangerous) - baby hr is slowly inc hr by end of contraction ie baby is not reacting when it should be reacting

variable deceleration; umbilical cord compression - inc fetal blood pressur e- deceleration via vagus nerve
fetal heart rate monitoring
when contracations start there is reduced flow into uterus and at maximum contraction there is no flow into uterus; so if the baby is compromised there will be manifestations in the heart rate

110-160 bpm = normal fetal hr; > 160 = tachy, <110 = brady - babies have severe problems and need to perform immediate delivery

short term variability; if you see no variability this is a bad sign (indicates nervous system is not responding or something)

early deceleration; fetal head compression within birth canal
late deceleration; sign of uteroplacental insufficiency (dangerous) - baby hr is slowly inc hr by end of contraction ie baby is not reacting when it should be reacting

variable deceleration; umbilical cord compression - inc fetal blood pressur e- deceleration via vagus nerve
position baby at same level as umbilical cord
if baby below -> too much flow -> hepatic congestion -> icterus

if baby above -> baby can be anemic

baby with 1 artery/1 vein when you examine the umbilical cord = intrauterine growth restriction
what to do if suspect of uterine tone
IV oxytocin, uterine massage, repair any episiotomys or lacerations
lochia rubra
similar to menstrual flow -> changes to serosa (pinkish) -> alba (fluid, transparent); part of post partum assessment

also have to assess uterine size/cramps, temp, bp, swelling of hands, ankles, face, breasts, bladder function, hemorrhoids
fetal bradycardia
It is important to remember that bradycardia is a late sign of fetal hypoxia (a
continued lack of oxygen). The heart rate slows in response to a depression of the
heart muscle activity caused by the continued decrease in needed oxyge
FHR variability
Absent variability indicates that the amplitude range is undetectable.
Minimal variability indicates an amplitude range that is detectable, but five beats per
minute or fewer.
Moderate, or normal variability shows an amplitude range 6 to 25 beats per minute.
Marked variability is characterized by an amplitude range greater than 25 beats per
minute.
fetal accelerations
Accelerations are
transient increases in the fetal heart rate caused by fetal movement. They are good
indications of fetal well-being and adequate oxygen reserve. Accelerations often
accompany contractions as a result of fetal movement in response to the pressure of
contracting uterine muscles. During an acceleration, the FHR increases by more than 15
BPM for more than 15 seconds (the 15 x15 rule). In the normal mature fetus, accelerations
can be triggered by fetal body motion, sounds, and other stimuli. They are considered
benign and are a reassuring sign that shows fetal responsiveness and the integrity of
mechanisms controlling the heart.
early deceleration
It appears almost as a mirror image of the
contractions; head compression during contractions
late decelerations
A late deceleration is a decrease is FHR from baseline that usually begins at the
middle of a contraction and remains below baseline until after the contraction is
complete (red arrows). The fetal heart rate will only improve after the contraction
has ended (in blue).

most severe, caused by HYPOXIA (uteroplacental insufficiency)
variable decelerations
Variable decelerations are a common type of fetal heart rate decelerations occurring with
up to 80% of fetuses.

CORD COMPRESSION
nonreassuring FHR patterns
fetal bradycardia, fetal tachycardia, loss of short-term
variability, late decelerations, and persistent late variable decelerations
common cause of fetal bradycardia
cord prolapse
"mirrors the shape and timing of contractions, thought to be benign, and is usually caused by head compression"
early deceleration
nonreassuring pattern, caused by placental insufficiency
late deceleration
on FHR graphs what does one square on the horizontal axis represent
10 seconds
on FHR graphs what does one square on the vertical axis represent
10 heart beats per minute