evaluate condition of fetus in high risk pregnancy
to provide baseline info like more accurate gestational age
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ultrasonography
high freq sound waves aimed in specific direction, deflected by objects in path and return echoes
converted to 2 or 3d images
real time scanning allows fetal heartbeat, breathing and body movements
widely used bc lots of into during any tri
* transvaginal done 1st tri * transabdominal 2nd and 3rd tri
Pros: clear visualization, safe, non invasive, immediate results
cons: no prenatal care in 1st tri lose accurate dating, can NOT identify every fetal structural defect, high cost w/o insurance, anxiety if abn findings
prenatal dx allows parents time to examine options/prepare
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disadvantages of quad/AFP
if abnormal, first step of many
benign conditions can result in apparently abn levels
limited time frame
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glucose tolerance test
screens for gestational diabetes, done at 24-28 weeks (earlier if high risk)
non fasting 50 g oral glucose load, 1hr venous G test
if >140 need further testing
(GDM caused by insulin resistance from hormones)
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amniocentesis
aspiration of amniotic fl from amniotic sac for examination; sterile needle inserted into uterine cavity through abdomen
done during 2nd (chromosomal or biochemical abn) or 3rd tri (fetal lung development)
placed in left lateral tilt position w wedge under right hip, no anesthesitic, guided by US, 20-30mL taken, FHR monitored 20-30min after, and right before, monitor TOCO, RH neg women need Rhogam\*
* Pros= simple, safe, painless * CONS= small time frame (15-20 wks), results take 2-4 weeks, risk of preterm labor, can NOT guarantee perfect baby
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indication of 2nd tri amniocentesis
identify chromosomal abnormalities
dx amnionitis (intrauterine infection)
test amniotic fl when AFP is abnormal
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indication for 3rd tri amniocentesis
fetal lung maturity
* if delivery probably < 37 wks * evaluates presence of lethicin/sphingomyelin (L:S ratio**)= lipoproteins that makeup surfactant (2:1 indicates mature fetal lungs**\*)
determine fetal hemolytic disease
* fetal bilirubin to determine Rh sensitization (rh neg antibodies destroy rh pos fetal RBCs and release bilirubin)
reduction amniocentesis
* in polyhydramnios
evaluation of amnionitis and fetal condition
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chorionic villus sampling (CVS)
microscopic projection from outer membrane (chorion) that develop and burrow into endometrial membrane as the placenta is formed
evaluation reflects chromosomal and genetic makeup of fetus
done by 10-12 wk
indicated for AMA, hx of previous anomalies, genetic defect carrier
procedure: transcervical or transabd, sample of placenta aspirated, rhogam given if rh neg
* Pros= results in 24-48 hrs, options for earlier decision making * Cons= risk of spontaneous abortion (2x of amnio), higher risk of limb reduction defects if done
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amniotic fluid index (AFI)
US measures vertical depth of largest pocket of amniotic fl in 4 uterine quadrants
5-20cm normal, measuring end organ perfusion\*
* Pros= noninvasive, less costly, outpatient, immediate results, nurses can perform * Cons= more research needed to refine interpretation of test
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kick counts
maternal assessment of fetal movement
starts at 28 wks (3rd tri)
\*10 in 2 most popular (count movement daily for an hour, if
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antepartum fetal surveillance
only high risk
3 types: NST, CST, BPP
equipment= bedside monitors, external TOCO, and fetal HR monitor, paper strip
looking at FHR in relation to braxton hicks, HR should inc/react to contraction/stressors of environment
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nonstress test (NST)
evaluates fetal heart ability to accelerate with fetal movement= well oxygenated fetus
done after 30-32 wks
fetal monitoring only/ fetus not challenged
indicated for: dec movement, postdates, high risk, maternal anemia, hx of stillborn
results: reactive, non-reactive
* pros= noninvasive, painless, no risk * cons= false positives (fetal sleep), may have to wait 40 min, acoustic stim may be needed, inc maternal glucose to wake up baby
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reactive NST
normal baseline
2 FHR accelerations within 20 min, lasting 15 sec and peak 15 BPM above baseline
extension of time to 40 min to account for fetal sleep
NO DECELERATIONS
before 32 wks= 10x10
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contraction stress test (CST)
contraction is stimulated (pitocin or nipple stimulation) for 2 min, 5 min resting period, watching for decels
follow up test of nonreactive NST
negative is normal
* pros= allows md to analyze options for STAT delivery * cons= can not be done if UCs contraindicated (placenta previa, previous classical c/s), uterine hyperstimulation reduce placental perfusion, time consuming, expensive, tedious, requires hospital setting, errors in interpretation are common
also gives accurate info about strength of ctx unlike toco
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factors required for adequate fetal oxygenation
1. normal maternal blood flow and volume 2. normal o2 sat and CO2 in placenta 3. open circulatory path between placenta and fetus through umbilical vessels (o2 blood in umbilical vein, deo2 blood in umbilical arteries) 4. normal fetal circulatory and o2 carrying functions 5. pathological influences on fetal o2= HTN, tachysystole, placental abruption
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effects of gradual hypoxemia and worsening fetal acidosis
late decels = 1st sign
accels disappear
fetal breathing movement stops
fetal movement stops (late sign)
fetal tone absent (fetus already compromised)
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variability
in normal fetus, there is interplay between sympathetic (accels) and parasympathetic (decels) in control of the heart
describes the flucuations in baseline FHR (irregular wavelike line rather than smooth line)
helps clarify how fetus is tolerating stress of labor and factors that cause hypoxia
\*\*SINGLE MOST IMPORTANT FACTOR OF ADEQUATELY OXYGENATED FETUS
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causes of decreases in variability
benign causes= fetal sleep, narcotics or sedative (MgSO4), alcohol, gestation
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accelerations
temporary inc in FHR at least 15bpm above baseline for 15 secs
often occur w fetal movement, show good oxygenation= reassuring, good variability
episodic= not associated w ctx; d/t fetal movement/stimulation, reassuring
periodic= assoc with utcs
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decelerations
dec in FHR by at least 15 bpm lasting 15 sec
early= d/t fetal head compression during ctx, benign
variable= abrupt dec below baseline U,V, W shaped, not consistent w ctx, suggest cord compression
late=occur after acme and cont past end of ctx, suggeset utero-placental insufficiency= FETAL DISTRESS
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interventions for variable decels
cord compression
trendelenburg position/ knee to chest position
administer O2
vag exam to feel for prolapsed cord and intervene
c/s may be necessary if not corrected
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interventions for late decels
fetal distress/uteroplacental insufficiency
place woman on left side
admin O2 at 8L/mask
inc IVF
vag exam
call MD if not resolved
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interventions for non-reassuring HR
identify cause of non-reassuring pattern (maternal VS, vag exam, narcotic given?)
4 additional tests to evaluate how fetus is tolerating labor
fetal scalp stimulation
vibroacoustic stimulation
fetal oxygen sat monitoring
fetal scalp blood sample
\*umbilical cord blood gasses after birth
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early term
37-38 6/7weeks
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full term
39-40 6/7 weeks
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late term
41-41 6/7 weeks
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postterm
>42 weeks
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preterm labor
labor between 20-37 weeks
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postterm labor
labor >42 weeks
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primigravida
woman pregnant for the first time
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gravida
pregnant women
any pregnancy regardless of duration, including current pregnancy
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para
woman who have given birth after 20 wks gestation, regardless if born dead or alive
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stillbirth
fetus born dead after 20 wks gestation
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abortion
birth occuring < 20 wks gestation, or the birth of a fetus who weighs
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Gravida/para method
G- number of pregnancies regardless of duration
P- number of pregancies of 20 weeks gestation or more \*multiple infants=single para
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GTPAL
gravida/term/ preterm/ abortions/ # of currently living children
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presumptive signs of pregnancy
least reliable
subjective things felt by woman: amenorrhea, N/V, fatigue, urinary frequency, breast changes, fetal movement
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probable signs of pregnancy
more reliable
usually observed by practitioner
uterine changes: Hegars sign (softening of lower uterine segment), ladin sign, Mcdonald sign, braun von fernwald sign, enlargement, ballotement (baby bounces up and down after vag exam), braxton hicks, palpation of fetal outline, uterine souffle (blood circulation through placenta)
skin changes: linea nigra, areola darkening, chloasma (face), abd striae
vaginal/cervical changes: chadwicks sign (blue color over cervix/labia) caused by increased vascularity; goodells sign (cervical softening)
abd enlargement
positive pregnancy test (hcg, still not certainty, drugs may affect accuracy, urine may be too dilute, ectopic pregnancy)
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positive signs of pregnancy
most reliable, woman is pregnant
only viable pregnancy is an IUP (intrauterine) confirmed by US (gestational sac) as early as 4-5 weeks, and fetal heart movement at 6 weeks
fetal heartbeat (detected w doppler at 10-12wks)
fetal movement felt by examiner at around 20 wks
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common antepartum labs
blood grouping with Rh factor and antibody screen= possible blood incompatibility
antibody titer (indirect coombs)= Rh neg women, determine if they have antibodies; if negative repeat at 28 weeks
CBC= infection and anemia
hemoglobin= anemia
VDRL/RPR= syphilis
Rubella titer= determine immunity, immunize PP if not immune
TB test= if positive refer to more testing
Hep B= HbsAg should be neg, if positive newborns should be given Hep immune globulin and vaccine after birth
HIV screen= voluntary,
UA= renal disease or infection, assess further is positive for trace protein (preeclampsia), ketones (dehydration, fasting), bacteria (infection)
PAP test= screen for cervical neoplasia
cervical culture= GBS and STIs, tx GBS during labor