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PERIODIC/EPISODIC CHANGES
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Transcribers: CALANO, LANGPUYAS | Page 1 of 7
______________________________________________ OBSTETRICS 2
c. Variable METHODS TO MONITOR FETAL HEALTH/
- Independent of contractions/based on shape and degree FETAL SURVEILLANCE
- V, U, W shape Fetal Movements
- Mild moderate or severe Fetal Breathing
Non-stress Tests
Contraction Stress Testing
Acoustic Stimulation Tests/ VAS (Vibroacoustic stimulation)
Biophysical Profile
Amniotic Fluid Volume
Doppler Velocimetry
NON-STRESS TEST
No uterine contraction
Test of fetal condition to assess fetal well being
Rationale:
o FETAL HEART REACTIVITY: presence of FHR
accelerations associated with fetal movement
o Indicator: Good Fetal Health
If you see acceleration, in your mind you know that the
baby is moving. If the baby is moving even in the
presence of stress to the mother which are contractions
during labor, you know that there is enough fetal
reserve. Kahit na squeeze na yung uterine blood flow,
still the baby is moving then the output in the CTG is
acceleration
o Absence / more than 40 mins; some books: >80 mins:
We have to remember that in reading a CTG: May suggest fetal distress/fetal hypoxia
Identify baseline FHR, the baseline variability, periodic changes Loss of fetal reactivity may mean hypoxia and
(whether acceleration or deceleration present then identify if neurologic depression and acidosis
early/late/variable). Identify any changes in the trends of fetal heart For fetal surveillance: test to know how is the baby inside the
rate patterns over time. Also check intensity and frequency of uterus. Is the baby at risk for hypoxia? Basis: presence of
uterine contractions acceleration. If intact/normal: (+) acceleration; if absent: no
Ex: Basal FHR report: 130/min, variability is normal, fetal reactivity: means neurologic depression
moderate variability 15 beats difference, 10 accelerations present, Physiology: Intact cortical function where fetal movement is
no decelerations elicited will result to FHR acceleration
o Fetal movement means intact cortical function: because
movement is developed in the cerebral cortex
Normally initiated at 32 weeks (for severe cases we can start
even at 26 weeks)
Interval/Frequency of NST tests
o 7 days
o Biweekly (DM, gestational diabetes, postterm, post dated,
preeclampsia, IUGR)
National Institute of Child Health and Human Development
Fetal Monitoring Workshop's definition of acceleration
depending on AOG
o >32 weeks (baseline rate 15 beats and duration
of 15 seconds or more)
o <32 weeks (10bpm/10seconds)
Advantage: done as outpatient
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NST interpretation VIBROACOUSTIC STIMULATION TEST (VAST)
Reactive: 2 or more accelerations in 20 mins Decrease time spent in doing NST
o Baby will do well within 1 week Use of artificial larynx (by Gagnon) applied over abdominal
o Sign of good fetal condition wall over fetal head for 1-3 seconds produce vibratory
sound stimulus of 100-110 db
Sounds of 100-105 db provoke fetal movement
Response: fetal startle as seen by a reactive NST or palpable
fetal movement or visible in the ultrasound called “fetal
recoil test”
Gestational age related
o <24 weeks: no response
The auditory system is not yet developed/mature
o 23-27 weeks: 30% will respond
o 27-30 weeks: 80% will respond
o >30 weeks: 96% will respond
Non-reactive: no acceleration/ 1 acceleration
o If non-reactive: Extend test (20 mins)/ Provoke fetal
movement via meal/manipulation of uterus/sound
o Not immediately suggestive of hypoxia (ask last meal of
mother or apply stimulation to awaken the baby and
provoke fetal movement)
o Absence of accelerations - does not mean fetal
compromise (healthy fetus may not move up to 75 mins)
o Nonreactive in 80-120 mins imposes a problem,
increase in neonatal morbidity (do additional tests like
BPP)
This reactive NST also shows a transition from the on reactive state (first half of
tracing) in which there are no movements and low FHR variability. The onset of
normal FHR variability accelerations, and fetal activity (spikes on lower channel)
correspond to VAS. The initial quiet state of the fetus does not signify fetal
compromise
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______________________________________________ OBSTETRICS 2
Indications Contraindications Three-Tier Fetal Heart Rate Interpretation System
DM PROM National Institute of Health Workshops
Post-maturity Placenta Previa: may bleed A. Category I trace
HPN disorder 3rd trimester bleeding Baseline rate of 110-160bpm
IUGR Previous CS: uterine rupture Baseline FHR variability: Moderate
Previous stillbirth Multifetal Pregnancy Late or Variable decelerations: absent
Collagen disease Incompetent Cervix: may dilate Accelerations: present or absent
Cervix
B. Category II trace
PolyHydramnios: may lead to
Accelerations
premature delivery
o Absence of induced accelerations after fetal stimulation
Periodic/episodic Decelerations
Interpretation of CST o Recurrent variable with minimal-moderate variability
Positive Persistent >50% of contractions has late o Prolonged deceleration >2mins but <10mins
deceleration o Recurrent late with moderate variability
Negative No late decelerations – GOOD o Variable deceleration with slow return to baseline,
Suspicious Inconsistent-intermittent overshoots, “shoulders”
Equivocal- Contraction every 2mins lasting for 90secs Baseline FHR
Hyperstimulatory or more. Can induce fetal hypoxia o Bradycardia not accompanied by absent variability
(iatrogenic). Stop the test! Not good for the o Tachycardia
baby Baseline FHR variability
Unsatisfactory No good contractions (no 3 contractions in o Minimal baseline variability
10 mins, stop the test) o Absent variability not accompanied by recurrent
decelerations
A healthy result: Reactive non-stress test and a o Marked baseline variability
negative contraction stress test C. Category III trace
Absent variability and any of the following:
o Recurrent late decelerations
o Recurrent variable decelerations
o Bradycardia
o Sinusoidal pattern
Should terminate pregnancy
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PHYSIOLOGIC CRITERIA OF FETAL BPP Modified (BPP NST/AFV)
(HYPOXIC CASCADE) Normal (NST/AFV): Repeat weekly
BPP CNS center AOG of development >36 weeks (Abnormal NST/AFV): Deliver
Tone center Cortex-subcortical area 7.5-8.5 weeks <36 weeks (individualized test) further testing
Movement Cortex 9 weeks NST (reactive) but is oligohydramnios: look for cause and
Breathing 4th ventricle 20-21 weeks biweekly testing
FHR Medulla, Posterior 24-26 weeks AFV (Normal) NST (Nonreactive): do CST or full BPP
reactivity hypothalamus
This is why Non-Stress Test (NST) cannot be performed at less than Amniotic Fluid Volume
26 weeks, because FHR reactivity is still under development AFI of <5
o Increased CS rate for fetal distress
BPP Cascade o Low 5min APGAR score
The most recently developed center is the earliest to be Causes:
affected by hypoxia (Theory of cascade of hypoxia) o Decreased uteroplacental perfusion
o Decreased renal blood flow
FHR reactivity (as seen in NST) is the first to be affected by
o Decreased urine production
hypoxia, then breathing, movement and tone
o Oligohydramnios - chances of CS is very high
Tone: Last to be affected (earliest to develop, so it should be o Ex: HTN → vasoconstriction → decreased uteroplacental
more established) perfusion → baby tends to shunt blood to the more
Chronic Marker of hypoxia : amniotic fluid volume (AFV) important organ (brain and adrenals) → decrease blood
Acute: movement, FHR reactivity flow to the kidneys → decrease renal blood flow →
Hindi naman agad mawawala yung fluid unless there is decrease urine prod → Oligohydramnios
ruptured BOW and the only anomaly that can lead to
oligohydramnios is Renal agenesis
Formation of AF volume is a function of the fetal kidney Fetal breathing is affected by infection. So if there is ruptured BOW
Decreased uteroplacental perfusion → decreased blood (noted from BPP) → if there is early sign of intra amniotic infection
flow to the kidney → blood is needed more in the brain → → check on the absence fetal breathing
less blood goes to the kidneys → lesser urine formation →
oligohydramnios (occurs within months → chronic) DOPPLER VELOCIMETRY
Other parameters: Acute Hypoxia Detects and measures blood flow (Doppler principle)
It measures the motion or velocity of the RBCs as it passes
Interpretation through the dilated blood vessels
Total Score: 10/10 if all 5 parameters fulfilled (w/ NST) Ex: problems in blood flow like vasoconstriction, HTN
w/o NST total score is: 8/8 3 fetal vascular circuits (fetal health to intervene for IUGR
If score is 8/8 or 10/10: Reassuring fetuses)
If score is 6/10: Equivocal (needs close monitoring) 1. Umbilical artery
If score is <4/10: Non-reassuring (Terminate/ 2. Middle Cerebral Artery
Deliver) 3. Ductus Venosus
Note: breathing is sometimes affected by meal. If 0: probably Assess fetus at risk for IUGR and hypoxia or acidosis
the mother did not take her meal so let her eat or drink a glass (called ARED flow)
of juice, then let her come back Assess risk for preeclampsia (diastolic notch: notching of
uterine arteries)
BPP Interpretation/Management
BPP Interpretation Management
Measurement
10/10 Normal Repeat test weekly (for
8/8 DM/Post term: twice weekly) S/D ratio (systolic/diastolic ratio)
8/10 Normal AFV Repeat weekly Pulsatility index
If oligohydramnios Deliver o S-D/mean
6/10 Possible asphyxia, Deliver Resistance index (Pourcelot’s index)
Abnormal AFV o S-D/S
Normal AFV and term Normal flow: good uteroplacental perfusion
Oligohydramnios and Deliver o Increased diastolic flow
close to term S/D ratio normally decreases from
Oligohydramnios and If L:S (lecithin- 4 at 20 weeks to 2 at term, it decreases as AOG advances
preterm sphingomyelin) ratio <2: S/D ratio is less than 3 after 30 weeks (beyond 3, it
repeat test in 24h becomes abnormal, Normally, ratio should be decreasing)
In 24h, if <6: deliver Abnormal S/D (above 95th percentile for AOG)
In 24h, if >6: repeat/observe ISUOG (International Society of Ultrasound in Obstetrics and
4/8 or Probable asphyxia Repeat test same day (repeat Gynecology): free loop of cord
4/10 <4: deliver) More diastolic flow (placental cord insertion) less at fetal cord
0 or 2 Fetal asphyxia Deliver insertion
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______________________________________________ OBSTETRICS 2
Maternal Uterine Artery 3. Ductus venosus
Predicts placental dysfunction Imaged as it branches from umbilical vein approximately at
DIASTOLIC NOTCH: predictive of IUGR and risk of the level of diaphragm
preeclampsia; Doppler done at 24 weeks, give Aspirin to Waveform is biphasic (first peak: systolic flow while second
prevent pre-eclampsia peak: diastolic flow) followed by a nadir; the a wave
Vascular resistance in uterine circulation normally decreases a wave: atrial contraction
in the first half of pregnancy (trophoblastic invasion) o Decreased, absent, or reversed in preterm IUGR fetus
High risk of uteroplacental insufficiency shows high (sustained irreversible multi-organ damage due to
resistance patterns HYPOXIA)
22-24 weeks
Worst scenario would be an abnormality in the ductus
Abruption, preeclampsia, FGR venosus
1. Umbilical Artery
About 60-70% of small placental vessels need to be
obliterated before umbilical artery becomes abnormal
A – Normal
B/C – ARED (Absent-Reversed Diastolic Blood Flow); poor
Antenatal fetal testing
outcome for the baby
Which is the best test? Every test has an end point so it’s more
S/D ratio above 95th % - Abnormal of a common sense. Each test should be supplementary to each
AEDBF (absent RDBF): Perinatal mortality of 10% other. No best test.
REDBF (reduced RDBF): Perinatal mortality of 33% o Good history taking
American College of OB-GYN: Umbilical artery Doppler o Inform mother the risks of hypoxia
velocimetry is beneficial for suspected fetal growth o Important: is to detect early problems and close
restriction monitoring of the mother
No benefit for Post-term, DM, SLE, APAS o For NST: acceleration
o For Contraction Stress Test: no late deceleration
2. Middle cerebral artery o Vibroacoustic Test: acceleration. What if acceleration is
absent? It’s okay. Maybe the baby is sleeping
In babies with growth restriction, there is increased blood flow
When is it done earliest?
to the brain, increased flow to the MCA
o At 32 weeks. If high risk: 26weeks
HYPOXIC FETUS attempts “Brain Sparing” by reducing o As early as 26-28 weeks, but usually most of the test is done
cerebrovascular impedance and increasing blood flow at 32 weeks. Why? Because prematurity can have different
If decreased blood flow to umbilical artery → decrease blood results. Ex: tachycardia at very premature AOG. This can
flow to brain → baby is in trouble → there is no compensatory be seen in fetuses below 32 weeks which is physiologic.
mechanism → hypoxia Because the sympathetic nervous system matures earlier
If there is compensatory (we call it brain sparing): decrease than parasympathetic system. That is why tachycardia
blood flow to umbilical artery → increase blood flow to the
is physiologic in premature fetuses. So it will depend
brain → brain sparing → good outcome
on the time that you will do the test
Such brain sparing growth restricted fetuses will undergo the
reversal What is the significance of these tests?
Risk of fetal death
Sensitive tool for assessing fetal anemia
Peak systolic velocity (increased-increased cardiac
output/blood viscosity)
MCA value of >1.5 multiple of median (MOM): Anemia
(alloimmunized pregnancy, erythroblastosis fetalis)
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______________________________________________ OBSTETRICS 2
Fetal Tachycardia
Baseline rate above 160 bpm
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