Module 2 Notes
Module 2 Notes
normal
Antepartum fetal surveillance procedures
▪ Done at least everyday at
- Fetal movement counting the same time of the day to
- Nonstress test compare
- Vibroacoustic stimulation o Rayburn, 1980 – 80% of all
- Contraction stress tests movements observed during
- Biophysical profile sonography monitoring were
- Doppler velocimetry perceived by the mother
o Johnson, 1992 – beyond 37
Fetal Movement Counting weeks, mothers perceived only
Fetal movements 16% of the fetal movements
- Use of uterine contraction
- Observed by ultrasound as early as 8 weeks tocodynamometer
AOG but the mother can start to feel it o Tocodynamometer – composed
around weeks AOG especially for of transducers attached to the
primigravid maternal abdomen (fundal end)
- Can be either: which can record the number of
o Weak movements and reflected on a
o Strong paper strip
o Rolling movements o Cardiotocography – similar to an
- Appreciated easily by multigravida (4 ECG where you need a thermal
months) mothers compared to primigravid paper to record the FHR. Uterine
(5 months) contractions are also recorded
- Weak movements decrease as pregnancy ▪ Device is usually set at
advances – due to declining amniotic fluid 3cm/ min
and space account for diminishing activity ▪ Important to determine
at term certain changes such as
Factors affecting motility acceleration and
deceleration in the FHR
- Sleep-awake cycle - Visualization with sonography
o Most important determinant of fetal
activity Nonstress test (NST)
o Independent of maternal sleep- - Simple to perform, relatively quick and
awake state non-invasive
o Sleep cyclicity: 20-75 mins (average - Describes FHR acceleration in response
sleep cycle is 20-30 mins only) to fetal movement as a sign of fetal
- Amniotic fluid volume health
o Decreased fetal activity with o Fetal heart rate acceleration – sign
diminished amniotic fluid volumes for fetal well-being; wellness
and suggested that a restricted rather than illness
intrauterine space might physically - Widely used for primary testing method
limit fetal movements for assessment of fetal well-being
Clinical methods to quantify fetal movements - Also incorporated into the biophysical
profile
- Maternal subjective perceptions
o Let the mother count the FHR Accelerations
movement - Fetal heart rate accelerations
o Cheapest and easiest way o For fetus > 32 weeks: the
o Count of 10 (Moore, 1989) acceleration peak is 15 bpm or
▪ Perception of 10 fetal more above the baseline rate;
movements in up to 2 lasts for 15 seconds or longer but
less than 2 minutes
▪ 2-10 mins: prolonged Interval between testing
acceleration
- Every 7 days: ideal
▪ >10mins: used as new
- In certain cases, it can be done more
baseline
frequently (patients with comorbidities)
o For fetuses < 32 weeks: normal
o Increased if mother has
accelerations are defined as having
uncontrolled HTN and DM, as well
an acme that is 10 bpm or more
as case wherein intrauterine growth
above the baseline for 10 seconds
restriction is considered
or longer
- ACOG, 2016
- Principle behind testing:
o Frequent testing should be done
o HR of a fetus will transiently
for patients with:
accelerate in response to fetal
▪ Post-term pregnancy
movement
▪ Multifetal gestation
- Factors that cause loss of reactivity:
▪ Diabetes
o Fetal sleep
▪ Fetal growth restriction
o Medications that cause central
▪ Pregnancy HTN (twice
depression
weekly)
o Cigarette smoking
- Note!! Causes of fetal death within 7 days of normal
o Absence does not invariably predict nonstress test
fetal compromise
o Determine the baseline FHR to - Meconium aspiration syndrome
determine increase or decrease. o Most common cause
Baseline is defined as the area that o Associated with umbilical cord
is a the most stable part or no abnormality → acute asphyxia
recording of movements insult → provokes fetal gasping
- Intrauterine infections
NST interpretations - Abnormal cord position
- Malformations
- Reactive
- Placental abruption
o Requires at least 2 or more
accelerations occurring within 20 Decelerations during nonstress testing
minutes of beginning of the test
o Accelerations with or without fetal - Take note!!
movements should also accepted; a o Variable decelerations if
40 minute or longer tracing should nonrepetitive and brief (<30
be performed before concluding seconds) do not indicate fetal
nonreactive status compromise or the need for
o Other criteria: normal fetal heart obstetrical interventions
beat (110-160 bpm) with normal o On the other hand, repetitive
variability variable decelerations (at least 3
- Non-reactive (abnormal) in 20 minutes), even if mild, have
o Reactive criteria not met been associated with greater
o A 40-minute or longer should be risk of CS delivery
performed before concluding ▪ Decelerations lasting > 1
nonreactive status minute have worse
o Note!! prognosis
▪ Not always ominous; baby ▪ Correlate w/ amniotic fluid
may be asleep volume
▪ Abnormal result may be Vibroacoustic Stimulation (VAS)
attributed to patients with
preeclampsia or with - Loud external sounds are used to startle
maternal HTN the fetus and thereby provoke heart
acceleration
- Positive (+): rapid appearance of a time when deceleration
qualifying acceleration following starts
stimulation o E.g.: 3 late decelerations in 5
- Shortens the average time of NST from 24 observed contractions
minutes to 15 minutes - Equivocal
o Suspicious
Contraction Stress Test (CST)
▪ Intermittent late
- Artificially induced decelerations or
- To observe changes to the FHR in significant variable
relation to uterine contractions decelerations; <50% of
- Rationale: evaluates the status of basal uterine contractions
fetal oxygen reserves by observing FHR o Hyperstimulatory
response to uterine contraction ▪ FHR decelerations that
- A test of uteroplacental function occur in the presence of
- Endpoint: contractions more
o Achievement of 3 uterine frequent than every 2
contractions of at least 40 seconds minutes or lasting >90
or longer duration in 10 minutes seconds
- Unsatisfactory
Ways to perform CST o Fewer than 3 contractions in 10
- Oxytocin Challenge Test minutes or an uninterpretable
o A dilute IV infusion of oxytocin (10 tracing
units in 1 L liquid) is slowly and Indications for CST
gradually initiated until the desired
uterine contractions are achieved - Vaginal delivery is CONTEMPLATED
o Usually not done, or a 2nd choice to o (-) CST = allow mother to go into
nipple stimulation test labor
- Nipple Stimulation Test o (+) = do not allow mother to go
into labor
Criteria for interpretation of CST ▪ Fetus may not tolerate the
- Negative (normal finding) stress of labor since the
o No late or significant variable uteroplacental reserves are
decelerations already compromised
- Positive ▪ Baby may get asphyxiated
o Late decelerations following → leading to death
50% or more contractions - Presence of the following prior to labor
▪ Late decelerations: decline or o Postdated pregnancy
decrease FHR in association o DM
with uterine contractions but o Severe HTN
the timing is late o Oligohydramnios
• The timing of the onset, Contraindications for CST
the nadir, and the end of
FHR is late with the onset, - Vertical uterine scar
peak, and end of the o Hx of classical CS
uterine contractions ▪ Types of CS:
o Nadir: lowest point of • Lower segment (transverse)
the tracing; time – not contraindicated
when the contraction • Classical (vertical)
ends, subsequently o Contraindicated
the FHR recovers o Risk of uterine rupture
• The peak of the uterine as scar from surgery is
contraction is only the located at fundus, area
of which the most active
during uterine Amniotic Fluid Normal: ≥ 1 pocket that
contraction Volume measures ≥ 2cm in 2
- Known placenta previa
(no. of
measurement
pocket/
in 2
perpendicular planes;
o Implantation of placenta at the perpendicular planes) polyhydramnios
lower part of the uterus below
the presenting part or head of the Abnormal: (-) or pocket < 2
cm in 2 perpendicular planes;
baby
oligohydramnios
o There is tendency to bleed
FHR Normal: ≥ 2 episodes of
during uterine contractions (episodes of acceleration
≥15bpm with fetal
FHR acceleration of ≥ 15
- Conditions at risk for preterm delivery movement w/in 30 mins) bpm of ≥ 15 second with
o Twins fetal movement within 30
o Polyhydramnios minutes
o Incompetent cervix
o Previous preterm labor Abnormal: < 2 episodes of
- Presence of spontaneous contractions acceleration or acceleration
of < 15 seconds duration
within 30 minutes
Biophysical Profile Testing (BPT)
Events during normal labor and delivery MAIN MECHANISMS OF PLACENTAL SEPARATION
- Shultz “Shiny Shultz”
- Ritgen maneuver
o Technique used to control - Duncan “Dirty Duncan”
delivery of baby’s head and Feature Shultz Duncan
minimize perineal trauma Site of Central Peripheral
separation
o Applying upward pressure on the
Hematoma Forms centrally, Blood escapes
fetal chin through the perineum formation pushes placenta as separation
while simultaneously guiding outward begins at the
edges
the head with the other hand
Presenting Fetal side (shiny, Maternal side
- Extension surface smooth) (rough
- External rotation cotyledons)
o Baby is facing the maternal thigh Amount of Minimal at first More obvious
external bleeding
o Nuchal cord – loop of cord found at bleeding
the neck of the baby; may hinder Appearance of Shiny Dirty, cotyledons
the delivery of the baby Placenta membranes/ visible
amnions left behind
- Expulsion
- Cord clamping
ACTIVE MANAGEMENT OF THE THIRD STAGE OF • Less pain
LABOR (AMTSL) • Better anatomical
results
- Protocols established by the Philippine
▪ Disadvantage
Board of Obstetrics and Gynecology to
• More prone to 4th
prevent maternal hemorrhage
degree laceration
- Attendance by providers with the
– involves the rectal
training and skills to actively manage the
lumen →
third stage
rectovaginal fistula
- Use of Uterotonics
(untreated)
o 10 units of oxytocin IM after the
o Mediolateral
delivery of the baby’s anterior
shoulder Lacerations
▪ Prevents excessive vaginal
- 1st degree: vaginal mucosa, fourchette,
bleeding by promoting
perineal skin
uterine contractions →
- 2nd degree: fascia and muscle surrounding
constricts vessels at the
the perineal body; most common
placental site
- 3rd degree: external anal sphincter
▪ Effective only in singleton
- 4th degree: rectal lumen
pregnancies; relatively CI
in multifetal gestations as it
may trap the other baby
during the process FOURTH STAGE OF LABOR
- Gentle traction on the umbilical cord - After the placenta has been delivered
o Prevents uterine inversion due to - Observe for postpartum hemorrhage
forceful pulling of the cord - Complications to observe:
- Timing of clamping of the umbilical o Vulvar hematoma – occurs when
cord a lacerated vestibular bulb vein
was not ligated properly
- Always check the episiotomy site if patient
EPISIOTOMY
complains of pain
- Surgical incision made in the mother’s
OXYTOCIC AGENTS
pudenda to assist in the delivery of the
baby and prevent severe lacerations - Promote uterine contractions
- Selective episiotomy: making the - Oxytocin
decision based in specific factors and o Given during pre-partum,
indications intrapartum, or postpartum period
o NOT ALL WOMEN in labor o Transient but marked fall in arterial
undergo episiotomy BP
- Routine episiotomy: performing the o Diluted IV or IM
incision regardless of individual ▪ Never give as IV bolus
circumstances o Directly to the uterus, vagina to
- Indications: control postpartum bleeding
o Expedite delivery o Antidiuretic action may lead to
o Spontaneous laceration is likely water intoxication
o Maternal/fetal distress o First line prophylactic uterotonic
o Breech position during 3rd stage labor
o Forceps delivery - Methylergometrine
o Large baby o Given only during the postpartum
o Maternal exhaustion period
- Types of incision o Ergot alkaloid
o Median/Midline o IM or Oral route
▪ Advantages o Side effects: IV route – HTN
• Easier to repair
- Misoprostol Qualities of smooth muscle aiding uterine
o Initially intended to manage contraction and fetal delivery
gastric symptoms; later found to
- Degree of smooth muscle shortening
stimulate uterine contractions
during contraction is greater
o Synthetic prostaglandin analogue
- Forces can be exerted in smooth muscle
o Not FDA approved
cells in multiple directions
▪ Used as abortifacient
- Thick and thin filaments of smooth
(abortive agent)
muscle are found in long, random
- Carbetocin
bundles
o Long-acting synthetic oxytocin
- Greater multidirectional force
analogue
generation in uterine fundus than lower
o Induces uterine contraction
uterine segment
Decidua
PARTURITION - Endometrium that is transformed by
- Encompasses the entire physiological pregnancy hormones
process of giving birth - Composed of stromal cells and maternal
- 4 phase process immune cells
- Maintain pregnancy by
LABOR immunoregulation that suppress
inflammatory signals during gestation
- Subset of parturition
o Prevents rejection of the foreign
- Begins with the onset of regular uterine
fetus
contractions and ends with delivery of
- At the end of pregnancy, transitions to
NB and expulsion of the placenta
induce inflammatory signals and withdraw
MATERNAL AND FETAL COMPARTMENTS immunosuppression
Uterus Cervix (function)
- Composed of 3 layers - Maintain epithelial barrier to protect
o Serosa from infection
o Myometrium - Sustain competence despite
▪ Composed of bundles of gravitational forces as the fetus grows
smooth muscle cells - Orchestrates ECM changes allowing
surrounded by connective greater tissue compliance
tissue
Placenta
▪ Smooth muscle cells are
not terminally - Area for nutrient and waste exchange
differentiated between mother and fetus
▪ Adaptable to - Source of steroid hormones, growth
environmental changes factors and other mediators that maintain
o Endometrium pregnancy
- Stimuli, such as stretch, inflammation, and - Amnion and chorion, and decidua serve as
hormones modulate transition of these shield against untimely parturition
cells into phenotypes that provide: initiation
o Cell growth
AMNION CHORION
o Proliferation
- Towards the fetal - Maternal side
o Secretion side - Provides
o Contractility - Provide tensile immunological
strength to fetal acceptance
membrane to resist - Rich with enzyme
tearing and rupture that inactivate
- Avascular; highly uterotonins in the
resistant to early part of pregnancy:
penetration by
leukocytes, o Prostaglandin
microorganisms, dehydrogenase
neoplastic cells o Oxytocinase FOUR PHASES OF PARTURITION
- Selective filter to o Enkephalinase
protect maternal - Phase 1: Quiescence
tissues from amniotic
fluid content
- Phase 2: Activation
o Prevents - Phase 3: Stimulation
amniotic fluid - Phase 4: Involution
embolism
PHASE 1: QUIESCENCE AND CERVICAL
SOFTENING – PRELUDE TO PARTURITION
ROLE OF HORMONES
- 95% of pregnancy
- Estrogen
- Myometrial cells are in a noncontractile
o Promotes parturition
state
o Enhance progesterone
o Uterine muscle is unresponsive to
responsiveness
natural stimuli
- Progesterone
- Braxton Hicks may occur
o Inhibits parturition
o Low amplitude contractions
o Removal of progesterone precedes
o Not cause cervical dilatation
progression of parturition
- Prostaglandins Quiescence is achieved through:
o Lipid-derived molecules
- ↓ intracellular crosstalk and ↓
o Role:
intracellular Ca2+ levels
▪ Myometrial contractility
o prevents muscle contraction by
▪ Relaxation
lowering calcium needed for actin-
▪ Inflammation
myosin interaction.
o Amnion is the major source of
- Ion channel regulation of cell
prostaglandins in amniotic fluid
membrane potential
Side note o Keeps the uterus electrically stable
and less excitable, preventing
Prostaglandin Synthesis
contractions
- Arachidonic acid in phospholipid stores is - Activation of stress-unfolded protein
released from membrane phospholipids by response by the uterine endoplasmic
Phospholipase A2 (PLA2) or Phospholipase reticulum
C (PLC) o ↑ caspase activity (anti-
- Arachidonic acid is converted into PGH2 contractile agent) → degrades actin
by: and gap junction Connexin 43
o Prostaglandin H synthetase – 1 ▪ Caspase 3: muscle
(PGHS-1/COX1) wasting and reduced
o Prostaglandin H synthetase – 2 muscle tension; degrades
(PGHS-2/COX2) connexin 43
- PGH2 is acted upon by PG isomerase to ▪ Connexin 43: cell-cell
convert it to: communication through
o Prostaglandin E2, F2a, and I2 – gap junctions
active prostaglandins involved in o Limits protein misfolding and
parturition inflammation, helping maintain a
- PGE2, PGF2a, PG12 are converted into relaxed state.
inactive metabolites mediated by - Uterotonin degradation
prostaglandin dehydrogenase (PGDH) o Decreases stimulatory hormones
o Ensures uterine quiescence is (e.g., prostaglandins, oxytocin),
maintained when labor is not reducing contraction signals.
imminent
Myometrial Contractility is achieved by: Uterine Relaxation
Exercise Coitus