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Intrapartum Assessment

This document discusses intrapartum assessment and electronic fetal monitoring. It describes direct and indirect fetal monitoring methods. Factors indicating the need for continuous electronic fetal monitoring include abnormal fetal heart rate, meconium staining, and certain maternal factors like fever or bleeding. The document outlines how to evaluate fetal status during monitoring using the DR BRAVADO method of determining risk, assessing contractions, baseline rate, variability, accelerations, and decelerations. Normal and abnormal findings for each parameter are defined. Monitoring provides information on fetal wellbeing during labor and delivery.

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Yanyan Panes
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0% found this document useful (0 votes)
63 views89 pages

Intrapartum Assessment

This document discusses intrapartum assessment and electronic fetal monitoring. It describes direct and indirect fetal monitoring methods. Factors indicating the need for continuous electronic fetal monitoring include abnormal fetal heart rate, meconium staining, and certain maternal factors like fever or bleeding. The document outlines how to evaluate fetal status during monitoring using the DR BRAVADO method of determining risk, assessing contractions, baseline rate, variability, accelerations, and decelerations. Normal and abnormal findings for each parameter are defined. Monitoring provides information on fetal wellbeing during labor and delivery.

Uploaded by

Yanyan Panes
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd
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INTRAPARTUM

ASSESSMENT
(CARDIOTOCOGR
OB Clinical Clerk Faigani

APHY-CTG)
OBJECTIVES
 Learn how to evaluate fetal status
 Enumerate and define different methods of
evaluating fetal status
 Discuss briefly the categories of FHR CTG traces
 Compare Non stress Test and Contraction Stress
Test
ELECTRONIC FETAL
MONITORING
 Direct / Internal electronic fetal
monitoring

 Indirect / External electronic fetal


monitoring
DIRECT / INTERNAL ELECTRONIC
FETAL MONITORING
 Direct fetal heart measurement is accomplished by
attaching a bipolar spiral electrode directly to the fetus
EXTERNAL (INDIRECT)
ELECTRONIC MONITORING
 The fetal heart rate is detected through the
maternal abdominal wall using the ultrasound
Doppler principle.
EXTERNAL (INDIRECT)
ELECTRONIC MONITORING
Consists of:

 Transducer
 Sensor
 Coupling gel
 Belt
Reflected ultrasound signals
from moving fetal heart
valves are analyzed through a
process, called
autocorrelation.
RECOMMENDATIONS FOR
INTRAPARTUM FHR
MONITORING
WHEN?
FACTORS THAT INDICATE USE OF
CONTINUOUS ELECTRONIC FETAL
MONITORING

Fetal Factors:

 Abnormal fetal heart rate on


auscultation or admission tracing (20-
minute strip)*
 Meconium-stained amniotic fluid

Liston R, Sawchuck D, Young D, for the Society of Obstetrics and Gynaecologists of Canada, and the British Columbia Perinatal Health Program. Fetal health surveillance: antepartum and
intrapartum consensus guideline. No. 197 (replaces No. 90 and No. 112) [published correction appears in  J Obstet Gynaecol Can. 2007;29(11):909]. J Obstet Gynaecol Can. 2007;29(9 suppl
4):S33.
FACTORS THAT INDICATE USE OF
CONTINUOUS ELECTRONIC FETAL
MONITORING

Maternal Factors:
 Hypertonic uterus
 Induced or augmented labor
 Intrauterine infection or
chorioamnionitis
 Post-term pregnancy (> 42 weeks'
gestation)
 Preterm labor (< 32 weeks' gestation)

Liston R, Sawchuck D, Young D, for the Society of Obstetrics and Gynaecologists of Canada, and the British Columbia Perinatal Health Program. Fetal health surveillance: antepartum and
intrapartum consensus guideline. No. 197 (replaces No. 90 and No. 112) [published correction appears in  J Obstet Gynaecol Can. 2007;29(11):909]. J Obstet Gynaecol Can. 2007;29(9 suppl
4):S33.
FACTORS THAT INDICATE USE OF
CONTINUOUS ELECTRONIC FETAL
MONITORING
 Maternal Factors:

 Previous cesarean delivery


 Prolonged membrane rupture > 24 hours at
term
 Regional analgesia, particularly after initial
bolus and after top-ups (continuous electronic
fetal monitoring is not required with mobile or
continuous-infusion epidurals)
 Vaginal bleeding in labor

Liston R, Sawchuck D, Young D, for the Society of Obstetrics and Gynaecologists of Canada, and the British Columbia Perinatal Health Program. Fetal health surveillance: antepartum and
intrapartum consensus guideline. No. 197 (replaces No. 90 and No. 112) [published correction appears in  J Obstet Gynaecol Can. 2007;29(11):909]. J Obstet Gynaecol Can. 2007;29(9 suppl
4):S33.
HOW?
NATIONAL INSTITUTE OF
CHILD HEALTH AND HUMAN
DEVELOPMENT (2008)
 DR C BRAVADO
DR - Determine risk
C - Contractions
BRA - Baseline rate
V - Variability
A - Accelerations
D - Decelerations
O - Overall assessment and written plan
DETERMINE RISK

High
Moderate
Low risk
CONTRACTIONS
Frequency – time between start of
contraction to start of next contraction

Duration – time from the start of


contraction to end of same contraction

Interval – amount of time between end of


one contraction to start of another
CONTRACTIONS
Intensity – measure of how strong a
contraction

Resting tone – measure of how relaxed


the uterus is between contractions
CONTRACTIONS

Normal - no more than (<5) five


contractions in a 10-minute
period.
Tachysystole
>5 contractions in a 10-minute
period, averaged over a 30-
minute window
TACHYSYSTOLE
CONTRACTIONS
 Montevideo units
 Uterine performance is the product of the
intensity – increased uterine pressure above
the baseline tone
 An MVU of >200 predicts normally
progressive labor 90% of the time
 An MVU < 200 suggest protraction of labor
or frank arrest of labor
CONTRACTIONS
 calculated by obtaining the peak uterine pressure
amplitude and subtracting the resting tone. Then
multiply the difference is multiplied to the # of
contractions within a 10-minute window.

 Example
 A patient has baseline of 15 mmHg with 4
contractions, each of which has a peak pressure of
70 mmHg.

 70-15=55
 MVU- 55x4= 220
CONTRACTIONS

 Contractions
 Clinically palpable after intensity
exceeds 10 mmHg
 Associated with pain if it exceeds 15
mmHg
CONTRACTIONS
First 30 weeks of pregnancy
 Quiescent
 Contractions seldom > 20 mmHg

After 30 weeks of pregnancy


 Increase in intensity and frequency
CONTRACTIONS
Last weeks of pregnancy
Further increase in uterine pregnancy –
prelabor

Clinical labor
- 80 to 12o montevideo units
DEFINITION OF
TERMS
 Baseline
 Baseline Variability
 Acceleration
 Early Deceleration
 Late Deceleration
 Variable Deceleration
 Prolonged Deceleration
 Sinusoidal Pattern
BASELINE
 The mean FHR rounded to increments of
5 bpm during a 10-min segment,
excluding:

 Periodic or episodic changes


 Segments of baseline that differ by >25bpm
BASELINE

 The baseline must be for a minimum of 2


min in any 10-min segment or the
baseline for that time period is
indeterminate
BASELINE
 With increasing fetal maturation, heart
rate decreases
 Corresponds to the maturation of the
parasympathetic (vagal) heart control

 Baseline decreased an average of 24 bpm


between 16 weeks and term (1 bpm/week)
Average FHR
 tonic balance between the
accelerator (sympathetic) and
decelerator (parasympathetic)
influences on pacemaker cells

 Control of arterial chemoreceptors


BASELINE
Normal FHR: 110-160 bpm

Tachycardia: >160 bpm

Bradycardia: <110 bpm


NORMAL BASELINE

 Normal baseline fetal heart rate (FHR), shown at 135 beats per minute (bpm). Normal baseline rate ranges
from 110 to 160 bpm for a 10-minute segment and duration ≥ 2 minutes. Excludes periodic and episodic
changes, marked variability, and segments differing by ≥ 25 bpm.
BRADYCARDIA
BRADYCARDIA
 Causes:
• Congenital heart block
• Serious fetal compromise
• Maternal hypothermia
• Severe pyelonephritis
TACHYCARDIA

 Tachycardia of fetal heart rate (FHR), shown at 170 beats per minute (bpm). Baseline rate with tachycardia is > 160 bpm.
TACHYCARDIA
 Causes:
• Maternal fever from chorioamnionitis
• Fetal compromise
• Cardiac arrhythmias
• Maternal administration of parasympathetic
(atropine) or sympathomimetic (terbutaline)
drugs
BASELINE VARIABILITY
An important index of
cardiovascular function and is
regulated by autonomic nervous
system

Fluctuations in the baseline FHR


that are irregular in amplitude and
frequency
BASELINE VARIABILITY
Quantified as the amplitude of
peak-to-trough in bpm

Absent – undetectable
Minimal - <5 bpm
Moderate - 6-25 bpm
Marked - >25 bpm
ABSENT

 Amplitude range of FHR tracing is undetectable.


MINIMAL

Amplitude range of FHR tracing ≤ 5 beats per minute.


MODERATE

 Amplitude range of FHR tracing is 6 to 25 beats per minute.


MARKED

 Amplitude range of FHR tracing > 25 beats per minute.


SHORT TERM VARIABILITY

instantaneous change in fetal heart


rate from one beat – or R wave – to the
next
LONG TERM VARIABILITY

oscillatory changes during 1 minute and


results in the waviness of baseline
INCREASED
VARIABILITY
Factors that causes increased
variability:
 Fetal breathing
 Fetal body movements
 Advancing gestational age
DECREASED
VARIABILITY

Factors that causes decreased variability:


 Hypoxemia
 A result of metabolic acidemia that
causes depression of the fetal
brainstem or the heart itself.
 analgesic drugs
 It is generally believed that reduced
baseline heart rate variability is
the single most reliable sign of fetal
compromise.
ACCELERATION
Visually apparent abrupt increase
(onset to peak in <30s) in the FHR

Prolonged acceleration was defined


as 2 minutes or more but less than
10 minutes.
Proposed mechanisms for
intrapartum accelerations
include:
- fetal movement
- stimulation by uterine
contractions
- umbilical cord occlusion
- fetal stimulation during pelvic
examination
DECELERATION
A decrease below the baseline
rate

Early
Late
Variable
 Early decelerations are termed head
compression

 Late decelerations are termed


uteroplacental insufficiency

 Variable decelerations become cord


compression patterns.
EARLY DECELERATION

This consists of a gradual


decrease and return to baseline
associated with a contraction.
Head
compression

Dural
stimulation

Vagal nerve
activation

Heart rate
deceleration
LATE DECELERATION

 A late deceleration is a smooth,


gradual, symmetrical decrease in
fetal heart rate beginning at or after
the contraction peak and returning to
baseline only after the contraction
has ended.
A gradual decrease is defined as
30 seconds or more from the
onset of the deceleration to the
nadir.

In most cases, the onset, nadir,


and recovery of the deceleration
occur after the beginning, peak,
and ending of the contraction,
respectively
VARIABLE DECELERATION

 Variable deceleration is defined as an


abrupt decrease in the fetal heart
rate beginning with the onset of the
contraction and reaching a nadir in less
than 30 seconds.
The decrease must last between
≥ 15 seconds and 2 minutes
and must be ≥ 15 bpm in
amplitude.
Partial or complete cord
occlusion

Increase in afterload (baroreceptor) and a


decrease in fetal arterial oxygen content
(chemoreceptor)

Vagal activity

DECELERATION
Variable decelerations represent
fetal heart rate reflexes that
reflect either blood pressure
changes due to interruption of
umbilical flow or changes in
oxygenation
American College of Obstetricians
and Gynecologists (2013)
 recurrent variable decelerations
with minimal to moderate
variability are indeterminate,
whereas those with absent
variability are abnormal.
PROLONGED DECELERATION

 An isolated deceleration greater than 15 bpm lasting 2 minutes


or longer but < 10 minutes from onset to return to baseline.

Common causes include:


 cervical examination
 uterine hyperactivity
 cord entanglement
 maternal supine hypotension
 Placental abruption
 Umbilical cord knots or prolapse
 Maternal seizures
SINUSOIDAL PATTERN
 Visually apparent, smooth, sine wave-line
undulating pattern in FHR baseline with a cycle
frequency of 3-5 per minute which persists for 20 min
or more
NATIONAL INSTITUTES OF HEALTH
WORKSHOPS
THREE-TIER CLASSIFICATION SYSTEM

Category I – Normal
Category II – Indeterminate
Category III – Abnormal
CATEGORY I—NORMAL

Include all of the following:


• Baseline rate: 110–160 bpm
• Baseline FHR variability: moderate
• Late or variable decelerations: absent
• Early decelerations: present or
absent
• Accelerations: present or absent
CATEGORY II –
INDETERMINATE
 Include all FHR tracings not categorized
as Category I or III
 Baseline rate:
 Bradycardia not accompanied by absent
baseline variability
 Tachycardia

 Baseline FHR variability:


 minimal, absent, marked
CATEGORY II –
INDETERMINATE
 Accelerations:
 absence of induced accelerations after fetal
stimulation
 Periodic or episodic decelerations
 Recurrent variable decelerations accompanied by
minimal or moderate baseline variability
 Prolonged decelerations >2min but <10 min
 Recurrent late decelerations with moderate
baseline variability
 Variable decelerations with other characteristics,
such as slow return to baseline, “overshoots” or
“shoulders”
CATEGORY III – ABNORMAL

 Include either
 Absent baseline FHR variability and
any of the following:
 Recurrent late decelerations
 Recurrent variable decelerations
 Bradycardia

 Sinusoidal pattern
 Category I – Normal; strongly
predictive of normal fetal acid-base
status.
 Category II – Indeterminate; Not
predictive of abnormal fetal acid-
base status, but evaluation and
continued surveillance and
reevaluations are indicated.
 Category III – Abnormal; predictive
of abnormal fetal acid-base status &
requires prompt evaluation and
mamangement
NON STRESS
TEST
VS
CONTRACTION
STRESS TEST
NON STRESS TEST
 Evaluates the response of FHR to fetal
movement
 Based on the premise that the heart rate
of the fetus that is not acidotic or
neurologically depressed and will
temporarily accelerate with fetal
movement
NON STRESS TEST
 REACTIVE:
 At least 2 FHR acceleration occur for at least 15 bpm
from baseline lasting for 15s within 20 min observation
time
NON STRESS TEST
 NON REACTIVE:
 <2 accelerations
 Loss of reactivity associated with fetal sleep
cycle, acidosis or CNS depression
CONTRACTION STRESS
TEST
 Goal: to identify a fetus at risk for
compromise by observing the fetus in
the presence of stress
 Evaluates the reaction of the FHR to
contraction induced by either nipple
stimulation or oxytocin administration
 Testing is stopped once 3 contraction/10
minutes has been established
CONTRACTION STRESS
TEST
 POSITIVE:
 Presence of late deceleration with at least
50% of the contraction
CONTRACTION STRESS
TEST
 NEGATIVE:
 No late or significant variable decelerations,
with at least 3 uterine contraction in 10
minutes
CONTRACTION STRESS
TEST
 EQUIVOCAL SUSPICIOUS
 Late deceleration with fewer than 50% of
contraction or significant variable
decelerations
CONTRACTION STRESS
TEST
 EQUIVOCAL UNSATISFACTORY
 <3 contractions occur within 10 minutes or
a tracing quality that cannot be interpreted
CONTRACTION STRESS
TEST
EQUIVOCAL TACHYSYSTOLE
 Contractions that occur more
frequently than every 2 minutes
or longer than 90s in the
presence of late decelerations
OTHER
INTRAPARTUM
ASSESSMENT
TECHNIQUE
OTHER INTRAPARTUM
ASSESSMENT TECHNIQUES
 Fetal Scalp Blood Sampling
 Scalp Stimulation
 Vibroacoustic Stimulation
 Fetal Pulse Oximetry
 Fetal Electrocardiography
 Intrapartum Doppler Velocimetry

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