ctg o&g
TRANSCRIPT
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Ali SungkarSub Bagian Fetomaternal
Bagian Obstetri dan Ginekologi FKUI/RSUPN - CM
Cardiotocography ( CTG )Electronic Fetal Monitoring
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Fetal Monitoring
• Track the baby’s heart rate during labor.
• Safe procedure that has saved the lives of many babies in high-risk situations.
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Electronic Monitoring
• Indirect (External monitoring)
•Direct (Internal monitoring)
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EFM-ISSUES
Detect fetal hypoxia i.e reduce and avoid harm to the fetus and improve fetal and baby out-come.
Severe acidosis may result in FHR changes.
Could occur in Normal physiological response in labor.
Misunderstanding the physiological and pathphysiological CTGs will improve the Mx ( management).
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EFM Problems and Realities
Electronic Intra-partum FHR Monitoring is now considered mandatory for high-risk pregnancies.
Difficulties with interpretation include over confidence and not-only difference in opinion between practitioners but, also when the same practitioner examines the same CTG twice.
Increases CS rates 1.41%rr. Increases operative vaginal delivery 1.20%rr. And no change in incidence of C Palsy. Reduction in Neonatal seizures rates 0.51% No difference in APGAR scores. ? About the efficacy.
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EFM- Facts
Reliability of interpretation-50-75% are false positive .
False positive Dx reduces to 105 with FBS.
FBS 93% sensitivity, 6% false positive.
PH Vs Lactate -39% Vs 2.3(rr 16.7).
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Electronic Fetal Monitoring-Indications
• Oligohydramnios
• Hypertension.
• Abnormal FHR detected.
• Malpresentation and in labour.
• DM,Multiple Gestation.
• Previous CS.
• Abdominal Trauma.
• Prolonged ROM.
• Meconium Liq.
• High risk pregnancies
• IOL and Augmentation of Labour.
• Reduced FM.
• Premature labour/TPL.
• APH/IPH
Indications for the continuous EFM
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EFM- Interpretation
Consider :
• Intrapartum / antepartum trace.
• Stage of labour.
• Gestation.
• Fetal presentation, ? Malpresentation.
• Any augmentation,? Induction labor Medications ?
• Direct or indirect monitoring
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EFM- 4 Basic Features of FH Trace
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EFM- 4 Basic Features.
• Baseline FHR - Mean level of FHR when this is stable, excluding Accelerations and Decelerations (110-160 bpm)
-Tachycardia
-Bradycardia Baseline Variability-5 bpm or greater than or
equal to 5bpm, between contractions
-Normal
-Non-reassuring-Less than 5 bpm or less but less than 30 min
-Abnormal-less than 5 bpm for 90 min or more.
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Uterine Contraction
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Baseline variability CTGBaseline variability
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FHR: Variability
• Definitions– Short term– Long term
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Baseline variability
• The minor fluctuations on baseline FHR at
3-5 cycles p/m produces Baseline
variability.
• Examine imin segment and estimate
highest peak and lowest trough.
• Normal is more than or equal to 5 bpm.
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Factors affecting Baseline variability.
• Para-Sympathetic affects short term
variability whilst Long Term is more Symp.
• CNS ,Drugs reduce Variability
• High gestation increases variability
• Mild Hypoxia may cause both S and para S
stimulation.
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Non-reassuring Baseline variability.
• NR CTGs- reduced or less than 5 bpm for 40
min or more but less than 90 mins..
• B-B or short Term V is varying intervals
between successive heart beats .
• Long Term v is irregular waves on the CTG
3-5 bpm.
• Normal is 5-25 bpm– this indicates N-CNS.
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EFM-Accelerations
• Accelerations- transient increase in FHR of
15 bpm or more lasting for 15 sec.
• Absence of accelerations on an otherwise
normal CTG remains un clear.
• Presence of FHR Accelerations have Good
outcome.
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EFM Decelerations
• Decelerations-
transient slowing of
FHR below the
baseline level of
more than 15 bpm
and lasting for 15 sec.
Or more.
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Electronic Fetal Monitoring
• a) Early Decelerations
Head compression
Begins on the onset of contraction and
returns to baseline as the contraction
ends.
Should not be disregarded if they
appear early in labor or Antenatal.
Clinical situation should be r/v
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Early Decelerations
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Late Decelerations.
• Uniform periodic slowing of FHR with the on
set of the contractions .
• Repetitive late decels increases risk of
Umbilical artery acidosis and Apgar score of
less than 7 at 5 mins and Increased risk of
CP.
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Electronic Fetal Monitoring
b) Late Decelerations • Due to acute and chronic feto-placental
vascular insufficiency Occurs after the peak and past the length of
uterine contraction, often with slow return to the baseline.
Are precipitated by hypoxemia Associated with respiratory and metabolic
acidosis Common in patients with PIH, DM, IUGR or
other form of placental insufficiency.
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Late Decelerations
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Late Decelerations
• Reduces Baseline variability together
with Late Decelerations or Variable
Decelerations is associated with
increased risk of CP.
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EFM- Variable Decelerations• Variable intermittent periodic slowing of FHR with
rapid onset recovery and isolation.• They can resemble other types of deceleration in
timing and shape.• Atypical VD are associated with an increased risk
of umbilical artery acidosis and Apgar score less than 7 at 5 min
• Additional components:• Loss of 1 degree or 2 degree rise in baseline Rate• Slow return to baseline FHR after and end of
contraction.• Prolonged secondary rise in Base FHR • Biphasic deceleration• Loss of variability during deceleration • Continuation of base line at a lower level.
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Electronic Fetal Monitoring
c) Variable Deceleration (Vagal activity)• Inconsistent in configuration, • No uniform temporal r-ship to the onset of
contraction, are variable and occur in isolation.• Worrisome when Rule of 60 is exceeded (i.e.
decrease of 60 bpm,or rate of 60 bpm and longer than 60 sec)
• Caused by cord compression of the umbilical cord• Often associated with Oligo-hydroaminos with or
without ROM• Can cause short lived RDS if they MILD• Acidosis if prolonged and Recurrent.
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Variable Decelerations
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References
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EFM Prolonged deceleration
Prolonged Deceleration
• Drop in FHR of 30 bpm or More lasting for at least 2 min
• Is pathological when crosses 2 contractions i.e 3 mins.
• Reduction in O2 transfer to placenta.
• Associated with poor neonatal outcome.
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EFM- Prolonged DecelerationsCAUSES
• Cord prolapse.
• Maternal hypertension
• Uterine Hypertonia
• Followed by a Vag Exam or ARM or SROM
with High PP.
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Prolonged Deceleration
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EFM Mx Prolonged Deceleration
• Maternal position
• IV fluids
• V.E to exclude cord prolapse
• Assess BP
• FBS if cx dilated and well applied PP
• Mx Depending on the clinical situation.
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Baseline Bradycardia
• FH below 110bpm(FIGO ).
• less than 100bpm (RANZCOG).
Causes.
Postdates, Drugs, Idiopathic,
Arrythmias, hypothermia(increased Vagal Tone)
Cord Compression (Acute Hypoxia, congenital H disease and Drugs).
Mx depends on the clinical situation.(FBS,Vag Exam, Observation or expedite delivery)
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Types
• Moderate Bradycardia 100-109 bpm
• Abnormal bradycardia less than 100bpm.
• Tachycardia 161-180 bpm
• Abnormal Tachycardia more than 180
bpm
• Ranzcog Australian more than 170 bpm
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Baseline tachycardia and Bradycardia.
• Uncomplicated baseline tachycardia
161-180 bpm or bradycardia 101-109
do not appear to be associated with
poor NN outcome.
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Causes of B Tachycardia.
• Asphyxia
• Drugs
• Prematurity
• Maternal Fever
• Maternal thyrotoxicosis
• Maternal Anxiety
• Idiopathy
• Mx depends on the clinical situation
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Electronic Fetal MonitoringBaseline Bradycardia
FH Rate below 110bpm (FIGO Recommended)
Postdates
Drugs
Idiopathic
Arrhythmia's
Hypothermia.(Increased Vagal tone),
Cord compression(Acute Hypoxia,Congenital H/disease, and drugs)
Mx depends on the clinical situation. (FBS, Vag Exam , Observation or expedite Delivery).
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Electronic Fetal Monitoring
Baseline Tachycardia Asphyxia Drugs Prematurity Maternal fever Maternal thyrotoxicosis Maternal Anxiety Idiopathy
Mx depends on the clinical situation
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Sinusoidal patternInterpretation of the CTG
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EFM-Sinusoidal Pattern
• Regular Oscillation of the Baseline long-term
Variability resembling a Sine wave ,with no B-
b Variability
• Has fixed cycle of 3-5 p min. with amplitude of
5-15 bpm and above but not below the
baseline.
• Should be viewed with suspicion as poor
outcome has been seen (eg Feto-maternal
haemorrhage)
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Electronic Fetal Monitoring
Sinusoidal pattern- distinctive smooth undulating
Sine-wave baseline with no B-b variability
• 0.3 % (Young 1980)
• cord compression
• hypovolemia
• ascites
• idiopathic(fetal thumb sucking)
• Analgesics
• Anaemia
• Abruption
• Mx r/v clinical situation
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EFM- Saltatory pattern
• Seen During Fetal thumb sucking.
• Could be associated with Hypoxia.
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NR CTGs
• Difficult to interpretation,leads to Increased
rate of C Section.
• 50% CTG in Labour have 1 abnormal feature
• 15-20% Nr CTGs (pathological).
• ?? To reduce CS….
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EFM-Summary
• Normal - CTG with all 4 Features
• Suspicious -one non reassuring category
and reminder are reassuring
• Pathological -2 or more non-reassuring
categories or one or more abnormal
categories.
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Caring for the Mom, Not the Monitor!
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References
• Manual Obs and Gyn. by Niswander, MD
• Fetal Monitoring RCOG UK
• CTGs RANZCOG
• Literature review articles American Family Physician
• CTG Made Easy
• D. Lata Sharma, MD, FRANZCOG, Senior Lecturer,
University Of Queensland, Australia
• Charles Kawada, M.D,Harvard Medical School