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INTRAPARTUM FETAL MONITORING




   DR MANAL BEHERY
 Zagazig University, EGYPT
The three unique risk factors for fetus
            during labor

Factor of uterine contraction


Factor of cord accident


Factor of head compression
Factor of uterine contraction

 Let us see what happen to oxygenation
 and blood supply of the fetal brain during
 a uterine contraction?
 De-oxy-Hb   0.79micromol/100Gm of brain
 Oxy –Hb 0.19 0.79micromol/100Gm of brain


 CerebralO2 saturation      9%

 Cerebral blood volume    0.33 ml/100Gm of
In spite of this slightly worrying picture,
Nothing harmful effect happen if
 fetus is healthy
 labor contraction are normal
 Placenta has adequate reserve
Fetal distress, birth asphxia are likely
               to occur if

 The fetus is already compromised
 antenatally---even with normal uterine
 contraction

 The uterine contraction are
 exaggerated------even with healthy
 fetus and adequate placental reserve
Factor of cord accident

 Only during labor cord prolaps ,presentation
 and entanglements (occult or overt) become
 apparent either by compression or stretch
 secondary to uterine contraction
Factor of head compression

 Some degree of compression is inevitable
  during normal labor But
 Excessive compression over long period
  causing supermoulding
as in obstructed labor
 may cause fetal hypoxia
Methods available for fetal monitering
              in labor
 Intermittent auscultation


 CTG Fetal electrocardiography
   Scalp stimulation

   Vibroacoustic stimulation

 Fetal scalp sampling  PH determination


 Fetal pulse oximetry
Important        definations

 Hypoxia: Decreased po2 level in tissues.


 Hypoxima: Decreased po2 level in blood.


 Acidosis: Decreased PH in tissues.


 Acidemia: Decreased PH in blood.


 Ashyxia: Hypoxia with acidosis.
Aim of intrapertum fetal monitering



 1- to detect the earliest stages of hypoxia or
 (hypoxic acidemia ) so therapy can be
 directed to prevent asphyxia and asphyxial
 damage

 2-To Improve perinatal morbidity &
 mortality
What is Cardiotocography(CTG)?

 It is a paper record of the continuous FHR
 blotted simultaneously with a record of
 uterine activity
 Ultrasound (cardio)
  transducer
 Tocotransducer
External monitoring

Doppler ultrasound transducer
   FHR
Tocotransducer(contraction)
Internal monitoring
What is ‘’Admission test ‘’?

 Ideally every fetus every fetus should be screened by
 CTG for a short period (20 min) right on admission
 in labor.
From nature of the trace determine
 Intensity of monitoring “Whether  the case
 should be monitored clinically or by CTG”
Duration and frequency of monitoring
 “Whether the case should be covered by CTG
 continuously or intermittently”
Interpreting FHR trace
 4 components


  Base   line FHR

  Baseline   variability

  Accelerations



  Decelerations
Baseline FHR

 The dominant reading taken ≥10 min
 Normal baseline FHR 110-160(pbm)


 Controlled by
atrial
pacemaker
Tachycardia FHR>160 bpm
Baseline bradycardia FHR<110bpm
Baseline varibility

The Oscaltatory pattern of FHR when
  recorded on a graph.
Short term(beat t0 beat)
 is the fluctuation of HR over short interval
Long term
 is the fluctuation over long interval(≥2 min)


Indicates mature fetal neurologic system
Baseline varibility

 Short term variability
(scalp electrode)




 Long term variability
 defined as 3-5 cycle/min
Baseline varibility
No variability (0-2   /   )




  Minimal variability (3-4          /       )




Moderate variability (11-25             /       )




Mark variability (>25           /   )
Changes in fetal HR

Peroidic changes: Occur with
 contraction

Episodic changes (non peroidic):do not
 occur with contraction
Accelaration

 Increase in FHR with contraction or
  with other activities
 Can be periodic or episodic
 Increase15pbm
 lasting 15 sec
 Return to base line <2 min
Accelaration
Decelerations
                 Decelerations
Transient slowing of
FHR below the
baseline level
more than 15 bpm

and lasting for 15 sec.
or more.
Early Decelerations

   Uniform

   Synchronous with contraction (mirror
    image)
   Rarely fall below 110 (pbm)
   Due to head compression

   Should not be disregarded

if they appear early in labor or Antenatal.
Early Decelerations
Late Deceleration

 Uniform
 Start after peak of contraction
 Associated with decreased
Variability
 Reflect a baroreceptor
response
 Indicate fetal hypoxia
Late Deceleration
Repetitive late decelration

increases risk of
 Umbilical artery acidosis


 Apgar score < 7 at 5 ms


 Cerebral palsy
 If associated with
decrease or loss of
 variability
Variable Deceleration (the most
                 common type)
 Varible in appearance and Timing.
 May be assoicated with
    increased variability .

 Reflect umbilical cord compres
 Observed in up to 50% of NSTs compression
• Of no clinical significance
    if non recurrent

.
Variable Deceleration
Prolonged Deceleration
               deceleration
 A deceleration that lasts more than 90
 seconds (but less than 10 minutes)


   Drop in FHR of 30 bpm or More


 Reduction in O2 transfer to placenta.


 Associated with poor neonatal outcome
Prolonged Deceleration
Sinusoidal pattern

 Regular Oscillation of the Baseline long-term
  Variability resembling a Sine wave ,with no beat
  to -beat Variability.

 Has fixed cycle of 3-5 pbm 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)
Sinusoidal pattern
What are the features of a normal
               tracing?
 Baseline FHR 110-160 BPM




 Baseline Variability > 5 pbm (10-25)


 2 Accelerations > 15 BPM > 15 sec / 20 min
 trace



 No decelrations
Normal -Reassuring CTG
Interpertation of CTG

 Normal -Reassuring(R)-   CTG with all 4
 Features

 Suspicious (equivocal)- one non reassuring
 category and reminder are reassuring

 Abnormsal -Non reasurring (NR) -  2 or
 more non-reassuring categories or one or
 more abnormal categories.
Is Normal   CTGs always Reassuring?

 With normal CTC the chance of fetus to
 develop hypoxia is 1.5% due to
 unpredictable acute events

 So a normal CTG is always Reassuring
Is NR CTGs always worrisome ?

60% CTG in Labour have 1 abnormal feature


Only 15-20% of NR CTGs are pathological.


High false positive rate with unnecessary
 operative intervention for fetal distress.

Thus NR CTG is not always worrisome.
?? To reduce CS….
Consider these factors with abnormal
                 CTG
 Clinical indication of doing CTG
 Abnormal patch of tracing from high risk case differ
  that from no risk case
 Maturity of the fetus
 Reduced variability and baseline tachycardia is
  conmen in preterm
 State of maternal pulse
Drugs may cause maternal tachycardia– fetal
  tachycaedia
 Check blood pressure for hypotension in patients
  on Epidural
Consider these factors with abnormal
                 CTG
 Posture of patient during CTG
o Supine position give abnormal tracing
o Some cord compression can get released by change
  posture and must be tried with variable deceleration
 Congenital fetal malformation
Color Doppler of fetal heart to exclude congenital
  heart block
Stage of labor and expected time of
 delivery Wether to deliver immediate or give
 sometime under close observation
Suspicious (Equivocal)CTG

 Do continuous monitoring for further
 development towards better or worse trace
 while instituting the corrective measures.

 Ideally check condition of fetus by FAS or
 FBS or scalp stimulation test.

 However ,if liquor is meconium stained ---
 Deliver immediately
Correct reversible causes

 Change mother position from supine to left
 lateral position-----increase uterine blood flow

 Improve maternal oxygenation—100% O2 by
 masK
Correct maternal hypotension –IV fluid

 Decrease or stop any oxytocin infusion


 Remove vaginal prostaglandins
Secondary tests of fetal well-being

 Vibro-acoustic stimulation


 Used as a substitute for scalp sampling when
  CTG –is NR
 Normal ----------if FHR acceleration > 15
  bpm for 15 seconds within 15 seconds after
  the stimulation with prolonged fetal
  movements.
 Abnormal ----Only 50% have acidotic PH
Fetal blood sampling

 If the pH >7.25 --- observe.


 If the pH 7.2 and 7.25---repeated
within 30 minutes.

 If the pH <7.2----repeat immediately


 If pH still low -- Prompt delivery
 Scalp stimulation.
 Firm digital pressure


 Gentile pinch by atramatic Allis forceps


 Fetal pulse oximetry.
THANK YOU

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intrapartum fetal monitoring for undergraduate

  • 1. INTRAPARTUM FETAL MONITORING DR MANAL BEHERY Zagazig University, EGYPT
  • 2. The three unique risk factors for fetus during labor Factor of uterine contraction Factor of cord accident Factor of head compression
  • 3. Factor of uterine contraction  Let us see what happen to oxygenation and blood supply of the fetal brain during a uterine contraction?
  • 4.  De-oxy-Hb 0.79micromol/100Gm of brain  Oxy –Hb 0.19 0.79micromol/100Gm of brain  CerebralO2 saturation 9%  Cerebral blood volume 0.33 ml/100Gm of In spite of this slightly worrying picture, Nothing harmful effect happen if  fetus is healthy  labor contraction are normal  Placenta has adequate reserve
  • 5. Fetal distress, birth asphxia are likely to occur if  The fetus is already compromised antenatally---even with normal uterine contraction  The uterine contraction are exaggerated------even with healthy fetus and adequate placental reserve
  • 6. Factor of cord accident  Only during labor cord prolaps ,presentation and entanglements (occult or overt) become apparent either by compression or stretch secondary to uterine contraction
  • 7. Factor of head compression  Some degree of compression is inevitable during normal labor But  Excessive compression over long period causing supermoulding as in obstructed labor  may cause fetal hypoxia
  • 8. Methods available for fetal monitering in labor  Intermittent auscultation  CTG Fetal electrocardiography  Scalp stimulation  Vibroacoustic stimulation  Fetal scalp sampling  PH determination  Fetal pulse oximetry
  • 9. Important definations  Hypoxia: Decreased po2 level in tissues.  Hypoxima: Decreased po2 level in blood.  Acidosis: Decreased PH in tissues.  Acidemia: Decreased PH in blood.  Ashyxia: Hypoxia with acidosis.
  • 10. Aim of intrapertum fetal monitering  1- to detect the earliest stages of hypoxia or (hypoxic acidemia ) so therapy can be directed to prevent asphyxia and asphyxial damage  2-To Improve perinatal morbidity & mortality
  • 11. What is Cardiotocography(CTG)?  It is a paper record of the continuous FHR blotted simultaneously with a record of uterine activity  Ultrasound (cardio) transducer  Tocotransducer
  • 12. External monitoring Doppler ultrasound transducer FHR Tocotransducer(contraction)
  • 14. What is ‘’Admission test ‘’?  Ideally every fetus every fetus should be screened by CTG for a short period (20 min) right on admission in labor. From nature of the trace determine  Intensity of monitoring “Whether the case should be monitored clinically or by CTG” Duration and frequency of monitoring “Whether the case should be covered by CTG continuously or intermittently”
  • 15. Interpreting FHR trace  4 components  Base line FHR  Baseline variability  Accelerations  Decelerations
  • 16. Baseline FHR The dominant reading taken ≥10 min  Normal baseline FHR 110-160(pbm)  Controlled by atrial pacemaker
  • 19. Baseline varibility The Oscaltatory pattern of FHR when recorded on a graph. Short term(beat t0 beat)  is the fluctuation of HR over short interval Long term  is the fluctuation over long interval(≥2 min) Indicates mature fetal neurologic system
  • 20. Baseline varibility  Short term variability (scalp electrode)  Long term variability  defined as 3-5 cycle/min
  • 22. No variability (0-2 / ) Minimal variability (3-4 / ) Moderate variability (11-25 / ) Mark variability (>25 / )
  • 23. Changes in fetal HR Peroidic changes: Occur with contraction Episodic changes (non peroidic):do not occur with contraction
  • 24. Accelaration  Increase in FHR with contraction or with other activities  Can be periodic or episodic  Increase15pbm  lasting 15 sec  Return to base line <2 min
  • 26. Decelerations Decelerations Transient slowing of FHR below the baseline level more than 15 bpm and lasting for 15 sec. or more.
  • 27. Early Decelerations  Uniform  Synchronous with contraction (mirror image)  Rarely fall below 110 (pbm)  Due to head compression  Should not be disregarded if they appear early in labor or Antenatal.
  • 29. Late Deceleration  Uniform  Start after peak of contraction  Associated with decreased Variability  Reflect a baroreceptor response  Indicate fetal hypoxia
  • 31. Repetitive late decelration increases risk of  Umbilical artery acidosis  Apgar score < 7 at 5 ms  Cerebral palsy  If associated with decrease or loss of  variability
  • 32. Variable Deceleration (the most common type)  Varible in appearance and Timing.  May be assoicated with increased variability .  Reflect umbilical cord compres  Observed in up to 50% of NSTs compression • Of no clinical significance if non recurrent .
  • 34. Prolonged Deceleration deceleration  A deceleration that lasts more than 90  seconds (but less than 10 minutes)  Drop in FHR of 30 bpm or More  Reduction in O2 transfer to placenta.  Associated with poor neonatal outcome
  • 36. Sinusoidal pattern  Regular Oscillation of the Baseline long-term Variability resembling a Sine wave ,with no beat to -beat Variability.  Has fixed cycle of 3-5 pbm 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)
  • 38. What are the features of a normal tracing?  Baseline FHR 110-160 BPM  Baseline Variability > 5 pbm (10-25)  2 Accelerations > 15 BPM > 15 sec / 20 min trace  No decelrations
  • 40. Interpertation of CTG  Normal -Reassuring(R)- CTG with all 4 Features  Suspicious (equivocal)- one non reassuring category and reminder are reassuring  Abnormsal -Non reasurring (NR) - 2 or more non-reassuring categories or one or more abnormal categories.
  • 41. Is Normal CTGs always Reassuring?  With normal CTC the chance of fetus to develop hypoxia is 1.5% due to unpredictable acute events  So a normal CTG is always Reassuring
  • 42. Is NR CTGs always worrisome ? 60% CTG in Labour have 1 abnormal feature Only 15-20% of NR CTGs are pathological. High false positive rate with unnecessary operative intervention for fetal distress. Thus NR CTG is not always worrisome.
  • 43. ?? To reduce CS….
  • 44. Consider these factors with abnormal CTG  Clinical indication of doing CTG Abnormal patch of tracing from high risk case differ that from no risk case  Maturity of the fetus Reduced variability and baseline tachycardia is conmen in preterm  State of maternal pulse Drugs may cause maternal tachycardia– fetal tachycaedia  Check blood pressure for hypotension in patients on Epidural
  • 45. Consider these factors with abnormal CTG  Posture of patient during CTG o Supine position give abnormal tracing o Some cord compression can get released by change posture and must be tried with variable deceleration  Congenital fetal malformation Color Doppler of fetal heart to exclude congenital heart block Stage of labor and expected time of delivery Wether to deliver immediate or give sometime under close observation
  • 46. Suspicious (Equivocal)CTG  Do continuous monitoring for further development towards better or worse trace while instituting the corrective measures.  Ideally check condition of fetus by FAS or FBS or scalp stimulation test.  However ,if liquor is meconium stained --- Deliver immediately
  • 47. Correct reversible causes  Change mother position from supine to left lateral position-----increase uterine blood flow  Improve maternal oxygenation—100% O2 by masK Correct maternal hypotension –IV fluid  Decrease or stop any oxytocin infusion  Remove vaginal prostaglandins
  • 48. Secondary tests of fetal well-being  Vibro-acoustic stimulation  Used as a substitute for scalp sampling when CTG –is NR  Normal ----------if FHR acceleration > 15 bpm for 15 seconds within 15 seconds after the stimulation with prolonged fetal movements.  Abnormal ----Only 50% have acidotic PH
  • 49. Fetal blood sampling  If the pH >7.25 --- observe.  If the pH 7.2 and 7.25---repeated within 30 minutes.  If the pH <7.2----repeat immediately  If pH still low -- Prompt delivery
  • 50.  Scalp stimulation.  Firm digital pressure  Gentile pinch by atramatic Allis forceps  Fetal pulse oximetry.